CHAPTER
He-W 500 MEDICAL ASSISTANCE
REVISION
NOTE:
Pursuant to RSA 161:4, VI, the
Division of Human Services (Division) in December, 1993 and January, 1994 filed
with the Office of Legislative Services renumbered and reorganized existing
rules under Chapter He-W 500 governing the Division's medical assistance
program. The Director of the Office of
Legislative Services (OLS) reviewed the changes pursuant to RSA 161:4,
VI(b). As certified by the agency, these
changes in numbering and organization of existing rules pursuant to RSA 161:4,
VI(b) were limited to title, chapter, part, section, and subsection changes and
non-substantive changes in the text so as to conform to the renumbering and
reorganization.
The renumbered and reorganized Chapter
He-W 500 supersedes all previous filings for rules in this chapter. However, these certified changes by the
Division do not affect the adoption, effective, or expiration dates of
the text of the rules in Chapter He-W 500.
Pursuant to RSA 161:4, VI(b), the changes in numbering and organization
were effective January 7, 1994 for citation purposes with a notice published in
the New Hampshire Rulemaking Register.
The Division with its certification
filed a conversion index to relate the new rule numbering to the former rule
numbering and section titles, and that index is included below. The index also includes the most recent
document numbers for rule filings under the former numbering, with the
effective and expiration dates, so that the reader can examine the dates
applicable to the respective rules in the renumbered and reorganized Chapter
He-W 500.
New
Part # |
Old
Section # |
Old
Section Title |
Doc.
# |
Eff.
Date |
Exp.
Date |
|
|
|
|
|
|
520 |
501.01 |
General Program Information |
5018 |
11/30/90 |
11/30/96 |
501 |
502.01 |
General Medical Eligibility (Int.
Rule #93-011) |
5749 |
12/1/93 |
3/31/94 |
502 |
502.02 |
Aid to the Needy Blind (ANB)
Program |
5019 |
11/30/90 |
11/30/96 |
502.04 |
502.02(d) |
|
5272 |
11/15/91 |
11/15/97 |
503 |
502.03 |
Aid to the Permanently and
Totally Disabled (Int. Rule #93-011) |
5749 |
12/1/93 |
3/31/94 |
|
502.04 |
(Reserved) |
|
|
|
505 |
502.05 |
Aid to Families with Dependent
Children Program |
5623 |
5/13/93 |
5/13/99 |
|
502.06 |
(Reserved) was: Notice
Requirement - Medicaid (EXPIRED) |
2918 |
11/30/84 |
11/30/90 |
507 |
502.07 |
Medical Assistance for Children
with Severe Disabilities |
4560-A |
1/1/89 |
1/1/95 |
508 |
502.08 |
Medical Assistance for Home Care
of Certain Children with Severe Disabilities |
4681 |
10/4/89 |
10/4/95 |
521 |
503.01 |
General Payment Information |
4488-a |
9/13/88 |
9/13/94 |
521.01 |
503.01(a) |
|
4560-B |
1/1/89 |
1/1/95 |
521.02(c)(1) |
503.01(b)(3)a |
|
4560-B |
1/1/89 |
1/1/95 |
521.02(c)(3) |
503.01(b)(3)c |
|
4560-B |
1/1/89 |
1/1/95 |
521.02(c)(9) |
503.01(b)(3)i |
|
4560-B |
1/1/89 |
1/1/95 |
519 |
503.02 |
Payments to Disproportionate
Share Psychiatric Hospitals |
5194 |
7/26/91 |
7/26/97 |
530 |
504.01 |
Service Limits, Non-Covered
Services and Co-Payments |
4863 |
7/12/90 |
7/12/96 |
530.03(d) |
504.01(c)(4) |
|
5714 |
10/1/93 |
10/1/99 |
533 |
504.02 |
Chiropractic Services |
4817 |
6/1/90 |
6/1/96 |
531 |
504.03 |
Physician Services |
4629 |
6/16/89 |
6/16/95 |
531.03 |
504.03(b) |
|
4694 |
11/9/89 |
11/9/95 |
531.05(h) |
504.03(d)(8) |
|
4694 |
11/9/89 |
11/9/95 |
531.05(m) |
504.03(d)(13) |
|
4779 |
3/1/90 |
3/1/96 |
531.05(s) |
504.03(d)(18) |
|
4630 |
6/16/89 |
6/16/95 |
531.05(s)(1) and (2) |
504.03(d)(18)a. and b. |
|
4694 |
11/9/89 |
11/9/95 |
531.05(s)(4) through (6) |
504.03(d)(18)d. through f. |
Physician Services (cont'd) |
4694 |
11/9/89 |
11/9/95 |
531.06 |
504.03(e) |
|
4694 |
11/9/89 |
11/9/95 |
531.06(b) |
504.03(e)(2) |
|
4779 |
3/1/90 |
3/1/96 |
531.08(f) through (h) |
504.03(g)(5) through (7) |
|
5181 |
7/22/91 |
7/22/97 |
537 |
504.04 |
Rural Health Clinics |
4884 |
8/1/90 |
8/1/96 |
532 |
504.05 |
Podiatrist Services |
4818 |
6/1/90 |
6/1/96 |
542 |
504.06 |
Abortion Services |
4968 |
11/7/90 |
11/7/96 |
536 |
504.07 |
Medical Services Clinic |
4690 |
12/1/89 |
12/1/95 |
535 |
504.08 |
Psychologist Services |
4794 |
3/30/90 |
3/30/96 |
535.05 |
504.08(e) |
|
5182 |
7/22/91 |
7/22/97 |
541 |
504.09 |
Family Planning Services |
4969 |
11/7/90 |
11/7/96 |
546 |
504.10 |
Early and Periodic Screening,
Diagnosis and Treatment Services |
5532 |
12/17/92 |
12/17/98 |
548 |
504.11 |
Extended Services to Pregnant
Women |
5578 |
2/11/93 |
2/11/99 |
|
504.12 |
(Reserved) |
4771 |
3/1/90 |
|
543 |
504.13 |
Hospital Services |
4488-a |
9/13/88 |
9/13/94 |
543.01 |
504.13(a) |
|
4560-B |
1/1/89 |
1/1/95 |
543.04(i) |
504.13(d)(8) |
|
4695 |
11/9/89 |
11/9/95 |
543.07 |
504.13(g) |
|
4560-B |
1/1/89 |
1/1/95 |
543.11(a) |
504.13(k)(1) |
|
4560-B |
1/1/89 |
1/1/95 |
543.11(c) |
504.13(k)(3) |
|
4560-B |
1/1/89 |
1/1/95 |
543.11(i) |
504.13(k)(9) |
|
4560-B |
1/1/89 |
1/1/95 |
|
504.14 |
(Reserved) |
4773 |
3/1/90 |
|
|
504.15 |
(Reserved) |
4774 |
3/1/90 |
|
565 |
504.16 |
Vision Care |
4819 |
6/1/90 |
6/1/96 |
550 |
504.17 |
Adult Medical Day Care |
4482 |
9/1/88 |
9/1/94 |
|
504.18 |
(Reserved) |
4908 |
8/17/90 |
|
540 |
504.19 |
Private Duty Nursing Services |
4691 |
12/1/89 |
12/1/95 |
552 |
504.20 |
Personal Care Attendant Services |
4993 |
11/30/90 |
11/30/96 |
566 |
504.21 |
Dental Services |
5639 |
6/17/93 |
6/17/99 |
576 |
504.22 |
Health Maintenance Organizations |
4907 |
9/1/90 |
9/1/96 |
576.06 |
504.22(f) |
|
5165 |
6/17/91 |
6/17/97 |
576.07 |
504.22(g) |
|
5165 |
6/17/91 |
6/17/97 |
576.08 |
504.22(h) |
|
5165 |
6/17/91 |
6/17/97 |
576.09 |
504.22(i) |
|
5165 |
6/17/91 |
6/17/97 |
553 |
504.23 |
Home Health Services |
5342 |
3/3/92 |
3/3/98 |
522 |
504.24 |
Interpreter Services |
5735 |
11/12/93 |
11/12/99 |
568 |
504.25 |
Therapy Services |
4995 |
11/30/90 |
11/30/96 |
569 |
504.26 |
Laboratory and Radiological
Services |
4886 |
8/1/90 |
8/1/96 |
569.08(f) through (h) |
504.26(g)(5) through (7) |
|
5183 |
7/22/91 |
7/22/97 |
|
504.27 |
(Reserved) |
4887 |
8/1/90 |
|
570 |
504.28 |
Pharmaceutical Services |
5742 |
12/1/93 |
12/1/99 |
567 |
504.29 |
Hearing Aid Services |
4778 |
3/1/90 |
3/1/96 |
567.05(a)(4) |
504.29(e)(4) |
|
4888 |
8/1/90 |
8/1/96 |
571 |
504.30 |
Durable Medical Equipment,
Prosthetic Devices and Medical Supplies |
4712 |
1/1/90 |
1/1/96 |
572 |
504.31 |
Ambulance Services |
5022 |
11/30/90 |
11/30/96 |
573 |
504.32 |
Wheelchair Van Services |
5023 |
11/30/90 |
11/30/96 |
574 |
504.33 |
General Medical Transportation |
4696 |
1/1/90 |
1/1/96 |
556 |
504.34 |
Supported Residential Care
Services |
5676 |
8/1/93 |
8/1/99 |
534 |
504.35 |
Advanced Registered Nurse Practitioner
Services |
4793 |
3/30/90 |
3/30/96 |
558 |
504.36 |
Home and Community-Based Care for
the Elderly and Chronically Ill |
4482 |
9/1/88 |
9/1/94 |
558.05(h), except (h) (1)a. and
b. |
504.36(e)(8), except (e)(8) a. 1.
and 2. |
|
4776 |
3/1/90 |
3/1/96 |
|
504.37 |
(Reserved) was: Preadmission
Screening Program (EXPIRED) |
4062 |
5/29/86 |
5/29/92 |
559 |
504.38 |
Case Management Services |
4482 |
9/1/88 |
9/1/94 |
590 |
505.01 |
Nursing Facility Services |
4908 |
8/17/90 |
8/17/96 |
590.01 |
505.01(a) |
|
5085 |
3/5/91 |
3/5/97 |
590.16 |
505.01(m) |
|
5085 |
3/5/91 |
3/5/97 |
590.02(d)(3) |
505.01(b)(1) d. 3. |
|
5164 |
6/12/91 |
6/12/97 |
593 |
505.02 |
Nursing Facility Reimbursement |
5058 |
1/31/91 |
1/31/97 |
593.09(g) |
505.02(b)(7) a. 7. |
|
5268 |
11/1/91 |
11/1/97 |
593.22 |
505.02(b)(7) j. 5. |
|
5268 |
11/1/91 |
11/1/97 |
593.27 |
505.02(b)(7)o. |
Nursing Facility Reimbursement
(cont'd) |
5268 |
11/1/91 |
11/1/97 |
593.28 |
505.02(b)(7)p. |
|
5268 |
11/1/91 |
11/1/97 |
593.37 |
505.02(b)(9)b. |
|
5531 |
12/16/92 |
12/16/98 |
593.38 |
505.02(b)(9)c. |
|
5531 |
12/16/92 |
12/16/98 |
593.39 |
505.02(b)(9) d. and e. |
|
5531 |
12/16/92 |
12/16/98 |
591 |
505.03 |
Nursing Home Enforcement Remedies |
4741 |
1/23/90 |
1/23/96 |
592 |
505.04 |
Nursing Assistant Training
Reimbursement |
5618 |
4/28/93 |
4/28/99 |
PART
He-W 501 GENERAL MEDICAL ELIGIBILITY -
EXPIRED
He-W
501.01 Definitions.
Source. (See Revision Note at chapter heading He-W
500); ss by #5806, eff 3-30-94; amd by #5941, eff
12-22-94, all EXPIRED: 3-30-00, except paragraph (c) EXPIRED: 12-22-02
He-W
501.02
Source. (See Revision Note at chapter heading He-W
500); ss by #5806, eff 3-30-94, EXPIRED: 3-30-00
He-W
501.03
Source. (See Revision Note at chapter heading He-W
500); ss by #5806, eff 3-30-94; amd by #5941, eff
12-22-94, all EXPIRED: 3-30-00, except paragraph (a)(3) EXPIRED: 12-22-02
He-W
501.04 - 501.12
Source. (See Revision Note at chapter heading He-W
500); ss by #5806, eff 3-30-94, EXPIRED: 3-30-00
PART
He-W 502 AID TO THE NEEDY BLIND PROGRAM
He-W
502.01 Definitions.
(a) “Aid to the Needy Blind (ANB)” means a
category of assistance for which eligibility is determined by the New Hampshire
department of health and human services, in accordance with RSA 167:6, IV.
(b) “Blindness” means “blindness” as defined in
Sections 216(i)(1) and 1614(a)(2) of the Social
Security Act, 42 USC 416 and 42 USC 1382c.
(c) “Department” means the New Hampshire
department of health and human services.
(d) “Medicaid” means the Title XIX and Title XXI
programs administered by the department, which makes medical assistance
available to eligible individuals.
(e) “Recipient” means any individual who is
eligible for and receiving medical assistance under the medicaid
program.
(f) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(g) “Title XXI” means the joint federal-state
program described in Title XXI of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
Source. (See Revision Note at chapter heading He-W
500); ss by #6112, eff 11-4-95; ss by #7132, eff 11-23-99; ss by #9011, eff
10-25-07; amd by #10139, eff 7-1-12; ss by #11027,
eff 1-26-16
He-W
502.02 Recipient Eligibility. ANB shall be available to recipients who:
(a) Meet the financial, categorical, technical,
and other eligibility requirements, pursuant to He-W 600 and He-W 800, as
applicable; and
(b) Meet the definition of blindness in He-W
502.01(b).
Source. (See Revision Note at chapter heading He-W
500); amd by #5272, eff 11-15-91; ss by #6112, eff
11-4-95; ss by #7132, eff 11-23-99; ss by #9011, eff 10-25-07; ss by #11027,
eff 1-26-16
He-W 502.03 Blindness Evaluation.
(a)
The recipient’s optometrist or ophthalmologist shall complete, sign, and
date Form 901 “Report of Eye Examination” (April 2015) and submit the form to
the department.
(b)
The department shall review the information provided on Form 901 in (a)
above, to determine if the criteria in He-W 502.02 have been met.
Source. (See Revision Note at chapter heading He-W
500); ss by #6112, eff 11-4-95; ss by #7132, eff 11-23-99; ss by #9011, eff
10-25-07; ss by #11027, eff 1-26-16
PART
He-W 503 AID TO THE PERMANENTLY AND TOTALLY
DISABLED (APTD) PROGRAM - EXPIRED AND RESERVED
Source. (See Revision Note at chapter heading He-W
500); ss by #5806, eff 3-30-94, EXPIRED: 3-30-00
PART
He-W 504 MEDICAID FOR EMPLOYED ADULTS
WITH DISABILITIES
He-W 504.01 Definition.
(a)
“Medicaid for employed adults with disabilities (MEAD)” means a category
of eligibility that allows certain individuals who are working to either retain
or obtain medicaid eligibility.
Source. #7644, eff
2-8-02; ss by #8292, eff 2-24-05; ss by #10321, eff 4-25-13
He-W
504.02 Medical Eligibility. To be medically eligible for MEAD:
(a) An individual who is currently a medicaid
recipient shall:
(1) Have been determined eligible
for aid to the permanently and totally disabled (APTD) according to RSA 167:6,
VI, or aid to the needy blind (ANB) according to RSA 167:6, IV, within the 12
months prior to application for MEAD; and
(2) Not have been terminated from
APTD or ANB due to medical improvement during the previous 12 months; or
(b)
An individual who is not currently an APTD or ANB recipient shall:
(1) Be employed, or self-employed,
for pay, pursuant to the provisions of He-W 641.03(b)-(c), on the date of
application and during the time eligibility for MEAD is being determined;
(2) Have a medical impairment that
meets the Social Security Administration’s Listing of Impairments in accordance
with 20 CFR 404, Subpart P, Appendix I; and
(3) Have a medical impairment that
has persisted or is expected to persist for a minimum of 48 consecutive months.
Source. #7644, eff 2-8-02; ss by #8292, eff 2-24-05;
ss by #10321, eff 4-25-13
PART
He-W 505 - RESERVED
He-W
505.01-505.04 - REPEALED
Source. (See Revision Note at chapter heading He-W 500);
ss by #5623, eff 5-13-93, EXPIRED: 5-13-99
New. #7134, eff 11-23-99; rpld
by #8973, eff 9-11-07
PART
He-W 506 MEDICAID CARE MANAGEMENT (MCM)
He-W 506.01 Purpose. The purpose of this part is to prescribe the
requirements of the New Hampshire medicaid care
management program as they pertain to medicaid
recipients, including individuals determined eligible for medicaid coverage through the granite advantage health care
program (granite advantage) in accordance with RSA 126-AA:2.
Source. #10410, eff 9-13-13; ss by #10631, eff 7-1-14;
ss by #13474, eff 10-24-22
He-W 506.02 Scope.
This part shall apply to all medicaid
recipients insofar as they are required to enroll in managed care. Those recipients who are not enrolled in
managed care shall receive medicaid services on a
fee-for-service basis in accordance with applicable rules in He-W 500.
Source. #10410, eff 9-13-13; ss by #10965, eff
11-1-15; ss by #13474, eff 10-24-22
He-W 506.03 Definitions.
(a)
“Action” means a managed care organization (MCO) activity including, but
not limited to, the following activities identified in the definition of
“adverse benefit determination” in 42 CFR 438.400(b):
(1) The denial or limited authorization of a
requested service, including the type or level of service, including
determinations based on the type or level of service, requirements for medical
necessity, appropriateness, setting, or effectiveness of a covered benefit;
(2) The reduction, suspension, or termination of
a previously authorized service;
(3) The denial, in whole or in part, of payment
for a service except when denial for payment for a service is solely because
the claim does not meet the definition of a “clean claim”;
(4) The failure to provide services in a timely
manner, as described in the contracts between the department and the MCO;
(5) The failure of an MCO to act within the
timeframes required for a service authorization, disposition of a grievance,
standard resolution of an appeal, or expedited resolution of an appeal, as
described in the contracts between the department and the MCO; or
(6) The denial of a member’s request to dispute a
financial liability, including cost sharing, copayments, premiums, deductibles,
coinsurance, or other enrollee financial liabilities.
(b) “Alternative Benefit Plan
(ABP) services” means the Secretary-approved coverage described in section 1937
of the Social Security Act and which aligns with and includes the traditional medicaid state plan services.
(c)
“Appeal” means a request to the MCO for the review of any action taken
by the MCO.
(d)
“Clean claim” means a claim that does not have any defect, impropriety,
lack of any required substantiating documentation, or particular circumstance
requiring special treatment that prevents timely payment.
(e)
“Department” means the New Hampshire department of health and human
services.
(f)
“Fair hearing” means an administrative appeal under He-C 200.
(g)
“Fee-for-service” means the reimbursement method used by the department:
(1) For all services to recipients who are not
enrolled in managed care; and
(2) For those services excluded from managed care
for all recipients.
(h)
“Granite Advantage Health Care Program (Granite Advantage)” means the
granite advantage health care program established under RSA 126-AA, which
authorizes medical assistance for individuals described in 42 U.S.C
§1396a(a)(10)(A)(i)(VIII).
(i) “Grievance” means an expression of
dissatisfaction about any matter other than an action that is communicated to
the MCO, such as with regard to the quality of care or services provided, and
aspects of interpersonal interactions with the MCO employees.
(j)
“Managed care organization (MCO)” means an entity that has a
comprehensive risk-based contract with the department to provide managed medicaid health care services.
(k)
“MCO grievance system” means the system through which members can
complain, express dissatisfaction, or challenge an action made by the MCO,
including:
(1) An MCO grievance process;
(2) An MCO appeal process; and
(3) Access to the department’s fair hearing
process after (k)(2) above has been exhausted.
(l)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(m)
“Member” means a recipient who has selected or who has been passively
enrolled into an MCO.
(n)
“Recipient” means any individual who is eligible for and is receiving
medical assistance under the New Hampshire medicaid
program.
(o)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(p)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. #10410, eff 9-13-13; amd
by #10631, eff 7-1-14; amd by #10965, eff 11-1-15; ss
by #12537, eff 5-24-18; ss by #13474, eff 10-24-22
He-W 506.04 Covered Services.
(a)
Covered services provided through an MCO shall include:
(1) All covered state plan and ABP services
except the following:
a. Dental services provided in the dental
setting;
b. Intermediate care facility for individuals
with intellectual disabilities;
c. Medicaid to schools program;
d. Skilled nursing facility;
e. Skilled nursing facility atypical care;
f. Inpatient hospital swing beds, intermediate
care facility;
g. Inpatient hospital swing beds, skilled
nursing facility;
h. Intermediate care facility nursing home;
i.
Intermediate care facility atypical care;
j. Glencliff Home;
k. Early supports and services;
l. The following drugs when billed by a
pharmacy:
1. Drugs used for the treatment of hemophilia;
2. Carbaglu; and
3. Raviciti;
m. Zolgensma®,
a gene therapy for spinal muscular atrophy ; and
n.
The following services which are only
offered to children involved with the division for children, youth and
families:
1. Home based therapy;
2.
Child health support service;
3. Placement services;
4. Intensive home and community services;
5. Private non-medical institutional care for
children; and
6. Crisis intervention; and
o. Section 1915(i) of
the Social Security Act, state plan home and community based services for high
risk children with severe emotional disturbances.
(b)
The services excluded in (a)(1) above shall be covered by medicaid on a fee-for-service basis except dental services
which are covered as described in He-W 566.
(c)
Covered services shall be provided by the MCO starting the same business
day as a member’s selection of or passive enrollment in an MCO.
(d)
Covered state plan and ABP services provided through an MCO shall be
furnished in an amount, duration, and scope that is no less than the amount,
duration, and scope for the same services furnished to recipients under
fee-for-service.
Source.
#10410, eff 9-13-13; ss by #10631, eff 7-1-14; amd by #11107, eff 7-1-16; amd by
#12016, eff 10-25-16; ss by #13474, eff 10-24-22
He-W 506.05 Enrollment in Managed Care.
(a)
All medicaid
recipients shall be enrolled in managed care unless the recipient is excluded
from managed care as described in (b) below.
(b)
The following individuals shall not be allowed to enroll in managed
care:
(1) Recipients receiving certain financial
benefits from the U.S. Department of Veterans Affairs;
(2) Recipients receiving in and out medically
needy assistance in accordance with 42 CFR 435.301 and He-W 878.01;
(3)
Recipients who are eligible under the qualified medicare
beneficiary (QMB), specified low-income medicare
beneficiary (SLMB), or qualified disabled working individual (QDWI) benefits
only, and are not eligible for full medicaid
coverage;
(4)
Recipients who are eligible under the family planning expansion category (FPEC)
in accordance with 1902(a)(10)(A)(ii) of the Social Security Act, 42 U.S.C.
1396a(a)(10)(A)(ii) and He-W 509;
(5)
Individuals during a presumptive eligibility period; and
(6)
Individuals in a retroactive eligibility period.
(c) Any recipient not enrolled in managed care shall receive medicaid services on a fee-for-service basis.
Source. #10410, eff 9-13-13; ss by #10631, eff 7-1-14;
ss by #10965, eff 11-1-15; ss by #13474, eff 10-24-22
He-W 506.06 Selection of a Managed Care Organization.
(a)
Recipients shall be passively enrolled in an MCO if they do not select a
plan at application.
(b)
Recipients shall select an MCO at application by:
(1) Utilizing the on-line NH
Electronic Application System (NH EASY);
(2)
A personal interview, as required in
He-W 636.01 and He-W 644.01;
(3)
A telephone application pursuant to He-W
802.03; or
(4)
Calling the medicaid
service center.
(c)
The department shall send a notice to all recipients not excluded from
managed care per He-W 506.05(b) specifying which MCO the recipient has been
enrolled into.
(d)
Passive enrollment shall be based on the following criteria:
(1) MCO participation of a primary care provider
with whom the recipient has a pre-existing relationship as demonstrated by past
claims history;
(2) MCO participation of a specialty care
provider with whom the enrollee has a pre-existing relationship as demonstrated
by past claims history;
(3) Family affiliation to an MCO;
(4) Previous enrollment with an MCO prior to a
loss of medicaid eligibility;
(5) Provider-member relationship, to the extent
obtainable; or
(6) If enrollment cannot be made utilizing
(1)-(5) above, enrollment shall be based on the terms of the contract agreed to
by the department and the MCO.
(e)
A member may request to change his or her MCO selection without cause,
by making a written or oral request to the department at any of the following
times:
(1) Once during the 90 days following the date of
the member’s initial medicaid eligibility;
(2) During the first 12 months of enrollment, if
the member has an established relationship with a primary care provider that is
only in-network of a non-assigned MCO;
(3)
During annual open enrollment periods and enrollments related to
renegotiation and re-procurement; and
(4) When the department imposes an intermediate
sanction specified in 42 CFR 438.702(a)(3).
(f)
A member may request to change his or her MCO with cause after seeking redress through
the MCO’s grievance system, by making a written or oral request to the
department at any time for any of the following reasons:
(1) The member requires related services
simultaneously that are not available in the MCO’s network and bifurcation of
the care creates unnecessary risk to the member as determined by the member’s
treating provider;
(2) Due to moral or religious
objections of the MCO, the MCO does not provide the covered service the member
needs;
(3) Poor quality of care;
(4) Lack of access to covered services;
(5) The member has experienced a violation of his
or her member rights, as established in 42 CFR 438.100; or
(6) The MCO’s network providers are not
experienced in the member’s unique healthcare needs.
(g)
If a request made pursuant to (e) or (f) above does not include the
selection of a different MCO, the department shall not act on the request
unless there are only 2 MCOs.
(h)
A member may request a department fair hearing of a denial of (e) or (f)
above in accordance with He-C 200 without first exhausting the MCO appeal
process.
(i) A member shall be locked into an MCO for a
period of 12 months or until the next open enrollment period, whichever comes
first, unless the member changes his or her MCO selection in accordance with
(e)(1)-(3) or (f) above.
(j)
A member shall disenroll from an MCO when the member has moved out of
state and is no longer NH medicaid eligible or
becomes exempt as described in He-W 506.05(b).
(k)
An MCO may request the department to disenroll a member who is
threatening or abusive such that the health or safety of other members, MCO
staff, or providers is jeopardized.
(l)
The department shall approve a request for disenrollment in (j) above
when no other option is available that would ensure the health and safety of
other members, MCO staff, or providers.
(m)
If the department approves an MCO request for involuntary disenrollment,
the member may request a department fair hearing of the disenrollment in
accordance with He-C 200 without first exhausting the MCO appeal process.
(n)
Members appealing involuntary disenrollment may request a continuation
of services pending appeal as outlined in 42 CFR 431.230.
Source. #10410, eff 9-13-13; ss by #10965, eff
11-1-15; ss by #13474, eff 10-24-22
He-W 506.07 MCO
Grievance Process.
(a) A member who is dissatisfied with any matter other than an
action, as defined in He-W 506.03(a), shall utilize the MCO grievance process
exclusively.
(b) The MCO grievance process shall address members’ expression
of dissatisfaction about any matter other than an action including, but not
limited to:
(1) The quality of care or services provided;
(2) Aspects of interpersonal interactions with providers or MCO employees; or
(3) Failure to respect the member’s rights.
(c) Actions, as defined in He-W 506.03(a), shall be subject to
the MCO appeal process but not subject to the MCO grievance process.
(d) A
member, or the member’s authorized
representative, appointed in accordance with He-W 803.01, shall file a
grievance with the MCO either orally or in
writing.
(e) Members shall be notified of the disposition of grievances
as follows:
(1) Either orally or in writing for grievances not
involving clinical issues; and
(2) In writing for grievances involving clinical issues.
(f) Members
shall not have the right to a department fair hearing in regard to the
disposition of a grievance.
(g) The
MCO grievance process shall not preclude a member’s ability to pursue client
rights protection under He-M 204.
Source. #10410, eff 9-13-13; ss by #13474, eff
10-24-22
He-W 506.08 MCO
Appeal Process.
(a) The
MCO appeal process shall address members’ requests for the appeal of any
adverse benefit determination or action taken by the MCO.
(b) A
member who wants to appeal an action taken by the MCO shall utilize the MCO
appeal process.
(c) A
member, the member’s authorized representative, the member’s legal guardian
appointed in accordance with He-W 803.01, or the member’s provider acting on
behalf of the member and with the member’s written consent may file an appeal
with the MCO. However, a provider acting as an authorized
representative shall not request continuation of benefits pending the appeal
even with written consent.
(d) All
requests for appeals shall be made within 60 calendar days of the date on the
MCO’s notice of action.
(e) All
requests for appeals shall be made either orally or in writing. An oral request
for an appeal shall be followed by a written request, unless the request is for
expedited resolution as described in (g) below.
(f) The
MCO shall resolve standard appeals within 30 calendar days from the day the MCO
receives the appeal.
(g) A
person in (c) above may request an expedited resolution of an appeal when
taking the time needed for a standard resolution could seriously jeopardize the
member’s life, physical or mental health, or ability to attain, maintain, or
regain maximum function.
(h) The
MCO shall resolve an expedited appeal within 72 hours of receiving the appeal.
(i) The MCO may extend the timeframes to resolve
standard and expedited appeals up to 14 calendar days if:
(1) The member requests the extension; or
(2) The MCO demonstrates that there is a need for additional
information in order to resolve the appeal and the extension is in the member’s
interest.
(j) If
the MCO extends the timeframes not at the request of the member in accordance
with (i)(2) above, then the MCO shall:
(1) Make reasonable efforts to give the
member prompt oral notice of the delay by providing a minimum of 3 oral attempts to contact
the member at various times of the day, on different days within 2 calendar
days of the MCO’s decision to extend the timeframe;
(2) Within 2 calendar days of the MCO’s
decision to extend, give the member written notice of the reason for the decision to extend
the timeframe and inform the member of the right to file a grievance if he or
she disagrees with that decision; and
(3) Resolve the appeal as expeditiously as the member’s health
condition requires and no later than the date the extension expires.
(k) A
member’s benefits shall be continued during an appeal if:
(1) The member requests a continuation of benefits on or before the
later of the following:
a. Within 10 calendar days of the date the MCO mails the
notice of action; or
b. The intended effective date of the MCO’s proposed action;
(2) The appeal involves the termination, suspension, or
reduction of previously authorized services;
(3) The services were ordered by an authorized provider;
and
(4) The period covered by the original authorization has
not expired.
(l) If
the MCO’s action is upheld in a hearing, the MCO may institute recovery
procedures against the member to recoup the cost of any continued benefits
furnished to the member.
(m) The
MCO grievance process shall not preclude a member’s ability to pursue client
rights protection under He-M 204.
Source. #10410, eff 9-13-13; ss by #12537, eff
5-24-18; ss by #13474, eff 10-24-22
He-W 506.09 Department
Fair Hearing Process.
(a) A
member shall exhaust the MCO appeal process prior to filing a request for a
fair hearing with the department, subject to the following:
(1) Grievances shall not be the subject of a department
fair hearing; and
(2) The MCO shall have resolved an appeal under He-W 506.08
and provided notice of that resolution prior to the member requesting a fair
hearing with the department, except that a member shall be deemed to have
exhausted the MCO’s appeal process if the MCO fails to adhere to the notice and
timing for expedited and standard appeals as described in He-W 506.08(f), (h),
and (j).
(b) If
the member does not agree with the MCO’s resolution of an appeal, the member
may file a request, in accordance with He-C 200, for a department fair hearing.
(c) Requests
for a department fair hearing shall be made in writing within 120 calendar days
of the date of the MCO’s notice of the resolution of the appeal.
(d) A
member in (b) above may request an expedited resolution of a department fair
hearing if the department determines that the time otherwise permitted for a
hearing could seriously jeopardize the member’s life, physical or mental
health, or ability to attain, maintain, or regain maximum function, and:
(1) The MCO adversely resolved the member’s appeal, wholly or
partially; or
(2) The MCO failed to resolve the appeal
within 72 hours and failed to extend the 72-hour deadline in accordance with 42
CFR 438.408(c) and He-W 506.08(i).
(e) The
department shall notify the member as expeditiously as possible as to whether
the request for an expedited department fair hearing is granted or
denied. If oral notice is provided, the department shall follow up
with written notice, which might be made through electronic means.
(f) If
the department denies the member’s request for an expedited department fair
hearing, the department shall schedule a department fair hearing within 90 days
from the date the member filed an MCO appeal not including the number of days
the member took to subsequently file for a department fair hearing.
(g) If
the department grants the member’s request for an expedited department fair
hearing, then the department shall resolve the appeal within 3 business days
after the department receives from the MCO the case file and any other
necessary information. The MCO shall have no more than 3 days from
the date the department notifies the MCO that it has granted the member’s
expedited appeal, to provide the case file to the department.
(h) A
member’s benefits shall be continued during a department fair hearing if:
(1) The member received benefits pending the MCO appeal; and
(2) The member requests a department fair hearing and continuation of
benefits within 10 calendar days of the date the MCO sends the notice of
adverse decision of an MCO appeal to the member.
(i) If the member did not receive benefits
pending the MCO appeal, then a member’s benefits shall be continued during a
department fair hearing if:
(1) The member requests a department fair hearing within 10 calendar days of the date the MCO mails the notice of decision
adverse to the member;
(2) The member requests continuation of benefits pending the
department fair hearing;
(3) The department fair hearing involves the
termination, suspension, or reduction of a previously authorized service;
(4) The service was ordered by an authorized provider; and
(5) The original authorization period for the service has not
expired.
(j) Only
the member, the member’s authorized representative, or the member’s legal
guardian may request benefits pending a department fair hearing of a MCO
decision.
(k) Providers
acting as an authorized representative shall not request continuation of
benefits pending the appeal even with written consent.
(l) If
the MCO’s adverse decision is upheld in a department fair hearing, the MCO may
institute recovery procedures against the member to recoup the cost of any
continued benefits furnished to the member.
Source. #10410, eff 9-13-13; ss by #12537, eff
5-24-18; ss by #13474, eff 10-24-22
PART
He-W 507 MEDICAL ASSISTANCE FOR CHILDREN
WITH SEVERE DISABILITIES
He-W 507.01 Definitions.
(a)
“Department” means the New Hampshire department of health and human
services.
(b)
“Medical review team (MRT)” means a team of medical professionals,
comprised of physicians and registered nurses with expertise in the care of
children with special health care needs, developmental disabilities and
behavioral issues, who determine medical eligibility for healthy kids-gold
medical assistance in accordance with the criteria set forth in He-W 507 and
He-W 508.
(c)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(d)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(e)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(f)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #5941, eff 12-22-94, EXPIRED: 12-22-02
New. #7867, eff 4-10-03; ss by #9866, eff 2-11-11;
amd by #10139, eff 7-1-12
He-W 507.02 Recipient Eligibility. Title XIX services shall be available to
children with disabilities who:
(a)
Are under the age of 19;
(b)
Meet the requirements of He-W 641.04;
(c)
Are chronically ill or impaired, whose illness or disability does not
require the level of care provided in an inpatient facility, but whose
condition requires ongoing and regular medical monitoring and treatment; and
(d)
Have a severe disability which includes at least one of the following:
(1) A developmental disability as defined in RSA
171-A:2,V;
(2) A chronic, degenerative, progressive, or
life-threatening condition causing impairment of a vital organ function which
requires ongoing and regular medical monitoring;
(3) A sensory impairment which is expected to
continue indefinitely, including a hearing loss established by audiometry which
functionally impacts the child;
(4) A mental illness, emotional disturbance or
behavioral disorder which functionally impacts his or her psychosocial
adjustment and the diagnosis for which is recognized by the American
Psychiatric Association;
(5) An acquired childhood disease which
functionally impacts the child; or
(6) A genetic disorder or congenital anomaly
requiring ongoing medical monitoring.
Source. (See Revision Note at chapter heading He-W
500); ss by #5941, eff 12-22-94, EXPIRED: 12-22-02
New. #7867, eff 4-10-03; ss by #9866, eff 2-11-11
He-W 507.03 Continued Eligibility.
(a)
The MRT shall conduct periodic redeterminations of medical eligibility
for Title XIX benefits based on current evidence of the child’s disability.
(b)
At the time of redetermination, the MRT shall first determine whether
the recipient meets the eligibility criteria in accordance with He-W 507.02.
(c)
The department shall issue a written notice to the recipient when a
medical eligibility determination is made.
(d)
If an adverse eligibility determination is made, the written notice to
the recipient shall include the following information:
(1) The recipient’s identifying information;
(2)
A listing of the medical and non-medical reports considered during the
disability determination process;
(3) A statement of the department’s action;
(4) The reasons for the department’s action;
(5) Citations from federal and state statutes and
regulations supporting the department’s actions; and
(6) An explanation of the individual’s rights to
appeal the department’s disability determination and to reapply for medical
assistance.
(e)
The department shall continue the recipient’s medical eligibility after
an adverse medical eligibility determination is made when the recipient:
(1) Submits a hearing request to the local
district office within 30 days from the date on the written notice of adverse
decision; and
(2) Submits a request to the local district
office for a continuation of benefits during the appeal process within 10 days
of the date on the written notice of adverse decision.
Source. (See Revision Note at chapter heading He-W
500); ss by #5941, eff 12-22-94, EXPIRED: 12-22-02
New. #7867, eff 4-10-03; ss by #9866, eff 2-11-11
He-W 507.04 Termination of Medical Eligibility. The department shall terminate medical
eligibility after an adverse medical eligibility determination is made when:
(a)
The MRT determines that the recipient no longer meets the eligibility
criteria specified in He-W 507.02; and
(b)
The recipient fails to submit a continuation of benefits request to the
local district office within 10 days from the date of written notice of adverse
decision.
Source. #7867, eff 4-10-03; ss by #9866, eff 2-11-11
He-W 507.05 Appeals.
(a) Individuals may appeal an adverse disability
determination, pursuant to RSA 541-A:31, III and He-C 200.
(b)
Individuals must submit the written request for a hearing to the local
district office pursuant to RSA 541-A:31, III and He-C 200 within 30 days from
the date of the notice of decision.
Source. #7867, eff 4-10-03; ss by #9866, eff 2-11-11
PART
He-W 508 MEDICAL ASSISTANCE FOR HOME
CARE OF CERTAIN CHILDREN WITH SEVERE DISABILITIES
He-W 508.01 Purpose. The purpose of family centered
community-based home care shall be to support, but not supplant, the
recipient’s family as the primary caregiver.
Source. (See Revision Note at chapter heading He-W
500); ss by #5941, eff 12-22-94, EXPIRED: 12-22-02
New. #8196, INTERIM, eff 10-29-04, EXIRED: 7-1-05
New. #9291, eff 7-1-09
He-W 508.02 Definitions.
(a)
“Degree of care” means the level of intensity or extent of medical care,
treatment, or intervention required by the child as determined by the medical
setting in which the child is being evaluated.
(b)
“Department” means the New Hampshire department of health and human
services.
(c)
“Family centered community-based home care” means an organized network
of integrated and coordinated services delivered at the local level which
promotes normal patterns of living and which recognizes the pivotal role of
families with respect to the provision of services for their children.
(d)
“Joint medical review team (MRT)” means a team of medical professionals,
comprised of physicians and registered nurses with expertise in the care of
children with special health care needs, developmental disabilities, and
behavioral issues, that determines if home care services are medically
appropriate in accordance with RSA 167:3-f, VI, and the most appropriate level
of care under which to evaluate the child in accordance with RSA 167:3-g,
III–VI.
(e)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(f)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(g) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(h) “Title XXI”
means the joint federal-state program described in Title XXI of the Social
Security Act and administered in New Hampshire by the department under the medicaid program.
Source.
(See Revision Note at chapter heading He-W 500); ss by #5941, eff
12-22-94; amd by #6198, eff 2-28-96, all EXPIRED:
12-22-02 except (b)(3) EXPIRED: 2-28-04
New.
#8196, INTERIM, eff 10-29-04, EXIRED: 7-1-05
New.
#9291, eff 7-1-09 (from He-W 508.01); amd by
#10139, eff 7-1-12
He-W 508.03 Recipient Eligibility.
(a)
In accordance with RSA 167:3-e, III, and RSA 167:3-f, III (a)–(f),
recipients shall be eligible for medical assistance for home care of children
with severe disabilities (HC-CSD), if the recipient:
(1) Resides in a place maintained as the
recipient’s home community;
(2) Is able to receive services in the home as
defined in 45 CFR 233.90(c)(1)(v)(B);
(3) Meets the program criteria described in
Section 1902(e)(3) of the Social Security Act;
(4) Meets the criteria described in He-W 641.04,
except that, pursuant to the prohibition in Section 1614(f)(2)(B) of the Social
Security Act, the criteria described in He-W 641.04(b)-(e) on the deeming of
parental income shall not apply;
(5) Has an impairment, or combination of
impairments, that meets, medically equals, or functionally equals the criteria
for an impairment as described in 20 CFR, Part 404, Subpart P, App. 1;
(6) Meets the medical criteria pursuant to RSA
167:3-f, III(e); and
(7) Requires the same degree of care that is
typically provided in a hospital, psychiatric hospital, nursing facility, or
intermediate care facility for the mentally retarded (ICF-MR), in accordance
with He-W 508.04.
(b) In addition to (a) above, recipients shall be
eligible only if the services proposed for the recipient are:
(1) Medically appropriate in accordance with He-W
508.05; and
(2) Cost effective in accordance with He-W
508.06.
Source. (See Revision Note at chapter heading He-W
500); ss by #5941, eff 12-22-94, EXPIRED: 12-22-02
New. #8196, INTERIM, eff 10-29-04, EXIRED 7-1-05
New. #9291, eff 7-1-09 (from He-W 508.02)
He-W 508.04 Degree of Care. The most appropriate degree of care under
which to evaluate the recipient’s eligibility per He-W
508.03(a)(7) above shall be determined as follows:
(a)
The MRT shall review, in accordance with RSA 167:3-g, II, the
recipient’s medical condition and community care needs; and
(b)
Based upon the review in (a) above, the MRT shall:
(1) Determine that the degree of care provided by
a hospital is appropriate for the recipient, if all of the criteria in RSA
167:3-g, III, are met;
(2) Determine that the degree of care provided by
a psychiatric hospital is appropriate for the recipient, if all of the criteria
in RSA 167:3-g, IV, are met;
(3) Determine that the degree of care provided by
a nursing facility is appropriate for the recipient, if any one of the criteria
in RSA 167:3-g, V, is met; or
(4) Determine that the degree of care provided by
an ICF-MR is appropriate for the recipient, if all of the criteria in RSA
167:3-g, VI, are met.
Source. #9291, eff 7-1-09 (from He-W 508.03)
He-W 508.05 Medically Appropriate
Services.
(a)
The medical services proposed for a recipient shall be medically
appropriate if the MRT, upon certification by the recipient’s physician,
determines in accordance with (b) below, that it is medically appropriate for
the recipient to receive family centered, community-based home care as opposed
to institutional care.
(b)
In accordance with RSA 167:3-f, VI, family centered, community-based
home care shall be medically appropriate if each of the following conditions is
met:
(1) The care can be provided in
the home without jeopardizing the medical needs of the recipient;
(2) Medical and psychological support services
are available in the community;
(3) The recipient’s treating physician recommends
home care and certifies the safety of home placement in accordance with (c)
below;
(4) The recipient’s family or guardian has
expressed a willingness and desire to assume responsibility as the primary
caregiver for the recipient in order to maintain the recipient at home; and
(5) The family and household members have been
trained to support the recipient’s needs in the home and have the ability to be
primary caregivers.
(c)
The treating physician’s recommendation of home care and certification
of the safety of home placement shall be submitted in writing by mail,
electronic mail, or facsimile to the department or via direct telephone
conversation with the MRT.
(d)
The written certification in (c) above, or MRT documentation of direct
telephone conversation with the treating physician as per (c) above, shall be
maintained in the recipient’s case file at the department.
Source. #9291, eff 7-1-09
He-W 508.06 Monitoring and
Determination of Cost Effectiveness.
(a)
In accordance with RSA 167:3-e, IV, the medical services proposed for a
recipient shall be cost effective if the estimated cost of care outside an
institution is no higher than the estimated medicaid
cost of appropriate institutional care.
(b)
For each recipient, cost effectiveness shall be monitored monthly and
determined annually by the department as follows:
(1) The department shall obtain Title XIX payment
data on the costs paid by Title XIX for the recipient’s home care from the
department’s cost reports generated for each recipient from the Medicaid
Management Information System (MMIS);
(2) For each recipient, the items or services
included in the home care cost data in (1) above shall include only those items
or services listed in (c) below;
(3) The items or services included in (d) below
shall not be included in home care cost data for (1) above, or in institutional
cost of care data in (c) below;
(4) The department shall utilize, as
institutional cost of care data, the most recently published inpatient per diem
Title XIX rates for hospitals, psychiatric hospitals, nursing facilities, or
ICF-MR;
(5) The department shall determine the per diem
rate to use as the recipient’s institutional cost of care by selecting the rate
for the facility in (4) above that most closely corresponds to the degree of
care determined and utilized for the recipient’s eligibility determination
pursuant to He-W 508.04; and
(6) The department shall compare the costs of the
recipient’s home care to the recipient’s institutional cost of care, as
determined in He-W 508.06(b)(1)–(b)(5).
(c) The
costs associated with the following categories of service, which are included
in an institution’s per diem
rate, shall be the only costs utilized in determining the costs incurred for
the recipient’s home care in accordance with He-W 508.06(b)(1) and (2) above:
(1) Mental health services,
including psychotherapy and community mental health center services;
(2) Family planning services;
(3) Drugs which are included in the per diem of
the institution in (b)(4) above that is utilized in the calculation in (b)(6)
above;
(4) Durable medical equipment;
(5) Medical supplies;
(6) Dental services;
(7) Private duty nursing services;
(8) Physical therapy;
(9) Occupational therapy;
(10) Speech therapy;
(11) Care provided through the Home and Community
Based Care for the Developmentally Disabled waiver in accordance with He-M 517,
with the exception of assistive technology support services, environmental
modifications, employment services, respite and specialty services that would
not otherwise be included in the institutional per diem rate;
(12) Home and community-based care provided
through the In Home Supports Waiver for Children with Developmental
Disabilities in accordance with He-M 524, with the exception of environmental
modifications, respite, and consultative services not otherwise included in the
institutional per diem rate;
(13) Case management services;
(14) Home health; and
(15) Early supports and services.
(d)
Costs associated with the following categories of service, which are not
included in an institution’s per diem rate, shall not
be included in home care cost data in (b)(1) above or in institutional cost of
care data in (c) above:
(1) Inpatient services, including acute
psychiatric admissions;
(2) Outpatient services;
(3) Laboratory services;
(4) X-ray services;
(5) Medical assistance services provided by
education agencies in accordance with He-M 1301;
(6) Ambulance services;
(7) Wheelchair van services;
(8) Audiology services;
(9) Ophthalmology services;
(10) Podiatry services;
(11) Chiropractic services;
(12) Physician services, including services of a
psychiatrist;
(13) Advanced registered nurse practitioner
services;
(14) DCYF/DJSS medicaid
funded services to include private non-medical institutional placement services
(PNMI) and residential placement;
(15) Youth development center or other youth
detention center placements;
(16) Rural health clinics and federally qualified
health centers;
(17) Short term stays of 30 days or less in an
intermediate care facility for the mentally retarded or in a nursing facility;
(18) Services provided on an acute or short-term
basis, in response to an illness or injury, rather than care for the chronic
condition which is the basis for the home care;
(19) Mileage reimbursement; and
(20) Medicaid health insurance premium payments.
Source. #9291, eff 7-1-09
He-W 508.07 Recipient
Notification of Cost Effectiveness Monitoring and Determination Results.
(a)
When the department’s monthly monitoring of cost effectiveness results
in an estimated, projected annual home care cost for a recipient which is
higher than the appropriate type of institutional care cost, the department
shall notify the recipient in writing.
(b)
The notification in (a) above shall include:
(1) A reminder of the requirement to maintain
annual home care costs at or below the cost of care for the appropriate type of
institution pursuant to state and federal law in order to maintain HC-CSD
eligibility;
(2) Medicaid payment data showing the recipient’s
monitored home care costs and estimated, projected annual home care costs,
including a copy of the report used;
(3) The calculated cost of care in an appropriate
type of institution for the same time period as in (2) above and the projected
annual institutional costs, including identification of the appropriate type of
institution; and
(4) Contact information for the department’s care
coordination services unit.
(c) Upon receipt of the notification in (a)
above, the recipient’s family or guardian may contact the department:
(1) For an explanation of the information
included in the notification pursuant to (b) above;
(2) To report costs they believe the department
should not include in the home care costs; and
(3) To request assistance with reducing the costs
of home care or achieving cost effectiveness pursuant to He-W 508.06(a).
(d)
For each state fiscal year ending June 30, the department shall complete
an annual determination of cost effectiveness for each recipient pursuant to
He-W 508.06(b).
(e)
If the department’s annual determination of cost effectiveness indicates
that home care costs are higher than the costs of the appropriate type of
institutional care, the department shall provide written notice to the
recipient within 30 days of the determination.
(f)
The written notice pursuant to (e) above shall include:
(1) A statement that annual cost effectiveness
has not been demonstrated;
(2) A statement that the recipient is required to
reduce and maintain annual home care costs at or below the cost of care for the
appropriate type of institution pursuant to state and federal law in order to
maintain HC-CSD eligibility;
(3) Medicaid payment data showing the recipient’s
annual home care costs and a copy of the report used;
(4) The calculated
annual cost of care in an appropriate type of institution, including
identification of the appropriate type of institution;
(5) A statement that the recipient’s family or
guardian shall submit and implement a written plan for reducing costs in accordance with (f)(2) within 3 months of the date
of the notice in (e) above;
(6) Contact information for the
department’s care coordination services unit which the recipient’s family
or guardian may use for assistance in identifying any billing errors and in
developing the cost reduction plan in (5) above; and
(7) Information that a fair hearing on the
requirement to reduce costs may be requested within 30 calendar days of the
date on the cost effectiveness annual determination notice, in accordance with
He-C 200.
(g)
If the recipient’s family or guardian requests assistance in accordance
with (f)(6) above, the department shall assign a care coordination manager to
assist the recipient’s family or guardian.
Source. #9291, eff 7-1-09
He-W 508.08 Cost Reduction Plans.
(a)
The department shall continue to monitor cost effectiveness monthly and
determine it annually in accordance with He-W 508.06, for recipients who submit
and implement a cost reduction plan in accordance with He-W 508.07(f)(5).
(b)
The department shall terminate a recipient’s medical eligibility for
HC-CSD if:
(1) The recipient submits a cost reduction plan
that does not demonstrate cost effectiveness in accordance with He-W
508.07(f)(2);
(2) The recipient submits a cost reduction plan
that demonstrates cost effectiveness, but does not implement the cost
effectiveness plan in accordance with He-W 508.07(f)(5); or
(3) The recipient does not submit a cost
reduction plan in accordance with He-W 508.07(f)(5).
(c)
A recipient’s termination of medical eligibility for HC-CSD, in
accordance with (b) above, shall be effective 30 days after the due date of the
written plan in He-W 508.07(f)(5).
(d)
The recipient shall receive a written notice of termination of medical
eligibility on department Form 272hc, “Termination of Medical Eligibility for
HC-CSD,” including:
(1) The reason for, and legal basis of, the termination;
(2) Information that a fair hearing on the
termination may be requested within 30 calendar days of the date on the notice
of termination, in accordance with He-C 200.
(e)
The department shall continue the recipient’s medical eligibility after
the termination date of medical eligibility in accordance with (b) above when
the recipient submits to the local district office both a request for a fair
hearing and for a continuation of benefits during the appeal process not later
than 10 calendar days from the date on the written notice of termination.
Source. #9291, eff 7-1-09
He-W 508.09 Continued Medical
Eligibility for HC-CSD.
(a)
The MRT shall conduct reviews of continued medical eligibility for Title
XIX benefits based on current evidence of the recipient’s disability or based
upon changes in eligibility.
(b)
At the time of medical eligibility review, the MRT shall determine
whether the recipient meets the eligibility standards in accordance with He-W
508.03 and He-W 508.04.
(c)
The department shall issue a written notice to the recipient when a
denial of continued medical eligibility is made following a medical eligibility
review.
(d)
The written notice in (c) above shall include:
(1) The recipient’s identifying information:
(2) A listing of the medical and non-medical
reports used for consideration during the medical eligibility review process;
(3) A description of the impairments used for
consideration during the medical eligibility review process;
(4) The reasons for the department’s decision;
(5) The legal basis supporting the department’s
decision(s);
(6) Information that a fair hearing on the denial
of continued medical eligibility may be requested within 30 calendar days of
the date on the notice of denial, in accordance with He-C 200; and
(7) Information on how to reapply for medical
assistance.
(e)
The department shall continue the recipient’s medical eligibility after
a denial of continued medical eligibility in accordance with (c) above when the
recipient submits to the local district office both a request for a fair
hearing and for a continuation of benefits during the appeal process not later
than 10 calendar days from the date on the written notice of denial.
Source. #9291, eff 7-1-09
He-W 508.10 Denial or Termination
of Medical Eligibility for HC-CSD.
The department shall deny or terminate medical eligibility for HC-CSD
if:
(a)
The MRT, in accordance with He-W 508.09(b), determines that the
recipient does not meet the eligibility criteria specified in He-W 508.03 and
508.04; or
(b)
Both the following occur:
(1) A cost reduction plan is not acceptable in
accordance with He-W 508.08(b); and
(2) The recipient fails to submit a request for a
fair hearing and for a continuation of benefits during the appeals process to
the local district office within 10 calendar days from the date of written
notice of adverse decision or termination.
Source. #9291, eff 7-1-09
PART He-W 509 FAMILY
PLANNING EXPANSION CATEGORY (FPEC)
He-W
509.01 Purpose. The purpose of this part is to describe the
family planning and family planning-related services and supplies available to
individuals who are determined eligible, in accordance with He-W 626, for this
expanded Title XIX eligibility category.
In accordance with Section 1902(a)(10)(A)(ii) of the
Social Security Act, 42 U.S.C. 1396a(a)(10)(A)(ii), FPEC recipients shall not be eligible for any other Title XIX
services, except as provided for in this part.
Source. #10357, eff 7-1-13
He-W
509.02 Definitions.
(a)
“Department” means the New Hampshire department of health and human
services.
(b)
“Family planning expansion category” means a category of recipients who meet the technical eligibility
requirements established by the department for the family planning services
and/or family planning-related services specified in this part, but who are not
eligible for any other Title XIX services not specified in He-W 509.
(c)
“Family planning-related services” means certain medical diagnosis and
treatment services and pharmaceutical supplies that are provided pursuant to a
family planning service in a family planning setting and that do not receive an
enhanced rate of 90% federal match.
(d) “Family planning services” means family
planning services and supplies described in section 1905(a)(4)(c) of the Social
Security Act, 42 U.S.C. 1396d(a)(4)(c), including medical services, medical
procedures, and pharmaceutical supplies and devices provided by or under the
supervision of a physician or other health professional that allow an
individual to prevent or delay pregnancy or to otherwise control family size,
and which receive an enhanced match rate of 90% federal match.
(e)
“Hysterectomy” means a surgical procedure for the purpose of removing
the uterus.
(f)
“Institutionalized individual” means “institutionalized individual” as
defined in 42 CFR 441.251.
(g)
“Mentally incompetent individual” means “mentally incompetent
individual” as defined in 42 CFR 441.251.
(h) “Sterilization”
means any medical procedure, treatment, or surgical procedure which is intended
to render an individual permanently incapable of reproducing.
(i) “Title XIX program” means the joint
federal-state program described in Title XIX of the Social Security Act.
Source. #10357, eff 7-1-13
He-W 509.03 Eligibility.
(a)
Individuals shall be eligible for family planning services and family
planning-related services, as described in He-W 509.06(b) and (c) below,
respectively, and in accordance with He-W 509 if the individual:
(1) Meets the division of family assistance
eligibility requirements specified in He-W 626;
(2) Once determined eligible in accordance with
(1) above, the FPEC recipient has reached reproductive maturity; and
(3) If female, is not known to be pregnant.
(b)
Acceptance of any family planning services shall be voluntary on the
part of the individual.
(c) FPEC recipients shall not be considered to be
Title XIX recipients for the purposes of receipt of services other than those
as described in He-W 509.
Source. #10357, eff 7-1-13
He-W 509.04 Provider Participation. All participating family planning providers
shall be:
(a)
Licensed by the state in which s/he practices or be a NH certified
midwife; and
(b)
A New Hampshire enrolled Title XIX provider.
Source. #10357, eff 7-1-13
He-W 509.05 Service Limits. Family planning services and family
planning-related services for FPEC recipients shall be subject to the limits
described in He-W 530.
Source. #10357, eff 7-1-13
He-W 509.06 Covered Services.
(a)
The services in (b) and (c) below shall be covered as family planning
services and family planning-related services, respectively, only if the
services, supplies, and procedures are clearly provided or performed for family
planning purposes.
(b) The following services shall be covered as
family planning services:
(1) Those physician services in accordance with
He-W 531, certified midwife services in accordance with He-W 538, and advanced
registered nurse practitioner services in accordance with He-W 534, provided
for family planning purposes;
(2) Contraceptive devices or drugs, both
prescription and non-prescription, in accordance with He-W 570;
(3) Pregnancy tests and screening for a sexually
transmitted disease (STD) only when performed routinely as part of an initial,
regular, or follow-up family planning visit; and
(4) Sterilization, in accordance with 42 CFR
441.253 and 42 CFR 441.254, as follows:
a. The FPEC recipient shall be at least 21 years
old at the time consent is obtained;
b. The FPEC recipient shall not be a mentally
incompetent individual;
c. The FPEC recipient shall not be an institutionalized
individual;
d. The FPEC recipient shall voluntarily give
informed consent in accordance with the requirements at 42 CFR 441.257 through
42 CFR 441.258;
e. The provider shall submit a sterilization
consent form meeting the requirements of 42 CFR 441, Subpart F, to the
department prior to the department’s payment for the sterilization claim;
f. At least 30 days, but not more than 180 days,
shall have passed between the date of informed consent and the date of
sterilization, with the exception of cases of premature delivery or emergency
abdominal surgery as described in g. below;
g. A FPEC recipient may consent to be sterilized
at the time of an emergency abdominal surgery if at least 72 hours have passed
since he or she gave informed consent for the sterilization; and
h. Treatment of surgical or anesthesia-related
complications resulting from or during a covered sterilization procedure shall
be covered; and
(5) Family planning-related services that were
provided as part of, or as follow-up to, a family planning visit in which a
sterilization procedure took place.
(c) The following services
shall be covered as family planning-related services:
(1) Services to treat adverse reactions to, or
medical complications of, family planning procedures, services, treatments, or
therapies including, but not limited to:
a. Treatment of perforated uterus due to an
intrauterine device insertion; and
b. Treatment of severe
menstrual bleeding caused by Depo-Provera injection;
(2) Drugs, in accordance with the following:
a. Drugs shall be for the treatment of STDs,
except for HIV/AIDS and hepatitis, when the STD is identified or diagnosed
during a routine or periodic family planning visit; and
b. Title
XIX providers shall comply with the provisions of He-W 570 regarding
pharmaceutical services when prescribing or dispensing drugs covered in a.
above;
(3) A follow-up visit after prescribing drugs for
the treatment of an STD, including a re-screen for the STD;
(4) Drugs and other treatment for lower genital
tract and genital skin infections/disorders, and urinary tract infections, when
the infection/disorder is identified/diagnosed during a routine/periodic family
planning visit;
(5) A follow-up
visit for drugs and other treatment of the lower genital tract and genital skin
infections or disorders where the infections or disorder is identified during a
family planning visit; and
(6) Vaccinations to prevent cervical cancer that
are routinely provided pursuant to a family planning service in a family
planning setting.
Source. #10357, eff 7-1-13
He-W
509.07 Non-Covered Services. The following services shall not be covered
as family planning or family planning-related services:
(a) Sterilizations
which do not meet the requirements of He-W 509.06(b)(4) above;
(b) Hysterectomies;
(c) Abortions;
(d) Medical, surgical,
or pharmaceutical treatment for the purpose of enhancing, promoting, or
restoring fertility;
(e) Diagnostic
examination of the cervix or vagina by means of a special microscope,
colposcopy, biopsy, or cryotherapy of the cervix or vagina; and
(f) Any medical
service, procedure, or pharmaceutical supply or device provided to a FPEC
recipient who is known to be pregnant.
Source. #10357, eff 7-1-13
He-W 509.08 Transportation.
(a) FPEC recipients shall be ensured assistance with locating or being
reimbursed for transportation to Title XIX providers in order to access
necessary family planning and family planning-related services described in
He-W 509.
(b) FPEC recipients who wish to be reimbursed for transportation shall:
(1) Enroll in the transportation provider system
in accordance with He-W 574.10(b)–(e); and
(2) Be known as a recipient driver only for
enrollment and payment purposes.
(c) FPEC recipients shall only be reimbursed for transportation under the
following circumstances:
(1) Transportation shall be to in-state or border
Title XIX enrolled providers, except as described in (2) below;
(2) Transportation to out-of-area providers shall
be authorized in advance in accordance with He-W 574.08;
(3) There is no transportation available free of
charge or payable by any other agency;
(4) Only one trip per day, whether one-way or
round-trip, shall be covered;
(5) Only the actual number of miles driven from
the individual’s residence to the Title XIX provider and return to individual’s
residence shall be reimbursed; and
(6) Transportation shall be to the nearest
available provider of the necessary
covered family planning services or family planning-related services via the
shortest, most economical route, as described in He-W 574.14(b).
(d) FPEC recipients shall submit transportation
claims in accordance with He-W 574.06.
(e) The above transportation claims shall be paid
in accordance with He-W 574.07.
(f) The provisions of He-W 574.12 and He-W 574.14
regarding hearings and utilization review and control shall apply to FPEC
recipients.
(g) FPEC recipients who request transportation
assistance via wheelchair van in order to access family planning services or
family planning-related services shall qualify for wheelchair van transportation
if they meet the requirements in He-W 573.02(a)(1) and (2), except that
eligibility as an FPEC recipient shall be substituted for the requirements in
He-W 573.02(a) to be a Title XIX recipient.
(h) FPEC recipients utilizing wheelchair van transportation
shall be subject to the provisions of He-W 573.04, He-W 573.10, He-W 573.11,
and He-W 573.12 regarding service limits, prior authorization to exceed service
limits, utilization review and control, and third party liability.
(i) FPEC recipient
shall utilize Title XIX enrolled wheelchair van providers who meet the
requirements of He-W 573.
(j) FPEC recipients shall be eligible to be
transported by volunteer drivers in accordance with He-W 574 only for the
purpose of accessing family planning services or family planning-related
services.
Source. #10357, eff 7-1-13
He-W 509.09 Co-Payments. Co-payments for family planning
pharmaceutical products shall not be required.
Source. #10357, eff 7-1-13
He-W
509.10 Utilization Review and Control. The department’s surveillance and utilization
review of subsystems unit (SURS) shall monitor utilization of family planning
services in accordance with 42 CFR 455 and 42 CFR 456.
Source. #10357, eff 7-1-13
He-W 509.11 Third Party Liability. All third party obligations shall be
exhausted before Title XIX shall be billed, in accordance with 42 CFR 433.139.
Source. #10357, eff 7-1-13
He-W 509.12 Payment for Services.
(a)
Rates of payment for family planning and family planning-related
services shall be established by the department in accordance with RSA 161:4,
VI(a).
(b)
The provider shall submit claims for payment to the department’s fiscal
agent.
(c)
The provider shall maintain supporting records, in accordance with He-W
520.
Source. #10357, eff 7-1-13
PART
He-W 510 - RESERVED
PART He-W 511
HEALTH INSURANCE PREMIUM PAYMENT PROGRAM (HIPP)
He-W
511.01 Purpose. The purpose of this part is to describe the
requirements for enrollment in the health insurance premium payment program
(HIPP), which uses medicaid funds to purchase group
health plan coverage on behalf of a medicaid
recipient, as allowed by 42 USC §1396e.
Source. #10632, eff 7-1-14
He-W
511.02 Scope. This part shall apply only to newly eligible
adults for whom enrollment in HIPP is a condition of medicaid
eligibility under 42 USC §1396a(a)(10)(A)(i)(VIII)
and RSA 126-A:5, XXIII. Enrollment in HIPP shall be voluntary for all other medicaid recipients.
Source. #10632, eff 7-1-14
He-W
511.03 Definitions.
(a) “Cost effective” means that the cost to
enroll an individual in a group health plan is likely to be less than the medicaid expenditures for an equivalent set of services.
(b) “Cost effectiveness test” means the method by
which the department determines if a recipient’s group health plan costs less
than the expected medicaid expenditure.
(c) “Department” means the New Hampshire
department of health and human services.
(d) “Group health plan” means any plan of, or
contributed to by, an employer, including a self-insured plan, to provide
health care to the employer’s employees, former employees, or the families of
employees or former employees, and which meets S. 5000(b)(1) of the Internal
Revenue Code of 1986, and includes continuation coverage pursuant to Title XXII
of the Public Health Services Act, S. 4980B of the Internal Revenue Code of
1986, or Title VI of the Employee Retirement Income Security Act of 1974.
(e) “Health insurance premium payment program
(HIPP)” means a premium assistance program administered by the department
consistent with section 1906 of the Social Security Act, which permits the use
of medicaid funds to purchase group health plan
coverage on behalf of eligible medicaid recipients.
(f) “Medicaid” means the Title XIX and Title XXI
programs administered by the department, which makes medical assistance
available to eligible individuals.
(g) “New Hampshire health protection program
(NHHPP)” means the program established by SB 413 (Chapter 3, Laws of 2014),
which authorizes medical assistance for adults up to 133% federal poverty
levels under 42 USC §1396a(a)(10)(A)(i)(VIII).
(h) “Newly eligible adult” means adults who are
eligible for medicaid under the New Hampshire health
protection program and the provision of section 1902(a)(10)(A)(i)(VIII) of the social security act of 1935 as amended, 42
USC §1396a(a)(10)(A)(i)(VIII).
(i) “Wrap-around
services” means to the extent that a group health plan does not cover a benefit
contained in the NH state medicaid benefit package
for newly eligible adults, the service is covered by traditional medicaid so that the individual has access to the same
services to which they are entitled if they were covered directly through the
state’s medicaid program.
Source. #10632, eff 7-1-14
He-W
511.04 Recipient Participation.
(a)
Participation in HIPP shall be mandatory when a newly eligible adult has
access to a group health plan and the department determines, in accordance with
He-W 511.05 below, that it is cost effective for the individual to enroll in
the group health plan.
(b)
Pending the determination of cost effectiveness, the newly eligible
adult shall be eligible to receive medicaid covered
services through the medicaid fee-for-service
program.
(c)
Premium assistance through the HIPP program shall not be available when:
(1) The
insurance plan is an indemnity plan that pays only a predetermined amount for
covered services, such as dental or vision only plans, or long-terms care
plans;
(2) The
insurance plan is a school-based plan offered based on attendance or school
enrollment;
(3) The
individual is only eligible for medicaid through in
and out medical assistance in accordance with He-W 678.01;
(4) The
insurance plan is only offered for a temporary time period;
(5) The
eligible individual does not qualify for full medicaid
benefits;
(6) The
insurance plan is through New Hampshire’s high-risk pool;
(7) The
insurance plan is a medicare supplemental policy, if
the HIPP application was filed after March 1, 1996;
(8) The
insurance plan is COBRA; or
(9) The newly
eligible adult is eligible for, but is not enrolled in Medicare Part B.
(d) The newly eligible adult shall inform the
department if he or she has access to group health plan coverage, at the time
of application, and within 10 days of any other such time as coverage becomes
available.
(e) Within 30 days of receiving a written request
from the department or the department’s vendor, the newly eligible adult shall
provide information necessary to establish the cost effectiveness of the group
health plan, including the following:
(1) Health
plan information, such as the plan name and policy number;
(2) Premium
liability, which is the portion of the premium that is paid by the policy
holder;
(3)
Co-insurance, which is the policy holder’s share of the cost of a
covered health care services, and is generally calculated as a percentage of
the total charge for the service;
(4)
Deductibles, which is the amount the policy holder must pay for health
care services before the group health plan begins to pay;
(5) Co-pay
liability, which is a fixed amount the policy holder pays for a health care
service, and generally paid for at the time the services are rendered;
(6) Covered
benefits and services;
(7) Any
service limits applied to the benefit and service use by the health plan; and
(8)
Demographic information relative to other individuals on the
policyholder’s plan, including gender and age.
(f) In addition to the information listed in
(e)(1)-(8) above, the newly eligible adult shall also provide employer and
employment information to the department within the 30-day timeframe described
in (e) above, to include:
(1) The
employer’s business name;
(2) The number
of hours worked by the employee per week; and
(3) Contact
information for the employer's human resource department.
(g)
The newly eligible adult shall be granted an additional 15 days to
provide the information required in (e) and (f) above when the individual
informs the department or the department’s vendor that the failure to comply
with (e) above was due to one of the following reasons:
(1) There was a serious illness or death in the
individual’s family;
(2) There was a family emergency or household
disaster, such as a fire, flood, or tornado;
(3) The individual offers a cause beyond the
individual’s control, such as the individual has made multiple unsuccessful
attempts to obtain the information; or
(4) There was a failure to receive the
department’s request for information or notification for a reason not
attributable to the individual’s lack of a forwarding address.
(h)
Except as allowed by (i) below, if the
department or the department’s vendor determines that the group health plan is
cost effective, the newly eligible adult shall:
(1) Enroll in the health plan within 15 days of
receiving notification from the department or the department’s vendor that the
plan is cost effective; and
(2) Upon enrollment, provide the department or
the department’s vendor with confirmation of the start date of coverage.
(i) In the event that the newly eligible adult is
already enrolled in cost effective group health plan prior to applying for medicaid, then the HIPP premium payments will begin in the
month following HIPP approval notification.
(j)
If the department or the department’s vendor determines that the group
health plan is not cost effective, the newly eligible adult shall be enrolled
in the medicaid care management program in accordance
with He-W 506.
(k)
Enrollment in a group health plan shall not change the individual’s
eligibility for medicaid benefits.
Source. #10632, eff 7-1-14
He-W 511.05 Cost
Effectiveness Determination. Cost
effectiveness shall be determined by the department applying the methodology
set forth in Chapter 3, Section 3910, Medicaid Payments for Recipients under
Group Health Plans, of the federal Centers for Medicare and Medicaid Services
(CMS), State Medicaid Manual, available as noted in Appendix A.
Source. #10632, eff 7-1-14
He-W
511.06 Cost Effectiveness
Redetermination.
(a) Cost effectiveness shall be redetermined annually concurrent with the recipient’s annual enrollment in the group health plan, or any time there is a change in the group health plan.
(b) The newly
eligible adult shall submit the current group health plan, as described in He-W
511.04(e) and (f) above, within 30 days of having receiving a notice of
redetermination from the department.
Source. #10632, eff 7-1-14
He-W
511.07 Wrap Around Coverage.
(a) If the group health plan does not cover the
full range of medicaid services, the newly eligible
adult shall receive wrap-around services.
(b) Non-medicaid
eligible family members shall not be eligible to receive wrap around services.
Source. #10632, eff 7-1-14
He-W
511.08 Payment of Cost Sharing.
(a) Recipient cost sharing obligations shall be
either paid directly by medicaid or reimbursed to the
recipient if the recipient paid out of pocket, such as for mail order
prescription medications.
(b) If a non-medicaid
family member is enrolled in the group health plan, then medicaid
funds shall be expended for payment of premiums, but not for any other cost
sharing expenses attributable to the non-medicaid
family members.
(c) The HIPP program shall pay for the minimum
coverage option that allows the medicaid-eligible
person/persons to be covered.
(d)
When more than one cost effective group health plan is available, the
department shall pay the premium for only one plan, but the newly eligible
adult may choose the cost effective plan in which to enroll.
(e)
If the newly eligible adult’s health plan offers more services than what
is covered under medicaid, the newly eligible adult
shall be responsible for any deductibles, coinsurance, and other cost sharing
obligations attributable to those services not covered by medicaid.
(f) The newly eligible adult shall be responsible
for payment of any nominal cost sharing amounts permitted under section 1916 of
the SSA.
Source. #10632, eff 7-1-14
He-W 511.09 Loss of Eligibility and Discontinuation of
Premium Payments.
(a)
Except as provided in (b) below, when the newly eligible adult loses medicaid eligibility, premium payments shall be
discontinued as of the month of medicaid ineligibility.
(b)
Premium payments shall continue for 6 months from the date the
department determines that the group health plan is cost effective, even if the
newly eligible adult loses medicaid eligibility
within that 6-month period.
(c) Coverage of any medicaid
benefits provided outside the group health plan, including any wrap around
services, shall end on the date the newly eligible adult loses medicaid eligibility.
(d)
If the department determines that the health plan is no longer cost
effective, HIPP premium payment shall be discontinued pending timely and
adequate notice, made in accordance with 42 CFR 431.211.
(e)
If the newly eligible adult fails to provide the information necessary
to determine the availability and cost effectiveness of group health insurance
in accordance with the timeframes set forth in He-W 511.04(e) or (f) above, he
or she shall be terminated from the medicaid program
within 15 days following the failure to comply.
(f)
If the newly eligible adult fails to provide the information necessary
to establish ongoing eligibility in accordance with the timeframes set forth in
He-W 11.06(b), he or she shall be terminated from the medicaid
program within 15 days for failure to comply.
(g)
If the newly eligible adult provides the necessary documentation within
the 15 day advance notice period stipulated in (e) or (f) above, his or her
termination from the medicaid program shall be voided
and a HIPP cost effective calculation shall be performed.
(h) If the newly eligible adult disenrolls from
their cost effective group health plan, the newly eligible adult shall lose
eligibility for medicaid until such time as the newly
eligible adult recipient re-enrolls in the cost effective group health plan and
reapplies for medicaid.
(i) If the health
plan is no longer available or the policy has lapsed, premium payments shall be
discontinued as of the effective date of the termination of the coverage.
Source. #10632, eff 7-1-14
He-W
511.10 Third Party Liability. All third party obligations shall be
exhausted before claims shall be submitted to the department’s fiscal agent in
accordance with 42 CFR 433.139.
Source. #10632, eff 7-1-14
He-W
511.11 Utilization Review &
Control. The department’s provider
program integrity unit shall monitor utilization of services
to identify, prevent, and correct potential occurrences of fraud, waste and
abuse in accordance with in accordance with He-W 520, 42 CFR 455, and 42 CFR
456.
Source. #10632, eff 7-1-14
PART He-W 512
ALTERNATIVE BENEFIT PLAN (ABP) AND PREMIUM ASSISTANCE PROGRAM
He-W 512.01 Purpose. The purpose of this part is to describe the
alternative benefit plan (ABP) services and the premium assistance program
(PAP)
available through the medicaid
program to the newly eligible population in accordance with the New Hampshire
Health Protection Program, RSA 126-A:5, XXIV.
Source. #10656, eff 8-15-14; ss by #11012, INTERIM,
eff 1-1-16, EXPIRES: 6-29-16; ss by #11119, eff 6-29-16
He-W
512.02 Definitions.
(a) “Alternative benefit plan (ABP)” means the medicaid benchmark or benchmark equivalent coverage
described in section 1937 of the Social Security Act.
(b) “Department” means the New Hampshire
department of health and human services.
(c) “Medicaid” means the Title XIX and Title XXI
programs administered by the department, which makes medical assistance
available to eligible individuals.
(d) “Medically frail” means a newly eligible
individual who is exempt from mandatory enrollment in the ABP or PAP in
accordance with the conditions set forth in 42 CFR § 440.315(f).
(e) “Newly eligible adult” means adults who are eligible for medicaid under
the New Hampshire health protection program and the provision of section
1902(a)(10)(A)(i)(VIII) of the Social Security Act of
1935 as amended, 42 USC §1396a(a)(10)(A)(i)(VIII).
(f) “Premium Assistance Program
(PAP)” means the Marketplace Premium Assistance Program, established by RSA
126-A:5 which requires that adults eligible for medical assistance under 42 USC
§ 1396a(a)(10)(A)(i)(VIII) enroll in a cost-effective
Qualified Health Plan offered on New Hampshire’s federally facilitated
Marketplace, authorized through the Section 1115(a) research and demonstration
waiver, # 11-W-00298/1 by the Centers for Medicare and Medicaid Services on
March 4, 2015.
(g) “Premium Assistance Program
participants (PAP participants)” means those newly eligible adults who are
mandatorily required to enroll in a qualified health plan, and those who
voluntarily enroll in a qualified health plan.
(h) “Qualified Health Plan
(QHP)” means an individual health insurance policy certified by the Centers for
Medicare and Medicaid Services (CMS) for sale through New Hampshire’s
individual health insurance Marketplace.
(i) “Subluxation”
means an incomplete dislocation, off centering, misalignment, fixation, or
abnormal spacing of the vertebrae.
(j) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department.
(k) “Title XXI” means the joint federal-state
program described in Title XXI of the Social Security Act and administered in
New Hampshire by the department.
(l) “Wrap
benefits” means:
(1) Non-emergency
medical transportation;
(2) Early
Periodic Screening Diagnosis and Treatment (EPSDT) services as described in
He-W 546, for individuals who are under the age of 21; and
(3) Family
planning services and supplies from a medicaid
enrolled provider, and adult dental in accordance with He-W 566.04(e) and adult
vision services in accordance with He-W 530.03(g).
Source. #10656, eff 8-15-14; ss by #11012, INTERIM, eff
1-1-16, EXPIRES: 6-29-16; ss by #11119, eff 6-29-16
He-W
512.03 Eligibility.
(a) All newly eligible individuals shall receive
services under the ABP, unless they are medically frail or identify as pregnant
after application and opt to receive Medicaid state plan services.
(b) Individuals who are eligible for medicaid through the New Hampshire Health Protection
Program (NHHPP) shall be in the PAP unless the individual is exempt or
voluntary as described in He-W 512.04(b) and (c) below.
Source. #10656, eff 8-15-14; ss by #11012, INTERIM,
eff
1-1-16, EXPIRES: 6-29-16; ss by #11119, eff 6-29-16
He-W 512.04 Enrollment.
(a)
For individuals who are eligible for PAP, enrollment in a QHP shall be
mandatory unless the individual is determined to be exempt as described in (b)
below or voluntary as described in (c) and (d) below.
(b)
Individuals
who are determined to be medically frail as defined in 42 CFR § 440.315(f)
shall be exempt from mandatory enrollment with a QHP.
(c)
The following individuals shall be considered voluntary for enrollment
with a QHP:
(1) Individuals who are members of a federally
recognized Indian tribe or Alaskan natives; and
(2) Individuals who are enrolled in PAP who
identify as pregnant after the point of application for medicaid.
(d)
The following shall apply to voluntary individuals described in (c)
above:
(1) Voluntary individuals shall be enrolled in a
QHP unless the individual identifies to the department that he or she is in a
voluntary eligibility group as noted in (c) above; and
(2) If, after identifying as being in a voluntary
eligibility group, a voluntary individual chooses not to enroll in a QHP, the
individual shall be notified by the department and required to choose a medicaid managed care organization (MCO) as described in
He-W 506.
(e)
The department shall send a notice of QHP plan selection to all
individuals eligible for PAP enrollment as indicated in (a) above except those
who are exempted from enrollment.
(f)
PAP participants shall have 30 days from the date of the QHP plan
selection notice in (e) above to select a QHP and to respond to the
department’s notice by using the on-line portal NH Electronic Application
System (NH EASY) at www.nheasy.nh.gov, calling via
telephone at 1-888-901-4999, or contacting the department in person.
(g)
Except for voluntary individuals described in (c) and (d) above, PAP
participants who fail to select a QHP within 30 days from the date of the
notice in (f) above shall be auto-assigned to a QHP.
(h)
Auto-assignments with a QHP shall be based on the following criteria:
(1) Personal or family affiliation to a QHP or
MCO, if the MCO offers a complementary QHP;
(2) Primary care provider affiliation with a QHP;
or
(3) If no assignment can be made utilizing
(1)-(2) above, assignment shall be equally distributed among the available
QHPs.
