Civilian Health and Medical Program of the Department of Veterans Affairs, 2396-2412 [2018-00332]
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effects of this rule elsewhere in this
preamble.
F. Environment
We have analyzed this proposed rule
under Department of Homeland
Security Management Directive 023–01,
which guides the Coast Guard in
complying with the National
Environmental Policy Act of 1969 (42
U.S.C. 4321–4370f), and have made a
preliminary determination that this
action is one of a category of actions that
do not individually or cumulatively
have a significant effect on the human
environment. This proposed rule
involves two safety zones lasting one
hour that would prohibit entry within a
one-mile section of the Lower
Mississippi River. They are categorically
excluded from further review under
paragraph L60(a) of Appendix A, Table
1 of DHS Instruction Manual 023–01–
001–01, Rev. 01. A preliminary Record
of Environmental Consideration
supporting this determination is
available in the docket where indicated
under ADDRESSES. We seek any
comments or information that may lead
to the discovery of a significant
environmental impact from this
proposed rule.
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G. Protest Activities
The Coast Guard respects the First
Amendment rights of protesters.
Protesters are asked to contact the
person listed in the FOR FURTHER
INFORMATION CONTACT section to
coordinate protest activities so that your
message can be received without
jeopardizing the safety or security of
people, places, or vessels.
V. Public Participation and Request for
Comments
We view public participation as
essential to effective rulemaking, and
will consider all comments and material
received during the comment period.
Your comment can help shape the
outcome of this rulemaking. If you
submit a comment, please include the
docket number for this rulemaking,
indicate the specific section of this
document to which each comment
applies, and provide a reason for each
suggestion or recommendation.
We encourage you to submit
comments through the Federal
eRulemaking Portal at https://
www.regulations.gov. If your material
cannot be submitted using https://
www.regulations.gov, contact the person
in the FOR FURTHER INFORMATION
CONTACT section of this document for
alternate instructions.
We accept anonymous comments. All
comments received will be posted
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without change to https://
www.regulations.gov and will include
any personal information you have
provided. For more about privacy and
the docket, visit https://
www.regulations.gov/privacyNotice.
Documents mentioned in this NPRM
as being available in the docket, and all
public comments, will be in our online
docket at https://www.regulations.gov
and can be viewed by following that
website’s instructions. Additionally, if
you go to the online docket and sign up
for email alerts, you will be notified
when comments are posted or a final
rule is published.
List of Subjects in 33 CFR Part 165
Harbors, Marine safety, Navigation
(water), Reporting and recordkeeping
requirements, Security measures,
Waterways.
For the reasons discussed in the
preamble, the Coast Guard proposes to
amend 33 CFR part 165 as follows:
PART 165—REGULATED NAVIGATION
AREAS AND LIMITED ACCESS AREAS
1. The authority citation for part 165
continues to read as follows:
Coast Guard assigned to units under the
operational control of USCG Sector New
Orleans.
(2) Vessels requiring entry into this
safety zone must request permission
from the COTP or a designated
representative. They may be contacted
on VHF–FM Channel 16 or 67.
(3) Persons and vessels permitted to
enter these safety zones must transit at
their slowest safe speed and comply
with all lawful directions issued by the
COTP or the designated representative.
(c) Information broadcasts. The COTP
or a designated representative will
inform the public through Broadcast
Notices to Mariners of any changes in
the planned schedule.
Dated: January 11, 2018.
Wayne R. Arguin,
Captain, U.S. Coast Guard, Captain of the
Port Sector New Orleans.
[FR Doc. 2018–00652 Filed 1–16–18; 8:45 am]
BILLING CODE 9110–04–P
DEPARTMENT OF VETERANS
AFFAIRS
■
38 CFR Part 17
Authority: 33 U.S.C. 1231; 50 U.S.C. 191;
33 CFR 1.05–1, 6.04–1, 6.04–6, and 160.5;
Department of Homeland Security Delegation
No. 0170.1.
RIN 2900–AP02
2. Add § 165.T08–1058 to read as
follows:
AGENCY:
§ 165.T08–1058 Safety Zones; Lower
Mississippi River, New Orleans, LA
SUMMARY:
■
(a) Safety Zones. The following areas
are a safety zone:
(1) Bayou Country Music Fest, New
Orleans, LA.
(i) Location: All navigable waters of
the Lower Mississippi River between
mile marker (MM) 95.4 and MM 96.4,
above Head of Passes.
(ii) Effective Period: This rule is
effective from 7:45 p.m. through 8:45
p.m. on May 25, 2018.
(2) NOLA Tricentennial 2018 Jazz and
Heritage Fest.
(i) Location: All navigable waters of
the Lower Mississippi River between
mile marker (MM) 94 and MM 95, above
Head of Passes.
(ii) Effective Period: This rule is
effective from 8 p.m. through 9 p.m. on
May 6, 2018.
(b) Regulations. (1) In accordance
with the general regulations in § 165.23
of this part, entry into these zones is
prohibited unless specifically
authorized by the Captain of the Port
Sector New Orleans (COTP) or a
designated representative. A designated
representative is a commissioned,
warrant, or petty officer of the U.S.
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Civilian Health and Medical Program of
the Department of Veterans Affairs
ACTION:
Department of Veterans Affairs.
Proposed rule.
The Department of Veterans
Affairs (VA) proposes to amend its
regulations governing the Civilian
Health and Medical Program of the
Department of Veterans Affairs
(CHAMPVA). The proposed revisions
would clarify and update these
regulations to conform to changes in law
and policy that control the
administration of CHAMPVA and
would include details concerning the
administration of CHAMPVA that are
not reflected in current regulations. The
proposed revisions would also expand
covered services and supplies to include
certain preventive services and
eliminate cost-share amounts and
deductibles for certain covered services.
DATES: Written comments must be
received on or before March 19, 2018.
ADDRESSES: Written comments may be
submitted through https://
www.Regulations.gov; by mail or handdelivery to the Director, Regulation and
Policy Management (00REG),
Department of Veterans Affairs, 810
Vermont Avenue NW, Room 1068,
Washington, DC 20420; or by fax to
(202) 273–9026. Comments should
indicate that they are submitted in
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response to ‘‘RIN 2900–AP02, Civilian
Health and Medical Program of the
Department of Veterans Affairs.’’ Copies
of comments received will be available
for public inspection in the Office of
Regulation Policy and Management,
Room 1063B, between the hours of 8:00
a.m. and 4:30 p.m. Monday through
Friday (except holidays). Please call
(202) 461–4902 for an appointment.
(This is not a toll-free number.) In
addition, during the comment period,
comments may be viewed online
through the Federal Docket Management
System at https://www.Regulations.gov.
FOR FURTHER INFORMATION CONTACT:
Joseph Duran, Director, Policy and
Planning, Office of Community Care
(OCC), 3773 Cherry Creek North Drive,
Denver, Colorado 80209,
Joseph.Duran2@va.gov, (303) 370–1637.
(This is not a toll-free number.)
SUPPLEMENTARY INFORMATION: The
Civilian Health and Medical Program of
the Department of Veterans Affairs
(CHAMPVA) is a health benefits
program in which the Department of
Veterans Affairs (VA) shares the cost of
covered medical care services and
supplies with spouses, children,
survivors, and certain caregivers of
veterans who meet eligibility criteria
under 38 U.S.C. 1781. CHAMPVA
beneficiaries must not be eligible for
TRICARE, a health care program
administered by the Department of
Defense (DoD) that is also authorized to
provide health care to certain family
members of veterans. Certain Primary
Family Caregivers designated under 38
U.S.C. 1720G(a)(7)(A) are eligible under
section 1781 as long as they are not
entitled to services under a health-plan
contract as that term is defined in 38
U.S.C. 1725(f).
Under section 1781, VA ‘‘shall
provide for medical care in the same or
similar manner and subject to the same
or similar limitations as medical care is
furnished to certain dependents and
survivors of active duty and retired
members of the Armed Forces under
chapter 55 of title 10 [United States
Code] (CHAMPUS).’’ 38 U.S.C. 1781(b).