(i) PAP participants may request to change the
QHP selection without cause, by making a written or oral request to the
department at any of the following times:
(1) During the first 30 days following the date
of the member’s initial selection of or the auto-assignment to the QHP, or the
date the department sends the member confirmation of the individual’s selection
or auto-assignment, whichever is later; and
(2) During annual open enrollment.
(j)
PAP participants may request to change the QHP selection for cause, by
making a written or oral request to the department within 60 days of the
occurrence of one of the following events:
(1) PAP participant loses access to the QHP he or
she is currently enrolled in because of a permanent move to a county where that
QHP is not available;
(2) PAP participant gains or becomes a dependent
through marriage, birth, adoption, foster care, child support order, or court
order;
(3) PAP participant loses a dependent or is no
longer considered a dependent through divorce or legal separation as defined by
state law in the state in which the divorce or legal separation occurs, or if
the enrollee’s dependent dies;
(4) The department confirms based on a PAP
participant’s complaint that the QHP in which the PAP participant is enrolled
violated a material provision of its contract in relation to the PAP
participant; or
(5) PAP participant’s enrollment or
non-enrollment in a QHP is unintentional, inadvertent, or erroneous and is the
result of the error, misrepresentation, misconduct, or inaction of an officer,
employee, or agent of the department, its instrumentalities, or a
non-departmental entity providing enrollment assistance or conducting
enrollment activities.
(k)
PAP participants shall be dis-enrolled from the PAP program if they
identify as medically frail after they were previously determined eligible.
(l)
Medically frail individuals shall have the option to enroll with a medicaid MCO to receive the ABP benefit or the state plan medicaid benefit.
(m)
Individuals who are voluntary as described in (c) and (d) above shall be
enrolled as follows:
(1) Individuals who are enrolled in PAP and
identify as pregnant after the point of application for medicaid
shall elect to receive either state plan medicaid
benefits delivered through a medicaid MCO or remain
enrolled in the PAP with a QHP; and
(2) Individuals who are members of a federally
recognized Indian tribe or Alaskan natives who elect to dis-enroll from their
QHP shall receive ABP benefits delivered through a medicaid
MCO.
(n)
For PAP participants eligible for medicaid
after October 1, 2015, the PAP participant shall receive coverage through
fee-for-service medicaid from the date of the
eligibility determination until the individual’s enrollment in the QHP becomes
effective.
(o)
If a PAP participant selects or is auto-assigned to a QHP on or before
the 15th of the month, coverage in the QHP shall be begin the first
day of the month following the month in which the selection or auto-assignment
was made.
(p)
If a PAP participant selects or is auto-assigned to a QHP any time after
the 15th of the month, coverage in the QHP shall be begin the first
day of the second month following the month in which the selection or
auto-assignment was made.
Source. #10656, eff 8-15-14; ss by #11012, INTERIM,
eff
1-1-16, EXPIRES: 6-29-16; ss by #11119, eff 6-29-16
He-W
512.05 Covered Services.
(a) ABP services for NHHPP participants who are
medically frail or identify as members of federally recognized Indian tribes or Alaskan
natives who choose to opt-out of the PAP shall include the following:
(1) Services described in He-W
506.04(a) and (b);
(2) Substance use disorder
(SUD) services as described in He-W 513; and
(3) Chiropractor services,
which shall be provided as follows:
a.
Chiropractic services shall consist of spinal manipulation and manual
medical intervention services, including:
1. Office
visits for:
(i) Assessment;
(ii)
Evaluation;
(iii) Spinal
adjustments;
(iv)
Manipulation; and
(v)
Physiological therapy before or in conjunction with spinal adjustments;
and
2. Medically
necessary diagnostic laboratory and x-ray tests;
b.
Chiropractic services shall not include wellness care; and
c.
Chiropractic services shall be limited to 12 visits per recipient, per
state fiscal year.
(b) Covered services for PAP participants enrolled with a QHP shall include the following
categories of services from a QHP:
(1) Ambulatory patient services;
(2) Emergency services;
(3) Hospitalization;
(4) Maternity and newborn care;
(5) Mental health and substance
use disorder services, including behavioral health treatment;
(6) Prescription drugs;
(7) Rehabilitative and
habilitate services and devices;
(8) Laboratory services;
(9) Preventive and wellness
services and chronic disease management; and
(10) Pediatric services
including oral and vision care.
(c) PAP
participants shall receive benefits described in (b) above from a QHP, and
shall be restricted to using the QHP provider networks except that PAP
participants shall not be restricted in their choice of family planning
providers if the family planning provider is enrolled with medicaid.
(d) PAP participants shall receive fee for
service wrap benefits as defined in He-W 512.02(l) above.
Source. #10656, eff 8-15-14; ss by #11012, INTERIM,
eff
1-1-16, EXPIRES: 6-29-16; ss by #11119, eff 6-29-16
He-W
512.06 Co-payments.
(a) Except as prohibited by 42 USC § 1396o-1(b)(3)(B), newly
eligible individuals who have an income greater than 100 percent of the FPL and
are PAP participants shall be subject to the following co-payments:
(1) A
co-payment in the amount of $8.00 for each non-preferred drug prescription and
refill dispensed;
(2) A co-payment in the amount of $4.00 for each
preferred drug prescription and refill dispensed;
(3) A
co-payment in the amount of $5.00 for each primary care provider visit to treat
illness or injury;
(4) A
co-payment in the amount of $125.00 for each inpatient mental health admission,
inpatient substance use disorder treatment admission or hospital admission,
excluding maternity admissions;
(5) A
co-payment in the amount of $50.00 for high-cost imaging such as CT/PET scans,
and MRIs;
(6) A
co-payment in the amount of $5.00 for each mental health outpatient visit;
(7) A
copayment in the amount of $5.00 for each substance use disorder outpatient
visit;
(8) A
co-payment in the amount of $8.00 for each physical therapy visit;
(9) A
co-payment in the amount of $8.00 for each occupational therapy visit;
(10) A
co-payment in the amount of $8.00 for each speech therapy visit;
(11) A
co-payment in the amount of $5.00 for each chiropractor visit;
(12) A
co-payment in the amount of $8.00 for each specialty physician visit;
(13) A
co-payment in the amount of $5.00 for each visit to other medical professionals
such as an advanced practice registered nurse or a physician’s assistant; and
(14) A
co-payment in the amount of $5.00 for each laboratory outpatient visit.
(b) Co-payment obligations shall be suspended for
the remainder of the calendar year quarter when the total co-payments made out
of pocket by the newly eligible individual reach 5 percent of the individual’s
household income for that quarter. Co-payment obligations shall resume at the
beginning of the next quarter. “Quarter” means one of 4 calendar periods ending
March 31, June 30, September 30, and December 31.
Source. #10656, eff 8-15-14; ss by #11012, INTERIM,
eff
1-1-16, EXPIRES: 6-29-16 (from He-W 512.05); ss by #11119, eff 6-29-16; ss by
#12438, eff 1-1-18
He-W 512.07 Appeals Process
for the Premium Assistance Program.
(a) The appeals
process for the PAP shall address PAP participants’ requests for the appeal of
any adverse decisions made by the QHP related to a PAP participant’s QHP
covered benefits and decisions made by the department related to eligibility or
wrap benefits related to the PAP.
(b) PAP
participants who want to appeal a decision made by the QHP regarding a QHP’s
covered benefits shall exhaust all private market appeals processes applicable
under RSA 420-J:5 and RSA 420-J:5-a through 5-e prior to requesting a state
fair hearing with the department. The
private market appeals processes include internal review conducted by the QHP
under RSA 420-J:5 with respect to both medical necessity and coverage issues,
and an independent external review conducted by an independent review organization
(IRO) under RSA 420-J:5-a through 5-e with respect to medical necessity issues
only.
(c) PAP
participants shall have the right to a state fair hearing in accordance with
(d) and (e) below when the enrollee has exhausted the private market appeals
processes without having the issue under appeal resolved in his or her favor.
PAP enrollees shall file a request for a fair hearing in accordance with He-C
200.
(d) PAP
participants shall have the right to a state fair hearing for the following
issues:
(1) For
medical necessity issues, at the conclusion of the external review process as
provided in RSA 420-J:5-a-5-e;
(2) For issues
not related to medical necessity, at the conclusion of a QHP internal review
process as provided in RSA 420-J:5; and
(3) For
decisions related to eligibility for medicaid or
decisions made regarding wrap benefits made by the department, without first
exhausting any private market appeals processes.
(e) Requests for a department fair hearing shall be made in writing within
30 calendar days of the date of the notice of the resolution of the appeal
through the private market appeals process.
(f) A PAP participant’s benefits shall be continued during a department
fair hearing if:
(1) The
individual requests a department fair hearing within 10 calendar days of the
notice of the disposition of the private market appeals process or the notice
of the department’s decision on eligibility or wrap benefits;
(2) The
individual requests continuation of benefits; and
(3) The individual
identifies a medicaid enrolled provider to provide
the benefit requested.
(g) If the QHP’s adverse decision is upheld in a
department fair hearing, the member shall be liable for the cost of continued
benefits.
Source. #10656, eff 8-15-14; ss by #11012, INTERIM,
eff 1-1-16, EXPIRES: 6-29-16; ss by #11119, eff 6-29-16
He-W
512.08 Utilization Review and Control. The department’s provider program integrity
unit shall monitor utilization of ABP services to identify, prevent, and
correct potential occurrences of fraud, waste and abuse in accordance with in
accordance with He-W 520, 42 CFR 455, and 42 CFR 456.
Source. #11012, INTERIM, eff 1-1-16, EXPIRES: 6-29-16
(from He-W 512.06); ss by #11119, eff 6-29-16
He-W 512.09 Third Party Liability. All third party obligations shall be
exhausted before claims shall be submitted to the department’s fiscal agent in
accordance with 42 CFR 433.139.
Source. #11012, INTERIM, eff 1-1-16, EXPIRES: 6-29-16
(from He-W 512.07); ss by #11119, eff 6-29-16
PART
He-W 513 SUBSTANCE USE DISORDER (SUD)
TREATMENT AND RECOVERY SUPPORT SERVICES
He-W 513.01 Purpose. The purpose of this part is to establish the
procedures and requirements for age and clinically appropriate substance use
disorders (SUDs) treatment and recovery support services that are provided to
the individuals who are eligible for medicaid.
Source. #10655, INTERIM, eff 8-15-14, EXPIRES:
2-11-15; ss by #10779, eff 2-11-15; ss by #10922, eff 9-1-15; ss by #11107, eff
7-1-16; ss by #12681, eff 11-27-18
He-W
513.02 Definitions.
(a) “Collaborative service model” means a model
whereby SUD treatment and recovery support services, health care services, and
mental health services are provided by practitioners from different programs
who work together via formalized relationships.
(b) “Comprehensive SUD program” means:
(1) An agency
under contract with or agreement with the department which provides specialty
SUD treatment and recovery support services on a residential and outpatient
basis and whose facility is:
a. Licensed as a residential
treatment and rehabilitation facility in accordance with He-P 807; or
b. A state-owned SUD
residential treatment and rehabilitation facility which is exempt from
licensure in accordance with RSA 151:2, II (i)and
He-P 807;
(2) A hospital
enrolled in medicaid both as a hospital in accordance
with He-W 543 and as a comprehensive SUD program in accordance with He-W 513,
which provides specialty SUD treatment and recovery support services on a
residential and outpatient basis; or
(3) Providers
enrolled in medicaid in the state in which they
practice to provide residential services consistent with criteria as set forth
in the American Society of Addiction Medicine (ASAM) Criteria: Treatment Criteria for Substance-Related,
Addictive, and Co-Occurring Conditions, Third Edition (2013), henceforth
referred to as “ASAM Criteria (2013)” available as noted in Appendix A, and who
are also enrolled in NH medicaid.
(c) “Crisis intervention” means a response to a
crisis or emergency situation experienced by an individual, family member, or
significant other(s) related to a recipient’s SUD.
(d) “Department” means the New Hampshire
department of health and human services.
(e) “Direct supervision” means that the
supervisor meets with the individual to review his or her clinical practice in
order to evaluate his or her performance.
(f) “Evaluation” means a clinical interview
conducted by a qualified individual using one or more standardized, evidence
based evaluation tools to determine the existence and severity of substance use
and specific problem areas.
(g) “Family treatment” means outpatient
individual or group treatment services provided by a clinician to assist
recipients and their families to achieve treatment objectives through the
exploration of SUDs and their ramifications, including an examination of
attitudes and feelings, and consideration of alternative solutions and decision
making with regard to substance misuse.
(h) “Integrated service model” means a model
whereby SUD treatment and recovery support services, health care services, and
mental health services are provided by a team of practitioners within a single
program.
(i) “Intensive
outpatient SUD services” means intensive and structured individual and group
alcohol or other drug treatment services and activities that are provided at least
9 hours a week for recipients age 21 and over, and at least 6 hours a week for
recipients under age 21, according to an individualized treatment plan that
include a range of outpatient treatment services and other ancillary alcohol or
other drug services.
(j) “Licensed mental health provider” means a
psychotherapist licensed by the NH board of mental health practice or the NH
board of psychologists, or an advanced practice registered nurse (APRN) with a
psychiatric specialty.
(k) “Lived Experience” means that an individual
has direct, personal experience with either their own recovery from a substance
use disorder or that of a family member.
(l) “Medicaid” means the Title XIX and Title XXI
programs administered by the department, which makes medical assistance
available to eligible individuals.
(m) “Office-based
medication assisted substance use disorder treatment” means medication
prescription and monitoring by a licensed prescriber for the purpose of
treating a SUD, including clinically appropriate referral to, and coordination
with, SUD treatment providers within the prescriber’s practice or externally.
(n) “Opioid treatment services” means treatment
for opioid use disorders using a combination of approved medications, limited
to methadone and buprenorphine, and behavioral health services which is
delivered by an agency certified as an opioid treatment program in accordance
with He-A 304.03.
(o) “Outpatient,
group treatment” means services provided by a clinician to assist 2 or more
individuals to achieve treatment objectives through the exploration of
substance use disorders and their ramifications, including an examination of
attitudes and feelings, and consideration of alternative solutions and decision
making with regard to substance misuse.
(p) “Outpatient, individual treatment” means
services provided by a clinician to assist an individual to achieve treatment
objectives through the exploration of substance use disorders and their
ramifications, including an examination of attitudes and feelings, and
consideration of alternative solutions and decision making with regard to
substance misuse.
(q) “Outpatient
SUD program” means an agency which provides specialty SUD treatment and
recovery support services on an outpatient basis and which is:
(1) Under
contract with or agreement with the department;
(2) A hospital
enrolled in medicaid both as a hospital in accordance
with He-W 543 and as an outpatient SUD program in accordance with He-W 513;
(3) A provider
enrolled in medicaid in the state in which they
practice to provide intensive outpatient services consistent with Level 2.1, as
set forth in ASAM Criteria (2013), available as noted in Appendix A, or partial
hospitalization consistent with Level 2.5, as set forth in ASAM Criteria
(2013), available as noted in Appendix A, and who is also enrolled in NH
Medicaid;
(4) Under
current primary care services contract obligation with the maternal and child
health section of the NH division of public health services;
(5) A medicaid enrolled community mental health center;
(6) A medicaid enrolled
Federally Qualified Health Center (FQHC), as defined in section 1905(l)(2)(B)
of the Social Security Act, or a medicaid enrolled
Rural Health Clinic (RHC), as defined in section 1905(l)(1) of the Social
Security Act; or
(7) An opioid
treatment program which is certified as such in accordance with He-A 304.03.
(r) “Partial hospitalization services” means
intensive and structured individual and group treatment of moderate to severe
co-occurring substance use and other mental health disorder(s) that are
provided at least 20 hours per week.
(s) “Peer
recovery coach” means an individual who meets the requirements set out in He-W
513.05(r)(4).
(t) “Peer recovery program” means a recovery community
organization or program that is accredited by the Council on Accreditation of
Peer Recovery Support Services (CAPRSS), is accredited by Clubhouse
International, is under contract with the department’s contracted facilitating
organization, or is under contract with the department’s BDAS to provide peer
recovery support services.
(u) “Peer recovery support services” means
non-clinical recovery support services which are recipient directed and
delivered by peers who have common life experiences with the
recipients they are serving.
(v) “Recipient” means any individual who is
eligible for and receiving medical assistance under the medicaid
program.
(w) “Recovery support services” means
non-clinical services that are provided to recipients to support their recovery
from substance use disorders and prevent relapse.
(x) “Rehabilitative services” means 24-hour per
day non-acute care in a non-hospital, residential treatment program where a
planned program of professionally directed evaluation, care, and treatment for
the restoration of functioning for persons with substance use disorders occurs.
(y) “Screening” means a brief process designed to
identify an individual who is misusing substances, or is at risk for developing
a substance use disorder, by using a screening instrument and evaluating
responses to questions about alcohol and other drug use.
(z) “Screening, brief intervention, and referral
to treatment (SBIRT)” means a comprehensive, integrated public health approach
for early identification and intervention with patients whose alcohol or drug
use may put their health at risk.
(aa)
“Substance use disorder (SUD)” means a cluster of symptoms meeting the
criteria for SUD as set forth in the Diagnostic and Statistical Manual of
Mental Disorders, 5th edition (DSM-5) (2013), available as noted in
Appendix A.
(ab) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(ac) “Title XXI” means the joint federal-state
program described in Title XXI of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(ad) “Treatment plan” means an action plan,
written in behavioral terms, which:
(1) Is consistent with the competencies described in
Section 2: Practice Dimensions, II. Treatment Planning of the “Addiction
Counseling Competencies, TAP 21” (2017 revision), available as noted in
Appendix A;
(2) Is based
on evaluation data;
(3) Identifies
the recipient’s clinical needs, treatment goals, and objectives;
(4) Defines
the strategy for providing services to meet those needs, goals, and objectives;
(5) Provides
the criteria for terminating specific interventions; and
(6) Includes
specification and description of the indicators to be used to assess the
individual’s progress.
Source. #10655, INTERIM, eff 8-15-14, EXPIRES:
2-11-15; ss by #10779, eff 2-11-15; ss by #10922, eff 9-1-15; ss by #11107, eff
7-1-16; amd by #12012, INTERIM, eff 10-25-16,
EXPIRES: 4-23-17; amd by #12131, eff 3-10-17; ss by
#12681, eff 11-27-18
He-W
513.03 Recipient Eligibility.
(a) All recipients shall be eligible for SUD
treatment and recovery support services in accordance with this part and He-W
506.
(b) In order to receive SUD treatment and
recovery support services, other than SBIRT pursuant to He-W 513.05(c),
substance use screenings pursuant to He-W 513.05(d), crisis intervention
pursuant to He-W 513.05(q), peer recovery support pursuant to He-W 513.05(r),
non-peer recovery support pursuant to He-W 513.05(s), continuous recovery
monitoring pursuant to He-W 513.05(t), and evaluations pursuant to He-W 513.05(u),
the recipient shall have been determined to have a SUD by undergoing a clinical
evaluation in accordance with He-W 513.05(u) to determine the level of care and
ensuing treatment plan to be followed.
Source. #10655, INTERIM, eff 8-15-14, EXPIRES:
2-11-15; ss by #10779, eff 2-11-15; ss by #10922, eff 9-1-15; ss by #11107, eff
7-1-16; ss by #12681, eff 11-27-18
He-W 513.04 Provider
Participation.
(a) All SUD treatment and recovery support
service providers shall be enrolled as a New Hampshire medicaid
provider.
(b) SUD treatment and recovery support service
practitioners shall meet the provider requirements in He-W 531.05 for the
services they are enrolling to provide.
(c) Individual practitioners delivering services
as part of a medicaid enrolled outpatient SUD program or medicaid
enrolled comprehensive SUD program
shall be allowed to delegate, in accordance with scope of law and practice, the
performance of SUD treatment and recovery support services to individuals under
their supervision in such program, and subject to the following restrictions:
(1) With the exception of those licensed alcohol and
drug counselors (LADCs) who are permitted to engage in independent practice in
accordance with Chapter Law 189:2, II, Laws of 2008, and Chapter Law 249:24, V,
Laws of 2010, LADCs shall only provide SUD treatment and recovery support
services under the supervision of:
a. A master licensed alcohol
and drug counselor (MLADC) who is on the staff of a medicaid
enrolled outpatient SUD program or comprehensive SUD program;
b. A LADC who is permitted to
engage in independent practice in accordance with Chapter Law 189:2, II, Laws
of 2008, and Chapter Law 249:24, V, Laws of 2010, who also is a licensed
clinical supervisor (LCS), and who is on the staff of a medicaid
enrolled outpatient SUD program or comprehensive SUD program; or
c. A licensed mental health
provider who is on the staff of a medicaid enrolled
outpatient SUD program or comprehensive SUD program;
(2)
Supervision requirements for SUD recovery support services shall be as
follows:
a. A
certified recovery support worker (CRSW) shall be supervised by one of the
following:
1. An MLADC
who is on the staff of or under contract with a medicaid
enrolled outpatient SUD program, comprehensive SUD program, or peer recovery
program;
2 A LADC who
is permitted to engage in independent practice in accordance with Chapter Law
189:2, II, Laws of 2008, and Chapter Law 249:24, V, Laws of 2010, who also is
an LCS and who is on the staff of or under contract with a medicaid
enrolled outpatient SUD program, comprehensive SUD program, or peer recovery
program;
3. A LADC who is on the staff of or under contract
with a medicaid enrolled outpatient SUD program,
comprehensive SUD program, or peer recovery program;
4. A CRSW who
has been certified for one year and has taken 6 hours of supervisory training
and 6 hours of practical training which has been approved by the board pursuant
to Alc 409.01; or
5. A licensed
mental health provider who is on the staff of or under contract with a medicaid enrolled outpatient SUD program, comprehensive SUD
program, or peer recovery program;
b. A LADC delivering recovery
support services shall be supervised by an MLADC who is on the staff of or
under contract with a medicaid enrolled outpatient
SUD program, comprehensive SUD program, or peer recovery program; and
c An MLADC delivering recovery
support services shall not require supervision;
(3)
Individuals who meet the following criteria shall only provide services
under the supervision of an MLADC or licensed mental health provider who is on
the staff of a medicaid enrolled outpatient SUD
program or comprehensive SUD program:
a. The individual shall be
enrolled in a formal internship for at least a master’s degree in a clinical
discipline that meets the requirements for initial licensing as an MLADC
pursuant to RSA 330-C:16, I, or
b. The individual shall:
1. Have
completed at least one year of work in the field of substance use disorders
treatment under the supervision of an MLADC or licensed mental health provider;
2. Have at
least a master’s degree in a clinical discipline that meets the requirements
for initial licensing as an MLADC pursuant to RSA 330-C:16, I; and
3. Be working
to accumulate the work experience required for licensure;
(4)
Individuals who meet the criteria below shall only provide services
under the supervision of a psychologist who is on the staff of a medicaid enrolled outpatient SUD program or comprehensive
SUD program:
a. The individual shall be
enrolled in a formal internship for at least a master’s program that meets the
requirements for initial licensure by the NH board of psychologists pursuant to
RSA 329-B; or
b. The individual shall:
1. Have
completed at least one year of work in the field of substance use disorders
treatment under the supervision of a person licensed by the NH board of
psychologists;
2. Have at
least a master’s degree that meets the requirements for initial licensure by
the NH board of psychologists pursuant to RSA 329-B; and
3. Be working
to accumulate the work experience required for licensure;
(5)
Individuals who meet the criteria below shall only provide services
under the supervision of a psychotherapist who is on the staff of a medicaid enrolled outpatient SUD program or comprehensive
SUD program:
a. The individual shall be
enrolled in a formal internship for at least a master’s program that meets the
requirements for initial licensure by the NH board of mental health practice
pursuant to RSA 330-A; or
b. The individual shall:
1. Have
completed at least one year of work in the field of substance use disorders
treatment under the supervision of a psychotherapist;
2. Have at least a master’s degree that meets the
requirements for initial licensure by the NH board of mental health practice
pursuant to RSA 330-A; and
3. Be working
to accumulate the work experience required for licensure;
(6)
Individuals who qualify to provide services pursuant to He-W
513.04(c)(3) – (5) above and who hold at least a master’s degree shall have
ongoing supervision of at least 2 hours per month as follows:
a. There shall be direct,
individual, or group supervision of at least one hour per month by the
supervising practitioner noted in (3) -(5) above; and
b. The second hour of
supervision may be peer review or case review, such as client-centered
conferences;
(7)
Individuals who qualify to provide services pursuant to He-W
513.04(c)(3) – (5) above and who are enrolled in a formal internship shall
receive direct supervision as follows:
a. There shall be direct
supervision of at least one hour per week;
b. The supervisor shall write and sign a weekly note in the intern’s
supervisory record stating his or her observations and recommendations relative
to the intern’s performance; and
c. The supervisor shall write
and sign a monthly note in the intern’s supervisory record summarizing his or
her evaluation;
(8) The medicaid program shall reimburse the
outpatient or comprehensive SUD program only if the supervision required in
accordance with He-W 513.04(c)(3) - (7) occurs and is documented;
(9) The
delegated services shall be billed by the outpatient or comprehensive SUD
program; and
(10) A LADC
who is permitted to engage in independent practice in accordance with Chapter
Law 189:2, II, Laws of 2008, and Chapter Law 249:24, V, Laws of 2010, shall not
provide supervision to an MLADC for the purposes of providing services under
He-W 513.
(d) SUD
treatment and recovery support service providers shall ensure that the
recipient has undergone a clinical evaluation, as required by He-W 513.03(b)
above, prior to the provider’s delivery of other SUD treatment and recovery support
services.
(e) SUD treatment and recovery support service
providers shall ensure that all SUD treatment and recovery support services are
provided and documented in accordance with the Health Insurance Portability and
Accountability Act (HIPAA) of 1996, 45 CFR 160, 45 CFR 164, Subparts A and E,
and 42 CFR, Part II.
(f) SUD treatment and recovery support service
providers shall ensure that any SUD group treatment and recovery support
services described in He-W 513.05 below are delivered in accordance with the
following:
(1) Services
shall only be covered when 2 or more individuals are present for a group
service;
(2) SUD treatment groups shall include no more than
12 individuals with one licensed practitioner present or no more than 16
individuals when that licensed practitioner is joined by a CRSW or a second
licensed practitioner;
(3) Recovery
support groups shall include no more than 8 individuals with one CRSW present
or no more than 12 individuals when that CRSW is joined by a second CRSW; and
(4) Peer recovery support groups shall include no
more than 8 individuals with one peer recovery coach present or no more than 12
individuals when that peer recovery coach is joined by a second peer recovery
coach.
(g) SUD treatment service providers shall ensure
that all covered services are provided in accordance with criteria as set forth
in ASAM Criteria (2013), available as noted in Appendix A, except for SBIRT
services provided in accordance with He-W 513.05(c), substance use screening
provided in accordance with He-W 513.05(d), crisis intervention provided in
accordance with He-W 513.05(q), and evaluations provided in accordance with
He-W 513.05(u).
(h) All SUD treatment and recovery support
service providers shall treat co-occurring disorders in accordance with scope
of law and practice.
(i) Except as in (j)
below, LADCs, and MLADCs who are delivering or supervising SUD treatment and
recovery support services shall be licensed by the NH board of licensing for
alcohol and other drug use professionals.
(j) Providers who hold a reciprocal international
certification and reciprocity consortium/alcohol and other drug abuse
(IC&RC) license shall be considered to have met the requirement in (i) above for the purpose of He-W 513.
(k) New
Hampshire enrolled out of state providers whose license or certification allows
them to provide SUD services in the state in which they practice shall be
considered to have met the requirements in (i) above.
(l) Hospitals enrolled in medicaid
as a hospital in accordance with He-W 543 shall also be enrolled in medicaid as an outpatient or comprehensive SUD program in
order to provide outpatient or comprehensive SUD services in accordance with
He-W 513.05.
(m) Providers
who are enrolled in other states and who meet the definition of outpatient or
comprehensive SUD programs in accordance with He-W 513.02 (b) or (q) shall also
be enrolled in NH medicaid in order to provide
outpatient or comprehensive SUD services in accordance with He-W 513.05.
(n) Providers
who are employed by, or under contract with, a comprehensive or outpatient SUD
program shall be considered to be on the staff of that program.
Source. #10655, INTERIM, eff 8-15-14, EXPIRES:
2-11-15; ss by #10779, eff 2-11-15; ss by #10922, eff 9-1-15; ss by #11107, eff
7-1-16; amd by #12131, eff 3-10-17; ss by #12681, eff
11-27-18
He-W
513.05 Covered Services.
(a) SUD treatment and recovery support services
shall be covered in accordance with this section.
(b) In order for the services described in this
section to be covered, they shall:
(1) Be
delivered in accordance with appropriate guidelines that are consistent with
generally accepted standards of care in the ASAM Criteria (2013), available as
noted in Appendix A;
(2) Include continuing care, transfer, and discharge
plans that address all domains in ASAM Criteria (2013), available as noted in
Appendix A, as follows:
a. Plans shall include the
process of transfer and discharge planning at the time of the recipient’s
intake to the program;
b. Plans for continuing care
shall include at least one of the 3 following criteria for continuing services:
1. The
recipient is making progress but has not yet achieved the goals articulated in
the individualized treatment plan, and continued treatment at the present level
of care is assessed as necessary to permit the recipient to continue to work
toward his or her treatment goals;
2. The
recipient is not yet making progress, but has the capacity to resolve his or
her problems, is actively working toward the goals articulated in the
individualized treatment plan, and continued treatment at the present level of
care is assessed as necessary to permit the recipient to continue to work
toward his or her treatment goals; or
3. New
problems have been identified that are appropriately treated at the present
level of care and that requires services at a frequency and intensity that can
only safely be delivered by the recipient’s continued stay in the current level
of care; and
c. Plans for transfer or
discharge planning shall include at least one of the 4 following criteria:
1. The
recipient has achieved the goals articulated in the individualized treatment
plan thus resolving the problem or problems that justified admission to the
present level of care and continuing chronic disease management of the
recipient’s condition at a less intensive level of care is indicated;
2. The
recipient has been unable to resolve the problem or problems that justified the
admission to the present level of care despite amendments to the treatment plan
and has been determined to have met the maximum possible benefit from
engagement in services at the current level of care, so transfer or discharge
from treatment is indicated;
3. The
recipient has demonstrated a lack of capacity due to diagnostic or co-occurring
conditions that limit his or her ability to resolve his or her problem, so
treatment at a qualitatively different level of care or type of service, or
discharge from treatment is indicated; or
4. The
recipient has experienced an intensification of his or her problem or problems
or has developed a new problem or problems and can be treated effectively at a
more intensive level of care;
(3) Be
evidence based, as demonstrated by meeting one of the following criteria:
a. The service shall be
included as an evidence-based mental
health and substance abuse intervention on the
SAMHSA Evidence-Based Practices Resource Center available at
https://www.samhsa.gov/ebp-resource-center;
b. The services shall be
published in a peer-reviewed journal and found to have positive effects; or
c. The SUD treatment and
recovery support service provider shall be able to document the services’ effectiveness
based on the following:
1. The service
is based on a theoretical perspective that has validated research; or
2. The service is supported by a documented body of
knowledge generated from similar or related services that indicate effectiveness;
(4) When
clinically appropriate, include referral to, and assistance in accessing,
medication assisted SUD treatment either on site or off site;
(5) Include an
assessment of all recipients for risk of self-harm at all phases of treatment,
such as at initial contact, during screening, intake, admission, on-going
treatment services, and at discharge;
(6) With the
exception of peer and non-peer recovery and continuous recovery monitoring, be
consistent with the “Addiction Counseling Competencies, TAP 21” (2017
revision), available as noted in Appendix A;
(7) Be
provided in accordance with the ASAM Level of Care service descriptions, as
applicable, noted in He-W 513.11; and
(8) Be
provided at a length of time and frequency of care based on individual client
need in accordance with ASAM Criteria (2013), available as noted in Appendix A,
and not on predetermined time or frequency limits.
(c) Screening, brief intervention, and referral
to treatment (SBIRT) shall be a covered service when provided as follows:
(1) The screening shall be
provided for the purpose of identifying individuals who have an alcohol or drug
use problem or who are at risk for developing one;
(2) The screening shall be
conducted by evaluating responses to questions as described in (3) below about
the context, frequency, and amount of alcohol and other drug use;
(3) The screening shall be
performed using a screening instrument listed in Appendix E of “Systems-Level
Implementation of Screening, Brief Intervention, and Referral to Treatment, TAP
33” (2013 edition), available as noted in Appendix A;
(4) SBIRT
shall be provided with and billed with another medical service;
(5) SBIRT shall be conducted by
a provider who has been trained in the SBIRT model and is either:
a. A medicaid
enrolled physician or APRN;
b. A medicaid enrolled physician assistant,
or other practitioner under a physician’s supervision; or
c. A practitioner working in an
outpatient SUD program as defined in He-W 513.02(q)(4) or He-W 513.02(q)(6) who
is either:
1. A physician or APRN; or
2. A physician assistant or
other practitioner under a physician’s supervision;
(6) SBIRT shall be performed in
the primary care practitioner’s office or other health care settings not
specific to the delivery of SUD treatment and recovery support services;
(7) The services provided by
the providers described in (5)a. above shall be billed by the medicaid enrolled practitioner; and
(8) The services provided by
the providers described in (5)b. above shall be billed by the supervising
physician.
(d) SUD screening shall be a covered service when
provided as follows:
(1) The screening shall be
provided for the purpose of identifying individuals who have an alcohol or drug
use problem or who are at risk for developing one;
(2) The screening shall be
conducted by evaluating responses to questions as described in (3) below about
the context, frequency, and amount of alcohol and other drug use;
(3) The screening shall be
performed using a screening instrument listed in Appendix E of “Systems-Level
Implementation of Screening, Brief Intervention, and Referral to Treatment, TAP
33” (2013 edition), available as noted in Appendix A;
(4) Except as allowed in (5)
and (6) below, the screening shall be performed by medicaid
enrolled psychotherapy providers licensed by the NH board of mental health
practice, medicaid enrolled psychotherapy providers
licensed by the NH board of psychology, medicaid
enrolled MLADCs licensed by the NH board of licensing for alcohol and other
drug use professionals, LADCs who
are permitted to engage in independent practice in accordance with Chapter Law
189:2, II, Laws of 2008, and Chapter Law 249:24, V, Laws of 2010, medicaid enrolled outpatient SUD programs,
or medicaid enrolled comprehensive SUD programs; and
(5) The screening may be
performed by individuals who are allowed to do such screenings under the
supervision of the providers in (4) above in accordance with RSA 329-B, RSA
330-A, or RSA 330-C as follows:
a. The
restrictions described in He-W 513.04(c) shall not apply; and
b. Such screenings shall be billed by the supervising
practitioner or the outpatient or comprehensive SUD program.
(e) Opioid treatment services shall be a covered
service when provided as follows:
(1) Opioid treatment services
shall be provided by medicaid enrolled providers who
meet the medical services clinic requirements in He-W 536 and are certified as
an opioid treatment program in accordance with He-A 304.03;
(2) Opioid treatment providers
shall operate and provide services in accordance with He-A 304;
(3) Opioid treatment services
shall be delivered in accordance with a treatment plan;
(4) Opioid treatment services
shall be limited to treatment with methadone or buprenorphine;
(5) Opioid treatment services
shall be inclusive of the necessary components of the daily opioid treatment
services, such as intake services, medication counseling, administration,
medical supervision of vitals, observation afterwards, urine testing, and blood
and lab work;
(6) SUD treatment and recovery
support services may be provided in conjunction with the opioid treatment
services and may be billed separately from the opioid treatment service; and
(7) Except as specified in (5)
above, opioid treatment services shall be billed in accordance with He-W 536.
(f)
Pharmaceuticals prescribed for SUD treatment services shall be covered
in accordance with He-W 570.
(g)
Office-based medication assisted SUD treatment shall be a covered
service when provided as follows:
(1) Office-based medication
assisted SUD treatment via buprenorphine shall be provided by medicaid enrolled providers who:
a. Have
obtained a waiver in accordance with the Drug Addiction Treatment Act of 2000
(DATA 2000), Title XXXV, Section 3502 of the Children’s Health Act of 2000, to
treat opioid addiction with Schedule III, IV, and V narcotic medications; and
b. Provide services in accordance with TIP 63: Medications for Opioid Use Disorder (2018), available at https://store.samhsa.gov/product/tip-63-medications-opioid-use-disorder-%E2%80%93-full-document-including-executive-summary-parts-1-5
and as noted in Appendix A;
(2) Office-based medication
assisted SUD treatment shall be provided by medicaid
enrolled providers who meet the physician requirements in He-W 531 or the
advanced practice registered nurse requirements in He-W 534;
(3) Office-based medication
assisted SUD treatment shall be delivered in accordance with a treatment plan;
(4) The writing of the
prescription shall be a component of an office visit;
(5) The provider shall:
a. Refer the
recipient to clinically appropriate SUD treatment and recovery services as
described in He-W 513; and
b. Coordinate
care with the SUD treatment and recovery provider within or external to the office
based practice;
(6) Office-based medication
assisted SUD shall be billed by the prescribing provider, outpatient SUD
program, or comprehensive SUD program; and
(7) The prescribing provider
shall be listed as the rendering provider on the claim.
(h) Outpatient, individual treatment consistent
with Level 1, as set forth in ASAM Criteria (2013), available as noted in
Appendix A, shall be a covered service when provided as follows:
(1) Outpatient, individual
treatment shall be delivered in accordance with a treatment plan;
(2) Outpatient, individual treatment shall be covered when provided by
medicaid enrolled psychotherapists licensed by the NH
board of mental health practice or the NH board of psychologists, medicaid enrolled MLADCs licensed by the NH board of
licensing for alcohol and other drug use professionals, LADCs who are permitted to engage in independent practice
in accordance with Chapter Law 189:2, II, Laws of 2008, and Chapter Law 249:24,
V, Laws of 2010, medicaid enrolled physicians or advanced practice registered nurses (APRNs), medicaid enrolled outpatient SUD programs, or medicaid enrolled comprehensive SUD programs; and
(3) Outpatient, individual
treatment shall be billed by the medicaid enrolled
individual or group practitioner or by the outpatient or comprehensive SUD
program.
(i) Group treatment
consistent with Level 1, as set forth in ASAM Criteria (2013), available as
noted in Appendix A, shall be a covered service when provided as follows:
(1) Group
treatment shall meet the requirements in He-W 513.04(f);
(2) Group
treatment shall be delivered in accordance with a treatment plan;
(3) Group treatment shall be covered when provided by
medicaid enrolled psychotherapists
licensed by the NH board of mental health practice or the NH board of
psychologists, medicaid enrolled MLADCs licensed by
the NH board of licensing for alcohol and other drug use professionals, LADCs who are permitted to engage in independent practice
in accordance with Chapter Law 189:2, II, Laws of 2008, and Chapter Law 249:24,
V, Laws of 2010, medicaid enrolled physicians or APRNs, medicaid
enrolled outpatient SUD programs, or medicaid
enrolled comprehensive SUD programs; and
(4) Group treatment shall be
billed by the medicaid enrolled individual or group
practitioner or by the outpatient or comprehensive SUD program.
(j) Family treatment consistent with Level 1, as
set forth in ASAM Criteria (2013), available as noted in Appendix A, shall be a
covered service when provided as follows:
(1) Family
treatment shall be provided to either:
a. The recipient; or
b. The recipient’s family members or significant others, either with
or without the recipient present, if treatment is related to the recipient’s
SUD;
(2) Family
treatment shall be delivered in accordance with a treatment plan;
(3) Family
treatment shall be covered when provided by medicaid enrolled psychotherapists licensed by the NH
board of mental health practice or the NH board of psychologists, medicaid enrolled MLADCs licensed by the NH board of
licensing for alcohol and other drug use professionals, LADCs who are permitted to engage in independent practice
in accordance with Chapter Law 189:2, II, Laws of 2008, and Chapter Law 249:24,
V, Laws of 2010, medicaid enrolled physicians or APRNs, medicaid
enrolled outpatient SUD programs, or medicaid
enrolled comprehensive SUD programs; and
(4) Family treatment shall be
billed by the medicaid enrolled individual or group
practitioner or by the outpatient or comprehensive SUD program.
(k) Intensive outpatient SUD services consistent
with Level 2.1, as set forth in ASAM Criteria (2013), available as noted in
Appendix A, shall be a covered service when provided as follows:
(1) Intensive
outpatient SUD services shall be covered when they are:
a. Provided by medicaid enrolled outpatient or comprehensive SUD programs;
and
b. Delivered by the following
practitioners:
1. Psychotherapists licensed by
the NH board of mental health practice or the
NH board of psychologists; or
2. MLADCs licensed by the NH
board of licensing for alcohol and other drug use professionals;
(2) Intensive
outpatient SUD services shall be comprised of a combination of individual and
group treatment services at least 9 hours per week for recipients age 21 and over
and at least 6 hours per week for recipients under age 21;
(3) Group
treatment shall meet the requirements in He-W 513.04(f);
(4) Intensive
outpatient SUD services shall be delivered in accordance with a treatment plan;
(5) Intensive
outpatient SUD services shall be comprised of a range of outpatient treatment
services and other ancillary alcohol or drug treatment services to include all
of the following:
a. Evaluation;
b. Individual, group, or family
treatment;
c. Crisis intervention;
d. Activity therapies; and
e. Substance use prevention
education; and
(6) Intensive
outpatient SUD services shall be billed by the outpatient or comprehensive SUD
program.
(l) Partial hospitalization services consistent
with Level 2.5, as set forth in ASAM Criteria (2013), available as noted in
Appendix A, shall be a covered service when provided as follows:
(1) Partial
hospitalization services shall be:
a. Provided to recipients with
moderate to severe co-occurring SUD and mental health disorders as described in
DSM-5 (2013), available as noted in Appendix A;
b. Provided by a medicaid enrolled outpatient or comprehensive SUD treatment
program; and
c. Delivered by the following
practitioners:
1. For all partial
hospitalization services, except medication management:
(i)
Psychotherapists licensed by the NH board of mental health practice or
the NH board of psychologists; or
(ii) MLADCs licensed by the NH
board of licensing for alcohol and other drug use professionals; and
2. For medication management
services:
(i)
Psychiatrists licensed by the NH board of medicine; or
(ii) APRNs with a psychiatric
specialty;
(2) Partial hospitalization
shall address both disorders and be comprised of a range of outpatient
treatment services and other ancillary mental health and alcohol or drug
treatment services to include all of the following:
a. Evaluation;
b. Individual, group, or family
treatment;
c. Crisis intervention;
d. Activities therapies;
e. Medication management, which shall include psychiatric services,
including psychotropic medication management services as applicable; and
f. Substance use prevention
education;
(3) Services shall be provided
at least 20 hours per week;
(4) Group
sessions shall meet the requirements in He-W 513.04(f); and
(5) Services shall be billed by
the outpatient or comprehensive SUD program.
(m) Rehabilitative services shall be a covered
service when provided as follows:
(1) Rehabilitative services
shall be:
a. Provided by a medicaid enrolled comprehensive SUD program;
b. Delivered by the following
practitioners:
1. Psychotherapists licensed by
the NH board of mental health practice or the NH board of psychologists;
2. MLADCs licensed by the NH
board of licensing for alcohol and other drug use professionals;
3. Physicians; or
4. Advanced practice registered
nurses (APRN); and
c. Provided as a planned program of professionally directed
evaluation, care, and treatment for the restoration of functioning for persons
with SUDs;
(2) Recipients who are being
treated at an ASAM 3.5 level of care shall be present in the facility at least
22 hours per day; and
(3) Recipients who are being
treated at an ASAM 3.1 level of care shall receive at least 5 hours of clinical
service per week..
(n) Medically monitored outpatient withdrawal
management (WM) consistent with Level 1-WM, as set forth in ASAM Criteria
(2013), available as noted in Appendix A, shall be a covered service when provided as
follows:
(1) Medically
monitored outpatient withdrawal management services shall be provided by a medicaid enrolled outpatient or comprehensive SUD program
and supervised by a licensed physician or
APRN who is on the staff of, or under contract with, the outpatient or comprehensive
SUD program;
(2) Medically monitored
outpatient withdrawal management services shall be organized and delivered by
SUD treatment and mental health personnel and other health care providers who
provide a planned regimen of care in the outpatient setting;
(3) Personnel required in (2)
above shall be:
a. Psychotherapists licensed by the NH board of mental health practice or
the NH board of psychologists on the staff of, or under contract with, the outpatient or comprehensive
SUD program;
b. MLADCs licensed by the NH board of licensing for alcohol and other
drug use professionals on the staff of, or under contract with, the outpatient or comprehensive
SUD program;
c. Licensed physicians on the staff of, or under contract with, the outpatient or comprehensive
SUD program; or
d. Licensed APRNs on the staff of, or under contract with, the outpatient or comprehensive
SUD program;
(4) Medically monitored outpatient withdrawal
management services shall be delivered in accordance with a treatment plan;
(5) Medically
monitored outpatient withdrawal management services shall be provided in
regularly scheduled sessions in accordance with defined policies and procedures
consistent with ASAM Criteria (2013) standards, available as noted in Appendix
A;
(6) Medically
monitored outpatient withdrawal management services shall be provided under an
integrated or collaborative service model; and
(7) Medically monitored outpatient withdrawal
management services shall be billed by the outpatient or comprehensive SUD
program.
(o) Medically monitored residential withdrawal
management consistent with Level 3.7-WM, as set forth in ASAM Criteria (2013),
available as noted in Appendix A, shall be a covered service when provided as
follows:
(1) Medically monitored
residential withdrawal management services shall be provided by a medicaid enrolled comprehensive SUD program;
(2) Medically monitored
residential withdrawal management services shall be organized and delivered by
SUD treatment and mental health personnel and other health care providers who
provide a planned regimen of care in a 24-hour live-in setting;
(3) Personnel required in (2)
above shall be:
a. Psychotherapists licensed by the NH board of mental health practice or
the NH board of psychologists on the staff of, or under contract with, the
comprehensive SUD program;
b. MLADCs licensed by the NH board of licensing for alcohol and other
drug use professionals on the staff of, or under contract with, the
comprehensive SUD program;
c. Licensed physicians on the
staff of, or under contract with, the comprehensive SUD program; or
d. Licensed APRNs on the staff
of, or under contract with, the comprehensive SUD program; and
(4) Medically monitored
residential withdrawal management services shall be billed by the comprehensive
SUD program.
(p) Medically managed withdrawal in an acute care
setting shall be covered for recipients in accordance with the provisions of
He-W 543.
(q) Crisis intervention shall be a covered
service when provided as follows:
(1) Crisis intervention shall
be covered when a recipient, family member, or significant other is facing a crisis or emergency situation and
the crisis intervention is related to the recipient’s SUD;
(2) Crisis
intervention shall be covered when provided by medicaid enrolled psychotherapists licensed by the NH
board of mental health practice or the NH board of psychologists, medicaid enrolled MLADCs licensed by the NH board of
licensing for alcohol and other drug use professionals, LADCs who are permitted to engage in independent practice
in accordance with Chapter Law 189:2, II, Laws of 2008 and Chapter Law 249:24,
V, Laws of 2010, medicaid enrolled physicians or APRNs, medicaid
enrolled outpatient SUD programs, or medicaid
enrolled comprehensive SUD programs; and
(3) Crisis intervention shall
be billed by the medicaid enrolled individual or
group practitioner or by the outpatient or comprehensive SUD program.
(r) Peer recovery support shall be a covered
service when provided as follows:
(1) Peer recovery support
services shall include non-clinical services delivered by peers who
self-identify as having lived experience to help recipients age 12 and above
and families identify and work toward strategies and goals around stabilizing
and sustaining recovery and, as applicable, providing links to professional
treatment and community supports;
(2) Peer recovery support
services shall include:
a. Skill restoration therapy intended to reduce or
remove barriers to achieving and maintaining recovery;
b. Emergency
or crisis services available by telephone;
c. Assistance in accessing transportation services for individuals who lack safe transportation;
d. Individual
skills development and restoration to prevent continuation or recurrence of
substance misuse;
e.
Psychoeducation interventions to support recovery;
f. Development
and periodic revision of a specific recovery plan based on the information
collected through the assessment that shall specify the goals and actions to
address the recovery goals and other services needed by the individual; and
g. Working
with the individual to develop and refine recovery goals;
(3) Peer
recovery support services shall be provided by a medicaid
enrolled peer recovery program;
(4) Peer recovery support
services shall be delivered by a peer recovery coach who shall have:
a. Completed
30 contact hours of recovery coach training approved by:
1. NH Training Institute on
Addictive Disorders;
2. The NH Board of Licensing
for Alcohol and Other Drug Use Professionals;
3. NAADAC, the Association for
Addiction Professionals;
4. AdCare
Education Institute, Inc., of New England;
5. Addiction Technology
Transfer Center; or
6. Connecticut Communities for Addiction Recovery (CCAR) Recovery
Coach Academy (RCA);
b. Completed a
minimum of sixteen contact hours of training in ethics approved by any of the
providers in (r)(4)a.1.-6.;
c. Completed a
minimum of 6 contact hours of training in suicide prevention approved by any of
the providers in (r)(4)a.1.-6.; and
d. Completed a
minimum of 3 contact hours of training on co-occurring mental health and
substance use disorders approved by any of the providers in (r)(4)a.1.-6.;
(5) The individual providing
the services shall be supervised by a practitioner in accordance with He-W
513.04 (c)(2) who is on the staff of, or under contract with, the peer recovery
program who shall have:
a. Completed
the training described in He-W 513.05(r)(4); and
b. Completed 6
contact hours of training in the supervision of individuals delivering peer
recovery support services approved by:
1. NH Training Institute on
Addictive Disorders;
2. The NH Board of Licensing
for Alcohol and Other Drug Use Professionals;
3. NAADAC, the Association for
Addiction Professionals;
4. AdCare
Education Institute, Inc., of New England;
5. Addiction Technology
Transfer Center; or
6. Connecticut Communities for Addiction Recovery (CCAR) Recovery
Coach Academy (RCA);
(6) Peer recovery support
services shall be billed by the peer recovery program; and
(7) The supervising practitioner in (5) above shall be listed as the
rendering provider when billing for services.
(s) Recovery support services shall be a covered
service when provided as follows:
(1) Recovery support services
shall include non-clinical group or individual services consistent with a
recipient’s treatment plan that help to prevent relapse and promote recovery
and community integration for the individual being served;
(2) Recovery support services
shall include:
a. Skill restoration therapy intended to reduce or
remove barriers to achieving and maintaining recovery;
b. Emergency
and crisis services available by telephone;
c. Assistance in accessing transportation services
for individuals who lack safe transportation;
d. Individual
skills development and restoration to prevent continuation or recurrence of
substance misuse;
e.
Psychoeducation interventions to support recovery;
f. Development
and periodic revision of a specific recovery plan based on the information collected
through the assessment that shall specify the goals and actions to address the
recovery goals and other services needed by the individual; and
g. Working
with the individual to develop and refine recovery goals;
(3) Recovery support services shall be provided by a medicaid enrolled outpatient, comprehensive SUD treatment
program, or peer recovery program;
(4) Recovery support services
shall be provided by a CRSW certified by the NH board of licensing for alcohol
and other drug use professionals, by a LADC or MLADC licensed by the board of
licensing for alcohol and other drug use professionals, or by a psychotherapist
licensed by the NH board of mental health practice or the NH board of
psychologists;
(5) The individual providing
the services shall be supervised by a practitioner in accordance with He-W
513.04(c)(2);
(6) Recovery support shall be
billed by the outpatient, comprehensive SUD program, or peer recovery program;
and
(7) The supervising
practitioner in (5) above shall be listed as the rendering provider when
billing for services.
(t) Continuous recovery monitoring shall be a
covered service when provided as follows:
(1) Continuous recovery
monitoring shall include recovery check-ups with recipients on a regular basis,
evaluations of the status of the recipient’s recovery, consideration of a broad
array of recipient needs, and provision of active referral to community
resources as applicable;
(2) Continuous recovery
monitoring shall be provided by a medicaid enrolled
outpatient or comprehensive SUD treatment program or a peer recovery program;
(3) When provided in a peer recovery program, continuous recovery
monitoring shall be provided by an individual described in He-W 513.05(r)(4)
above who is supervised in accordance with He-W 513.04(c)(2) above;
(4) When provided in an outpatient or comprehensive SUD program,
continuous recovery monitoring shall be provided by an individual described in
He-W 513.05(s)(4) who is supervised in accordance with He-W 513.04(c)(2) above;
(5) Continuous recovery
monitoring shall be billed by the outpatient or comprehensive SUD program or
peer recovery program; and
(6) The supervising
practitioner in (3) above shall be listed as the rendering provider when
billing for services.
(u) Evaluations to determine the existence and
severity of the SUD and appropriate level of care for the recipient shall be a
covered service when provided as follows:
(1) An evaluation shall be
covered when provided by a medicaid enrolled
psychotherapist licensed by the NH board of mental health practice or the NH
board of psychologists, medicaid enrolled MLADCs
licensed by the NH board of licensing for alcohol and other drug use
professionals, LADCs who are permitted to engage
in independent practice in accordance with Chapter Law 189:2, II, Laws of 2008
and Chapter Law 249:24, V, Laws of 2010, or medicaid enrolled outpatient or comprehensive SUD programs;
(2) The results of the
evaluation, which shall include the following, shall be maintained in the
recipient’s file:
a. Client identified
problem(s);
b. Summary of data gathered;
c. Diagnostic evaluation interpretive summary, including signs,
symptoms, and progression of the recipient’s involvement with alcohol and other
drugs;
d. Statement regarding provision
of an HIV/AIDS screening and referrals made; and
e. Documentation of the level
of care recommended in accordance with ASAM Criteria (2013), available as noted
in Appendix A;
(3) Evaluations shall be billed
by the medicaid enrolled individual or group
practitioner or by the outpatient or comprehensive SUD program; and
(4) Evaluations shall be
completed within 3 sessions or within 3 days of client admission to services,
whichever is longer.
Source. #10655, INTERIM, eff 8-15-14, EXPIRES:
2-11-15; ss by #10779, eff 2-11-15; ss by #10922, eff 9-1-15; ss by #11107, eff
7-1-16; amd by #12012, INTERIM, eff 10-25-16,
EXPIRES: 4-23-17; amd by #12131, eff 3-10-17; ss by
#12681, eff 11-27-18
He-W 513.06 Non-Covered
Services.
(a) Services that are delivered at a higher level
than the recipient’s level of care, as described in ASAM Criteria (2013),
available as noted in Appendix A, shall not be covered.
(b) Services that are non-evidence based in
accordance with He-W 513.05(b) shall not be covered.
(c) Services that are not specified as covered in
He-W 513.05 shall not be covered.
Source. #10655, INTERIM, eff 8-15-14, EXPIRES:
2-11-15; ss by #10779, eff 2-11-15; ss by #10922, eff 9-1-15; ss by #11107, eff
7-1-16; ss by #12681, eff 11-27-18
He-W
513.07 Utilization Review and Control.
(a) The department’s provider program integrity
unit shall monitor utilization of SUD treatment services to identify, prevent,
and correct potential occurrences of fraud, waste, and abuse, in accordance
with 42 CFR 455, 42 CFR 456, and He-W 520.
(b) Failure to maintain records in accordance
with He-W 520 and He-W 513 shall entitle the department to recoupment of state
and federal medicaid payments made as permitted by 42
CFR 455, 42 CFR 447, and 42 CFR 456.
Source. #10655, INTERIM, eff 8-15-14, EXPIRES:
2-11-15; ss by #10779, eff 2-11-15; ss by #10922, eff 9-1-15; ss by #11107, eff
7-1-16; ss by #12681, eff 11-27-18; ss by #12681, eff 11-27-18
He-W 513.08 Third Party Liability. All third party obligations shall be
exhausted before medicaid may be billed, in
accordance with 42 CFR 433.139.
Source. #10655, INTERIM, eff 8-15-14, EXPIRES:
2-11-15; ss by #10779, eff 2-11-15; ss by #10922, eff 9-1-15; ss by #11107, eff
7-1-16; ss by #12681, eff 11-27-18
He-W
513.09 Payment for Services.
(a) Payment for SUD treatment and recovery
support services shall be made in accordance with rates of reimbursement
established by the department in accordance with RSA 161:4, VI(a).
(b) The rate of reimbursement for rehabilitative
services in a comprehensive SUD program shall:
(1) Be on a per diem basis that
takes into account the ASAM level of care and is inclusive of all component
services rendered;
(2) Not include room and board;
and
(3) Be established by the
department in accordance with RSA 161:4, VI(a).
(c) The rate of reimbursement established by the
department in accordance with RSA 161:4, VI(a) for partial hospitalization,
medical monitored residential withdrawal management, and intensive outpatient
SUD services shall be on a per diem basis inclusive of all component services
rendered.
(d) The rate of reimbursement established by the
department in accordance with RSA 161:4, VI(a), for medically monitored
outpatient withdrawal management shall be on a per visit basis inclusive of all
component services rendered.
(e) SUD providers may bill separately for drug
testing utilizing rapid read tests, except when in conjunction with opioid
treatment services in accordance with He-W 513.05(e).
(f) The SUD treatment and recovery support
services provider shall submit claims for payment to the department’s fiscal
agent.
Source. #10655, INTERIM, eff 8-15-14, EXPIRES:
2-11-15; ss by #10779, eff 2-11-15; ss by #10922, eff 9-1-15; ss by #11107, eff
7-1-16; ss by #12681, eff 11-27-18
He-W
513.10 Documentation.
(a) With the exception of peer recovery programs,
SUD treatment and recovery support services providers shall maintain supporting
records, in accordance with He-W 520 and (b) - (f) below.
(b) Supporting documentation shall include:
(1) A complete record of all
physical examinations, laboratory tests, and treatments including drug and
counseling therapies, whether provided directly or by referral;
(2) A progress note for each
treatment session, including:
a. The treatment modality and
duration;
b. The signature of the primary
therapist for each entry;
c. The primary therapist’s
professional discipline; and
d. The date of each treatment
session; and
(3) A copy of the treatment
plan that is:
a. Updated at least every 4
sessions or 4 weeks, whichever is less frequent;
b. Signed by the provider and
the recipient prior to treatment being rendered; and
c. Signed by the clinical
supervisor, prior to treatment being rendered, if the service is an outpatient
or comprehensive SUD program.
(c) The recipient’s individual record shall
include at a minimum:
(1) The recipient’s name, date
of birth, address, and phone number; and
(2) A copy of the evaluation
described in He-W 513.05(u)(2).
(d) SUD providers that close their treatment and
recovery support programs shall arrange for continued management of all medicaid recipient records as follows:
(1) The provider shall notify
the department in writing of the address where records will be stored;
(2) The provider shall specify
to the department the person who will be managing the records and the person’s
contact information; and
(3) The provider shall arrange
for storage of each record through one or more of the following measures:
a. The provider shall continue
to manage the records and give written assurance to the department that it will
respond to authorized requests for copies of client records within 10 working
days;
b. The provider shall transfer
records of clients who have given written consent to another medicaid enrolled provider; or
c. The provider shall enter
into an agreement with a medicaid enrolled provider
to store and manage records.
(e) All electronic or written documentation shall
be legible and written in English.
(f) The SUD treatment and recovery support
services provider shall provide documentation to the department upon request.
(g) Peer recovery programs shall maintain
supporting records in accordance with He-W 520 and(d), (e), and (f) above, and
shall include the following supporting documentation:
(1). Progress on goals for each
recovery contact including:
a. The type of support received
and duration;
b. The topics addressed with
the recipient;
c. The signature of the person
delivering services; and
d. The date of each recovery
contact;
(2) Where applicable, a copy of
the recovery plan that is:
a. Updated a every session; and
b. Signed by the provider and
the recipient prior to services being rendered; and
(3) The recipient’s name, date
of birth, address, and phone number.
Source. #10655, INTERIM, eff 8-15-14, EXPIRES:
2-11-15; ss by #10779, eff 2-11-15; ss by #10922, eff 9-1-15; ss by #11107, eff
7-1-16; ss by #12681, eff 11-27-18
He-W
513.11 ASAM Level of Care Service
Descriptions. The covered services
in He-W 513.05 above that are required to be provided in accordance with the
levels of care in ASAM Criteria (2013), available as noted in Appendix A, shall
include the following:
(a) Services required to be provided consistent
with Level 1, ASAM Criteria (2013), shall include:
(1) Affiliation with other
levels of care, including:
a. Other levels of specialty substance use disorder treatment for
additional problems identified through a comprehensive biophysical assessment;
and
b. Coordination of services and service planning within a provider
agency, with other providers, and with other human service agencies and systems
such as local health and social services departments;
(2) Continued treatment
planning individualized to the recipient’s needs;
(3) Medical, psychiatric,
psychological, laboratory, and toxicology services on-site or through
consultation or referral, and in accordance with He-W 513.11(h);
(4) Coordinating discharge or
transfer planning an referrals for counseling and community recovery support
groups;
(5) Random drug screening to
monitor and reinforce treatment gains as appropriate to the recipient’s
treatment plan;
(6) Stabilization of imminent
risk;
(7) Services in an amount,
frequency, and intensity appropriate to the objectives of the treatment plan;
(8) For recipients with mental
health conditions, the addressing of the issues of psychotropic medication,
mental health treatment, and their relationship to substance use and addictive
disorders as the need arises;
(9) Skill restoration therapy
to reduce or remove barriers to recipients who are achieving and maintaining
recovery;
(10) Emergency services by
telephone 24 hours a day, 7 days a week;
(11) Assistance in accessing
transportation services for recipients who lack transportation;
(12) Motivational enhancement
and engagement strategies appropriate to the recipient’s stage of readiness and
desire to change;
(13) Family therapy for the
direct benefit of the recipient in accordance with the recipient’s needs and treatment
goals identified in the treatment plan and for the purpose of assisting in the
recipient’s recovery; and
(14) Skilled treatment services
which may include evaluation, individual and group counseling, motivational
enhancement, family therapy with recipient present, psychoeducational groups,
psychotherapy, addiction pharmacotherapy, medication management, or other
skilled therapies;
(b) Services required to be provided consistent
with Level 2.1, ASAM Criteria (2013), shall include:
(1) The services in (a)(1) -
(13) above;
(2) A planned format of
therapies delivered on an individual and group basis and adapted to the
recipient’s developmental stage and comprehension level; and
(3) Skilled treatment services
which:
a. May include evaluation,
individual and group counseling, motivational enhancement, family therapy with individual present,
psychoeducational groups, psychotherapy, addiction pharmacotherapy,
medication management, or other skilled therapies; and
b. Shall be provided a minimum of
9 hours per week for individuals age 21 and over and a minimum of 6 hours per
week for individuals under age 21;
(c) Services required to be provided consistent
with Level 2.5, ASAM Criteria (2013), shall include:
(1) The services in (a)(1) -
(13) above;
(2) A planned format of
therapies delivered on an individual and group basis and adapted to the
patient’s developmental stage and comprehension level; and
(3) Skilled treatment services
which:
a. May include evaluation,
individual and group counseling, motivational enhancement, family therapy with
individual present, psychoeducational groups, psychotherapy, addiction
pharmacotherapy, medication management, or other skilled therapies; and
b. Shall be provided a minimum
of 20 hours per week;
(d) Services required to be provided consistent
with Level 3.1, ASAM Criteria (2013), shall include:
(1) The services in (a)(1) -
(9) and (a)(12) - (13) above;
(2) A planned format of
therapies delivered on an individual and group basis and adapted to the
patient’s developmental stage and comprehension level;
(3) Daily clinical services to
improve the individual’s ability to structure and organize tasks of daily
living and recovery to include individual skills development and restoration to
prevent continuation or recurrence of substance misuse;
(4) Planned clinical program
activities which:
a. Shall be adapted to the
individual’s developmental stage, level of comprehension, level of
understanding, and physical abilities for the purpose of stabilizing and
maintaining the stability of the individual’s substance use disorder symptoms
and to help him or her develop and apply recovery skills;
b. May include relapse
prevention, exploring interpersonal choices, medication education and management, addiction pharmacotherapy,
psychoeducational groups, skill development services, health education,
family reintegration, recovery support services, or development of a social
network supportive of recovery; and
c. Consist of at least 5 hours
per week of professionally directed treatment; and
(5) Monitoring of the
individual’s adherence to taking any prescribed medications or permitted over
the counter medications or supplements;
(e) Services required to be provided consistent
with Level 3.5, ASAM Criteria (2013), available as noted in Appendix A, shall
include:
(1) The services in (a)(1) -
(9) and (a)(12) - (13) above;
(2) A planned format of
therapies delivered on an individual and group basis and adapted to the
patient’s developmental stage and comprehension level;
(3) Daily clinical services to
improve the individual’s ability to structure and organize tasks of daily
living and recovery to include individual skills development and restoration to
prevent continuation or recurrence of substance misuse;
(4) Planned clinical program
activities which:
a. Shall be adapted to the
individual’s developmental stage, level of comprehension, level of
understanding, and physical abilities for the purpose of stabilizing and
maintaining the stability of the individual’s substance use disorder symptoms
and to help him or her develop and apply recovery skills; and
b. May include relapse
prevention, exploring interpersonal choices, medication education and management, addiction pharmacotherapy,
psychoeducational groups, skill development services, health education,
family reintegration, recovery support services, or development of a social
network supportive of recovery; and
(5) Monitoring of the
individual’s adherence to taking any prescribed medications or permitted over
the counter medications or supplements;
(f) Services required to be provided consistent
with Level 1-WM, ASAM Criteria (2013), available as noted in Appendix A, shall
include:
(1) The services in (a)(1) -
(8) and (a)(10) - (11) above;
(2) A comprehensive medical
history and physical examination of the individual at admission;
(3) A range of cognitive, behavioral, medical, mental health, and
other skilled therapies administered to the individual on a group or individual
basis which:
a. Shall be designed to enhance the individual’s understanding of
addiction, the completion of the withdrawal management process, and referral to
an appropriate level of care for continuing treatment;
b. Shall be clinically necessary based on the individual’s progress
through withdrawal management and the assessed needs in ASAM Dimensions 2
through 6; and
c. May include multidisciplinary individualized assessment and
treatment, health education services, and medical nursing care and observation;
(4) Family
involvement in the withdrawal management process for the direct benefit of the
individual in accordance with the individual’s needs and treatment goals
identified in the individual’s treatment plan and for the purpose of assisting
in the individual’s recovery;
(5) Individual
assessment, medication or non-medication methods of withdrawal management,
patient education, non-pharmacological clinical support, and involvement of
family members or significant others in the withdrawal management process with
the individual present; and
(6) Inclusion
in therapies of physician or nurse monitoring, assessment, and management of
signs and symptoms of intoxication and withdrawal;
(g) Services required to be provided consistent
with Level 3.7-WM, ASAM Criteria (2013), available as noted in Appendix A,
shall include:
(1) The services in (a)(1) -
(8) above;
(2) A comprehensive medical
history and physical examination of the individual at admission;
(3) A range of cognitive, behavioral, medical, mental health, and
other skilled therapies administered to the individual on a group or individual
basis which:
a. Shall be designed to enhance the individual’s understanding of
addiction, the completion of the withdrawal management process, and referral to
an appropriate level of care for continuing treatment;
b. Shall be clinically necessary based on the individual’s progress
through withdrawal management and the assessed needs in ASAM Dimensions 2
through 6; and
c. May include multidisciplinary individualized assessment and
treatment, health education services, and medical nursing care and observation;
(4) Family
involvement in the withdrawal management process for the direct benefit of the
individual in accordance with the individual’s needs and treatment goals
identified in the individual’s treatment plan and for the purpose of assisting
in the individual’s recovery;
(5) Daily clinical services to
assess and address the needs of each individual which may include:
a. Appropriate medical
services;
b. Individual and group
therapies; and
c. Withdrawal support; and
(6) Hourly nurse monitoring of
the individual’s progress and medication administration as needed; and
(h) Services described in He-W 513.11(a)(3) shall
be provided in accordance with the following:
(1) Medical and psychiatric
consultation shall be available within 24 hours by telephone or, if in person,
within a time frame appropriate to the severity and urgency of the consultation
requested for services provided at Level 1, ASAM Criteria (2013), available as
noted in Appendix A;
(2) Psychiatric and other
medical consultation shall be available within 24 hours by telephone and within
72 hours in person for services provided at Level 2.1, ASAM Criteria (2013),
available as noted in Appendix A;
(3) Psychiatric and other
medical consultation shall be available within 8 hours by telephone and within
48 hours in person for services provided at Level 2.5, ASAM Criteria (2013),
available as noted in Appendix A; and
(4) Telephone or in-person consultation
with a physician or any other
practitioner licensed to perform the duties designated for a physician shall be
available 24 hours a day, 7 days a week for emergency services provided at
Level l-WM and Level 3.7-WM, ASAM Criteria (2013), available as noted in
Appendix A.
Source. #12681, eff 11-27-18
He-W
513.12 Waivers.
(a) Medicaid providers or the director of the
bureau of drug and alcohol services (BDAS) seeking waivers of specific rules in
He-W 513 shall submit a written request for a waiver to the commissioner that
shall include:
(1) The specific reference to the rule for which
a waiver is being sought;
(2) A full
explanation of why a waiver is necessary;
(3) The time
period for which the waiver is requested and a full explanation of why this
time period is being requested; and
(4) A full
explanation of alternatives proposed which shall detail how the intent of the
rule will be satisfied if the waiver is granted.
(b)
A request for waiver shall be granted if the commissioner determines
that the waiver would:
(1) Meet the objective or intent of the rule;
(2) Rectify problems unforeseen by the rule;
(3) Meet the provider requirements of the federal
regulations and the medicaid state plan; and
(4) Not waive or modify any state statute or
federal requirement unless such statute or requirement allows for such waiver.
(c)
The duration of the waiver shall be based on the information in (a)(3)
above.
(d)
The medicaid provider’s or BDAS’ subsequent
compliance with the alternatives approved in the waiver shall be considered
equivalent to complying with the rule from which the waiver was sought.
(e)
Waivers shall not be transferable.
(f)
When a medicaid provider or BDAS wishes to
renew a non-permanent waiver beyond the approved period of time, they shall
apply for a new waiver at least 60 days prior to the expiration of the existing
waiver by submitting the information required by (a) above.
(g)
The request to renew a waiver shall be subject to (b) through (f) above.
Source. #12681, eff 11-27-18
PARTS
He-W 514 THROUGH 518 RESERVED
PART He-W
519 PAYMENTS TO DISPROPORTIONATE SHARE
PSYCHIATRIC HOSPITALS
Source. (See Revision Note at chapter heading He-W
500); ss by #6642, eff 11-27-97; moved by #8432, eff 11-27-05 (see He-M 601)
PART He-W 520 GENERAL PROGRAM INFORMATION
He-W 520.01 Definitions.
(a)
“Department” means the New Hampshire department of health and human
services.
(b) “Direct ownership interest” means the
possession of equity of 5% or greater in capital, stock, or profits of the
provider or provider applicant.
(c)
“Early and periodic screening, diagnosis, and treatment (EPSDT)” means a
program pursuant to 42 CFR 440.40, designed to provide medical care to
recipients under the age of 21.
(d)
“High
risk provider or high risk provider applicant” means an individual or entity
which meets one of the criteria in He-W 520.06(c).
(e) “Indirect ownership interest” means an
ownership interest of 5% or greater in an entity that has a direct ownership
interest in the provider or provider applicant.
(f) “Medicaid” means the Title XIX and Title XXI
programs administered by the department, which makes medical assistance
available to eligible individuals.
(g) “Medicaid management information system
(MMIS)” means the general system for mechanized claims processing and
information retrieval recommended by the Centers for Medicare and Medicaid
Services (CMS) for the implementation of the requirements of state fiscal
administration pursuant to 42 CFR 433, Subpart C.
(h) “Presumptive eligibility” means an
eligibility period as described in Section 1920A of the Social Security Act
during which eligibility for a child is determined for the medicaid
program.
(i) “Provider” means
an entity or individual who furnishes health care services or supplies to medicaid recipients under an agreement with the department.
(j) “Provider applicant” means an individual or
entity who is undergoing the provider enrollment or re-enrollment process to
become a New Hampshire medicaid provider.
(k) “Qualified entity” means an entity authorized
and trained by the department to determine presumptive eligibility pursuant to
the provisions of Section 1920A(b)(3)(A) of the Social Security Act, including
providers that are:
(1) Title V-funded family and community health
agencies;
(2) Title X family planning agencies;
(3) Hospitals;
(4) Agencies authorized to determine eligibility
for the Head Start program;
(5) Agencies authorized to determine eligibility
for child care services provided under the Child Care and Development Block
Grant Act;
(6) Agencies participating in the Early
Intervention Program; and
(7) Agencies participating in the Special
Supplemental Nutrition Program for Women, Infants, and Children (WIC).
(l)
“Recipient” means any individual who is
eligible for and receiving medical assistance under the medicaid
program.
(m) “Revalidation” means the process through
which the provider verifies the accuracy of, and updates if necessary, its
current provider enrollment information.
(n)
“Termination” means that the department revoked a provider’s medicaid billing privileges.
(o) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(p)
“Title
XXI” means the joint federal-state program described in Title XXI of the Social
Security Act and administered in New Hampshire by the department under the medicaid program.
(q)
“Utilization review and control” means the monitoring of medicaid program services pursuant to 42 CFR 455 and 42 CFR
456.
Source. (See Revision Note at chapter heading He-W
500); ss by #6574, eff 9-12-97; ss by #6745, eff 5-1-98, EXPIRED: 12-31-98; ss
by #6925, eff 1-1-99; amd by #7666, eff 4-1-02; ss by
#8781, eff 1-1-07; amd by #10139, eff 7-1-12; paras
(a), (b), (d), (g), (j), & (k), EXPIRED: 1-1-15; amd
by #10776, INTERIM, eff 1-31-15, EXPIRES: 7-30-15; ss by #10887, eff 7-17-15; amd by #12023, INTERIM, eff 11-1-16, EXPIRES: 4-30-17; amd by #12166, eff 4-29-17
He-W 520.02 Program Administration.
(a) The department shall:
(1) Administer and maintain the federal medicaid State Plan, pursuant to 42 CFR 430.10 and RSA
161:2, VI;
(2) Provide the mandatory medicaid
services pursuant to 42 CFR 440.210 and 42 CFR 440.220;
(3) Provide the medicaid
optional services which are specified in the medicaid
State Plan;
(4) Describe the provider and recipient
requirements for the medicaid services found in He-W 530
through He-W 577, and pursuant to RSA 161:4-a, X; and
(5) Authorize and train qualified entities to
determine presumptive eligibility.
(b) The provider shall:
(1) Be a NH enrolled medicaid
provider; and
(2) Request and obtain prior authorization from
the department before providing any medicaid covered
services requiring prior authorization.
(c) The recipient of covered services shall be an
eligible medicaid recipient at the time the service
is rendered.
Source. (See Revision Note at chapter heading He-W
500); ss by #6574, eff 9-12-97; ss by #6745, eff 5-1-98, EXPIRED: 12-31-98; ss
by #6925, eff 1-1-99; ss by #8781, eff 1-1-07, EXPIRED: 1-1-15
New. #10776, INTERIM, eff 1-31-15, EXPIRES:
7-30-15; ss by #10887, eff 7-17-15
He-W 520.03 Record Keeping Requirements. Providers shall maintain clinical records to
support claims submitted for reimbursement for a period of at least 6 years
from the date of service or until the resolution of any legal action(s)
commenced in the 6 year period, whichever is longer.
Source. (See Revision Note at chapter heading He-W
500); ss by #6574, eff 9-12-97; ss by #6925, eff 1-1-99; ss and moved by #8781,
eff 1-1-07 (from He-W 520.05), EXPIRED: 1-1-15
New. #10776, INTERIM, eff 1-31-15, EXPIRES: 7-30-15;
ss by #10887, eff 7-17-15
He-W 520.04 Surveillance and Utilization Review and
Control.
(a)
The purpose of a surveillance and utilization review and control program
is for the department to:
(1) Assess the quality of the care, services, and
supplies received by recipients and for which a medicaid
program has reimbursed providers;
(2) Detect, correct, and prevent occurrences of
unnecessary or inappropriate medical care, service, or supply usage by
recipients, or provision by providers, for which a medicaid
program has reimbursed providers; and
(3) Ensure that accurate and proper reimbursement
has been made for the care, services, or supplies provided.
(b)
The department shall be responsible for surveillance and utilization
review and control activities by:
(1) Performing the utilization reviews directly,
or contracting with professional organizations for the performance of reviews;
and
(2) Monitoring the results of reviews to ensure
appropriate corrective action has been taken.
(c)
Reviews described in (b)(1) and (2) above shall include:
(1) Reviewing recipient utilization and provider
service profiles generated quarterly by the MMIS in accordance with 42 CFR
456.23;
(2) Reviewing provider claims selected randomly;
(3) Reviewing claims for all or selected services
for a given period of time;
(4) Application of the Centers for Medicare and
Medicaid Services’ National Correct Coding Initiative (CMS NCCI) to review
claims processed by the fiscal agent to ensure:
a. That the provider has coded claims properly;
and
b. That the claims processing system has made
proper payment through application of edits based upon the CMS NCCI;
(5) An on-site review of hospital, office, or
other provider records to establish the accuracy of claims data and to ensure
other documentation supports the claim for services rendered;
(6) Contacting recipients to verify that services
or supplies claimed for reimbursement by providers were actually rendered;
(7) Contacting providers in order to recover
overpayments or correct underpayments; and
(8) Referring cases of potential fraud for
further investigation and possible criminal action, pursuant to 42 CFR 455.15.
Source. (See Revision Note at chapter heading He-W
500); ss by #6574, eff 9-12-97; ss by #6925, eff 1-1-99; ss and moved by #8781,
eff 1-1-07 (from He-W 520.06); ss by #9365, eff 1-17-09; ss by #12188, eff
5-25-17
He-W 520.05 Fraud Detection and Investigation.
(a) In accordance with 42 CFR 455.14, if the department
receives a complaint of medicaid fraud or abuse from
any source or identifies any questionable practices, it shall conduct a
preliminary investigation.
(b) Cases where potential fraud has been detected
as a result of a preliminary investigation pursuant to (a) above, shall be
referred for a full investigation to the appropriate agency, in accordance with
42 CFR 455.15.
(c) A full investigation and resolution shall be
conducted in accordance with 42 CFR 455.16.
Source. (See Revision Note at chapter heading He-W
500); ss by #6574, eff 9-12-97; ss by #6925, eff 1-1-99; ss by #8781, eff
1-1-07, EXPIRED: 1-1-15
New. #10776, INTERIM, eff 1-31-15, EXPIRES:
7-30-15; ss by #10887, eff 7-17-15
He-W 520.06 Provider Requirements.
(a) NH medicaid
providers and provider applicants shall meet the provider participation
requirements contained in He-W 530 through He-W 577, as applicable, for
providers of the type of services they will be providing, as well as
requirements in He-W 520.06.
(b) The following
individuals and entities shall be subject to a risk determination described in
(c) below:
(1) NH medicaid
providers enrolled as of November 1, 2016 who submitted their provider
enrollment application to the department’s fiscal agent on or after August 1,
2015 through October 31, 2016;
(2) NH medicaid
provider applicants;
(3) NH medicaid
providers who are applying to enroll a new practice location(s);
(4)
NH medicaid
providers who are re-enrolling; and
(5) NH medicaid
providers being revalidated in accordance with 42 CFR 455.414.
(c) Individuals and entities in (b) above who
meet either of the following criteria shall be determined to be high risk providers
or high risk provider applicants:
(1) The individual or entity, with the exception
of those who are undergoing revalidation in accordance with 42 CFR 455.414,
provides home health services or durable medical equipment services; or
(2) The individual’s or entity’s risk level was
adjusted to high by the department as required by 42 CFR 455.450(e)(1) because
any of the following occurred:
a. The department imposed a payment
suspension on the individual or entity based on credible allegation of fraud,
waste, or abuse;
b. The individual or entity has an existing medicaid overpayment;
c. The individual or entity was excluded from
participation in a federally funded program by the office of inspector general
or another state’s medicaid program within the
10 years preceding the date of application or date of revalidation; or
d. In accordance with 42 CFR 455.450(e)(2), NH medicaid or the Centers for Medicare and Medicaid Services
(CMS) in the previous 6 months lifted a temporary moratorium for the particular
provider type and a provider that was prevented from enrolling based on the
moratorium applies for enrollment as a provider within 6 months from the date
the moratorium was lifted.