CHAMPUS was the original program
administered by DoD to provide civilian
health benefits for active duty military
personnel, military retirees, and their
dependents. 32 CFR 199.1. Although the
CHAMPUS program is still referenced
in DoD regulations, DoD effectively
replaced the CHAMPUS program with
what is commonly known as the
‘‘TRICARE Standard’’ plan
(‘‘TRICARE’’). See 32 CFR 199.1(r),
199.17(a)(6)(ii)(C) (identifying
‘‘TRICARE Standard’’ as the basic
CHAMPUS program). TRICARE’s
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current benefit structure offers varying
degrees of medical benefits under
multiple plan options beyond its
Standard plan, but we administer
CHAMPVA in the same or similar
manner as TRICARE Standard only,
because that basic program is the one
that is referenced by the CHAMPUS
authority. Thus, all references in this
rulemaking to ‘‘TRICARE’’ are to the
TRICARE Standard plan, which we refer
to simply as ‘‘TRICARE’’ throughout
most of this rulemaking for ease of
reference.
VA interprets the mandate in 38
U.S.C. 1781(b) to administer CHAMPVA
in the ‘‘same or similar manner . . . as
medical care is furnished . . . under
title 10 chapter 55 (CHAMPUS)’’ to
mean that we must generally administer
CHAMPVA in a ‘‘same or similar
manner’’ as the TRICARE Standard
plan. The phrase ‘‘same or similar
manner’’ does not require the programs
to be administered in an identical
manner. Rather, we broadly interpret
this language as affording us needed
flexibility to administer the program for
CHAMPVA beneficiaries. For this
reason, not every aspect of CHAMPVA
will find a corollary in the TRICARE
Standard Plan.
TRICARE has undergone changes in
legal authority and policy that have
prompted these proposed revisions to
our CHAMPVA regulations. This
rulemaking is intended to ensure that
our regulations continue to be, again
broadly speaking, the same or similar to
the regulations and policies governing
TRICARE. As noted throughout this
proposed rule, there are necessary
variations from TRICARE, particularly
due to TRICARE’s current benefit
structure with varying degrees of
medical benefits under multiple plan
options, but we believe these variations
satisfy the same or similar requirement
in 38 U.S.C. 1781(b).
This rulemaking also proposes
clarifications and revisions that will
improve our ability to effectively
administer CHAMPVA, as well as
technical revisions to make our
regulations more understandable.
17.270 General Provisions and
Definitions
Current § 17.270(a) broadly discusses
general administrative provisions of
CHAMPVA, and current § 17.270(b)
establishes certain definitions for the
CHAMPVA regulations. We would
revise the title of § 17.270 to clearly
indicate that it contains both general
provisions as well as definitions and
would revise and reorganize the current
definitions as well as add new
definitions. Finally, we would add a
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new paragraph (c) to permit VA to
waive, under certain circumstances, any
requirements in the CHAMPVA
regulations that are not otherwise
required by statute, as is allowed under
TRICARE. See 32 CFR 199.1(n). Waiver
would be limited to very unusual and
limited circumstances when waiver was
determined to be in the best interests of
VA; would not set a precedent for future
decisions; and would not be used to
deny any individual any right, benefit,
or privilege provided to him or her by
statute or these regulations.
Proposed § 17.270(a) would continue
to provide an overview of CHAMPVA,
including a general summary of the
manner in which CHAMPVA is
administered. We would refer to
CHAMPUS, as we do in the current
regulation, but would also reference
TRICARE because the reference to
CHAMPUS is outdated, as explained
above, and may be misunderstood by
CHAMPVA beneficiaries. Current
§ 17.270(a) states that CHAMPVA is
administered by the ‘‘Health
Administration Center’’ (HAC) (referred
to now as the Office of Community Care
(OCC)), which is located in Denver,
Colorado. We propose to delete this
statement because that fact is not
substantively relevant to the regulations.