(d) The following individuals and entities shall
be subject to a state and federal criminal background check, including
fingerprinting, in accordance with this section:
(1) Persons with a direct or indirect ownership
interest in a high risk provider or high risk provider applicant described in
(c)(1) above; and
(2)
High risk providers or high risk
provider applicants described in (c)(2) above.
(e) Those who meet the criteria in (d) above
shall not be subject to an additional criminal background check, including
fingerprinting, if, within the previous 36 months, they have undergone a
criminal background check as required by:
(1) A Medicare administrative contractor;
(2) NH medicaid;
(3) Any other state’s medicaid
agency, and the department is able to access the information from the other
state’s medicaid agency; or
(4) Any other state’s children’s health insurance
program (CHIP), and the department is able to access the information from the
other state’s CHIP.
(f) Those who meet the criteria in (d) above, and
who are not excluded in (e) above, shall be notified in writing of the
following by the department:
(1) That a state and federal criminal background
check, including fingerprinting, is required;
(2) Where the criminal background check,
including fingerprinting, can be conducted as specified in (h)(1) below; and
(3) The deadline by which the criminal background
check, including fingerprinting, shall be conducted as specified in (g) below.
(g) The deadline for undergoing a criminal
background check, including fingerprinting, shall be 30 days from the date of
the notification in (f) above.
(h) Those who meet the criteria in (d) above, and
who are not excluded in (e) above, shall undergo a state and federal criminal
background check by:
(1) Having a complete set of electronic
fingerprints taken at any location maintained by the NH state police criminal
records unit that has electronic fingerprinting capability, or by any other in
or out of state law enforcement agency that conducts fingerprinting
electronically; and
(2) Completing and submitting to the location in
(1) above a notarized Form DSSP 417, “New Hampshire Health and Human Services
Criminal History Record Information Authorization,” incorporated by reference
in Saf-C 5703.10, Table 5700-1, which authorizes the
release of the individual’s criminal history record, if any, to the department.
(i) Those who meet
the criteria in (d) above shall be terminated from, or denied enrollment in,
the NH medicaid program if:
(1) The individual fails to get fingerprinted by
the deadline in (g) above, as applicable; or
(2) The results of the criminal background check
indicate that the individual has been convicted of any of the following federal
or state felony offenses within the 10 years preceding the date of application
or date of revalidation of enrollment:
a. Felony crimes against persons, such as
murder, sexual assault, assault, interference with freedom, destruction of
property, unauthorized entries, robbery and theft, fraud and corruption, and
other similar crimes for which the individual was convicted, including guilty
pleas;
b. Financial crimes, such as extortion,
embezzlement, income tax evasion, insurance fraud, and other similar crimes for
which the individual was convicted, including guilty pleas; or
c. Any felony that placed the medicaid program or its recipients at immediate risk, such
as a malpractice suit that results in a conviction of criminal neglect or
misconduct.
(j) An individual or entity being terminated
from, or denied enrollment in, the NH medicaid
program in accordance with (i) above shall receive a
written notice from the department of the denial or termination.
(k)
The notice in (j) above shall contain:
(1) The reason for, and legal basis of, the
denial or termination; and
(2) Information that an appeal of the denial or
termination may be requested, in accordance with He-C 200, within 30 calendar
days of the date on the notice of the denial or termination.
(l) Appeals of the results of the criminal
background check shall be made in accordance with the department of safety
rules at Saf-C 5703.12.
Source. #12023, INTERIM, eff 11-1-16, EXPIRES:
4-30-17; ss by #12166, eff 4-29-17
PART
He-W 521 GENERAL PAYMENT INFORMATION -
EXPIRED AND RESERVED
Source. (See Revision Note at chapter heading He-W
500); ss by #5888, eff 8-31-94, EXPIRED: 8-31-00
PART
He-W 522 INTERPRETER SERVICES - EXPIRED
AND RESERVED
Source. (See Revision Note at chapter heading He-W
500); ss by #5735, eff 11-12-93, EXPIRED: 11-12-99
PART
He-W 529 INDEPENDENT COVERAGE REVIEW -
RESERVED
He-W 529.01 – 529.07
Source. #8983, INTERIM, eff 9-21-07, EXPIRES: 3-19-08;
ss by #9103, eff 3-12-08; rpld by #10031, eff
11-19-11
PART
He-W 530 SERVICE LIMITS, CO-PAYMENTS,
AND NON-COVERED SERVICES
He-W 530.01 Definitions.
(a) “Co-payment” means an amount to be paid by
the recipient to an enrolled New Hampshire medicaid
provider.
(b) “Department” means the New Hampshire
department of health and human services.
(c) “Generally accepted standards of medical
practice” means standards that are based on credible scientific evidence
published in peer-reviewed medical literature generally recognized by the
relevant medical community, or the recommendations of physician specialists
practicing in relevant clinical areas or of various physician specialty
societies.
(d) “Medicaid” means the Title XIX and Title XXI
programs administered by the department, which makes medical assistance
available to eligible individuals.
(e) “Medically necessary” means health care
services that a licensed health care provider, exercising prudent clinical
judgment, would provide, in accordance with generally accepted standards of
medical practice, to a recipient for the purpose of evaluating, diagnosing,
preventing, or treating an acute or chronic illness, injury, disease, or its
symptoms, and that are:
(1) Clinically
appropriate in terms of type, frequency of use, extent, site, and duration, and
consistent with the established diagnosis or treatment of the recipient’s
illness, injury, disease, or its symptoms;
(2) Not primarily for the
convenience of the recipient or the recipient’s family, caregiver, or health
care provider;
(3) No more costly than other
items or services which would produce equivalent diagnostic, therapeutic, or
treatment results as related to the recipient’s illness, injury, disease, or
its symptoms; and
(4) Not experimental,
investigative, cosmetic, or duplicative in nature.
(f) “Multi-source pharmaceutical product” means a
product which is available from more than one manufacturer.
(g) “Non-preferred prescription drug” means a
medication that has been determined to have an alternative drug available that
is clinically equivalent and has been clinically reviewed and approved by the
NH Pharmacy and Therapeutics Committee or the NH Drug Use Review Board
established in He-C 5010 and has been included in the department’s preferred
drug list as non-preferred.
(h) “Preferred prescription drug” means a
medication that has been clinically reviewed and approved by the NH Pharmacy
and Therapeutics Committee or the NH Drug Use Review Board established in He-C
5010 and has been included in the department’s preferred drug list based on its
proven clinical and cost effectiveness.
(i) “Preferred Drug
List (PDL)” means a formal published list of specific prescription drug
products by brand and generic name divided into 2 separate categories as either preferred or
non-preferred.
(j) “Provider”
means an entity or individual who furnishes health care services or supplies to
medicaid recipients under an agreement with the
department, and is licensed or certified pursuant to applicable state law to
provide such services and supplies.
(k) “Recipient” means any individual who is eligible
for and receiving medical assistance under the medicaid
program.
(l) “Service” means medical care or a medical
product for which payment is made by New Hampshire medicaid.
(m) “Service limit” means a finite number of
visits or units of service per recipient per specified time period for which
payment is made by New Hampshire medicaid.
(n) “Single source pharmaceutical product” means
a brand name product which is available from only one manufacturer.
(o) “State fiscal year” means July 1 through June
30.
(p) “Third party entity” means the agency under
contract with the department to collect and process premium payments for medicaid recipients.
(q) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(r) “Title XXI” means the joint federal-state
program described in Title XXI of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(s) “Unit” means a determinate quantity for which
a particular service is rendered.
(t) “Visit” means all services provided to a
recipient per appointment or encounter with a provider.
Source. (See Revision Note at chapter heading He-W
500); ss by #5914, eff 11-1-94; ss by #6745, eff 5-1-98, EXPIRED: 12-31-98; ss
by #6925, eff 1-1-99; ss by #8780, INTERIM, eff 1-1-07, EXPIRES: 6-30-07; ss by
#8929, eff 6-30-07; amd by #8983, INTERIM, eff
9-21-07, EXPIRES: 3-19-08; ss by #9103, eff 3-12-08; amd
by #10139, eff 7-1-12; ss by #11101, eff 5-25-16
He-W
530.02 Recipients Subject to Service
Limits, Co-Payments, and Non-Covered Services.
(a) All recipients shall be subject to service
limits in accordance with He-W 530.03.
(b) All recipients shall be subject to the
co-payments specified in He-W 530.04, except for:
(1) Recipients with income at
or below 100% of the federal poverty level (FPL);
(2) Recipients residing in a
nursing facility, hospital, intermediate care facility for individuals with
intellectual disabilities, or other medical institution;
(3) Recipients participating in
the home and community based care (HCBC) waiver programs;
(4) Recipients receiving services that relate to pregnancy, in
accordance with 42 CFR 447.53(b)(2), or any other medical condition that might
complicate the pregnancy;
(5) Recipients under the age of
18;
(6) Women eligible through the
Breast and Cervical Cancer Treatment Program, pursuant to 42 CFR 435.213;
(7) Recipients receiving
hospice care pursuant to He-W 544; and
(8) Individuals who are members
of a federally recognized Indian tribe or Alaskan natives who have ever been
served through the Indian Health Services Programs, pursuant to 42 CFR
447.56(a)(x).
(c)
All recipients shall be subject to non-covered services provisions in accordance
with He-W 530.05.
Source. (See Revision Note at chapter heading He-W
500); ss by #4863, eff 7-12-90, EXPIRED: 7-12-96
New. #6745, eff 5-1-98, EXPIRED: 12-31-98; ss by
#6925, eff 1-1-99; ss by #8780, INTERIM, eff 1-1-07, EXPIRES:
6-30-07; ss by #8929, eff 6-30-07; amd by #10016, eff
11-1-11; amd by #10716, eff 11-18-14; ss by #10915,
eff 8-26-15; ss by #11101, eff 5-25-16
He-W 530.03 Service Limits. The following service limits shall apply to
each recipient who is subject to service limits, per state fiscal year, with
exceptions noted:
(a)
The hearing aid evaluation or a hearing aid consultation shall be
limited to one service every 2 years since the last date of service;
(b)
Hospital services shall be limited as follows:
(1) Outpatient hospital services shall be limited
to 12 visits per state fiscal year;
(2) Services provided in an emergency department
(ED) or an urgent care setting shall not be considered outpatient hospital
services, and shall not apply toward the limit established in (1) above;
(3) Physician services shall be unlimited except
when associated with an outpatient hospital visit, in which case they shall be
limited to 12 visits per state fiscal year; and
(4) Services that are described individually in
component parts of this chapter, such as therapy services or radiology
services, and that are associated with an outpatient hospital, ED or urgent
care visit shall be subject to the service limits which apply to that
individual service;
(c)
Physician and advanced practice registered nurse (APRN) services
performed in the inpatient hospital setting shall be limited to one visit per
each day of stay approved by the department or its designated quality
improvement organization (QIO) as defined in He-W 531.01(h);
(d)
Podiatry services shall be limited to 4 visits;
(e)
Therapy services, including physical, occupational and speech therapy,
shall be limited to 80, 15-minute units per recipient. The 80 units may be used
for one type of therapy or for any combination of therapies;
(f)
Vision care services shall be limited as follows:
(1) One refraction to determine the need for
glasses, no more frequently than every 12 months;
(2) Replacement of lenses or at the discretion of
the recipient, lenses and frames, when the refractive error changes .50 diopter
or more in both eyes;
(3) Replacement of nickel frames after 12 months,
if the recipient has a documented allergy to nickel demonstrated by skin
irritation and wearing down of the frame in the affected area; and
(4) One repair of glasses every 12 months,
including replacement of the broken part(s) only;
(g)
Wheelchair van services shall be limited to 24 trips, either one-way or
round trip;
(h)
X-ray services shall be limited as follows:
(1) X-ray services for diagnostic purposes shall
be limited to 15 x-rays; and
(2) X-ray services provided for radiation therapy
shall not be limited; and
(i) If a recipient is covered by medicare and medicare pays at
least half the medicaid program rate for a covered
service which is subject to limits, that service shall not be counted against
such limits.
Source. (See Revision Note at chapter heading He-W
500); ss by #4863, eff 7-12-90; amd He-W 530.03(d) by
#5714, eff 10-1-93; amd He-W 530.03(f) by #6050, eff
6-17-95; ss by #6925, eff 1-1-99; ss by #8780, INTERIM, eff 1-1-07, EXPIRES:
6-30-07; ss by #8929, eff 6-30-07; amd by #8983,
INTERIM, eff 9-21-07, EXPIRES: 3-19-08; amd by #9103,
eff 3-12-08; amd by #9366, eff 1-17-09; amd by #9622, eff 1-1-10; amd by
#9736, eff 6-25-10; amd by #10017, eff 11-1-11; amd by #10090, eff 3-1-12; amd by
#10427, eff 9-28-13; amd by #10657, eff 8-15-14; ss
by #10915, eff 8-26-15; amd by #12818, eff 7-1-19
He-W 530.04 Co-Payments.
(a) Recipients subject to co-payments
shall make co-payments to the pharmacy provider for pharmaceutical products as
follows, except as noted in (3) below:
(1) For recipients eligible for medicaid through the New Hampshire Health Protection
Program (NHHPP) co-payments as required in He-W 512.
(2) For all other recipients subject to
co-payments as required by this part:
a. A
co-payment in the amount of $1.00 shall be required for each preferred
prescription drug and each refill of a preferred prescription drug dispensed;
b. A co-payment in the amount of $2.00 shall
be required for each non-preferred prescription drug and each refill of a
non-preferred prescription drug dispensed unless the prescribing provider determines that a preferred drug
will be less effective for the recipient, will have adverse effects for the
recipient, or both, in which case, the co-payment shall be $1.00; and
c. A
co-payment in the amount of $1.00 shall be required for a prescription drug
that is not identified as either a preferred or non-preferred prescription
drug; and
(3) Co-payments for pharmaceutical products shall
not be required:
a. Of
recipients exempt from co-payments in accordance with He-W 530.02(b);
b.
For family planning products; and
c.
For Clozaril (Clozapine) prescriptions.
(b)
Recipients subject to co-payments shall make co-payments to the provider
for services as follows, except as noted in (2) below:
(1) For recipients eligible for medicaid through the NHHPP, co-payments as described in
He-W 512; and
(2) Recipients shall not be responsible for a
co-payment for the following services:
a.
Emergency services needed to evaluate or stabilize an emergency medical
condition as defined in 42 CFR 438.114(a);
b.
Provider-preventable services as described in 42 CFR §447.26(b);
c.
Services furnished to pregnant women, including counseling and
pharmacotherapy for cessation of tobacco use;
d.
Family planning services and supplies; and
e.
Preventive services.
(c)
Pursuant to 42 CFR 447.56(f), co-payment obligations shall be suspended
for the remainder of the calendar year quarter when the total co-payments made
out of pocket by the recipient reaches 5 percent of the recipient’s household
income.
(d)
All recipients subject to co-payments required by this part shall not be denied
services by any medicaid enrolled provider on account
of the recipient’s inability to pay the co-payments required by this part.
Source. (See Revision Note at chapter heading He-W
500); ss by #4863, eff 7-12-90, EXPIRED: 7-12-96
New. #6925, eff 1-1-99; ss by #7976, eff 10-22-03;
ss by #8780, INTERIM, eff 1-1-07, EXPIRES: 6-30-07; ss by #8929, eff 6-30-07; amd by #10017, eff 11-1-11; ss by #10716, eff 11-18-14; ss
by #11101, eff 5-25-16
He-W 530.05 Non-Covered Services.
(a)
Non-covered services shall be those services for which the Medicaid
program shall make no payment.
(b)
Non-covered services shall include:
(1) Acupuncture;
(2) Services ancillary to, or directly related
to, a non-covered service or procedure;
(3) Biofeedback;
(4) Experimental or investigational procedures
described as such in the National Coverage Determinations (NCD) found in the
Centers for Medicare and Medicaid Services “Medicare Coverage Database” at http://www.cms.gov/medicare-coverage-database/ (under the
“Quick Search” function, select “National Coverage Documents”, optionally enter
a filter by entering a “keyword” to narrow the search results, and select the
“Search by Type” button, or, if a keyword is not entered, the entire list of
NCD titles will appear alphabetically and may be selected), including
thermogenic therapy and electrosleep therapy;
(5) Reversal of voluntary sterilization;
(6) Operations for impotency;
(7) Operations, devices, and procedures for the
purpose of contributing to or enhancing fertility or procreation;
(8) Plastic surgery, to include cosmetic surgery,
for the purpose of preserving or improving appearance or disfigurement, except
when required for the prompt repair of accidental injury or for the improvement
in functioning of a malformed body part;
(9) Hypnosis, except when performed by a
psychiatrist as part of an established treatment plan;
(10) Routine foot care, except as described in
He-W 532;
(11) Services or items that are free to the
public;
(12) Physician care in a non-medical government or
public institution;
(13) Dietary services, including commercial weight
loss, nutritional counseling, and exercise programs, except as otherwise
allowed in He-W 500;
(14)
Homemaker services, except when provided as part of an authorized Choices for
Independence (CFI) program support plan to CFI recipients as described in He-E
801;
(15) Academic performance testing not related to a
medical condition;
(16) Detoxification services provided outside an
acute care facility or a medical services clinic;
(17) Services provided by halfway houses;
(18) Hospital inpatient care which is not
medically necessary;
(19) Autopsies;
(20) Auditory training, except for auditory
trainer devices which are covered;
(21) Respite, except as a service under a home and
community based care waiver in accordance with 42 CFR 400.180 and 440.181;
(22) Child care;
(23) Chiropractor services;
(24) Institutions for Mental Diseases, in
accordance with Section 1905(a)(24)(B) of the Social Security Act;
(25) Duplicative services, which are services that deliver the same functionality to the
same recipient during the same period
of time, regardless of whether those services are provided solely under medicaid or by medicaid in
combination with another program or entity;
(26) Services provided outside the United States
and its territories;
(27) Vaccinations for out of country travel;
(28) Services provided by individuals who are not
licensed, certified or otherwise recognized by the provisions of He-W 500 to
provide such services;
(29) Personal clothing or footwear;
(30) Service and therapy animals;
(31) Equine-assisted psychotherapy;
(32) Any service which is not specifically listed
elsewhere in He-W 522 through He-W 589 as covered, or covered with prior
authorization, and which is not covered as follows:
a. The service is not covered by Medicare, as
indicated by the National Coverage Determinations (NCD) found in the Centers
for Medicare and Medicaid Services “Medicare Coverage Database” at http://www.cms.gov/medicare-coverage-database/ (under the
“Quick Search” function, select “National Coverage Documents”, optionally enter
a filter by entering a “keyword” to narrow the search results, and select the
“Search by Type” button, or, if a keyword is not entered, the entire list of
NCD titles will appear alphabetically and may be selected); or
b. The service is not covered by New Hampshire
or New England commercial insurance policies and coverage criteria as follows:
1.
Anthem Medical Policies and Clinical UM Guidelines, http://www.anthem.com/wps/portal/ahpprovider?content_path=provider/wi/f5/s1/t4/pw_ad080065.htm&state=wi&rootLevel=0&label=Anthem%20Medical%20Policies
(select the “Continue” button to confirm that the page has been read and
proceed to the “Overview” page, then select the “Click Here to Search” button
in the middle of this page to continue to the search engine, enter search
criteria for the specific coverage policy, and then select the specific
coverage policy);
2. Cigna Coverage Policies, https://cignaforhcp.cigna.com
(select “RESOURCES” at the top of the page, then select “Coverage Policies”,
then select “Medical A-Z Index” for an alphabetical list of policies, and then
select the specific coverage policy);
or
3.
Aetna Clinical Policy Bulletins, http://www.aetna.com/healthcare-professionals/policies-guidelines/cpb_alpha.html
(select specific bulletin from the alphabetical listing of clinical policy
bulletins);
and
(33) Any service for
which coverage is not specified within the New Hampshire
Medicaid State Plan, and as such the department is unable to claim federal financial participation
(FFP) for said service.
Source. #6745, eff 5-1-98, EXPIRED: 12-31-98; ss by
#6925, eff 1-1-99; ss by #8780, INTERIM, eff 1-1-07, EXPIRES: 6-30-07; ss by
#8929, eff 6-30-07; amd by #9103, eff 3-12-08; amd by #9366, eff 1-17-09; amd by
#9622, eff 1-1-10; amd by #9836, eff 12-18-10; ss by
#10504, eff 1-9-14; amd by #10561, eff 3-29-14
He-W 530.06 Recipient Responsibility for Payment.
(a)
The recipient shall be responsible for payment of the entire cost of a
service if:
(1) The individual is not eligible for medicaid on the date of service;
(2) The service is not covered by medicaid;
(3) The provider is not a NH enrolled medicaid provider; or
(4) The provider is no longer taking additional medicaid recipients, but the recipient chooses to receive
the service anyway as a private patient.
(b)
The recipient shall be informed of these provisions verbally at the
initial determination of eligibility and at each redetermination of eligibility
by the department.
Source. (See Revision Note at chapter heading He-W
500); ss by #5874, eff 8-1-94; ss by #6925, eff 1-1-99; ss by #8780, INTERIM,
eff 1-1-07, EXPIRES: 6-30-07; ss by #8929, eff
6-30-07; ss by #10915, eff 8-26-15
He-W 530.07 Prior Authorization of Services Which
Exceed Service Limits.
(a)
When the individual medical care plan of a recipient who is under 21
years of age indicates the need for services in excess of the service limits
described in He-W 530.03, authorization to exceed the service limit shall be
requested in accordance with He-W 546.
(b)
When the individual medical care plan of a recipient who is 21 years of
age or older indicates the need for services in excess of the service limits
described in He-W 530.03, the provider shall request from the department
additional visits or units of covered service(s).
(c)
All requests in (b) above shall be in advance of the service(s) being
rendered, except that services provided during a retroactive eligibility period
shall be exempt from this requirement.
(d)
Requests for additional units of covered service(s) may be made by the
following providers:
(1) Advanced practice registered nurses;
(2) Associate psychologists;
(3) Occupational therapists;
(4) Optometrists;
(5) Osteopathic physicians;
(6) Psychotherapy providers licensed by the board
of mental health practice;
(7) Physicians;
(8) Physician’s assistants;
(9) Podiatrists;
(10) Psychologists;
(11) Physical therapists; and
(12) Speech and language therapists.
(e)
Providers shall direct requests for prior authorization of services in
excess of the limits described in He-W 530.03 to the department.
(f)
Prior to payment by the department, requests for prior authorization of
covered services in excess of the limits described in He-W 530.03 shall:
(1) With the exception of services provided
during a retroactive eligibility period, be submitted in advance of rendering
additional services;
(2) Be submitted in writing to the department via
mail, e-mail or fax;
(3) Be signed by a provider described in (d)
above; and
(4) Be based on the provider’s medical care plan
developed for the recipient.
(g)
Except as allowed by He-W 573.10, requests for prior authorization shall
include, at a minimum:
(1) The recipient’s name;
(2) The recipient’s Title XIX program
identification number;
(3) The recipient’s diagnosis;
(4) A copy of the recipient’s medical care plan;
(5) The number of additional visits or units of
service being requested;
(6) The provider number of the individuals or
agencies to whom the recipient is being referred for these additional services;
(7) Clinical documentation that addresses how the
requested additional services meet the definition of medically necessary;
(8) Except as provided by (9) below, if the
requested additional services do not meet the definition of medically
necessary, clinical documentation that addresses:
a. Any extenuating circumstances unique to the
recipient that would make denial of the additional services clinically
contraindicative; or
b. Any new scientific evidence in the medical
literature or by experts in the field about the efficacy or medical
appropriateness of the services;
(9)
If the requested additional
services are for therapy services, as described in He-W 568, documentation
demonstrating that the request meets the clinical criteria set forth in the
Milliman Care Guidelines, 17th edition (February/March 2013), available as noted
in Appendix A;
(10) A statement of the anticipated medical
outcome if the requested additional services are provided; and
(11) A statement of the anticipated medical
outcome, and either the estimated cost of such outcome or a description of
medical services that might be required as the result of such outcome, if the
requested additional services are not provided.
(h)
Except as allowed by He-W 573.10, prior authorization requested in
accordance with (b) through (g) above shall be approved by the department if
the department determines that the requested additional services meet the
definition of medically necessary or that coverage is supported by clinical
documentation provided in accordance with (g)(8) above.
(i) If the department approves the prior
authorization request in accordance with (h) above, the state’s fiscal agent
shall send written confirmation of the approval to the provider.
(j)
The provider shall be responsible for determining that the recipient is
Title XIX eligible on the date of service.
(k)
Providers may monitor the number of services used by a recipient based
on claims processed and paid by contacting the department’s fiscal agent for
this information.
(l)
With the exception of requests for services provided during a
retroactive eligibility period and wheelchair van services requested in
accordance with He-W 573.10, requests for retroactive authorization for
services rendered prior to the authorization request shall be denied by the
department.
(m)
Except as allowed by He-W 573.10, the department shall deny a prior
authorization request when the department determines that the requested
additional services do not meet the definition of medically necessary and that
the coverage is not supported by clinical documentation provided in accordance
with (g)(8) or (9) above.
(n)
If the department denies the prior authorization request, the department
shall forward a notice of denial to the recipient and the wheelchair van
provider.
(o)
The notice of denial
shall contain the information required by 42 CFR 431.210, including:
(1) The reason for, and legal basis of, the
denial; and
(2) Information that an appeal of the denial may
be requested, in accordance with He-C 200, within 30 calendar days of the date
on the notice of the denial.
Source. (See Revision Note at chapter heading He-W
500); ss by #4863, eff 7-12-90, EXPIRED: 7-12-96
New. #6745, eff 5-1-98, EXPIRED: 12-31-98; ss by
#6925, eff 1-1-99; ss by #8780, INTERIM, eff 1-1-07, EXPIRES:
6-30-07; ss by #8929, eff 6-30-07; ss by #9366, eff 1-17-09; amd by #9622, eff 1-1-10; amd by
#10017, eff 11-1-11; amd by #10031, eff 11-19-11; amd by #10342, eff 6-1-13; ss by #10605, eff 5-23-14; amd by #11101, eff 5-25-16
PART
He-W 531 PHYSICIAN SERVICES
He-W 531.01 Definitions.
(a) “Cosmetic
purpose” means a procedure done for the sole purpose of changing a physical
appearance.
(b) “Current
procedural terminology (CPT) code” means a unique identifying code in the field
of medical nomenclature and designated by the United States Department of
Health and Human Services as the national coding standard utilized in
government and private health insurance programs for reporting medical services
and procedures.
(c)
“Department” means the New Hampshire department of health and human
services.
(d) “Healthcare Common Procedure
Coding System (HCPCS)” means a standardized coding system used by Medicare that
describes services and procedures. HCPCS includes CPT codes that are used
primarily to identify products, supplies, and services not included in the
normal CPT code list, such as ambulance services and durable medical equipment,
prosthetics, orthotics, and supplies (DMEPOS), when used outside a physician’s
office.
(e)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(f) “National
Correct Coding Initiative (NCCI) edits” means standardized coding edits
developed by the Centers for Medicare and Medicaid Services (CMS) to reduce
improper coding and prevent inappropriate payments when incorrect code combinations are reported.
(g) “Prior authorization agent” means an
individual or organization contracted by the department, responsible for
reviewing all prior authorization requests.
(h) “Quality improvement organization
(QIO)” means an organization or
agency established in accordance with 42 CFR 475 that performs utilization and
quality control peer reviews in accordance with 42 CFR 476 when contracted by
the department for the performance of such reviews.
(i)
“Recipient” means any individual who is eligible for and receiving medical
assistance under the medicaid program.
(j)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(k)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #6051, eff 6-17-95; ss by #7895, eff 5-21-03; ss by #9915, INTERIM,
eff 5-15-11, EXPIRES: 11-14-11; ss by #10018, eff 11-14-11; amd
by #10139, eff 7-1-12; amd by #10561, eff 3-29-14; amd by #12818, eff 7-1-19; ss by #12999, eff 3-5-20
He-W 531.02 Recipient Eligibility. All medicaid
recipients shall be eligible for physician services in accordance with He-W
531.
Source. (See Revision Note at chapter heading He-W
500); ss by #6051, eff 6-17-95; ss by #7895, eff 5-21-03; ss by #9915, INTERIM,
eff 5-15-11, EXPIRES: 11-14-11; ss by #10018, eff 11-14-11;
ss by #12999, eff 3-5-20
He-W 531.03 Provider Participation.
(a)
Each participating physician provider shall:
(1) Be licensed to practice by the state in which
he or she practices;
(2) Be a New Hampshire enrolled medicaid provider; and
(3) Request and obtain prior authorization in
accordance with He-W 531.07.
(b)
Medicaid enrolled physicians and physician practices shall not charge a membership
fee to medicaid recipients or a recipient’s parent,
family member, agent or legal guardian.
Source. (See Revision Note at chapter heading He-W
500); ss by #6051, eff 6-17-95; ss by #7895, eff 5-21-03; ss by #9915, INTERIM,
eff 5-15-11, EXPIRES: 11-14-11; ss by #10018, eff 11-14-11; ss by #12999, eff
3-5-20
He-W 531.04 Service Limits. All physician services shall be subject to
the service limits set forth in He-W 530.03.
Source. (See Revision Note at chapter heading He-W
500); ss by #6051, eff 6-17-95; ss by #7895, eff 5-21-03; ss by #9915, INTERIM,
eff 5-15-11, EXPIRES: 11-14-11; ss by #10018, eff 11-14-11; ss by #12999, eff
3-5-20
He-W 531.05 Covered Services.
(a)
The following physician services, subject to the prior authorization
requirements in He-W 531.07, as applicable, shall be covered services:
(1) Anesthesia not administered by the operating
surgeon;
(2) Care provided by 2 or more physicians on the
same day for unrelated diagnoses regardless of the setting, for example,
inpatient or outpatient;
(3) Consultation services, as documented in a
written report, provided by a physician whose opinion or advice regarding
evaluation and management of a specific problem is requested by another
physician or health care professional;
(4) Second opinion;
(5) Eye care provided by ophthalmologists as
described in He-W 565;
(6) Family planning services as described in He-W
541;
(7)
Inpatient hospital visits for acute care days of stay approved in accordance
with He-W 543.11;
(8) Laboratory and radiology services as
described in He-W 577 and He-W 569;
(9) Obstetrical or gynecological procedures that
relate to care and treatment of pregnant women and the female reproductive
system, except for those procedures for which the sole purpose is to contribute
to, promote, or restore fertility, procreation, or sexual activity;
(10)
Face-to-face services rendered by a physician in any setting, including walk-in
clinics, urgent care centers, emergency departments, outpatient hospital
settings, nursing facilities, and recipients’ homes;
(11)
Surgical procedures, subject to the prior authorization requirements in He-W
531.07, as applicable, including:
a. Operative procedures for the treatment of
illnesses, injuries and congenital anomalies;
b. The treatment of fractures and dislocations;
c. The treatment of burns; and
d. Invasive diagnostic and treatment services;
(12) Services in addition to those usually and
customarily carried out to treat preoperative or postoperative complications,
provided that the physician has followed the procedures described in He-W
531.07;
(13) The following tissue transplants:
a. Cornea transplants;
b. Skin transplants with the exception of hairplasty; and
c. Bone grafts; and
(14) Immunizations.
(b) The following organ transplants
from a human donor to a recipient performed at facilities described in He-W
543.05(f) shall be covered subject to the prior authorization requirements in
He-W 531.07 and in accordance with the applicable coverage criteria in Interqual Connect Clinical Guidelines,
2019 Edition,
available as noted in Appendix A:
(1) Kidney transplants;
(2) Heart transplants;
(3) Heart and lung transplants;
(4) Lung transplants;
(5) Allogenic bone marrow transplants;
(6) Autologous bone marrow transplants;
(7) Liver transplants;
(8) Pancreas transplants; and
(9)
Pancreas and kidney transplants.
(c) Bariatric surgical procedures shall be
covered, subject to the prior authorization requirements in He-W 531.07 and in
accordance with the coverage criteria in Interqual
Connect Clinical Guidelines,
2019 Edition , available as noted in Appendix A, except that the
recipient shall also have lost at least 15% of body weight prior to scheduling
bariatric surgery as documented in the recipient’s medical record.
(d)
Breast reduction surgery shall be covered, subject to the prior
authorization requirements in He-W 531.07 and in accordance with the coverage
criteria in Interqual Connect Clinical Guidelines,
2019 Edition
, available as noted in Appendix A.
(e)
Blepharoplasty shall be covered, subject to the prior authorization
requirements in He-W 531.07 and in accordance with the coverage criteria in Interqual Connect Clinical Guidelines,
2019 Edition
, available as noted in Appendix A.
(f)
Panniculectomy shall be covered, subject to the prior authorization
requirements in He-W 531.07 and in accordance with the coverage criteria in Interqual Connect Clinical Guidelines,
2019 Edition
, available as noted in Appendix A.
(g)
Septoplasty and rhinoplasty shall be covered, subject to the prior
authorization requirements in He-W 531.07 and in accordance with the coverage
criteria in Interqual Connect Clinical Guidelines,
2019 Edition,
available as noted in Appendix A.
(h) Coverage of routine visits to nursing
facilities for non-acute services shall be limited to one visit per calendar
month.
Source. (See Revision Note at chapter heading He-W
500); ss by #6051, eff 6-17-95; ss by #7895, eff 5-21-03; ss by #9915, INTERIM,
eff 5-15-11, EXPIRES: 11-14-11; ss by #10018, eff 11-14-11; amd
by #10091, eff 2-24-12; ss by #10561, eff 3-29-14; ss by #12999, eff 3-5-20
He-W 531.06 Non-Covered Services.
(a)
Physician services for the surgery, inpatient hospital services for the
surgical admission(s), and organ procurement services related to the following
types of transplants shall be non-covered services:
(1) Any type of organ transplant not specified in
He-W 531.05(b) or tissue transplant not specified in He-W 531.05(a)(13);
(2) Organ
transplants requiring prior authorization but which are not prior authorized;
or
(3) More than 2 transplants of the same type of
organ per recipient per lifetime.
(b)
Psychiatric services when provided at or through a community mental
health center shall be non-covered as a physician service.
(c)
Treatment shall be non-covered when the sole purpose is to contribute
to, promote, or restore fertility, procreation, or sexual activity.
(d)
Procedures
or surgery for the sole purpose of preserving or improving appearance shall be
non-covered, except when required for the prompt repair of accidental injury or
for the improvement of the functioning of a malformed body member.
(e)
With the exception of procedures covered in accordance with the coverage
criteria in He-W 531.05(b)-(g), experimental or investigational procedures
described as such in the National Coverage Determinations (NCD) found in the Centers
for Medicare and Medicaid Services “Medicare Coverage Database” at http://www.cms.gov/medicare-coverage-database/
(under the “Quick Search” function, select “National Coverage Documents”,
optionally enter a filter by entering a “keyword” to narrow the search results,
and select the “Search by Type” button, or, if a keyword is not entered, the
entire list of NCD titles will appear alphabetically and may be selected) shall
be non-covered.
(f)
Thermogenic therapy, which treats certain types of resistant infectious
diseases through the production of artificial fever, shall be non-covered.
(g)
Electrosleep therapy, which consists of the
application of pulses of direct current to the recipient’s brain through
external electrodes, shall be non-covered.
(h)
Any services directly related to a non-covered service or procedure
shall be non-covered.
(i) Inpatient hospital visits for non-acute
inpatient stays shall be non-covered, including but not limited to:
(1) Visits to recipients who are in an inpatient
hospital setting awaiting placement to a long term care facility; and
(2) Visits for days that have not been approved
by the department or its
designated Quality Improvement Organization (QIO) in accordance with He-W 543.
(j)
Components of surgical preparatory regimens that are not described as
covered services in accordance with He-W 520 through He-W 577 shall be
non-covered, including:
(1) Services rendered by dieticians or
nutritionists; and
(2) Exercise regimens.
Source. (See Revision Note at chapter heading He-W
500); ss by #6051, eff 6-17-95; ss by #7895, eff 5-21-03; ss by #9915, INTERIM,
eff 5-15-11, EXPIRES: 11-14-11; ss by #10018, eff 11-14-11; ss by #10561, eff
3-29-14; amd by #12403, eff 10-20-17; amd by #12818, eff 7-1-19; ss by #12999, eff 3-5-20
He-W 531.07 Prior Authorization.
(a) The following services and procedures, as
described in He-W 531.05, shall require prior authorization from the
department’s prior authorization agent:
(1)
All organ transplants, except kidney
transplants;
(2) Bariatric surgical procedures;
(3) Breast reduction surgery;
(4) Blepharoplasty;
(5) Panniculectomy; and
(6) Septoplasty and rhinoplasty.
(b) Prior to payment by the department, requests
for prior authorization of services and procedures described in He-W 531.05
shall:
(1) Be submitted in advance of rendering the
service;
(2) Be submitted in writing to the department’s
prior authorization agent via mail or fax on Form 273S “Physician Request for
Prior Authorization for Certain Surgical Procedures, Including Organ
Transplants” (02/2020), along with any supporting documentation;
(3) Be signed by the provider; and
(4) Be based on the provider’s medical care plan
developed for the recipient.
(c) Requests for prior authorization shall
include a physician’s order, letter of medical necessity, and clinical notes to
enable the department’s prior authorization agent to evaluate the request.
(d) Prior authorization requested in accordance
with (a) through (c) above shall be approved by the department’s prior
authorization agent if the department’s prior authorization agent determines
that the submitted documentation supports the applicable requirements in He-W
531.05.
(e) If the department approves the prior
authorization request, the department’s fiscal agent shall send written
confirmation of the approval to the provider.
(f) The provider shall be responsible for
determining that the recipient is Title XIX eligible on the date of service.
(g) If the
department’s prior authorization agent denies the prior authorization request,
the department’s prior authorization agent shall forward a notice of denial to
the recipient and the ordering provider on the department Form 272a, “Medical
Assistance Program Denial for Prior Authorized Services,” including the
following:
(1) The reason for, and legal basis of, the
denial; and
(2) Information that a fair hearing on the denial
may be requested within 30 calendar days of the date on the notice of the
denial, in accordance with He-C 200.
Source. (See Revision Note at chapter heading He-W
500); ss by #6051, eff 6-17-95; ss by #7895, eff 5-21-03; ss by #9915, INTERIM,
eff 5-15-11, EXPIRES: 11-14-11; ss by #10018, eff 11-14-11; ss by #10561, eff
3-29-14; ss by #12999, eff 3-5-20
He-W
531.08 Utilization Review and Control.
(a) The department’s provider integrity unit
shall monitor utilization of physician services, to identify, prevent, and
correct potential occurrences of fraud, waste, and abuse, in accordance with 42
CFR 455, CFR 456, 42 CFR 1001, and He-W 520.
(b) The department shall recoup state and federal
medicaid payments as permitted by 42 CFR 455, 42 CFR
447, and 42 CFR 456 for a provider’s failure to maintain supporting records in
accordance with He-W 520 and He-W 531.
Source. (See Revision Note at chapter heading He-W
500); ss by #6051, eff 6-17-95; ss by #7895, eff 5-21-03; ss by #9915, INTERIM,
eff 5-15-11, EXPIRES: 11-14-11; ss by #10018, eff 11-14-11; ss by #10561, eff
3-29-14; ss by #12999, eff 3-5-20
He-W 531.09 Third Party Liability. All third party obligations shall be
exhausted before medicaid shall be billed, in
accordance with 42 CFR 433.139.
Source. #10018, eff 11-14-11; ss by #12999, eff
3-5-20
He-W
531.10 Payment for Services.
(a) Payment to physicians shall be made in
accordance with rates established by the department in accordance with RSA
161:4, VI(a).
(b) The payment rates for surgery, established by
the department in accordance with RSA 161:4, VI(a), shall be at a global rate
in accordance with the CPT codes and National Correct Coding Initiative (NCCI)
edits, inclusive of the following:
(1) Local infiltration,
metacarpal/metatarsal/digital block, or topical anesthesia;
(2) Subsequent to the decision for surgery, any
related evaluation and management encounter that occurs up to 5 days prior to
or on the date of procedure, including history and physical;
(3) Immediate postoperative care, including
dictating operative notes, and talking with the family and other physicians;
(4) Writing orders;
(5) Evaluating the patient in the post anesthesia
recovery area; and
(6) Typical post-operative follow-up care up to
30 days post surgery.
(c) Rates established by the department in
accordance with (a) above shall be considered to include all costs of doing
business including, but not limited to:
(1) Missed or cancelled appointments; and
(2) Administrative services such as:
a. Copying records;
b. Referrals;
c. Renewing prescriptions; and
d. Providing medical documents for schools,
sports, and camps.
(d) Payment for second surgical opinions shall be
made in accordance with rates established by the department in accordance with
RSA 161:4, VI(a).
(e) Physicians who request reimbursement for
clinical laboratory services, in accordance with He-W 577, shall receive
reimbursement provided that a contract or agreement exists between the
physician and the laboratory and requests for reimbursement shall be made by
the physician.
(f) The provider shall use CPT and HCPCS
procedure codes when billing.
(g) The provider shall submit claims for payment
to the department’s fiscal agent.
(h) The provider shall maintain supporting
records in accordance with He-W 520.
Source. #10018, eff 11-14-11 (from He-W 531.08); ss
by #10561, eff 3-29-14; ss by #12999, eff 3-5-20
PART He-W 532 PODIATRY SERVICES
He-W 532.01 Definitions.
(a) “Current procedural terminology (CPT) code”
means a unique identifying code in the field of medical nomenclature and
designated by the United States Department of Health and Human Services as the
national coding standard utilized in government and private health insurance
programs for reporting medical services and procedures.
(b) “Department (DHHS)” means the New Hampshire
department of health and human services.
(c) “Medicaid” means the Title XIX and Title XXI
programs administered by the department which makes medical assistance
available to eligible individuals.
(d) “Mycotic nail” means a fungus infection of a
toenail.
(e) “Pathological condition” means any disease,
trauma, tumors, or deformities affecting anatomy or physiology.
(f) “Podiatry service” means the diagnosis and
treatment of ailments of the human foot and lower leg by any medical,
mechanical, electrical, and surgical means available and performed by a
podiatrist.
(g) “Recipient” means any individual who is
eligible for and receiving medical assistance under the medicaid
program.
(h) “Routine foot care” means preventive and
hygienic maintenance of the feet, of the type which is ordinarily considered
self-care, including observation and cleansing of the feet, and the use of skin
creams to maintain skin tone.
(i) “State fiscal year” means July 1 through June
30.
(j) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(k) “Title XXI” means the joint federal-state
program described in Title XXI of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(l) “Visit” means all podiatry services provided
to a recipient on one day by one podiatrist.
Source. (See Revision Note at chapter heading He-W
500); ss by #4818, eff 6-1-90, EXPIRED: 6-1-96
New. #6756, eff 5-22-98, EXPIRED: 5-22-06
New. #8642, INTERIM, eff 5-26-06, EXPIRES: 11-22-06;
ss by #8745, eff 10-24-06; amd by
#10139, eff 7-1-12; ss by #10814, eff 4-21-15
He-W 532.02 Recipient Eligibility. All medicaid
recipients, including those confined to medical care institutions, including
hospitals or nursing facilities, shall be eligible for podiatry services in
accordance with this part.
Source. (See Revision Note at chapter heading He-W
500); ss by #4818, eff 6-1-90, EXPIRED: 6-1-96
New. #6756, eff 5-22-98, EXPIRED: 5-22-06
New. #8642, INTERIM, eff 5-26-06, EXPIRES:
11-22-06; ss by #8745, eff 10-24-06; ss by #10814,
eff 4-21-15
He-W 532.03 Provider Participation. Each participating podiatrist shall:
(a) Be licensed by the state in which he or she
practices; and
(b) Be a New Hampshire enrolled medicaid provider.
Source. (See Revision Note at chapter heading He-W
500); ss by #4818, eff 6-1-90, EXPIRED: 6-1-96
New. #6756, eff 5-22-98, EXPIRED: 5-22-06
New. #8642, INTERIM, eff 5-26-06, EXPIRES:
11-22-06; ss by #8745, eff 10-24-06; ss by #10814,
eff 4-21-15
He-W 532.04 Service Limits. Podiatry services shall be limited to 4
visits per recipient per state fiscal year.
Source. (See Revision Note at chapter heading He-W
500); ss by #4818, eff 6-1-90, EXPIRED: 6-1-96
New. #6756, eff 5-22-98, EXPIRED: 5-22-06
New. #8642, INTERIM, eff 5-26-06, EXPIRES:
11-22-06; ss by #8745, eff 10-24-06; ss by #9736, eff 6-25-10;
ss by #10814, eff 4-21-15
He-W 532.05 Covered Services. The following podiatry services shall be
covered only if they are medical or surgical treatments of the human foot and
lower leg for pathological conditions of the foot due to localized illness,
injury, or symptoms involving the foot:
(a) Routine foot care, and trimming and burring
of nails, including mycotic nails, performed by a podiatrist, provided that:
(1) The recipient’s primary health care provider
has documented in the recipient’s medical record that the recipient’s current
medical condition justifies the need for such foot care to be performed by a
podiatrist;
(2) The recipient’s primary health care provider
has written a referral to a podiatrist for such care, documenting in the
recipient’s medical record that the referral was made; and
(3) The referral is documented as received by,
and is retained by, the podiatrist in the recipient’s medical record;
(b) Prevention and reduction of corns, calluses,
and warts shall be covered by cutting or surgical means only; and
(c) Casting, strapping, and taping when performed
by a podiatrist for the treatment of fractures, dislocations, sprains, strains,
and open wounds of the ankle, foot, and toes.
Source. (See Revision Note at chapter heading He-W
500); ss by #4818, eff 6-1-90, EXPIRED: 6-1-96
New. #6756, eff 5-22-98, EXPIRED: 5-22-06
New. #8642, INTERIM, eff 5-26-06, EXPIRES:
11-22-06; ss by #8745, eff 10-24-06; ss by #10814,
eff 4-21-15
He-W 532.06 Non-Covered Services. The following podiatry services shall not be
covered:
(a) Routine foot care, and trimming and burring
of nails, except as described in He-W 532.05 above;
(b) Prevention and reduction of corns, calluses,
and warts other than by cutting or surgical means only;
(c) Nail care not involving surgery, except as
specified in He-W 532.05(a);
(d) Any podiatry service performed in the absence
of pathological conditions of the foot due to localized illness, injury or
symptoms involving the foot; and
(e) Office visits occurring on the same date of
service as a podiatry surgical procedure, except where additional non-podiatry
related medical conditions are addressed.
Source. (See Revision Note at chapter heading He-W
500); ss by #4818, eff 6-1-90, EXPIRED: 6-1-96
New. #6756, eff 5-22-98, EXPIRED: 5-22-06
New. #8642, INTERIM, eff 5-26-06, EXPIRES:
11-22-06; ss by #8745, eff 10-24-06; ss by #10814,
eff 4-21-15
He-W
532.07 Documentation. The podiatrist shall maintain:
(a) Supporting clinical records in accordance
with He-W 520;
(b) Specific written documentation in the
recipient’s medical record justifying the need for podiatry care in accordance
with He-W 532.05(a);
(c) Specific written documentation in the
recipient’s medical record, by the podiatrist, specifying the frequency of the
podiatry service(s) being performed;
(d) Specific written documentation in the
recipient’s podiatry medical record of all podiatry services performed; and
(e) A completed recipient medical history maintained in the
recipient’s podiatry medical record.
Source. (See Revision Note at chapter heading He-W
500); ss by #4818, eff 6-1-90, EXPIRED: 6-1-96
New. #6756, eff 5-22-98, EXPIRED: 5-22-06
New. #8642, INTERIM, eff 5-26-06, EXPIRES:
11-22-06; ss by #8745, eff 10-24-06; ss by #10814,
eff 4-21-15
He-W 532.08 Utilization Review and Control. The department’s provider integrity unit
shall monitor utilization of podiatry services to identify, prevent, and correct
potential occurrences of fraud, waste and abuse, in accordance with 42
CFR 455, 42 CFR 456
and He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #4818, eff 6-1-90, EXPIRED: 6-1-96
New. #6756, eff 5-22-98, EXPIRED: 5-22-06
New. #8642, INTERIM, eff 5-26-06, EXPIRES:
11-22-06; ss by #8745, eff 10-24-06; ss by #10814,
eff 4-21-15
He-W 532.09 Third Party Liability. All third party obligations shall be
exhausted before claims shall be submitted to the department’s fiscal agent in
accordance with 42 CFR 433.139.
Source. (See Revision Note at chapter heading He-W
500); ss by #4818, eff 6-1-90, EXPIRED: 6-1-96
New. #6756, eff 5-22-98, EXPIRED: 5-22-06
New. #8642, INTERIM, eff 5-26-06, EXPIRES:
11-22-06; ss by #8745, eff 10-24-06; ss by #10814,
eff 4-21-15
He-W 532.10 Payment for Services.
(a) Rates of payment for podiatry services shall
be established by the department in accordance with RSA 161:4, VI(a).
(b) The payment rates for podiatry surgical
procedures shall include:
(1) Pre-operative visits and consultations,
regardless of the treatment location;
(2) The podiatry surgical procedure;
(3) Casting at the time of surgery, if required;
and
(4) Normal uncomplicated follow-up for 30 days
following the podiatry surgical procedure, regardless of treatment location.
(c) The podiatrist shall submit claims for payment
to the department’s fiscal agent.
(d) Providers of podiatry services shall bill for
podiatry services utilizing CPT codes.
Source. (See Revision Note at chapter heading He-W
500); ss by #4818, eff 6-1-90, EXPIRED: 6-1-96
New. #6756, eff 5-22-98, EXPIRED: 5-22-06
New. #8642, INTERIM, eff 5-26-06, EXPIRES:
11-22-06; ss by #8745, eff 10-24-06; ss by #10814,
eff 4-21-15
PART
He-W 533 - RESERVED
He-W 533.01 - 533.09
Source. (See Revision Note at chapter heading He-W
500); ss by #4817, eff 6-1-90, EXPIRED: 6-1-96
New. #6700, eff 2-28-98, EXPIRES: 2-29-05; ss by #8573, eff 2-24-06;
rpld by #9622, eff 1-1-10
PART
He-W 534 ADVANCED REGISTERED NURSE
PRACTITIONER SERVICES
He-W
534.01 Definitions.
(a)
“Advanced practice registered nurse (APRN)” means a registered nurse
currently licensed by the New Hampshire board of nursing under RSA 326-B:18 or,
in states other than New Hampshire, a registered professional nurse
practitioner who, in accordance with 42 CFR 440.166, meets that state’s
advanced educational and clinical practice requirements, if any, beyond the 2
to 4 years of basic nursing education required of all registered nurses.
(b) “Current procedural terminology (CPT) code”
means a unique identifying code in the field of medical nomenclature and
designated by USDHHS as the national coding standard utilized in government and
private health insurance programs for reporting medical services and
procedures.
(c)
“Department” means the New Hampshire department of health and human
services.
(d)
“Healthcare Common Procedure Coding System (HCPCS)” means a standardized
coding system used by Medicare that describes services and procedures. HCPCS
includes CPT codes that are used primarily to identify products, supplies, and
services not included in the normal CPT code list, such as ambulance services
and durable medical equipment, prosthetics, orthotics, and supplies (DMEPOS),
when used outside a physician’s office.
(e)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department, which makes medical assistance available to eligible
individuals.
(f)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(g)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(h)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #4793, eff 3-30-90, EXPIRED: 3-30-96
New. #6701, eff 2-28-98, EXPIRES: 2-28-05; ss by
#8574, eff 2-24-06; amd by #10139, eff 7-1-12; ss by
#10512, eff
1-24-14
He-W
534.02 Recipient Eligibility. All NH medicaid
recipients shall be eligible to receive APRN services, in accordance with He-W
534.
Source. (See Revision Note at chapter heading He-W
500); ss by #4793, eff 3-30-90, EXPIRED: 3-30-96
New. #6701, eff 2-28-98, EXPIRES: 2-28-05; ss by
#8574, eff 2-24-06; ss by #10512, eff 1-24-14
He-W
534.03 Provider Participation. Each participating APRN shall:
(a) Be a New Hampshire (NH) enrolled medicaid provider;
(b) If practicing in NH, be licensed as an APRN
by the NH board of nursing in accordance with RSA 326-B:18; and
(c) If practicing in another state, submit
current proof of meeting that state’s advanced education and clinical
requirements to practice as a registered nurse in an advance practice role.
Source. (See Revision Note at chapter heading He-W
500); ss by #4793, eff 3-30-90, EXPIRED: 3-30-96
New. #6701, eff 2-28-98, EXPIRES: 2-28-05; ss by
#8574, eff 2-24-06; ss by #10512, eff 1-24-14
He-W 534.04 Service Limits. All services shall be subject to the service
limits set forth in He-W 530.
Source. (See Revision Note at chapter heading He-W
500); ss by #4793, eff 3-30-90, EXPIRED: 3-30-96
New. #6701, eff 2-28-98, EXPIRES: 2-28-05; ss by
#8574, eff 2-24-06; ss by #10512, eff 1-24-14; ss by #10657, eff
8-15-14
He-W 534.05 Covered Services. Covered services shall be those services set
forth in Nur 304.05.
Source. (See Revision Note at chapter heading He-W
500); ss by #4793, eff 3-30-90, EXPIRED: 3-30-96
New. #6701, eff 2-28-98, EXPIRES: 2-28-05; ss by
#8574, eff 2-24-06; ss by #10512, eff 1-24-14
He-W 534.06 Utilization Review & Control. The department’s provider program integrity
unit shall monitor utilization of APRN services to identify, prevent, and
correct potential occurrences of fraud, waste and abuse in accordance with in
accordance with He-W 520, 42 CFR 455, and 42 CFR 456.
Source. (See Revision Note at chapter heading He-W
500); ss by #4793, eff 3-30-90, EXPIRED: 3-30-96
New. #6701, eff 2-28-98, EXPIRES: 2-28-05; ss by
#8574, eff 2-24-06; ss by #10512, eff 1-24-14
He-W
534.07 Third Party Liability. All third party obligations shall be
exhausted before medicaid may be billed, in
accordance with 42 CFR 433.139.
Source. (See Revision Note at chapter heading He-W
500); ss by #4793, eff 3-30-90, EXPIRED: 3-30-96
New. #6701, eff 2-28-98, EXPIRES: 2-28-05; ss by
#8574, eff 2-24-06; ss by #10512, eff 1-24-14
He-W 534.08 Payment for Services.
(a)
The payment rates for APRN services shall be established by the
department in accordance with RSA 161:4, IV.
(b)
The APRN shall submit claims for payment to the department’s fiscal
agent.
(c)
The APRN shall use CPT and HCPCS codes and coding guidelines established
for use with these procedure codes when billing.
(d)
The APRN shall maintain supporting records, in accordance with He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #4793, eff 3-30-90, EXPIRED: 3-30-96
New. #6701, eff 2-28-98, EXPIRES: 2-28-05; ss by
#8574, eff 2-24-06; ss by #10512, eff 1-24-14
PART
He-W 535 PSYCHOTHERAPY SERVICES -
EXPIRED
Source. (See Revision Note at chapter heading He-W
500); ss by #6050, eff 6-17-95, EXPIRED: 6-17-03
PART
He-W 536 MEDICAL SERVICES CLINIC
He-W 536.01 Definitions.
(a)
“Department” means the New Hampshire department of health and human
services.
(b)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(c)
“Medical services clinic” means a facility or a mobile immunization
provider that is not part of a hospital but is organized to provide preventive,
diagnostic, therapeutic, rehabilitative, or palliative services to outpatients.
(d)
“Mobile immunization provider” means an agency organized to provide
immunizations at host facilities.
(e)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(f)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(g)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #6133, eff 11-30-95; ss by #7825, eff 2-8-03; ss by #9860, eff
2-8-11; amd by #10139, eff 7-1-12; ss by #12732,
INTERIM, eff 2-22-19, EXPIRED: 8-21-19
New. #12877, eff 9-25-19
He-W 536.02 Recipient Eligibility. All recipients shall be eligible for services
delivered by a medical services clinic in accordance with He-W 536.
Source. (See Revision Note at chapter heading He-W
500); ss by #6133, eff 11-30-95; ss by #7825, eff 2-8-03; ss by #9860, eff
2-8-11, EXPIRED: 2-8-19
New. #12732, INTERIM, eff 2-22-19, EXPIRED:
8-21-19
New. #12877, eff 9-25-19
He-W 536.03 Provider Participation. All participating medical services clinics
shall meet the following criteria in either (a) or (b) below:
(a)
Medical services clinics that are not mobile immunization providers
shall meet the following criteria:
(1) Be composed of New Hampshire licensed
practitioners who meet the provider requirements for the particular medical
service being performed as set forth in He-W 511 through He-W 577;
(2) Provide recipient care that is under the
supervision of a licensed physician affiliated with the clinic which shall mean
that:
a. The physician is readily available to provide
direction either by phone or in person;
b. The physician has seen the recipient as a
patient at least once and assesses the need for continuing care as necessary;
and
c. The physician assumes professional
responsibility for the services provided to the recipient;
(3) Provide medical care on an outpatient basis;
(4) Be organized and operated independently from
a hospital pursuant to 42 CFR 440.90;
(5) Be an enrolled New Hampshire medicaid provider; and
(6) Request and obtain prior authorization from
the department before providing services which require prior authorization as
specified in He-W 511 through He-W 577; or
(b)
Medical services clinics that are mobile immunization providers shall
meet the following criteria:
(1) Be composed of, and provide immunizations by,
New Hampshire licensed practitioners whose licensure allows them to provide
immunizations;
(2) Be under contract with, or have a current
vaccine provider agreement with, the department’s division of public health
services;
(3) Provide immunizations to recipients in
settings such as walk-in clinics, retail stores and outlets, pharmacies, and
schools;
(4) Provide immunizations as medicaid
services only in those settings and for those types or ages of recipients
addressed in the contract or agreement in (2) above;
(5) Provide services “under the direction of a
physician”, which means through standing orders or other indirect supervision
where the physician is not necessarily on site but who assumes professional
responsibility for the services provided to the recipient;
(6) Affiliate with the directing physician
through a contractual agreement or any other formal arrangement which obligates
the physician to supervise the care provided to the recipient by the clinic;
(7) Be organized and operated independently from
a hospital pursuant to 42 CFR 440.90; and
(8) Be an enrolled New Hampshire medicaid provider.
Source. (See Revision Note at chapter heading He-W
500); ss by #6133, eff 11-30-95; ss by #7825, eff 2-8-03; ss by #9860, eff
2-8-11, EXPIRED: 2-8-19
New. #12732, INTERIM, eff 2-22-19, EXPIRES:
8-21-19
He-W 536.04 Service Limits. The services provided by a medical services
clinic shall be subject to each of the specific service limits and provider
requirements for the services delivered and which are set forth in He-W 511
through He-W 577.
Source. (See Revision Note at chapter heading He-W
500); ss by #6133, eff 11-30-95; ss by #7825, eff 2-8-03; ss by #9860, eff
2-8-11; ss by #9860, eff 2-8-11, EXPIRED: 2-8-19
New. #12732, INTERIM, eff 2-22-19, EXPIRED:
8-21-19
New.
#12877, eff 9-25-19
He-W 536.05 Covered Services.
(a)
Except for those clinic providers who meet the mobile immunization
criteria in He-W 536.03(b), covered services provided by a medical services
clinic shall include medicaid covered services that
are referenced in He-W 511 through He-W 577.
(b)
Covered services provided by clinic providers who meet the mobile
immunization criteria in He-W 536.03(b) shall include only medically necessary
immunizations ordered by the directing physician.
Source. (See Revision Note at chapter heading He-W
500); ss by #6133, eff 11-30-95; ss by #7825, eff 2-8-03; ss by #9860, eff
2-8-11; ss by #9860, eff 2-8-11, EXPIRED: 2-8-19
New. #12732, INTERIM, eff 2-22-19, EXPIRED:
8-21-19
New. #12877, eff 9-25-19
He-W 536.06 Utilization Review and Control.
(a)
The department’s program integrity unit shall monitor utilization of
medical services clinics to identify, prevent, and correct potential
occurrences of fraud, waste, and abuse in accordance with 42 CFR 455, 42 CFR
456, 42 CFR 1001, and He-W 520.
(b)
The department shall recoup state and federal medicaid
payments as permitted by 42 CFR 455, 42 CFR 447, and 42 CFR 456 for a
provider’s failure to maintain supporting records in accordance with He-W 520
and He-W 536.
Source. (See Revision Note at chapter heading He-W
500); ss by #6133, eff 11-30-95; ss by #7825, eff 2-8-03; ss by #9860, eff
2-8-11, EXPIRED: 2-8-19
New. #12732, INTERIM, eff 2-22-19, EXPIRED:
8-21-19
New. #12877, eff 9-25-19
He-W 536.07 Third Party Liability. All third party obligations shall be
exhausted before medicaid shall be billed in
accordance with 42 CFR 433.139.
Source.
(See Revision Note at chapter heading He-W 500); ss by #6133, eff
11-30-95; ss by #7825, eff 2-8-03; ss by #9860,
eff 2-8-11, EXPIRED: 2-8-19
New. #12732, INTERIM, eff 2-22-19, EXPIRED:
8-21-19
New. #12877, eff 9-25-19
He-W 536.08 Payment for Services.
(a)
Payment for the services provided to recipients shall be made in
accordance with the rates established by the department for the individual
services provided in accordance with RSA 161:4, VI(a).
(b)
The provider shall submit claims for payment to the department’s fiscal
agent.
(c)
The provider shall maintain supporting records in accordance with He-W
520.
Source. (See Revision Note at chapter heading He-W
500); ss by #6133, eff 11-30-95; ss by #7825, eff 2-8-03; ss by #9860, eff
2-8-11, EXPIRED: 2-8-19
New. #12732, INTERIM, eff 2-22-19, EXPIRED:
8-21-19
New. #12877, eff 9-25-19
PART
He-W 537 RURAL HEALTH CLINICS/FEDERALLY
QUALIFIED HEALTH CENTERS
He-W
537.01 Definitions.
(a) “Encounter code” means a procedure code
assigned to each provider by the medicaid
administration bureau which reflects the individual payment rate and is
utilized by the rural health clinic and federally qualified health center
service providers for billing purposes.
(b) “Federally qualified health center (FQHC)”
means “federally qualified health center” as described in 42 CFR 491, Subpart
A, which is located in a rural or urban area that is designated as either a
shortage area or an area that has a medically underserved population.
(c) “Hospital based rural health clinic” means
“rural health clinic” as described in 42 CFR 491, Subpart A, which is an
integral part of a hospital that is participating in medicare,
and is licensed, governed, and supervised with other departments of the
hospital.
(d) “Independent rural health clinic” means
“rural health clinic” as described in 42 CFR 491, Subpart A, which is a
freestanding facility not administered by another facility.
(e) “Medically underserved population” means a
population of an urban or rural area which ahs a
shortage of personal health services as described in 42 CFR 491, Subpart A.
(f) “Rural health clinic (RHC),” means a primary
care facility or agency, either independent or hospital based, which is not a
rehabilitation agency nor a facility primarily for the care and treatment of
mental diseases and which is certified by medicare
pursuant to 42 CFR 491, Subpart A.
(g) “Shortage area” means “shortage area” as
defined by 1302(7) of the Public Health Services Act.
(h) “Visit” means a face-to-face encounter which
takes place on a single day, at a single location, between a recipient and a
health professional in a rural health clinic or FQHC.
Source. (See Revision Note at chapter heading He-W
500); ss by #4884, eff 8-1-90, EXPIRED: 8-1-96
New. #6725, eff 4-1-98, EXPIRED: 4-1-06
He-W
537.02 Recipient Eligibility. All medicaid
recipients shall be eligible for services delivered by a RHC or FQHC, in
accordance with He-W 537.
Source. (See Revision Note at chapter heading He-W
500); ss by #4884, eff 8-1-90, EXPIRED: 8-1-96
New. #6725, eff 4-1-98, EXPIRED: 4-1-06
He-W
537.03 Provider Participation. All participating RHCs and FQHCs shall:
(a) Be composed of licensed and N.H. board
certified practitioners;
(b) Be certified to participate in medicare as RHC and FQHC;
(c) Provide medical care on an outpatient basis;
(d) Be an enrolled New Hampshire medicaid provider; and
(e) Request and obtain prior authorization from
the medicaid administration bureau before providing
service which requires prior authorization, as specified in He-W 521.
Source. (See Revision Note at chapter heading He-W
500); ss by #4884, eff 8-1-90, EXPIRED: 8-1-96
New. #6725, eff 4-1-98
He-W
537.04 Service Limits. The individual services which compromise a
RHC and a FQHC visit shall be subject to the applicable limits, in accordance
with He-W 530.
Source. (See Revision Note at chapter heading He-W
500); ss by #4884, eff 8-1-90, EXPIRED: 8-1-96
New. #6725, eff 4-1-98, EXPIRED: 4-1-06
He-W
537.05 Covered Services.
(a) Covered
services for FQHCs and independent RHCs shall include the following outpatient
services:
(1) The services of a physician, when the
physician has an agreement to be paid by the clinic for such services;
(2) The services of a nurse practitioner, or
physician assistant, provided within the scope of his/her training or
certification;
(3) The services and supplies that are furnished
as incidental to the professional services of a physician, nurse practitioner,
or physician assistant;
(4) Laboratory services essential to the
immediate diagnosis and treatment of the patient; and
(5) Other ambulatory services provided within the
scope of the FQHC or RHC practice.
(b) Covered services for hospital-based RHCs
shall include the following outpatient services:
(1) The services of a physician, when the
physician has an agreement to be paid by the clinic for such services;
(2) The services of a nurse practitioner, or
physician assistant, provided within the scope of his/her training or
certification; and
(3) The services and supplies that are furnished
as incidental to the professional services of a physician, nurse practitioner,
or physician assistant.
Source. (See Revision Note at chapter heading He-W
500); ss by #4884, eff 8-1-90, EXPIRED: 8-1-96
New. #6725, eff 4-1-98, EXPIRED: 4-1-06
He-W
537.06 Utilization Review and Control. The department of health and human services
shall monitor utilization of RHC and FQHC services, in accordance with He-W
520.
Source. (See Revision Note at chapter heading He-W
500); ss by #4884, eff 8-1-90, EXPIRED: 8-1-96
New. #6725, eff 4-1-98, EXPIRED: 4-1-06
He-W
537.07 Third Party Liability. All third party obligations shall be
exhausted before medicaid may be billed in accordance
with He-W 521.
Source. (See Revision Note at chapter heading He-W
500); ss by #4884, eff 8-1-90, EXPIRED: 8-1-96
New. #6725, eff 4-1-98, EXPIRED: 4-1-06
He-W
537.08 Payment for Services.
(a) Payment for the RHC and FQHC services described
in He-W 537.05 above shall be made on the basis of an all-inclusive rate per
visit.
(b) RHC and FQHC providers shall bill for the
services described in He-W 537.05 above utilizing the encounter code assigned
by the department of health and human services.
(c) RHC and FQHC providers shall bill for
services other than the outpatient RHC/FQHC services described in He-W 537.05
above utilizing the appropriate procedure code listed in the current edition of
Current Procedural Terminology.
(d) Recipient encounters with more than one
health professional, or multiple encounters with the same health professional,
which take place on the same day for the same diagnosis or treatment, shall be
counted as one visit.
(e) RHCs and FQHCs shall bill for only one visit
per recipient per day, except for cases in which the patient, subsequent to the
first visit, suffers an illness or injury requiring additional diagnosis and
treatment.
(f) Payment shall be made in accordance with
encounter code rates established by the department of health and human
services.
(g) Independent RHCs and RQHCs shall submit
claims for payment to the department of health and human services’ fiscal agent
on form HCFA 1500.
(h) Hospital-based RHCs shall submit claims for
payment to the department of health and human services’ fiscal agent on form UB
92, also known as HCFA 1450.
(i) The RHC and FQHC
shall maintain supporting records, in accordance with He-W 520.
(j) The form HCFA 1500 in (g) above, and the form
UB 92, also know as HCFA 1450 in (h) above, pursuant
to 42 CFR 424.32, shall include:
(1) Patient and insured information;
(2) Physician or supplier information; and
(3) Carrier information.
Source. (See Revision Note at chapter heading He-W
500); ss by #4884, eff 8-1-90, EXPIRED: 8-1-96
New. #6725, eff 4-1-98, EXPIRED: 4-1-06
PART
He-W 538 CERTIFIED MIDWIFE SERVICES
He-W 538.01 Definitions.
(a)
“Department” means the NH department of health and human services.
(b)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(c)
“Midwifery” means the practice of providing the necessary supervision,
care, and advice to women during pregnancy, labor, and the postpartum period,
pursuant to RSA 326-D:2, V.
(d)
“New Hampshire certified midwife (NHCM)” means a person who is certified
to practice midwifery in accordance with RSA 326-D:6.
(e)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(f)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(g)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. #7657, eff 3-5-02, EXPIRED: 3-5-10
New. #9737, eff 6-25-10; amd
by #10139, eff 7-1-12, paras (a), (c), (d), and (g) EXPIRED: 6-25-18; ss by
#12783, eff 5-21-19
He-W 538.02 Recipient Eligibility. All recipients shall be eligible for NHCM
services, in accordance with this part.
Source. #7657, eff 3-5-02, EXPIRED: 3-5-10
New. #9737, eff 6-25-10, EXPIRED: 6-25-18
New. #12783, eff 5-21-19
He-W 538.03 Provider Participation. All NHCM providers shall:
(a)
Be enrolled New Hampshire medicaid providers;
and
(b)
Be certified to practice midwifery in New Hampshire pursuant to RSA
326-D:6.
Source. #7657, eff 3-5-02, EXPIRED: 3-5-10
New. #9737, eff 6-25-10, EXPIRED: 6-25-18
New. #12783, eff 5-21-19
He-W 538.04 Covered Services. Pursuant to RSA 326-D:2, V, covered NHCM services
shall include:
(a)
Providing supervision and advice during the recipient's:
(1) Pregnancy;
(2) Labor; and
(3) Postpartum period;
(b)
Providing care during the recipient's:
(1) Pregnancy, including:
a. Preventive care;
b. The detection of abnormal conditions of the
mother and fetus; and
c. The execution of emergency measures in the
absence of medical help;
(2) Labor, including:
a. The conduction of vaginal deliveries on their
own responsibility; and
b. The execution of emergency measures in the
absence of medical help; and
(3) Postpartum period, including:
a. Preventive care for the mother and newborn;
b. The detection of abnormal conditions of the
mother and newborn; and
c.
The execution of emergency measures for the
mother and newborn in the absence of medical help; and
(c)
Administering medications in accordance with RSA 326-D:12.
Source. #7657, eff 3-5-02, EXPIRED: 3-5-10
New.
#9737, eff 6-25-10, EXPIRED: 6-25-18
New. #12783, eff 5-21-19
He-W 538.05 Non-Covered Services. Non-covered services shall be those services
which a NHCM is not legally recognized to perform, pursuant to RSA 326-D:1, V,
including:
(a)
Operative obstetrics;
(b)
Cesarean sections;
(c)
General and conductive anesthesia;
(d)
Contraction stress tests;
(e)
Treatment to enhance fertility or procreation;
(f)
Any artificial, forcible, or mechanical means to assist the delivery;
and
(g)
Induced abortions.
Source. #7657, eff 3-5-02, EXPIRED: 3-5-10
New. #9737, eff 6-25-10, EXPIRED: 6-25-18
New. #12783, eff 5-21-19
He-W 538.06 Utilization Review and Control.
(a)
The department’s provider integrity unit shall monitor utilization of
NHCM services to identify, prevent, and correct potential occurrences of fraud,
waste, and abuse in accordance with 42 CFR 455, 42 CFR 456, 42 CFR 1001, and
He-W 520.
(b)
Failure to maintain supporting records in accordance with He-W 520 and
He-W 538 shall entitle the department to recoupment of state and federal medicaid payments pursuant to 42 CFR 455, 42 CFR 447, and
42 CFR 456.
Source. #7657, eff 3-5-02, EXPIRED: 3-5-10
New. #9737, eff 6-25-10, EXPIRED: 6-25-18
New. #12783, eff 5-21-19
He-W 538.07 Third Party Liability. All third party obligations shall be
exhausted before medicaid shall be billed, in
accordance with 42 CFR 433.139.
Source. #7657, eff 3-5-02, EXPIRED: 3-5-10
New. #9737, eff 6-25-10, EXPIRED: 6-25-18
New. #12783, eff 5-21-19
He-W 538.08 Payment for Services.
(a)
Payment for services to NHCM’s shall be made in accordance with rates
established by the department in accordance with RSA 161:4, VI(a).
(b)
The NHCM shall submit claims for payment to the department’s fiscal
agent.
(c)
The NHCM shall maintain supporting records, in accordance with He-W 520.
(d)
All electronic or written documentation shall be legible and written in
English.
(e)
All NHCM’s shall provide documentation to the department upon request.
Source. #7657, eff 3-5-02, EXPIRED: 3-5-10
New. #9737, eff 6-25-10, EXPIRED: 6-25-18
New. #12783, eff 5-21-19
PART
He-W 539 - RESERVED
PART
He-W 540 PRIVATE DUTY NURSING SERVICES
He-W
540.01 Definitions.
(a) “Clinically appropriate” means care that is:
(1) Provided in a timely manner and meets
professionally recognized standards of acceptable medical care;
(2) Delivered in the appropriate medical setting;
and
(3) The least costly of multiple, equally effective
alternative treatments or diagnostic modalities.
(b) “Department”
means the New Hampshire department of health and human services.
(c) “Medicaid”
means the Title XIX and Title XXI programs administered by the department which
makes medical assistance available to eligible individuals.
(d) “Order” means a written authorization issued by a licensed
practitioner for medications, treatments, recommendations, and referrals, and
signed by the licensed practitioner using terms such as authorized by,
authenticated by, approved by, reviewed by, or any other term that denotes
approval by the licensed practitioner.
(e) Licensed
practitioner” means:
(1) Physician;
(2) Physician's assistant;
(3) Advanced practice registered nurse (APRN); or
(4) Any practitioner with diagnostic and prescriptive powers licensed by
the appropriate state licensing board.
(f) “Plan of care” means a plan of care
prepared in accordance with 42 CFR 484.60.
(g) “Prior authorization agent” means an
individual or organization contracted by the department, responsible for
reviewing prior authorization requests.
(h) “Private duty nursing
(PDN)” means the provision of skilled nursing services for recipients who
require more individual
and continual skilled nursing observation, judgment, assessment, or
interventions than are available from a visiting nurse, in contrast to
part-time or intermittent care, such as wound care.
(i) “Reasonable attempt” means
such action taken to accomplish the purpose as may be customary, appropriate,
and suitable to the circumstances and that is in the best interests of the
recipient.
(j) “Recipient” means any individual who
is eligible for and receiving medical assistance under the medicaid program.
(k) “Skilled
nursing
services” means services that are provided by a registered nurse (RN) or a
licensed practical nurse (LPN) because the nature of the service is inherently
complex or the recipient’s condition is such that the service can be safely and
effectively provided only by a licensed nurse in accordance with the nurse practice act,
RSA 326-B.
(l) “Title
XIX program” means the joint federal-state program described in Title XIX of
the Social Security Act (SSA) and administered in New Hampshire by the department under the medicaid program.
(m) “Title
XXI” means the joint federal-state program described in Title XXI of the Social
Security Act and administered
in New Hampshire by the department under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #6134, eff 11-30-95, EXPIRED: 11-30-03
New. #8069, eff 4-17-04; ss by #10107, INTERIM,
eff
4-17-12, EXPIRES: 10-15-12; amd by #10139, eff 7-1-12;
ss by #10186, eff 10-15-12; ss by #13544, eff 1-28-23
He-W 540.02 Recipient
Eligibility. All recipients shall be eligible for PDN in
accordance with He-W 540 if the recipient:
(a) Requires
continual skilled nursing observation, judgment, assessment, or interventions
for more than a 2 hour duration
which can only be provided by an RN or LPN, to maintain or improve the
recipient’s health status; and
(b) Is
receiving nursing care
under a written plan of care established or approved by the recipient’s
physician or other licensed practitioner.
Source. (See Revision Note at chapter heading He-W
500); ss by #6134, eff 11-30-95, EXPIRED: 11-30-03
New. #8069, eff 4-17-04; ss by #10107, INTERIM,
eff
4-17-12, EXPIRES: 10-15-12; ss by #10186, eff 10-15-12; ss by #13544, eff
1-28-23
He-W 540.03 Provider
Participation. Each participating provider of PDN shall:
(a) Be a home health care provider licensed in accordance with RSA
151:2, and He-P 809;
(b) Require all staff providing PDN to be an RN
or an LPN licensed by the state in which the RN or LPN practices;
(c) Request and obtain prior authorization from the department or its
prior authorization agent, in accordance with He-W 540.07, before providing
PDN; and
(d) Provide to each recipient, or the recipient’s
caregiver if the recipient is a minor, the home health care provider’s written grievance policy that includes the phone number of
the department’s ombudsman’s office upon the initiation of PDN.
New. #8069, eff 4-17-04; ss by #10107, INTERIM,
eff
4-17-12, EXPIRES: 10-15-12; ss by #10186, eff 10-15-12; ss by #10186, eff
10-15-12; ss by #13544, eff 1-28-23
He-W
540.04 Covered Services. PDN shall be a covered
service when:
(a) It is part of the recipient’s medical regimen
and rendered under the order and general direction of the
recipient’s physician or other
licensed practitioner;
(b)
It is provided in one of the
following locations:
(1) The
recipient’s home; or
(2) In locations
other than the recipient’s home when routine life activities take the recipient
outside of the home if the services would have otherwise been provided in the
recipient’s home; and
(c) Prior authorization in accordance
with He-W 540.07 has been requested and obtained.
Source. (See Revision Note at chapter heading He-W
500); ss by #6134, eff 11-30-95, EXPIRED: 11-30-03
New. #8069, eff 4-17-04; ss by #10107, INTERIM,
eff
4-17-12, EXPIRES: 10-15-12; ss by #10186, eff 10-15-12; ss by #13544, eff
1-28-23
He-W
540.05 Non-covered
Services.
(a) PDN
shall not be a covered service when the recipient resides in any one of the
following:
(1) A
nursing facility licensed pursuant to RSA 151:2 and He-P 803;
(2) A
hospital licensed pursuant to RSA 151:2 and He-P 802;
(3) An
assisted living residence-supported residential health care (ALR-SRHC) facility
licensed pursuant to RSA 151:2 and He-P 805;
(4) A
private non-medical institution as defined in 42 CFR 434.2, and licensed
pursuant to RSA 151:2 and He-P 800;
(5) An
intermediate care facility for individuals with intellectual disabilities
(ICF/IID) as defined in 42 CFR 440.150; and
(6) An
institution for mental diseases (IMD) as defined in 42 CFR 435.1010.
(b) Services
that consist only of assistance with activities of daily living or other
non-skilled services needed to live at home that do
not require a nurse, including but not limited to assistance
with grooming, toileting, eating, dressing, getting into or out of a bed
or chair, and walking shall not be covered as PDN.
Source. (See Revision Note at chapter heading He-W
500); ss by #6134, eff 11-30-95, EXPIRED: 11-30-03
New. #8069, eff 4-17-04; ss by #10107, INTERIM, eff
4-17-12, EXPIRES: 10-15-12; ss by #10186, eff 10-15-12; ss by #13544, eff
1-28-23
He-W 540.06 Required
Documentation. For each recipient,
PDN service providers shall maintain complete and timely records as follows:
(a) A
written, signed, and
dated physician’s or other licensed practitioner’s order for care
provided, updated and signed every 60 days, which shall include:
(1) The recipient’s
diagnosis, with a description of the severity of the illness or condition; and
(2) A
detailed explanation of the medical need for PDN, including:
a. The
specific nursing
services that are required; and
b. A description of the specific
medical complications necessitating PDN;
(b) A
nursing
assessment with information that supports the need for PDN including, but not
limited to, the following:
(1) Recipient
identification information including:
a. Recipient name;
b. Medicaid identification number
(MID); and
c. Date
of birth;
(2) Contact
information of the recipient’s parent, guardian, or primary caregiver including
addresses and phone numbers;
(3) Private
health insurance information including coverage dates;
(4)
Information regarding the recipient’s participation in any medicaid program,
including medicaid to schools, waiver
programs, and licensed nursing assistant (LNA) services, or participation in
the special medical services program;
(5) Name
and contact information of the recipient’s treating physician or other licensed practitioner,
including the primary care physician, and any specialists;
(6) A
summary of the recipient's physical and behavioral health status including:
a. A list of the
recipient’s current conditions; and
b. A history of the conditions
leading to the need for PDN;
(7) An
assessment of the recipient’s body systems including a medication profile;
(8) A
functional assessment of the recipient’s physical and cognitive status
including a list of any durable medical equipment being utilized;
(9) A
description of the household make-up including the nature of the household
member’s relationship with the recipient and their ability and availability to
provide care and support to the recipient;
(10) Information
about the recipient’s school participation including the number of hours per
week the recipient attends and whether a nurse or aide is available to assist
the recipient while at school;
(11) The
recipient’s emergency plan in the event that the primary caregiver is
unable to provide care; and
(12) Any
additional medical or social information, such as family stressors and their
impact on the mental and emotional health of the recipient that the recipient
wants to provide that supports the need for PDN.
(c) A
plan of care documenting the extent of the recipient’s nursing needs, prepared
by the PDN service provider, signed and dated by the
recipient’s physician or other licensed practitioner, and updated
every 60 days in accordance with 42 CFR 484.60(c)(1);
(d) Nurses’
notes that fully document, for each date of service, the provision of services
and the care and treatment provided to the recipient,
including:
(1) The location of where the care was provided,
and the time that the nursing shift began and ended;
(2) A
description of each nursing service provided, including the type of nursing service,
the time of the service delivery, and the recipient’s response to the service
so that an independent reviewer can replicate what happened during
the shift;
(3) Details showing that the
nursing services are consistent with the care plan and orders of the
recipient’s physician or other
licensed practitioner;
(4) Any adverse findings
and, if so, a plan of action to address those findings; and
(5) The recipient’s
progress towards established goals; and
(e) Documentation
of a face-to-face encounter between the recipient’s physician or other licensed practitioner and the recipient
within 90 days prior to, or within 30 days following the start of, the PDN
service provision, as established in 42 USC 1395n of the SSA and in accordance with 42 CFR 440.
Source. (See Revision Note at chapter heading He-W
500); ss by #6134, eff 11-30-95, EXPIRED: 11-30-03
New. #8069, eff 4-17-04; ss by #10107, INTERIM,
eff
4-17-12, EXPIRES: 10-15-12; amd by #10139, eff 7-1-12;
ss by #10186, eff 10-15-12; ss by #13544, eff 1-28-23
He-W
540.07 Prior Authorization and Review.
(a) All
requests for PDN shall require written prior authorization from the department
or its prior authorization agent
before the recipient receives PDN.
(b) The
PDN
service provider shall submit a prior authorization request to the department
or its prior authorization agent, along with sufficient current medical and
psychosocial information to enable the department or its prior authorization
agent to evaluate the request and make a determination.
(c) The
information
required by (b) above shall include, but not be limited to:
(1) A
written, signed, and dated physician’s or other
licensed practitioner’s order, as described in He-W 540.06(a);
(2) The
nursing assessment, as described in He-W 540.06(b); and
(3) The
plan of care, as described in He-W 540.06(c).
(d) If
further medical information is necessary, the department or its prior
authorization agent shall contact the recipient’s physician, other
licensed practitioner, or PDN service provider directly by letter, fax, or
telephone and request the additional information.
(e) The
department
or its prior authorization agent shall determine if PDN is appropriate, and if
so, the number of hours authorized and the start and end date of the PDN
authorization period, based on an evaluation of the following clinical
information provided or gathered in accordance with (b)-(d) above:
(1) The
order and direction of the recipient’s physician or other licensed practitioner;
(2) The
frequency of the recipient’s need for skilled nursing observation,
judgment, assessment, or interventions;
(3) The
nursing assessment;
(4) The
identified problems and goals in the plan of care; and
(5) For
authorization extensions in (o) below, as applicable, the assessment of needs
based on the face-to-face nursing visit in (k) and (l) below.
(f)
The term of prior authorized services
shall be valid for no less than 6 months, unless a shorter term is identified
by the practitioner ordering the PDN services, from the start date and may be
longer based on the clinical prognosis of the recipient,
(g) Requests
for prior authorization shall be denied by the department or its prior
authorization agent if, based on the evaluation in (e) above:
(1) Any
of the requirements in He-W 540 are not met, including eligibility requirements
in He-W 540.02, coverage requirements in He-W 540.04 and 540.05, documentation
requirements in He-W 540.06, or prior authorization requirements in He-W
540.07; or
(2) It
is determined that:
a. The
recipient does not require skilled nursing services;
b.
The recipient does not require continual skilled nursing observation, judgment,
assessment, or interventions for more than a 2 hour duration; or
c. There
are less costly and equally effective alternatives available, such as care
provided by alternative providers including personal care attendants, licensed
nursing assistants, or homemakers, which will provide the recipient with the
same level of service.
(h) If
a request for prior authorization is denied by the department or its prior
authorization agent, notice of denial shall be forwarded to the recipient, to include:
(1) The
reason for, and legal basis of, the denial; and
(2) Information
that an administrative appeal on the denial may be requested within 30 calendar
days of the date on the notice of the denial, in accordance with He-C 200.
(i) If an initial request for authorization is
approved, the department or its prior authorization agent shall issue a temporary
initial authorization for a 90-day period.
(j)
Notice
of the initial authorization in (h) above shall be sent to the recipient and
the PDN service provider and include a face-to-face or virtual nursing visit
between the department, or its designated party, and the recipient shall be
completed within a 90-day period
(k) If
the
department or its prior authorization agent approves the prior authorization
request, then the PDN service provider shall receive notification, which
confirms the approval, includes the number of hours authorized and, documents
the start
and end date of the PDN authorization period.
(l) Within the 90 days in (i) above, and at least once annually for all approved
authorization requests, the department or its designated party shall conduct a face-to-face or virtual
nursing visit with the recipient in order to:
(1) Assess
the recipient’s needs;
(2) Identify
other supports in the home;
(3) Verify
the clinical appropriateness of the initial authorization or subsequent authorization
extensions made based on the clinical evaluation in (e) above; and
(4) Provide
education to the recipient.
(m) The face-to-face nursing visit may be
conducted in person virtually by electronic means.
(n) The
requirements of (i) through (m) above shall not apply
to recipients being discharged from any of the locations listed in He-W
540.05(a) when the department has participated in the recipient’s discharge
planning, except that the requirements for an annual nursing visit as described
in (l) above shall still apply.
(o) The department shall review subsequent
authorization requests within 90 days for continued approval.
(p) If
the face-to-face or virtual nursing visit confirms the initial authorization
was clinically appropriate, the department or its prior authorization agent
shall issue notification which confirms the approval, includes the number of
hours authorized, and documents the start and end date of the PDN
authorization period.
(q) For
PDN
to extend beyond the authorized duration, the PDN service provider shall
request and obtain prior authorization in accordance with this section.
Source. (See Revision Note at chapter heading He-W
500); ss by #6134, eff 11-30-95, EXPIRED: 11-30-03
New. #8069, eff 4-17-04; ss by #10107, INTERIM,
eff
4-17-12, EXPIRES: 10-15-12; ss by #10186, eff 10-15-12; ss by #13544, eff
1-28-23
He-W
540.08 Utilization
Review and Control.
(a) The department’s program integrity unit shall
monitor utilization of PDN, in accordance with 42 CFR 455, 42 CFR 456, 42 CFR
1001 and He-W 520; and
(b) The department shall recoup state and federal medicaid payments as permitted by 42 CFR 455, 42 CFR 447,
and 42 CFR 456 for a provider’s failure to maintain supporting records in
accordance with He-W 520 and He-W 540.
Source. (See Revision Note at chapter heading He-W
500); ss by #6134, eff 11-30-95, EXPIRED: 11-30-03
New. #8069, eff 4-17-04; ss by #10107, INTERIM,
eff
4-17-12, EXPIRES: 10-15-12; ss by #10186, eff 10-15-12; ss by #13544, eff
1-28-23
He-W
540.09 Third Party Liability.
(a) All third
party obligations shall be exhausted before medicaid shall
be billed, in accordance with 42 CFR 433.139.
(b) PDN
service providers shall request information from the recipient regarding other
insurance coverage.
(c) If
other insurance coverage is available, providers shall contact the insurer to
verify benefits initially and at least annually thereafter or when the
insurance carrier changes.
(d) PDN
service providers shall maintain a record of any other insurance verifications
in the recipient’s medical record in accordance with He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #6134, eff 11-30-95, EXPIRED: 11-30-03
New. #8069, eff 4-17-04; ss by #10107, INTERIM,
eff
4-17-12, EXPIRES: 10-15-12; ss by #10186, eff 10-15-12; ss by #13544, eff
1-28-23
He-W
540.10 Payment
for Services.
(a) Payment
for PDN shall be made in accordance with rates established by the department in
accordance with RSA 161:4, VI(a).
(b) Payments for services
billed shall be for direct care only, and shall not include
administrative work or travel time.
(c) The
provider shall submit claims for payment to the department’s
fiscal agent.
(d) The
provider shall maintain supporting records, in accordance with
He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #6134, eff 11-30-95, EXPIRED: 11-30-03
New. #8069, eff 4-17-04; ss by #10107, INTERIM,
eff 4-17-12, EXPIRES: 10-15-12; ss by #10186, eff 10-15-12; ss by #13544, eff
1-28-23
He-W 541.01 Definitions.
(a) “Clean claim(s)” means a claim that can be
processed without obtaining additional information from the provider or from a
third party, including a claim with errors originating in the state’s claims
system, but not including a claim from a dispensing provider who is under
investigation for fraud or abuse or a claim under review for medical necessity.
(b)
“Department” means the New Hampshire department of health and human
services.
(c) “Family planning services” means medical
services, medical procedures, and pharmaceutical supplies and devices provided
by or under the supervision of a physician or other health professional that
allow a recipient to prevent or delay pregnancy or to otherwise control family
size, and which receive an enhanced match rate of 90% federal match.
(d)
“Hysterectomy” means a surgical procedure for the purpose of removing
the uterus.
(e)
“Institutionalized individual” means an individual who:
(1) Is involuntarily confined or detained under a
civil or criminal statute, in a correctional or rehabilitative facility,
including a mental hospital or other facility for the care and treatment of
mental illness; or
(2) Is confined under a voluntary commitment in a
mental hospital or other facility for the care and treatment of mental illness.
(f) “Medicaid” means the Title XIX and Title XXI
programs administered by the department which makes medical assistance available
to eligible individuals.
(g)
“Mentally incompetent individual” means a mentally incompetent
individual as defined in 42 CFR 441.251.
(h) “Recipient” means any individual who is
eligible for and receiving medical assistance under the medicaid
program.
(i) “Sterilization” means any medical procedure,
treatment or surgical procedure which is intended to render an individual
permanently incapable of reproducing.
(j) “Title XIX program” means the joint
federal-state program described in Title XIX of the Social Security Act and
administered in New Hampshire by the department under the medicaid
program.
(k) “Title XXI” means the joint federal-state
program described in Title XXI of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
Source. (See Revision Note at chapter heading He-W
500); ss by #5874, eff 8-1-94; ss by #7329, eff 8-1-00, EXPIRED: 8-1-08
New. #9272, eff 9-19-08;
amd by #10139, eff 7-1-12; ss by #12053, eff 11-19-16
He-W 541.02 Recipient Eligibility.
(a)
All Medicaid recipients of child bearing age and not known to be
pregnant shall be eligible for family planning services, in accordance with
He-W 541.
(b)
Acceptance of any family planning services shall be voluntary on the
part of the recipient and shall not be a prerequisite or impediment to
eligibility for any other service or assistance program administered by the
department.
Source. (See Revision Note at chapter heading He-W
500); ss by #5874, eff 8-1-94; ss by #7329, eff 8-1-00, EXPIRED: 8-1-08
New. #9272, eff 9-19-08; ss by #12053, eff
11-19-16
He-W 541.03 Provider Participation. All family planning providers shall be:
(a)
Licensed by the state in which she or he practices or be a NH certified
midwife; and
(b)
A New Hampshire enrolled Medicaid provider.
Source. (See Revision Note at chapter heading He-W
500); ss by #5874, eff 8-1-94; ss by #7329, eff 8-1-00, EXPIRED: 8-1-08
New. #9272, eff 9-19-08; ss by #12053, eff
11-19-16
He-W 541.04 Service Limits. Family planning services for recipients shall
be subject to the limits described in He-W 530.
Source. (See Revision Note at chapter heading He-W
500); ss by #5874, eff 8-1-94; ss by #7329, eff 8-1-00, EXPIRED: 8-1-08
New. #9272, eff 9-19-08; ss by #12053, eff
11-19-16
He-W 541.05 Covered Services. The following services shall be covered as
family planning services only if the items and procedures are clearly provided
or performed for family planning purposes:
(a)
Physician services, in accordance with He-W 531, certified midwife
services in accordance with He-W 538, and advanced practice registered nurse
services in accordance with He-W 534;
(b)
Contraceptive devices or drugs, both prescription and non-prescription,
in accordance with He-W 570;
(c)
Pregnancy tests and screening for sexually transmitted diseases only
when performed routinely as part of an initial, regular, or follow-up family
planning visit; and
(d) Sterilization, in accordance with 42 CFR
441.253 and 42 CFR 441.254, as follows:
(1) The recipient shall be at least 21 years old
at the time consent is obtained;
(2) The recipient shall not be a mentally
incompetent individual;
(3) The recipient shall not be an
institutionalized individual;
(4) The recipient shall voluntarily give informed
consent in accordance with the requirements at 42 CFR 441.257 through 42 CFR
441.258;
(5) The provider shall submit the federal health
and human services office of management and budget form HHS-687 “Consent for
Sterilization” (OMB No. 0937-0166) to the department prior to the department’s
payment for the sterilization claim;
(6) At least 30 days, but not more than 180 days,
shall have passed between the date of informed consent and the date of
sterilization, with the exception of cases of premature delivery or emergency
abdominal surgery as described in (7) below; and
(7) A recipient may consent to be sterilized at
the time of a premature delivery or emergency abdominal surgery if at least 72
hours have passed since the recipient gave informed consent for the
sterilization and, in the case of premature delivery, if the informed consent
was given at least 30 days before the expected date of delivery.
Source. (See Revision Note at chapter heading He-W
500); ss by #5874, eff 8-1-94; ss by #7329, eff 8-1-00, EXPIRED: 8-1-08
New. #9272, eff 9-19-08; ss by #12053, eff
11-19-16
He-W 541.06 Non-Covered Services.
(a)
The following services shall not be covered as family planning services:
(1) Sterilizations which do not meet the
requirements of He-W 541.05(d) above;
(2) Hysterectomies;
(3) Medical, surgical, or pharmaceutical
treatment for the purpose of enhancing, promoting or restoring fertility;
(4) Medical procedures performed for medical
reasons such as the removal of an IUD due to an infection, diagnostic
examination of the cervix or vagina by means of a special microscope,
colposcopy, biopsy, or cryotherapy of the cervix or vagina;
(5) Treatment of medical complications caused by,
or following, a family planning procedure;
(6) Any medical service, procedure, or
pharmaceutical supply or device provided to a recipient who is known to be
pregnant; and
(7) Pregnancy and sexually transmitted disease
tests, except for those performed as part of an initial or annual family
planning examination.
(b)
The services in (a)(2) and (a)(4) through (a)(7) above which are non-covered
as family planning services shall be covered in accordance with He-W 531, He-W
534, He-W 538, He-W 570, and 42 CFR 441, Subpart F.
Source. (See Revision Note at chapter heading He-W
500); ss by #5874, eff 8-1-94; ss by #7329, eff 8-1-00, EXPIRED: 8-1-08
New. #9272, eff 9-19-08; ss by #12053, eff
11-19-16
He-W 541.07 Co-Payments. In accordance with He-W 570, co-payments for
family planning pharmaceutical products shall not be required.
Source. (See Revision Note at chapter heading He-W
500); ss by #5874, eff 8-1-94; ss by #7329, eff 8-1-00, EXPIRED: 8-1-08
New. #9272, eff 9-19-08; ss by #12053, eff
11-19-16
He-W 541.08 Utilization Review and Control. The department’s program integrity unit shall
monitor utilization of family planning services to identify, prevent, and
correct potential occurrences of fraud, waste, and abuse, in accordance with 42
CFR 455, 42 CFR 447, 42 CFR 456, and He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #5874, eff 8-1-94; ss by #7329, eff 8-1-00, EXPIRED: 8-1-08
New. #9272, eff 9-19-08 (from He-W 541.07); ss by
#12053, eff 11-19-16
He-W 541.09 Third Party Liability. All third party obligations shall be
exhausted before medicaid shall be billed, in
accordance with 42 CFR 433.
Source. (See Revision Note at chapter heading He-W
500); ss by #5874, eff 8-1-94; ss by #7329, eff 8-1-00, EXPIRED: 8-1-08
New. #9272, eff 9-19-08 (from He-W 541.08); ss by
#12053, eff 11-19-16
He-W 541.10 Payment for Services.
(a)
Rates of payment for family planning services shall be established by
the department in accordance with RSA 161:4, VI(a).
(b)
The provider shall submit clean claims for payment.
(c)
The provider shall maintain supporting records in accordance with He-W
520 and shall keep documentation supporting claims and records necessary to
disclose the extent of services the provider furnishes to medicaid
recipients in accordance with He-W 520.
Source.
#9272, eff 9-19-08 (from He-W 541.09); ss by #12053, eff 11-19-16
PART
He-W 542 ABORTION SERVICES - EXPIRED
Source. (See Revision Note at chapter heading He-W
500); ss by #4968, eff 11-7-90, EXPIRED: 11-7-96
PART
He-W 543 HOSPITAL SERVICES
He-W 543.01 Definitions.
(a)
“Acute care” means those services provided to recipients, other than
swing bed patients, in a hospital.
(b)
“Border hospital” means a hospital which is located in a state bordering
New Hampshire and which has not requested, and been granted, enrollment as an out-of-state
hospital.
(c)
“Budget neutrality factors” means adjustments applied to rate-setting
methodology to reduce spending growth.
(d) “Centers for Medicare and Medicaid Services
(CMS)” means the division of the federal Department of Health and Human
Services that administers medicare, medicaid, the children’s health insurance program, and the
health insurance marketplace.
(e)
“Day outlier” means those cases for which the actual length of stay
exceeds the trim point per diagnosis related group.
(f)
“Department” means the New Hampshire department of health and human
services.
(g)
“Diagnosis related group (DRG)” means the taxonomy of diagnoses as
classified in the medicare DRG classification system
which groups hospital inpatient cases according to factors such as principal
diagnosis, age, and sex, and assigns a relative weight which represents
hospital resource use associated with treatment for the diagnosis, pursuant to
42 CFR 412.60.
(h)
“Generally accepted standards of medical practice” means standards that
are based on credible scientific evidence published in peer-reviewed medical
literature generally recognized by the relevant medical community, or the
recommendations of physician specialists practicing in relevant clinical areas
or of various physician specialty societies.
(i) “Hospital” means any hospital providing acute
care services, to include acute care rehabilitation services, not operating as
a psychiatric hospital or an institution for mental diseases and which meets
the requirements of 42 CFR 440.10.
(j) “In-state hospital” means a
hospital which is located within the physical boundaries of New Hampshire.
(k)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(l)
“Medically necessary” means:
(1) For individuals under age 21, reasonably
calculated to prevent, diagnose, correct, cure, alleviate, or prevent the
worsening of conditions that endanger life, cause pain, result in illness or
infirmity, threaten to cause or aggravate a handicap, or cause physical
deformity or malfunction, and no other equally effective course of treatment is
available or suitable for the EPSDT recipient requesting a medically necessary
service; and
(2) For individuals age 21 and over, health care
services that a licensed health care provider, exercising prudent clinical
judgment, would provide, in accordance with generally accepted standards of
medical practice, to a recipient for the purpose of evaluating, diagnosing,
preventing, or treating an acute or chronic illness, injury, disease, or its
symptoms, and that are:
a. Clinically appropriate in extent, site, and
duration, and consistent with the established diagnosis or treatment of the recipient’s
illness, injury, disease, or its symptoms;
b. Not primarily for the convenience of the
recipient or the recipient’s family, caregiver, or health care provider;
c. No more costly than other items or services
which would produce equivalent diagnostic, therapeutic, or treatment results as
related to the recipient’s illness, injury, disease, or its symptoms; and
d. Not experimental, investigative, cosmetic, or
duplicative in nature.
(m)
“Observation services” means services furnished by a hospital on the
hospital’s premises, including the use of a bed and periodic monitoring by a
hospital’s nursing or other staff, which are reasonable and necessary to
evaluate an outpatient’s condition or determine the need for a possible
admission to the hospital as an inpatient.
(n)
“Out-of-state hospital” means a hospital located in a state not
bordering New Hampshire, or a border hospital that has requested, and been
granted, enrollment as an out-of-state hospital.
(o)
“Quality improvement organization (QIO)” means an organization or other
agency established in accordance with 42 CFR 475 that performs utilization and
quality control peer reviews in accordance with 42 CFR 476 when contracted by
the department for the performance of such reviews.
(p)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(q)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(r)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #5897, eff 9-19-94; amd by #6548, eff
7-26-97; ss by #7399, eff 11-2-00, EXPIRED: 11-2-08
New. #9324, eff 11-21-08;
amd by #10139, eff 7-1-12; ss by #12103, eff 2-9-17; amd by #12818, eff 7-1-19
He-W 543.02 Recipient Eligibility. All recipients shall be eligible to receive
inpatient and outpatient hospital services in accordance with He-W 543, and within the
service limits described in He-W 530.
Source. (See Revision Note at chapter heading He-W
500); ss by #5897, eff 9-19-94, EXPIRED: 9-19-00
New. #7399, eff 11-2-00, EXPIRED: 11-2-08
New. #9324, eff 11-21-08; ss by #12103, eff 2-9-17
He-W 543.03 Provider Participation.
(a)
All in-state, out-of-state, and border hospital providers shall:
(1) Be licensed by the department in accordance
with RSA 151, or by the relevant state licensing authority in the state within
which the provider operates;
(2) Meet medicare participation
requirements; and
(3) Be a New Hampshire enrolled medicaid provider in accordance with the following:
a. In-state hospitals shall be enrolled as
in-state hospital providers;
b. Out-of-state hospitals shall be enrolled as
out-of-state hospital providers; and
c. Border hospitals shall be enrolled as border
hospitals except as follows:
1. Enrollment as an out-of-state hospital shall
be granted to any border hospital that requests such enrollment, either upon
initial enrollment or at a later date; and
2. Border hospitals that are enrolled as
out-of-state hospitals shall be subject to all out-of-state hospital
requirements.
Source. (See Revision Note at chapter heading He-W
500); ss by #5897, eff 9-19-94, EXPIRED: 9-19-00
New. #7399, eff 11-2-00, EXPIRED: 11-2-08
New. #9324, eff 11-21-08; ss by #12103, eff 2-9-17
He-W 543.04 Prior Authorization.
(a)
Out-of-state hospitals shall obtain prior authorization (PA) from the
department before providing inpatient hospital services to recipients, except
that authorization for emergency hospital services shall be obtained within 72
hours of admission.
(b)
Inpatient hospital services at out-of-state hospitals shall be limited
as follows:
(1) For recipients who are absent from the state,
one of the following conditions shall be met:
a. Medical services are needed because of a
medical emergency;
b. Medical services are needed and the
recipient’s health would be endangered if he or she were required to travel to
his or her state of residence; or
c. Needed medical services, or necessary
supplementary resources, are more readily available in the other state; or
(2) For recipients who are in state but request
to receive services out of state, one of the following conditions shall be met:
a. Medical services are needed because of a
medical emergency;
b. The recipient’s attending physician has:
1. Proposed out-of-state hospitalization;
2. Determined that the proposed treatment plan
is medically necessary; and
3. Determined that the proposed treatment is not
available from resources and facilities within the state;
c. The recipient’s attending physician has:
1. Proposed out-of-state hospitalization;
2. Determined that the proposed treatment plan
is medically necessary; and
3. Determined that redirection to an in-state
facility would jeopardize either the treatment of an episode of care or a long
standing medical relationship between the recipient and a specific physician;
d. The recipient is age 18 or younger and the
recipient’s attending physician has:
1. Proposed out-of-state hospitalization;
2. Determined that the proposed treatment plan
is medically necessary; and
3. Determined that referral to a pediatric
specialist is appropriate and there is no such pediatric specialist available
in New Hampshire;
e. The out-of-state hospital is an enrolled
provider and only the medicare deductible and
co-insurance are to be billed to NH medicaid;
f. The out-of-state hospital care is provided
prior to a recipient’s eligibility determination and coverage is retroactive to
the time period in which the hospitalization occurred and the hospital is a medicaid enrolled provider; or
g. It is the general practice for recipients in
a particular NH locality to use medical resources in another state and the
costs of obtaining care at the out-of-state hospital will result in no higher
costs than the costs of obtaining in state hospital care.
(c)
Prior authorization requests shall be submitted as follows:
(1) On Form 272H, “Request for Prior
Authorization for Out of State Inpatient Admission” (10/2015 edition);
(2) The form shall be signed and dated by a
primary care physician, treating physician, or advanced practice registered
nurse requesting the service;
(3) The person in (2) above shall certify that
“…the requested treatments and/or procedures are medically necessary and cost
effective in obtaining measurable, realistic goals for the above-named recipient”;
and
(4) The form shall be submitted with physician’s
notes and clinical notes supporting the medical necessity for the requested
services, including, but not limited to, the medical care plan, relevant
diagnostic tests, and progress notes.
(d)
The department shall grant prior authorization if the documentation on
Form 272H supports the requirements in (b) above.
(e)
If the department approves the PA request, the state’s fiscal agent
shall send written confirmation of the approval to the provider.
(f)
The provider shall be responsible for determining that the recipient is medicaid eligible on the date of service.
(g)
If the department denies the PA request, the department shall forward a
notice of denial to the recipient and the ordering provider on the department
Form 272a, “Medical Assistance Program Denial for Prior Authorized Services,”
which includes the following information:
(1) The reason for, and legal
basis of, the denial; and
(2) Information that a fair hearing on the denial
may be requested within 30 calendar days of the date on the notice of the
denial, in accordance with He-C 200.
Source. (See Revision Note at chapter heading He-W
500); ss by #5897, eff 9-19-94, EXPIRED: 9-19-00
New. #7399, eff 11-2-00, EXPIRED: 11-2-08
New. #9324, eff 11-21-08; amd
by #10031, eff 11-19-11; ss by #12103, eff 2-9-17
He-W 543.05 Covered Services.
(a)
Covered services shall include those services described in the various
service component rules found in this chapter which may be provided in a
hospital setting as either an inpatient or outpatient hospital service.
(b)
Inpatient hospital services shall be covered when those services are
rendered:
(1) By or under the direction of a physician or
dentist;
(2) To a recipient who has been admitted to a
hospital as an inpatient;
(3) For a continuous period of 24 hours or longer;
(4) By a hospital offering room, board, and
professional services; and
(5) By a NH medicaid
participating hospital which meets the requirements set forth in He-W 543.03.
(c)
Outpatient hospital services shall be covered when those services are rendered:
(1) As preventive, diagnostic, therapeutic,
rehabilitative, emergency, or palliative outpatient services;
(2) Within the service limits set forth in He-W
530;
(3) By or under the direction of a physician or
dentist;
(4) To a recipient who has not been admitted as
an inpatient;
(5) For a period of time less than 24 hours; and
(6) By a NH medicaid
participating hospital which meets the requirements set forth in He-W 543.03.
(d)
Observation services, as defined in He-W 543.01(m), shall be covered in
accordance with He-W 543.05(c), above.
(e)
Inpatient hospital services provided at an out-of-state hospital shall
be covered pursuant to the prior authorization requirements of He-W 543.04.
(f)
Organ transplant procedures and procurements shall be covered when
performed as an inpatient service at an organ transplant facility approved by
CMS and in accordance with the requirements and limits at He-W 531.
Source. (See Revision Note at chapter heading He-W
500); ss by #5897, eff 9-19-94, EXPIRED 9-19-00
New. #7399, eff 11-2-00, EXPIRED: 11-2-08
New. #9324, eff 11-21-08 (from He-W 543.04); ss by
#12103, eff 2-9-17
He-W 543.06 Non-Covered Services.
(a) Services which are not described in the
various service component rules in this chapter shall be non-covered in a
hospital setting as either inpatient or outpatient hospital services.
(b)
Services provided to recipients by psychiatric hospitals or in institutions
for mental diseases shall be non-covered services under He-W 543.
Source. (See Revision Note at chapter heading He-W
500); ss by #5897, eff 9-19-94, EXPIRED 9-19-00
New. #7399, eff 11-2-00, EXPIRED: 11-2-08
New.
#9324, eff 11-21-08; ss by #12103, eff 2-9-17
He-W 543.07 Readmission to Hospital. A separate payment shall not be made for
readmission to any hospital for the same diagnosis if the readmission occurs
within 30 days of discharge, except for those cases where the department or its
designated QIO have given medical necessity approval in accordance with He-W
543.11.
Source.
(See Revision Note at chapter heading He-W 500); ss by #5897, eff
9-19-94, EXPIRED 9-19-00
New. #7399, eff 11-2-00, EXPIRED: 11-2-08
New. #9324, eff 11-21-08 (from He-W 543.05); ss by
#12103, eff 2-9-17; ss by #12818, eff 7-1-19
He-W 543.08 Transfer of Recipient.
(a)
A hospital which transfers or discharges a recipient from a unit in a
hospital to the same type of unit in another hospital for continued inpatient
hospital services shall be paid 100 percent of the per diem for each day of
care, not to exceed the DRG rate, except for rehabilitative and newborn cases,
which shall be paid in accordance with He-W 543.13(a).
(b) A hospital which transfers or discharges a
recipient to a different type of unit in another hospital, or different type of
unit within the same hospital for continued inpatient hospital services, shall
be paid according to the DRG payment designated for the type of services
provided, plus day outlier payments, if applicable.
(c)
The receiving hospital which does not transfer a recipient to another
hospital shall be paid the DRG rate, plus day outlier payments, if applicable,
when the recipient is discharged.
(d)
If a recipient is transferred back, or readmitted to the original
admitting hospital unit for continuing treatment, only one DRG payment, plus
day outlier payments if applicable, shall be paid for the combined initial
admission and subsequent readmission to that hospital unit.
(e)
The hospital unit which receives and then transfers a recipient back to
the original admitting hospital unit shall also be considered a transferring
hospital and shall be paid in accordance with He-W 543.08(a) or He-W 543.08(b),
as applicable, above.
Source. (See Revision Note at chapter heading He-W
500); ss by #5897, eff 9-19-94, EXPIRED 9-19-00
New. #7399, eff 11-2-00, EXPIRED: 11-2-08
New.
#9324, eff 11-21-08; ss by #12103, eff 2-9-17
He-W 543.09 Split Eligibility. When a recipient is eligible for only part of
a hospital stay, the medicaid payment shall be made
at 100 percent of the per diem for each day of care on which the recipient is medicaid eligible, not to exceed the DRG rate, except for
rehabilitative cases, which shall be paid in accordance with He-W 543.13(a).
Source. (See Revision Note at chapter heading He-W
500); ss by #5897, eff 9-19-94, EXPIRED 9-19-00
New. #7399, eff 11-2-00, EXPIRED: 11-2-08
New. #9324, eff 11-21-08 (from He-W 543.07); ss by
#12103, eff 2-9-17
He-W 543.10 Medicare Participation. For inpatient services, the 60-day lifetime
reserve medicare inpatient hospital benefit for medicare-eligible recipients shall be used before medicaid inpatient hospital payments are made.
Source. (See Revision Note at chapter heading He-W
500); ss by #5897, eff 9-19-94, EXPIRED 9-19-00
New. #7399, eff 11-2-00, EXPIRED: 11-2-08
New.
#9324, eff 11-21-08 (from He-W 543.08); ss by #12103, eff 2-9-17
He-W 543.11 Utilization Review.
(a)
Evaluations of the quality, medical necessity, appropriateness of care,
and length of stay determinations for all inpatient hospital services at
in-state and border hospitals shall be made by the department or its designated
QIO in accordance with 42 CFR 456.100 and those sections of 42 CFR 456
described therein.
(b)
The department’s program integrity unit shall monitor utilization of
hospital services to identify, prevent, and correct potential occurrences of
fraud, waste, and abuse, in accordance with 42 CFR 455, 42 CFR 447, 42 CFR 456,
and He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #5897, eff 9-19-94; amd by #6548, eff
7-26-97; ss by #7399, eff 11-2-00; ss by #7558, eff 10-1-01; ss by #9324, eff 11-21-08
(from He-W 543.09); ss by #12103, eff 2-9-17; amd by
#12818, eff 7-1-1-19
He-W 543.12 Third Party Liability. All third party obligations shall be
exhausted before medicaid may be billed, in
accordance with 42 CFR 433.139.
Source.
#9324, eff 11-21-08 (from He-W 543.10); ss by #12103, eff 2-9-17
He-W 543.13 Payment for Services.
(a)
Payment for hospital services shall be made at rates established by the
department in accordance with RSA 161:4, VI(a).
(b)
Hospital providers shall submit claims for payment to the department’s
fiscal agent using the form currently designated and approved by CMS for this
purpose.
(c)
Hospital providers billing for newborns who do not have their own medicaid identification number shall complete the claim
form as follows:
(1) The newborn’s name shall be entered in the
patient field;
(2) The medicaid
identification number field shall be left blank; and
(3) The mother’s name and medicaid
identification number shall be entered in the remarks section.
(d)
Payment for inpatient hospital services shall be made for acute care days
of stay only when approved by the department or its designated QIO.
(e)
All outpatient hospital services rendered to a medicaid
recipient within 3 calendar days prior to his or her inpatient admission, with
a calendar day beginning at 12:00 AM and ending at 11:59 PM, shall be inclusive
of the inpatient payment and not be billed separately, with the exception of:
(1) Prenatal outpatient services; and
(2) Diagnostic and
nondiagnostic outpatient services that are unrelated to the recipient’s inpatient
hospital admission.
Source.
#9324, eff 11-21-08 (from He-W 543.11); ss by #12103, eff 2-9-17; amd by #12818, eff 7-1-19
PART
He-W 544 HOSPICE SERVICES
He-W 544.01 Definitions.
(a)
“Agent” means an adult to whom authority to make health care decisions
is delegated under an activated durable power of attorney for health
care executed in accordance with RSA 137-J.
(b) “Attending physician” means the
doctor of medicine or osteopathy or the advance practice registered nurse who
is identified by the recipient at the time of election of hospice care as
having the most significant role in the determination and delivery of medical
care to the recipient.
(c)
Bereavement counseling” means emotional, psychosocial, and spiritual
support and services provided before and after death of the recipient to assist
with issues related to grief, loss, and adjustment.
(d)
“Continuous home care” means hospice care consisting of primarily
nursing care provided by hospice personnel on a continuous basis at home.
(e)
“Day” means the 24-hour period starting at 12:00AM and ending at 11:59PM
of the same day.
(f)
“Department” means the New Hampshire department of health and human services.
(g) “Dietary counseling” means
education and interventions provided to the recipient and family regarding
appropriate nutritional intake as the recipient’s condition progresses and
provided by qualified individuals including a registered nurse, dietician, or
nutritionist, when identified in the recipient’s plan of care.
(h)
“Election period” means one or more periods for which a recipient may
elect to receive medicaid coverage for hospice care,
as follows:
(1) Two 90-day periods; and
(2) An unlimited number of subsequent 60-day
periods.
(i) “Employee” means:
(1) An employee of the hospice;
(2) If the hospice is a subdivision of an agency
or organization, an employee of the agency or organization who is appropriately
trained and assigned to the hospice unit; or
(3) A volunteer under the jurisdiction of the
hospice.
(j)
“General inpatient care” means hospice care received in an inpatient
facility for pain control or symptom management, which cannot be managed in
other settings.
(k)
“Hospice” means a comprehensive set of services described in section
1861(dd)(1) of the Social Security Act, identified and coordinated by an
interdisciplinary group to provide for the physical, psychosocial, spiritual,
and emotional needs of a terminally ill recipient and/or family members, as
delineated in a specific recipient plan of care.
(l)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(m)
“Palliative care” means recipient and family-centered care that
optimizes quality of life by anticipating, preventing, and treating suffering.
Palliative care throughout the continuum of illness involves addressing
physical, intellection, emotional, social, and spiritual needs and to
facilitate recipient autonomy, access to information, and choice.
(n)
“Physician” means “physician” as defined in 42 CFR 410.20.
(o)
“Quarter” means one of 4 calendar periods ending March 31, June 30,
September 30, and December 31.
(p)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(q)
“Respite care” means short-term inpatient care provided to the recipient
only when necessary to relieve the family members or other persons caring for
the recipient.
(r)
“Room and board services” includes performance of personal care
services, including assistance in the activities of daily living, in
socializing activities, administration of medication, maintaining the
cleanliness of a resident’s room, and supervision and assistance in the use of
durable medical equipment and prescribed therapies.
(s)
“Routine home care” means hospice care received at the place of
residence and which is not continuous home care as defined in (d) above.
(t)
“Terminally ill” means a condition for which the recipient has a medical
prognosis of a life expectancy of 6 months or less if the illness runs its normal
course.
(u)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(v)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. #9726-A,
eff 7-1-10; amd by #10139,
eff 7-1-12
He-W 544.02 Recipient Eligibility Requirements.
(a)
To be eligible to receive hospice care, recipients age 21 and over
shall:
(1) Be certified as terminally ill in accordance
with He-W 544.06;
(2) Elect hospice care in accordance with He-W
544.04; and
(3) Upon election of hospice care pursuant to (2)
above, agree to waive all rights to the following Title XIX services:
a. Hospice care provided by a hospice other than
the one designated by the recipient on the hospice care provider’s hospice
election form, unless provided under arrangements made by the designated
hospice;
b. Title XIX services that are:
1. Related to the treatment of the terminal
illness for which hospice care was elected;
2. Related to the treatment of a condition or
complication related to the terminal illness for which hospice care was
elected; or
3. Equivalent to, or duplicative of, hospice
services; and
c. Title XIX home and community-based care
waiver services that are equivalent to, or duplicative of, hospice services.
(b)
To be eligible to receive hospice care, recipients under the age of 21:
(1) Shall be certified as terminally ill in
accordance with He-W 544.06;
(2) Shall elect hospice care in accordance with
He-W 544.04; and
(3) Shall not, in accordance with 42 U.S.C.
1396d(o)(1), be required to waive rights to Title XIX services that are related
to treatment of the recipient's condition for which a diagnosis of terminal
illness has been made.
(c)
A recipient shall not be required to waive rights to the following
services, which shall be covered in addition to hospice services:
(1) Services provided by the recipient’s Title
XIX attending physician if that physician is not an employee of the designated
hospice or is not receiving compensation from the hospice for those services;
and
(2) Room and board services provided by a nursing
facility if the recipient meets nursing facility level of care.
Source. #9726-A,
eff 7-1-10; ss by #9867-A, eff 2-11-11
He-W 544.03 Provider Participation. Each participating hospice provider shall:
(a) Be medicare
certified as a hospice provider;
(b)
Be a NH enrolled Title XIX provider;
(c)
Hold a current
NH state license as a home hospice care provider or hospice house in accordance
with RSA 151:2 and He-P 823 or He-P 824, or be licensed as such by the state in
which they practice; and
(d)
Notify the department of a recipient’s discharge from the hospice provider
due to the recipient’s death, within 5 state business days of the recipient’s
death, via Form 282A, “Medicaid Hospice Care Notification Form,” incorporated
by reference in He-W 544.17.
Source. #9726-A,
eff 7-1-10
He-W 544.04 Election of Hospice Care.
(a)
If a recipient seeks to elect hospice care, the hospice provider shall
obtain an election statement via the hospice care provider’s hospice care
election form signed and dated by the recipient or his or her agent or legal
guardian.
(b)
The election statement obtained by the hospice provider on the hospice
care provider’s hospice care election form shall:
(1) Specify the hospice provider designated by
the recipient to provide care;
(2) Specify the effective date of the election,
which shall not be earlier than the date the recipient or his or her agent or
legal guardian signs the election statement; and
(3) Specify that by waiving rights in accordance
with He-W 544.02(a)(3), the recipient or the recipient’s agent or legal
guardian acknowledges that he or she has been given a full understanding of the
palliative rather than curative nature of hospice care, as it relates to the
recipient’s terminal illness specified on the form.
(c)
If a recipient elects hospice care in accordance with (a) and (b) above,
the designated hospice provider shall notify the department of the effective
date of the election in (b)(2) above, within 5 state business days of the
election, via the applicable sections of Form 282A, “Medicaid Hospice Care
Notification Form,” incorporated by reference in He-W 544.17.
Source. #9726-A,
eff 7-1-10
He-W 544.05 Hospice Election Periods.
(a)
The recipient shall be allowed hospice coverage divided into election
periods as follows:
(1) An initial 90-day period;
(2) A subsequent 90-day period; and
(3) An unlimited number of subsequent 60-day
periods.
(b)
Election of hospice care in accordance with He-W 544.04 shall be
considered to continue through the election periods specified in (a) above
without a break in care if the recipient:
(1) Remains in the care of the hospice provider;
and
(2) Does not revoke the election under the
provisions of He-W 544.08.
Source. #9726-A,
eff 7-1-10
He-W 544.06 Certification of Terminal Illness. The hospice provider shall obtain certification
of terminal illness as follows:
(a)
For the first 90-day election period, the hospice provider shall obtain,
within 2 calendar days after hospice care is initiated, written certification
of terminal illness signed and dated by:
(1) The medical director of the hospice provider
or the physician member of the hospice interdisciplinary group; and
(2) The recipient’s Title XIX attending
physician, if the recipient has an attending physician, except that an advance
practice registered nurse shall not be allowed to sign;
(b)
For subsequent election periods of coverage specified in He-W
544.05(a)(2) and (3) above, the hospice provider shall obtain, within 2
calendar days after the beginning of each election period, a written
certification of terminal illness signed and dated by the medical director of
the hospice provider or the physician member of the hospice interdisciplinary
group;
(c)
If the written certification in (a) or (b) above cannot be obtained
within 2 days, a verbal certification shall be:
(1) Obtained within 2 days;
(2) Documented in the recipient’s medical
records; and
(3) Followed by a written certification pursuant
to (a) or (b) above within 30 calendar days; and
(d)
No Title XIX payment shall be made for days prior to certification in
accordance with (a) – (c) above.
Source. #9726-A,
eff 7-1-10
He-W 544.07 Change in Designated Hospice Provider.
(a)
A recipient or his or her agent or legal guardian may change the
designated hospice provider once in each of the election periods specified in
He-W 544.05(a).
(b)
The recipient or his or her agent or legal guardian shall complete the
hospice care provider’s change of designated provider form and provide it to
the current hospice provider and the newly designated hospice provider.
(c) The recipient’s current
hospice provider shall notify the department within 5 state business days of a
recipient changing his or her designated hospice provider via the applicable
sections of Form 282A, “Medicaid Hospice Care Notification Form,” incorporated
by reference in He-W 544.17
(d)
The recipient’s current hospice provider shall forward the following to
the newly designated hospice provider:
(1) A copy of the election statement obtained by
the current hospice provider in accordance with He-W 544.04; and
(2) A copy of the certification of terminal
illness obtained by the current hospice provider in accordance with He-W
544.06.
(e)
The newly designated hospice provider shall comply with all requirements
of He-W 544, except that the forms forwarded pursuant to (d) above may be used
in place of completing new documents.
Source. #9726-A,
eff 7-1-10
He-W 544.08 Revocation of Hospice Care.
(a)
The recipient or his or her agent or legal guardian may revoke the
recipient’s election of hospice care at any time by completing and signing the
hospice care provider’s hospice care revocation form.
(b)
If the revocation form in (a) above cannot be signed at the time of
revocation, the following shall occur:
(1) The recipient or his or her agent or legal
guardian shall verbally revoke the recipient’s election of hospice care, the
date of which shall be documented in the recipient’s medical record; and
(2) The recipient or his or her agent or legal
guardian shall complete and sign the revocation form in (a) above.
(c)
A recipient or his or her agent or legal guardian shall not designate a
revocation effective date earlier than the date the revocation is made as
allowed in (a) and (b)(1) above.
(d)
Within 5 state business days of a recipient revoking his or her election
of hospice care, the designated hospice shall notify the department of the date
that the revocation is to be effective, via the applicable sections of Form
282A, “Medicaid Hospice Care Notification Form,” incorporated by reference in
He-W 544.17.
(e)
Effective with the revocation date specified, the recipient shall no
longer be covered under the hospice benefit and shall resume eligibility for
all Title XIX benefits previously waived pursuant to He-W 544.02(a)(4).
(f)
A recipient who revokes his or her election of hospice care shall be
eligible to elect hospice care for any remaining election periods in accordance
with He-W 544.04.
Source. #9726-A,
eff 7-1-10
He-W 544.09 Covered Hospice Services.
(a)
The designated hospice provider shall create a plan of care for the
recipient in accordance with 42 CFR 418.56 a.2(b) that specifies the services
to be provided to the recipient, which are reasonable and necessary for the
palliation or management of the symptoms of the terminal illness and conditions
or complications related to the terminal illness.
(b)
Services covered as part of the hospice benefit shall include:
(1) Nursing care
provided by or under the supervision of a registered nurse;
(2) Medical social services provided by a
social worker who has at least a bachelor’s degree from a school
accredited or approved by the Council on Social Work Education, and who is
working under the direction of a physician;
(3) The following services performed by hospice
physicians:
a. General supervisory services of the medical
director;
b. Participation in the establishment of plans
of care, supervision of care and services, periodic review and updating of
plans of care, and establishment of governing policies by the physician member
of the interdisciplinary group; and
c. Physician services described in He-W
544.16(b)(2)a.;
(4) Counseling services, including
dietary counseling, provided to the recipient, family members,
and others caring for the recipient for the purpose of training the recipient’s
family or caregivers to provide care;
(5) General inpatient
care as follows:
a. Such care shall be provided in a Title XIX
enrolled hospice house, licensed in accordance with RSA 151 and He-P 824,
hospital, or nursing facility that meets that meets the requirements in 42 CFR
418.110 regarding staffing and patient areas; and
b. Care shall be for pain control or symptom
management which cannot be provided in an outpatient setting;
(6) Inpatient respite care
provided to the recipient as follows:
a. Only for recipients who are not residing in a
nursing facility;
b. Only when necessary to relieve the family
members or other caregivers of caring for the recipient;
c. Not for more than one period of 5 consecutive
days at a time per election period, except that the sixth and any subsequent
consecutive days shall be covered and paid at the routine home care rate; and
d. Only in those intermediate care facilities
that meet the requirements of 42 CFR 418.100 (a) and (e) regarding 24-hour
nursing and patient areas;
(7) Durable medical equipment and
supplies for self help and personal comfort related
to the palliation or
management of the recipient’s terminal illness or conditions related to the
terminal illness while the recipient is under hospice care;
(8) Drugs for the palliation and
management of the recipient’s terminal illness or conditions related to the
terminal illness;
(9) Home health aide and
homemaker services;
(10) Physical therapy, occupational therapy, and
speech language pathology services for the purpose of symptom control or to
enable the recipient to maintain activities of daily living and basic
functional skills;
(11) Ambulance and wheelchair van transportation;
(12) Any other service that is specified in the
recipient’s plan of care as reasonable and necessary for the palliation and
management of the recipient’s terminal illness and related conditions; and
(13) Continuous home care, which shall be:
a. Provided only during a period of crisis,
which is a period in which a recipient requires continuous care which is primarily
nursing care to achieve palliation or management of acute medical symptoms;
b. Provided by a registered nurse or licensed
practical nurse, who shall provide care for more than half the period of care;
and
c. A minimum of 8 hours of care during a 24-hour
day, which shall not be required to be consecutive hours.
(c)
The recipient’s plan of care shall include bereavement counseling for
the recipient’s family after the recipient’s death.
(d)
Bereavement counseling in (c) above shall not be billable to Title XIX
nor to the recipient’s family.
Source. #9726-A,
eff 7-1-10
He-W 544.10 Documentation of Hospice Services.
(a)
Hospice providers shall maintain documentation in their records to fully
support each claim billed for services.
(b)
Hospice providers’ records shall include forms created by the providers
which address the following:
(1) Recipient election of hospice care in
accordance with He-W 544.04;
(2) Provider certification of terminal illness in
accordance with He-W 544.06;
(3) Change in designated hospice provider in
accordance with He-W 544.07; and
(4) Revocation of hospice care in accordance with
He-W 544.08.
(c)
Hospice
provider records shall also include copies of any forms submitted to the
department.
(d)
Hospice
providers shall maintain any other supporting records in accordance with He-W
520.
(e) Hospice providers shall submit to the department a copy of the
provider’s annual Medicare Cost Report, by November 30 of each year.
(f) Within 30 days following the end of each quarter, for each
recipient who died within that quarter, hospice providers shall notify the department of hospice service utilization via
Form 282B, “Service Utilization within Hospice by Recipient,” incorporated by
reference in He-W 544.17, except that this form shall not be required for
dual-eligible hospice recipients who reside in a nursing facility.
Source. #9726-A, eff 7-1-10
He-W 544.11 Utilization Review and Control. The department’s surveillance and utilization
review of subsystems unit
(SURS) shall monitor utilization of hospice services in accordance with 42 CFR
455, 42 CFR 456, He-W 520, and documentation of hospice services as required by
He-W 544.
Source. #9726-A,
eff 7-1-10
He-W 544.12 Third Party Liability.
(a)
All third party obligations shall be exhausted before Title XIX shall be
billed, in accordance with 42 CFR 433.139.
(b)
Recipients who elect or revoke the medicaid
hospice benefit shall also elect or revoke the hospice benefit under medicare and/or other insurance, as applicable.
Source. #9726-A,
eff 7-1-10
He-W 544.13 Payment for Hospice Services.
(a)
Hospice
providers shall submit claims for payment to the department’s fiscal agent.
(b)
Payment
for hospice care, with the exception of physician services which are paid in
accordance with He-W 544.16, shall be at a per diem rate for each day that the
recipient is under the care of the hospice provider.
(c)
The
per diem rate shall:
(1) Be determined in accordance with medicare regulations at 42 CFR 418, Subpart G;
(2) For continuous home care, be calculated based
upon the number of hours of continuous home care furnished to arrive at a per
diem rate, in accordance with 42 CFR 418.302(e)(4); and
(3) Be based upon the level of care as follows:
a. Routine home care;
b. Continuous home care;
c. Inpatient respite care; and
d. General inpatient care.
(d)
Payment for inpatient respite care shall be limited to one period of no
more than 5 consecutive days in each election period.
(e)
Inpatient respite care provided in excess of the 5 day limit per
election period shall be paid at the routine home care rate.
(f)
If there is a change in designated provider, admission status, or level
of care, payment shall be made as follows:
(1) If admission occurs on the same day as
discharge, revocation or death, the day shall be considered a hospice care day
and the hospice shall be paid in accordance with (c) above;
(2) If the level of care changes, payment shall
be made for the new level of care beginning with the day it commences;
(3) If a change of hospice provider occurs,
payment shall not be made to the discharging hospice for the day of discharge,
but payment shall be made to the newly designated hospice; and
(4) If the recipient is discharged from an
inpatient unit, the routine home care rate shall be paid, unless the recipient
dies as an inpatient, in which case the general inpatient or respite care rate
shall be paid for the discharge date.
(g)
If certification is not obtained in accordance with the provisions of
He-W 544.06(a)–(c), payment shall not be made for days prior to certification.
(h)
Bereavement counseling pursuant to He-W 544.09(c) shall not be billable
to Title XIX nor to the recipient’s family pursuant to He-W 544.09(d).
Source. #9726-A,
eff 7-1-10
He-W 544.14 Hospice Payment Limitations and
Adjustments.
(a)
Hospice payments for inpatient care shall be limited and paid in
accordance with Medicare regulations 42 CFR 418.302(f).
(b) Acquired Immunodeficiency Syndrome (AIDS)
cases shall be included in the limitation calculation.
(c) On an annual basis, by November 30, hospice
providers shall submit to the department a copy of their Medicare cap report.
(d)
Hospice payments for inpatient care shall be considered to be interim
payments with adjustments made during the end of the November 1 to October 31
cap period for any payments over the limit.
(e)
Hospice providers shall refund any excess reimbursement as determined
and requested by the department in accordance with (a) and (d) above.
Source. #9726-A,
eff 7-1-10
He-W 544.15 Hospice Payment for Recipients in Nursing
Facilities.
(a)
No Title XIX payments shall be made directly to a nursing facility.
(b)
When hospice services are provided to a recipient residing in a nursing
facility, the hospice provider shall:
(1) Bill for, in addition to routine or
continuous home care, room and board; and
(2) Be reimbursed
by Title XIX at a room and board rate which is, in accordance with 1902(a)(13)
of the Act, at
least 95% of the per diem rate that would have been paid to the nursing
facility for the recipient for the same dates of service under rates
established in accordance with He-E 803.
Source. #9726-A,
eff 7-1-10
He-W 544.16 Payment for Physicians’ Services.
(a)
If a recipient’s attending physician, who is not an employee of the
designated hospice or providing services under arrangement
with the designated hospice, provides physician services related or unrelated
to the treatment of the terminal illness:
(1) These physician services shall not be
considered as part of the per diem rate described in He-W 544.13; and
(2) He or she shall bill for these physician
services separately and be reimbursed at the regular physician
services rate in accordance with He-W 531.
(b)
If a recipient does not have an attending physician at the time of
electing the hospice benefit, the medical director of the
designated hospice provider or the physician member of the hospice
interdisciplinary group shall:
(1) Be the recipient’s attending physician; and
(2) Bill and receive payment as follows:
a. Physician services that are
related to the treatment of the terminal illness shall be considered hospice
services and be included in the per diem rate described in He-W 544.13; and
b. Physician services that are
unrelated to treatment of the terminal illness shall be considered physician
services and shall be billed separately by the physician and be reimbursed at
the regular physician services rate in accordance with He-W 531. These services
shall not be billed by the hospice provider.
(c)
If a recipient’s attending physician, who is not an employee of the
designated hospice or providing services under arrangement with the designated
hospice, requests through an order that the medical director or hospice
physician provide physician services not described in He-W 544.09(b)(3), these
physician services shall be billed as in (a)(1) and (2) above.
Source. #9726-A,
eff 7-1-10
He-W 544.17 Required Forms.
(a)
Each participating hospice provider notifying the department under He-W
544.03, 544.04, 544.07, and 544.08 shall complete, as applicable, and submit
Form 282A, “Medicaid Hospice Care Notification Form” (05/2014 edition).
(b)
Each participating hospice provider notifying the department under He-W
544.10 shall complete and submit Form 282B, “Service Utilization within Hospice
by Recipient” (09/2010 edition).
Source. #9726-B, eff 7-1-10; amd
by #9867-B, eff 2-11-11
PART
He-W 545 – RESERVED
PART
He-W 546 EARLY AND PERIODIC SCREENING,
DIAGNOSIS AND TREATMENT SERVICES
He-W 546.01 Definitions.
(a) “Department” means the New Hampshire
department of health and human services.
(b) “Early and Periodic Screening, Diagnosis and
Treatment (EPSDT) services” means a program, pursuant to 42 CFR 440.40,
designed to provide preventative health care, diagnostic services, and early
detection and treatment of disease or abnormalities to medicaid
eligible individuals under age 21.
(c) “Medicaid” means the Title XIX and Title XXI
programs administered by the department which makes medical assistance
available to eligible individuals.
(d) “Medical” means related to the following:
(1) Treatment
of disease;
(2)
Maintenance of health; or
(3)
Prevention, alleviation, or curing of disease.
(e) “Medically necessary” means reasonably
calculated to prevent, diagnose, correct, cure, alleviate or prevent the
worsening of conditions that endanger life, cause pain, result in illness or
infirmity, threaten to cause or aggravate a handicap, or cause physical
deformity or malfunction, and no other equally effective course of treatment is
available or suitable for the EPSDT recipient requesting a medically necessary
service.
(f) “Periodicity schedule” means a regularly
recurring schedule of preventive health care, dental care, or screening
services as determined by standards of practice.
(g) “Primary care physician” means the physician
who routinely provides health care to the recipient.
(h) “Recipient” means any individual who is
eligible for and receiving medical assistance under the medicaid
program.
(i) “Title XIX
program” means the joint federal-state program described in Title XIX of The
Social Security Act and administered in New Hampshire by the department under
the medicaid program.
(j) “Title XXI” means the joint federal-state
program described in Title XXI of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(k) “Treating physician” means the physician who
is managing a present illness or condition, in conjunction with or aside from
the recipient’s primary care physician.
Source. (See Revision Note at chapter heading He-W
500); ss by #5532, eff 12-17-92, EXPIRED: 12-17-98
New. #6940, eff 1-30-99; ss by #8782, eff 1-1-07; amd by #10139, eff 7-1-12; ss by #10829, eff 5-19-15
He-W 546.02 Recipient Eligibility. All recipients under the age of 21 shall be
eligible for EPSDT services.
Source. (See Revision Note at chapter heading He-W
500); ss by #5532, eff 12-17-92, EXPIRED: 12-17-98
New. #6940, eff 1-30-99; ss by #8782, eff 1-1-07;
ss by #10829, eff 5-19-15
He-W 546.03 Provider Participation. All participating EPSDT providers shall:
(a) Meet the state licensing or board
certification requirements to provide medical or dental care;
(b) Be a New Hampshire enrolled medicaid provider;
(c) Perform the necessary components whether in whole or in part required for each
EPSDT examination; and
(d) Request and obtain prior authorization from
the department before providing services which require prior authorization, in
accordance with He-W 530 and He-W 546.06.
Source. (See Revision Note at chapter heading He-W
500); ss by #5532, eff 12-17-92, EXPIRED: 12-17-98
New.
#6940, eff 1-30-99; ss and moved by
#8782, eff 1-1-07 (from He-W 546.04); ss by #10829, eff 5-19-15
He-W
546.04 Informing Requirements. The department shall carry out the informing
requirements specified in 42 CFR 441.56 as follows:
(a) The department shall inform all
pregnant women and children who are eligible for a medicaid
program, or the parent(s) or legal representative(s) of eligible children,
about EPSDT services within 60 days of the individual’s initial eligibility
determination for a medicaid program, and, in the
case of families which have not utilized EPSDT services, annually thereafter,
pursuant to 42 CFR 441.56(a)(4);
(b)
The department shall complete the requirements set out in this section through
written communications, oral communications, or any combination of both; and
(c) The department shall provide to recipients,
or their parent(s) or legal representative(s), information about:
(1) The services available under the EPSDT
program;
(2) The location of, and the requirements to
obtain and use the health care or dental services available under the EPSDT
program;
(3) The benefits of preventative health and
dental care;
(4) The availability of medicaid
payment for medical and dental services provided under the EPSDT program;
(5) The existence of other medical or social
agencies available to assist a recipient, or to which a recipient may be
referred, such as the department’s bureau of maternal and child health services
or bureau of special medical services;
(6) The availability of assistance in locating
and accessing medical and dental services, upon request; and
(7)
The availability of assistance with scheduling of medical or dental
appointments and obtaining transportation, upon request.
Source. (See Revision Note at chapter heading He-W
500); ss by #5532, eff 12-17-92, EXPIRED: 12-17-98
New. #6940, eff 1-30-99; ss and moved by #8782,
eff 1-1-07 (from He-W 546.03); ss by #10829, eff 5-19-15
He-W 546.05 Covered
Services.
(a) The
department shall cover the following EPSDT screening services:
(1) Comprehensive and age-appropriate medical
assessments and screenings of a child’s physical and mental status in
accordance with the 2014 periodicity schedule entitled “Recommendations for
Preventive Pediatric Health Care” of the American Academy of Pediatrics/Bright
Futures, available as noted in Appendix A, including:
a.
Comprehensive health and developmental history;
b.
Comprehensive unclothed physical examination;
c.
Developmental and behavioral assessment with a standardized validated
tool of the provider’s choice;
d. Measurements of the child’s height and weight,
head circumference, and blood pressure;
e. Appropriate
immunizations;
f. Appropriate
laboratory tests to include:
1. Testing for lead toxicity for EPSDT eligible
children at 12 and 24 months of age; and
2. Testing for
lead toxicity for EPSDT eligible children between 36 and 72 months of age, if
not previously screened for lead poisoning;
g. Appropriate
vision testing;
h. Appropriate
hearing testing;
i. Assessment
of nutritional status;
j. Dental screening services furnished by direct
referral to a dentist for diagnosis and treatment, and in accordance with the
periodicity schedule contained in “Guideline on Periodicity of Examination,
Preventive Dental Services, Anticipatory Guidance/Counseling, and Oral
Treatment for Infants, Children, and Adolescents” (2013 revision), of the
American Academy of Pediatric Dentistry, available as noted in Appendix A;
k. Health
education about the benefits of healthy lifestyles and practices; and
l.
Anticipatory guidance about child safety and injury prevention.
(b) The
department shall cover the following EPSDT diagnostic and treatment services,
if medically necessary as a result of assessment and screening:
(1)
Urinalysis;
(2) Sickle
cell screening;
(3) Tuberculin
testing;
(4) Blood
testing for hematocrit and/or hemoglobin levels;
(5)
Immunizations provided in accordance with the U.S. Department of Health
and Human Services, Centers for Disease Control and Prevention “Recommended
Immunization Schedules for Persons Aged 0 Through 18 Years, United States
2015,” available as noted in Appendix A; and
(6) Any other
Medicaid services as specified in He-W 522 through He-W 589, to treat
conditions discovered during a screen.
(c) Any
services not listed in He-W 522 through He-W 589 as covered services shall be
given independent review by the department for coverage based on medical
necessity in accordance with He-W 546.06.
(d)
Transportation services, pursuant to He-W 574, 42 CFR 43.153, and 42 CFR
441.62, shall be covered for EPSDT-eligible children.
(e) Services
in excess of the service limits in He-W 530 shall be covered for EPSDT-eligible
children, if medically necessary, in accordance with the requirements in He-W
546.06
Source. (See Revision Note at chapter heading He-W
500); ss by #5532, eff 12-17-92, EXPIRED: 12-17-98
New. #6940, eff 1-30-99; ss by #8437, eff 9-24-05;
ss by #8782, eff 1-1-07; ss by #10829, eff 5-19-15
He-W 546.06 Prior Authorization for
Coverage Based on Medical Necessity.
(a) Prior authorization shall
be required for services described in He-W 546.05(c) and (e).
(b) Requests for prior
authorization shall include the following:
(1) The recipient’s name,
address, and medicaid identification number;
(2) The recipient’s diagnosis
and prognosis, including an indication of whether the diagnosis is a
pre-existing condition or a presenting condition;
(3) An estimation of the effect
on the recipient if the requested service is not provided;
(4) The medical justification
for the services or equipment being requested;
(5) The recommended timetable
of the prescribed treatment;
(6) A discussion of why the
service is medically necessary as relates to He-W 546.01(e);
(7) The expected outcome of
providing the requested service;
(8) The recommended timeframe
to achieve the expected outcome;
(9) A summary of any previous
treatment plans, including outcomes, which were used to treat the diagnosed
condition for which the requested service is being recommended;
(10) Listings of individuals or
agencies to whom the recipient is being referred; and
(11) Assurance that the
requested service is the least restrictive, most cost-effective service
available to meet the recipient’s needs.
(c) Requests for prior
authorization shall include a statement signed by at least one of the following
indicating that they concur with the request:
(1) Treating physician or
primary care provider;
(2) Treating advanced practice
registered nurse; or
(3) Primary treating
psychotherapist.
(d) Prior authorizations for
coverage of services requested in accordance with He-W 546.06 shall be approved
by the department if the department determines that the information provided in
(b) above demonstrates medical necessity.
(e) Confirmation of department
approvals shall be sent to the treating physician in writing.
(f) Providers shall be
responsible for determining that the recipient is medicaid
eligible on the date of service.
(g) If the requested service is
denied, or denied in part, by the department, the department shall forward a notice
of denial to the recipient and the treating provider with the following
information:
(1) The reason for, and the
legal basis of, the denial; and
(2) Instructions that a fair
hearing on the denial may be requested by the recipient within 30 calendar days
of the date on the notice of the denial, in accordance with He-C 200.
(h) Decisions made by the
department in accordance with (d) and (g) above shall not be superseded by the
treating or consultative health care professional’s prescription, orders, or
recommendations.
Source. (See Revision Note at chapter heading He-W
500); ss by #5532, eff 12-17-92, EXPIRED: 12-17-98
New. #6940, eff 1-30-99; ss by #8782, eff 1-1-07;
ss by #10829, eff 5-19-15
He-W 546.07 Support
Services. The department shall
provide support services to enhance recipients’ participation in the EPSDT
program, including, but not limited to:
(a) Inter- or
intra-departmental coordination of programs;
(b) Providing
information to recipients about other available community services;
(c) Making
recipient referrals to human service agencies or social services, as requested
by the recipient or as appropriate; and
(d) Assisting
the recipient to access health care or dental services.
Source. (See Revision Note at chapter heading He-W
500); ss by #5532, eff 12-17-92, EXPIRED: 12-17-98
New. #6940, eff 1-30-99; ss by #8782, eff 1-1-07;
ss by #10829, eff 5-19-15
He-W 546.08 Non-Covered
Services.
(a) The
following services shall not be covered:
(1) Any
service for which there is no medical necessity or for which the medical
necessity has not been established;
(2) Services which are not medical or dental in
nature, except that transportation shall be covered in accordance with He-W
546.05(d);
(3)
Experimental or investigational procedures in accordance with He-W 530;
(4) Services
that have not been proven to be safe or effective, as documented in medical
peer review literature; and
(5) Services
which are more costly than other services which could be expected to provide
the recipient with the same outcome.
(b) Services
listed in He-W 522 through He-W 589 as non-covered services shall not be
covered unless the service is determined to be medically necessary for the
recipient pursuant to He-W 546.06.
Source. (See Revision Note at chapter heading He-W
500); ss by #5532, eff 12-17-92, EXPIRED: 12-17-98
New. #6940, eff 1-30-99; ss by #8782, eff 1-1-07;
ss by #10829, eff 5-19-15
He-W 546.09 Utilization
Review and Control. The department’s
provider program integrity unit shall monitor utilization of EPSDT services to
identify, prevent, and correct potential occurrences of fraud, waste, and
abuse, in accordance with 42 CFR 455, 42 CFR 456, and He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #5532, eff 12-17-92, EXPIRED: 12-17-98
New. #6940, eff 1-30-99; ss by #8782, eff 1-1-07;
ss by #10829, eff 5-19-15
He-W 546.10 Third
Party Liability.
(a) All third
party obligations shall be exhausted before medicaid
is billed, in accordance with 42 CFR 433.139, except as noted in (b) below.
(b) The
following services shall be exempt from third party billing requirements:
(1) Services
provided to children who are covered by third party liability enforced by the
department’s division of child support services; and
(2) All
preventive pediatric care services, in accordance with 42 CFR 433.139(b)(3)(i).
(c) Providers
may bill medicaid directly for the services described
in (b) above and medicaid shall then seek
reimbursement from the third party.
Source. (See Revision Note at chapter heading He-W
500); ss by #5532, eff 12-17-92, EXPIRED: 12-17-98
New. #6940, eff 1-30-99; ss by #8782, eff 1-1-07;
ss by #10829, eff 5-19-15
He-W 546.11 Payment
for Services.
(a) Payment
for services provided to recipients participating in the EPSDT program shall be
made in accordance with rates established by the department in accordance with
RSA 161:4, VI(a).
(b) The
provider shall submit claims for payment to the department’s fiscal agent.
(c) The
provider shall maintain supporting records, in accordance with He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #5532, eff 12-17-92, EXPIRED: 12-17-98
New. #6940, eff 1-30-99; ss by #8782, eff 1-1-07;
ss by #10829, eff 5-19-15
PART He-W 547 HOME VISIT FOR POSTPARTUM AND NEWBORN
ASSESSMENT
He-W
547.01 Definitions.
(a) “Department” means the New Hampshire
department of health and human services.
(b) “Health promotion and anticipatory guidance”
means services provided by a registered nurse to a newborn’s parent or guardian
within 60 days of the child’s birth in accordance with He-W 547.04(c).
(c) “Home visit for postpartum and newborn
assessment (home visit) services” means services rendered to newborns and their
birth mothers within the first 60 days of life at their residences.
(d) “Maternal postpartum assessment” means
services provided to a woman within 60 days postpartum by a registered nurse,
in accordance with He-W 547.04(b).
(e) “Medicaid” means the Title XIX and Title XXI
programs administered by the department, which makes medical assistance
available to eligible individuals.
(f) “Newborn health assessment” means services
provided by a registered nurse to a newborn within 60 days of birth, which
includes a determination of whether or not the newborn’s health is within
normal limits, in accordance with He-W 547.04(a).
(g) “Recipient” means any individual who is
eligible for and receiving medical assistance under the medicaid
program.
(h) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(i) “Title XXI” means
the joint federal-state program described in Title XXI of the Social Security
Act and administered in New Hampshire by the department under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #6018, eff 4-1-95, EXPIRED: 4-1-03
New. #8446, eff 10-7-05; amd
by #10139, eff 7-1-12; ss by #10428, eff 10-7-13
He-W
547.02 Recipient Eligibility. Recipients who are within 60 days postpartum
shall be eligible for home visit services.
Source. (See Revision Note at chapter heading He-W
500); ss by #6018, eff 4-1-95, EXPIRED: 4-1-03
New. #8446, eff 10-7-05; ss by #10428, eff 10-7-13
He-W
547.03 Provider Participation. All providers of home visit services shall:
(a) Be licensed as a home health care provider by
the department’s health facilities administration in accordance with RSA 151
and He-P 809;
(b) Be a NH enrolled medicaid
provider;
(c) Employ registered nurses, licensed by the
board of nursing in the state in which they practice, to perform the service;
and
(d) Require the registered nurses in (c) above to
have:
(1) A minimum of 2 years of maternal and child
health care experience, which shall include:
a. At least 6 months in child health; and
b. At least 6 months in maternal postpartum
care; or
(2) One year of maternal and child health care
experience and one year of community health experience.
Source. (See Revision Note at chapter heading He-W
500); ss by #6018, eff 4-1-95, EXPIRED: 4-1-03
New. #8446, eff 10-7-05; ss by #10428, eff 10-7-13
He-W
547.04 Covered Services. The following services shall be covered when
provided during a home visit:
(a) Newborn health assessment of the:
(1) Skin, including color, condition and
birthmarks;
(2) Head, including fontanelles;
(3) Neck, including mobility;
(4) Eyes, including appearance, movement and
evidence of sight;
(5) Ears, including evidence of hearing;
(6) Nose, including patency and septum;
(7) Mouth, including lips, mucosa, palate, and gums;
(8) Chest and lungs, including appearance,
respiration, auscultation, and breasts;
(9) Heart, including rate and rhythm;
(10) Abdomen, including appearance, palpation, umbilicus,
and femoral pulses;
(11) Skeleton, including upper and lower structure,
and range of upper and lower motion;
(12) Genitourinary system, including genitalia,
urine stream and circumcision;
(13) Back, including spine and anus;
(14) Neurological
and behavioral systems, including general appearance, cry, motor system,
reflexes, signs and symptoms of neonatal abstinence syndrome; and
(15) Weight;
(b) Maternal postpartum assessment services
including:
(1) A determination of whether the following
health characteristics and functions are within normal limits:
a. Diet;
b. Rest, activity, and exercise;
c. Breast feeding;
d. Abdominal cramping and tenderness;
e. Urinating and bowels;
f. Emotional response, including postpartum
depression screening;
g. Bonding;
h. General appearance;
i.
Blood pressure;
j. Temperature;
k. Heart and lungs;
l. Breasts and nipples;
m. Abdomen and fundus;
n. Perineum and episiotomy;
o. Lochia;
p. Wound care and healing; and
q. Substance use, including:
1. Alcohol;
2. Tobacco; and
3. Illicit and illegal drug use;
(2) Postpartum education including, but not
limited to:
a. Family planning;
b. Breast care;
c. Hygiene;
d. Sexuality;
e. Perineal care for stitches and hemorrhoids;
f. Psychological adjustment and postpartum
depression;
g. Exercising; and
h. Sleep safety measures;
(3) The provision of referrals to other community
agencies as appropriate, including, but not limited to:
a. Supplemental nutrition program for women,
infants and children (WIC);
b. Mental health services;
c. Domestic violence resources;
d Breastfeeding support;
e. Home visiting New Hampshire (HVNH) program
for continued support;
f. Local Family Resource Center; and
g. Safe transportation programs to include car
seat fitting; and
(4) The discussion of other health, social, or
environmental concerns; and
(c) Parent or guardian education including:
(1) Nutrition, including:
a. Breastfeeding;
b. Preparation and storage of formula;
c. Feeding problems; and
d. Supplements;
(2) Behavioral issues, including:
a. Crying patterns;
b. Colic;
c. Consolability;
d. Sleep patterns;
e. Elimination; and
f. Individuality;
(3) Family relationships and interactions, including:
a. Parent/guardian-child;
b. Sibling rivalry;
c. Parent/guardian-to-parent/guardian; and
d. Relatives;
(4) Safety, and injury prevention, including:
a. Home environment including, but not limited
to:
1. Fire safety;
2. Maintaining a smoke-free environment; and
3. Gun safety;
b. Use and placement of an appropriate infant
car seat;
c. Poison control;
d. Safe water temperature;
e. Drowning;
f. Falling;
g. Crib safety, including safe sleeping
environment;
h. Pets;
i.
Sleep positioning and current safe sleep practices;
j. Choking;
k. Younger siblings;
l. Abusive head trauma, formally known as shaken
baby syndrome; and
m.
Sudden infant death syndrome (SIDS) risk prevention and sudden unexplained
infant death safe sleep initiatives (SUID);
(5) Resources, including:
a. The supplemental nutrition program for women,
infants and children (WIC);
b. Family planning programs;
c. Respite care;
d. Support from family and friends;
e. Mental health services;
f. Domestic violence programs;
g. Breastfeeding support services;
h. Home visiting programs for continued support;
i.
Family Resource Centers, and
j. Programs that assist with car seat selection
and fitting;
(6) Health promotion and related concerns,
including:
a. Immunizations;
b. Rashes and jaundice;
c. When to call the newborn’s primary health
care provider for advice and concerns;
d.
The importance of keeping appointments with the primary health care provider
for the newborn’s health check-ups, in accordance with the recommendations set
forth in “Bright Futures: Guidelines for
Health Supervision of Infants, Children and Adolescents,” 3rd edition, 2008,
available as noted in Appendix A;
e. The medicaid
program and the importance of maintaining continued medicaid
coverage through the infant’s first birthday;
f. Bathing and skin care;
g. Urinary tract infections;
h. Temperature taking;
i.
The care of the umbilical cord and circumcision; and
j. Oral health care and the importance of bringing
the child for his or her first dental visit with a dental provider no later
than the child’s first birthday, in accordance with the periodicity schedule
contained in “Clinical Guideline on Periodicity of Examination, Preventive
Dental Services, Anticipatory Guidance, and Oral Treatment for Children”, of
the American Academy of Pediatric Dentistry, 81 Reference Manual 2004-2005,
Originating Committee- Clinical Affairs Committee, Review Council- Council on Clinical
Affairs, adopted 1991, Revised, 1992, 1996, 2000, and 2003, available as noted
in Appendix A;
(7) Identifying if the newborn is at risk for, or
has, a nutritional problem or unstable housing;
(8) Ensuring follow-up appointments are scheduled
with their primary health care providers; and
(9) Information regarding the child health
assurance program, as described in He-W 546, Early and Periodic Screening,
Diagnosis and Treatment Services.
Source. (See Revision Note at chapter heading He-W
500); ss by #6018, eff 4-1-95, EXPIRED: 4-1-03
New. #8446, eff 10-7-05; ss by #10428, eff 10-7-13
He-W
547.05 Non-Covered Services. Medical services covered under the NH medicaid program pursuant to He-W 522 through 590, or He-M
419 through 701 shall not be covered as part of a home visit.
Source. (See Revision Note at chapter heading He-W
500); ss by #6018, eff 4-1-95, EXPIRED: 4-1-03
New. #8446, eff 10-7-05; ss by #10428, eff 10-7-13
He-W
547.06 Required Documentation.
(a) Providers shall document home visit referrals
in the recipient’s medical record.
(b) Providers conducting home visits shall
document the results of newborn health assessments, health promotion and
anticipatory guidance, describing the assessment results and the provision of
the services provided, and report them to the child’s primary health care
provider within 5 business days of the home visit.
(c)
Providers conducting home visits shall document the results of the maternal
postpartum assessments, describing the assessment results, and report the
results to the mother’s primary health care provider or ob-gyn provider within
5 business days of the home visit.
Source. (See Revision Note at chapter heading He-W
500); ss by #6018, eff 4-1-95, EXPIRED: 4-1-03
New. #8446, eff 10-7-05; ss by #10428, eff 10-7-13
He-W
547.07 Utilization Review and Control. The department’s provider integrity unit
shall monitor utilization of home visit services to identify, prevent, and
correct potential occurrences of fraud, waste, and abuse in accordance with 42
CFR 455, 42 CFR 456, and He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #6018, eff 4-1-95, EXPIRED: 4-1-03
New. #8446, eff 10-7-05; ss by #10428, eff 10-7-13
He-W
547.08 Third Party Liability. All third party obligations shall be
exhausted before medicaid may be billed, in
accordance with 42 CFR 433.139.
Source. (See Revision Note at chapter heading He-W 500);
ss by #6018, eff 4-1-95, EXPIRED: 4-1-03
New. #8446, eff 10-7-05; ss by #10428, eff 10-7-13
He-W
547.09 Payment for Services.
(a) Payment rates of home visit services shall be
established by DHHS in accordance with RSA 541-A:21, III.
(b) Home visit service providers shall submit
claims for payment to DHHS’ fiscal agent.
(c) Home visit service providers shall maintain
supporting records.
Source. (See Revision Note at chapter heading He-W
500); ss by #6018, eff 4-1-95, EXPIRED: 4-1-03
New. #8446, eff 10-7-05; ss by #10428, eff 10-7-13
PART
He-W 548 EXTENDED SERVICES TO PREGNANT
WOMEN
He-W 548.01 Definitions.
(a) “Department” means the New Hampshire department
of health and human services.
(b) “Extended services” means services rendered
to pregnant and postpartum women in addition to routine medical prenatal and
postpartum care with the purpose of improving birth outcomes and parenting
skills.
(c) “Medicaid” means the Title XIX and Title XXI
programs administered by the department, which makes medical assistance
available to eligible individuals.
(d) “Postpartum period” means the period that
begins on the last day of pregnancy and extends through the end of the month in
which the 60-day period following termination of pregnancy ends.
(e) “Recipient” means any individual who is
eligible for and receiving medical assistance under the medicaid
program.
(f) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(g) “Title XXI” means the joint federal-state
program described in Title XXI of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
Source. (See Revision Note at chapter heading He-W
500); ss by #5578, eff 2-11-93; ss by #6939, Interim, eff. 1-30-99, EXPIRED
5-30-99
New. #7036, eff 6-25-99; ss by #8904, eff 6-25-07;
amd by #10139, eff 7-1-12; ss by #10914, eff 8-26-15
He-W 548.02 Recipient Eligibility. All medicaid
recipients shall be eligible for extended services during pregnancy and through
the postpartum period.