These revisions are not substantively
different from current § 17.270(a).
Proposed § 17.270(a)(1) would state
that an authorized non-VA provider
may provide medical services and
supplies that are covered by
CHAMPVA. This is current practice and
would reflect in regulation VA’s
authority to provide CHAMPVAcovered services and supplies under 38
U.S.C. 1781(b)(2). As explained in
greater detail below in connection with
proposed § 17.272(b)(3), CHAMPVAcovered services and supplies are those
provided by authorized non-VA
providers who agree to provide covered
services and supplies to CHAMPVA
beneficiaries in exchange for payment of
the CHAMPVA determined allowable
amount. Proposed § 17.270(a)(2) would
also reference VA’s alternate authority
under section 1781(b) to provide
medical care to CHAMPVA beneficiaries
through VA medical facilities equipped
to provide the care and services if such
resources are not being used for the care
of eligible veterans. This initiative is
called the CHAMPVA In-house
Treatment Initiative (CITI) and would be
referenced as such in proposed
§ 17.270(a)(2). CITI affords beneficiaries
the same medical services available to
veterans. CITI claims submitted to OCC
are processed in the same manner as all
other CHAMPVA claims. However, a
monthly transfer of funds, or Transfer
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Dispersing Authority (TDA), from OCC
to the providing VA facility is used to
reimburse CITI claims whereas
electronic funds transfer or paper
checks are used to reimburse
beneficiaries and providers for non-CITI
claims.
With regards to CHAMPVA
beneficiaries receiving care in VA
medical facilities through CITI, we have
historically interpreted section 1781(b)
to mean that such care may be provided
only if the CHAMPVA beneficiary is not
also eligible for Medicare benefits. We
base this interpretation on the fact that
CHAMPVA has always been the last
payer for CHAMPVA-covered medical
services and supplies when a
CHAMPVA beneficiary has Medicare
(included in this rulemaking’s
definition of ‘‘other health insurance’’
(OHI), see 38 U.S.C. 1781(d)(2)). The
mandated coordination of benefits
found in section 1781(d)(2) is
essentially the same as the requirement
in TRICARE codified at 32 CFR 199.8,
which provides that if a TRICARE
beneficiary is eligible for both Medicare
and TRICARE, Medicare is the primary
payer and TRICARE is the secondary
payer. In addition, this policy limitation
for CITI is reasonable because VA is a
publicly funded health care system that
cannot bill Medicare (see section
1814(c) and section 1835(d) of the
Social Security Act, codified at 42
U.S.C. 1395f(c) and 1395n(d)).
Moreover, Medicare is an entitlement
program, whereas the provision of
CHAMPVA medical benefits is subject
to the availability of appropriations
which, for any given time period, might
or might not be sufficient to cover all
CHAMPVA-covered medical services
and supplies in a VA medical facility.
Requiring beneficiaries to use their
Medicare benefits first accomplishes our
goal of protecting all patients’ access to
care. Therefore, we would further clarify
in proposed § 17.270(a)(2) that any
CHAMPVA beneficiary who is also
eligible for Medicare benefits may not
receive medical services and supplies
through CITI.
Proposed § 17.270(a)(3) would newly
indicate in regulation that outpatient
prescription medications may be
provided to certain CHAMPVA
beneficiaries through Medications by
Mail (MbM), administered by VA.
Proposed paragraph (a)(3)(i) would
further provide that VA’s MbM provides
prescription medications through the
mail to CHAMPVA beneficiaries who do
not have any OHI that pays for
prescriptions, including Medicare Part
D. This restriction largely is consistent
with TRICARE policy on the provision
of medications by mail, except that
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TRICARE covers prescribed medications
for beneficiaries with OHI in two
instances: When the prescribed
medication is not covered by the OHI or
when the beneficiary’s OHI prescription
benefit has been exhausted. See
TRICARE Pharmacy Program Handbook
(October 2015), pages 18–19.