Source. (See Revision Note at chapter heading He-W
500); ss by #5578, eff 2-11-93; ss by #6939, Interim, eff. 1-30-99, EXPIRED
5-30-99
New. #7036, eff 6-25-99; ss by #8904, eff 6-25-07;
ss by #10914, eff 8-26-15
He-W 548.03 Provider
Participation. All providers of
extended services shall:
(a) Be under current contract
obligation with the maternal and child health section, division of public
health services as a prenatal program or as a primary care agency providing
prenatal care; and
(b) Be a NH enrolled medicaid provider.
Source. (See Revision Note at chapter heading He-W
500); ss by #5578, eff 2-11-93; ss by #6939, Interim, eff. 1-30-99, EXPIRED
5-30-99
New. #7036, eff 6-25-99; ss by #8904, eff 6-25-07;
ss by #10914, eff 8-26-15
He-W 548.04 Covered Services. The following services shall be covered,
rendered singularly or in any combination during a calendar month, and in accordance
with the recipient’s plan of care:
(a) Social services including:
(1) An initial assessment;
(2) Assisting the recipient in
identifying her ongoing needs and referring her to appropriate services; and
(3) Home visits;
(b) Care coordination between a
recipient and any other individuals or agencies involved in the recipient’s
care, including:
(1) Communicating outcomes or
status to appropriate providers;
(2) Providing liaison
assistance during the transition process to ongoing health, mental health, or
social services;
(3) Assisting with arrangements
for transportation, childcare, or community services;
(4) Making referrals to other
agencies, programs, and community services, including the federal special
supplemental food program for women, infants and children;
(5) Follow-up to ensure the delivery of necessary services, including
tracking missed appointments, rescheduling, and the identification and resolution
of care barriers; and
(6) Intra-agency consultations
concerning the recipient’s care needs;
(c) Individual or group
education including:
(1) Education about the health
implications of risk behavior, such as smoking, and use of alcohol and other drugs;
(2) Education about infant
health, mental health, and development, including positive parenting and its
role in infant and child development; and
(3) Individual instruction
about the course of pregnancy, delivery and child care; and
(d) Nutritional services
including:
(a) An initial assessment of
the recipient’s current nutritional status;
(b) Nutritional counseling; and
(c) Assisting the recipient in
identifying her ongoing needs and appropriate services.
Source. (See Revision Note at chapter heading He-W
500); ss by #5578, eff 2-11-93; ss by #6939, Interim, eff. 1-30-99, EXPIRED
5-30-99
New. #7036, eff 6-25-99; ss by #8904, eff 6-25-07;
ss by #10914, eff 8-26-15
He-W 548.05 Non-Covered
Services. Any other medical services
that are covered under the NH medicaid program,
pursuant to He-W 522 through 577 or He-M 426 through 701 shall not be covered
as part of extended services to pregnant women.
Source. (See Revision Note at chapter heading He-W
500); ss by #5578, eff 2-11-93; ss by #6939, Interim, eff. 1-30-99, EXPIRED
5-30-99
New. #7036, eff 6-25-99; ss by #8904, eff 6-25-07;
ss by #10914, eff 8-26-15
He-W 548.06 Required
Documentation. The provider shall
maintain the following documentation for all extended services care provided:
(a) A plan of care containing:
(1) The initial assessment,
which shall contain:
a. The recipient’s name and medicaid identification number;
b. The date of entry into
clinic service;
c. The number of weeks of
gestation at the date of entry;
d. The recipient’s medical,
nutritional, and social needs and risks;
e. A listing of services and
types of providers to be used, to address the recipient’s needs and risks, as
well as the frequency of services;
f. A dated signature on the
plan of care by the physician or advanced practice registered nurse, or a
physician assistant if so delegated by a physician in accordance with Med
603.01, along with the signature of the recipient, approving the plan of care;
g. A statement signed by the
recipient which gives the agency staff permission to discuss the recipient’s
needs with other medical and social service caregivers; and
h. The date of, and reason for,
discharge from the program;
(2) Ongoing plan of care notes,
relating to the original plan of care, containing:
a. Date(s) of service(s); and
b. Description of service(s);
and
(3) Changes to the original
plan of care described in (1)d. and (1)e. above, to be attached to the original
plan of care;
(b) Attendance records for any
group education attended by a recipient;
(c) An extended services
summary sheet listing the recipient’s name and medicaid
identification number, and the date(s) and type(s) of extended service(s)
rendered;
(d) Supporting records in
accordance with He-W 520 and this part, and failure to maintain records in
accordance with He-W 520 and this part shall entitle the department to
recoupment of state and federal medicaid payments
made as permitted by 42 CFR 455 and 42 CFR 447; and
(e) Documentation required by
He-W 520 and this part for a minimum of 6 years or until the resolution of any
legal action(s) commenced within the 6 year period, whichever is longer.
Source. (See Revision Note at chapter heading He-W
500); ss by #5578, eff 2-11-93; ss by #6939, Interim, eff. 1-30-99, EXPIRED
5-30-99
New. #7036, eff 6-25-99; ss by #8904, eff 6-25-07;
ss by #10914, eff 8-26-15
He-W 548.07 Utilization
Review and Control. The department’s
provider integrity unit shall monitor utilization of extended services to
pregnant women to identify, prevent, and correct potential occurrences of
fraud, waste, and abuse, in accordance with 42 CFR 455, 42 CFR 456, and He-W
520.
Source. (See Revision Note at chapter heading He-W 500);
ss by #5578, eff 2-11-93; ss by #6939, Interim, eff. 1-30-99, EXPIRED 5-30-99
New. #7036, eff 6-25-99; ss by #8904, eff 6-25-07;
ss by #10914, eff 8-26-15
He-W 548.08 Third Party
Liability. All third party
obligations shall be exhausted before the medicaid
program is billed, in accordance with 42 CFR 433.139.
Source. (See Revision Note at chapter heading He-W
500); ss by #5578, eff 2-11-93; ss by #6939, Interim, eff. 1-30-99, EXPIRED
5-30-99
New. #7036, eff 6-25-99; ss by #8904, eff 6-25-07;
ss by #10914, eff 8-26-15
He-W 548.09 Payment for
Services. Payment for extended
services to pregnant women shall be made as follows:
(a) Rates of payment shall be at
a monthly rate established by the department in accordance with RSA 161:4,
VI(a);
(b) At least one of the
services described in He-W 548.04 shall be provided each month, in order for
the monthly rate to be billed by the provider;
(c) The provider shall submit
claims for payment to the department’s fiscal agent; and
(d) The provider shall maintain
supporting records, in accordance with He-W 520 and He-W 548.06, and the
department shall be entitled to recoupment of state and federal medicaid payments made in violation of 42 CFR 455 and 42
CFR 447.
Source. (See Revision Note at chapter heading He-W
500); ss by #5578, eff 2-11-93; ss by #6939, Interim, eff. 1-30-99, EXPIRED
5-30-99
New. #7036, eff 6-25-99; ss by #8904, eff 6-25-07;
ss by #10914, eff 8-26-15
He-W 549.01 Definitions.
(a) “Caregiver” means a parent, grandparent or any
other individual identified as having primary responsibility for the child.
(b) “Child/family health care support” means
services that are rehabilitative and preventive in nature and which, in
addition to medical care, are rendered to recipients for the purpose of
improving their health status and function within the family and community.
(c) “Department” means the New Hampshire
department of health and human services.
(d) “First time mother” means a pregnant woman
who has had no previous live births.
(e) “Home
Visiting New Hampshire (HVNH)” means the maternal and child health preventive
program that provides health education, support and linkages to community
services to Title XIX eligible, pregnant women together with their families in
their homes.
(f) “Low birth weight” means an infant weighed
2500 grams or less at birth.
(g) “Medicaid” means the Title XIX and Title XXI
programs administered by the department which makes medical assistance
available to eligible individuals.
(h) “Premature” means an infant born before 37
weeks gestation.
(i) “Recipient” means
any individual who is eligible for and receiving medical assistance under the medicaid program.
(j)
“Special
health care needs” means having or being at risk for chronic physical,
developmental, behavioral, or emotional conditions requiring health and related
services of a type or amount beyond what is generally required.
(k) “Title V” means the program described in
Title V of the Social Security Act, and administered by the maternal and child
health section (MCH) of the NH division of public health services or by the
special medical services (SMS) section of the NH division of community based
care services as part of the health resources and services administration,
United States department of health and human services.
(l) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(m) “Title XXI” means the joint federal-state
program described in Title XXI of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(n) “Unit” means a 15-minute period of time for
which a service is rendered.
Source. #7775, eff 10-8-02; ss by #9768, eff 10-8-10;
ss by #10092, eff 3-1-12; amd by #10139, eff 7-1-12; amd by #10398, eff 8-20-13
He-W
549.02 Recipient Eligibility.
(a) The following individuals shall be eligible
for HVNH, as described in He-W 549.05(a):
(1) A medicaid recipient who:
a. Is a first time mother; and
b. Is under age 21 at the time of enrollment;
(2) An infant, up to
one year of age, who is born to a recipient in (1) above; and
(3) An infant, up to one year of age, who:
a. Is no older than 2
weeks of age at the time of enrollment in the program; and
b. Is born to a first time mother who is under the age of 21
at the time of the infant’s enrollment in the program.
(b) All Title XIX recipients who are under age 21
shall be eligible to receive child/family health care support services, as
specified in He-W 549.05(b), if any one of the following 4 conditions are met:
(1) At least 2 primary
criteria outlined in (c) below;
(2) At least 3
secondary criteria outlined in (d) below;
(3) At least one
primary and 2 secondary criteria outlined in (c) and (d) below; or
(4) The recipient is
eligible for Title V services through the special medical services section, in
accordance with He-M 520.03 and He-M 520.04(b).
(c) For child/family health care support
services, primary criteria for eligibility shall include:
(1) The caregiver,
child or a household member has:
a. A diagnosed mental illness;
b. Known substance abuse; or
c. A disability or developmental delay, except
that a child shall not be a recipient of family-centered early supports and
services pursuant to He-M 510;
(2) The caregiver has
been referred by a protective services agency or has a finding of child neglect
or abuse;
(3) The caregiver or
child has special health care needs;
(4) The child’s family
is homeless; or
(5) One of the child’s
parents or parent’s partner is absent for circumstances including, but not
limited to, death, missing, incarceration, military deployment, or as a result
of a protective/restraining order.
(d) For child/family health care support
services, secondary criteria for eligibility shall include:
(1) The child’s
caregiver is under 21 years of age;
(2) The caregiver is a
first time parent;
(3) The caregiver has
limited English proficiency;
(4) The caregiver is
single without any identified social supports;
(5) The caregiver has
less than a high school education;
(6) The child was
premature or had a low birth weight and is not a recipient of family-centered
early supports and services pursuant to He-M 510;
(7) There is
documentation of family trauma, including, but not limited to:
a. An unexpected or untimely death in the
family;
b. Domestic violence in the family;
c. Caregiver is an adult victim of child abuse or
neglect; or
d. The family has been the victim of a crime;
(8) There is
documentation of a disrupted or problematic parent-child relationship, such as,
but not limited to, insecure attachment;
(9) The family’s
income is less than 125% of the most recent federal poverty level as published
annually in the Federal Register by the Secretary of the U.S. Department of
Health and Human Services; or
(10) One or more
grandparents is raising the child.
Source. #7775, eff 10-8-02; ss by #9768, eff 10-8-10;
ss by #10092, eff 3-1-12; amd by #10398, eff 8-20-13
He-W 549.03 Amount of Services.
(a)
Child/family health care support services shall consist of 12 units of
service per state fiscal year, including the units making up the assessment
visits in He-W 549.05(a)(2).
(b)
Recipients identified in He-W 549.02(b)(4) shall be eligible for 16
units of service per state fiscal year, including the units making up the
assessment visits in He-W 549.05(a)(2).
Source. #7775, eff 10-8-02; ss by #9768, eff 10-8-10;
ss by #10092, eff 3-1-12
He-W
549.04 Provider Participation.
(a) Each participating provider shall:
(1)
Be under current services contract obligation:
a. With the maternal and child health (MCH)
section of the NH division of public health services;
b.
With the special medical services (SMS) section of the NH division of
community based care services, as a Title V agency; or
c. With the department’s division for
children, youth, and families (DCYF);
(2) Be a New Hampshire
enrolled Title XIX provider; and
(3) Deliver HVNH or
child/family health care support services through the following health care
providers:
a. Advanced practice
registered nurses (APRN) licensed to practice by the states in which they
practice;
b. Registered nurses
(RN) licensed to practice by the states in which they practice;
c. Licensed practical
nurses (LPN) licensed to practice by the states in which they practice;
d. Licensed dietitians
who are licensed under RSA 326-H:12;
e. Social workers with
a baccalaureate or master’s degree in social services, psychology, education or
public health; or
f. Para-professionals
who:
1. Have a high school diploma or general
equivalency diploma;
2. Have 2 years’ experience working with
families in a health care support capacity; and
3. Work in coordination with a licensed
multidisciplinary team, including but not limited to APRNs, licensed clinical
social workers (LCSW), licensed marriage and family therapists, and/or other
licensed health care professionals.
(b) Participating providers under current
services contract obligation with SMS in accordance with (a)(1)b. above shall
bill only for nutrition-related services identified in He-W 549.05(b)(5)a.
Source. #7775, eff 10-8-02; ss by #9768, eff 10-8-10;
ss by #10092, eff 3-1-12 (from He-W 549.03); amd by
#11124, eff 6-22-16
He-W
549.05 Covered Services. Covered HVNH and child/family health care
support services shall include the following services delivered in accordance
with a plan of care as described in He-W 549.07:
(a) HVNH services which shall:
(1) Focus on healthy
birth outcomes;
(2) Include initial
assessment, not to exceed 2 visits, and subsequent visits;
(3) Be conducted
through face-to-face visits at:
a. The pregnant
woman’s or child’s home;
b. The participating
provider or health care provider agency; or
c. Any other location,
as documented in the pregnant woman’s or child’s progress notes; and
(4) Include the
following:
a. Prenatal
assessment, support and education including, but not limited to:
1. Nutrition assessment and education;
2. Networking with social support services;
3. Accessing and receiving continuous prenatal
care; and
4. Health implications of risk behavior, such as
smoking;
b. Parenting skills
and child development education;
c. Parental
assessment, support and education to encourage parental coping and the parent’s
ability to develop attachment and nurturing skills;
d. Family planning;
e. Community support
guidance for the purpose of securing and maintaining a safe and healthy home;
f. Education and
support to assure recipient has access to, and obtains, preventive and acute
health care; and
g. Follow-up
activities related to any of the above services; and
(b) Child/family health care support services
which:
(1) Shall include
initial assessment and subsequent visits;
(2) Shall be
family-centered and child-focused;
(3) Shall be conducted
through a face-to-face visit with the recipient’s parent or guardian at:
a. The recipient’s
home;
b. The participating
provider or health care provider agency; or
c. Any other location,
as documented in the recipient’s progress notes;
(4) May be conducted
on a limited basis by telephone or via a video conference in lieu of a
face-to-face visit if the service can be provided over the phone or via a video
conference and provision of the service over the phone or via a video
conference would not compromise the intent or anticipated result of the
service; and
(5) Shall include any
of the following:
a. Nutrition assessment
and education;
b. Family support
activities geared towards developing and maintaining family support systems,
including, but not limited to, education and consultation;
c. Child-focused,
family-centered education to a recipient’s parents or guardians in the areas of
physical and behavioral health, social support, parenting education, and
household and environmental safety;
d. Child development
screening, education, and guidance;
e. Community support guidance for the purpose of securing and
maintaining a safe and healthy home;
f. Parental assessment, support and education to encourage
parental coping and the parent’s ability to develop attachment and nurturing
skills;
g. Education and
support to assure recipient has access to, and obtains, preventive and acute
health care; and
h. Follow-up
activities related to any of the above services.
Source. #7775, eff 10-8-02; ss by #9768, eff 10-8-10;
ss by #10092, eff 3-1-12 (from He-W 549.04)
He-W
549.06 Non-Covered Services. The following services shall be non-covered
as HVNH and child/family health care support services:
(a) Any covered service listed in He-W 549.05, or
component thereof, which duplicates a service already being provided, such as,
but not limited to:
(1) Services provided
though other Title XIX-funded department programs;
(2) Services provided through private programs such as a
health maintenance organization (HMO); and
(3) Services which are
free to the public;
(b) Travel;
(c) Phone
calls or video conferences, other than those in lieu of a visit, as described
in He-W 549.05(b)(4);
(d) Administrative services; and
(e) Services that do not meet the documentation
requirements in He-W 549.07.
Source. #7775, eff 10-8-02; ss by #9768, eff 10-8-10;
ss by #10092, eff 3-1-12 (from He-W 549.05)
He-W
549.07 Required Documentation. Each participating provider shall develop and
maintain on file the following documentation for each recipient:
(a) A plan of care which shall be developed
following the initial assessment, in accordance with the following:
(1) The plan of care
shall include:
a. The recipient’s
name, date of birth and Title XIX identification number;
b. The recipient’s
identified needs and/or risk factors;
c. The recommended
HVNH or child/family health care support services; and
d. The frequency of
the recommended HVNH or child/family health care support services;
(2) The plan of care shall be approved, dated,
and signed by:
a. A physician or
APRN, when the plan of care contains a nursing or SMS nutrition component; or
b.
A physician, APRN, LCSW, psychologist, associate psychologist, licensed
clinical mental health counselor, or licensed marriage and family therapist,
when the plan of care does not contain a nursing component; and
(3) The plan of care
shall be reviewed and updated at least annually and as necessary, including
being approved, dated, and signed in accordance with (2) above;
(b) A family support plan which shall:
(1) Be required only
of participating HVNH providers;
(2) Be developed, in
conjunction with the family, based on initial assessment and the plan of care;
(3) Be updated at
least quarterly, in conjunction with the family, based on the health care
provider’s assessment of progress or lack of progress towards the goals in (4)
below; and
(4) Specify
family-specific goal information including, but not limited to:
a. Family-specific
goals, including the date each goal is identified;
b. Action steps to
achieve each family-specific goal;
c. Frequency of
services required to achieve each family-specific goal;
d. Sources of support
resources for the family to utilize to achieve each family-specific goal;
e. Name and
goal-related role of each anticipated and involved health care provider;
f. Dates on which
progress toward each goal is to be reviewed, which shall be at least quarterly;
and
g. Status of goal at
review date;
(c) Progress notes, which shall be prepared at
the time of each visit, or at the time of a telephone call made or video
conference conducted in lieu of a face-to-face visit, by the health care
provider, to include, but not be limited to:
(1) The date of each
visit, telephone call or video conference;
(2) The location of
each visit, if other than the recipient’s home or the participating provider or
health care provider agency, and the reason therefor;
(3) The reason for a
telephone call or video conference if in lieu of a visit;
(4) The individuals
present at the time of the visit;
(5) The start time and
end time of each visit, telephone call or video conference;
(6) For HVNH only,
documentation of the service(s) provided at each visit, or via telephone call
or video conferencing and how the service(s) provided relates to a specific
goal contained in the family support plan;
(7) For MCH providers
of child/family health care support services, documentation of which service(s)
specified in He-W 549.05(b)(5), as related to the plan of care, were provided
at each visit, or via telephone call or video conference;
(8) For participating
providers under contract obligation with SMS, documentation of the service(s)
provided at each visit or via telephone call or via video conference; and
(9) The dated
signature and credentials of the health care provider;
(d) For HVNH only, documentation in the
recipient’s chart as follows:
(1) Family/household
information, including, but not limited to:
a. Names of family
members;
b. Dates of birth of
family members; and
c. Relationship of
family members to recipient;
(2) Family support
team information, including, but not limited to the name and role of each
health care provider providing services; and
(3) The names and
types of other sources of support being received by the recipient, such as, but
not limited to:
a. Primary care,
dental, and mental health providers; and
b. Support from such
programs as women, infants and children nutrition services, and the division
for children, youth and families; and
(e) For child/family health care support services
only, documentation verifying that the recipients served met the eligibility
criteria in He-W 549.02(b).
Source. #7775, eff 10-8-02; ss by #9768, eff 10-8-10;
ss by #10092, eff 3-1-12 (fr5om He-W 549.06); amd by
#11124, eff 6-22-16
He-W
549.08 Utilization Review and Control. The department shall monitor utilization of
HVNH and child/family health care support services, in accordance with 42 CFR
455, 42 CFR 456, and He-W 520.
Source. #7775, eff 10-8-02; ss by #9768, eff 10-8-10;
ss by #10092, eff 3-1-12 (from He-W 549.07)
He-W
549.09 Third Party Liability.
(a) All third party obligations shall be
exhausted before Title XIX shall be billed, in accordance with 42 CFR 433.139,
with the exception of the following:
(1) Pregnant women and
children who are covered by third party liability, enforced by the New
Hampshire division of child support services, shall be exempt from third party
billing practices; and
(2) All preventive
pediatric and prenatal care services shall be exempt from third party billing
practices.
(b) Participating providers may bill medicaid directly for (a)(1) and (a)(2) above, and medicaid shall then seek reimbursement from the third
party.
Source. #7775, eff 10-8-02; ss by #9768, eff 10-8-10;
ss by #10092, eff 3-1-12 (from He-W 549.08)
He-W
549.10 Payment for Services.
(a) Payment for HVNH and child/family health care
support services shall be made, per 15 minute unit of service, in accordance
with rates established by the department in accordance with RSA 161:4, VI(a).
(b) For billing purposes:
(1) Any period of time
that consists of 8 minutes or less shall not be billed; and
(2) Any period of time
that consists of more than 8 minutes shall be billed as one unit.
(c) The participating provider shall submit
claims for payment to the department’s fiscal agent.
(d) The participating provider shall maintain
supporting records, in accordance with He-W 520.
Source. #10092, eff 3-1-12 (from He-W 549.09)
PART
He-W 550 ADULT MEDICAL DAY CARE SERVICES
- EXPIRED (Now He-E 803)
He-W
550.01 - 550.08 - EXPIRED
Source. (See Revision Note at chapter heading He-W
500); ss by #5889, eff 8-31-94; ss by #7355, INTERIM, eff 8-31-00, EXPIRED:
2-27-01
PART
He-W 551 - RESERVED
PART
He-W 552 PERSONAL CARE ATTENDANT
SERVICES
He-W 552.01 Purpose. The purpose of this chapter
is to set forth the procedures and requirements of personal care attendant
services provided by personal care attendants to the severely physically
disabled pursuant to RSA 161-E.
Source. (See Revision Note at chapter heading He-W
500); ss by #4993, eff 11-30-90, EXPIRED: 11-30-96
New. #6742, eff 4-30-98; ss by #7941, eff 8-23-03;
ss by #8597, eff 3-30-06; amd by #10139, eff 7-1-12;
ss by #10562, INTERIM, eff 3-30-14, EXPIRES: 9-26-14; ss by #10676, eff 9-26-14
He-W 552.02 Definitions.
(a)
“Chronically wheelchair mobile” means the recipient, due to a physical
disability, must use a wheelchair for mobility.
(b)
“Department” means the New Hampshire department of health and human
services.
(c) “Legally responsible relative” means a
spouse, or the parent(s) of a minor child, including step-parents, foster
parents and legal guardians, who are legally responsible to provide care for
another person.
(d)
“Medicaid” means the Title XIX and Title XXI programs, administered by
the department, which make medical assistance available to eligible
individuals.
(e)
“Member of the recipient’s family” means an individual related to the
recipient within the second degree of kinship, including:
(1) A spouse, parent, step-parent, sister, or
brother; or
(2) A grandparent, aunt, or uncle residing in the
same household.
(f)
“Natural supports” means the help and care that an individual receives
from his or her family, friends, significant others, roommates, neighbors, and
other community resources, including unpaid voluntary services.
(g)
“Personal care attendant (PCA)” means a person who meets the
requirements set forth in He-W 552.04(b) and is an employee of or is under
contract with a personal care service provider(s) to provide personal care
attendant services.
(h)
“Personal care attendant services (PCA services)” means medically oriented
personal care services as more fully described in He-W 552.05(b) which are
provided by a personal care attendant in the recipient’s home, workplace, or
other non-institutional setting to gain greater control over his or her life in
accordance with RSA 161-E.
(i) “Provider” means an entity that employs or
contracts with the personal care attendant to provide PCA services and meets
the requirements set forth in He-W 552.04(a).
(j)
“Recipient” means any individual who is eligible for and receiving medical
assistance under the medicaid program.
(k)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(l)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #4993, eff 11-30-90, EXPIRED: 11-30-96
New. #6742, eff 4-30-98; ss by #8597, eff 3-30-06;
ss by #10562, INTERIM, eff 3-30-14, EXPIRES: 9-26-14;
ss by #10676, eff 9-26-14 (from He-W 552.01)
He-W 552.03 Recipient Eligibility.
(a) Medicaid recipients shall be eligible for PCA
services when the recipient:
(1) Is at least 18 years of age;
(2) Is his/her own legal guardian;
(3) Is chronically wheelchair-mobile;
(4) Is approved to participate in an independent
living program by provider of PCA services;
(5) Is able to participate fully in activities of
daily living (ADLs), which are the basic self-care tasks of everyday life, such
as eating, bathing, dressing, toileting, and transferring;
(6) Is able to self direct,
which means the recipient is capable of:
a. Making informed choices about his or her PCA
services; and
b. Selecting, directing, supervising and
managing the personal care attendant in the implementation of a plan of care;
(7) Is living in a non-institutional environment,
but requires a minimum of 2 hours of medically oriented PCA services per day;
and
(8)
Has a demonstrated need for PCA services as required by (c) below.
(b)
The requirements in (a)(6) above shall not preclude the recipient from
obtaining assistance with the task of selecting and directing the personal care
attendant.
(c)
A demonstrated need for PCA services shall be documented by:
(1) Documentation from the recipient’s physician
that includes:
a. A statement certifying that, based on the
physician’s assessment of the recipient’s abilities and of the frequency and
scope of the acute medical interventions needed by the recipient, PCA services
are necessary and appropriate;
b. A description of the specific PCA services
and tasks that the recipient needs assistance with; and
c. The number of hours of PCA services needed on
a daily or weekly basis; and
(2) Documentation signed by the recipient
indicating that the recipient’s needs cannot be fully met with natural
supports, and includes:
a. A statement attesting that the PCA services
are intended to assist, not replace or supplant the help already available to
the recipient from family members, community resources, or other natural
supports; and
b. Information detailing why the legally
responsible relative is not able to provide the care that is needed, such as physical
limitations or a work schedule that limits their availability.
Source. (See Revision Note at chapter heading He-W
500); ss by #4993, eff 11-30-90, EXPIRED: 11-30-96
New. #6742, eff 4-30-98; ss by #8597, eff 3-30-06; ss by #10562,
INTERIM, eff 3-30-14, EXPIRES: 9-26-14; ss by #10676,
eff 9-26-14 (from He-W 552.02)
He-W 552.04 Provider Participation.
(a)
All providers of PCA services shall be enrolled as a New Hampshire medicaid provider to provide PCA services.
(b)
All personal care attendants shall:
(1) Be employed by or under contract with a New
Hampshire medicaid provider in (a) above;
(2) Meet the training and experience requirements
specified in He-W 552.07; and
(3) Not be a member of the recipient’s family, per
42 CFR 440.167(a)(2).
Source. (See Revision Note at chapter heading He-W
500); ss by #4993, eff 11-30-90, EXPIRED: 11-30-96
New. #6742, eff 4-30-98; ss by #7941, eff 8-23-03;
ss by #8597, eff 3-30-06;
ss by #10562, INTERIM, eff 3-30-14, EXPIRES: 9-26-14;
ss by #10676, eff 9-26-14 (from He-W 552.03)
He-W 552.05 Covered Services.
(a)
PCA services shall be covered when they are:
(1) PCA services as defined by He-W 552.02(h) and
as further described in (b) below;
(2) Documented by the recipient’s physician who
certifies to the necessity of the PCA services in accordance with He-W
552.03(c);
(3) Part of a plan of care developed by a
registered nurse as provided for in He-W 552.09(b);
(4) Provided in the home or in locations other
than the home, such as school and work, if the PCA services would have
otherwise been provided in the home;
(5) Of a type, frequency, and duration that is
consistent with the recipient’s demonstrated needs for PCA services as
documented in the plan of care; and
(6) Provided in accordance with the requirements
of this part.
(b)
PCA services, provided in accordance with the plan of care, shall
include, as applicable:
(1) Personal hygiene, such as providing or
assisting an individual with bathing, washing hair, grooming, shaving, nail
care, foot care, skin care, mouth care, and oral hygiene, including special
mouth care;
(2) Assistance with toileting, or a bowel and
bladder care program, such as assisting the recipient getting to and from the
bathroom, on and off the toilet, or assistive device used for toileting,
changing incontinence supplies, following a toileting schedule, cleansing an
individual or adjusting clothing relate to toileting, emptying a catheter
drainage bag or assistive device, ostomy care, and bowel care;
(3) Assistance with movement and mobility,
transfers or repositioning, such as transferring a recipient from a bed to a
wheelchair, turning an individual or adjusting padding for physical comfort or
pressure relief, and assisting with range-of-motion exercises;
(4) Under the direction of the recipient,
assistance with medications to the extent allowable under RSA 326-B;
(5) Assistance with dressing;
(6) Meal preparation and clean-up when such
activities are not otherwise being provided, and may include preparing meals
for modified diets, assisting with eating, and monitoring to prevent choking or
aspiration; and
(7) The performance of light household tasks
related to the recipient’s needs, such as but not limited to, changing and washing
the recipient’s bed linens, doing the recipient’s laundry, cleaning of
recipient occupied space, or moving furniture to remove obstacles and hazards
to enable the recipient to move easily in the home.
(c)
The recipient shall be
responsible for informing the personal care attendant about his or her
preferences regarding the PCA services, and how they are to be performed.
Source. (See Revision Note at chapter heading He-W
500); ss by #4993, eff 11-30-90, EXPIRED: 11-30-96
New. #6742, eff 4-30-98; ss by #8597, eff 3-30-06; ss by #10562,
INTERIM, eff 3-30-14, EXPIRES: 9-26-14; ss by #10676, eff 9-26-14 (from He-W
552.04)
He-W 552.06 Non-covered Services.
(a)
Non-covered services shall be those services for which the NH Medicaid
program shall make no payment.
(b)
The following activities shall not be considered PCA services:
(1) Services that are not medically oriented,
including:
a. Shopping, except for grocery shopping;
b. Managing finances;
c. Care, grooming, or feeding of pets or other
animals, with the exception of service animals as defined by the Americans with
Disabilities Act (ADA), Title III Subpart A 36.104, or assistance
animals as defined by the Fair Housing Act Section 504; and
d. Social integration
activities, such as accompanying the recipient to a restaurant, to the movies,
to a ball game or to any other community or social activity;
(2) Chore services, which are tasks that exceed
light housekeeping and include:
a. Cleaning of floors, shampooing carpets,
cleaning walls, and cleaning furniture in areas not occupied by the recipient,
such as cleaning the entire home rather than the area the recipient occupies;
b. Doing laundry, other than the recipient’s
personal laundry, such as doing laundry for the household as opposed to just
the recipient’s personal laundry;
c. Cleaning windows; and
d. Doing yard work, gardening, home
repairs, or shoveling snow unless needed to ensure the recipient’s and the
PCA’s safe access to and from the recipient’s home when the recipient has no
natural supports;
(3) Services provided outside the recipient’s
home for the convenience of the personal care attendant, such as care provided
at the personal care attendant’s home, or any other location where the
recipient would not normally go within the community;
(4) Services performed for the convenience of the
recipient, or the recipient’s family member(s), or intended to otherwise
replace assistance available through the recipient’s natural supports system;
(5) Time spent with the recipient when no actual
hands on care or other covered services are being provided, including but not
limited to supervision, companion care, baby-sitting the recipient’s dependents,
or social visits;
(6) Services provided to a recipient while the
recipient is:
a. An inpatient or resident of a hospital,
nursing facility, intermediate care facility for the mentally retarded, or
institution for mental disease, in accordance with 42 CFR 440.167;
b.
An inmate of a public institution in accordance with 1905(a)(27)(A) of the
Social Security Act; or
c. Attending a program for which personal care
services are already provided, such as adult medical day care;
(7) Services provided to the recipient outside
the United States;
(8) Duplicative PCA services;
(9) Any services not listed as covered under He-W
552.05;
(10) Services which are not included in the
approved plan of care;
(11) Services provided to someone other than the
recipient; and
(12) Care requiring the technical or professional
skill that a state statute or regulation mandates must be performed by a health
care professional licensed or certified by the state.
Source. (See Revision Note at chapter heading He-W
500); ss by #4993, eff 11-30-90, EXPIRED: 11-30-96
New. #6742, eff 4-30-98; ss by #8597, eff 3-30-06; ss by #10562,
INTERIM, eff 3-30-14, EXPIRES: 9-26-14; ss by #10676, eff 9-26-14 (from He-W
553.06)
He-W
552.07 Training Requirements.
(a)
The provider shall ensure that, within 30 days of the date of hire, the
personal care attendant has,
through training or experience, the skills required to perform the PCA services
including competency in the following areas:
(1) Roles, responsibilities and expectations of a
personal care attendant, including knowledge of activities that do and do not
qualify as PCA services;
(2) Personal care and nutrition;
(3) Infection control and universal precautions
designed to prevent the transmission of infectious diseases;
(4) Safety and emergency procedures, including
basic first aid and 911 protocols;
(5)
Proper lifting techniques;
(6) Recipient rights, and reporting of abuse and
neglect; and
(7) Record-keeping and documentation, including
the penalties associated with improper recordkeeping and documentation.
(b) The provider shall maintain documentation in
the personnel file indicating that the personal care attendant meets the
requirements of (a) above, including the name and signature of the person
making the competency determination.
Source. (See Revision Note at chapter heading He-W 500);
ss by #4993, eff 11-30-90, EXPIRED: 11-30-96
New. #6742, eff 4-30-98; ss by #8597, eff 3-30-06; ss by #10562,
INTERIM, eff 3-30-14, EXPIRES: 9-26-14; ss by #10676, eff 9-26-14
He-W 552.08 Provider and PCA Responsibilities.
(a)
The provider shall:
(1) Ensure that the recipient receives
independent living skills training as stated in the recipient’s individualized
independent living plan of care;
(2) Coordinate independent living resources and
supports; and
(3) Perform on-going assessments to evaluate the
recipient’s psychosocial, physical, and environmental status to prevent
hospitalization and to promote wellness.
(b)
The personal care attendant shall document a detailed written daily
record to include:
(1) Specific tasks performed;
(2) Condition and changes in condition or status
of the recipient, such as a reported change in sleep patterns, an injury, or
development of a decubitus ulcer; and
(3) The dates worked, total number of hours
and/or 15 minute units worked for each day, including the in and out times.
(c)
When the personal care attendant has concerns regarding the recipient’s
health, he or she shall:
(1) Raise the concerns with the recipient;
(2) Note the concerns in their daily report; and
(3) If raising the issue with the recipient does
not alleviate the concern, bring the concern to the attention of the registered
nurse employed by the provider to oversee the recipient’s care.
(d)
When the personal care attendant brings a concern to the nurse’s
attention in accordance with (c)(3), the nurse shall follow-up and document the
outcome in the provider’s record for the recipient.
Source. #10676, eff 9-26-14 (from He-W 552.03)
He-W 552.09 Personal Care Assessments and the Plan of
Care.
(a)
A personal care assessment shall be conducted by the provider’s licensed
registered nurse and used to develop the plan of care.
(b)
The personal care assessment shall include the following:
(1) The recipient’s functional level;
(2) The adaptability of the recipient’s place of
residence to the provision of PCA services;
(3)
The capability of the recipient to participate in his or her own care and to
determine the degree of support needed; and
(4)
The extent of, and need for, any natural supports taking into account the
potential contributions of natural supports.
(c)
The plan of care shall:
(1) Be based on the recipient’s physician’s
documentation described in He-W 552.03(c) and the personal care assessment as
described in (a) above;
(2) Include the information from the personal
case assessment as well as the following:
a. Diagnosis;
b. Recipient status, including:
1. Behavioral health status;
2. Physical health status;
3. Functional limitations; and
4. Rehabilitative prognosis;
c. PCA services needed, including:
1. The type, frequency, and number of hours
and/or 15 minute units per day or week;
2. Any equipment requirements;
3. Any nutritional requirements; and
4. Medications;
d. Discharge planning or referral; and
e. Other identified appropriate PCA services;
(3) Be signed by the licensed registered nurse
responsible for the oversight of the recipient’s care, and incorporated in the
provider’s record for the recipient; and
(4) Be reviewed by the provider’s licensed
registered nurse who is responsible for the oversight of the recipient’s care
every 3 months, and the prescribing physician every 6-months, or more often if
warranted by the severity of the recipient’s functional limitations.
(d)
The provider’s licensed registered nurse who is responsible for the
oversight of the recipient’s PCA services shall make a face-to-face visit to
the recipient’s residence at least once every 3-months to:
(1) Reassess the PCA services in light of the
recipient’s needs as described in the plan of care, and note any need for
changes to the plan of care;
(2) Confirm that the recipient is satisfied with
the PCA services being provided;
(3) Verify that the PCA services being provided
in accordance with the recipient’s needs, preferences and the plan of care; and
(4) Ensure that documentation and recordkeeping
are being performed in an accurate and appropriate manner.
(e)
All assessments required in (a) and (d) above shall be conducted using a
standardized assessment tool of the provider’s choice, which has been reviewed
by the department.
(f)
Any revisions to the plan of care as a result of a review as described
in (d) above, shall be in writing, and approved by the recipient’s physician.
Source. #10676, eff 9-26-14
He-W 552.10 Utilization Review and Control. The department’s provider program integrity
unit shall monitor utilization of the PCA services to identify, prevent, and
correct potential occurrences of fraud, waste and abuse, in accordance with 42
CFR 455 and 42 CFR 456 and He-W 520.
Source. #10676, eff 9-26-14 (from He-W 552.05)
He-W 552.11 Third Party Liability. All third party obligations shall be
exhausted before medicaid may be billed, in
accordance with 42 CFR 433.139.
Source. #10676, eff 9-26-14 (from He-W 552.06)
He-W 552.12 Payment for Services. Payment for PCA services shall be made as
follows:
(a)
Payment for PCA services shall be made in accordance with fee schedules
established by the department in accordance with RSA 161:4, VI(a); and
(b)
The provider shall submit claims for payment to the department’s fiscal
agent.
Source. #10676, eff 9-26-14 (from He-W 552.07)
He-W 552.13 Documentation.
(a)
The provider shall maintain supporting records, in accordance with He-W
520.
(b)
The supporting records described in (a) above shall include, but not be
limited to:
(1) Documentation from the recipient’s physician
that includes documentation of the need for PCA services in accordance with
He-W 552.03(c);
(2) Results of the personal care assessment
completed in accordance with He-W 552.09;
(3) The plan of care, as described in He-W
552.09(b);
(4) Documentation describing any changes in either
the type of PCA services to be provided or the number of hours of PCA services
provided, including an explanation of the basis for the change;
(5) Documentation of the time during which PCA
services were provided to each recipient, including the date of service, number
of hours and/or units worked, including specific in and out times, and
confirmed by the recipient in writing, verbally, or electronically that PCA
services were performed;
(6) Documentation of the PCA services for which
reimbursement has been requested, including a detailed description of the
specific PCA services provided;
(7) Documentation of the face-to-face visits
conducted in accordance with He-W 552.09(c), including any related notes and
outcomes; and
(8) Documentation of oversight measures taken by
the provider to ensure PCA services are being provided when they are being
provided outside the state of New Hampshire for longer than a 30-day period of
time.
(c) All electronic or written documentation
submitted in accordance with (b) above shall be legible and written in English.
(d)
The provider shall provide such documentation to the department upon request.
Source. #10676, eff 9-26-14 (from He-W 553.04)
PART He-W 553 HOME HEALTH SERVICES
REVISION NOTE:
Document
# 11127, effective 7-1-16, contained Part He-W 553 on home health agencies,
comprising rules He-W 553.01 through He-W 553.07. Document #11127 adopted He-W 553.01 and
readopted with amendments and renumbered the former He-W 553.01 through 553.06
as He-W 553.02 through He-W 553.07. Most
of the former He-W 553.01 and all of the former He-W 553.02 through He-W 553.06
were scheduled to expire 9-11-15 but were extended pursuant to RSA 541-A:14-a
until replaced by the rules He-W 553.02 through He-W 553.07 in Document #11127.
The
former He-W 553.07 on payment for services had originally been adopted by
Document #8972, effective 9-11-07, until superseded by Document #9105,
effective 3-18-08. The former He-W
553.08 on rate setting methodology had originally been adopted by Document
#9105, effective 3-18-08. The former
He-W 553.07 and He-W 553.08 were both “suspended for the biennium ending June
30, 2017” as rules relative to rate setting pursuant to 2015, 276:145,
effective 7-1-15. But the rules were
allowed by the Department of Health and Human Services to expire on
3-18-16. The former He-W 553.09 on third
party liability and former He-W 553.10 on utilization review and control had
also originally been adopted by Document #8972, effective 9-11-07, until
superseded by Document #9105, effective 3-18-08. These rules were also allowed by the
Department of Health and Human Services to expire on 3-18-16.
He-W 553.01 Purpose. The purpose of this part is
to prescribe the requirements of home health services under the New Hampshire medicaid state plan.
Source. (See Revision Note at part heading for He-W
553) #11127,
eff 7-1-16
He-W 553.02 Definitions.
(a) “Department” means the New Hampshire department of health and human
services.
(b) “Direct care time” means the time a licensed nursing assistant (LNA),
registered nurse (RN), or licensed practical nurse (LPN) spends with one
recipient during which home health services are provided only to that
individual recipient during a visit.
(c) “Home health aide” means an LNA, licensed in
accordance with RSA 326-B.
(d) “Home health aide services” means services
provided to a recipient which constitute hands-on care and are required to maintain the recipient’s health, facilitate treatment of
the recipient’s medical condition, illness, or injury, and when performed by a LNA, provided under the
supervision of a RN or LPN.
(e) “Home health care provider” means any
organization or business entity engaged in arranging for or providing home health
services as described in RSA 151:2-b(I) and 42 CFR 440.70(d) and which is a NH
enrolled medicaid provider in accordance with He-W
553.04.
(f) “Home health services” means skilled nursing
services, home health aide services, and physical therapy, occupational
therapy, speech pathology, and audiology services provided by a licensed
therapy provider in accordance with He-W 568.
(g) “Independent nurse” means an RN who is not an
employee with or an independent contractor of a home health care provider and
is qualified to provide skilled nursing services.
(h) “Light housekeeping” means preparing meals
for the recipient, cleaning the recipient’s bedroom and bathroom, and changing
the recipient’s bed linens.
(i) “Medicaid” means
the Title XIX and Title XXI programs administered by the department, which
makes medical assistance available to eligible individuals.
(j) “Non-routine
supplies” means those supplies necessary to complete specific medical
treatments ordered by a physician, such as ostomy supplies, IV
supplies, catheters and catheter supplies, syringes and needles, sterile
dressings, and wound care supplies, and does not include routine supplies.
(k) “Recipient” means an individual who is
eligible for and receiving medical assistance under the medicaid
program.
(l) “Routine supplies” means those supplies used incidentally
in the course of a visit and include gloves, alcohol wipes, blood drawing supplies,
adhesive and paper tape, and non-sterile dressings.
(m) “Skilled nursing services” means services
that must be provided by an RN or a LPN because the nature of the service is inherently complex or
the recipient’s condition is such that the service can be safely and
effectively provided only by a RN or LPN.
(n) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(o) “Title XXI” means the joint federal-state
program described in Title XXI of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(p) “Unit” means 15 minutes.
(q) “Visit” means a personal encounter with the
recipient by staff of a home health care provider for the purpose of providing a covered service(s).
Source. (See Revision Note at chapter heading He-W
500); ss by #5342, eff 3-3-92, EXPIRED: 3-3-98
New. #8972, eff 9-11-07; amd
by #9105, eff 3-18-08; amd by
#10139, eff 7-1-12; ss by #11127, eff 7-1-16 (formerly He-W 553.01) (See
Revision Note at part heading for He-W 553)
He-W 553.03 Recipient Eligibility. A recipient shall be eligible to receive home
health services in accordance with 42 CFR 441.15(c) if all of the following
criteria are met:
(a) The recipient is under the care of a
physician;
(b) The recipient requires home health services
as ordered by his or her physician and documented in a written plan of care;
and
(c) The recipient resides in his or her primary or temporary
residence, excluding a hospital, nursing facility, or intermediate care facility for individuals with intellectual
disabilities (ICF/IID), in accordance with 42 CFR 440.70(c).
Source.
#8972, eff 9-11-07; ss by #11127, eff 7-1-16
(formerly He-W 553.02) (See Revision Note at part heading
for He-W 553)
He-W 553.04 Provider Participation.
(a) All home health care providers
shall:
(1) Hold a current New Hampshire
state license as a home health care provider, in accordance with RSA 151:2-b,
I, and He-P 809;
(2) Be certified to participate in
the medicare program; and
(3) Be a New
Hampshire enrolled medicaid provider.
(b) When there is no licensed and certified home
health care provider in the area, an independent nurse may provide skilled
nursing services if the independent nurse:
(1) Is currently licensed to practice in the
state in which he or she practices;
(2) Receives written orders from the recipient’s
physician;
(3) Documents the care and services provided in accordance with He-W 553.05; and
(4) Is a NH enrolled medicaid
provider.
Source.
#8972, eff 9-11-07; ss by #11127, eff 7-1-16
(formerly He-W 553.03) (See Revision Note at part heading
for He-W 553)
He-W 553.05 Required
Documentation.
(a) Home health care providers
and independent nurses shall maintain complete and timely records for each
recipient receiving services in accordance with He-W 520, and this part.
(b) Where a home health care provider or independent nurse has failed
to maintain records pursuant to (a) above , the department shall be entitled to
recoupment of state or federal medicaid payments
made, as permitted by 42 CFR 455, 42 CFR 456 and 42 CFR 447.
(c) In addition to the
requirement set forth in (a) above, home health care providers and independent
nurses shall maintain the documentation required by this part and He-W 520 to
support claims submitted for reimbursement for a minimum of 6 years or until
the resolution of any legal action(s) commenced within the 6 year period,
whichever is longer.
(d) Recipient records shall
include all of the following:
(1) Written orders for initial
home health services and certification of the need for home health services
signed by the recipient’s physician specifying:
a. The frequency of medication
and treatment to be administered; and
b. The period of time to be
covered by the orders;
(2) Documentation of the
occurrence of a face-to-face encounter which is related to the primary reason
the recipient requires home health services indicating the time frame the
encounter took place, the date, the practitioner who conducted the encounter,
and the practitioner’s findings in accordance with He-W 553.06(a) below;
(3) For recipients under the
age of 21, a recipient history and a health assessment with an appropriate
pediatric tool completed upon admission by the RN or appropriate rehabilitation
skilled professional in accordance with 42 CFR 484.55;
(4) For recipients over the age
of 21, a recipient history and a health assessment, completed upon admission by
the RN or appropriate rehabilitation skilled professional in accordance with 42
CFR 484.55, except that the homebound assessment of 42 CFR 484.55 is not
required;
(5) Documentation at least
every 60 days to indicate review of the recipient’s health assessment by the RN
or appropriate rehabilitation skilled professional in accordance with 42 CFR
484.55;
(6) A written individualized
plan of care which shall include the following:
a. The diagnosis related to the
recipient’s need for home health services;
b. Other diagnoses;
c. An assessment of the
recipient’s mental alertness and cognitive level;
d. Measurable recipient goals;
e. Types of services and
equipment required;
f. Frequency of home health
services;
g. Anticipated length of
treatment;
h. General prognosis;
i. Rehabilitation potential;
j. Functional limitations
including activities of daily living;
k. Activities permitted;
l. Nutritional requirements;
m. Medications;
n. Treatments;
o. Safety measures required to
protect the recipient from potential injury;
p. Services being provided by
non-paid caregivers involved in the recipient’s treatment and any related
education or training needs of the caregivers; and
q. Discharge plans;
(7) Documentation at least
every 60 days, to indicate review of the written plan of care by the
recipient’s physician;
(8) Documentation at least
every 60 days that indicates the locations of service delivery other than the
recipient’s home for services already provided;
(9) Auditable, paper, or
electronic service notes for each service provided to the recipient
identifying:
a. Name of recipient;
b. Date of service;
c. Location(s) where service
was provided, if other than the recipient’s primary residence;
d. Primary purpose of the home
health services;
e. Description of services
provided;
f. Amount of direct care time
spent providing each home health service;
g. Condition of the recipient
at the time the service was provided, and any significant change in recipient’s
mental or physical condition;
h. Any progress the recipient
has made towards goals identified on the written plan of care;
i. An explanation of any variation from the
written plan of care; and
j. Name, title, and written or
electronic signature of the individual providing the home health service; and
(10) Documentation of any consults
or meetings regarding the recipient’s care, which also indicates the results of
the consult or meeting.
(e) Home health care providers
and independent nurses shall make the documentation required by this part and
He-W 520 available for review to the department upon the request of the
department.
Source.
#8972, eff 9-11-07; ss by #11127, eff 7-1-16
(formerly He-W 553.04) (See Revision Note at part heading
for He-W 553)
He-W 553.06 Covered Services.
(a) Services shall be covered when:
(1) A physician orders services
as part of a written plan of care; and
(2) A face-to-face encounter
with the recipient, which may occur within 90 days before the initial start of
the home health services or within 30 days after the start of services, is documented
in compliance with He-W 553.05(d)(2) above, and is performed by one of the
following medicaid enrolled providers:
a. The recipient’s physician;
or
b. The following non-physician
practitioners when the requirements in (b) below are met:
(i) A
nurse practitioner or clinical nurse specialist working in collaboration with
the recipient’s physician;
(ii) A certified nurse midwife;
or
(iii) A physician assistant
under the supervision of the recipient’s physician.
(b) Non-physician practitioners in (a)(2)b. above
who perform the face-to-face encounter shall communicate the clinical findings
of the face-to-face encounter to the recipient’s physician who shall incorporate
the clinical findings into the recipient’s medical record.
(c) Covered services shall be
those home health services, regardless of diagnosis, the need for which is
consistent with the nature of the recipient’s condition and accepted standards
of medical and nursing practice.
(d) Covered home health
services shall include:
(1) Skilled nursing services in
accordance with the written plan of care including:
a. Skilled observation and
assessment of the recipient’s status, including available support system and
physical environment;
b.
Administration of medications, including intramuscular and intravenous
medications;
c. Insertion and irrigation of
indwelling urinary catheters;
d. Administration of enemas, providing ostomy care, and other related
procedures to provide assistance with bowel evacuation;
e. Skilled respiratory care including suctioning, tracheostomy care,
administration of inhalation therapies, and chest physiotherapy;
f. Wound care, care of
decubitus ulcers, and treatment of other extensive skin disorders;
g. Administration of enteral
feedings;
h. Rehabilitative nursing
procedures such as the initiation and supervision of bowel and bladder training
programs;
i. Education, specific to the recipient’s
condition, provided to the recipient and significant others involved with the
recipient;
j. Pre-filling of medication
administration devices such as pill planners;
k. Medication reconciliation;
and
l. Education about medication
therapeutic effects, side effects, and adherence to prescribed regimen;
(2) Home health aide services,
in accordance with the written plan of care, including assistance provided to a
recipient for the following:
a. Personal hygiene, including
bathing, grooming, dressing, and changing bed linens, when there is a medical
need and it is documented in the care plan;
b. Ambulation and movement,
including range of motion exercises, turning, positioning, and transferring;
c. Nutritional care, including
feeding and hydration;
d. Elimination, including
toileting and bowel or bladder training;
e. Assistance with the use of adaptive
prosthetic and orthotic devices;
f. Assistance with
self-administering medications, when the assistance provided by the aide does
not require the skill of a licensed nurse;
g. Administration of
medications by a medication LNA or by an LNA if delegated by a RN in accordance
with RSA 326-B:14, II-a;
h. Activities that are directly
supportive of skilled therapy services;
i. Other medically related activities which can safely
and effectively be provided by a LNA, including simple dressing changes;
j. Light housekeeping when
there is documentation that no other support in the home exists at the time of
the visit, and when such services are directly related to the recipient’s
medical condition and care needs and is documented in the written plan of care;
and
k. Tasks properly delegated to
the LNA by the supervising RN pursuant to RSA 326-B:28;
(3) Physical therapy, speech
therapy, occupational therapy, speech
pathology and audiology services provided a licensed therapy provider and subject to the limits specified in He-W 530;
(4) Durable medical equipment,
medical supplies, prosthetics, and orthotic devices, when prescribed by the
attending physician and in accordance with the requirements in He-W 571; and
(5) Office visits, when the
recipient receives services provided by an advanced practice registered nurse
(APRN) at the location of the home health care provider as an alternative to
visiting a physician’s office for treatment.
Source.
#8972, eff 9-11-07; ss by #11127, eff 7-1-16
(formerly He-W 553.05) (See Revision Note at part heading
for He-W 553)
He-W 553.07 Non-Covered
Services. Non-covered home health
services shall include:
(a) Physician services;
(b) Social worker services;
(c) Nutritionist services;
(d) Visits provided solely for
the purpose of supervising the LNA;
(e) Services provided by an
LNA, RN, or LPN or other licensed therapy provider which are not medically
related and which constitute routine household activities, day care, or
recreational services;
(f) Services rendered without a
physician’s signed order;
(g) Any service whose primary
purpose is providing emotional support;
(h) Any service whose primary
purpose is the care or supervision that would be required by any individual of
the recipient’s chronological age;
(i)
Drugs and biologicals;
(j) Meals delivered to the
home; and
(k) Homemaker services
considered to be general household activities, except as described in He-W
553.06(d)(2)j., including:
(1) Keeping a safe environment
in areas of the home used by the recipient;
(2) Performing house cleaning;
(3) Rearranging furniture to assure
that the recipient can safely reach necessary supplies or medication;
(4) Completing laundry tasks;
and
(5) Assisting the recipient
with purchasing food and helping with the preparation of meals and special
diets.
Source.
#8972, eff 9-11-07; ss by #11127, eff 7-1-16
(formerly He-W 553.06) (See Revision Note at part heading
for He-W 553)
PARTS
He-W 554 and He-W 555 - RESERVED
PART
He-W 556 SUPPORTED RESIDENTIAL HEALTH
CARE FACILITY SERVICES - EXPIRED AND RESERVED
Source. (See Revision Note at chapter heading He-W
500); ss by #5676, eff 8-1-93, EXPIRED: 8-1-99
PART
He-W 557 - RESERVED
PART
He-W 558 HOME AND COMMUNITY-BASED
SERVICES FOR THE ELDERLY AND CHRONICALLY ILL - EXPIRED
He-W
558.01 – 558.09
Source. (See Revision Note at chapter heading He-W
500); ss by #5890, eff 8-31-94; ss by #7356, INTERIM, eff 8-31-00, EXPIRED:
2-27-01
PART He-W 559 CASE
MANAGEMENT OF ADVANCE CARE PLANNING AND DIRECTIVES - EXPIRED
He-W 559.01 - 559.02
Source. (See Revision Note at chapter heading He-W
500); ss by #5891, eff 8-31-94, EXPIRED: 8-31-00
New. #7700, eff 7-1-02, EXPIRED: 7-1-10
He-W
559.03 - 559.08
Source. #7700, eff 7-1-02, EXPIRED: 7-1-10
PARTS
He-W 560 through He-W 564 - RESERVED
PART
He-W 565 VISION CARE SERVICES
He-W 565.01 Definitions.
(a)
“Department” means the New Hampshire department of health and human
services.
(b)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department, which makes medical assistance available to eligible
individuals.
(c)
“Ophthalmologist” means a physician who specializes in the diagnosis and
treatment of disorders of the eye.
(d)
“Optometrist” means a doctor of optometry (OD), a primary health care provider
who diagnoses, manages, and treats conditions and diseases of the eye.
(e)
“Optician” means “optician” as defined in RSA 327-A:1,VII, namely
“anyone who sells or dispenses, upon prescription, spectacles, eyeglasses or
contact lenses.”
(f)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(g)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire under the medicaid program.
(h)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #4819, eff 6-1-90, EXPIRED: 6-1-96
New. #6705, eff 3-3-98, EXPIRED: 3-3-06
New. #8603, eff 4-10-06;
amd by #10139, eff 7-1-12; ss by #10638, eff 7-12-14
He-W 565.02 Recipient Eligibility. All medicaid
recipients shall be eligible to receive vision care services, in accordance
with He-W 565.
Source. (See Revision Note at chapter heading He-W
500); ss by #4819, eff 6-1-90, EXPIRED: 6-1-96
New. #6705, eff 3-3-98, EXPIRED: 3-3-06
New. #8603, eff 4-10-06;
ss by #10638, eff 7-12-14
He-W 565.03 Provider Participation. Vision care providers shall meet the criteria
specified below:
(a)
Ophthalmologists and optometrists shall be licensed by the state in
which they practice;
(b)
Opticians practicing in New Hampshire (NH) shall be registered in accordance
with RSA 327-A:2, or, if practicing in another state, meet the requirements of
the state in which they practice;
(c)
Opticians who fit contact lenses shall have a statement of delegation
from an ophthalmologist or optometrist in accordance with RSA 327-A:2;
(d)
Ophthalmologists, optometrists and opticians shall be NH-enrolled medicaid providers; and
(e)
Ophthalmologists, optometrists and opticians shall request and obtain
prior authorization from the department before providing services which require
prior authorization.
Source. (See Revision Note at chapter heading He-W
500); ss by #4819, eff 6-1-90, EXPIRED: 6-1-96
New. #6705, eff 3-3-98, EXPIRED: 3-3-06
New. #8603, eff 4-10-06;
ss by #10638, eff 7-12-14
He-W 565.04 Service Limits. Vision care services shall be subject to the
limits described in He-W 565 and He-W 530.
Source. (See Revision Note at chapter heading He-W
500); ss by #4819, eff 6-1-90, EXPIRED: 6-1-96
New. #6705, eff 3-3-98, EXPIRED: 3-3-06
New. #8603, eff 4-10-06;
ss by #10638, eff 7-12-14
He-W 565.05 Covered Services. Covered services shall include:
(a)
Eye examination procedures to diagnose and monitor medical conditions of
the eye, including:
(1) Complete eye examinations including:
a. Visual acuity testing;
b. Gross visual fields;
c. Muscle balance;
d. Slit lamp examinations; and
e. Ophthalmoscopy and tonometry;
(2) Interior extended testing of visual fields
only;
(3) Ophthalmoscopy, fundoscopy only; and
(4) Routine tonometry;
(b)
Eye examinations, performed in:
(1) A provider’s office;
(2) A recipient’s home; or
(3) A nursing facility in which the recipient
resides;
(c)
One refraction to determine the need for eyeglasses, no more frequently
than every 12 months;
(d)
One pair of single vision lenses with frames following an eye
examination as described in (a) and (b) above when the initial or change in
correction is as follows:
(1) For recipients 21 years of age and older, the
refractive error is at least plus or minus .50 diopter, according to the
refractive error, which may be calculated as a combined total of the spherical
and cylindrical errors, in both eyes; and
(2) For recipients under 21 years of age, the
refractive error is at least plus or minus .50 diopter, according to the
refractive error, which may be calculated as a combined total of the spherical
and cylindrical errors, in at least one eye;
(e)
One pair of eyeglasses with bifocal corrective lenses or one pair of
eyeglasses with corrective lenses for close vision and one pair of eyeglasses
with corrective lenses for distant vision if there is a refractive error of at
least .50 diopter for both close and distant vision;
(f)
Transition lenses for recipients with ocular albinism;
(g)
Contact lenses for ocular pathology in cases where the visual acuity is
not correctable to 20/70 or better without contact lenses, or when required to
correct aphakia or to treat corneal disease;
(h)
Replacement of the component eyeglasses parts due to breakage or damage,
subject to the following:
(1) Replacements may be in the form of a single
lens, both lenses, frame only or a complete pair of corrective lenses;
(2) Each component part or complete pair of
corrective lenses may only be replaced one time within a 12-month period; and
(3) When the recipients has 2 pairs of eyeglasses
in lieu of bifocals as allowed in (e) above, each pair of eyeglasses is subject
to replacement in accordance with (1) and (2) above;
(i) Only one replacement of lost eyeglasses per
lifetime for recipients under 21 years of age;
(j)
Trifocal lenses provided that the recipient:
(1) Is employed and the trifocal lenses are
required for the work involved in the recipient’s employment;
(2) Is a full time student and the trifocal
lenses are required for the work involved in the recipient’s education; or
(3) Currently has trifocals;
(k)
Ocular prostheses including:
(1) Artificial eyes; and
(2) Replacing the lens of an eye; and
(l)
Replacement of nickel frames after 12 months, if the recipient has a
documented allergy to nickel demonstrated by skin irritation and wearing down
of the frame in the effected area.
Source. (See Revision Note at chapter heading He-W
500); ss by #4819, eff 6-1-90, EXPIRED: 6-1-96
New. #6705, eff 3-3-98, EXPIRED: 3-3-06
New. #8603, eff 4-10-06; amd
by #10342, eff 6-1-13; ss by #10638, eff 7-12-14
He-W
565.06 Non-Covered Services. Non-covered services shall include:
(a) Replacement of lost eyeglasses, as follows:
(1) For recipients age 21 and over; and
(2) More than once per lifetime for recipients
under age 21;
(b) Progressive lenses;
(c) Photochromatic lenses, including Transition
lenses, except for recipients diagnosed with ocular albinism;
(d) Contact lenses, except as described in He-W
565.05(g) above, which shall be limited to a 60-day supply at a time;
(e) Orthopics and
vision therapy, such as muscle training;
(f) Low vision aids, such as magnifying glasses;
(g) Sunglasses and eyeglass tinting;
(h) Polarized lenses and anti-reflective
coatings;
(i) Titanium frames;
(j) High-index lenses;
(k) Lasiks surgery;
(l) Low vision aids;
(m) Items or services for which a less costly
alternative is available; and
(n) Any other item or service not listed in He-W
565.05.
Source. (See Revision Note at chapter heading He-W
500); ss by #4819, eff 6-1-90, EXPIRED: 6-1-96
New. #6705, eff 3-3-98, EXPIRED: 3-3-06
New. #8603, eff 4-10-06; ss by #10342, eff 6-1-13;
ss by #10638, eff 7-12-14
He-W 565.07 Utilization Review and Control. The department’s provider integrity unit
shall monitor utilization of vision care services to identify, prevent, and
correct potential occurrences of fraud, waste, and abuse in accordance with 42
CFR 455, 42 CFR 456, and He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #4819, eff 6-1-90, EXPIRED: 6-1-96
New. #6705, eff 3-3-98, EXPIRED: 3-3-06
New.
#8603, eff 4-10-06; ss by #10638, eff 7-12-14
He-W 565.08 Third Party Liability. All third party obligations shall be
exhausted before NH medicaid may be billed, in
accordance with 42 CFR 433.139.
Source. (See Revision Note at chapter heading He-W
500); ss by #4819, eff 6-1-90, EXPIRED: 6-1-96
New. #6705, eff 3-3-98, EXPIRED: 3-3-06
New.
#8603, eff 4-10-06; ss by #10638, eff 7-12-14
He-W 565.09 Payment for Services.
(a)
Payment for vision care services shall be made in accordance with rates
established by the department in accordance with RSA 161:4, VI(a).
(b)
The vision care provider shall submit claims for payment to the department’s
fiscal agent.
(c)
Vision frames and lenses shall be ordered from and billed by the
department’s sole source vision provider.
(d)
The provider shall maintain supporting records, in accordance with He-W
520.
Source. (See Revision Note at chapter heading He-W
500); ss by #4819, eff 6-1-90, EXPIRED: 6-1-96
New. #6705, eff 3-3-98, EXPIRED: 3-3-06
New.
#8603, eff 4-10-06; ss by #10638, eff 7-12-14
PART
He-W 566 DENTAL SERVICES
He-W 566.01 Definitions.
(a)
“By report” means a written description of the service provided and the
medical necessity of same as required by the department to be submitted with
certain claims for payment of such claims.
(b)
“Comprehensive orthodontic treatment” means diagnosis, long-term
treatment, periodic evaluations, and retention, leading to improvement of a
recipient’s malocclusion.
(c)
“Deciduous teeth”, also known as primary teeth, means the 20 teeth that
erupt first and are normally shed and replaced by secondary teeth.
(d)
“Department” means the New Hampshire department of health and human
services.
(e)
“Destruction of tissue” means demonstrable, traumatic alteration of soft
or hard tissue architecture with history of treatment of pain.
(f)
“Diagnostic model” means a model or representation that demonstrates all
erupted teeth, the gingival tissue surrounding the anterior and posterior
arches, and the true occlusal relationships of the teeth and tissues.
(g)
“Differential diagnosis” means a condition or disorder consistent with
and reasonably thought to be the cause of the history, signs, and symptoms
presented by the recipient which is determined by a process that differentiates
it from other conditions or disorders with similar signs or symptoms.
(h)
“Early and Periodic Screening, Diagnosis and Treatment (EPSDT) services”
means a program, pursuant to 42 CFR 440.40, designed to provide preventative
health care, diagnostic services, and early detection and treatment of disease
or abnormalities to Title XIX eligible individuals under age 21.
(i) “Interceptive orthodontic treatment” means an
intervention in the initial stages of a developing problem related to the
dentition, to lessen severity of the malformation and to eliminate its cause.
(j)
“Limited orthodontic treatment” means orthodontic treatment not
involving the entire dentition.
(k)
“Malocclusion” means improper alignment of the biting or chewing
surfaces of upper and lower teeth that results from a deviation of the
alignment of the teeth from the ideal alignment.
(l)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(m)
“Medically necessary” means:
(1) For individuals under age 21, reasonably
calculated to prevent, diagnose, correct, cure, alleviate, or prevent the
worsening of conditions that endanger life, cause pain, result in illness or
infirmity, threaten to cause or aggravate a handicap, or cause physical
deformity or malfunction, and no other equally effective course of treatment is
available or suitable for the EPSDT recipient requesting a medically necessary
service; and
(2) For individuals age 21 and over, health care
services that a licensed health care provider, exercising prudent clinical
judgment, would provide, in accordance with generally accepted standards of
medical practice, to a recipient for the purpose of evaluating, diagnosing,
preventing, or treating an acute or chronic illness, injury, disease, or its
symptoms, and that are:
a. Clinically appropriate in terms of type,
frequency of use, extent, site, and duration, and consistent with the
established diagnosis or treatment of the recipient’s illness, injury, disease,
or its symptoms;
b. Not primarily for the convenience of the
recipient or the recipient’s family, caregiver, or health care provider;
c. No more costly than other items or services
which would produce equivalent diagnostic, therapeutic, or treatment results as
related to the recipient’s illness, injury, disease, or its symptoms; and
d. Not experimental, investigative, cosmetic, or
duplicative in nature.
(n)
“Palliative treatment” means minor treatment to reduce the pain of a
disease, illness, or injury of the tooth or teeth excluding non-treatment
activities such as writing a prescription, dispensing a drug or medication, or
telephone consultation with or about a recipient.
(o)
“Radiograph” means an image or picture produced by exposure to ionizing
radiation of a radiation-sensitive film, phosphorous plate, emulsion, or digital
sensor.
(p)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(q)
“Severe handicapping malocclusion” means a malocclusion resulting from
severe skeletal discrepancies that can be objectively documented as causing the
following:
(1) Tissue injury;
(2) Significantly impaired speech, mastication,
breathing or swallowing; or
(3) Severe psychological trauma or severe
antisocial behavior.
(r)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(s)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #5639, eff 6-17-93; ss by #7012, eff 6-15-99; ss by #7912, eff
7-1-03; ss by #9902, eff 6-1-11; amd by #10139, eff
7-1-12; ss by #12782, INTERIM, eff 5-21-19, EXPIRED: 11-18-19
New. #12937, eff 12-7-19
He-W 566.02 Recipient Eligibility. All Title XIX recipients shall be eligible to
receive dental services, in accordance with He-W 566.
Source. (See Revision Note at chapter heading He-W
500); ss by #5639, eff 6-17-93; ss by #7012, eff 6-15-99; ss by #7912, eff
7-1-03; ss by #9902, eff 6-1-11; ss by #12782, INTERIM, eff 5-21-19, EXPIRED: 11-18-19
New. #12937, eff 12-7-19
He-W 566.03 Provider Participation. Each participating dental provider shall:
(a)
Hold an active license to practice dentistry in the state in which he or
she practices;
(b)
Be a New Hampshire enrolled Title XIX provider; and
(c)
Request and obtain prior authorization from the department, in
accordance with He-W 566.07.
Source. (See Revision Note at chapter heading He-W
500); ss by #5639, eff 6-17-93; ss by #7012, eff 6-15-99; ss by #7912, eff
7-1-03; ss by #9902, eff 6-1-11; ss by #12782, INTERIM,
eff 5-21-19, EXPIRED: 11-18-19
New. #12937, eff 12-7-19
He-W 566.04 Covered Services.
(a)
The following dental services shall be covered for recipients who are
under 21 years of age:
(1) Prophylaxis, no more frequently than every
150 days;
(2) Restorative treatment;
(3) Periodic examinations, no more frequently
than every 150 days, unless they are medically necessary to diagnose an illness
or condition;
(4) Vital pulpotomy, which consists of removal of
diseased or involved pulp in an effort to retain the remaining pulp in a
healthy, vital condition;
(5) Extractions of symptomatic teeth associated
with diagnosed pathology, such as tumor, cyst, or infection, except third
molars as described in (7) below;
(6) Extractions of asymptomatic teeth, except
third molars as described in (7) below, subject to prior authorization in
accordance with He-W 566.07, as follows:
a. When associated with diagnosed pathology,
such as tumor, cyst, or infection; or
b. When extraction is part of an orthodontic
treatment plan that has been approved through prior authorization by the
department in accordance with He-W 566.07;
(7) Third molar extraction, subject to prior
authorization in accordance with He-W 566.07;
(8) General anesthesia when medically necessary
and documented in the recipient’s dental records;
(9) Nitrous oxide analgesia and intravenous
therapy sedation;
(10) Comprehensive orthodontic treatment for
severe handicapping malocclusion in accordance with He-W 566.05(a), subject to
prior authorization in accordance with He-W 566.07;
(11) Interceptive orthodontic treatment in
accordance with He-W 566.05(b), subject to prior authorization in accordance
with He-W 566.07;
(12) Space maintainers when medically necessary to
replace a prematurely lost deciduous or permanent molar or bicuspid;
(13) Limited orthodontic treatment in accordance
with He-W 566.05(c);
(14) Radiographs as follows:
a. Complete series or panographic
survey, once every 5 years;
b. Bitewings every 12 months if medically
necessary; and
c. All types of dental radiographs regardless of
limits in a. and b. above, as may be required to complete a differential
diagnosis;
(15) Palliative treatment when the claim is
submitted in accordance with He-W 566.10(f);
(16) Removable prosthetic replacement of permanent
teeth subject to prior authorization in accordance with He-W 566.07;
(17) Topical fluoride treatment applied twice per
year until age 21;
(18) If moderate or high risk of caries is documented,
2 applications of silver diamine per tooth, provided that no more than 18 total
silver diamine treatments shall be administered per year and no application of
silver diamine shall be administered after the recipient reaches the age of 21;
(19) Endodontia, including root canal therapy,
excluding third molars, when the claim is accompanied by a radiograph, and the
endodontia treatment is deemed complete when all radiographs demonstrate that
the canals are completely filled to the apex of the root(s) of the tooth in
accordance with He-W 566.10(e);
(20) Crowns;
(21) Periodontal treatment limited to prophylaxis,
scaling, and root planing;
(22) Surgical periodontal treatment subject to
prior authorization in accordance with He-W 566.07;
(23) Sealants for permanent and deciduous molars
every 5 years, until age 21;
(24)
Diagnostic and preventive dental
services, with the exception of orthodontic treatment as allowed in (b) below,
available for EPSDT-eligible children in accordance with He-W 546.05; and
(25) Other services determined by the department
to be medically necessary, in accordance with He-W 546.06.
(b)
Orthodontic treatment for malocclusions that do not meet the criteria
set forth in He-W 566.05(b) shall be considered for orthodontic treatment under
the EPSDT prior authorization for coverage based on medical necessity
provisions at He-W 546 when documentation of the following is submitted to the
department:
(1) Principal diagnosis;
(2) Prognosis with and without treatment;
(3) Date of onset of the illness or condition and
etiology, if known;
(4)
Clinical significance or functional impairment or pathology caused by the
illness or condition resulting from the malocclusion;
(5) Demonstration of evidence of the degree to
which the malocclusion contributes to the illness or condition;
(6)
Specific types of services to be rendered by each discipline associated with
the total treatment plan;
(7) Therapeutic goals to be achieved by each
discipline and anticipated time for achievement of goals;
(8) Explanation of any existing conditions that
are likely to limit efficacy of treatment;
(9) Extent to which health care services have
been previously provided to address the illness or condition and summary of
results demonstrated by prior care;
(10) Orthodontic records as described in He-W
566.05(g)(1), (2) and (4); and
(11)
Any additional documentation in accordance with He-W 546.06(b) or any other
documentation available which might assist in making a determination of medical
necessity of the proposed orthodontic treatment.
(c)
The documentation submitted in accordance with (b) above shall be
completed by health professionals who are sufficiently trained and duly
licensed to diagnose and treat the illness or condition arising from the
malocclusion and creating the medical necessity for treatment.
(d) The documentation described in (b) and (c)
above shall be submitted to the department by the medicaid
enrolled provider who will complete the orthodontic treatment along with a request
for prior authorization in accordance with He-W 546.06.
(e)
The following dental services shall be covered for recipients 21 years
of age or over for relief of acute pain or elimination of acute infection or
diagnosed pathology:
(1) Palliative treatment when the claim is
submitted in accordance with He-W 566.10(f);
(2) Extraction of the causative tooth or teeth
and biopsy of the tooth or teeth;
(3) Treatment of severe trauma, when a
determination is made by the attending clinician using standard medical
parameters for emergency conditions, which shall include, but not be limited
to:
a. Hemorrhage;
b. Laceration requiring suturing;
c. Abrasion requiring debridement; or
d. Bone fracture requiring reduction; and
(4) Radiographs and examinations as necessary to
assess conditions described in (1)-(3) above.
Source. (See Revision Note at chapter heading He-W
500); ss by #5639, eff 6-17-93; ss by #7012, eff 6-15-99; ss by #7912, eff
7-1-03; ss by #9902, eff 6-1-11; ss by #12782, INTERIM, eff 5-21-19, EXPIRED:
11-18-19
New. #12937, eff 12-7-19
He-W 566.05 Orthodontic Treatment.
(a)
Comprehensive orthodontic treatment shall be covered for recipients
under 21 years of age who demonstrate severe handicapping malocclusion, which
limits function and if left untreated would result in damage to the dental
structures or surrounding tissue, due to one or more of the following
conditions:
(1) Crowding of teeth greater than 12 mm in a
single arch;
(2) Deep impinging overbite with destruction of
tissue;
(3) Crossbite of anterior teeth with destruction
of tissue;
(4) Overjet greater than 9 mm;
(5) Reverse overjet greater than 3.5 mm; or
(6) Severe traumatic deviations demonstrated by
gross pathology.
(b)
Interceptive orthodontic treatment shall be covered for recipients under
21 years of age who have at least one of the following conditions:
(1) Constricted palate;
(2) Deep impinging overbite with demonstration of
destruction of tissue;
(3) Anterior crossbite; or
(4) Dentition exhibiting results of harmful
habits.
(c)
Limited orthodontic treatment shall be covered for recipients under 21
years of age, by report, and no more than once per arch per recipient per
lifetime.
(d)
Comprehensive and interceptive orthodontic treatment shall:
(1) Each be covered once per recipient per
lifetime; and
(2) Require prior authorization in accordance
with He-W 566.07.
(e) Sealants shall be present on all
permanent molars prior to the provider requesting prior authorization in (d)(2)
above.
(f)
Any dental provider who undertakes orthodontic treatment for children
with severe handicapping malocclusions shall be qualified by training and
experience in accordance with Den 302.04.
(g) In addition to the information
required at He-W 566.07, prior authorization requests for comprehensive and
interceptive orthodontic treatment shall include the following:
(1) A treatment plan, which shall address and
include the following:
a.
Diagnosis and explanation describing the nature of the severe handicapping
malocclusion or functional limitation associated with the malocclusion with
sufficient detail and documentation to support and demonstrate the existence of
conditions described in (a)-(b) above or He-W 546.05;
b.
Justification for early treatment if the request is for comprehensive treatment
and deciduous teeth are present or not all of the permanent teeth have erupted;
c. Name of the referring dentist;
d.
Description of the chief complaint expressed by the referring dentist or the recipient
or legal representative;
e. Specific treatment objectives;
f. Description of the plan for comprehensive
oral care during orthodontic treatment;
g. Signed statement from the provider attesting
that:
1.
The recipient has received an oral examination and was found to be free of
untreated oral disease;
2. The recipient demonstrates oral hygiene
habits consistent with being able to prevent inflammation and dental decay
during orthodontic treatment; and
3. Sealants are in place on all of the
recipient’s unrestored erupted molars; and
h.
Signed statement from the recipient or legal representative acknowledging the
recipient’s understanding and acceptance:
1.
Of the provider’s treatment plan including, but not limited to, the recipient’s
willingness to adhere to an oral hygiene regimen necessary to prevent
inflammation and decay, to attend any scheduled appointments, and to properly
wear and maintain the appliance;
2. Of the provider’s right to discontinue
treatment for non-compliance, including, but not limited to, the recipient’s
failure to adhere to oral hygiene expectations, missed appointments, and
failure to properly wear or maintain appliances;
3. That the Title XIX program will not pay for
the cost of orthodontic treatment beyond the recipient’s 21st birthday; and
4. That the Title XIX program will not pay for
the cost of orthodontic treatment more than once per recipient per lifetime if
treatment is terminated due to non-compliance with the treatment plan as
documented by the provider;
(2) Diagnostic model taken within 30 days of
submitting the prior authorization request;
(3) Treatment cost estimate;
(4) Except as allowed by (h) below, radiographs
that are current and of adequate quality to allow for an accurate diagnosis of
the malocclusion; and
(5) Assurance that the requested treatment is the
least restrictive, most cost-effective treatment for the malocclusion.
(h)
When requesting interceptive treatment, photographs may be submitted in
lieu of radiographs, provided the photographs clearly demonstrate the criteria
being considered for approval.
(i) Banding shall occur within 60 days of the
receipt of the prior authorization approval.
(j)
Comprehensive orthodontic treatment shall be covered only if the
recipient adheres to the treatment plan of care specified at (g)(1) above.
(k)
Treatment may be terminated by the provider for non-compliance,
including, but not limited to, the recipient’s failure to adhere to oral
hygiene expectations, missed appointments, and failure to properly wear or
maintain appliances.
(l)
Providers shall supply the department with treatment progress reports at
the following intervals:
(1) A progress
report immediately following the 12th month of treatment, including a
description of recipient compliance with the provider’s treatment plan and a
report of objectives achieved to date;
(2) A final treatment report, including
diagnostic models or post treatment photographs of the dentition in centric
relation from center, right and left sides, submitted at the conclusion of
treatment which demonstrate that the treatment goals have been met; and
(3) Immediate report of any patterns of
non-compliance, if applicable.
Source. (See Revision Note at chapter heading He-W
500); ss by #5639, eff 6-17-93; ss by #7012, eff 6-15-99; ss by #7912, eff
7-1-03; ss by #9902, eff 6-1-11; ss by #12782, INTERIM, eff 5-21-19, EXPIRES:
11-18-19
New. #12937, eff
12-7-19
He-W 566.06 Non-Covered Services. Non-covered services shall include:
(a)
A dental procedure, which is attempted but cannot be completed;
(b)
Behavior management or the administration of psychotropic medication to
modify the recipient’s behavior in the dental office;
(c)
Experimental, investigational, or cosmetic dental procedures;
(d) Dental and orthodontic treatment
or surgery for the purpose of preserving or improving appearance, except when
required for the prompt repair of accidental injury;
(e)
Services that have not been proven to be safe or effective, as
documented in dental peer review literature;
(f)
Fixed prostheses of more than one unit;
(g)
Implants and procedures associated with implants such as bone grafting;
(h)
Dental services rendered in locations other than the dental office, such
as in outpatient hospital settings or ambulatory surgical centers, when such
services could be performed in a dentist’s office and there is no medical need
for the use of an acute care, outpatient hospital, or ambulatory facility;
(i) Orthodontic treatment for recipients who have
failed to comply with a prescribed treatment plan that has been approved
through prior authorization by the department, including non-compliance with
appointments, hygiene, or care of appliances, with such failure documented by
the provider;
(j)
Periodic examinations for recipients age 21 or over;
(k)
Services that are not dental in nature;
(l)
Services that are more costly than other services but are expected to
provide the recipient with the same functional outcome;
(m)
Replacement or repair of dental appliances required as a result of
recipient neglect, wrongful disposition, intentional misuse or abuse;
(n)
Extractions of asymptomatic teeth and third molars, unless prior
authorized in accordance with He-W 566.07;
(o) Periodontal treatment consisting
of subgingival placement of biological materials or chemotherapeutic agents;
(p)
Periodontal surgery, unless prior authorized in accordance with He-W
566.07;
(q) The portion of the orthodontic treatment plan
carried out after the recipient reaches 21 years of age;
(r) Any treatment, such as
extractions, radiographs, examinations, and other services, that are ancillary
to an orthodontic treatment plan that has not been prior authorized for medicaid coverage;
(s)
Dental records, including casts and radiographs, when such records do
not meet the criteria set forth in He-W 566.05(a)-(b) above or He-W 546.05; and
(t)
Endodontics, including root canal therapy, that has not been deemed
complete in accordance with He-W 566.04(a)(18) and He-W 566.10(e).
Source. (See Revision Note at chapter heading He-W
500); ss by #5639, eff 6-17-93; ss by #7012, eff 6-15-99; ss by #7912, eff
7-1-03; ss by #9902, eff 6-1-11; ss by #12782, INTERIM, eff 5-21-19, EXPIRES:
11-18-19
New. #12937, eff 12-7-19
He-W 566.07 Prior Authorization.
(a)
The following dental services and procedures, as described in He-W
566.04, shall require prior authorization from the department:
(1) Comprehensive and interceptive orthodontic
treatment;
(2) Dental orthotic device;
(3) Surgical periodontal treatment;
(4) Extraction of asymptomatic teeth and third
molars; and
(5) Removable prosthesis.
(b)
Procedures for prior authorization shall be as follows:
(1) The prior authorization shall be for the item
or treatment requested and be obtained prior to providing the item or
treatment;
(2) Notwithstanding (1) above, for extractions
that warrant immediate action, both the prior authorization request and the
claim for payment shall be submitted to the address in (4) below after the
extraction is performed;
(3) The recipient
shall have the primary responsibility for obtaining prior authorization and may
do this with the assistance of the provider, who requests authorization on
behalf of the recipient; and
(4) Requests for dental prior authorizations
shall be addressed to:
New
Hampshire Department of Health and Human Services
Office
of Medicaid Business and Policy
Dental
Director’s Office
Attn:
Dental Consultant
129
Pleasant Street
Concord,
NH 03301
(c)
Requests for prior authorization shall include sufficient, current
medical information to enable the department to evaluate the request.
(d)
Prior authorization requests for services in (a) above, shall include:
(1)
An explanation describing the illness, special care, or specific condition, to
enable the department to understand the physical and/or emotional problem of
the recipient and the specified goal for which the item or treatment is being
requested;
(2) Assurance that the required treatment is the
least restrictive, most cost-effective alternative;
(3) Cost of the treatment, if known;
(4) Diagnosis;
(5) Expected outcome and recommended timetable of
the prescribed item or treatment;
(6) Name and address of the intended provider;
(7) Name and address of person or agency making
the request;
(8) Radiographs;
(9) Periodontal charting when surgical
periodontal treatment is requested; and
(10) Recipient name, address, date of birth, and medicaid identification number (MID).
(e) In addition to (d) above, prior
authorization requests for the extraction of third molars and asymptomatic
teeth shall also include an explanation describing the specific conditions or
illness that requires tooth removal and a radiograph supporting the rationale
for removal, and shall include the diagnosed pathology, if present, for each
tooth requested.
(f) Prior authorization requests for
comprehensive and interceptive orthodontic treatment shall include, in addition
to the information specified in (c) and (d) above, information specified in
He-W 566.05(g).
(g)
Prior authorizations shall be approved by the department upon
determination that the treatment requested is appropriate, cost effective and
supported by the documentation submitted in accordance with (b) through (f)
above.
(h)
If the department approves the prior authorization request, the state’s
fiscal agent shall send written notification of the approval to the provider.
(i) Prior authorization requests for
comprehensive and interceptive orthodontic treatment that do not have enough
information as required in accordance with He-W 566.05(g) and (c) through (f)
above for an approval or denial decision shall be returned to the provider.
(j)
All prior authorizations approved shall be provider-specific and shall
be non-transferable between providers.
(k)
Prior authorization requests for services and procedures specified in
(a)(2)-(5) above that do not have enough information as required in accordance
with (c) through (e) above for an approval or denial decision shall be returned
to the provider.
(l)
Providers shall be responsible for determining that the recipient is medicaid eligible on the date of service.
(m)
If the department denies the prior authorization request, the department
shall forward a notice of denial to the recipient and the provider on the
department’s Form 272a, “Medical Assistance Program Denial for Prior Authorized
Services,” which includes the following information:
(1) The reason for, and legal basis of, the
denial; and
(2) Information that a fair hearing on the denial
may be requested within 30 calendar days of the date on the notice of the
denial, in accordance with He-C 200.
(n) Decisions made by the department in
accordance with (g)-(i) and (k) above shall not be
superseded by the treating or consultative health care professional’s
prescription, orders, or recommendations.
Source.
(See Revision Note at chapter heading He-W 500); ss by #5639, eff
6-17-93; ss by #7012, eff 6-15-99; ss by #7912, eff 7-1-03;
ss by #9902, eff 6-1-11; amd by #10031, eff
11-19-11; ss by #12782, INTERIM, eff 5-21-19, EXPIRED: 11-18-19
New. #12937, eff
12-7-19
He-W 566.08 Utilization Review and Control.
(a)
The department’s program integrity unit shall monitor utilization of
dental services to identify, prevent, and correct potential occurrences of
fraud, waste, and abuse in accordance with 42 CFR 455, 42 CFR 456, 42 CFR 1001,
and He-W 520.
(b)
The department shall recoup state and federal medicaid
payments as permitted by 42 CFR 455, 42 CFR 447, and 42 CFR 456 for a
provider’s failure to maintain supporting records in accordance with He-W 520
and He-W 566.
Source.
(See Revision Note at chapter heading He-W 500); ss by #5639, eff
6-17-93; ss by #7012, eff 6-15-99; ss by #7912, eff 7-1-03;
ss by #9902, eff 6-1-11; ss by #12782, INTERIM, eff 5-21-19, EXPIRED: 11-18-19
New. #12937, eff 12-7-19
He-W 566.09 Third Party Liability. All third party obligations shall be
exhausted before the Title XIX program shall be billed, in accordance with 42
CFR 433.139, except that if the recipient is under age 21 and is an EPSDT
participant or has other medical insurance provided by an absent parent, the
Title XIX program shall pay the provider for the service rendered and pursue
reimbursement from the other medical insurance.
Source.
(See Revision Note at chapter heading He-W 500); ss by #5639, eff
6-17-93; ss by #7012, eff 6-15-99; ss by #7912, eff 7-1-03;
ss by #9902, eff 6-1-11; ss by #12782, INTERIM, eff 5-21-19, EXPIRESD 11-18-19
New. #12937, eff 12-7-19
He-W 566.10 Payment for Services.
(a)
Payment for dental services shall be made in accordance with rates
established by the department in accordance with RSA 161:4, VI(a).
(b)
Dental providers shall submit claims for payment to the department’s fiscal
agent.
(c)
Pursuant to He-W 566.07(b)(2), for extractions that warrant immediate
action, both the prior authorization request and the claim for payment shall be
submitted to the address in He-W 566.07(b)(4).
(d)
Dental providers shall maintain supporting records, in accordance with
He-W 520 and this part.
(e)
Payments for endodontic treatments, including root canal treatment,
shall be made only when the provider submits a radiograph that demonstrates
that the endodontic therapy was successful, effective, and complete when
completely filled to the apex of the root(s) of the tooth.
(f)
Payment for palliative treatments shall be made only when the provider
submits documentation by report that demonstrates that the treatment was
completed and the services provided were consistent with palliative treatment
as defined in He-W 566.01(n).
(g)
Payment for comprehensive orthodontic treatment shall be inclusive of,
but not limited to:
(1)
All examinations associated with the orthodontic treatment including periodic
and emergency examinations;
(2) All periodic adjustments associated with the
orthodontic treatment;
(3) All radiographs, diagnostic models, images,
and other records associated with the orthodontic treatment;
(4)
Space maintenance, when performed by the orthodontic provider within 2 years of
the banding;
(5) Appliances as applied;
(6) Application and removal of appliances;
(7) Replacement and repair of brackets, bands,
and arch wires;
(8) Retainers and follow-up examinations;
(9)
Treatment ancillary to the orthodontia, including, but not limited to,
separators and radiographs;
(10) Orthodontically related palliative treatment;
and
(11) Closing records.
(h)
Payment for interceptive orthodontic treatment shall be inclusive of,
but not limited to:
(1)
All examinations associated with the orthodontic treatment including periodic
and emergency examinations;
(2) All periodic adjustments associated with the
orthodontic treatment;
(3) All radiographs, diagnostic models, images,
and other records associated with the orthodontic treatment;
(4) Space maintenance, if applicable;
(5) Appliances as applied;
(6) Application and removal of appliances;
(7) Replacement and repair of brackets, bands,
and arch wires;
(8) Retainers and follow-up examinations, if
applicable;
(9)
Treatment ancillary to the orthodontia, including but not limited to separators
and radiographs;
(10) Orthodontically related palliative treatment;
and
(11) Closing records.
(i) Payments for comprehensive orthodontic
treatment for services prior authorized shall be made to the provider in 3
equal installments upon the department’s receipt of an orthodontic claim and as
follows:
(1) A payment shall be made following the
application of appliances;
(2) A payment shall be made following the
completion of the 12th month of treatment and the submission of a progress
report as described in He-W 566.05(l)(1); and
(3) A payment shall be made following case
completion and the submission of the final treatment report and photographs as
described in He-W 566.05(l)(2).
(j)
In the event of termination, provider payment for comprehensive
treatment shall be prorated as follows:
(1)
If the appliances have been applied and the recipient is terminated or transferred
before completing 12 months of treatment, the provider shall receive payment in
accordance with (i)(1) above plus a payment equal to
the reimbursement rate for each periodic adjustment the recipient received; and
(2)
If the recipient has completed 12 months of treatment and is terminated prior
to case completion, the provider shall receive payment in accordance with (i)(1)-(2) above plus a payment equal to the reimbursement
rate for each periodic adjustment the recipient received following the 12th
month of treatment, up to 10 adjustments.
(k)
If treatment of the recipient is transferred to another provider, the
new provider shall:
(1) Request prior authorization for treatment in
accordance with He-W 566.07; and
(2) Receive payment based on the terms of the
treatment plan that has been approved through prior authorization by the
department in accordance with He-W 566.07.
(l)
Prior to terminating orthodontic treatment of a recipient, the provider
shall remove the appliances and provide retention.
Source.
#7012, eff 6-15-99; ss by #7912, eff 7-1-03;
ss by #9902, eff 6-1-11; ss by #12782, INTERIM, eff 5-21-19, EXPIRED: 11-18-19
New. #12937, eff 12-7-19
PART He-W 567 HEARING AID SERVICES
He-W 567.01 Definitions.
(a)
“Audiogram” means a specific hearing test which charts a person’s
hearing sensitivity utilizing an audiometer or other specialized equipment,
such as:
(1) Pure tone air audiometry;
(2) Bone conduction testing;
(3) Speech audiometry, including speech reception
threshold and speech recognition; and
(4) Auditory
brainstem response (ABR) testing which includes measurements of frequency
specific thresholds.
(b)
“Department” means the New Hampshire department of health and human
services.
(c) “Hearing aid” means “hearing aid”
as defined in RSA 137-F:2, IV, namely “any wearable instrument or device
designed for or offered for the purpose of or represented as aiding or
compensating for impaired human hearing and any parts or attachments, including
ear molds, but excluding batteries and cords or accessories thereto, or
equipment, devices, and attachments used in conjunction with services provided
by a public utility company.”
(d)
“Hearing aid consultation” means discussion with an audiologist of
hearing aid options regarding degree, type, and configuration of hearing loss
to determine an appropriate make and model of hearing aid.
(e)
“Hearing aid evaluation” means real ear evaluation of the current aids
to determine if the aids are adequate to meet the recipient’s needs, or sound
field evaluation for devices that cannot be measured via real ear, such as
cochlear implants, bone anchored or bone conduction hearing aids.
(f)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(g)
“Pocket talker” means a portable, personal amplification device that is
used to amplify sound and speech or to adjust tone to enhance comprehension of
speech, including, but not limited to, a generic device or a device with the
brand name “Pocketalker”, “Riezen”,
“Listen Up”, or “Super Ear”.
(h)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(i) “Statutory
blindness” means “blindness” as defined in Sections 216(i)(1)
and 1614(a)(2) of the Social Security Act, 42 USC 416, and 42 USC 1382c.
(j)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(k) “Title XXI” means the joint
federal-state program described in Title XXI of the Social Security Act and
administered in New Hampshire by the department under the medicaid
program.
Source.
(See Revision Note at chapter heading He-W 500); ss by #6157, eff
12-29-95, EXPIRED: 12-29-03
New. #9480, eff 5-23-09, amd by
#10139, eff 7-1-12;
paras (a)-(e), (g), and (i);
EXPIRED
5-23-17; ss by #12538, eff
5-25-18
He-W 567.02 Recipient Eligibility. All medicaid
recipients shall be eligible for hearing aid services, in accordance with He-W
567.
Source.
(See Revision Note at chapter heading He-W 500); ss by #6157, eff
12-29-95, EXPIRED: 12-29-03
New. #9480, eff 5-23-09, EXPIRED: 5-23-17
New. #12538, eff 5-25-18
He-W 567.03 Provider Participation. Each participating hearing aid services
provider shall be:
(a)
One of the following:
(1) An audiologist licensed in accordance with
RSA 137-F:11 or licensed by the state in which he or she practices; or
(2) A hearing aid
dealer registered in accordance with RSA 137-F:8 or credentialed in accordance
with applicable law in the state in which he or she practices; and
(b)
A New Hampshire enrolled medicaid provider.
Source.
(See Revision Note at chapter heading He-W 500); ss by #6157, eff
12-29-95, EXPIRED: 12-29-03
New. #9480, eff 5-23-09, EXPIRED: 5-23-17
New. #12538, eff 5-25-18
He-W 567.04 Service Limits. All hearing aid services shall be subject to
the limits set forth in He-W 567 and He-W 530.03.
Source.
(See Revision Note at chapter heading He-W 500); ss by #6157, eff
12-29-95, EXPIRED: 12-29-03
New. #9480, eff 5-23-09, EXPIRED: 5-23-17
New. #12538, eff 5-25-18
He-W 567.05 Covered Services. With the exception of those items specified
in He-W 567.06, the following hearing aid services and items shall be covered:
(a)
When provided by an audiologist or hearing aid dealer:
(1) The hearing aid evaluation or a hearing aid
consultation, which shall be limited to one service every 2 years since the
last date of service for recipients age 21 or over and as needed for recipients
under age 21;
(2) The ear mold(s);
(3) The least costly hearing aid(s) or pocket talker
as determined by the audiologist or hearing aid dealer to achieve appropriate
access to speech in all of the recipient’s communication settings;
(4) The dispensing or fitting of the hearing
aid(s) or pocket talker, including real ear verification for conventional
hearing aids, adjustment, and instruction;
(5) Follow-up to
include verification of hearing aid or pocket talker performance, if not
completed at the fitting, and monitoring of hearing thresholds, as needed; and
(6) The audiogram;
(b)
Monaural hearing aids:
(1) For recipients under 21 years of age when:
a. The audiogram indicates a unilateral hearing
loss of one or more thresholds of 25 decibels (dB) hearing level (HL) or poorer
at any frequency from 1000 hertz (Hz) to 4000 Hz; and
b. The audiologist or hearing aid dispenser
deems the loss communicatively significant; and
(2) For recipients 21 years of age or over when
the audiogram indicates a bilateral hearing loss with an average threshold of
35 dBHL or poorer for 1000 Hz, 2000 Hz, 3000 Hz, and
4000 Hz by pure tone air conduction;
(c)
Binaural hearing aids:
(1) For recipients under 21 years of age when:
a. The audiogram indicates a bilateral hearing
loss of one or more thresholds of 25 dBHL or poorer
at any frequency from 1000 Hz to 4000 Hz; and
b. The audiologist or hearing aid dispenser
deems the loss communicatively significant; and
(2) For recipients 21 years of age or over, when:
a.
A prior authorization has been requested and obtained from the department in
accordance with He-W 567.07 in advance of the hearing aid(s) being rendered;
and
b. One of the following applies:
1. The coverage criteria for monaural hearing
aids per He-W 567.05(b), and one of the following criteria have been met:
(i) The recipient is
attending post-secondary school at any educational level for the purpose of
obtaining employment or is receiving vocational training, as documented in
accordance with He-W 567.08(d); or
(ii) The recipient is employed and is likely to be
determined as unable to meet the audiometric requirements of the job without
the use of binaural hearing aids, as documented in accordance with He-W
567.08(c); or
2. The recipient meets the definition of
statutory blindness per He-W 567.01(i) and as
documented in accordance with He-W 567.08(b), and an audiogram indicates a
unilateral hearing loss with an average threshold of 35 dBHL
or poorer for 1000 Hz, 2000 Hz, 3000 Hz, and 4000 Hz by pure tone air
conduction;
(d)
Hearing aid batteries for the life span of the hearing aid(s);
(e)
Replacement of hearing aids:
(1) If there is an increase in the recipient’s
hearing loss, as established by the most recent audiogram, which makes the
existing hearing aid ineffective;
(2) If an audiologist or hearing aid dealer determines
that the hearing aid can no longer be repaired, or that it is not cost
effective to do so; or
(3) If the replacement is due to loss and is
coverable under He-W 546 for recipients under age 21;
(f)
Hearing aid repairs, which shall not require:
(1) A physician referral; or
(2) An initial purchase by medicaid;
(g)
Frequency modulation (FM) systems for recipients under age 21, when a
hearing aid on its own does not meet the recipient’s personal amplification
needs, or when a traditional hearing aid is not an appropriate option, as
determined by an audiologist;
(h)
Pocket talkers, to accommodate hearing loss and enhance communications,
when:
(1) The audiogram indicates that
a recipient has a bilateral hearing loss with an average threshold of 35 dBHL or poorer
for 1000 Hz, 2000 Hz, 3000 Hz, and 4000 Hz by pure tone air conduction; and
(2) A hearing aid is not already covered by medicaid;
(i) Replacement of a pocket talker:
(1) With hearing aid(s) or a more effective
pocket talker if there is an increase in the recipient’s hearing loss, as
established by the most recent audiogram, which makes the existing pocket
talker ineffective; or
(2) Once every 5 years; and
(j) Replacement of a headset, earbuds,
or neckloop for a pocket talker once every year if an
audiologist determines that such accessories are malfunctioning.
Source. (See
Revision Note at chapter heading He-W 500); ss by #6157, eff 12-29-95, EXPIRED:
12-29-03
New. #9480, eff 5-23-09; ss by #9739, eff 6-25-10;
amd by #10342, eff 6-1-13; ss by #12538, eff 5-25-18
He-W 567.06 Non-Covered Services. Non-covered services shall include, but not
be limited to:
(a)
Replacement of hearing aids due to loss, misuse, or abuse, except as
noted in He-W 567.05(e)(3);
(b)
FM systems, if the systems are for the sole purpose of recipient use in
an educational setting and are coverable under He-M 1301;
(c)
Repair of hearing aids which are covered under a warranty;
(d)
Pocket talker repairs, batteries, accessories, except those listed in
He-W 567.05(j) above, and optional telelinks;
(e)
A pocket talker if a hearing aid is already covered by medicaid;
(f)
A hearing aid if a pocket talker is already covered by medicaid, unless the criterion in He-W 567.05(i)(1) is met; and
(g)
Binaural hearing aids for recipients 21 years of age or over when the
requirements set forth in He-W 567.05(c)(2) or He-W 567.07 have not been met.
Source.
(See Revision Note at chapter heading He-W 500); ss by #6157, eff
12-29-95, EXPIRED: 12-29-03
New. #9480, eff 5-23-09; amd
by #10342, eff 6-1-13; ss by #12538, eff 5-25-18
He-W 567.07 Prior Authorization of Binaural Hearing
Aids for Recipients 21 Years of Age or Older.
(a)
Providers shall direct requests for prior authorization, as required in
He-W 567.05(c)(2)a. above, to the department.
(b)
Requests for prior authorization shall be submitted in writing and
include, at a minimum:
(1) The recipient’s name;
(2) The recipient’s medicaid
program identification number;
(3) The recipient’s diagnosis;
(4) The provider’s medicaid
ID number;
(5) Clinical documentation that addresses how the
request for binaural hearing aids meets the criteria outlined in He-W
567.05(c)(2)b.; and
(6) The signature of the provider.
(c)
Prior authorization requested in accordance with (b) above shall be
approved by the department if the department determines that the request
demonstrates the criteria outlined in He-W 567.05(c)(2)b. have been met.
(d)
If the department approves the prior authorization request in accordance
with (c) above, the state’s fiscal agent shall send written confirmation of the
approval to the provider.
(e)
If the department denies the prior authorization request, the department
shall forward a notice of denial to the recipient and the provider on the
department’s Form 272a, “Medical Assistance Program Denial for Prior Authorized
Services,” which includes the following information:
(1) The reason for, and legal basis of, the
denial; and
(2) Information that an appeal of the denial may
be requested, in accordance with He-C 200, within 30 calendar days of the date
on the notice of the denial.
(f)
The provider shall be responsible for determining that the recipient is medicaid eligible on the date of service.
Source.
#10342, eff 6-1-13; ss by #12538, eff 5-25-18
He-W 567.08 Documentation. The hearing aid services provider shall
maintain supporting records, including:
(a)
An audiogram;
(b)
Audiological and medical data, documenting the required criteria, as
established in accordance with He-W 567, to support the request for the hearing
aid(s) or pocket talker;
(c)
For those recipients 21 years of age or over requesting binaural hearing
aids in accordance with He-W 567.05(c)(2)b.1.(ii):
(1) A statement from the recipient’s employer
verifying the recipient’s employment status, and including the employer's
audiometric requirements for the particular position in which the recipient is
employed;
(2)
A statement from the audiologist that
the recipient cannot meet the employer’s audiometric requirements in (1)
without the use of binaural hearing aids; and
(3) An audiogram which supports the audiologist's
statement in (2) above; and
(d)
A letter from the recipient’s school verifying attendance or
documentation confirming the recipient is receiving vocational training, if
applicable.
Source.
(See Revision Note at chapter heading He-W 500); ss by #6157, eff
12-29-95, EXPIRED: 12-29-03
New. #9480, eff
5-23-09; ss by #9739, eff 6-25-10; renumbered by #10342 (from He-W 567.07); ss
by #12538, eff 5-25-18
He-W 567.09 Utilization Review and Control. The department’s program integrity unit shall
monitor utilization of hearing aid services to identify, prevent, and correct
potential occurences of fraud, waste, and abuse, in
accordance with 42 CFR 455, 42 CFR 456, and He-W 520.
Source.
(See Revision Note at chapter heading He-W 500); ss by #6157, eff
12-29-95, EXPIRED: 12-29-03
New. #9480, eff 5-23-09, EXPIRED: 5-23-17;
renumbered by #10342 (from He-W 567.08); ss by #12538, eff 5-25-18
He-W 567.10 Third Party Liability. All third party obligations shall be
exhausted before medicaid shall be billed, in
accordance with 42 CFR 433.139.
Source.
(See Revision Note at chapter heading He-W 500); ss by #6157, eff
12-29-95, EXPIRED: 12-29-03
New. #9480, eff 5-23-09, EXPIRED: 5-23-17;
renumbered by #10342 (from He-W 567.09); ss by #12538, eff 5-25-18
He-W 567.11 Payment for Services.
(a)
Payment for hearing aid services shall be made in accordance with rates
established by the department in accordance with RSA 161:4, VI(a).
(b)
The hearing aid services provider shall submit claims for payment to the
department’s fiscal agent.
(c)
The hearing aid services provider shall maintain supporting records, in
accordance with He-W 520.
Source.
(See Revision Note at chapter heading He-W 500); ss by #6157, eff
12-29-95, EXPIRED: 12-29-03
New. #9480, eff 5-23-09, EXPIRED: 5-23-17;
renumbered by #10342 (from He-W 567.10); ss by #12538, eff 5-25-18
PART He-W 568 PHYSICAL THERAPY, OCCUPATIONAL THERAPY AND
SERVICES FOR INDIVIDUALS WITH SPEECH, HEARING AND LANGUAGE DISORDERS
He-W 568.01 Definitions.
(a)
“Department” means the New Hampshire department of health and human
services.
(b)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(c) “Modalities” means methods of prescribed
therapy.
(d)
“Occupational therapy (OT)” means “occupational therapy” as defined in
RSA 326-C:1, III.
(e)
“Occupational therapy assistant” means “occupational therapy assistant”
as defined in RSA 326-C:1, IV.
(f)
“Physical therapy (PT)” means the “practice of physical therapy” as defined
in RSA 328-A:2, XI.
(g)
“Physical therapy assistant” means “physical therapy assistant” as
defined in RSA 328-A:2, VIII.
(h)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(i) “Services for speech, hearing and language
disorders” means diagnostic, screening, preventive, or corrective
speech-language pathology.
(j)
“Speech-language pathology (SLP)” means “speech-language pathology” as
defined in RSA 326-F:1, IV.
(k)
“Speech-language assistant” means “speech-language assistant” as defined
in RSA 326-F:1, II-a.
(l)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(m)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(n)
“Visits” are defined as a meeting scheduled by an individual to see an
occupational therapist, physical therapist, or a speech-language pathologist
for evaluation, treatment, or advice.
Source. (See Revision Note at chapter heading He-W
500); ss by #4995, eff 11-30-90, EXPIRED: 11-30-96
New. #7909, eff 6-24-03; ss by #9929, INTERIM, eff
6-19-11, EXPIRES: 12-16-11; ss by #10042, eff 12-16-11; amd
by #10139, eff 7-1-12; ss by #13355, eff 3-19-22
He-W 568.02
Recipient
Eligibility.
All
Title XIX recipients shall be eligible for physical therapy, occupational
therapy, and services for speech, hearing and language disorders, in accordance
with He-W 568.
Source. (See Revision Note at chapter heading He-W
500); ss by #4995, eff 11-30-90, EXPIRED: 11-30-96
New. #7909, eff 6-24-03; ss by #9929, INTERIM, eff
6-19-11, EXPIRES: 12-16-11; ss by #10042, eff 12-16-11; ss by #13355, eff
3-19-22
He-W
568.03 Provider Participation.
(a)
Each participating physical therapist, occupational therapist, and
speech-language pathologist shall:
(1) Be licensed by the state in which they
practice; and
(2) Be a NH enrolled Title XIX provider.
(b) Occupational therapy
assistants, physical therapy assistants, and speech-language assistants shall
not be eligible to enroll as a Title XIX provider but may provide services to Title
XIX recipients in accordance with He-W 568.05 below.
Source. (See Revision Note at chapter heading He-W
500); ss by #4995, eff 11-30-90, EXPIRED: 11-30-96
New. #7909, eff 6-24-03; ss by #9929, INTERIM, eff
6-19-11, EXPIRES: 12-16-11; ss by #10042, eff 12-16-11; ss by #13355, eff
3-19-22
He-W 568.04 Service Limits.
(a) The service limits for
physical therapy, occupational therapy, and services for speech, hearing and
language disorders shall apply to all such services, regardless of whether
these services are provided through a hospital outpatient department, another
provider, such as a home health agency, or by the individual therapists.
(b) Physical therapy, occupational
therapy, and services for speech, hearing and language disorders shall be
limited to 20 visits per recipient per state fiscal year.
(c) The 20 visits described
in (b) above may be used for physical therapy, occupational therapy, services
for speech, hearing and language disorders, or any combination of these
services.
Source. (See Revision Note at chapter heading He-W
500); ss by #4995, eff 11-30-90, EXPIRED: 11-30-96
New. #7909, eff 6-24-03; ss by #9929, INTERIM, eff
6-19-11, EXPIRES: 12-16-11; ss by #10042, eff 12-16-11; ss by #13355, eff
3-19-22
He-W 568.05 Covered
Services.
(a) Physical therapy,
occupational therapy and services for individuals with speech, hearing and
language disorders shall be covered when prescribed, in writing, by a physician
or other licensed practitioner, for each recipient treated.
(b) Services in (a) above
shall be covered:
(1) When
performed by the physical therapist, occupational therapist, or speech-language
pathologist; or
(2) When
performed by a physical therapy assistant, an occupational therapy assistant,
or a speech-language assistant working under the direction of a physical
therapist, occupational therapist, or a speech-language pathologist, as
applicable and in accordance with applicable requirements in Phy 400, Occ 400, or Spe 600.
(c) When services are
provided in accordance with (b)(2) above, the individual responsible for the
oversight of the assistant shall, in addition to any applicable requirements
in Phy 400, Occ 400, or Spe 600:
(1) See
the recipient first to conduct the initial assessment and develop a plan of
care;
(2) See
the recipient periodically thereafter;
(3) Specify
the type of care to be provided by the physical therapy assistant, occupational
therapy assistant, or speech-language assistant;
(4) Review
the need for continued services;
(5) Assume
professional responsibility for services provided by the physical therapy
assistant, occupational therapy assistant, or speech-language assistant; and
(6) Ensure
that services provided are within the scope of the prescribed services.
(d) Hearing aid services
and related auditory devices shall be covered subject to the requirements and
limits in He-W 567.
Source. (See Revision Note at chapter heading He-W
500); ss by #4995, eff 11-30-90, EXPIRED: 11-30-96
New. #7909, eff 6-24-03; ss by #9929, INTERIM, eff
6-19-11, EXPIRES: 12-16-11; ss by #10042, eff 12-16-11; ss by #13355, eff 3-19-22
He-W 568.06 Prior Authorization.
(a)
The provider shall request prior authorization, as specified in He-W
530, for therapy services prescribed in excess of the limits described in He-W
568.04.
(b)
Providers of hearing aid services and devices shall request prior
authorization in accordance with He-W 567.
Source. (See Revision Note at chapter heading He-W
500); ss by #4995, eff 11-30-90, EXPIRED: 11-30-96
New. #7909, eff 6-24-03; ss by #9929, INTERIM, eff
6-19-11, EXPIRES: 12-16-11; ss by #10042, eff 12-16-11; ss by #13355, eff
3-19-22
He-W 568.07 Utilization
Review and Control. The department’s program integrity unit
shall monitor utilization of physical therapy, occupational therapy and
services for individuals with speech, hearing and language disorders, in
accordance with 42 CFR 455, 42 CFR 456, 42 CFR 1001, and He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #4995, eff 11-30-90, EXPIRED: 11-30-96
New. #7909, eff 6-24-03; ss by #9929, INTERIM, eff
6-19-11, EXPIRES: 12-16-11; ss by #10042, eff 12-16-11; ss by #13355, eff
3-19-22
He-W 568.08 Documentation.
(a) Therapy service described
in He-W 568.05 above shall be documented, including:
(1) The
date of
each therapy service provided;
(2) The
amount
of time spent rendering each therapy service;
(3) A description of the
therapeutic modality used during the therapy service;
(4) Measurable short-term and
long-term goals;
(5) Objectives of the therapy
service provided;
(6) Modalities to be utilized
during the therapy service;
(7) Frequency
of therapy services prescribed;
(8) An
estimation of the duration of treatment;
(9) Ongoing
progress notes evaluating the recipient’s progress in relation to the
established goals and estimated duration of treatment; and
(10) An
indication as to whether the services provided were for
individual or group therapy.
(b) The provider shall
maintain records to support claims submitted for reimbursement for a period of
at least 6 years from the date of service, or until the resolution of any legal
action(s) commenced in the 6-year period, whichever is longer.
Source. (See Revision Note at chapter heading He-W
500); ss by #4995, eff 11-30-90, EXPIRED: 11-30-96
New. #7909, eff 6-24-03; ss by #9929, INTERIM, eff
6-19-11, EXPIRES: 12-16-11; ss by #10042, eff 12-16-11;
ss by #13355, eff 3-19-22
He-W 568.09 Third Party
Liability. All third party obligations shall be exhausted before
Title XIX shall be billed in accordance with 42 CFR 433.139.
Source. (See Revision Note at chapter heading He-W
500); ss by #4995, eff 11-30-90, EXPIRED: 11-30-96
New. #7909, eff 6-24-03; ss by #9929, INTERIM, eff
6-19-11, EXPIRES: 12-16-11; ss by #10042, eff 12-16-11;
ss by #13355, eff 3-19-22
He-W 568.10 Payment for
Services.
(a) Reimbursement to
providers of physical therapy, occupational therapy and services for
individuals with speech, hearing and language disorders shall be made in
accordance with fee schedules established by the department, in accordance with
RSA 161:4, VI(a).
(b)
The provider shall bill with a therapy procedure code as defined by the
American Medicaid Association’s “Current Procedural Terminology (CPT) 2022
Professional Edition” available as noted in Appendix A, and submit claims for
payment to the department’s fiscal agent.
(c)
The provider shall maintain supporting records, in accordance with He-W
520 and He-W 568.08.
(d)
Providers shall submit claims for payment for services in accordance
with the following:
(1) Only direct treatment by a therapist or a
physical therapy assistant, occupational therapy assistant, or speech-language
assistant shall be billed, meaning the time the therapist or physical therapy
assistant, occupational therapy assistant, or speech-language assistant spends
providing direct treatment to one recipient;
(2) Therapists working as a team to treat one or
more recipients shall not each bill separately for the same or different
service provided at the same time to the same recipient; and
(3) If a recipient requires co-treatment
simultaneously by 2 therapists, visits shall be billed separately by each
provider for the total time the recipient was receiving actual therapy
services.
(e)
The time a recipient spends not being treated, for any reason, shall not
be billed.
(f)
Services provided by a physical therapy assistant, occupational therapy
assistant, or speech-language assistant, in accordance with He-W 568.05(b) and
(c) above, shall be billed by the enrolled therapist providing oversight of the
physical therapy assistant, occupational therapy assistant, or speech-language
assistant.
Source. (See Revision Note at chapter heading He-W
500); ss by #4995, eff 11-30-90, EXPIRED: 11-30-96
New. #7909, eff 6-24-03; ss by #9929, INTERIM, eff
6-19-11, EXPIRES: 12-16-11; ss by #10042, eff 12-16-11;
ss by #13355, eff 3-19-22
PART
He-W 569 RADIOLOGICAL SERVICES
He-W 569.01 Definitions.
(a)
“Current procedural terminology (CPT) code” means a unique identifying
code in the field of medical nomenclature and designed by US Department of
Health and Human Services as the national coding standard utilized in
government and private health insurance programs for reporting medical services
and procedures.
(b)
“Department” means the New Hampshire department of health and human
services, unless otherwise specified.
(c)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department, which makes medical assistance available to eligible
individuals.
(d)
“Prior authorization (PA) agent” means the individual or organization
contracted by the department responsible for approving requests for outpatient
diagnostic radiological services.
(e)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(f)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(g)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #6575, eff 9-12-97; ss by #8400, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8562,
eff 2-7-06; amd by #10139, eff 7-1-12; ss by #10517,
eff 2-7-14
He-W 569.02 Recipient Eligibility. All medicaid
recipients shall be eligible for radiological services, in accordance with He-W
569.
Source. (See Revision Note at chapter heading He-W
500); ss by #6575, eff 9-12-97; ss by #8400, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8562,
eff 2-7-06; ss by #10517, eff 2-7-14
He-W 569.03 Provider Participation. All participating radiological service
providers shall:
(a)
Be licensed by the states in which they practice;
(b)
Provide radiological services under the direction of a physician in
accordance with 42 CFR 440.30; and
(c)
Be an enrolled New Hampshire medicaid provider.
Source. (See Revision Note at chapter heading He-W
500); ss by #6575, eff 9-12-97; ss by #8400, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8562,
eff 2-7-06; ss by #10517, eff 2-7-14
He-W 569.04 Service Limits. All services shall be subject to the limits
set forth in He-W 530.
Source. (See Revision Note at chapter heading He-W
500); ss by #6575, eff 9-12-97; ss by #8400, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8562,
eff 2-7-06; ss by #10517, eff 2-7-14
He-W 569.05 Covered Services. The following radiological services shall be
covered when ordered by a physician or other licensed practitioner within the
scope of his or her practice:
(a)
Therapeutic radiological services, such as radiation therapy; and
(b)
Diagnostic radiological services in accordance with the prior
authorization requirements of He-W 569.06.
Source. (See Revision Note at chapter heading He-W
500); ss by #6575, eff 9-12-97; ss by #8400, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8562,
eff 2-7-06; ss by #10517, eff 2-7-14
He-W 569.06 Prior Authorization and Review.
(a)
The following diagnostic radiological services shall require prior
authorization:
(1) Computerized tomography (CT);
(2) Magnetic resonance imaging (MRI);
(3) Magnetic resonance angiography (MRA);
(4) Positive emission tomography (PET); and
(5) Nuclear cardiology.
(b)
Diagnostic radiological services specified in (a) above shall be exempt
from prior authorization requirements when services are provided:
(1) As part of a hospital emergency department
visit;
(2) As part of a recipient’s inpatient
hospitalization; or
(3) Concurrently with, or on the same day as, an
urgent care facility visit.
(c)
The ordering practitioner shall initiate the prior authorization process
on behalf of the recipient by submitting a completed Form 272X, Request for
Prior Authorization for Diagnostic Imaging (January 2014), and clinical
information supporting the medical necessity for the request, including, but not
limited to, the medical care plan, relevant diagnostic tests, and progress
notes, to the PA agent by mail, fax, or via the agent’s website.
(d)
When a completed prior authorization request is submitted in accordance
with (c) above, the department’s PA agent shall:
(1) Make a decision on the prior authorization
request based on Milliman Care Guidelines, 17th edition (February/March 2013),
available as noted in Appendix A;
(2) Respond to the prior authorization request by
telephone or other telecommunication device within 2 business days of the initial
request, by:
a. Approving the request if it meets the
criteria as set forth in the Milliman Care Guidelines, 17th edition
(February/March 2013), available as noted in Appendix A;
b. Suggesting an alternative imaging service
other than the one requested to better meet the clinical need based on the
clinical guidelines as set forth in the Milliman Care Guidelines, 17th edition
(February/March 2013), available as noted in Appendix A;
c. Denying the request if it does not meet the
criteria as set forth in the Milliman Care Guidelines, 17th edition
(February/March 2013), available as noted in Appendix A; or
d. Requesting more information from the provider
to better determine whether the criteria for approval have been met as set
forth in the Milliman Care Guidelines, 17th edition (February/March 2013),
available as noted in Appendix A; and
(3) Send a written notice of decision to the
recipient and the ordering practitioner within 2 business days of the decision
being made.
(e)
Written denial notices, provided in accordance with (d)(2)c. above shall
include the following:
(1) The reason for, and the legal basis of, the
denial;
(2) A copy of the clinical guidelines used to
make the decision; and
(3) Information that a fair hearing on the denial
may be requested within 30 calendar days of the date on the notice of the
denial, in accordance with He-C 200.
Source. (See Revision Note at chapter heading He-W
500); ss by #6575, eff 9-12-97; ss by #8400, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8562,
eff 2-7-06; amd by #10342, eff 6-1-13; ss by #10517,
eff 2-7-14
He-W 569.07 Utilization Review and Control. The
department’s provider integrity unit shall monitor utilization of radiological
services, to identify, prevent, and correct potential occurrences of fraud,
waste, and abuse, in accordance with 42 CFR 455, 42 CFR 456, and He-W 520.
Source.
(See Revision Note at chapter heading He-W 500); ss by #6575, eff
9-12-97; ss by #8400, INTERIM, eff 8-20-05, EXPIRES: 2-16-06; #8562, eff 2-7-06;
ss by #10517, eff 2-7-14
He-W 569.08 Third Party Liability. All third party obligations shall be
exhausted before medicaid may be billed, in
accordance with 42 CFR 433.139.
Source. (See Revision Note at chapter heading He-W
500); ss by #6575, eff 9-12-97; ss by #8400, INTERIM, eff 8-20-05, EXPIRES:
2-16-06;
#8562, eff 2-7-06; ss by #10517, eff 2-7-14
He-W 569.09 Payment for Services.
(a)
Radiological services providers shall bill utilizing the complete
radiological examination CPT code to include the following modifiers as
described below:
(1)
The radiological professional CPT code modifier, which shall include
supervision, interpretation, and written report of the radiological examination
only;
(2)
The technical CPT code modifier which shall include the taking of the
radiological examination film only; and
(3) Informational modifiers, if more than one
procedure code is billed per day.
(b)
Payments to radiological services providers shall be made in accordance
with rates established by the department pursuant to RSA 161:4, VI.
(c)
Radiological services providers shall submit claims for payment to the
department’s fiscal agent.
(d)
Radiological services providers shall maintain supporting documentation,
in accordance with He-W 520.
Source.
#8562, eff 2-7-06; ss by #10517, eff 2-7-14
PART
He-W 570 PHARMACEUTICAL SERVICES
He-W 570.01 Definitions.
(a)
“Actual acquisition cost (AAC)” means actual acquisition cost as defined
at 42 CFR 447.502, namely, the agency’s determination of the pharmacy
providers’ actual prices paid to acquire drug products marketed or sold by
specific manufacturers.
(b) “Compound drug” means a drug
product prepared by the pharmacist using more than one ingredient.
(c)
“Controlled substance” means a “controlled substance” as defined under
21 USC 802 (6).
(d) “Co-payment” means the amount paid
by a recipient to a NH medicaid enrolled pharmacy
provider for each prescription filled.
(e)
“Department” means the New Hampshire department of health and human
services.
(f)
“Dispensing fee” means a payment for the pharmacist’s service of
dispensing drugs.
(g) “Drug efficacy study
implementation (DESI) drugs” means drugs found to lack substantial evidence of
effectiveness as determined by the Food and Drug Administration (FDA) and also
includes identical, related, or similar (IRS) drugs.
(h)
“Federal upper limit (FUL)” means the maximum cost allowed by the
federal government for certain multiple source drugs.
(i) “General public” means individuals purchasing
drugs at the usual and customary retail price.
(j)
“Generic equivalent” means an equivalent AB rated drug product that is
suitable for drug interchange, approved by the FDA as safe and effective, with
the same established generic name, active ingredient, strength, quantity, and
dosage form as the drug product identified in the prescription.
(k)
“Healthcare common procedure coding system (HCPCS)” means a uniform
method for health care providers and medical suppliers to report professional
services, procedures, and supplies.
(l)
“Identical, related, or similar (IRS) drugs” means a drug interchange or
substitution as it applies to DESI drugs.
(m) “Legend drug” means a drug which
is dispensed only with a prescription from a licensed practitioner.
(n) “Licensed practitioner” means any
person who is lawfully entitled to prescribe, administer, dispense, or
distribute legend drugs to patients.
(o)
“Maintenance medication” means a drug prescribed for routine continuous
daily therapy for at least 120 days.
(p)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(q) “National average drug acquisition cost
(NADAC)” means a national price benchmark that represents the national average
invoice price derived from retail community pharmacies for drug products based
on invoices from wholesalers and manufacturers, and which is updated and
published weekly by the Centers for Medicare and Medicaid Services (CMS) and
available at https://www.medicaid.gov/medicaid/prescription-drugs/pharmacy-pricing/index.html.
(r)
“National drug code (NDC)” means the unique 11-digit code number
assigned to any drug by the manufacturer identifying drug manufacturer or
distributor, drug name, and package size.
(s)
“New Hampshire maximum allowable cost (NHMAC)” means the maximum cost
allowed by the department for certain multiple source drugs.
(t)
“Non-legend drug” means a drug prescribed by a licensed practitioner
which is normally purchased over the counter.
(u) “Non-preferred prescription drug”
means a drug that has been determined to have an alternative drug available
that is clinically equivalent and more cost effective, and which has been clinically reviewed and approved by
the NH drug use review board established in He-C 5010 and has been included on
the department’s preferred drug list as non-preferred.
(v)
“Parenteral” means drug administration other than by the mouth or
rectum, such as by injection, infusion, or implantation.
(w)
“Patient profile” means a record, whether paper or electronic, of each
recipient’s drug history.
(x)
“Pharmacist” means “pharmacist” as defined in RSA 318:1, VII.
(y)
“Pharmacy benefit manager (PBM)” means the representative designated by
the department to administer the drug plan for the medicaid
population.
(z)
“Pharmacy lock-in program” means a program established to prevent
recipients from obtaining excessive quantities of, or from inappropriately
using, prescription drugs through multiple pharmacies.
(aa)
“Preferred drug list (PDL)” means a formal published list of specific
prescription drug products by brand and generic name divided into 2
separate categories as either preferred or non-preferred.
(ab)
“Preferred prescription drug” means a drug that has been clinically
reviewed and approved by the NH drug use review board established in He-C 5010
and has been included on the department’s preferred drug list based on its
proven clinical and cost effectiveness.
(ac)
“Prescription” means “prescription” as defined in RSA 318:1, XVI.
(ad) “Primary pharmacy” means the sole
pharmacy that is responsible for dispensing and, in accordance with Ph 706,
monitoring the drug utilization of a recipient assigned to the pharmacy lock-in
program.
(ae) “Prior authorization” means the
process by which a prescriber seeks approval from the department, through its
designated agent, to make payments for drugs which are considered to have a
high potential for misuse or abuse, are high cost, or should be monitored for
correct adherence to clinical protocols.
(af) “Recipient” means any individual who is
eligible for and receiving medical assistance under the medicaid
program.
(ag)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(ah)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(ai)
“Unit dose drug” means the individually packaged dosage form of a drug.
(aj) “Usual and customary” means “usual and
customary” as defined in RSA 126-A:3 III(b).
(ak) “Wholesale
acquisition cost (WAC)” means the drug manufacturer’s list price to wholesale
distributors or direct purchasers, not including prompt pay or other discounts,
rebates, or reductions in price, as reported in wholesale price guides or other
publications of drug or biological pricing data.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93, EXPIRED: 12-1-99
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #9831, eff
12-21-10; amd by #10139, eff 7-1-12; amd by #11101, eff 5-25-16; amd
by #12140, eff 4-1-17; ss by #12529, eff 5-22-18
He-W 570.02 Recipient Eligibility. All medicaid
recipients shall be eligible for pharmaceutical services, in accordance with
He-W 570.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93, EXPIRED: 12-1-99
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #9831, eff
12-21-10; ss by #12529, eff 5-22-18
He-W 570.03 Provider Participation. Each participating pharmacy provider shall
be:
(a)
One of the following:
(1) A registered
or licensed pharmacy in the state in which the pharmacy is located; or
(2) A mail-order pharmacy registered or licensed in
a state outside New Hampshire that is registered in New Hampshire and has been
issued a permit by the NH pharmacy board pursuant to RSA 318:37, II;
(b)
A licensed practitioner authorized to dispense drugs, pursuant to RSA
318 or applicable state law in which the pharmacy is located; and
(c)
A NH enrolled medicaid provider.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93, EXPIRED: 12-1-99
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #9831, eff
12-21-10; ss by #12529, eff 5-22-18
He-W 570.04 Covered Items. With the exception of those items specified
in He-W 570.05, the following FDA approved drugs, if rated effective, and if
produced by manufacturers who are participating in the United States Department
of Health and Human Services' (USDHHS) drug rebate agreement, shall be covered
when prescribed by a licensed practitioner and subject to the prior
authorization requirements in He-W 570.06:
(a)
Legend drugs, only when prescribed as part of the course of medical
treatment for a specific illness, injury, or disease for use specified by the
FDA, or for non-experimental purposes, as supported by accepted medical
practice, and in accordance with He-W 570.08;
(b) Non-legend drugs, with the
exception of those specified in He-W 570.05, and only when prescribed as part
of the course of medical treatment for a specific illness, injury, or disease
for use specified by the FDA, or for non-experimental purposes, as supported by
accepted medical practice, and in accordance with (c) below and He-W 570.08;
(c)
Non-legend drugs, only when prescribed or dispensed as generic drugs
including:
(1) Antihistamines;
(2) Antacids
and H2-Receptor Agonists;
(3)
Analgesics, salicylates, and antipyretics;
(4)
Magnesium, iron, niacin, and calcium;
(5)
Ganglionic stimulants;
(6) Laxatives
and cathartics;
(7) Hyperglycemics;
(8) Topical
steroids;
(9) Vaginal
and topical antifungals;
(10) Topical
antimicrobials; and
(11) Lice
treatments;
(d)
Compound drugs when at least one ingredient can be identified by a rebatable NDC; and
(e)
Nutritional supplements when needed to sustain life.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93, EXPIRED: 12-1-99
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #8372, eff 8-1-05;
ss by #9586, eff 11-4-09, EXPIRED: 11-4-17
New. #12421, INTERIM, eff 11-21-17, EXPIRED:
5-20-18
New. #12529, eff 5-22-18
He-W 570.05 Non-Covered
Items. Non-covered items shall
include:
(a)
Experimental or investigational drugs not approved by the FDA;
(b)
Drugs listed by the FDA as being DESI drugs or IRS drugs;
(c)
Legend and non-legend drugs that are not part of a medical treatment for
a specific illness, injury, or disease;
(d)
Non-legend drugs when:
(1) A legend
drug effecting the same health outcome is available and:
a. Is more
clinically effective; or
b. Is
therapeutically equivalent and more cost effective; or
(2) The
non-legend drug is being used to primarily treat discomfort or to maintain
comfort, including, but not limited to:
a.
Antidiarrheals;
b. Antiflatulants;
c. Nasal
decongestants;
d. Eye and
ear preparations; and
e. Topical antipruitics;
(e)
Non-legend drugs and supplies, which are household and medicine chest
items, including, but not limited to:
(1)
Band-aids;
(2) Corn
plasters;
(3) Contact
lens products;
(4) Cough
drops and lozenges;
(5)
Mouthwash;
(6) Nursery
supplies;
(7)
Nutritional supplements when not needed to sustain life;
(8) Odor
barrier products;
(9) Personal
hygiene items;
(10)
Sunscreen;
(11) Soaps
and cleansers;
(12) Acne
products;
(13) Products
to mitigate seborrheic dermatitis; and
(14) Fluoride
preparations;
(f)
Legend and non-legend drugs used for the symptomatic relief of cough and
colds, pursuant to Section 1396r-8(d)(2)(D) of the Social Security Act;
(g)
Legend and non-legend drugs used for cosmetic purposes or hair growth,
pursuant to Section 1396r-8(d)(2)(C) of the Social Security Act;
(h)
Legend and non-legend drugs which enhance or promote fertility or
procreation, or for which the labeled use is ovulation stimulation, pursuant to
Section 1396r-8(d)(2)(B) of the Social Security Act;
(i) Legend and non-legend drugs without a
prescription from a licensed practitioner;
(j)
Legend and non-legend drugs when used for the treatment of sexual or
erectile dysfunction, unless such agents are used to treat a condition, other
than sexual or erectile dysfunction, for which the agents have been approved by
the FDA, pursuant to Section 1396r-8(d)(2)(k); and
(k)
Items which are free to the general public.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93; amd by #5874, eff
8-1-94; ss by #7392, eff 10-28-00; ss by #7680, eff 4-20-02; ss by #7712,
INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #8372, eff 8-1-05;
ss by 8628, eff 5-6-06; ss by #9831, eff 12-21-10; ss by #12529, eff 5-22-18
He-W 570.06 Prior Authorization.
(a)
Coverage of drugs subject to prior authorization shall be in accordance
with this section.
(b)
Drugs shall be subject to prior authorization based on the following:
(1) The recommendations of the NH drug use review
board made pursuant to He-C 5010.07;
(2) The abuse potential of the drug;
(3) Whether the drug is new to the market;
(4) The possibility for off-label use of the
drug;
(5) The cost of the drug; and
(6) Any other safety or efficacy concerns.
(c)
A list of drugs subject to prior authorization shall be posted on the
department’s website.
(d)
Prior authorization requests for a drug shall be approved or denied
based on the following:
(1) Diagnosis;
(2) Whether or not the drug is prescribed for on
or off label use;
(3) Dosage;
(4) The recipient’s age;
(5) The drug class; and
(6) Any other factor concerning safety, efficacy,
or individual recipient medical concerns.
(e)
The criteria in (d) above shall be posted on the department’s website.
(f)
The procedure for requesting prior authorization shall be as follows:
(1)
The licensed practitioner or their designated agent shall initiate the prior
authorization process on behalf of the recipient by contacting the PBM by
telephone or other telecommunication device;
(2) The certified pharmacy technician at the PBM
shall collect information from the requestor in (f)(1) above regarding the drug
prescribed, to determine whether the criteria for approval have been met;
(3) The certified pharmacy technician at the PBM
shall then either:
a.
Grant immediate approval when all criteria, as approved by the department, in
accordance with (d) above have been met; or
b. Transfer the request to a pharmacist at the
PBM when the information furnished does not satisfy the criteria approved by
the department in (d) above or when it cannot be determined whether the
criteria approved by the department in (d) above have been met; and
(4) If the request or caller is transferred to
the pharmacist at the PBM pursuant to (f)(3)b. above, the pharmacist shall
further discuss the recipient’s specific needs with the requestor in (f)(1)
above and either:
a.
Grant immediate approval when all criteria approved by the department in (d)
above have been met; or
b. Issue a denial in accordance with (i) below.
(g)
The PBM shall respond to prior authorization requests by telephone or
other telecommunication device within 24 hours of the initial request, in
accordance with Section 1927(d)(5) of the Social Security Act.
(h)
While the prior authorization is being considered, a 72-hour supply of
medication shall be provided to the recipient in an emergency, in accordance
with Section 1927(d)(5) of the Social Security Act.
(i) When a prior authorization request is denied,
the department shall forward a written letter of denial to the recipient and
the licensed practitioner that states the following:
(1) The drug being denied;
(2) The reason for the denial;
(3) The legal basis for the denial;
(4) Information on how the recipient can file an
appeal in accordance with He-C 200; and
(5) That a denial may be appealed by the
recipient within 30 calendar days from the date the denial was issued.
(j)
When a subsequent prior authorization request is denied for a drug for
which a prior authorization was granted in accordance with (g)(1) above, the
department shall forward a written notice of denial to the recipient and the
prescribing, licensed practitioner that states the following:
(1) The drug being denied;
(2) The reason for the denial;
(3) The legal basis for the denial;
(4) Information on how the recipient can file an
appeal in accordance with He-C 200;
(5) That a denial may be appealed by the
recipient within 30 calendar days from the date the denial was issued; and
(6) That the recipient has 10 days from the date
of the written notification to request the continuation of the original drug
for which an initial prior authorization request was granted, pending the
completion of the appeal process.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93; ss by #5875, eff 7-27-94, EXPIRED: 7-27-00
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #9586, eff 11-4-09,
EXPIRED: 11-4-17
New. #12421, INTERIM, eff 11-21-17, EXPIRED:
5-20-18
New. #12529, eff 5-22-18
He-W 570.07 Pharmacy Lock-In Program.
(a)
The department shall conduct recipient utilization reviews in accordance
with He-W 520.04 and in consideration of the recommendations of the DUR board
pursuant to He-C 5010.07(j) to determine if prescribed drugs are being utilized
at a frequency or amount that results in a demonstrated pattern of excessive or
inappropriate utilization of services.
(b)
If it is determined from the utilization review in (a) above that the
recipient utilized excessive or inappropriate pharmaceutical services, the
recipient shall be enrolled into the pharmacy lock-in program pursuant to 42
CFR 431.54(e), for a 12-month period.
(c)
Recipients shall be notified by the department in writing of their enrollment
into the pharmacy lock-in program at least 30 days prior to the effective date
of their enrollment.
(d)
The written notification to the recipient shall include:
(1) The date of their enrollment into the
pharmacy lock-in program;
(2) Instructions for the recipient to choose a
primary pharmacy, within 21 days of the date of the written notification, as
their only source for obtaining all prescribed drugs;
(3) Notification that if the recipient fails to
choose a primary pharmacy in accordance with (d)(2) above, or if the pharmacy
is unwilling or unable to be the primary pharmacy, the department shall select
a primary pharmacy for the recipient based on the recipient’s previous pharmacy
use and geographical location; and
(4) The recipient's rights to appeal pharmacy
lock-in and request a fair hearing within 30 days of the date on the written
notification, pursuant to 42 CFR 431.54(e), and in accordance with He-C 200, if
the recipient disagrees with the department’s decision.
(e)
If the primary pharmacy is selected by the recipient pursuant to (d)(2)
above, the department shall notify the primary pharmacy in writing of its
selection at least 7 business days prior to the effective date of the
recipient's enrollment into the pharmacy lock-in program.
(f)
If the primary pharmacy is selected by the department pursuant to (d)(3)
above, the department shall notify the recipient and the primary pharmacy in
writing of its selection at least 7 business days prior to the effective date
of the recipient's enrollment into the pharmacy lock-in program.
(g)
Recipients enrolled in the pharmacy lock-in program shall have the
following service restrictions:
(1) Recipients shall be identified through a
claims transaction from the PBM to the non-primary pharmacy as having a service
restriction that states “Medication Control.
Recipient Restricted to Primary Pharmacy”;
(2) Except as set forth in (g)(3) below, only the
recipient’s primary pharmacy may receive payment from the department for drugs
dispensed to a recipient with the restriction set forth in (g)(1) above; and
(3) If a pharmacy other than the primary pharmacy
determines that a recipient is unable to access his or her primary pharmacy due
to the recipient being out of area, or due to the primary pharmacy not being
open or not having the prescribed drug available, the non-primary pharmacy may
contact the PBM to request permission to dispense a 72-hour emergency supply of
a drug to a restricted recipient in accordance with 42 CFR 431.54(e)(3).
(h)
Recipients enrolled in the pharmacy lock-in program may change their
primary pharmacy only:
(1) Upon the request of the primary pharmacy;
(2) If the recipient moves; or
(3) If the primary pharmacy disenrolls from the medicaid program.
(i) If the department implements a change
pursuant to (h) above, the department shall notify the new primary pharmacy and
the recipient, in writing, of the effective date of the change.
(j)
Eligible recipients who become ineligible for medicaid
services during their 12-month pharmacy lock-in enrollment period, shall be
reinstated into the pharmacy lock-in program for the balance of the enrollment
period, lasting until the originally calculated ending date, should they again
become eligible for medicaid services prior to the
originally calculated lock-in end date.
(k)
Within the last 3 months of the
12 month lock-in period, the department shall conduct a review of the
recipient's prior 6 months of utilization of pharmaceutical services pursuant
to (a) above and in consideration of the recommendations of the DUR board
pursuant to He-C 5010.07(j), to determine whether the recipient has continued
to utilize excessive or inappropriate pharmaceutical services.
(l)
If the utilization review in (k) above no longer shows a demonstrated
pattern of excessive or inappropriate utilization of pharmacy services, the
recipient shall be released from the lock-in.
(m)
Recipients shall be notified by the department in writing of their
release from the pharmacy lock-in program within 30 days after the end date of
their lock-in.
(n)
The written notification to the recipient shall include:
(1) The date that the recipient’s lock-in ended;
and
(2) Notification that the recipient may utilize
any medicaid enrolled pharmacy.
(o)
If the utilization review in (k) above shows no improvement in the recipient’s
pattern of excessive or inappropriate utilization of pharmacy services, the
recipient shall continue to be enrolled in the lock-in program for an
additional 24 months.
(p)
Recipients shall be notified by the department in writing of of their continued enrollment into the pharmacy lock-in
program in accordance with He-W 570.07(c) and (d).
(q)
Within the last 3 months of the 24 month lock-in period, the department
shall conduct a review in accordance with (k) above.
(r) If the utilization review in (k)
above shows some improvement in the recipient’s pattern of excessive or
inappropriate utilization of pharmacy services, the recipient shall continue to
be enrolled in the lock-in program for an additional 12 months after completion
of the prior 12-month lock-in.
(s)
Recipients shall be notified by the department in writing of their
continued enrollment into the pharmacy lock-in program in accordance with He-W
570.07(c) and (d).
(t)
Within the last 3 months of the 12 month lock-in period, the department
shall conduct a review in accordance with (k) above.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93, EXPIRED: 12-1-99
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #8636, eff 5-26-06;
ss by #9586, eff 11-4-09, EXPIRED: 11-4-09
New. #12421, INTERIM, eff 11-21-17, EXPIRED: 5-20-18
New. #12529, eff 5-22-18
He-W 570.08 Prescription Drug Dispensing Limitations. The following dispensing limitations shall
apply to prescriptions drugs:
(a)
Pharmacists shall follow current standards of practice in accordance
with Ph 501.01;
(b)
Non-controlled drug prescriptions shall be refilled pursuant to Ph
704.14;
(c)
Controlled drug substances shall follow dispensing requirements pursuant
to RSA 318-B:9, IV;
(d)
Controlled drug substances shall follow refill requirements pursuant to
21 CFR 1306.22;
(e)
Refill extensions authorized by the prescribing, licensed practitioner
shall be treated as a new prescription; and
(f)
Maintenance drugs shall be dispensed in a quantity sufficient to treat
the recipient as follows:
(1) Solid
oral drugs shall be dispensed as:
a. A minimum supply of 28 days and a maximum supply
of 12 months for oral contraceptives; and
b. A minimum
supply of 30 days and a maximum supply of 90 days for solid oral drugs with the
exception of oral contraceptives, as described in (f)(1)a. above;
(2) If the
prescribing, licensed practitioner’s professional judgment indicates possession
of the minimum supply of solid oral drugs, as described in (f)(1) above, would
not be in the patient’s best medical interest, the prescribing, licensed
practitioner shall clearly indicate, on the prescription, that an exception to
the minimum supply is being made; and
(3) For
non-solid drugs, such as ointments, aerosols, injectables, and liquids, the
drug shall be dispensed in the most commonly dispensed sized container to cover
a minimum of 7 days of therapy.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93, EXPIRED: 12-1-99
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #9831, eff
12-21-10; ss by #12529, eff 5-22-18; amd by #12698,
eff 12-28-18
He-W 570.09 Certification of Prescriptions. Certification for specific brand, NHMAC, and
FUL drugs, shall conform to the following:
(a) The certification shall be in the
licensed practitioner’s own handwriting, or the pharmacist’s own handwriting if
a telephone order;
(b) The hand-written certification shall state
the term “brand necessary” or “brand medically necessary”;
(c)
The certification shall be hand-written directly on the face of the
prescription blank; and
(d)
Drugs certified as “brand necessary” or “brand medically necessary”
shall be subject to prior authorization in accordance with He-W 570.06.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93, EXPIRED: 12-1-99
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #9831, eff
12-21-10; ss by #12529, eff 5-22-18
He-W 570.10 Documentation and
Retention. The following requirements shall apply to documentation
maintained for pharmaceutical services pursuant to RSA 318:47:
(a) The pharmacy provider shall maintain
supporting records for all drugs dispensed, in accordance with He-W 520,
including specific refill orders documented at the time of original fill; and
(b) Prescription documentation and retention
shall meet the requirements of RSA 318:47-c, except that such records shall be
retained for at least 6 years.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93, EXPIRED: 12-1-99
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #9831, eff
12-21-10; ss by #12529, eff 5-22-18
He-W 570.11 Utilization Review and Control. The department’s provider integrity unit
shall monitor utilization of pharmaceutical services to identify,
prevent, and correct potential occurrences of fraud, waste, and abuse in
accordance with 42 CFR 455, 42 CFR 456, and He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93, EXPIRED: 12-1-99
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRES: 12-19-02
New. #7805, eff 12-21-02; ss by #9831, eff
12-21-10; ss by #12529, eff 5-22-18
He-W 570.12 Third Party Liability. All third party obligations shall be
exhausted before claims shall be submitted to the department’s PBM or its
fiscal agent.
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93, EXPIRED: 12-1-99
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #9831, eff
12-21-10; ss by #12529, eff 5-22-18
He-W 570.13 Prescription Co-payment. Recipients shall make co-payments to the pharmacy provider for drug
products as follows:
(a) A co-payment in the amount of $1.00 shall be
required for each preferred prescription drug and each refill of a preferred
prescription drug dispensed;
(b) A co-payment in the
amount of $2.00 shall be required for each non-preferred prescription drug and
each refill of a non-preferred prescription drug dispensed unless the
prescribing provider determines that a preferred prescription drug will be less
effective for the recipient, will have adverse effects for the recipient, or
both, in which case the co-payment shall be $1.00;
(c) A co-payment in the amount of $1.00 shall be
required for a prescription drug that is not identified as either a preferred
or non-preferred prescription drug; and
(d) Co-payments for drug products shall not be
required:
(1)
Of recipients
with income at or below 100% of the federal poverty level (FPL);
(2)
Of recipients in a nursing facility, hospital, intermediate care facility
for individuals with intellectual disabilities, or other medical institution;
(3)
Of recipients participating in the home and community based care (HCBC)
waiver programs;
(4)
Of recipients receiving services that relate to pregnancy in accordance
with 42 CFR 447.53 (b)(2), or any other medical condition that might complicate
the pregnancy;
(5)
Of recipients under the age of 18;
(6)
For family planning products;
(7)
For clozaril or clozapine prescriptions;
(8) Of women eligible through the Breast and Cervical Cancer Treatment
Program, pursuant to 42 CFR 435.213;
(9)
Of recipients receiving hospice care pursuant
to He-W 544; and
(10) Of individuals who are members of a
federally recognized Indian tribe or Alaskan natives who have ever been served through the Indian Health Services Program,
pursuant to 42 CFR 447.56(a)(x).
Source. (See Revision Note at chapter heading He-W
500); ss by #5742, eff 12-1-93, EXPIRED: 12-1-99
New. #7392, eff 10-28-00; ss by #7680, eff
4-20-02; ss by #7712, INTERIM, eff 6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #7976, eff
10-22-03; ss by #9831, eff 12-21-10; ss by #10716, eff 11-18-14; ss by #11101,
eff 5-25-16; ss by #12529, eff 5-22-18; ss by #12698, eff 12-28-18
He-W 570.14 Payment for Drugs.
(a)
Payment for drugs shall be:
(1) Made for
products whose manufacturer has a signed rebate agreement with the USDHHS, or
for single or innovator multiple-source products exempt from such agreements,
pursuant to Section 4401 of P.L. 101-508, OBRA ‘90;
(2)
Reimbursed at the lesser of the following:
a. The AAC
using NADAC files when available, plus
the dispensing fee;
b. The WAC,
when a NADAC is not available, plus the dispensing fee;
c. The usual
and customary charge to the general public;
d. The NHMAC
plus the dispensing fee; or
e. The FUL
plus the dispensing fee; and
(3) Subject
to the following conditions and restrictions:
a. The
payment for multiple source drugs, listed as having a FUL by the USDHHS, shall
be reimbursed at a rate which does not exceed the FUL plus the dispensing fee,
except as determined by the CMS of the USDHHS;
b. The
payment for multiple source drugs, listed as having a NHMAC by the department,
shall be reimbursed at a rate which does not exceed the maximum allowable cost
plus the dispensing fee;
c. The NHMAC
and FUL shall not apply when a licensed practitioner certifies on the face of
the prescription in his or her own handwriting, pursuant to He-W 570.09, that a
specific brand of drug, which is a NHMAC or FUL drug, is medically necessary
for a particular recipient;
d. The payment for any refill prescriptions for the
same recipient for solid oral maintenance drugs within a time period that does
not allow for usage of 75% of the supply of the drug shall be only for the cost
of the drug unless the reason for the exception is documented on the prescription
or the licensed practitioner’s order; and
e. The
payment for compound drugs and sterile preparations for parenteral use shall be
at the rate established by the department in accordance with RSA 161:4, VI(a).
(b)
For a unit dose drug:
(1) The unit
dose form of tablets and capsules shall be reimbursable only for medicaid recipients residing in nursing facilities and
other facilities licensed under RSA 151;
(2) Unused
portions of unit dose drugs shall be returned by the licensed facility in (b)(1)
above to the pharmacy provider when allowed in accordance with 21 CFR 1306 or
applicable state law;
(3) Unit dose
credit shall be submitted by the pharmacy provider to the department, within 90
days of such return;
(4) The
original claim shall be voided by the pharmacy provider and a new claim
submitted for the actual amount used;
(5) A
pharmacy provider shall use the manufacturer’s unit dose package or his or her
own unit dose package which meets the requirements of US pharmacopoeia
dispensing information (USPDI) unit dose packages; and
(6) Claims
for unit dose packages shall be submitted only at the end of any monthly
period.
(c)
The pharmacy provider shall submit drug claims for payment to the PBM.
(d)
The pharmacy provider shall submit medical supply and equipment claims
with NDCs for payment to the PBM.
(e)
The pharmacy provider shall submit medical supply and equipment claims
with HCPCS codes for payment to the department’s fiscal agent.
(f)
The pharmacy provider shall make available to the department the
following documents for utilization and review purposes:
(1) All
prescriptions for both medicaid recipients and non-medicaid recipients filled during the time period specified
by the department, with all identifying information blocked out;
(2) All price
lists that were in effect for such time period; and
(3) Invoices
showing the actual acquisition cost of the drugs and supplies.
Source. #7680, eff 4-20-02; ss by #7712, INTERIM, eff
6-22-02, EXPIRED: 12-19-02
New. #7805, eff 12-21-02; ss by #9831, eff
12-21-10; amd by #12140, eff 4-1-17; ss by #12529,
eff 5-22-18
PART
He-W 571 DURABLE MEDICAL EQUIPMENT,
PROSTHETIC AND ORTHOTIC DEVICES, AND MEDICAL SUPPLIES
He-W 571.01 Definitions.
(a) “Apnea of
prematurity” means that one of the following has occurred to an infant:
(1) The sudden
cessation of breathing that lasts for at least 20 seconds;
(2) The sudden cessation of breathing for any length of time,
which is accompanied by bradycardia, which means a heart rate less than 80
beats per minute;
(3) O2
desaturation, which means O2 saturation of less than 90% with
cyanosis or pallor in an infant younger than 37 weeks gestation; or
(4) The presence of
marked hypotonia.
(b) “Apparent
life-threatening event (ALTE)” means one or more of the following conditions
affecting an infant:
(1) Apnea;
(2) Change in skin
color;
(3) Marked change in
muscle tone, usually marked limpness; or
(4) Choking and
gagging.
(c) “Clean claim(s)”
means a claim that can be processed without obtaining additional information
from the dispensing provider or from a third party, including a claim with
errors originating in the state’s claims system, and not including a claim from
a dispensing provider who is under investigation for fraud or abuse or a claim
under review for medical necessity.
(d) “Date of service”
means the date that the item is delivered to or received by the recipient
except:
(1) For custom
wheelchairs, the date the custom wheelchair is ordered;
(2) For custom fabricated
prosthetic and orthotic devices, the date of fabrication;
(3) For frame and
seating systems to pediatric and adult wheelchairs, the date of the order; or
(4) For medical
supplies that are dropped shipped, the date of shipment.
(e) “Department” means
the New Hampshire department of health and human services.
(f) “Dispensing
provider” means the company or the company’s authorized representative
providing the item to the recipient.
(g) “Durable medical
equipment (DME)” means a type of item that is:
(1) Non-disposable and
able to withstand repeated use;
(2) Primarily used to
serve a medical purpose for the treatment of an acute or chronic medically
diagnosed health condition, illness, or injury; and
(3) Not useful to an
individual in the absence of an acute or chronic medically diagnosed health
condition, illness, or injury.
(h) “Item(s)” means
any DME, prosthetic devices, mobility devices, orthotic devices, or medical
supplies.
(i) “Letter of medical necessity (LMN)” means a
letter, signed by the ordering physician, physician assistant, or advanced
practice registered nurse (APRN) certifying the need for the item being
requested.
(j) “Life
sustaining” means medical
interventions that utilize mechanical or other artificial means to sustain,
restore, or supplant a vital function, which serve only or primarily to prolong
the moment of death, and where, in the judgment of the attending and consulting
physicians, as reflected in the recipient’s medical records, death is imminent
if such interventions are not utilized.
(k) “Medicaid” means
the Title XIX and Title XXI programs administered by the department, which
makes medical assistance available to eligible individuals.
(l) “Medical supplies”
means a type of consumable or disposable item appropriate for relief or
treatment of a specific medically diagnosed health condition, illness, or
injury.
(m)
“Mobility devices” means a type of item specifically designed for use by
individuals with a mobility-related injury, illness, or disability
that helps the individual walk or move from place to place, and includes manual
and power wheelchairs, strollers, scooters, walkers, gait trainers, crutches, canes, or
similar devices.
(n) “Monthly quantity”
means the amount of medical supplies allowed per month.
(o) “Orthotic devices” means a type of orthopedic
item that is applied externally to the limb or body to:
(1) Protect against
injury;
(2) Support a weak or
deformed portion of the body; or
(3) Prevent or correct
a physical deformity or malfunction.
(p) “Prosthetic
devices” means a non-dental, artificial type of replacement, corrective or
supportive device or part of a device used to:
(1) Replace a missing
portion of the body; or
(2) Replace a missing
function of the body.
(q) “Provider” means a
New Hampshire licensed ordering physician, APRN, physician assistant, or an
ordering occupational or physical therapist specializing in rehabilitation
medicine.
(r) “Recipient” means
any individual who is eligible for and receiving medical assistance under the medicaid program.
(s) “Title XIX” means
the joint federal-state program described in Title XIX of the Social Security
Act and administered in New Hampshire by the department under the medicaid program.
(t) “Title XXI” means
the joint federal-state program described in Title XXI of the Social Security
Act and administered in New Hampshire by the department under the medicaid program.
Source. (See Revision Note at chapter heading He-W
500); ss by #6158, eff 12-29-95, EXPIRED: 12-29-03
New. #8961, eff 8-20-07; amd
by, INTERIM, #8983, eff 9-21-07, EXPIRES: 3-19-08 (deletion of former paras.
(d) & (h) and renumbering remaining paragraphs);
amd by #10139, eff 7-1-12; ss by #11046, eff 2-27-16
He-W 571.02 Recipient
Eligibility.
(a) Except as
specified in (b) below, all NH medicaid recipients
shall be eligible to receive items in accordance with and subject to the
limitations set forth in this part.
(b) Medicaid recipients residing in nursing
facilities shall be eligible to receive only customized items not already
included in the nursing facility rate, which is determined in accordance with
He-E 806.
Source. (See Revision Note at chapter heading He-W
500); ss by #6158, eff 12-29-95, EXPIRED: 12-29-03
New. #8961, eff 8-20-07;
ss by #11046, eff 2-27-16
He-W 571.03 Dispensing
Provider Participation. Each
dispensing provider shall be enrolled with NH medicaid.
Source. (See Revision Note at chapter heading He-W
500); ss by #6158, eff 12-29-95, EXPIRED: 12-29-03
New. #8961, eff 8-20-07;
ss by #11046, eff 2-27-16
He-W 571.04 Covered
Services.
(a) The purchase of
medical supplies, except incontinence supplies, for continuous use or on an
as-needed basis, shall not require prior authorization and shall be covered
when prescribed, except as follows:
(1) Specialty formulas
and food products shall only be covered in accordance with (b)(3)a. and b.
below;
(2) Enteral formulas
and supplies shall only be covered in accordance with (b)(3)c. below; and
(3) Medical supplies
that are listed as non-covered services in He-W 571.06 shall not be covered.
(b) The following
items shall be covered when prescribed and supported by an LMN:
(1) The purchase of,
or repairs to, prosthetic devices, including prosthetic fingers, thumbs, and
toes when they are part of a covered prostheses except as prohibited in He-W
571.06(v);
(2) The purchase of,
or repairs to, orthotic devices;
(3) The purchase of
the following medical supplies:
a. Specialty formulas
prescribed for life-sustaining purposes;
b. Specialty formulas
and food products prescribed for metabolic diseases described in RSA 415:6-c;
c. Enteral formulas
and supplies when oral feeds are contraindicated; and
d. Disposable
incontinence products for recipients between 3 and 20 years of age;
(4) The purchase of
one standard manual breast pump per pregnancy;
(5) Bed cradle when
necessary to prevent contact with the bed covering for conditions such as
burns, decubitis, diabetic ulcers, and gout; and
(6) Except as
specified in (c)(5) below, repairs to a purchased, non-rental, wheelchair when
such repairs do not exceed a total of $800 within a given state fiscal year,
which begins July 1st and ends June 30th.
(c) Unless a requested
item is considered non-covered as specified in He-W 571.06, all items that are
not otherwise indicated as covered in (a)-(b) above, shall be covered when
prescribed, supported by an LMN, and prior authorized in accordance with He-W
571.05, and as follows:
(1) Infant home apnea
monitors shall be covered when at least one of the following criteria is met:
a. Within the past 30
days from the date the completed PA request is submitted to the department, the
infant has experienced an ALTE; and
b. The infant has one
or more of the following conditions:
1. Tracheostomy or
anatomic abnormalities of the face, tongue, jaw, or airway that make the infant
vulnerable to airway compromise;
2. Neurologic or
metabolic disorders affecting respiratory control;
3. Chronic lung disease, such as bronchopulmonary dysplasia, which
requires supplemental oxygen (O2), continuous positive airway
pressure, or mechanical ventilation;
4. Apnea of
prematurity;
5. Bradycardia on
caffeine, theophylline, or similar agents;
6. Diagnosis of
pertussis, with positive laboratory results;
7. Diagnosis of
gastroesophageal reflux disease (GERD) that results in apnea of at least 20
seconds, bradycardia, or O2 saturation; or
8. Discharged home on
a schedule of weaning narcotics;
(2) A PA approved for
an infant home apnea monitor shall be issued as follows:
a. The initial
approval shall be valid for 3 months;
b. PA requests for
additional coverage beyond the initial 3-month period shall be granted until
the infant is ALTE-free for 2 months or until the child reaches 12 months of
age, whichever comes first; and
c. PA requests for
coverage after the infant reaches 12 months of age shall be granted when
supported by physician documentation recommending the continuation of
monitoring based on the child’s condition;
(3) An external insulin
pump for the treatment of insulin-dependent diabetes (Type 1) shall be limited
to one pump per recipient every 4 years or more frequently if technology
evolves so that the pump can no longer be used, and shall be approved when the
following criteria are met:
a. The recipient has
received 3 or more daily insulin injections for at least 6 consecutive months;
b. The recipient has
self-monitored his or her own blood sugar at least 4 times per day for the past
2 consecutive months;
c. The recipient and
the recipient’s family demonstrate to the recipient’s physician or to the
recipient’s diabetic educator the ability to carbohydrate count using
insulin-to-carbohydrate ratios as well as insulin correction factors;
d. The recipient has a documented history of recurrent
hypoglycemia with wide fluctuations in blood glucose, despite recipient
compliance;
e. The recipient has
dawn phenomenon with fasting sugars frequently exceeding 200 mg/dl;
f. The recipient has a
history of severe glycemic excursions; and
g. An endocrinologist,
or a physician with similar skills and training as an endocrinologist in the
management of external insulin pumps, prescribes the pump and is involved with
the medical care of the recipient;
(4) The purchase of a
wig shall be covered with approval being subject to RSA 415:18-d;
(5) The purchase of
any wheelchair or wheelchair accessory, as well as all repairs and
modifications made to purchased wheelchairs that exceed the $800 limit set
forth in (b)(6) above, shall be covered when the following criteria are met:
a. The need for a
wheelchair, accessory, repair, or modification has been evaluated by a physical
therapist (PT) or occupational therapist (OT), in consultation with the
ordering physician;
b. The recipient has a
condition for which there is a disease process, injury, or disability:
1. That would
contraindicate weight bearing or ambulation; and
2. Where there is a
decrease in neuromuscular function that prevents the recipient from being able
to ambulate without assistance;
c. When the PA request
is for a power wheelchair, the recipient:
1. Is unable to propel
a manual wheelchair because of a disease process, injury, or disability; and
2. Is able to safely
and independently operate a power wheelchair;
d. The wheelchair is
not solely for the convenience of the recipient, or the recipient’s family or
caregivers;
e. The recipient does
not already have another mobility device that meets the recipient’s mobility
needs; and
f. When the PA request
is to replace an existing wheelchair, the following criteria are met:
1. It is not possible
to repair or modify the existing wheelchair or replacement of the existing
wheelchair is found to be the least costly alternative;
2. The current
wheelchair no longer meets the recipient’s mobility needs; and
3. The request is not
being made solely as a result of changing technology, age of the current
wheelchair, or a desire for a new wheelchair;
(6) Customized
strollers shall be covered only for recipients who:
a. Are non-ambulatory;
b. Meet the criteria
for wheelchair approval as set forth in (5) above;
c. Do not already have
a wheelchair or customized stroller, and are not expected to be prescribed a
wheelchair within 24 months; and
d. Have mobility needs
that will not be met by a commercially available stroller with adaptations;
(7) Gait trainers
shall be covered only for recipients who:
a. Are able to stand
upright with assistance and have some lower-extremity and trunk strength to be
supported in the gait trainer;
b. Are not able to
ambulate independently due to a condition such as, but not limited to,
neuromuscular or congenital disorders, including acquired skeletal abnormalities;
c. Do not have
lower-extremity contractures that would preclude ambulation, and have adequate
range of motion to support mobility;
d. Have alignment of
the lower extremities such that the foot and ankle can tolerate a standing or
upright position as well as reciprocal movement;
e. Do not have
complete paralysis of the lower extremities;
f. Have demonstrated
improved mobility, ambulation, function, or physiologic symptoms, or have
maintained status with the use of the selected gait trainer, and are able to
follow a home therapy program incorporating the use of the gait trainer, as
documented by a clinical program or home trial with the requested gait trainer;
and
g. Have a written home
therapy plan outlining the use of the requested gait trainer and for whom there
is a caretaker who can appropriately supervise use of the gait trainer;
(8) Standers shall be
covered only for recipients who:
a. Do not already have
a stander or gait trainer;
b. Are unable to stand or ambulate independently due to a
condition such as, but not limited to, a neuromuscular or congenital disorder,
including acquired skeletal abnormalities;
c. Are at high risk
for lower extremity contractures that cannot be appropriately managed by other
treatment modalities, such as stretching, active therapy, and home programs;
d. Have an alignment
of the lower extremities such that they can tolerate a standing or upright
position;
e. Do not have
complete paralysis of the lower extremities;
f. Do not have orthostatic hypotension, postural tachycardia
syndrome, osteogenesis imperfecta, osteoporosis or other brittle bone diseases,
or hip and knee flexion contractures of more than 20°;
g. Have demonstrated
improved mobility, function, and physiologic symptoms, or have maintained
status with the use of the requested stander, when other alternatives have
failed, and are able to follow a home standing program incorporating the use of
the stander, as documented by clinical standing program or home trial with the
requested stander;
h. Are unable to stand
or ambulate with caregiver assistance or an ambulatory assistive device at
sufficient duration or distance to achieve a medical benefit;
i. Have a home therapy plan outlining the use of
the requested stander; and
j. Have a request for
a stander using code E0642, and are able to self-propel the stander;
(9) Cranial remolding
helmets shall be covered when the following criteria are met:
a. The recipient is at
least 3 months of age, but not older than 18 months of age;
b. The recipient has
marked asymmetry that has not been substantially improved following
conservative therapy of at least 2 months duration with cranial repositioning
therapy and/or physical therapy; and
c. The asymmetry of
the cranial base is documented by one of the following:
1. Skull base
asymmetry of at least 6 mm right or left discrepancy, measured subnasally to the tragus, which is the cartilaginous
projection of the auricle at the front of the ear; or
2. Cranial vault
asymmetry of at least 10 mm right or left discrepancy, measured obliquely from
the supraorbital point to the parietooccipital scalp at the midpoint of maximal
convexity and from the supraorbital point to the parietooccipital scalp at the
midpoint of the flattened area, or a ratio of these 2 measurements is greater
than 1:1;
(10) A continuous
positive air pressure (CPAP) machine to treat obstructive sleep apnea (OSA) in
recipients up to the age of 21 shall be covered when all of the following
criteria are met:
a. Adenotonsillectomy
is contraindicated, delayed, or unsuccessful in relieving symptoms of OSA;
b. There is an OSA
diagnosis established by polysomnography (PSG) performed by a medicare certified sleep study center, or a children’s
hospital; and
c. The recipient is 7
years of age or older and weighs 40
pounds or more;
(11) A CPAP machine to
treat OSA in a recipient 21 years of age or older shall be covered when all of
the following criteria are met:
a. The recipient has a
diagnosis of OSA established by PSG performed by a medicare
certified sleep study center; and
b. At least one of the
following clinical criteria has been met:
1. The apnea-hypopnea
index (AHI), which assesses the severity of sleep apnea, is moderate to severe,
which is defined as 15 or more events per hour; or
2. The AHI is from 5
to 14 events per hour with documentation of symptoms of daytime sleepiness,
impaired cognition, mood disorders, or insomnia that impairs the recipient’s
ability to carry out activities of daily living, and one of the following
conditions is met:
(i) A diagnosis of hypertension, ischemic heart
disease, or a history of stroke; or
(ii) More than 20 episodes of O2
desaturation, measuring less than 85%, or any one episode of O2
desaturation, measuring less than 70%, during a full-night sleep study;
(12) A CPAP machine
covered in accordance with (10) or (11) above shall be prior authorized as
follows:
a. The initial
authorization shall be limited to a 2-month trial rental of the CPAP machine to
ensure the recipient uses the machine daily and will receive a sufficient
benefit from use of the machine;
b. The recipient’s
daily use shall be documented by a compliance report indicating that the
recipient is gaining sufficient benefit from the CPAP machine, as evidenced by
a downloaded recording from the machine showing usage of a daily minimum of 4
hours per night;
c. Following the
2-month trial period, if the recipient demonstrates daily use as described in
b. above during the 2-month trial rental period, the requesting dispensing
provider may submit a subsequent PA request, which shall include the
documentation described in b. above, for the purchase of the CPAP machine;
d. If the recipient
does not use the machine as required in b. above during the trial period, but
the non-compliance is correctable, such as by adjusting the fit of the mask,
the requesting dispensing provider may submit a subsequent PA request for an
additional rental period; and
e. Following the trial
rental period, if it is demonstrated that the CPAP machine is not providing a
sufficient benefit to the recipient, and the failure is not due to
non-compliance, abuse, or neglect, the requesting dispensing provider may
submit a PA request for a bi-level positive airway pressure (BiPAP) machine;
(13) The department
shall approve a request for a BiPAP machine when it has been determined, in
accordance with (12) above, that a CPAP machine is not effective in treating
the recipient’s OSA;
(14) A BiPAP machine
shall be covered as follows:
a. The initial
authorization shall be limited to a 2-month trial rental of the BiPAP machine
to ensure the recipient uses the machine daily and will receive a sufficient
benefit from use of the machine;
b. The recipient’s
daily use shall be documented by a compliance report indicating that the
recipient is gaining sufficient benefit from the BiPAP machine, as evidenced by
a downloaded recording from the machine showing usage of a daily minimum of 4
hours per night; and
c. Following the
2-month trial period, if the recipient demonstrates daily use during the trial
rental period as required in b. above, the requesting item provider may submit
a subsequent PA request, which shall include the documentation described in b.
above, for the purchase of the BiPAP machine;
(15) High-frequency
chest compression (HFCC) devices shall be covered when the following criteria
are met:
a. The recipient is at
least 2 years of age at the time the device is being used;
b. The recipient has a
documented need of airway clearance;
c. The recipient has
one of the following documented diagnoses:
1. Cystic fibrosis;
2. Chronic
bronchiectasis that:
(i) Is characterized by a daily productive cough
that has been confirmed by high resolution, spiral, or a standard CT scan;
(ii) Lasts for at least 6 consecutive months; or
(iii) Results in exacerbation, at least 2 times in
a one year period, that requires antibiotic therapy; or
3. Chronic
neuromuscular disorder affecting the ability to cough or clear respiratory
secretions with a prior history of pneumonia or other significant worsening of
pulmonary function, which exists when at least 2 of the following criteria are
met:
(i) Forced expiration capacity (FEC) of 80%
predicted;
(ii) Forced vital capacity (FVC) of less than 50%
predicted;
(iii) Small airway score (FEP 25-75%) decrease in
one year of 25% or more;
(iv) Pattern of annual or more
hospitalizations for acute pulmonary exacerbations; or
(v)
Demonstration of reduction of pulmonary function while on steroids for a
year;
d. The recipient’s physician provides documentation
demonstrating that standard treatments have failed to adequately mobilize
retained secretions, as indicated by one of the following:
1. Other airway
clearance therapies, including chest physical therapy or the use of a flutter
device, cannot be performed at least twice daily, or as would be appropriate
for the recipient’s age, because:
(i) There are no
available parental or partner resources to perform chest physical therapy;
(ii)
The caregiver is physically or mentally incapable of performing chest physical
therapy at the required frequency; or
(iii) There are 2 or more
individuals with cystic fibrosis, chronic bronchiectasis, or chronic
neuromuscular disorder in the same household; or
2. There is a significant deterioration of the recipient’s
clinical conditions, as described in c.3. above; and
e. The recipient is
under the care of a pulmonologist;
(16) A HFCC device
covered in accordance with (15) above shall be prior authorized as follows:
a. The initial
authorization shall be limited to a 2-month trial rental of the HFCC device to
ensure the recipient uses the device daily and will receive a sufficient
benefit from use of the device;
b. The recipient’s
daily use and sufficient benefit from usage during the 2-month trial rental
period shall be documented by:
1. A report completed
by a pulmonologist documenting the recipient’s comfort, tolerance, and
willingness to use the device;
2. A report completed
by a pulmonologist demonstrating that the recipient has sufficiently benefited
from the use of the HFCC device as evidenced by clinical indications,
including:
(i)
Improvement in forced expiratory volume (FEV1); or
(ii) A reduction in
the number of hospitalizations per year;
3. A statement signed
by the pulmonologist, which may be part of the report in 2. above, stating that
the recipient has sufficiently benefited from the use of the HFCC device, and
that the pulmonologist recommends continued usage of the HFCC device; and
4. A usage meter
report generated by the dispensing provider documenting usage at least 67% of
the prescribed time;
c. Following the
2-month trial rental period specified in a. above, the requesting dispensing
provider may submit a prior authorization request for an additional rental
period, not to exceed one year, by submitting a prior authorization request
along with documentation demonstrating the recipient’s use as described in b.
above;
d. A request for an
additional rental period or to purchase the device through a rent-to-own
arrangement, submitted in accordance with c. above, shall be approved by the
department when the clinical evidence of the recipient’s use and sufficient
benefit supports continued use of the HFCC device; and
e. Approvals shall be
limited to only one HFCC device and one vest per size per family;
(17) Oximeters shall
be covered when the recipient has been assessed by his or her physician or
pulmonary specialist to determine if supplemental O2 is required,
and either:
a. The recipient has
been on supplemental O2 and an oximeter is requested to determine if
he or she can be weaned from the supplemental O2; or
b. The recipient is
receiving supplemental O2 and is experiencing widely fluctuating O2
saturation levels and an oximeter is required to assist in determining the
cause, frequency, and duration of the fluctuation to properly determine the O2
flow rate;
(18) Disposable
incontinence supplies, including chux underpads, incontinence briefs, pull-ups, diapers, pads or
liners, and gloves and toileting wipes used for this condition, for recipients
21 years of age or older shall be covered in accordance with the following:
a. The PA shall be
approved for a period of one year if the recipient’s type of incontinence is:
1. Secondary to a
disease process or injury to the bladder, which results in irreversible loss of
control of the urinary bladder and/or rectal sphincter;
2. Secondary to an
injury to the brain or spinal cord;
3. Secondary to a
disease or condition that causes incontinence; or
4. Attributed to a
profound cognitive disability or progressive neurological disorder, such as
severe intellectual disability, dementia, or tardive dyskinesia, that results
in an inability to achieve continence through bladder training;
b. The PA shall be
approved for a period of 6-months if the recipient’s type of incontinence is:
1. Secondary to a
surgical procedure, such as prostatectomy, resulting in temporary urinary
incontinence; or
2. Secondary to an
injury to the bladder and/or urinary sphincter, including nerve injury and
detrusor muscle instability, resulting in temporary urinary incontinence; and
c. The following
quantity limits shall apply, unless the prior authorization request specifies
and medically justifies a greater quantity:
1. Disposable chux underpads shall be limited
to a total of 3 per day, up to 93 per month, except that if package sizes
necessitate dispensing a greater monthly quantity, the monthly quantity shall
not exceed 105 per month;
2. Incontinence
briefs, pull-ups, and diapers shall be limited to a total of 6 per day, up to
186 per month, except as follows:
(i) If package sizes necessitate dispensing a
monthly quantity which is greater than 186, the monthly quantity shall not
exceed 216 per month; and
(ii) The dispensing provider shall dispense the
fewest number of packages that result in a quantity as close as possible to the
186 limit without going under, for example, if a package size is 10 diapers per
package, then 19 packages equaling 190 diapers shall be dispensed, not 20 nor
21 packages; and
3. Pads and liners
used to line undergarments shall be limited to a total of 3 per day, up to 93
per month, except as follows:
(i) If package sizes necessitate dispensing a
monthly quantity which is greater than 93, the monthly quantity shall not
exceed 144 per month; and
(ii) The dispensing provider shall dispense the
fewest number of packages that result in a quantity as close as possible to the
93 limit without going under, for example, if a package size is 16 liners per
package, then 6 packages equaling 96 liners shall be dispensed, not 17, 18, nor
19 packages;
(19) Functional
electric stimulation (FES), which is used to enable a recipient with spinal
cord injury to ambulate, shall be covered when the recipient meets all of the
following:
a. Has intact lower
motor units, L1 and below, both muscle and peripheral nerve;
b. Can bear weight on upper and lower extremities to maintain
an upright posture independently;
c. Demonstrates brisk muscle contraction in response to
neuromuscular electrical stimulation through a trial use of the equipment by
the recipient’s physical therapist, and has sensory perception of electrical
stimulation sufficient for muscle contraction;
d. Is motivated and
has the cognitive ability to use such devices for walking;
e. Can transfer
independently and stand for at least 3 continuous minutes;
f. Possesses hand and
finger function to manipulate the controls;
g. Is at least
6-months post-recovery of spinal cord injury and restorative surgery;
h. Does not have hip
or knee degenerative disease and has no history of long bone fracture secondary
to osteoporosis; and
i. Has successfully completed a training
program, which consists of at least 32 physical therapy sessions with the
device over a 3-month period;
(20) Pediatric specialty
beds shall be covered for infants and children up to the age of 12, as follows:
a. The recipient has
one or more of the following diagnoses:
1. Traumatic brain
injury;
2. Moderate or severe
cerebral palsy;
3. Seizure disorder
with daily seizure activity, characterized by loss of consciousness or lack of
awareness to surroundings;
4. Pervasive
developmental disorder;
5. Psychiatric,
neurological, or metabolic diagnosis with documented risk of self-injury; or
6. Severe behavioral
disorder;
b. The recipient has
cognitive and communication impairment;
c. There is
documentation of medical necessity that includes at least one of the following:
1. Daily seizure activity
as described in a.3. above;
2. Uncontrolled
perpetual involuntary movement related to a medical diagnosis; or
3. Self-injurious
behavior, such as head banging, where a helmet was tried and was not successful
at reducing the self-injurious behavior;
d. There is evidence
of a safety risk that includes at least one of the following:
1. The recipient
demonstrates unsafe mobility that will put the recipient at risk for serious
injury, not just a possibility of injury, such as climbing out of bed;
2. The recipient has
balance problems or vertigo; or
3. The recipient has
history of injury that has occurred prior to the request;
e. There is documented
use of more cost effective alternatives for which the outcomes were
unsuccessful, such as:
1. Positional aids and
side rails with padding around the regular bed;
2. Alternative
bedding, such as moving the mattress to the floor with surrounding padding;
3. Management of
seizure disorder;
4. Pharmacotherapy;
5. Helmet for head
protection;
6. Behavioral therapy;
7. Environmental
assessment and removal of safety hazards and use of appropriate child
protective devices, such as on the door knob or use of a baby gate to prevent
the child from leaving the room; or
8. Use of portable monitoring
devices, such as a baby monitor to listen in on the child’s activities; and
f. The LMN includes
the following:
1. The recipient’s
medical, psychiatric, neurological, metabolic, and behavioral diagnosis;
2. The recipient’s
needs that are a result of the diagnosis that shows the medical need for the
specialty bed;
3. The specific name,
type, and bed model that addresses each of the recipient’s needs with specific
requirements such as full safety rails, height required for safety, or the necessity
of articulation to raise the head or feet of the child to feed, medicate, or
provide mobility;
4. Documentation as to
how the recipient’s current bed or crib or modifications to the bedroom fail to
address the clinical need and which states whether the recipient has the
capacity to climb;
5. Current and
previous treatment modalities, including an explanation why these modalities
were not successful;
6. Assessment of
cognitive function including developmental age equivalent for motor function,
cognitive function, and habilitation potential; and
7. Detailed history of
safety issues including incidence and resulting injury;
(21) Coverage of other
items that are not specifically listed elsewhere in this rule, such as those
listed below, shall be based on the National Coverage Determinations (NCD)
criteria published in the Medicare Coverage Database (MCD) at the time of the
coverage determination, as found at http://www.cms.gov/medicare-coverage-database/,
including:
a. Pressure-reducing
surfaces;
b. Enteral feeding
pumps;
c. Hospital beds and
accessories;
d. External infusion
pumps, with the exception of insulin pumps, which shall be subject to the
criteria set forth in He-W 571.04(c)(3) above;
e. Negative pressure
wound therapy pumps;
f. Pneumatic
compression devices;
g. Hoyer type lifts
and other patient lift transfer systems;
h. Transcutaneous
electrical nerve stimulators (TENS);
i. Trapeze bars;
j. Osteogenesis
stimulators;
k. Parenteral
nutrition pumps;
l. Suction machines;
m. Airway clearance
devices, such as inexsufflators;
n. Voice activated
home glucose monitors;
o. Seat lift
mechanisms that are not part of a wheelchair;
p. Continuous passive
motion machines; and
q. Oxygen compressors
and humidification devices; and
(22) For items that
are not specifically listed elsewhere in this rule and are also not listed in
the MCD, the department shall review the recipient’s medical information and
shall cover the item when the department determines that coverage of the item:
a. Is clinically appropriate in terms of type,
frequency of use, extent, site, and duration, and consistent with the
established diagnosis or treatment of the recipient’s illness, injury, disease,
or its symptoms as determined by a review of the coverage criteria set forth in
the New Hampshire or New England commercial insurance coverage as listed in
He-W 530.05(b)(32)b.;
b. Is not primarily for the convenience of the
recipient or the recipient’s family, caregiver, or health care provider;
c. Is no more costly than other items or
services that would produce equivalent diagnostic, therapeutic, or treatment
results as related to the recipients’ illness, injury, disease, or its symptoms;
d. Is not experimental, investigative, cosmetic,
or duplicative in nature; and
e. Is allowable under
Medicaid and does not otherwise conflict with the New Hampshire Medicaid State
Plan.
(d) All items billed
with any Healthcare Common Procedure Coding System (HCPCS) miscellaneous
procedure code shall be covered when prescribed, supported by an LMN, and prior
authorized in accordance with He-W 571.05, and as follows:
(1) Customized car
seats shall be covered for recipients who have a neuromotor diagnosis and whose
needs cannot be met by a commercially available car seat with minor adaptations
that do not reduce the effectiveness or safety of the car seat nor make the
manufacturer’s warranty null and void; and
(2) Protective helmets
for recipients with drop seizures or severe head-banding
disorders.
Source. (See Revision Note at chapter heading He-W
500); ss by #6158, eff 12-29-95, EXPIRED: 12-29-03
New. #8961, eff 8-20-07; amd
by #8983, INTERIM, eff 9-21-07, EXPIRES: 3-19-08 (deletion of former paragraphs
(b)-(f) and renumbering remaining paragraph (a) as (a)-(f)); amd by #9103, eff 3-12-08; ss by
#11046, eff 2-27-16
He-W 571.05 Prescription,
LMN, and Prior Authorization Requirements.
(a) The prescription
required in He-W 571.04(a)-(c) above shall be written by the provider and
include the following:
(1) The recipient’s
name, address, date of birth, and NH medicaid identification
number (MIN);
(2) The specific
monthly quantity(s) to be dispensed, not to exceed the limits set forth in this
rule;
(3) The specific type
of item(s) to be dispensed;
(4) The frequency of
use for the medical supply(s) being dispensed; and
(5) The dated
signature or electronic signature of the provider.
(b) The LMN required
in He-W 571.04(b)-(c) above shall be written by the provider and include the
following:
(1) The recipient’s
name, address, date of birth, and NH MIN;
(2) A narrative
description of the recipient’s medically diagnosed health condition, illness,
or injury, including an indication of whether the diagnosis is a pre-existing
condition or a presenting condition;
(3) The recipient’s
prognosis;
(4) An estimation of the
effect on the recipient if the requested item(s) is not provided;
(5) The medical
justification for the item(s) being requested, including its contribution to
the treatment of the recipient’s illness or injury or to the improvement of the
recipient’s physical condition;
(6) The anticipated
length of time the item(s) is expected to be needed;
(7) The expected
outcome of providing the requested item(s);
(8) The recommended
timeframe to achieve the expected outcome;
(9) A summary of any
previous treatment plans, including outcomes, which were used to treat the
diagnosed condition for which the requested item(s) is being recommended;
(10) A statement, with
supporting documentation, assuring that the requested item(s) is the least
restrictive, least costly item available
to meet the recipient’s needs;
(11) Supporting
documentation that demonstrates the medical need for the item(s); and
(12) The dated
signature, or electronic signature, of the provider.
(c) The prescription
and LMN described in (a) and (b) above shall:
(1) Not be written
retroactively; and
(2) Be valid for one
year from the date written so long as the medical treatment remains unchanged.
(d) All PA requests
shall be sent to the department for review and approval, and include the
following documentation:
(1) A copy of the
prescription, as described in (a) above;
(2) An LMN containing
all of the information specified in (b) above; and
(3) A completed PA
form specific to the item being requested, as follows:
a. For all DME, a completed Form 272D, “Durable Medical
Equipment Prior Authorization Request” form (January 2016) shall be signed and
dated by an authorized representative of the NH medicaid
enrolled dispensing provider;
b. For all disposable
incontinence supplies, a completed Form 272DIA, “Incontinence Products Prior
Authorization Request Form” (January 2016) shall be completed by an authorized
representative of the NH medicaid enrolled dispensing
provider;
c. In addition to
submitting the forms required by a. above, requests for all wheelchairs,
scooters, and customized strollers must also include a completed Form 272M,
“Mobility Evaluation Form” (January 2016), including the following:
1. A dated signature
and printed name of the provider completing the evaluation;
2. A dated signature
and printed name of the recipient or the recipient’s parent or legal guardian,
if applicable;
3. A dated signature
and printed name of an authorized representative of the NH medicaid
enrolled dispensing provider; and
4. A copy of the
manufacturer’s invoice or quote, which includes the Manufacturer’s Suggested
Retail Price (MSRP) and acquisition cost;
d. In addition to the
requirements specified in (3)c. above, PA request for the purchase of
accessories for a wheelchair shall also include the following documentation
from the ordering physician:
1. Documentation that
the ordering physician has assessed the recipient for the accessory within 60
days of making the PA request;
2. A written
diagnosis, including a brief medical history justifying the need for the
accessory; and
3. When applicable, an
estimate of the length of time the accessory will be required; and
e. In addition to
submitting the form required by a. above, requests for all standers, gait
trainers, and bath and toileting items shall also include a completed Form
272EQ, “Medical Equipment Request Evaluation Form Non-Wheelchair” (January
2016), including the following:
1. A dated signature
and printed name of the provider completing the evaluation;
2. A dated signature
and printed name of the recipient or the recipient’s parent or legal guardian,
if applicable;
3. A dated signature
and printed name of an authorized representative of the NH Medicaid enrolled
dispensing provider; and
4. A copy of the
manufacturer’s invoice or quote, which includes the MSRP and acquisition cost.
(e) A dispensing provider may complete and submit
Form 272REV “Incontinence Products Prior Authorization Revision Request Form”
(October 2015) in order to provide products which better suit a recipient’s
needs when such changes are to:
(1) Product size that
will result in a new T-code or modifier;
(2) Product absorbency
that will result in a new T-code or modifier; or
(3) Product style that
will result in a new T-code or modifier.
(f) Requests for PA shall be approved by the
department if the department determines the following:
(1) With the exception
of disposable incontinence supplies, the item meets the definition of DME,
prosthetic devices, medical supplies, or orthotic devices as defined in He-W
571.01;
(2) The medical
documentation was completed and submitted in accordance with (d) above;
(3) The PA request
demonstrates that the item is consistent with the established diagnosis or
treatment of the recipient’s illness, injury, disease, or its symptoms as
determined by a review of the coverage criteria set forth in He-W 571.04 above;
and
(4) The item is cost
effective, as determined by a finding that:
a. There is no other
less costly item, as identified by the department that would effectively meet
the recipient’s needs; or
b. Less expensive,
appropriate alternatives are not covered or generally not available.
(g) A dispensing
provider shall request and obtain prior authorization from the department
before providing the item(s).
(h) A provider shall
conduct and document a face-to-face encounter with the recipient no earlier
than 60 days prior to submitting a prior authorization request and the
provider’s written order shall include the date of the encounter and the
primary clinical reason the recipient needs the item(s).
(i) Requests for a PA
shall be denied by the department if the department determines that the
requirements set forth in (f) above have not been met.
(j) Decisions made by the department in
accordance with this section shall not be superseded by the treating, ordering,
or consultative health care provider’s prescription, orders, or
recommendations.
(k) If the department approves the PA request,
the state’s fiscal agent shall send written confirmation of the approval to the
dispensing provider.
(l) If the department denies the PA request or
partially denies it, the state’s fiscal agent shall forward a notice of denial
to the recipient and the provider, which includes the following information:
(1) The reason for,
and legal basis of, the denial or partial denial; and
(2) Information that a
fair hearing on the denial may be requested within 30 days of the date on the
notice of the denial, in accordance with He-C 200.
(m) The dispensing provider shall be responsible
for determining that the recipient is eligible for NH medicaid
on the date of service as defined in He-W 571.01(a).
Source. (See Revision Note at chapter heading He-W
500); ss by #6158, eff 12-29-95, EXPIRED: 12-29-03
New. #8961, eff 8-20-07; amd
by #8983, INTERIM, eff 9-21-07, EXPIRES: 3-19-08 (deletion of former
subparagraph (b)(6) and renumbering remaining subparagraphs);
ss by #11046, eff 2-27-16
He-W 571.06 Non-Covered
Services. The following items shall
not be covered:
(a) Items that do not meet the coverage criteria
set forth in He-W 571.04;
(b) Specialty formulas when not needed for
life-sustaining purposes, or as the sole source of nutrition, except as allowed
under He-W 546;
(c) Common, over-the-counter, household and
medicine-chest items that can be purchased without a prescription, including,
but not limited to:
(1) Corn plasters and
foot pads;
(2) Nursery supplies;
(3) Hand cleaners or
sanitizers, such as Hygenall or Purell;
(4) Personal hygiene
items including body lotions, toothbrushes, electric shavers, razors, and other
hair removal devices and services;
(5) Thermometers;
(6) Odor barrier
products;
(7) Toileting wipes,
except as allowed by He-W 571.04(c)(18) above;
(8) First aid kits and
supplies, including adhesive bandages and scissors;
(9) Mechanical heated
water circulating pads and pumps, including hydrocollator heating units;
(10) Non-legend
medications specified in accordance with He-W 570.05(d); and
(11) Nutritional
supplements or formula as follows:
a. Dietary or food
supplements;
b. Lactose-free foods
or products that aid in lactose digestion;
c. Gluten-free
products;
d. Low carbohydrate
diets;
e. Weight-loss foods,
formulas, and related products intended to aid in weight loss;
f. Normal grocery
items, including over-the counter infant formulas;
g. Baby food and
banked breast milk;
h. Grocery items that
can be prepared in a blender and used with an enteral feeding system;
i. High protein powders and mixes;
j. Medical food
products that:
1. Are prescribed
without a diagnosis requiring such foods;
2. Used for
convenience purposes;
3. Have no proven
therapeutic benefit without an underlying disease, condition, or disorder;
4. Used as a
substitute for acceptable standard dietary interventions; or
5. Are used
exclusively for nutritional supplementation; and
k. Enteral nutrition
when the recipient has food allergies or dental problems, but has the ability
to meet his or her nutritional requirements through an alternative store-bought
food source;
(d) Environmental modifications and controls,
including:
(1) Wheelchair ramps;
(2) Tub rails;
(3) Space heaters and
heat lamps;
(4) Air conditioners
and fans;
(5) Air purifiers,
including HEPA and vacuum filters;
(6) Vaporizers,
humidifiers, and dehumidifiers;
(7) Aromatherapy;
(8) Stairway lifts and
elevators;
(9) Lifting devices
including electric patient lifts and hydraulics and ceiling tract lifting
devices;
(10) Power generators;
and
(11) Adaptive or
computer switch toys;
(e) Items typically not used by the general
public for a medical purpose, including:
(1) Furniture for
non-mobility purposes including, but not limited to:
a. Corner seats;
b. Positioning chairs;
c. High chairs or
other feeding type chairs;
d. All beds, except
hospital beds as allowed by He-W 571.04(c)(20)c., and the pediatric specialty
beds as allowed in He-W 571.04(c)(20) above;
e. Toddler beds,
bassinets, portable cribs, or playpens; and
f. Massage and therapy
tables and related equipment;
(2) Lumbar support
cushions;
(3) Bedding, including
electric or weighted blankets;
(4) Clothing items,
including sportswear such as neoprene shorts;
(5) Hot Tubs,
whirlpool equipment, aqua massagers, and sauna baths;
(6) Recreational, therapeutic, or exercise equipment
including, but not limited to, bicycles, treadmills, weights, tables, mats, and
swings; and
(7) Video, computer
games, or computer applications intended for the purpose of exercise,
recreation, education, or instruction;
(f) Items that contribute to or enhance fertility
or procreation;
(g) Items typically used by the general public
for preventing injury or ensuring safety, including:
(1) Car seats, except
as allowed by He-W 571.04(d)(1);
(2) Helmets, including
protective helmets used for sports and recreation, except as allowed by He-W
571.04(d)(2); and
(3) Pneumatic vests
and lumbar supports;
(h) Disposable incontinence supplies for:
(1) Recipients younger
than 3 years of age, except as allowed by He-W 546; and
(2) Recipients 21 years of age or older who do not meet the
criteria set forth in He-W 571.04(c)(18);
(i) Bed wetting
alarms;
(j) Sleep positioning wraps;
(k) Computer controlled and programmable lateral
rotation therapy bed systems;
(l) Chewelry, and
similar non-toxic jewelry, intended to be chewed;
(m)
Magnets, crystals, gemstones, and similar non-evidenced based, experimental, or
investigational healing items;
(n) Glucowatches;
(o) Auto-feeders;
(p) Automated medication reminder systems;
(q) Cast bags, such as Aquashield;
(r) Electric resuscitators and portable
defibrillators;
(s) Bi-directional static progressive stretch
devices, including, but not limited to, Joint Active Systems (JAS) splints;
(t) Service or therapy animals and related
expenses;
(u) Apnea monitors, except when the criteria in
He-W 571.04(c)(2) have been met;
(v) Prosthetic fingers, thumbs, and toes when not
part of a covered prosthesis;
(w) Commercially available strollers;
(x) Wheelchairs requested within 24 months of the
purchase of a customized stroller;
(y) The following accessories and options for
wheelchairs, customized strollers, or other mobility devices:
(1) Wheelchair remote
controls and attendant control switches;
(2) Power assist
devices or equipment to modify a manual wheelchair into a power wheelchair;
(3) Air suspension
systems;
(4) Power standers and
seat lift mechanisms;
(5) Grade aids and
anti-roll devices for manual wheelchairs;
(6) Wheelchairs with
stair climbing options;
(7) Titanium framed
and sport-type wheelchairs;
(8) Custom wheels for
off-road use or for sport and recreational purposes;
(9) Any wheelchair
accessory or option for purposes of allowing the recipient to perform leisure,
social, or recreational activities;
(10) Lights, horns,
mirror, baskets, pouches, backpacks, and similar accessories; and
(11) Back-up or spare
wheelchairs for recipients who already have a wheelchair, power scooter, or
customized stroller;
(z) Any back-up or spare equipment, with the
exception of ventilators;
(aa) Replacement, repair, or modifications of an
item when the need for which is the result of:
(1) Recipient abuse,
misuse, or neglect;
(2) Failure to protect
the item from the elements;
(3) Using the item
inappropriately or contrary to its designed and intended use;
(4) Making improper
repairs to the item, which would void any manufacturer’s warranty;
(5) Loss of the item
when basic safeguarding measures could have been instituted;
(6) Failure to
maintain the item through proper routine maintenance by an authorized dealer;
or
(7) Taking any action
that would otherwise void the manufacturer’s written warranty or is contrary to
the manufacturer’s recommendations for care, use, and maintenance;
(ab) Repairs, modifications, or adjustments to any
rented item, including wheelchairs;
(ac) Repairs to recipient owned items, when the
recipient does not meet the criteria for coverage of the item, or when such
repairs, modifications, or adjustments are:
(1) Within the
dispensing provider’s or manufacturer’s warranty; or
(2) Within one year of
the purchase of the item or accessory, unless written documentation from the
provider demonstrates a significant change in the recipient’s medical condition
that meets the coverage criteria for the item and the repair or modification is
warranted;
(ad) Upgrades to or replacement of any functioning
item that still meets the recipient’s needs, but is being requested solely as a
result of changing technology;
(ae) Items which are more costly than other
available items which could be expected to provide the same, similar, or
duplicate outcome;
(af) Any items that
are primarily intended for use at a school, are part of a child’s care plan at
school, and could be obtained through the “Medicaid to Schools” program in
accordance with He-M 1301, and the child and the child’s school participate in
the “Medicaid to Schools” program; and
(ag) Any items that are experimental,
investigational, or non-FDA approved.
Source. (See Revision Note at chapter heading He-W 500);
ss by #6158, eff 12-29-95, EXPIRED: 12-29-03
New. #8961, eff 8-20-07; amd
by #8983, INTERIM, eff 9-21-07, EXPIRES: 3-19-08; amd
by #9103, eff 3-12-08; amd by #9637, eff 1-16-10; amd by #9836, eff 12-18-10; ss by
#11046, eff 2-27-16 (from He-W 571.05)
He-W 571.07
Requirements for Maintaining Documentation.
(a) The dispensing provider shall maintain
supporting records in accordance with He-W 520 and this part, and failure to
maintain records in accordance with He-W 520 and this part shall entitle the
department to recoupment of state or federal medicaid
payments made as permitted by 42 CFR 455, 42 CFR 447, and 42 CFR 456.
(b) In addition to the requirement set forth in
(a) above, the dispensing provider shall maintain the following documentation for
a minimum of 6 years or until the resolution of any legal action(s) commenced
within the 6 year period, whichever is longer:
(1) All letters of
medical necessity (LMN) described in He-W 571.05(b);
(2) Documentation of
adjustments made to and inspections of items or related accessories;
(3) Documentation showing:
a. The date and proof
of delivery of all items to the recipient;
b. For custom
wheelchairs and customized strollers, the date of the order;
c. For custom
prosthetic and orthotic devices, the date of fabrication;
d. For frame and
seating systems to pediatric and adult wheelchairs, the date of order; and
e. For medical
supplies shipped, the date of shipment;
(4) Documentation of a
face-to-face encounter between the recipient and the recipient’s provider no
earlier than 60 days of the PA request as described in He-W 571.05(h) above;
and
(5) All other
supporting documentation needed to justify monthly quantity(s) and type of
item(s) dispensed.
Source. (See Revision Note at chapter heading He-W
500); ss by #6158, eff 12-29-95, EXPIRED: 12-29-03
New. #8961, eff 8-20-07; amd
by #9103, eff 3-12-08; amd by #9637, eff 1-16-10; amd by #10031, eff 11-19-11; ss by
#11046, eff 2-27-16
He-W 571.08 Third Party Liability.
(a) All third party obligations shall be
exhausted before medicaid shall be billed, in
accordance with 42 CFR 433.
(b) Dispensing providers shall request
information from the recipient regarding other insurance coverage.
(c) If other insurance coverage is available,
dispensing providers shall contact the insurer to verify benefits initially and
at least annually thereafter or when the insurance carrier changes.
(d) Dispensing providers shall maintain a record
of any other insurance verifications in the recipient’s medical record.
Source. (See Revision Note at chapter heading He-W
500); ss by #6158, eff 12-29-95, EXPIRED: 12-29-03
New. #8961, eff 8-20-07;
ss by #11046, eff 2-27-16 (from He-W 571.09)
He-W 571.09 Utilization Review and Control. The department’s provider program integrity
unit shall monitor utilization of items to identify, prevent, and correct
potential occurrences of fraud, waste, and abuse, in accordance with 42 CFR
455, 42 CFR 456, and He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #6158, eff 12-29-95, EXPIRED: 12-29-03
New. #8961, eff 8-20-07; ss by #11046, eff 2-27-16
(from He-W 571.10)
He-W 571.10 Payment for Items.
(a) The department shall establish rates for all
items in accordance with RSA 161:4, VI(a).
(b) All dispensing providers shall submit clean
claim(s) as defined in He-W 571.01(c).
(c) All dispensing providers shall submit clean
claims for payment to the department’s fiscal agent, and the department shall
be entitled to recoupment of state and federal medicaid
payments as permitted in 42 CFR 455, 42
CFR 456, and 42 CFR 447.
(d) All dispensing providers shall maintain
supporting records supporting submitted claims in accordance with He-W 520 and
He-W 571.07.
(e) Payment shall not be made for items that require
prior authorization when prior authorization was not received and approved
before the items were provided, in accordance with He-W 571.05. Retroactive
prior authorization requests shall be denied.
(f) Payment for disposable incontinence supplies,
including gloves and toileting wipes used for this condition, provided to
recipients shall be made only for supplies obtained from the exclusive supplier
of incontinence supplies contracted through the department.
(g) Billing of and payment for items and repair
parts shall be made at the lesser of:
(1) The dispensing
provider’s usual and customary charge to the public, as defined in RSA 126-A:3,
III(b);
(2) The lowest amount
the dispensing provider accepts from any other third party payor; or
(3) The rate
established by the department in accordance with RSA 161:4, VI(a).
(h) Payment for labor costs for repairs shall be
at a rate established by the department in accordance with RSA 161:4, VI(a).
(i) Payment shall be
denied or recouped if the dispensing provider bills for and is paid for
disposable incontinence supplies, including gloves and toileting wipes used for
such condition, which are not obtained from the exclusive supplier of
incontinence supplies contracted through the department.
(j) Except as allowed by (k) below, payment shall
be denied if the recipient is not eligible on the date of service, even when a
prior authorization request has been approved.
(k) For the following items only, payment shall
be denied if the recipient is not medicaid eligible
on the date of service as defined in He-W 571.01(a).
(l) No item shall be paid for prior to delivery
to the recipient and dispensing providers shall maintain documentation in
accordance with He-W 571.07 and 571.10 which demonstrates that the items were
delivered to the recipient.
(m) No payment shall be made for items left
unattended which results in the item(s) destruction or damage to the item so
that it is unusable.
(n) In accordance with the payment rates
established in (a) above, the rate for wheelchairs shall include the following
required services:
(1) Delivery and
assembly of the wheelchair;
(2) Training to the
recipient and recipient’s family and other caregiver(s) in the use of the
equipment, maintenance care, and equipment diagnostics; and
(3) Wheelchair
adjustments and any follow-up training within 30 days following the delivery of
the chair.
(o) Dispensing providers shall supply a
comparable substitute wheelchair at no additional cost for 2 weeks during the
repair of the original wheelchair. For
repairs that require more than 2 weeks to complete, the dispensing provider may
request PA for a rental fee.
Source. (See Revision Note at chapter heading He-W
500); ss by #6158, eff 12-29-95, EXPIRED: 12-29-03
New. #8961, eff 8-20-07;
ss by #11046, eff 2-27-16 (formerly He-W 571.11)
PART He-W 572
AMBULANCE SERVICES
He-W 572.01 Definitions.
(a) “Acute care hospital” means a hospital that
provides short-term medical treatment for patients who have an acute illness or
injury, or who are recovering from surgery.
(b) “Advanced life support (ALS) services” means
“advanced life support (ALS)” as defined by Saf-C
5901.04, namely, “medical
procedures and the scope of practice rendered by advanced emergency medical
care providers in accordance with RSA 153-A:12.”
(c) “Air ambulance” means a fixed-wing or
rotary-wing aircraft that is certified by the Federal Aviation Administration
as an air ambulance and which is designed and equipped for the provision of
medically necessary supplies and services.
(d) “Ambulance” means any vehicle designed,
equipped, and used for the transport of sick or injured individuals and which
are licensed to do so in the state in which they operate.
(e) “Basic life support (BLS) services” means “basic
life support (BLS)” as defined by Saf-C 5901.09,
namely, “fundamental medical procedures and the scope of practice in which
emergency medical care providers at the first responder or emergency medical
technician-basic levels are trained.”
(f) “Department” means the New Hampshire
department of health and human services.
(g) “Emergency medical condition” means:
(1) A medical condition manifesting itself by
acute symptoms of sufficient severity, including severe pain, such that a
prudent layperson, with an average knowledge of health and medicine, could
reasonably expect the absence of immediate medical attention to result in:
a. Placing the health of the recipient, or, with
respect to a pregnant woman, the health of the woman or her unborn child, in
serious jeopardy;
b. Serious impairment to bodily functions; or
c. Serious dysfunction of any bodily organ or
part; or
(2) With respect to a pregnant woman who is
having contractions:
a. That there is inadequate time to effect a
safe transfer to another hospital before delivery; or
b. That transfer may pose a threat to the health
or safety of the woman or unborn child.
(h) “Medicaid” means the Title XIX and Title XXI
programs administered by the department which makes medical assistance available
to eligible individuals.
(i) “Prior
authorization agent” means an individual or agency contracted by the department
responsible for reviewing all scheduled and routine ambulance transportation
requests.
(j) “Recipient” means an individual who is eligible
for and receiving medical assistance under the medicaid
program.
(k) “Scheduled and routine ambulance
transportation” means transportation by an ambulance for the purpose of
attending an appointment to obtain a medicaid covered
service from a medicaid enrolled provider when the
use of any other mode of transportation would likely endanger the health and
safety of the recipient and when the medicaid covered
service is not to treat an emergency medical condition as defined in (g) above.
(l) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(m)
“Title XXI” means the joint
federal-state program described in Title XXI of the Social Security Act and
administered in New Hampshire by the department under the medicaid
program.
Source. (See Revision Note at chapter heading He-W
500); ss by #6641, eff 11-27-97; EXPIRED: 11-27-05
New. #8502, INTERIM, eff 12-2-05, EXPIRES:
5-31-06; ss by #8638, eff 5-30-06; amd by #10139, eff
7-1-12; ss by #10294, eff 12-1-13
He-W
572.02 Recipient Eligibility. All recipients shall be eligible for
ambulance services, in accordance with He-W 572.
Source. (See Revision Note at chapter heading He-W
500); ss by #6641, eff 11-27-97; EXPIRED: 11-27-05
New. #8502, INTERIM, eff 12-2-05, EXPIRES: 5-31-06;
ss by #8638, eff 5-30-06; ss by #10294, eff 12-1-13
He-W
572.03 Provider Participation. All participating ambulance providers shall:
(a) Be licensed in the state in which they
operate; and
(b) Be an enrolled New Hampshire medicaid provider.
Source. (See Revision Note at chapter heading He-W
500); ss by #6641, eff 11-27-97; EXPIRED: 11-27-05
New. #8502, INTERIM, eff 12-2-05, EXPIRES: 5-31-06;
ss by #8638, eff 5-30-06; ss by #10294, eff 12-1-13
He-W
572.04 Covered Services.
(a) The following ambulance services, in the case
of an emergency medical condition, shall be covered:
(1) Transportation to the nearest acute care
hospital with appropriate treatment facilities, including loaded mileage and
routine disposable supplies used en-route;
(2) Transportation from one acute care hospital
to another acute care hospital when the necessary treatment or diagnostic
testing cannot be provided by the originating hospital and the recipient is
discharged from the originating hospital; and
(3) Waiting time for transportation as follows:
a. Prior to transporting the recipient while the
recipient is being stabilized; and
b. Up to a maximum of 2 hours, rounded to the
nearest half-hour.
(b) Air ambulance services, in the case of an
emergency medical condition, shall be covered if the recipient’s condition is
such that:
(1) The recipient
cannot be safely transported in a timely basis via an ALS ground transportation
with appropriate staff; and
(2) The recipient is
at imminent risk of losing life or limb if the fastest means of transport is
not utilized to move the recipient to the nearest facility capable of treating
the recipient.
(c) Scheduled and routine ambulance
transportation, as defined in He-W 572.01(k), to and from the destination,
including loaded mileage and routine disposable supplies used en-route, shall be covered when the service is authorized
in accordance with He-W 572.06.
(d) Waiting time for scheduled and routine
ambulance transportation authorized pursuant to He-W 572.06 shall be covered up
to a maximum of 2 hours, rounded to the nearest half hour.
Source. (See Revision Note at chapter heading He-W
500); ss by #6641, eff 11-27-97; EXPIRED: 11-27-05
New. #8502, INTERIM, eff 12-2-05, EXPIRES: 5-31-06;
ss by #8638, eff 5-30-06; ss by #10294, eff 12-1-13; ss by #10294, eff 12-1-13
He-W
572.05 Non-Covered Services. Non-covered ambulance services shall include:
(a) Transportation for a recipient whose
condition permits transport in any type of vehicle other than an ambulance,
such as a private vehicle or a wheelchair van, without endangering the
recipient’s health;
(b) Transportation in an ambulance which is not:
(1) Scheduled and
routine ambulance transportation, as defined in He-W 572.01(k); or
(2) For an emergency
medical condition, as defined in He-W 572.01(g);
(c) Transportation by ambulance only for the
recipient’s or his or her family’s convenience;
(d) Transportation to and from medical providers,
unless authorized in accordance with He-W 572.06;
(e) Transportation from one acute care hospital
to another acute care hospital for necessary treatment or diagnostic testing
while the recipient maintains inpatient status with the originating hospital;
(f) Waiting time, as follows:
(1) Waiting time that exceeds 2 hours; and
(2) Waiting time for transportation in the case
of an emergency medical condition when the wait is not due to the recipient
needing to be stabilized.
Source. (See Revision Note at chapter heading He-W
500); ss by #6641, eff 11-27-97; EXPIRED: 11-27-05
New. #8502, INTERIM, eff 12-2-05, EXPIRES: 5-31-06;
ss by #8638, eff 5-30-06; ss by #10294, eff 12-1-13
He-W
572.06 Authorization Requirements for
Scheduled and Routine Ambulance Transportation.
(a) Scheduled and routine ambulance transportation
shall require authorization to be a covered service.
(b) A complete authorization request shall:
(1) Be submitted by the ambulance provider to the
department or its prior authorization agent by either fax or mail; and
(2) Include the following forms, completed and
legible:
a. Form 272AMB “Scheduled and Routine Ambulance
Transportation Authorization Request Form” (3/13) signed and dated by the
ambulance provider; and
b. Form 272MN “Medical Necessity for Ambulance
Services Form” (3/13) dated and signed by the recipient’s attending physician,
doctor of osteopathy, physician assistant, clinical nurse specialist, advanced
practice registered nurse, registered nurse, licensed practical nurse, or
discharge planner employed by the facility where the recipient is being
treated.
(c) Authorization requests shall be submitted
prior to or within 30 days of the service being delivered.
(d) A complete authorization request shall be
approved by the department or its prior authorization agent if:
(1) The recipient is bed confined, as described
in (e) below; or
(2) The recipient has a condition such that all
other methods of transportation are contraindicated by the recipient’s condition,
and therefore, the recipient cannot
be transported by any other means from the origin to the destination without
endangering the recipient’s health.
(e) In order to be considered bed confined, a
recipient shall be:
(1) Unable to get up from bed without assistance;
(2) Unable to ambulate; and
(3) Unable to sit in a chair or wheelchair.
(f) Authorizations shall be approved for a
specified number of trips over a specified period of time, not to exceed a
maximum of 3 months, after which a new complete authorization request shall be
submitted in accordance with (b) above.
(g) If the department or its prior authorization
agent denies the authorization request, it shall forward a notice of denial to
the recipient and the requesting provider on the department Form 272a, “Medical
Assistance Program Denial for Prior Authorized Services,” including the
following:
(1) The reason for, and legal basis of, the
denial; and
(2) Information that a fair hearing on the denial
may be requested within 30 calendar days of the date on the notice of the
denial, in accordance with He-C 200.
Source. (See Revision Note at chapter heading He-W
500); ss by #6641, eff 11-27-97; EXPIRED: 11-27-05
New. #8502, INTERIM, eff 12-2-05, EXPIRES:
5-31-06; ss by #8638, eff 5-30-06; ss by #10294, eff 12-1-13
He-W 572.07 Documentation.
(a) Each ambulance provider shall maintain
supporting records in accordance with He-W 520.
(b) Each ambulance provider shall maintain
documentation in their records to fully support each claim billed for services,
including:
(1) For emergency transportation, documentation
of the nature of the recipient’s emergency medical condition; and
(2) For all ambulance transportation,
documentation that justifies the level of service, whether ALS or BLS, claimed.
(c) For each trip billed in (b) above, the
ambulance provider shall maintain a run sheet or patient care report that
includes at a minimum the following information, which is legibly written:
(1) Recipient name and medicaid
identification number;
(2) Date of service;
(3) Origin and destination;
(4) Recipient vital signs;
(5) Recipient signs and symptoms upon arrival at
the point of pick-up;
(6) Recipient status en-route;
(7) Services provided;
(8) The name of the person who provided the
service or care in the ambulance, including signature and credentials; and
(9) The response code that indicates the mode of
response for the ambulance making the trip.
Source. (See Revision Note at chapter heading He-W
500); ss by #6641, eff 11-27-97; EXPIRED: 11-27-05
New. #8502, INTERIM, eff 12-2-05, EXPIRES: 5-31-06;
ss by #8638, eff 5-30-06; ss by #10294, eff 12-1-13 (from He-W 572.06)
He-W 572.08 Utilization Review and Control. The department shall monitor utilization of
ambulance services, in accordance with 42 CFR 455, 42 CFR 456, and He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #6641, eff 11-27-97; EXPIRED: 11-27-05
New. #8502, INTERIM, eff 12-2-05, EXPIRES: 5-31-06;
ss by #8638, eff 5-30-06; ss by #10294, eff 12-1-13 (from He-W 572.06)
He-W
572.09 Third Party Liability. All third party obligations shall be
exhausted before medicaid may be billed, in
accordance with 42 CFR 433.139.
Source.
#8638, eff 5-30-06; ss by #10294, eff 12-1-13 (from He-W 572.08)
He-W
572.10 Payment for Services.
(a) Payment for ambulance services shall be made
in accordance with the rates established by the department in accordance with
RSA 161:4, VI(a).
(b) Payment shall consist of the following
separate components, as applicable:
(1) A base rate;
(2) A mileage rate, which shall be paid for the most direct route to and from a destination
and for loaded miles only, which:
a. Shall be the distance traveled while
transporting a recipient from a pick-up point to a drop-off point; and
b. Does not include mileage incurred on the way
to pick up a recipient or after dropping off a recipient;
(3) Payment for waiting time, as allowed by He-W
572.04(a)(3) and (d); and
(4) Payment for routine disposable supplies used en-route.
(c) Payment shall be made for only one mileage
charge per trip regardless of the number of recipients transported.
(d) Payment shall be based on the level of
service provided, not on the vehicle used, even if the local government
requires an ALS response for all calls.
(e) The ambulance provider shall not bill medicaid for transporting a recipient from an acute care
hospital to another acute care hospital or medical provider to obtain necessary
treatment or diagnostic testing not available while the recipient is still an
inpatient of the originating acute care hospital.
(f) The ambulance provider shall submit claims
for payment to the department’s fiscal agent.
Source. #10294,
eff 12-1-13 (from He-W 572.09)
PART He-W 573
WHEELCHAIR VAN SERVICES
He-W 573.01 Definitions.
(a) “Department”
means the New Hampshire department of health and human services.
(b) “Medicaid” means
the Title XIX and Title XXI programs administered by the department, which
makes medical assistance available to eligible individuals.
(c) “Recipient” means an individual who is
eligible for and receiving medical assistance under the medicaid
program.
(d) “Round trip”
means transportation from a pick-up point, to a medical provider waiting for
the recipient, and transporting the recipient back to the point of pick-up.
(e) “Title XIX
program” means the joint federal-state program described in Title XIX of the
Social Security Act and administered in New Hampshire by the department under
the medicaid program.
(f) “Title XXI
program” means the joint federal-state program described in Title XXI of the
Social Security Act and administered in New Hampshire by the department under
the medicaid program.
(g) “Wait time”
means the time a wheelchair van drivers may have to wait for a recipient to complete
a medical appointment.
Source. (See Revision Note at chapter heading He-W
500); ss by #6598, eff 10-8-97; ss by #8401, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8563,
eff 2-7-06; amd by #10139, eff 7-1-12; ss by #10605,
eff 5-23-14
He-W 573.02 Recipient Eligibility. All medicaid
recipients, including all home and community-based care (HCBC) waiver
recipients and recipients residing in nursing facilities, shall be eligible to
receive wheelchair van services, in accordance with this part, when:
(a) The recipient is confined to a wheelchair for
mobility, which means:
(1) At the time of a wheelchair van service, the
recipient is unable to ambulate without the use of a wheelchair; and
(2) The recipient is unable to be transported in
a private vehicle without special equipment or modifications to the vehicle;
and
(b) The wheelchair van services are required as
certified on Form 975 “Documentation to Support the Use of Wheelchair Van
Services” (May 2014) by the signature of the recipient’s treating physician,
physician assistant (PA), advanced practice registered nurse (APRN), or
registered nurse (RN).
Source. (See Revision Note at chapter heading He-W
500); ss by #6598, eff 10-8-97; ss by #8401, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8563,
eff 2-7-06; ss by #10605, eff 5-23-14
He-W
573.03 Provider Participation. All participating wheelchair van service
providers shall:
(a) Be enrolled as a NH medicaid
provider;
(b)
At the time of enrollment, provide proof of vehicle registration in accordance
with He-W 573.07(a);
(c) At the time of enrollment, provide proof of
vehicle insurance in accordance with He-W 573.07(b); and
(d) Comply with
all applicable requirements of RSA 153-A:1, Saf-C
5919, 49 CFR 37, and 49 CFR 38.
Source. (See Revision Note at chapter heading He-W
500); ss by #6598, eff 10-8-97; ss by #8401, INTERIM, eff 8-20-05, EXPIRES: 2-16-06;
ss by #8563,
eff 2-7-06; ss by #10605, eff 5-23-14
He-W
573.04 Service Limits.
(a) Except as provided by He-W 573.10 below,
wheelchair van services shall be limited to 24 trips, per recipient per state
fiscal year.
(b) A one way trip and a round trip each shall
count as one trip towards the service limit described in (a) above.
Source. (See Revision Note at chapter heading He-W
500); ss by #6598, eff 10-8-97; ss by #8401, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8563,
eff 2-7-06; amd by #10016, eff 11-1-11; ss by #10605,
eff 5-23-14
He-W
573.05 Covered Services.
(a) Wheelchair van services shall be covered to
transport eligible recipients to and from an enrolled NH Medicaid provider to
receive necessary medical and dental services that are covered by the NH
Medicaid program.
(b) Wait times shall be covered for round trips
only and for up to a maximum of 2 hours, rounded to the nearest half hour.
(c) Transportation shall be to the nearest available
NH medicaid enrolled provider of the necessary
medical or dental service, unless the department determines that:
(1) The cost to transport the recipient is less
than double the cost to transport the recipient to the nearest available NH medicaid enrolled provider; or
(2) The recipient has an established relationship
with a provider.
Source. (See Revision Note at chapter heading He-W
500); ss by #6598, eff 10-8-97; ss by #8401, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8563,
eff 2-7-06; amd by #9622, eff 1-1-10; ss by #10605,
eff 5-23-14
He-W
573.06 Non-Covered Services. The following services shall not be covered
as wheelchair van services:
(a) Transportation for purposes of recipient or
provider convenience;
(b) Transportation that is otherwise available
free of charge or payable by another agency, or when the item can be obtained
using a free delivery service;
(c) Transportation for any purpose other than to
receive NH medicaid covered services from an enrolled
NH medicaid provider;
(d) Transportation that does not meet the
requirements of He-W 573.05(c);
(e) Any wait time associated with one way trips;
(f) Wait time that exceeds 2 hours for round
trips;
(g) The payment of tolls; and
(h) The payment of parking fees and fines.
Source. (See Revision Note at chapter heading He-W
500); ss by #6598, eff 10-8-97; ss by #8401, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8563,
eff 2-7-06; ss by #10605, eff 5-23-14
He-W
573.07 Provider Requirements. Wheelchair van service providers shall:
(a) Ensure that all vehicles used for wheelchair
van services are registered in accordance with RSA 261:40 and have been
inspected in accordance with RSA 266:1;
(b) Obtain and maintain vehicle insurance for
general and professional liability in accordance with Saf-C
5919.01(a)(1)b;
(c) Ensure that all drivers they employ, or
otherwise engage, possess a valid NH driver’s license in accordance with RSA
263:1 and RSA 263:1-a; and
(d) Provide proof of compliance with (a)-(c)
above, when requested by the department or the medicaid
fraud control unit (MFCU) of the New Hampshire department of justice (NHDOJ).
Source. (See Revision Note at chapter heading He-W
500); ss by #6598, eff 10-8-97; ss by #8401, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8563,
eff 2-7-06; ss by #10605, eff 5-23-14
He-W
573.08 Documentation.
(a) When wheelchair van services are required, a
Form 975, “Documentation to Support the
Use of Wheelchair Van Services” (May 2014), shall be completed prior to the
services being provided, and as follows:
(1) The wheelchair van provider shall complete
section 1 of the form by providing information specific to the wheelchair van
provider;
(2) The recipient’s treating physician, doctor of
osteopathic (DO), physician assistant (PA), advanced practice registered nurse
(APRN), or registered nurse (RN) shall complete section 2 of the form and
certify by signature that the services are necessary; and
(3) When submitting a request for a service limit
override, the wheelchair van provider shall complete section 3 of the form, and
submit the form in accordance with He-W 573.10 below.
(b)
Wheelchair van service providers shall obtain and retain copies of the
signed and completed Form 975 “Documentation
to Support the Use of Wheelchair Van Services” (May 2014), and provide
copies of said documentation upon request to the department or the MFCU.
(c)
Wheelchair van service providers shall retain, and provide when
requested by the department or MFCU, copies of the trip logs, which shall contain
the following documentation for each trip:
(1) Origin;
(2)
Destination;
(3) Date of
service;
(4) Driver’s
name;
(5) Time of
pick-up and drop off;
(6) Whether the
trip was one-way or round-trip;
(7) Amount of
wait time if applicable;
(8) Loaded
mileage incurred; and
(9) Names and
number of recipients transported concurrently during each trip.
(d)
Wheelchair van service providers shall retain, and provide when
requested by the department or MFCU, the following documentation concerning the
safety of wheelchair vans used for transporting recipients:
(1) Proof
that the vehicle was registered in accordance with RSA 261:40 and inspected in
accordance with RSA 266:1, during the time of medicaid
wheelchair van service; and
(2) Proof of
insurance in accordance with He-W 573.07(b) during the time period that
services were delivered.
Source. (See Revision Note at chapter heading He-W
500); ss by #6598, eff 10-8-97; ss by #8401, INTERIM, eff 8-20-05, EXPIRES:
2-16-06; ss by #8563,
eff 2-7-0606; ss by #10605, eff 5-23-14
He-W
573.09 Safety Requirements.
Wheelchair van providers shall comply with all of the applicable parts of Saf-C 5919.19 and 49 CFR 38.23 to ensure that all
wheelchair vans are properly equipped and supplied.
Source.
#8563, eff 2-7-06; ss by #10605, eff 5-23-14
He-W
573.10 Service Limit Override and
Review.
(a) All requests for consideration of additional
wheelchair van services beyond the 24 trip limit shall require prior
authorization from the department before the recipient receives the additional
services in accordance with He-W 530.07(a)-(f) and this section.
(b) The wheelchair van provider shall make
requests for additional wheelchair van services beyond the 24 trip limit by
submitting a copy of Form 975 “Documentation to Support the Use of Wheelchair
Van Services” (May 2014), completed in accordance with He-W 573.08(a) above, to
the department’s prior authorization agent.
(c) A request for a service limit override
submitted in accordance with (a) through (b) above shall be approved by the
department’s prior authorization agent when the department’s prior
authorization agent determines that the recipient meets the eligibility
requirements described in He-W 573.02.
(d) If the department’s prior authorization agent
approves the service limit override request in accordance with (c) above, the
state’s fiscal agent shall send written confirmation of the approval to the
provider.
(e) The department’s prior authorization agent
shall deny a request for a service limit override when the department's prior
authorization agent determines that the recipient does not meet the eligibility
requirements of He-W 573.02.
(f) If the department’s prior authorization agent
denies the request for a service limit override, the department’s prior authorization
agent shall forward a notice of denial to the recipient and the wheelchair van
provider.
(g) The notice of denial shall contain the
information required by 42 CFR 431.210, including:
(1) The reason for, and legal basis of, the
denial; and
(2) Information that an appeal of the denial may
be requested, in accordance with He-C 200, within 30 calendar days of the date
on the notice of the denial.
Source.
#8563, eff 2-7-06; amd by #10016, ef 11-1-11; ss by #10605, eff 5-23-14
He-W
573.11 Utilization Review and Control. The department’s provider program integrity
unit shall monitor utilization of wheelchair van services, to identify,
prevent, and correct potential occurrences of fraud, waste and abuse, in
accordance with 42 CFR 455, 42 CFR 456, and He-W 520.
Source.
#8563, eff 2-7-06; ss by #10605, eff 5-23-14
He-W
573.12 Third Party Liability. All third party obligations shall be
exhausted before medicaid may be billed, in
accordance with 42 CFR 433.139.
Source.
#8563, eff 2-7-06; ss by #10605, eff 5-23-14
He-W
573.13 Payment for Services.
(a)
Payments for wheelchair van services shall be made in accordance with
rates established by the department, in accordance with RSA 161:4, VI(a).
(b)
Payments for wheelchair van services shall consist of the following
components:
(1) A base rate, which shall:
a. Include the first 5 miles of travel;
b. Be paid once only for a single one-way trip
or round trip; and
c. Be paid twice for 2 one-way trips for the
same recipient on the same day;
(2) A mileage rate, which shall:
a. Be based on the most direct route to and from
a destination, and not necessarily the route used;
b. Be paid for loaded miles only, which:
1. Shall be the distance traveled while
transporting recipients from a pick-up point to a drop-off point; and
2. Does not include mileage incurred on the way
to pick up a recipient or after dropping off a recipient;
c. Not include the first 5 miles; and
d. Be paid only once per trip regardless of the
number of recipients transported; and
(3) A payment for the wait time described in He-W
573.05(b).
(c)
The wheelchair van provider shall submit claims for payment to the
department’s fiscal agent.
(d)
The wheelchair van provider shall maintain supporting records, in
accordance with He-W 573.08 and He-W 520.03.
Source.
#8563, eff 2-7-06; ss by #10605, eff 5-23-14
PART He-W 574 GENERAL
MEDICAL TRANSPORTATION
He-W
574.01 Definitions.
(a)
“Assistance group” means the individuals living together with or without
benefit of a dwelling pursuant to He-W 630.01(a), whose needs and income,
resources, or both are considered and combined together when determining
eligibility or the amount of benefits for financial or medical assistance.
(b)
“Commissioner” means the commissioner of the NH department of health and
human services, or his or her designee.
(c)
“Department” means the New Hampshire department of health and human
services.
(d)
“Driver(s)” means a person, company, or entity, including volunteer and
recipient drivers, that submit claims for reimbursement for providing general
medical transportation services for a recipient and is enrolled with or
contracted by the department.
(e)
“General medical transportation” means non-emergency transportation for
the purpose of accessing medicaid covered medical or
dental services via motorized public or private transportation pursuant to 42
CFR 441.62(a), 42 CFR 431.53, and 42 CFR 440.170.
(f)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department which makes medical assistance available to eligible
individuals.
(g)
“Out of area” means a state other than New Hampshire, Massachusetts,
Vermont, or Maine.
(h)
“Point of origin” means the recipient’s residence as listed on file at
the department or the volunteer driver’s residence as it appears on the
completed Form 14 as provided for in He-W 574.03(c).
(i) “Private transportation” means transportation
via a recipient’s own vehicle or other vehicle that does not meet the
definition of public transportation.
(j)
“Public transportation” means transportation via commercial buses,
boats, airplanes, helicopters, or trains.
(k)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(l)
“Recipient driver” means someone who provides transportation in
accordance with He-W 574 and is:
(1) A recipient who transports him/herself and
members of his/her assistance group for medical or dental appointments;
(2) The parent/guardian of the recipient being
transported; or
(3) Residing in the same household as the
recipient being transported.
(m)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(n)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(o)
“Transit company” means an entity that provides or brokers
transportation via private transportation.
(p)
“Usual and customary” means “usual and customary” as defined in RSA
126-A:3, III(b).
(q)
“Volunteer driver(s)” means individuals who provide general medical
transportation services in accordance with He-W 574 and are not:
(1) The recipient who transports him/herself or
members of his/her assistance group;
(2) A parent/guardian of the recipient being
transported; or
(3) Residing in the same household as the
recipient being transported.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; amd
by #10139, eff 7-1-12; ss by #10810, eff 4-9-15
He-W
574.02 Recipient Eligibility. All recipients shall be ensured assistance to
locate transportation or be reimbursed for miles traveled, in order to access medicaid covered medical and dental services as required by
42 CFR 441.62(a), 42 CFR 431.53, and 42 CFR 440.170.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New.
#8732, eff 9-30-06; ss by #10810, eff 4-9-15
He-W
574.03 Driver Participation.
(a) All drivers shall be enrolled with the
department as:
(1) A recipient driver;
(2) A volunteer driver;
(3) Both a. and b.; or
(4) A transit company driver.
(b) All recipient drivers shall submit to the
department:
(1) A copy of a valid New Hampshire driver’s
license; and
(2) A completed, signed, and dated Form 14,
“Medicaid Transportation Enrollment Form” (03/15), attesting to the following:
“I
agree to accept up to the maximum New Hampshire Medicaid mileage allowance per
trip as payment in full.”
(c) All volunteer drivers shall submit the
following information to the department:
(1) A completed, signed, and dated Form 14,
“Medicaid Transportation Enrollment Form” (03/15), attesting to the following:
“I
agree to accept up to the maximum New Hampshire Medicaid mileage allowance per
trip as payment in full.”
(2) A copy of a valid driver’s license;
(3)
Proof of automobile liability insurance;
and
(4) Updated proof of licensure and insurance at
the time each is renewed, and at any other time when a change in status has
occurred.
(d) Transit company drivers shall submit the
following information to the department:
(1) A completed, signed, and dated Form 14b,
“Medicaid Transportation Enrollment Form – Transit Company” (03/15), certifying
the following:
a.
“For the purpose of establishing eligibility to receive direct payment for
transportation provided to recipients of the New Hampshire (NH) Medicaid
Program, I certify that the information furnished in this application is true,
accurate, and complete to the best of my knowledge. I understand that, per 42 CFR 455, Subpart B,
it is my responsibility to notify the NH Medicaid Transportation office of any
changes to the information on this application, including but not limited to:
name, address, group affiliation, or change in ownership.”;
b. “I understand that payment of all claims will
be from federal and state funds, and that any falsification, or concealment of
a material fact, may be prosecuted under federal and state laws.”; and
c.
“I agree to accept up to the maximum NH Medicaid mileage allowance per trip as
payment in full.”;
(2) A copy of the document received from the IRS
which provided the applicant’s federal tax ID number;
(3) A completed IRS W-9 form at the time of
enrollment;
(4) A copy of the document received from the IRS
which indicates the applicant’s non-profit tax-exempt status, if applicable;
(5) Proof of automobile liability insurance; and
(6) Updated proof of insurance at the time it is
renewed, and at any other time when a change in status has occurred.
(e) Volunteer and transit company drivers shall
submit a completed IRS form 1099 to the IRS at the end of the calendar year if
the yearly total of contracted services exceeds $600.00.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; ss by #10810, eff 4-9-15
He-W
574.04 Covered Services.
(a) General medical transportation shall be
covered for the purpose of allowing a recipient to access medicaid
covered medical or dental services from a medicaid
enrolled provider pursuant to 42 CFR 441.62(a) and 42 CFR 440.170.
(b) When general medical transportation is
arranged by the department, the covered service shall be the least costly
available to meet the recipient’s needs.
(c) The costs of tolls and parking fees shall be
covered when the total cost for these is $3.00 or more per trip.
(d) Driver reimbursement, except for volunteer or
transit company drivers, shall be limited to one trip per day unless as provided
for in He-W 574.09.
(e) Only the actual number of miles traveled from
point of origin and return to point of origin shall be reimbursable and as
described in He-W 574.07(a).
(f) General medical transportation shall be to
the nearest available medicaid enrolled provider of
the covered medical or dental service, unless as authorized in accordance with
He-W 574.08, via the least costly route, as described in He-W 574.10(d).
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; ss by #10810, eff 4-9-15
He-W 574.05 Non-Covered
Services. General medical
transportation shall be a non-covered service when it:
(a) Is being provided for a purpose other than
for the recipient to access medicaid covered medical
or dental services;
(b) Is to a medicaid
enrolled provider who transports recipients to his or her own location of
service;
(c) Is to a pharmacy which provides free delivery
service to the recipient’s residence;
(d) Can be obtained free of charge to the
recipient;
(e) Is being provided to a resident of a nursing
facility;
(f) Was provided prior to the volunteer,
recipient, or transit company driver being enrolled as a general medical
transportation driver in accordance with He-W 574.03(c); or
(g) Was performed by a driver who has not
complied with the requirements of He-W 574.03.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; ss by #10810, eff 4-9-15
He-W
574.06 Submission of Claims.
(a) All drivers seeking reimbursement for general
medical transportation services shall complete and submit a Form 13A, “Medicaid
Transportation Reimbursement Form” (03/15).
(b) Form 13A shall be completed in the following
manner:
(1) The recipient shall obtain the medicaid enrolled provider’s signature on the Form 13A at
the time of the service provision, certifying the following: “I certify that NH
Medicaid covered services were rendered for this recipient on the trip date
indicated.”; and
(2) The recipient, or the recipient’s parent or
legal guardian, and the volunteer driver if applicable, shall sign and date the
Form 13A prior to submitting the form to the department, as follows:
a. If the driver is the recipient, the recipient
shall sign and date the “Driver Signature” line;
b. If the driver is a volunteer driver:
1. The recipient shall sign and date the
“Recipient Signature” line; and
2. The volunteer driver shall sign the “Driver
Signature” line; and
c. The individual(s) in a. and b. above shall
certify the following:
“This
is to certify that the information above is true, accurate and complete. I
understand that payment of this claim may be from Federal and State funds and
that any false claims, statements, documents or the concealment of material
fact may be prosecuted under applicable Federal and State Laws (42 CFR
455.18)”.
(c) All drivers shall include copies of receipts
for tolls, parking, and public transportation with the completed Form 13A, as
applicable.
(d) All completed Form 13A forms shall be
submitted to the department within 90 calendar days of the date transportation
services were provided or performed.
(e) Submission of claims for multiple trips in
one day shall be limited to the submission of one claim per trip regardless of
the number of passengers. A driver shall not submit separate claims for each
passenger.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; ss by #10810, eff 4-9-15
He-W
574.07 Payment for Services.
(a) Except as provided by (c) below, claims for
general medical transportation delivered via private transportation shall be
reimbursed at the lesser amount of:
(1) Actual number of miles billed multiplied by
rate per mile; or
(2) The maximum allowable mileage for the trip,
multiplied by the rate per mile.
(b)
All reimbursements shall be made by one of the following methods:
(1) By direct deposit to a checking account;
(2) By direct deposit to a money bank card; or
(3) By paper check.
(c) Public transportation claims shall be
reimbursed in the following manner:
(1) To either the recipient or to the
transportation provider; and
(2) At the usual and customary charge made to the
general public if receipts are attached to the Form 13A.
(d) Reimbursement for tolls and parking fees
shall paid if the total cost is $3.00 or more per trip and receipts are
submitted with the completed Form 13A.
(e) Reimbursement for volunteer drivers when a
trip includes multiple passengers shall be as follows:
(1) For multiple trips in one day this shall be
limited to the submission of one claim per trip regardless of the number of
passengers;
(2) For the total miles from the volunteer driver’s
point of origin to the farthest distanced medical provider and return to the
volunteer driver’s point of origin; and
(3) For total miles in the claim submission
described in (2) above shall be paid at the actual mileage traveled or the
maximum mileage allowance per trip, in accordance with He-W 574.10(c),
whichever is less.
(f) Reimbursement shall not be made:
(1) For trips provided prior to the enrollment
date of the provider;
(2) For claims submitted 90 days or more from the
date of the trip;
(3) If the medicaid
enrolled provider’s signature as described in He-W 574.06(b) is missing on the
Form 13A;
(4) If the signature of the driver or the
recipient, or both, as described in He-W 574.06(b), is missing on the Form 13A;
(5) For general medical transportation provided
prior to the enrollment date of the volunteer, recipient, or transit company
driver; or
(6) For waiting time, which is defined as the
total time for which the driver must be in attendance for a recipient while the
recipient is receiving a medicaid covered medical or
dental service.
(g) If a recipient is dual enrolled,
transportation of members of his or her assistance group shall require
submission of a claim for the costs of transportation as a recipient driver
only.
(h)
Any claims submitted by a recipient
driver which are submitted for payment as a volunteer driver shall be denied
unless:
(1) The recipient driver is also enrolled as a
volunteer driver; and
(2) The recipient driver is providing general
medical transportation for a medicaid recipient who
was unable to provide transportation him/herself.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; ss by #10810, eff 4-9-15
He-W
574.08 Prior Authorization.
(a) All drivers shall contact the department to
obtain prior authorization for general medical transportation services when:
(1) Transportation is needed out of area;
(2) Transportation is to a medicaid
enrolled provider that is not the nearest available provider of the covered
medical or dental service;
(3) Transportation is by means other than private
transportation or bus; or
(4) The recipient requires assistance from the
department because all other transportation resources have been exhausted by
the recipient.
(b) The recipient shall provide the following
information for out of area transportation as described in (a)(1) above:
(1) The recipient’s name and address;
(2) The recipient’s medicaid
identification number; and
(3) A letter from the recipient’s primary care
physician or referring physician with the following information:
a.
Details describing the illness or condition sufficient to enable the department
to understand the physical and/or emotional condition of the recipient and the
reason(s) for which the medical or dental service is required;
b. That the needed medical or dental services
cannot be obtained in New Hampshire, Vermont, Massachusetts, or Maine;
c. The expected outcome and recommended timetable
of the prescribed medical or dental service; and
d. The name and address of the medicaid enrolled provider.
(c) The recipient shall provide the following
information for prior authorization of transportation as described in (a)(2)
above:
(1) The recipient’s name and address;
(2) The recipient’s medicaid
identification number; and
(3) A letter from the recipient’s primary care
physician or referring physician with the following information:
a.
Details describing the illness or condition sufficient to enable the department
to understand the physical and/or emotional condition of the recipient and the
reason(s) for which the medical or dental service cannot be obtained closer to
the recipient’s home;
c. The expected outcome and recommended timetable
of the prescribed medical or dental service; and
d. The name and address of the medicaid enrolled provider.
(d) The recipient shall provide the following
information for prior authorization by means other than private transportation
or bus as described in (a)(3) above:
(1) The recipient’s name and address;
(2) The recipient’s medicaid
identification number; and
(3) A letter from the recipient’s primary care or
referring physician which includes the following information:
a. Details describing the illness or condition
sufficient to enable the department to understand the physical and/or emotional
condition of the recipient and the reason(s) for which the medical or dental
service is required;
b. That the type of specialized transportation service
is medically necessary;
c. The expected outcome and recommended
timetable of the prescribed medical or dental service; and
d. The name and address of the medicaid enrolled provider.
(e) The recipient shall provide following
information when requesting assistance from the department as described in
(a)(4) above:
(1) The recipient’s name and address;
(2) The recipient’s medicaid
identification number;
(3) Information that explains how the recipient
has attempted to obtain transportation and has been unable to do so; and
(4) The name and location of the medicaid enrolled provider the recipient is trying to
access.
(f) Requests for prior authorization shall be approved
if:
(1) All of the required information described in
(b), (c), (d), or (e) above is received; and
(2) The department determines, based on the
information provided, that the transportation is necessary and appropriate for
the recipient’s medical or dental condition, as supported by the information
provided in the request.
(g) The department shall deny requests for prior
authorization if the provisions set forth in (f) above are not met.
(h) If prior authorization is approved, payment
for general medical transportation shall still comply with all of the
provisions of He-W 574.
(i) If advanced
authorization is denied, the recipient may appeal this decision pursuant to
He-W 574.11.
(j) If a recipient requires general medical
transportation for which advanced authorization as described in (a) is
required, but the need arises outside of the department’s normal working hours,
the request to the department for prior authorization shall be made within 3
business days of the trip.
(k) If the request for prior authorization in (j)
above is not made within 3 business days of the trip, the transportation claim
shall be denied.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; ss by #10810, eff 4-9-15
He-W
574.09 Extenuating Circumstances.
(a) Notwithstanding He-W 574.04(d) and (e),
respectively, the department shall allow general medical transportation
reimbursement payments under the following conditions and in accordance with
this section:
(1) The recipient found it necessary to take more
than one trip per day; and
(2) The point of origin of the medical
transportation is not the recipient’s residence.
(b) The recipient shall provide following
documentation when the recipient found it necessary to take more than one trip
in a day:
(1) The recipient’s name and address;
(2) The recipient’s medicaid
identification number; and
(3) Either:
a. A letter from the medicaid
enrolled provider which includes details regarding the necessity of the second
trip sufficient to enable the department to understand the necessity of the
second trip; or
b. A letter from the medicaid
enrolled provider which includes details regarding a referral made to another medicaid enrolled provider who was able to see the
recipient the same day.
(c) The recipient shall provide following
documentation when the point of origin is not the recipient’s address:
(1) The recipient’s name and address;
(2) The recipient’s medicaid
identification number; and
(3) Either:
a. A statement, signed by the recipient and the medicaid enrolled provider, containing sufficient detail to
enable the department to understand the need for medical or dental services and
why the point of origin was not the recipient’s residence; or
b. If the recipient must provide care for
another party at the residence of the other party, and this is the reason why
the transportation was not the recipient’s residence:
(i) A statement from
the other party’s medicaid enrolled provider of the
necessity of and the amount of time of the care provided by the recipient for
the other party; and
(ii)
A statement, signed by the recipient and the recipient’s medicaid
enrolled provider, containing sufficient detail to enable the department to
understand that the need for medical or dental services.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; ss by #10810, eff 4-9-15
He-W
574.10 Mileage Limits and Rate.
(a) The rate paid shall be that established by
the commissioner in accordance with RSA 161:4, VI(a).
(b) The maximum allowed traveled round trip
mileage to medicaid enrolled providers by recipient
drivers shall not exceed the following limits:
(1) 75 miles to a hospital;
(2) 45 miles to a physician or mental health
provider;
(3) 300 miles to a dentist;
(4) 75 miles to a physical, speech, or
occupational therapist;
(5) 90 miles to a dialysis provider;
(6) 400 miles to a referred medical provider; and
(7) 20 miles to a pharmacy.
(c) The maximum allowed billable round trip
mileage for travel to medicaid enrolled providers by
volunteer drivers shall not exceed the following limits:
(1) 95 miles to a hospital;
(2) 65 miles to a physician or mental health
provider;
(3) 320 miles to a dentist;
(4) 95 miles to a physical, speech, or occupational
therapist;
(5) 110 miles to a dialysis provider;
(6) 420 miles to a referred medical provider; and
(7) 40 miles to a pharmacy.
(d) Determination of the least
costly route shall be by the use of a web-based mapping tool containing a mileage
calculator, which has the functionality to allow the input of addresses and the
calculation of distance between them and to identify toll roads.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; ss by #10810, eff 4-9-15
He-W
574.11 Hearings. Any recipient who has been denied
reimbursement for general medical transportation services may appeal an adverse
decision by requesting a fair hearing in accordance with He-C 200. Requests for fair hearings shall be submitted
no later than 30 days after the date the notice of decision being appealed is
issued.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; ss by #10810, eff 4-9-15
He-W
574.12 Third Party Liability. All third party obligations shall be
exhausted before the NH medicaid program may be
billed, in accordance with 42 CFR 433.139.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; ss by #10810, eff 4-9-15
He-W
574.13 Utilization Review and Control. The department’s provider integrity unit
shall monitor utilization of general medical transportation services to
identify, prevent, and correct potential occurrences of fraud, waste, and
abuse, in accordance with 42 CFR 455, 42 CFR 456, and He-W 520.
Source. (See Revision Note at chapter heading He-W
500); ss by #6163, eff 1-4-96, EXPIRED: 1-4-04
New. #8732, eff 9-30-06; ss by #10810, eff 4-9-15
(formerly He-W 574.14)
PART
He-W 575 AUGMENTATIVE AND ALTERNATIVE
COMMUNICATION AID SERVICES
He-W 575.01 Definitions.
(a)
“Augmentative and alternative communication (AAC)” means all forms of
communication other than oral speech that are used to express thoughts, needs,
wants, and ideas.
(b)
“Augmentative and alternative communication (AAC) aids” means electronic
or non-electronic aids, devices or systems that assist an individual to
overcome or ameliorate the communication limitations that preclude or interfere
with meaningful participation in current and projected daily activities, such
as communication boards or books, speech amplifiers, electronic devices that
produce speech and/or written output.
(c)
“Augmentative and alternative communication (AAC) consultant” means the
speech language pathologist who participates in the AAC evaluation and who
provides ongoing consultation to the recipient regarding AAC implementation.
(d) “Augmentative and alternative
communication (AAC) evaluation” means an evaluation
that assesses the recipient’s communication skills and abilities, and their AAC
needs.
(e)
“Date of service” means the date the AAC provider orders the prior
authorized AAC aid or accessory.
(f)
“Department” means the NH department of health and human services.
(g)
“Functionally communicate” means to share information, to impart
knowledge, and/or to have interchanges of thoughts.
(h) “Medicaid” means the Title XIX and Title XXI
programs administered by the department, which makes medical assistance
available to eligible individuals.
(i) “Recipient” means
any individual who is eligible for and receiving medical assistance under the medicaid program.
(j) “Title XIX” means the joint federal-state
program described in Title XIX of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
(k) “Title XXI” means the joint federal-state
program described in Title XXI of the Social Security Act and administered in
New Hampshire by the department under the medicaid
program.
Source.
#10636, eff 7-12-14
He-W 575.02 Recipient Eligibility. A recipient
shall be eligible to receive AAC aids as prescribed by a physician when:
(a)
The recipient has a significant,
expressive communication or language comprehension impairment such as apraxia
of speech, dysarthria, and cognitive communication disabilities, and the
impairment or disability either temporarily or permanently causes communication
limitations that preclude or interfere with the recipient's meaningful
participation in current and projected daily activities;
and
(b)
The prescribed AAC aid is coverable in accordance with this rule.
Source.
#10636, eff 7-12-14
He-W 575.03 Provider Participation. All participating AAC providers shall:
(a)
Be an enrolled New Hampshire Medicaid durable medical equipment (DME)
provider;
(b)
Request and obtain prior authorization from the department in accordance
with He-W 575.06 below; and
(c)
Provide the recipient and caregiver with equipment training and related
supports, including equipment set-up,
training in the use and maintenance of the AAC aid, and technical support.
Source.
#10636, eff 7-12-14
He-W 575.04 Covered Services. The following AAC aids, accessories, and
services shall be covered:
(a)
The purchase, repair, and modifications of AAC aids and accessories when
they:
(1) Meet the definition of durable medical
equipment (DME) per He-W 571.01;
(2) Are medically necessary;
(3) Are the most clinically appropriate and least
costly alternative;
(4) Are a dedicated communication device used
only for communication purposes;
(5) Are to be used solely by the recipient; and
(6) Have been prior authorized in accordance with
He-W 575.06 below;
(b)
Rental of AAC aids for up to 2 months when prior authorized in
accordance with He-W 575.06 below, and at least one of the following is true:
(1) Time is needed to assess the appropriateness
of the AAC aid, and whether it will
meet the person’s current needs and accommodate reasonable anticipated future
needs;
(2) Rental is needed because the recipient’s AAC
aid is out for authorized repair and no loaner equipment is available from the
AAC provider or manufacturer; or
(3) Rental is needed during the time period
between order and delivery of the aid approved for purchase, and no loaner
equipment is available from the AAC provider or manufacturer; and
(c)
Computer equipment and accessories when such items are:
(1)
Identified in the AAC evaluation,
conducted in accordance with He-W 575.07 below, as the recipient’s only AAC aid
allowing for functional communication;
(2) Are medically necessary;
(3) Are the most clinically appropriate and least
costly alternative;
(4) Are a dedicated communication device used
only for communication purposes;
(5) Are to be used solely by the recipient; and
(6) Have been prior authorized in accordance with
He-W 575.06 below.
Source.
#10636, eff 7-12-14
He-W
575.05 Non-Covered Services. The following equipment, accessories, items,
and services shall not be covered:
(a) Computer equipment and accessories that do
not meet the criteria in He-W 575.04(c) above;
(b) Software or computer equipment that is not
specifically integral to communication devices;
(c) Multiple AAC aids and accessories unless such
items together expand the functional capability of the aid, such as increased
recording time or vocabulary, and represent the most clinically appropriate and
least costly alternative in equipment options for the recipient;
(d)
Equipment that duplicates equipment already funded by medicaid, per He-W 530.05(b)(25);
(e) More than one charger per AAC aid;
(f) Extended warranty and maintenance agreements;
(g) Shipping and handling fees on purchased
equipment, except as allowed by He-W 575.11(e)-(f) below;
(h) Repair of original AAC aids once a
replacement has been provided;
(i) Replacement or repair of rented AAC aids;
(j)
Replacement of AAC aids when the replacement is requested solely as a
result of changing technology, or when
the existing device effectively addresses the beneficiary’s needs;
(k) Replacement of
AAC aids when the replacement occurs within 5 years from the date of purchase
of the original equipment unless there is a clinical justification for a
replacement in less time, such as a significant change in the recipient’s needs
and abilities relative to AAC use such that the current aid limits
communication, or no longer provides access to communication;
(l)
Environmental control equipment;
(m)
Equipment or appliances that are not considered medical equipment in
nature, such as tape recorders, fans, lights, radios, and toys, with the
exception of computer equipment and accessories covered in accordance with He-W
574.04(c) above;
(n) Internet access, including costs associated
with initial and recurring internet service provider fees, purchase or rental
of modems, mobile device data plans, or network access for mobile devices;
(o) Subscriptions for mobile device applications,
also known as “apps”; and
(p) Replacement, repair, or modifications of an
item when the need is the result of:
(1)
Abuse, misuse, or inappropriate use or neglect of the AAC aid;
(2)
Failure to protect the item from the elements;
(3)
Using the item inappropriately or contrary to its designed and intended
use;
(4)
Making improper repairs to the item, which would void any manufacturer’s
warranty;
(5)
Loss of the item when basic safeguarding measures could have been
instituted;
(6)
Failure to maintain the item through proper routine maintenance by an
authorized dealer; or
(7)
Taking any action that would otherwise void the manufacturer’s written
warranty or is contrary to the manufacturer’s recommendations for care, use,
and maintenance.
Source.
#10636, eff 7-12-14
He-W 575.06 Prior Authorization.
(a)
An AAC provider shall request and obtain a prior authorization from the
department on behalf of a recipient for the purchase, rental, or repair of AAC
aids and accessories.
(b)
Prior authorization requests for purchases and rentals shall include the
following:
(1) A statement from the recipient’s physician
that includes:
a. An explanation of the medical need of the AAC
aid being requested;
b. A statement that the physician concurs with
the recommendation of the AAC evaluation, conducted in accordance with He-W
575.07; and
c. When the request is for a rental, an
indication of which of the coverage criteria has been met per He-W 575.04(b)
above;
(2) An AAC evaluation as described in He-W
575.07; and
(3) A completed Form #288-Q, “Quote for
Augmentative and Alternative Communication (AAC) Aids Funding Request” (June
2014), completed and signed by a NH Medicaid DME provider.
(c)
Prior authorization requests for repairs shall include the following:
(1) The all-inclusive cost of the repair;
(2) Replacement cost of the current AAC aid;
(3) A letter from a licensed speech language
pathologist (SLP) that establishes the recipient’s prognosis for continued
use of the current AAC aid, including the expected life-span of the AAC aid
with repair;
(4) A copy of the safeguarding plan, as described
in He-W 575.07(c)(10)b., that is less than one year old and contains current
contact information; and
(5) A signed statement from the recipient
attesting that the need for the repair is not the result of any of the
condition listed in He-W 575.05(q).
(d)
Prior authorization requests for modification of an existing AAC aid
shall include the following:
(1) The all-inclusive cost of the modification;
(2) A justification of need, as described in He-W
575.07(c)(6), from a licensed SLP, including updated clinical information; and
(3) The results of an AAC evaluation completed in
accordance with He-W 575.07 within the last 3 years.
(e)
In addition to the requirements of (c) and (d) above, prior
authorization requests for the repair or modification of an existing AAC aid
shall include current clinical information regarding the recipient’s use of the
AAC aid, as well as current contact information of the individuals listed in
He-W 575.07(c)(2).
(f)
Prior authorization requests shall be approved when the department’s
prior authorization agent determines that the purchase, rental, or repair of
the AAC aid being requested is determined to be the most clinically appropriate
and least costly
alternative, as supported by the documentation submitted in accordance
with (b), (c), or (d) above.
(g)
The department’s prior authorization agent shall forward written
confirmation of the department’s approval of a prior authorization request to
the provider.
(h)
The AAC provider shall be responsible for determining that the recipient
is Medicaid eligible on the date of service.
(i) The department’s
prior authorization agent shall deny a PA request if the agent determines that
the requirements set forth in this part have not been met.
(j) If the department’s prior
authorization agent denies the prior authorization request, the department’s
prior authorization agent shall forward a notice of denial to the recipient and
the AAC provider.
(k)
The notice of denial shall contain the information required by 42 CFR
431.210, including:
(1) The reason for, and legal basis of, the
denial; and
(2) That a fair hearing on the denial may be
requested within 30 calendar days of the date on the notice of the denial.
Source.
#10636, eff 7-12-14
He-W
575.07 AAC Evaluation.
(a)
An AAC evaluation shall be required for prior authorization of all AAC
aids.
(b)
An AAC evaluation shall be completed by a SLP licensed as such by the state
in which he or she practices, and who has one of the following credentials:
(1)
Has at least 3 years’ experience in the provision of AAC aids; or
(2)
Has completed an accredited training in AAC.
(c)
The AAC evaluation shall include the following:
(1)
The recipient’s identifying information including name and medicaid identification (MID) number;
(2) A Form #288-F, “Augmentative and Alternative
Communication (AAC) Aids Funding Information” (June 2014) that has been signed
by the SLP who conducted the AAC evaluation;
(3) The recipient’s medical and communication
diagnoses;
(4) An explanation of the medical need of the
recommended AAC aid, and how it will allow the recipient the ability to
functionally communicate, including the recipient’s communication prognosis
both with and without the use of the AAC aid;
(5) The recipient’s past and current
communication skills, including information about past AAC use;
(6)
A justification of need which indicates the need for modified equipment
including information about any of the following areas:
a. The recipient’s environment;
b. The recipient’s behavior, cognitive skills,
motor skills, perceptual skills, and sensory impairments;
c. The recipient’s ability to access and activate
the AAC aid including activation through touch, eye gaze, or scanning; and
d. The need for the AAC aid to be positioned and
mounted;
(7) A comparison of at least 3 different AAC
aids from the same device code category using features match, simulation, or
trial, and the results of the comparison including:
a. Identification of the chosen aid and the
rationale as to why it was chosen over the others;
b. An explanation of how the
chosen aid meets the recipient’s communication needs including data demonstrating
improvement over baseline using the selected equipment; and
c. An explanation as to how the AAC aid
represents the least costly, most clinically appropriate alternative given the
recipient’s demonstrated cognitive and linguistic abilities;
(8) Except as allowed by (d) below, the results
of a one-month long trial of the AAC aid identified in (7)a. above, which shall
be provided on Form #288-T, “Augmentative and Alternative Communication (AAC)
Aids Trial Summary” (June 2014), showing that the recipient’s ability to
communicate has been maintained or has improved over baseline, and signed by a
SLP who completed the evaluation;
(9) A detailed list of recommended AAC aids and
accessories to be ordered as a result of the completed evaluation;
(10) A plan of care for the recipient’s use of the
AAC aid, which shall include:
a. Training of the recipient and the
caregiver(s) in the use, maintenance, and care of the AAC aid;
b.
A safeguarding plan, which shall be provided on Form #288-SG, “Augmentative
and Alternative Communication (AAC) Aids Safeguarding Plan” (June 2014), and signed by the SLP who completed the evaluation; and
c. The frequency of direct treatment and/or
consultation by the licensed SLP responsible for integration of the AAC aid or
by the AAC consultant;
(11) Documentation indicating that the use of the
AAC aid will be supported in the home, school, and work settings as
applicable;
(12) Signature of the SLP who completed the evaluation who
attests to his or her agreement with the findings of the evaluation and its
recommendations; and
(13) Signatures of any individuals who, as part of
the plan of care, are responsible for ensuring that the plan is effectively
implemented at home, at school, or at work, and their acknowledgement that they
understand their role in the implementation of the plan.
(d)
When an AAC aid has 8 minutes of recording time or less and can be
accessed by direct selection or scanning and light tech materials, a trial
period shall not be required.
(e)
None of the individuals signing the evaluation in (c) above shall have
any financial affiliation with the manufacturer or the supplier of the AAC
aids.
(f)
The AAC evaluation shall be valid for 3 years from the date it was
completed.
Source.
#10636, eff 7-12-14
He-W 575.08 Documentation.
(a)
In accordance with He-W 520, the AAC provider shall maintain supporting
records to substantiate claims
submitted for reimbursement for a period of at least 6 years from the date of
service or until the resolution of any legal action(s) commenced in the 6 year
period, whichever is longer.
(b)
The
AAC provider shall maintain records of equipment training and related support provided in accordance with He-W 575.03(c) above.
Source.
#10636, eff 7-12-14
He-W
575.09 Third Party Liability. All third party obligations shall be
exhausted before medicaid may be billed in accordance
with 42 CFR 433.129.
Source.
#10636, eff 7-12-14
He-W 575.10 Utilization Review and Control. The
department’s provider integrity unit shall monitor utilization of AAC aids and
services to identify, prevent, and correct potential occurrences of fraud,
waste, and abuse in accordance with 42 CFR 455, 42 CFR 456, and He-W 520.
Source.
#10636, eff 7-12-14
He-W 575.11 Payment for AAC Aids. Payment for AAC aids shall be made as
follows:
(a)
The DME provider of AAC aids shall submit claims for payment to the
department’s fiscal agent;
(b)
Claims shall not be submitted prior to the date the AAC aid is delivered
to the recipient;
(c)
The payment amount for rental shall be based on the manufacturer’s
customary rental charge to the public;
(d)
Payment for the purchase of AAC aids shall be made at the lesser of the
following amounts:
(1) Usual and customary charge to the public, as
established by the provider; or
(2) Provider acquisition cost, plus a mark-up,
which shall be determined as follows:
a. For purchases from providers who have a
program in place for ongoing education and technical support for the use of the
AAC aid(s) after purchase, the mark-up shall be no greater than 35%; and
b. For purchases from providers who do not have
a program in place for ongoing education and technical support for the use of
the AAC aid(s) after purchase, the mark-up shall be as follows:
1. For AAC aids with a total cost of less than
$301, the mark up shall be no greater than 35%;
2. For AAC aids with a total cost from $301 to
$750, the mark-up shall be no greater than 30%;
3. For AAC aids with a total cost from $751 to
$1,200, the mark-up shall be no greater than 25%; and
4. For AAC aids with a total cost of $1,201 and
above, the mark-up shall be no greater than 20%;
(e)
Payment as calculated in (d) above shall not include shipping costs,
except for cases in which the AAC aids are purchased from multiple vendors, or
the provider would receive less than $35 per vendor over their cost when
shipping is included;
(f)
When the AAC provider receives less than $35 over the acquisition cost
when shipping is included, then an amount shall be included in the total
payment to account for the cost of shipping;
(g)
In the case of an AAC aid that has been rented before purchase, the cost
of one month’s rental shall be deducted from the purchase amount computed in
(d) above;
(h)
For rental of AAC aids:
(1) No prepayment shall be made; and
(2) The provider shall submit claims at the end
of the rental period;
(i) Payment for repairs of purchased AAC aids shall
be the all-inclusive usual and customary charge to the public, except that:
(1) The allowable labor costs shall not exceed
$50.00/hour; and
(2) Payment shall not include the cost of
shipping and handling;
(j)
Recipients shall not be liable for shipping and handling costs
associated with repairs, rentals, and purchases; and
(k)
Payment shall be denied if the recipient is not eligible for NH Medicaid
on the date the authorized AAC aid is ordered.
Source.
#10636, eff 7-12-14
PART
He-W 576 MANAGED CARE ORGANIZATIONS -
EXPIRED
He-W
576.01 – 576.05
Source. (See Revision Note at chapter heading He-W
500); ss by #4907, eff 9-1-90, EXPIRED: 9-1-96
New. #6926, eff 12-30-98
He-W
576.06 – 576.09
Source. (See Revision Note at chapter heading He-W
500); ss by #5165, eff 6-17-91, EXPIRED: 6-17-97
New.
#6926, eff 12-30-98
PART
He-W 577 LABORATORY SERVICES
He-W 577.01 Definitions.
(a)
“Current procedural terminology (CPT) code” means a unique identifying
code in the field of medical nomenclature and designated by the US Department
of Health and Human Services as the national coding standard utilized in
government and private health insurance programs for reporting medical services
and procedures.
(b)
“Department” means the New Hampshire department of health and human
services.
(c)
“Medicaid” means the Title XIX and Title XXI programs administered by
the department, which makes medical assistance available to eligible individuals.
(d)
“Recipient” means any individual who is eligible for and receiving
medical assistance under the medicaid program.
(e)
“Title XIX” means the joint federal-state program described in Title XIX
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
(f)
“Title XXI” means the joint federal-state program described in Title XXI
of the Social Security Act and administered in New Hampshire by the department
under the medicaid program.
Source.
#8564, eff 2-7-06; amd by #10139, eff 7-1-12;
ss by #10513, eff 1-24-14
He-W 577.02 Recipient Eligibility. All medicaid
recipients shall be eligible for laboratory services, in accordance with He-W
577.
Source.
#8564, eff 2-7-06; ss by #10513, eff 1-24-14
He-W 577.03 Provider Participation.
(a)
All participating laboratory service providers shall:
(1) Be licensed by the states in which they
practice;
(2) Be certified to participate in the medicare program if the provider is an independent
laboratory;
(3) Be Clinical Laboratory Improvement Amendments
(CLIA) certified in accordance with 42 U.S.C. 263a; and
(4) Be an enrolled New Hampshire Medicaid
provider.
(b)
If a laboratory test cannot be performed within the capabilities of the
participating laboratory services provider, the specimens may be referred to
another laboratory that is certified in the appropriate specialties and
subspecialties of services in accordance with the requirements of 42 CFR 493.
Source.
#8564, eff 2-7-06; ss by #10513, eff 1-24-14
He-W 577.04 Covered Services. Laboratory services shall be covered when:
(a)
Ordered and provided under the direction of a physician or other
licensed practitioner within the scope of his or her practice; or
(b)
Ordered by a physician but provided by a referral laboratory in
accordance with 42 CFR 440.30.
Source.
#8564, eff 2-7-06; ss by #10513, eff 1-24-14
He-W
577.05 Utilization Review and Control. The department’s provider program integrity
unit shall monitor utilization of laboratory services to identify, prevent, and
correct potential occurrences of fraud, waste and abuse, in accordance with 42
CFR 455, 42 CFR 456 and He-W 520.
Source.
#8564, eff 2-7-06; ss by #10513, eff 1-24-14
He-W 577.06 Third Party Liability. All third party obligations shall be
exhausted before medicaid may be billed, in
accordance with 42 CFR 433.139.
Source.
#8564, eff 2-7-06; ss by #10513, eff 1-24-14
He-W 577.07 Payment for Services.
(a)
Laboratory service providers shall bill:
(1) Utilizing the appropriate CPT code and code
guidelines established for use with these procedure codes;
(2)
For services referred to and provided by another laboratory in accordance with
He-W 577.03(b); and
(3) For tests performed as groups and
combinations utilizing the CPT codes for automated multichannel procedures.
(b)
All laboratory tests shall be included in the panel if:
(1) A panel
procedure code is utilized for billing; and
(2) The panel
procedure code is listed in the National Correct Coding Initiative (NCCI), found
at the Centers for Medicare and Medicaid Services, at www.cms.hhs.gov.
(c)
Payments to laboratory service providers shall be made in accordance
with rates established by the department pursuant to RSA 161:4, VI.
(d)
The department shall directly reimburse a physician for laboratory
services provided by a laboratory service provider with which the physician has
a contract or agreement.
(e) Laboratory service providers shall submit
claims for payment to the department’s fiscal agent.
(f)
Laboratory service providers shall maintain supporting documentation, in
accordance with He-W 520.
Source.
#8564, eff 2-7-06; ss by #10513, eff 1-24-14
PARTS
He-W 578 through He-W 589 - RESERVED
PART
He-W 590 NURSING FACILITY SERVICES
He-W
590.01 Definitions.
Source. (See Revision Note at chapter heading He-W
500); ss by #5085, eff 3-5-91; amd by #6159, eff
12-29-95; rpld by #7749, eff 8-17-02
He-W
590.02 Recipient Eligibility. -
EXPIRED
Source. (See Revision Note at chapter heading He-W
500); ss by #4908, eff 8-17-90; amd by #5164, eff
6-12-91, EXPIRED: 8-17-96 and 6-12-97
He-W
590.03 through He-W 590.14 - EXPIRED
Source. (See Revision Note at chapter heading He-W
500); ss by #4908, eff 8-17-90, EXPIRED: 8-17-96
He-W
590.15 Absence from the Facility.
Source. (See Revision Note at chapter heading He-W
500); ss by #5965, eff 1-27-95; rpld by #7749, eff 8-17-02
He-W
590.16 Resident Assessment System.
Source. (See Revision Note at chapter heading He-W
500); ss by #6159, eff 12-29-95; rpld by #7749, eff
8-17-02
PART
He-W 591 NURSING FACILITY ENFORCEMENT
REMEDIES - EXPIRED
Source. (See Revision Note at chapter heading He-W
500); ss by #6082, eff 8-22-95; ss by #7936, INTERIM, eff 8-22-03, EXPIRED:
2-18-04
PART
He-W 592 NURSING ASSISTANT TRAINING
REIMBURSEMENT
He-W
592.01 Definitions. - EXPIRED
Source. (See Revision Note at chapter heading He-W
500); ss by #5618, eff 8-1-93, EXPIRED: 8-1-99
He-W
592.02 Requirements, Conditions and
Limitations.
Source. (See Revision Note at chapter heading He-W
500); ss by #5618, eff 4-28-93; amd by #6033, eff
5-1-95; rpld by #7750, eff 8-17-02
He-W
592.03 Payment to CAN.
Source. (See Revision Note at chapter heading He-W
500); ss by #5618, eff 4-28-93; amd by #6033, eff
5-1-95; rpld by #7750, eff 8-17-02
PART He-W 593 NURSING FACILITY REIMBURSEMENT - EXPIRED (Now
He-E 806)
Source.
(See Revision Note at chapter heading He-W 500); ss by #6547, eff
7-26-97; amd by #8185, eff 10-2-04; ss by #8391,
INTERIM, eff 7-26-05, EXPIRED: 1-22-06
PARTS
He-W 594 through He-W 599 – RESERVED
APPENDIX A: Incorporation by Reference Information
Rule |
Title |
Publisher; How
to Obtain; and Cost |
He-W 511.05 |
Chapter 3, Section 3910, Medicaid
Payments for Recipients under Group Health Plans, of the federal Centers for
Medicare and Medicaid Services (CMS), State Medicaid Manual |
Publisher: Centers for Medicare and Medicaid Services
(CMS). This document is available for free on the CMS website at: |
He-W 513.02(b)(2), (p)(3);
513.04(f); 513.05(b)(1), (h)-(l), (m)(3)-(4), (n) intro, (n)(6), (o) intro,
(u)(3)e.; and 513.06(a) |
ASAM
Criteria: Treatment Criteria for Substance-Related, Addictive, and
Co-Occurring Conditions, 3rd edition (2013) |
Publisher: American
Society of Addiction Medicine (ASAM). The ASAM Criteria (2013) can be purchased online through the ASAM
website at: http://www.asamcriteria.org/. Cost = $95
(non-members) or $85 (members). Discounts are available for large purchases. |
He-W 513.02(b)(3), (q)(3);
513.04(g); 513.05(b)(1), (h)intro.-(l)intro, (n) intro, (n)(5), (o) intro,
(u)(2)e.; 513.06(a), and 513.11 |
ASAM
Criteria: Treatment Criteria for Substance-Related, Addictive, and
Co-Occurring Conditions, 3rd edition (2013) |
Publisher: American
Society of Addiction Medicine (ASAM). The ASAM Criteria (2013) can be purchased online
through the ASAM website at: http://www.asamcriteria.org/. Cost = $95 (non-members) or $85 (members). Discounts are available for
large purchases. |
He-W 513.02(x), 513.05(l)(1)a. |
The Diagnostic and Statistical Manual of Mental
Disorders, 5th Edition (2013) (DSM-5) |
Publisher: The American Psychiatric Association
(APA). The DSM-5 can be purchased on line at:
http://www.appi.org/SearchCenter/Pages/SearchDetail.aspx?ItemId=2554 Cost = $199 |
He-W 513.02(aa), 513.05(l)(1)a. |
The Diagnostic and
Statistical Manual of Mental Disorders, 5th Edition (2013) (DSM-5) |
Publisher: The American
Psychiatric Association (APA). The DSM-5 can be purchased on line at: https://www.appi.org/Diagnostic_and_Statistical_Manual_of_Mental_Disorders_DSM-5_Fifth_Edition Cost = $157.50 -$210 depending upon APA affiliation |
He-W 513.02(ad)(1) and He-W
513.05(b)(6) |
Addiction Counseling
Competencies, TAP 21 (2017 revision) |
Publisher:
U.S. Department of Health and Human Services, Substance Abuse and Mental
Health Services Administration, Center for Substance Abuse Treatment,
www.samhsa.gov Available free
of charge at: |
He-W 513.02(aa)(1) |
Addiction Counseling Competencies,
TAP 21 (2011 revision) |
Publisher: U.S. Department of Health and
Human Services, Substance Abuse and Mental Health Services Administration,
Center for Substance Abuse Treatment, www.samhsa.gov Available free of charge at: http://store.samhsa.gov/shin/content//SMA12-4171/SMA12-4171.pdf |
He-W 513.02(aa), 513.05(l)(1)a. |
The Diagnostic and
Statistical Manual of Mental Disorders, 5th Edition (2013) (DSM-5) |
Publisher: The American
Psychiatric Association (APA). The DSM-5 can be purchased on line at: https://www.appi.org/Diagnostic_and_Statistical_Manual_of_Mental_Disorders_DSM-5_Fifth_Edition Cost = $157.50 -$210 depending upon APA affiliation |
He-W 513.02(ad)(1) and He-W
513.05(b)(6) |
Addiction Counseling
Competencies, TAP 21 (2017 revision) |
Publisher:
U.S. Department of Health and Human Services, Substance Abuse and Mental
Health Services Administration, Center for Substance Abuse Treatment,
www.samhsa.gov Available free
of charge at: |
He-W 513.05(c)(3), 513.05(d)(3) |
Systems-Level Implementation of
Screening, Brief Intervention, and Referral to Treatment, TAP 33 (2013
edition) |
Publisher:
U.S. Department of Health and Human Services, Substance Abuse and Mental
Health Services Administration, Center for Substance Abuse Treatment,
www.samhsa.gov Available free
of charge at: |
He-W 513.05(g)(1)b. |
TIP 63: Medications for Opioid Use Disorder (2018) |
Publisher: The U.S. Department
of Health and Human Services, Substance Abuse and Mental Health Services Administration. The document is included in the Clinical Guidelines for the Use of
Buprenorphine in the Treatment of Opioid Addiction, Treatment Improvement
Protocol (Tips) #40. The document can be accessed online at |
He-W 513.05(g)(1)c. |
Federation of
State Medical Boards – Model Policy Guidelines for Opioid Addiction Treatment
in the Medical Office (2004) |
Publisher:
The U.S. Department of Health and Human Services, Substance Abuse and
Mental Health Services Administration. The document is included in the Clinical
Guidelines for the Use of Buprenorphine in the Treatment of Opioid Addiction,
Treatment Improvement Protocol (Tips) #40. The document can be accessed online at http://buprenorphine.samhsa.gov/Bup_Guidelines.pdf |
He-W 530.05(b)(4) |
Medicare Coverage Database |
Publisher: Centers for Medicare and Medicaid Services.
National Coverage Determinations can be
found in the “Medicare Coverage Database” at http://www.cms.gov/medicare-coverage-database/
(under the “Quick Search” function, select “National Coverage Documents”,
optionally enter a filter by entering a “keyword” to narrow the search
results, and select the “Search by Type” button, or, if a keyword is not
entered, the entire list of NCD titles will appear alphabetically and may be
selected). There is no cost to access the website
or print the material contained therein. |
He-W 530.05(b)(32)a. |
Medicare Coverage Database |
Publisher: Centers for Medicare and Medicaid Services.
National
Coverage Determinations can be found in the “Medicare Coverage Database” at http://www.cms.gov/medicare-coverage-database/
(under the “Quick Search” function, select “National Coverage Documents”,
optionally enter a filter by entering a “keyword” to narrow the search
results, and select the “Search by Type” button, or, if a keyword is not
entered, the entire list of NCD titles will appear alphabetically and may be
selected). There
is no cost to access the website or print the material contained therein. |
He-W 530.05(b)(32)b.1. |
Anthem Medical Policies and Clinical UM
Guidelines |
Publisher: Anthem Insurance Companies Anthem Medical Policies and Clinical UM
Guidelines can be obtained from: http://www.anthem.com/wps/portal/ahpprovider?content_path=provider/wi/f5/s1/t4/pw_ad080065.htm&state=wi&rootLevel=0&label=Anthem%20Medical%20Policies (select the
“Continue” button to confirm that the page has been read and proceed to the
“Overview” page, then select the “Click Here to Search” button in the middle
of this page to continue to the search engine, enter search criteria for the
specific coverage policy, and then select the specific coverage policy). There is no cost to access the website or
print the material contained therein. |
He-W 530.05(b)(32)b.2. |
Cigna Coverage Policies |
Publisher: Cigna Insurance Company Cigna Coverage Policies can be obtained
from https://cignaforhcp.cigna.com (select “RESOURCES”
at the top of the page, then select “Coverage Policies”, then select “Medical
A-Z Index” for an alphabetical list of policies, and then select the specific
coverage policy). There is no cost to access the website
or print the material contained therein. |
He-W 530.05(b)(32) b.3. |
Aetna Clinical Policy Bulletins |
Publisher: Aetna Insurance Company Aetna Clinical Policy Bulletins can be
obtained from http://www.aetna.com/healthcare-professionals/policies-guidelines/cpb_alpha.html (select
specific bulletin from the alphabetical listing of clinical policy
bulletins). There is no cost to access the website
or print the material contained therein. |
He-W 530.07(g)(9) |
Milliman Clinical Guidelines, |
Publisher: MCG Health, LLC. 901 Fifth
Avenue, Suite 2000, Seattle, WA 98164. Phone: 206-389-5300; Toll-Free:
888-464-4746. Fax: 206-464-7813. http://www.careguidelines.com/.
Cost per guideline: approximately $6,000. NH Medicaid
providers and recipients may obtain relevant portions of the guidelines
(e.g., the specific criteria related to a prior authorization denial) free of
charge and upon request by contacting the Department’s Prior Authorization
Agent, KeyPro, at 2810 N. Parham Rd., Suite 305,
Henrico, VA 23294 PHONE: (800)
299-5921 FAX: (800) 922-9847. |
He-W |
Interqual Connect
Clinical Guidelines, |
Publisher: Change Healthcare (McKesson),
3055 Lebanon Pike, Nashville, TN 37214. Phone:615-932-3000; Toll-Free:
1-800-274-8374. Fax: 615-231-4843. interqualsupport@changehealthcare.com
Cost $367,475 NH Medicaid providers and recipients may
obtain relevant portions of the guidelines (e.g., the specific criteria
related to a prior authorization denial) free of charge and upon request by
contacting their managed care organization: AmeriHealth Caritas https://www.amerihealthcaritasnh.com/
Member Services: 1-833-704-1177 (TTY:
1-855-534-6730) New Hampshire Healthy Families, http://www.nhhealthyfamilies.com/
Member Services: 1-866-769-3085 (TTY/TDD:
1-855-742-0123) Well Sense Health Plan, http://www.wellsense.org/ Member
Services: 1-877-957-1300 (TTY/TDD: 711) |
He-W 531.06(e) |
Medicare Coverage Database |
Publisher: Centers for Medicare and Medicaid Services.
National Coverage Determinations can be
found in the “Medicare Coverage Database” at http://www.cms.gov/medicare-coverage-database/
(under the “Quick Search” function, select “National Coverage Documents”,
optionally enter a filter by entering a “keyword” to narrow the search
results, and select the “Search by Type” button, or, if a keyword is not
entered, the entire list of NCD titles will appear alphabetically and may be
selected). There is no cost to access the website
or print the material contained therein. |
He-W 546.05(a)(1) intro. |
Recommendations for Preventive
Pediatric Health Care (2014) |
Publisher: American Academy of Pediatrics/Bright
Futures. Available free of charge at: |
He-W 546.05(a)(1)j. |
Guideline on Periodicity of
Examination, Preventive Dental Services, Anticipatory Guidance/Counseling,
and Oral Treatment for Infants, Children, and Adolescents (2013 revision) |
Publisher: American Academy of Pediatric Dentistry. Available free of charge at: http://www.aapd.org/media/Policies_Guidelines/G_Periodicity.pdf |
He-W 546.05(b)(5) |
Recommended Immunization Schedules
for Persons Aged 0 Through 18 Years, United States 2015 |
Publisher: U.S. Department of
Health and Human Services, Centers for Disease Control and Prevention. Available free of charge at: http://www.cdc.gov/vaccines/schedules/downloads/child/0-18yrs-child-combined-schedule.pdf
|
He-W |
“Bright
Futures: Guidelines for Health Supervision of Infants, Children and
Adolescents,” 3rd edition, 2008. |
Published by the American Academy of
Pediatrics. PDFs of each chapter of the guidelines can
be downloaded free of charge from: http://brightfutures.aap.org/3rd_Edition_Guidelines_and_Pocket_Guide.html.
The complete document can be ordered from
the AAP Bookstore at a cost of $64.95 at https://www.nfaap.org/, or by writing to: Bright Futures |
He-W |
“Clinical
Guideline on Periodicity of Examination, Preventive Dental Services,
Anticipatory Guidance, and Oral Treatment for Children”, of the American
Academy of Pediatric Dentistry, 81 Reference Manual 2004-2005, Originating
Committee- Clinical Affairs Committee, Review Council- Council on Clinical
Affairs, adopted 1991, Revised, 1992, 1996, 2000, and 2003. |
Published by the American Academy of
Pediatric Dentistry. Available on-line, at: http://www.aapd.org/media/Policies_Guidelines/G_Periodicity.pdf. Free of charge. |
He-W 568.10(b) |
American Medicaid Association’s “Current
Procedural Terminology (CPT) 2022 Professional Edition” |
Publisher:
American Medical Association Cost:
$109.76 The
incorporated document is available for purchase at
https://www.amazon.com/stores/page/112D63A3-2DF2-490B-A8CA-79D03F0F0E99 |
He-W 569.06(d)(1) & (d)(2)a.-d. |
Milliman Clinical Guidelines, 17th Edition (February/March 2013) |
Publisher: MCG Health, LLC. 901 Fifth
Avenue, Suite 2000, Seattle, WA 98164. Phone: 206-389-5300; Toll-Free:
888-464-4746. Fax: 206-464-7813. http://www.careguidelines.com/.
Cost per guideline: approximately $6,000. NH Medicaid providers and recipients may obtain relevant portions of
the guidelines (e.g., the specific criteria related to a prior authorization
denial) free of charge and upon request by contacting the Department’s Prior
Authorization Agent (currently KePro) at
1-800-299-5921. |
He-W 571.04(c)(21) |
Medicare Coverage Database |
Publisher: Centers for Medicare and Medicaid Services.
National Coverage Determinations can be
found in the “Medicare Coverage Database” at http://www.cms.gov/medicare-coverage-database/
(under the “Quick Search” function, select “National Coverage Documents”,
optionally enter a filter by entering a “keyword” to narrow the search
results, and select the “Search by Type” button, or, if a keyword is not
entered, the entire list of NCD titles will appear alphabetically and may be
selected). There is no cost to access the website
or print the material contained therein. |
APPENDIX B
RULE |
STATE OR FEDERAL STATUTE THE RULE
IMPLEMENTS |
He-W 506.01 |
RSA
126-A:5, XIX; 42 U.S.C. 1396u–2(a); 42 U.S.C. 1396u-2; RSA 126-A:5,
XXIII-XXV |
He-W 506.02 |
RSA 126-A:5,
XIX; §1932(a) of the SSA [42 USC 1396u-2(a)]; 42 USC 1396u-2 |
He-W 506.03 |
1932(a) of the
SSA [42 USC 1396u-2(a)]; 42 USC 1396u-2; 42 CFR 438.2; RSA 126-A:5,
XXIII-XXV |
He-W 506.04 |
§1903(m) of the SSA [42 USC 1396b(m)]; 1932(a) of the SSA [42
USC 1396u-2(a)]; 42 USC 1396u-2; 42 CFR 438.210; §1932(a)(3) of the SSA; 42 U.S.C.
1396u-2(a)(3) |
He-W 506.05 |
§1932(a)(4) of
the SSA [42 USC 1396u-2(a)(4)]; §1915(b)(1) of the SSA [42 USC 1396n(b)(1)];
§1915(b)(4) of the SSA [42 USC 1396n(b)(4)]; 42 CFR 438.56 and .226 |
He-W 506.06 |
§1932(a)(4) of
the SSA [42 USC 1396u-2(a)(4)]; 42 CFR 438.52; 42 CFR 438.700 |
He-W 506.07 |
42 CFR 438
Subpart F; 42 CFR 438.228 |
He-W 506.08 |
42 CFR 438
Subpart F; §1932(a)(5)(iii) of the SSA |
He-W
506.09 |
42 CFR 438
Subpart F; §1932(a)(5)(iii) of the SSA |
He-W 507.01 |
42 CFR 435.540 |
He-W 507.02 |
42 CFR 435.222,
42 CFR 435.540 |
He-W 507.03 |
RSA 171-A:2, V,
42,CFR 435.222, 42 CFR 435.540 |
He-W 507.04 |
42 CFR 435.211,
42 CFR 435.541(f)(3), 42 CFR 435.916 |
He-W 507.05 |
42 CFR 435.919,
42 CFR 435.912, 42 CFR 431.211 |
He-W 507.06 |
42 CFR 431.200,
42 CFR 435.220, 42 CFR 435.221 |
He-W 508.01 |
RSA 167:3-f, II |
He-W 508.02 |
RSA 167:3-f, I;
42 CFR 435.225; 42 CFR 435.217; 42 CFR 435.540; 42 CFR
483.440(a) |
He-W 508.03 |
RSA 167:3-e,
III; RSA 167:3-f, III and IV; 42 CFR 435.225; 42 CFR 435.217;
42 CFR 435.540; 45 CFR 233.90(c)(1)(v)(B) |
He-W 508.04 |
RSA 167:3-g; 42
CFR 435.225; SS Act 1902 (e)(3); 42 CFR 435.217; 42 CFR
483.102(b)(2) RSA 171-A:2, V |
He-W 508.05 |
RSA 167:3-f, V
and VI |
He-W 508.06 |
RSA 167:3-e, IV |
He-W 508.07 |
RSA 167:3-e, IV |
He-W 508.08 |
RSA 167:3-e, IV |
He-W 508.09 |
RSA 167:3-e,
III; RSA 167:3-f, III and IV; 42 CFR 435.225; 42 CFR 435.217;
42 CFR 435.540; 45 CFR 233.90(c)(1)(v)(B) |
He-W 508.10 |
RSA 167:3-e,
III; RSA 167:3-f, III and IV; 42 CFR 435.225; 42 CFR 435.217;
42 CFR 435.540; 45 CFR 233.90(c)(1)(v)(B) |
He-W 509.01 |
Section
1902(a)(10)(A)(ii) of the Social Security Act (42 U.S.C. 1396a(a)(10)(A)(ii));
42 U.S.C 1396d |
He-W 509.02 |
Section 1902(a)(10)(A)(ii) of the
Social Security Act (42 U.S.C. 1396a(a)(10)(A)(ii)); 42 U.S.C 1396d; 42 CFR
441.251
|
He-W 509.03 |
Section 1902(a)(10)(A)(ii) of the
Social Security Act (42 U.S.C. 1396a(a)(10)(A)(ii))
|
He-W 509.04 |
42 CFR 440.50; 42 CFR 440.60
|
He-W 509.05 |
42 CFR 440.230
|
He-W 509.06 |
42 CFR 441
Subpart F; 42 U.S.C 1396d |
He-W 509.07 |
42 CFR 441 Subpart F; 42 U.S.C 1396d
|
He-W 509.08 |
42 CFR 431.53 |
He-W 509.09 |
42 CFR
447.53(b)(5) |
He-W 511.01 |
RSA 126-A:5, XXIII;
42 U.S.C. 1396e |
He-W 511.02 |
RSA 126-A:5,
XXIII; 42 U.S.C. 1396e |
He-W 511.03 |
RSA 126-A:5,
XXIII; 42 U.S.C. 1396e |
He-W 511.04 |
RSA 126-A:5,
XXIII; 42 U.S.C. 1396e |
He-W 511.05 |
RSA 126-A:5,
XXIII; 42 U.S.C. 1396e |
He-W 511.06 |
RSA 126-A:5,
XXIII; 42 U.S.C. 1396e |
He-W 511.07 |
RSA 126-A:5,
XXIII; 42 U.S.C. 1396e |
He-W 511.08 |
RSA 126-A:5,
XXIII; 42 U.S.C. 1396e |
He-W 511.09 |
RSA 126-A:5,
XXIII; 42 U.S.C. 1396e |
He-W 511.10 |
RSA 126-A:5,
XXIII; 42 CFR 433.139 |
He-W 511.11 |
RSA 126-A:5,
XXIII; 42 CFR 455; and 42 CFR 456 |
He-W 512.01 |
RSA 126-A:5,
XXIV; 42 U.S.C. 1396u-7 |
He-W 512.02 |
RSA 126-A:5,
XXIV; 42 U.S.C. 1396u-7 |
He-W 512.03 |
RSA 126-A:5,
XXIV; 42 U.S.C. 1396u-7 |
He-W 512.04 |
RSA 126-A:5,
XXIV; 42 U.S.C. 1396u-7; RSA 420-J:5 |
He-W 512.05 |
RSA 126-A:5,
XXIV; 42 U.S.C. 1396u-7 |
He-W 512.06 |
RSA 126-A:5,
XXIV; 42 U.S.C. 1396u-7 |
He-W 512.07 |
RSA 126-A:5,
XXIV; 42 U.S.C. 1396u-7; RSA 420-J:5 |
He-W 512.08 |
RSA 126-A:5,
XXIV; 42 CFR 433.139 |
He-W 512.09 |
RSA 126-A:5,
XXIV; 42 CFR 455; and 42 CFR 456 |
He-W 513.01 |
42 USC 1396u-7(b)(5),
RSA 126-A:5, XXIII-XXV, 42 CFR 440.347 |
He-W 513.02 |
42 USC
1396u-7(b)(5), RSA 126-A:5, XXIII-XXV, 42 CFR 440.347 |
He-W 513.03 |
42 USC
1396u-7(b)(5), RSA 126-A:5, XXIII-XXV, 42 CFR 440.347 |
He-W 513.04 |
42 USC
1396u-7(b)(5), RSA 126-A:5, XXIII-XXV, 42 CFR 440.347, Chapter Law 189:2,
II, Laws of 2008, Chapter Law 249:24, V, Laws of 2010 |
He-W 513.05 |
42 USC
1396u-7(b)(5), RSA 126-A:5, XXIII-XXV, 42 CFR 440.347 |
He-W 513.06 |
42 USC
1396u-7(b)(5), RSA 126-A:5, XXIII-XXV, 42 CFR 440.347 |
He-W 513.07 |
42 CFR 455 and
42 CFR 456 |
He-W 513.08 |
42 CFR 433.139 |
He-W 513.09 |
RSA 161:4, VI |
He-W 513.10 |
42 CFR 455 and
42 CFR 456 |
He-W 513.11 |
42 CFR 455 and
42 CFR 456 |
He-W 513.12 |
RSA 161:4-a, X |
He-W 520.01 |
42 CFR 433,
Subpart C; Section 1920A of the SSA Section 1920A(b)(3)(A)
of the SSA; 42 CFR 440.40 |
He-W 520.01
(b), (d), (e), (j), (m), and (n) |
42 CFR 433,
Subpart C; Section 1920A of the SSA; 42 USC 1396a(a)(10); 42 USC 1396d(a);
42 CFR 455; 42 CFR 457 |
He-W
520.02 |
42
CFR 430.10, 42 CFR 440.210, 42 CFR 440.220; RSA 161:2, VI; RSA
161:4-a, IX |
He-W
520.03 |
42
CFR 431.107 |
He-W 520.04 |
42 CFR 455; 42
CFR 456 |
He-W
520.05 |
42
CFR 455.14; 42 CFR 455.15; 42 CFR 455.16 |
He-W 520.06 |
42
U.S.C. 1395cc(j)(2); 42
CFR 433.139; 42 CFR 424; 42 CFR Part 455; RSA 161:4-a,X; 42 U.S.C.
1396a(a)(77); 42 U.S.C. 1396a(kk) ; RSA 126-A:5, VIII |
He-W 520.07 |
RSA
161:4, VI(a); 42 CFR 447.15 |
He-W 530.01 |
RSA 318:1; 21
CFR 310.6; 42 CFR 440.120; 21 USC 802(6), 42 CFR 447.53; 42 CFR 456 subpart
K; Chapter Law 188 and 281:9, 2004, SB 383-FN, 2004. |
He-W 530.01(a)-(c),
(e) |
RSA 318:1; 21
CFR 310.6; 42 CFR 440.120; 21 USC 802(6) |
He-W 530.01(d),
(h), (i), (o) |
RSA 318:1; 21
CFR 310.6; 42 CFR 440.120; 21 USC 802(6); RSA 318:1; 21
CFR 310.6; 42 CFR 440.120; 21 USC 802(6) |
He-W 530.01(f) |
RSA 167:3-h, II |
He-W 530.01(g),
(j)-(n), (p)-(r) |
RSA 318:1; 21
CFR 310.6; 42 CFR 440.120; 21 USC 802(6) |
He-W 530.02 |
42 USC 1396o;
42 CFR 447.53, 42 CFR 447.56 |
He-W 530.03 |
RSA 167:3-h, IV; 42 CFR 440.230(d); 42 CFR 447.53-55; RSA 326-B:2, I;
RSA 326-B:11 |
He-W 530.04 |
42 USC 1396o;
42 CFR 447.53, 42 CFR 438.114(a), 42 CFR 447.26(b), 42 CFR 447.56 |
He-W 530.05 |
42 CFR
440.230(d) |
He-W
530.05(b)(4) & (b)(32) |
RSA 541-A:21,
VIII |
He-W 530.06 |
42 CFR 447.15 |
He-W 530.07 |
42 CFR
440.230(d); 42 CFR 431.107; RSA 126-A:5, VII |
He-W 531.01 |
42 USC 1396 |
He-W 531.02 |
42 CFR 440.210,
42 CFR 440.220 & 42 CFR 440.225 |
He-W 531.03 |
42 CFR 440.50 |
He-W 531.04 |
42 CFR 440.230
& 42 CFR 440.250 |
He-W 531.05 |
42 CFR 441.30; 42
CFR 441.35 |
He-W 531.06 |
42 CFR
440.230(d) |
He-W 531.06(e) |
RSA 541-A:21, VIII |
He-W 531.06(i) |
42 CFR 447.15 |
He-W 531.07 |
42 CFR
440.230(d) |
He-W 531.08 |
42 CFR 455; 42
CFR 456 |
He-W 531.09 |
42 CFR 433.139 |
He-W 531.10 |
42 CFR 447.15;
RSA 161:4, VI(a) |
He-W 543.01(o) |
42 CFR 412.60;
42 CFR 440.210; 42 CFR 440.220; 42 CFR 440.225; 42 CFR 476.1; 42 CFR 475 |
He-W 531.07 |
42 CFR
440.230(d) |
He-W 531.08 |
42 CFR 455; 42
CFR 456 |
He-W 531.09 |
42 CFR 433.139 |
He-W 531.10 |
42 CFR 447.15;
RSA 161:4, VI(a) |
He-W 532.01 |
42 CFR 440.110 |
He-W 532.02 |
42 CFR 440.210;
42 CFR 440.220; 42 CFR 440.225 |
He-W 532.03 |
42 CFR 440.50;
RSA 315 |
He-W 532.04 |
42 CFR 440.230 |
He-W 532.05 |
42 CFR
440.10-50; RSA 315 |
He-W 532.06 |
42 CFR
440.230(d) |
He-W 532.07 |
42 CFR 431.107 |
He-W 532.08 |
42 CFR 455 |
He-W 532.09 |
42 CFR 433.139 |
He-W 532.10 |
42 CFR 447.200;
42 CFR 447.202; 42 CFR 447.204; RSA 541-A:21, III |
He-W 534.01 |
RSA 326 B:2; 42
CFR 440.166 |
He-W 534.02 |
42 CFR 440.210;
42 CFR 440.220 |
He-W 534.03 |
42 CFR 440.166 |
He-W 534.04 |
42 CFR 440
Subpart B |
He-W 534.05 |
42 CFR 440.166 |
He-W 534.06 |
42 CFR 456 |
He-W 534.07 |
42 CFR 433.139 |
He-W 534.08 |
RSA 541-A:21;
42 CFR 447 Subpart B |
He-W 536.01 |
42 CFR 440.90 |
He-W 536.02 |
42 CFR 440.210,
42 CFR 440.220 & 42 CFR 440.225 |
He-W 536.03 |
42 CFR 440.90 |
He-W 536.04 |
42 CFR 440.230
and 42 CFR 440.240 |
He-W 536.05 |
42 CFR 440.90,
42 CFR 440.230 & 42 CFR 440.240 |
He-W 536.06 |
42 CFR 455, 42
CFR 456 |
He-W 536.07 |
42 CFR 433.139 |
He-W 536.08 |
42 CFR 447.15,
42 CFR 430.0, 42 CFR 447.204 & 42 CFR 431.107; RSA 161:4, VI(a) |
He-W 538.01 |
RSA 326-D:2; RSA
326-D:6 |
He-W 538.02 |
42 CFR 440.210,
42 CFR 440.220, 42 CFR 440.225 |
He-W 538.03 |
RSA 326-D:2, 42
CFR 440.165, 42 CFR 440.210, 42 CFR 440.220, 42 CFR 440.225 |
He-W 538.04 |
RSA 326-D:1 and
RSA 326-D:12 |
He-W 538.05 |
RSA 326-D:1, V |
He-W 538.06 |
42 CFR 455,42
CFR 456, 42 CFR 447, 42 CFR 1001 |
He-W 538.07 |
42 CFR 433.139 |
He-W 538.08 |
42 CFR 447.15,
RSA 161:4, VI(a) |
He-W 540.01 |
42 CFR 484.60;
Nurse Practice Act, RSA 326-B; 42 CFR 440.80 |
He-W 540.02 |
42 CFR 440.210;
42 CFR 440.220 |
He-W 540.03 |
RSA 151:2,
I(b); 42 CFR 440.80 |
He-W 540.04 |
42 CFR 440.80 |
He-W
540.05 |
RSA 151:2; 42
CFR 434.2; 42 CFR 440.150; 42 CFR 435.1010 |
He-W 540.06 |
42 CFR 484.60;
42 U.S.C. 1395n; 42 CFR 440 |
He-W 540.07 |
42 CFR 431.107;
42 CFR 440.230 |
He-W 540.08 |
42 CFR 447; 42
CFR 455; 42 CFR 456; 42 CFR 1001 |
He-W 540.09 |
42 CFR 433.139 |
He-W 540.10 |
RSA 161:4,
VI(a) |
He-W
541.01 |
42
CFR 441.251, 42 CFR 447 |
He-W
541.02 |
42
CFR 440.220; 42 CFR 440.225 |
He-W
541.03 |
42
CFR 431.51(b); 42 CFR 431.51(c)(2); 42 CFR 431.107(b) |
He-W
541.04 |
42
CFR 440.230; 42 CFR 440.240 |
He-W
541.05 |
42
CFR 441.253; 42 CFR 441.254; 42 CFR 441.255; 42 CFR 441.257; 42 CFR 441.258 |
He-W
541.06 |
42
CFR 441.254; 42 CFR 441.255 |
He-W
541.07 |
42
CFR 447.53(b)(5) |
He-W
541.08 |
42
CFR 456.3; 42 CFR 455, 42 CFR 447, 42 CFR 456 |
He-W
541.09 |
42
CFR 433 |
He-W
541.10 |
42
CFR 447.204; 42 CFR 431.107 |
He-W 543.01 |
42 CFR 412.60;
42 CFR 440.210; 42 CFR 440.220; 42 CFR 440.225; 42 CFR 476.1; 42 CFR 475 |
He-W 543.02 |
42 CFR 440.210;
42 CFR 440.220; 42 CFR 440.225 |
He-W 543.03 |
42 CFR 431.52;
42 CFR 476 Subpart C; 42 CFR 482.1,2,11,24,30; RSA 151; 42 CFR
440.10; 42 CFR 431.107, 108 |
He-W 543.04 |
42 CFR 431.15;
42 CFR 431.52; 42 CFR 440.230 |
He-W 543.05 |
42 CFR 440.2;
42 CFR 440.10; 42 CFR 440.20; 42 CFR 440.50; 42 CFR 440.130 |
He-W 543.06 |
42 CFR 440.10;
42 CFR 440.140; 42 CFR 440.160 |
He-W 543.07 |
42 CFR 456 |
He-W 543.08 |
42 CFR 412,
Subpart A - F,H |
He-W 543.09 |
42 CFR 440.210;
42 CFR 440.220; 42 CFR 440.225 |
He-W 543.10 |
42 CFR 433.139 |
He-W 543.11 |
42 CFR 455; 42
CFR 447; 42 CFR 456 |
He-W 543.12 |
42 CFR 433,
Subpart D |
He-W 543.13 |
42 CFR 431.107;
42 CFR 447.204; 42 CFR 447.250-255 |
He-W 544.01 |
RSA 137-J, 42
CFR 418.3, SSA Sec. 1905(o)[42 USC 1396d(o)], SSA Sec. 1861(dd)[42 USC
1395x] |
He-W 544.02 |
SSA
Sec 1905(o)(1)(C) [42 USC 1396d], as amended by Section 2302 of the
Affordable Care Act, SSA
Sec. 1812(d)(2)[42 USC 1395d], SSA Sec. 1905(o)[42 USC 1396d(o)], SSA Sec.
1861(dd)[42 USC 1395x], 42 CFR 418.20, 42 CFR 418.24 |
He-W 544.03 |
SSA Sec.1861
(dd)(1)[42 USC1395x], RSA 151:2, 42 CFR Part 418, Subparts C & D |
He-W 544.04 |
SSA Sec.
1905(o)[42 USC 1396d(o)], 42 CFR 418, Subpart B |
He-W 544.05 |
SSA Sec. 1905(o)(2)(B) [42 USC
1396d(o)], SSA Sec. 1812(d)(1)[ 42 USC 1395d], 42 CFR 418.21, 42 CFR 418.24 |
He-W 544.06 |
42 CFR 418.22 |
He-W 544.07 |
42 CFR 418.30 |
He-W 544.08 |
42 CFR 418.28 |
He-W 544.09 |
SSA, Sec.
1861(dd)[42 USC1395x], 42 CFR 418.200, 42 CFR 418.202, 42 CFR 418.204,
42 CFR 418.58 |
He-W 544.10 |
42 CFR 431.107,
42 CFR 455, 42 CFR 456 |
He-W 544.11 |
42 CFR 455; 42
CFR 456 |
He-W 544.12 |
42 CFR 433.139 |
He-W 544.13 |
SSA, Sec.
1861(dd)[42 USC1395x], SSA, Sec. 1814(a)[42 USC 1395(a)], SSA, Sec.
1905(o)[42 USC 1396d(o)], 42 CFR 418, Subpart G |
He-W 544.14 |
SSA, Sec.
1905(o)[42 USC 1396d(o)], 42 CFR 418.302(f) |
He-W 544.15 |
SSA, Sec.
1902(a)(13)[42 USC 1396a(a)(13)] |
He-W 544.16 |
SSA, Sec.
1812(d)(1)[42 USC 1395d], 42 CFR 418.304 |
He-W 544.17(b) |
RSA
541-A:19-b |
He-W 546.01 |
42 CFR 441,
Subpart B |
He-W 546.02 |
42 CFR
440.40(b), 42 CFR 441.50 |
He-W 546.03 |
42 CFR 441.56 |
He-W 546.04 |
42 CFR 441.61,
42 CFR 431.107 |
He-W 546.05 |
42 CFR 440.230;
42 CFR 441.56, 42 CFR 441.58, 42 CFR 441.62 |
He-W 546.06 |
42 CFR 440.230,
42 CFR 456.3 |
He-W 546.07 |
42 CFR 441.61 |
He-W 546.08 |
42 CFR
440.230(d) |
He-W 546.09 |
42 CFR 455, 42
CFR 456 |
He-W 546.10 |
42 CFR 433.139 |
He-W 546.11 |
42 CFR 447.15,
42 CFR 447, Subpart B |
He-W 547.01 |
RSA 167:66-68 |
He-W 547.02 |
RSA 167:68, I |
He-W 547.03 |
RSA 167:68,
II(e) |
He-W 547.04 |
RSA 167:68, II(e) |
He-W 547.05 |
RSA 167:66-68 |
He-W 547.06 |
RSA 167:66-68 |
He-W 547.07 |
42 CFR 456 |
He-W 547.08 |
42 CFR 433.139 |
He-W 547.09 |
RSA 541-A:21,
III |
He-W 548.01 |
42 CFR
440.250(p) |
He-W 548.02 |
42 CFR 440.210,
42 CFR 440.220, 42 CFR 440.225, 42 CFR 440.250(p) |
He-W 548.03 |
42 CFR 440.50,
42 CFR 440.60(a), 42 CFR 440.70, 42 CFR 440.90, 42 CFR 440.130, 42 CFR
440.165, 42 CFR 440.166 |
He-W 548.04 |
42 CFR
440.250(p), 42 CFR 440.210(a)(2) |
He-W 548.05 |
42 CFR 440.250(p) |
He-W 548.06 |
42 CFR
440.250(p), 42 CFR 455, 42 CFR 447 |
He-W 548.07 |
42 CFR 456.3 |
He-W 548.08 |
42 CFR 433.139 |
He-W 548.09 |
42 CFR 455, 42
CFR 447; RSA 161:4, VI(a) |
He-W 549.01 |
42 USC 1396; 42
USC 702 |
He-W 549.02 |
42 CFR 440.210;
42 CFR 440.220; 42 CFR 440.225; 42 CFR 440.250(p) |
He-W 549.03 |
42 CFR
440.230(d) |
He-W 549.04 |
RSA 326-B:1; RSA
326-B:10; RSA 326-B:6; RSA 326-H:12; 42 CFR 440.166;
42 CFR 440.60(a) |
He-W 549.04(a)
intro and (a)(1) |
42 CFR 440.166;
42 CFR 440.60(a) |
He-W 549.05 |
42 CFR 440.210(a)(2);
42 CFR 440.250(p); 42 CFR 440.220; 42 CFR 440.225;
42 CFR 440.130; 42 CFR 441.20 |
He-W 549.06 |
42 CFR
440.230(d) |
He-W 549.07 |
RSA 132:12 |
He-W 549.07(a)
intro, (a)(2) intro and (a)(2)b. |
RSA 132:12 |
He-W 549.08 |
42 CFR 455; 42
CFR 456.33 |
He-W 549.09 |
42 CFR 433.139 |
He-W 549.10 |
42 CFR 447.15 |
He-W
550.01-550.08 |
RSA 161:2, VI
& VIII, 42 CFR Section 440.130(c) & (d) |
He-W 552.01 |
42 CFR 440.167,
RSA 161-E:1 |
He-W 552.02 |
42 CFR 440.167,
RSA 161-E:1 |
He-W 552.03 |
42 CFR 440.167,
42 CFR 440.210, 42 CFR 440.220, RSA 161-E:1 |
He-W 552.04 |
42 CFR 440.167,
RSA 161-E:1 |
He-W 552.05 |
42 CFR 440.167,
RSA 161-E:1 |
He-W 552.05 |
42 CFR 440.167,
RSA 161-E:1 |
He-W 552.06 |
42 CFR 440.167,
RSA 161-E:1 |
He-W 552.07 |
42 CFR 440.167,
RSA 161-E:1 |
He-W 552.08 |
42 CFR 440.167,
RSA 161-E:1 |
He-W 552.09 |
42 CFR 440.167,
RSA 161-E:1 |
He-W 552.10 |
42 CFR 455, 42
CFR 456 |
He-W 552.11 |
42 CFR 433.139 |
He-W 552.12 |
42 CFR 440.167,
RSA 161-E:1 |
He-W 552.13 |
42 CFR 440.167,
RSA 161-E:1 |
He-W 553.01 |
42 CFR 440.70;
RSA 326-B:18 |
He-W 553.02 |
42 CFR 440.70;
42 CFR 440.210; 42 CFR 440.220; 42 CFR 441.15; RSA 326-B |
He-W 553.03 |
42 CFR 440.70;
42 CFR 440.210; 42 CFR 440.220 |
He-W 553.04 |
42 CFR
440.70(d); RSA 151:2-b,I |
He-W 553.05 |
42 CFR 440.70;
42 CFR 440.230; 42 CFR 484.55 |
He-W 553.06 |
42 CFR 440.70; 42
CFR 441.15; RSA 326-B |
He-W 553.07 |
42 CFR
440.230(d) |
He-W 558.01-558.09 |
Section 1915 (c)
of the Social Security Act |
He-W 559.01 |
Section
1905(a)(19) and Section 19115(g)(2) Social Security Act |
He-W 559.02 |
42 CFR 440.210,
42 CFR 440.220 and 42 CFR 440.225 |
He-W 559.03 |
42 CFR 440.70
and 42 CFR 440.60 |
He-W 559.04 |
42 CFR 440.70
and 42 CFR 440.230 |
He-W 559.05 |
42 CFR 441.15
and 42 CFR 440.230 |
He-W 559.06 |
42 CFR 456.30 |
He-W 559.07 |
42 CFR 433.139 |
He-W 559.08 |
42 CFR 447.15
and 42 CFR 430.0 |
He-W 565.01 |
RSA 327-A:1 |
He-W 565.01(a),
(e) & (f) |
42 CFR 440.210;
42 CFR 440.220 |
He-W 565.02 |
42
CFR 440.210; 42
CFR 440.220 |
He-W 565.03 |
42 CFR 440.120 |
He-W 565.04 |
42 CFR 440
Subpart B |
He-W 565.05 |
42 CFR 440.120 |
He-W 565.06 |
42 CFR 440.120 |
He-W 565.07 |
42
CFR 455; 42 CFR 456 |
He-W 565.08 |
42 CFR 433.139 |
He-W 565.09 |
RSA 541-A:21; 42CFR
447 Subpart B |
He-W 566.01 |
42 CFR 440.100,
and 42 CFR 440.40 |
He-W 566.02 |
42 CFR 440.210,
42 CFR 440.220, and 42 CFR 440.225 |
He-W 566.03 |
42 CFR 440.100,
42 CFR 431.107, and 42 CFR 431.108 |
He-W 566.04 |
42 CFR 440.100,
42 CFR 440.40, 42 CFR 441.56, 42 CFR 440.225, and 42 CFR 440.50 |
He-W 566.05 |
42 CFR 440.225,
42 CFR 440.40, and 42 CFR 441.56 |
He-W 566.06 |
42 CFR 440.230 |
He-W 566.07 |
42 CFR 440.230 |
He-W 566.08 |
42 CFR 455, 42
CFR 456, 42 CFR 447, and 42 CFR 1001 |
He-W 566.09 |
42 CFR 433,
Subpart D |
He-W 566.10 |
42 CFR Subpart
B, and RSA 161:4,VI(a) |
He-W
567.01 |
RSA
137-F:2, IV; Section 216(i)(l) of the SSA; Section
1614(a)(2) of the SSA, 42 USC 416, 42 USC 1382c |
He-W
567.02 |
42
CFR 440.210; 42 CFR 440.220 |
He-W
567.03 |
RSA
137-F:11; RSA 137-F:8; 42 CFR 440.110; 42 CFR 440.120; 42 CFR 440.70 |
He-W
567.04 |
42
CFR 440.230 |
He-W
567.05 |
42
CFR 440.110; 42 CFR 440.120; 42 CFR 440.70; 42 CFR 441.57 |
He-W
567.06 |
42
CFR 440.110; 42 CFR 440.120; 42 CFR 440.70; 42 CFR 440.230 |
He-W
567.07 |
42
CFR 440.230 |
He-W
567.08 |
42
CFR 431.107 |
He-W
567.09 |
42
CFR 455; 42 CFR 456 |
He-W
567.10 |
42
CFR 433, Subpart D |
He-W
567.11 |
42
CFR 447.204 |
He-W 568.01 |
RSA 161:4-a, IX
|
He-W 568.02 |
42 CFR 440.210;
42 CFR 440.220; 42 CFR 440.225 |
He-W 568.03 |
42 CFR 440.110 |
He-W 568.04 |
42 CFR 440 Subpart
B |
He-W 568.05 |
42 CFR 440.10 |
He-W 568.06 |
42 CFR 440.110 |
He-W 568.07 |
42 CFR 455; 42
CFR 456; 42 CFR 1001 |
He-W 568.08 |
42 CFR 440.10 |
He-W 568.09 |
42 CFR 433.139 |
He-W 568.10 |
42 CFR 447 Subpart
B |
He-W 569.01 |
42 CFR 440.30 |
He-W 569.02 |
42 CFR 440.210;
42 CFR 440.220 |
He-W 569.03 |
42 CFR 440.30; 42 CFR 441.17
|
He-W 569.04 |
42 CFR 440,
Subpart B |
He-W 569.05 |
42 CFR 440.30
|
He-W 569.06 |
42 CFR 440.230; 42 CFR 456.3
|
He-W 569.07 |
42 CFR 455; 42
CFR 456 |
He-W 569.08 |
42 CFR 433.139 |
He-W 569.09 |
42 CFR 447,
Subpart B; RSA 161:4, VI; RSA 541-A:21, III, |
He-W
570.01 |
RSA 318:1, VII;
RSA 318:1, XV, RSA 318:1, XVI, RSA 318:21; |
He-W
570.01(a), (p), (q) |
42 CFR 447.502;
RSA 541-A:21, VIII |
He-W
570.01(a) & (q) |
42
CFR 447.502; RSA 541-A:21, VIII |
He-W
570.01(s) |
RSA
318:1, VII; RSA 318:1, XV, RSA 318:1, XVI, RSA 318:21; RSA 126-A:3, III(b),
21CFR 310.6, 42 CFR 440.120, 42 CFR 447.53; 42 CFR 456 subpart K; Chapter 188
and 281:9, 2004, SB 383-FN, 2004 |
He-W 570.01(u),
(aa), (ab) |
RSA 318:1, VII;
RSA 318:1, XV, RSA 318:1, XVI, RSA 318:21; RSA 126-A:3, III(b), 21CFR 310.6,
42 CFR 440.120, 42 CFR 447.53; 42 CFR 456 subpart K; Chapter 188 and 281:9,
2004, SB 383-FN, 2004 |
He-W 570.02 |
42 CFR 440.210,
42 CFR 440.220; 42 CFR 440.225 |
He-W 570.03 |
42 CFR 440.120,
RSA 318 |
He-W 570.04 |
42 CFR 440.120,
42 CFR 441.25, 42 CFR 440.225, 42 CFR 440.230(d), 42 CFR 431 Subpart E, 42
USC 1396r-8(d), 42 USC 1396r-8(k)(2) |
He-W 570.05 |
42 USC
1396r-8(d)(2)(k) |
He-W 570.06 |
42 CFR
431.54(e), 42 CFR 431 Subpart E, 42 CFR 440.230(d), 42 USC 1396r-8(d)(5) and
(6); RSA 126-A:5, VIII |
He-W 570.07 |
42 CFR 431.54(e) |
He-W 570.08 |
RSA 318-B:9, IV,
21 CFR 1306.22; 42 USC 1396r-8(d)(7) |
He-W 570.09 |
RSA 318:47-c |
He-W 570.10 |
RSA 146-B:5; RSA
318:47 |
He-W 570.11 |
42 CFR 456 |
He-W 570.12 |
42 USC
1396r-8(g), 42 CFR 456.3 |
He-W 570.13 |
42 USC 1396o; 42
CFR 447.53, 42 CFR 447.56 |
He-W 570.14 |
42 CFR 447 |
He-W 570.14 (a)
intro, (a)(2) intro, and (a)(2)a. & b. |
42 CFR 447.512(b) |
He-W
570.15 |
RSA 151:2, 42 USC 1396r-8 |
He-W 571.01 |
42 CFR 440.120 |
He-W 571.02 |
42 CFR 440.210;
42 CFR 440.220 |
He-W 571.03 |
42
CFR 440.50; 42 CFR 440.60; 42 CFR 440.166; 42 CFR 431.107; RSA 328-D:1 |
He-W 571.04 |
RSA
415:6-c; RSA 415:18-n; RSA 415:18-d; RSA 126-A:5,VII;42 CFR 440.230; 42 CFR
440.130(a); RSA 541-A:21, VIII; |
He-W 571.05 |
42 CFR
440.230(d); 42 CFR 456.3 |
He-W 571.06 |
42 CFR
440.230(d); 42 CFR 456.3 |
He-W 571.07 |
42 CFR 431.107;
42 CFR 455 Subparts A and B; 42 CFR 447 Subparts A and B; 42 CFR 456 Subparts
A and B |
He-W 571.08 |
42 CFR 431.107,
42 CFR 433 Subpart D |
He-W 571.09 |
42 CFR 455 Subparts A and B; 42 CFR 456
Subparts A and B |
He-W 571.10 |
42 CFR 455
Subparts A and B; 42 CFR 456 Subparts A and B, 42 CFR 447.45; RSA 161:4,
VI(a); RSA 126-A:3, III(b) |
He-W 572.01 |
42 CFR 440.170 |
He-W 572.02 |
42 CFR 440.210,
42 CFR 440.220 |
He-W 572.03 |
42 CFR 440.60,
RSA 153A-11, 42 CFR 440.170 |
He-W 572.04 |
42 CFR 440.170 |
He-W 572.05 |
42 CFR 440.170 |
He-W 572.06 |
42 CFR 440.230 |
He-W 572.07 |
42 CFR 431.107 |
He-W 572.08 |
42 CFR 455 |
He-W 572.09 |
42 CFR 433.139 |
He-W 572.10 |
RSA 541-A:21,
III, 42 CFR 447.200, 42 CFR 447.202, 42 CFR 447.204 |
He-W 573.01 |
42 CFR 440.170 |
He-W 573.02 |
42 CFR 440.210,
42 CFR 440.220 |
He-W 573.03 |
42 CFR 440.170 |
He-W 573.04 |
42 CFR 440,
Subpart B |
He-W 573.05 |
42 CFR 440.170 |
He-W 573.06 |
42 CFR 456 |
He-W 573.07 |
42 CFR 433.139 |
He-W 573.08 |
RSA 541-A:21,
III, 42 CFR 447, Subpart B |
He-W 573.09 |
42 CFR 456.4 |
He-W 573.10 |
42 CFR 431.107;
42 CFR 440.230 |
He-W 573.11 |
42 CFR 456 |
He-W 573.12 |
42 CFR 433.139 |
He-W 573.13 |
RSA 541-A:21,
III; 42 CFR 447, Subpart B |
He-W 574.01 |
42 CFR 441.62;
42 CFR 431.53 |
He-W 574.02 |
42 CFR 441.62;
42 CFR 431.53; 42 CFR 440.170 |
He-W 574.03 |
42 CFR 441.62;
42 CFR 431.53; 42 CFR 431.107; 42 CFR 455; RSA 161:4-a, XI |
He-W
574.03(b)(2), (c)(1) & (d)(5) |
42 CFR
455.104(b)(1)(ii) |
He-W 574.04 |
42 CFR 441.62;
42 CFR 431.53; 42 CFR 440 Subpart B; 42 CFR 440.170 |
He-W 574.05 |
42 CFR 441.62;
42 CFR 431.53; 42 CFR 440 Subpart B |
He-W 574.06 |
RSA 541-A:21,
III; 42 CFR 447, Subpart B |
He-W 574.07 |
RSA 541-A:21,
III; 42 CFR 447, Subpart B |
He-W 574.08 |
42 CFR 431.107;
42 CFR 440.230 |
He-W 574.09 |
42 CFR 431.107;
42 CFR 440.230 |
He-W 574.10 |
42 CFR 431.53 |
He-W 574.11 |
42 CFR 431.220 |
He-W 574.12 |
42 CFR 433.139 |
He-W 574.13 |
42 CFR 455; 42 CFR
456 |
He-W
575.01 |
42 CFR 440.120 |
He-W
575.02 |
42 CFR 440.210; 42 CFR 440.220 |
He-W
575.03 |
42 CFR 440.50; 42 CFR 440.60; 42 CFR 440.166; RSA 328-D:1 |
He-W
575.04 |
RSA 415:6-C; RSA 415:18-n; 42 CFR 440.230; 42 CFR
440.130(a) |
He-W
575.05 |
42 CFR 440.230(d) |
He-W
575.06 |
42 CFR 440.230(d) |
He-W
575.07 |
42 CFR 440.230(d) |
He-W
575.08 |
42 CFR 431.107 |
He-W
575.09 |
42 CFR 433.139 |
He-W
575.10 |
42 CFR 455; 42 CFR 456 |
He-W
575.11 |
42 CFR 447.15 |
He-W 577.01 |
42 CFR 440.30 |
He-W
577.02 |
42
CFR 440.210; 42 CFR 440.220 |
He-W
577.03 |
42 CFR 440.30;
42 CFR 441.17 |
He-W
577.04 |
42 CFR 440.30 |
He-W
577.05 |
42 CFR 455; 42
CFR 456 |
He-W
577.06 |
42 CFR 433.139 |
He-W
577.07 |
42 CFR 447,
Subpart B; RSA 161:4, VI |
He-W
591.01(a) |
42 CFR 488.442 |
He-W 591.01(b) |
42 CFR 488.3 |
He-W 591.01(c) –
(e) |
42 CFR 488.400 -
488.456 |
He-W 591.01(f) |
42 USC 1396r(b) |
He-W 591.01(g) |
42 CFR 488.402 |
He-W 591.01(h) |
42 USC 1396r(a) |
He-W 591.01(i) – (l) |
42 CFR 488.400 -
488.456 |
He-W 591.02(a) |
42 CFR
488.11(b), 42 USC 1396r(h) |
He-W 591.02(b) |
42 CFR
488.110(j) |
He-W 591.02(c) |
42 CFR 488.402-
488.406 |
He-W 591.03 |
42 CFR 488.404-488.446 |
He-W 591.04(a) |
42 CFR
488.402(f)(3) |
He-W 591.04(b) |
42 CFR
488.402(f)(4) |
He-W 591.04(c) |
42 CFR
488.402(f); 42 CFR 488.406(a) |
He-W 591.04(d) |
42 CFR 488.454 |
He-W 591.05 |
42 CFR 488.415;
42 CFR 488.454 |
He-W 591.06 |
42 CFR
488.430-488.444 |
He-W 591.07 |
42 CFR 488.442 |
He-W 591.08 |
42 CFR
448.442(f) |
He-W 591.09 |
42 CFR 488.330;
42 CFR 488.454 |
He-W 591.10 |
42 CFR 488.454 |
He-W 591.11 (a)
and (b) |
RSA 541-A:31 |
He-W 591.11(c) |
42 CFR 431.153(g) |
He-W 591.11(d) |
42 CFR
488.404(b), 42 CFR 431.151(d) |
He-W 591.11(e) |
42 CFR 488.438 |
He-W 591.11(f) |
42 CFR
431.151(c) |
He-W 591.11(g) –
(k) |
RSA 541-A:31 |
He-W 591.11(l) |
42 CFR 488.438
(e) and (f) |
He-W 591.11(m) |
RSA 541-A:31 |
He-W 591.12 (a)
– (c) |
RSA 541-A:31 |
He-W 591.12 (d) |
42 CFR
431.153(k) |
He-W 591.13 |
42 CFR 488.426 |
He-W 591.14 |
42 CFR 488.452 |
He-W 593.01 |
RSA 541-A:7; RSA
161:4, VI(a) |
He-W 593.02 - 593.34 |
RSA 161:4,
VI(a); 1902 (a)(13) of the SSA |
He-W 593.35 |
1902 (a)(13) of
the SSA, RSA 161:4, VI(a) |
He-W 593.36 |
RSA 161:4,
VI(a), 1902 (a)(13) of the SSA |
He-W 593.37 |
1902 (a)(13) of
the SSA, RSA 161:4, VI(a) |
He-W 593.38 - 593.40 |
RSA 161:4,
VI(a), 1902 (a)(13) of the SSA |
He-W 593.41 |
RSA 541-A:31-36 |
He-W 593.42 |
RSA 161:4,VI(a),
1902 (a)(13) of the SSA |