CHAMPVA is unable to duplicate these
two exceptions due to system
limitations, meaning that CHAMPVA
will only provide prescription
medications through the mail to
beneficiaries who do not have any OHI
prescription coverage. Despite this,
CHAMPVA’s inclusion of prescription
medications is, broadly speaking,
sufficiently similar to TRICARE that VA
remains in substantial compliance with
the requirements of section 1781(b).
Proposed paragraph (a)(3)(ii) would
provide that smoking cessation
pharmaceutical supplies are available
only through MbM. Section 713 of the
Duncan Hunter National Defense
Authorization Act for Fiscal Year 2009,
Public Law 110–417 (October 14, 2008)
(‘‘2009 NDAA’’) required DoD to
establish a smoking cessation program
under TRICARE under which specified
smoking cessation benefits are to be
made available to beneficiaries who are
not also eligible for Medicare. This
TRICARE benefit is codified at 32 CFR
199.4(e)(30). As to the pharmaceutical
component of this TRICARE benefit,
smoking cessation pharmaceutical
agents (which VA refers to as
pharmaceutical supplies) are available
only through Military Treatment
Facility (MTF) pharmacies or the
TRICARE Mail Order Program. See 32
CFR 199.4(e)(30)(ii)(A) and
199.21(h)(2)(iii). Similar to 32 CFR
199.4(e)(30)(i), proposed
§ 17.270(a)(3)(ii) would provide that the
same smoking cessation supplies will be
made available to CHAMPVA
beneficiaries who are not eligible for
Medicare. Additionally, smoking
cessation pharmaceutical supplies
would be available only through MbM.
For purposes of CITI, we would not
provide smoking cessation
pharmaceutical supplies through VA
facility pharmacies because it is
administratively more efficient for
CHAMPVA to provide these through
MbM, and because, in complying with
the requirements of section 1781(b), as
discussed above, VA facility pharmacies
would be required to administer any
needed smoking cessation
pharmaceutical supplies first to veterans
before providing them to CHAMPVA
beneficiaries. We would also remove the
restriction on smoking cessation
services and supplies in current
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§ 17.272(a)(57), as discussed later in this
proposed rule.
For clarity, we would establish
abbreviations for the Civilian Health
and Medical Program of the Department
of Veterans Affairs as ‘‘CHAMPVA’’ and
the Department of Veterans Affairs as
‘‘VA.’’ The current regulations refer to
the part of VA that administratively
handles CHAMPVA claims as the
‘‘Center’’ in several places (see current
§§ 17.275–17.277), and to the ‘‘Health
Administration Center’’ in other places
(see current §§ 17.270, 17.275–17.276),
and we believe that referring to ‘‘VA’’ is
more appropriately descriptive and
would eliminate ambiguity.
Proposed § 17.270(b) would establish
definitions for the CHAMPVA
regulations. We would define ‘‘accepted
assignment’’ as the action of an
authorized non-VA provider who
accepts responsibility for the care of a
CHAMPVA beneficiary and thereby
agrees to accept the CHAMPVA
determined allowable amount as full
payment for services and supplies
rendered to the beneficiary. This
extinguishes the beneficiary’s payment
liability to the provider with the
exception of applicable cost shares and
deductibles. This definition is
consistent with our explanation for
proposed § 17.272(b)(3), which further
outlines the necessity for defining
‘‘accepted assignment.’’ Our current
regulations do not define the term
‘‘authorized provider,’’ but the term
‘‘authorized provider’’ (and variations
thereof) is used throughout current
§ 17.272 to refer to an institutional or
individual provider of CHAMPVAcovered services and supplies. The term
is used to describe persons or
institutions that are considered
appropriately licensed or credentialed
to competently provide medical services
and supplies to CHAMPVA
beneficiaries and that VA will pay to
provide such services and supplies. In
addition, an ‘‘authorized provider’’ has
historically been interpreted in
CHAMPVA to be a non-VA medical
provider. To capture this historical
interpretation in full, we would define
an ‘‘authorized non-VA provider’’ to
mean an individual or institutional nonVA provider of CHAMPVA-covered
medical services and supplies who is
licensed or certified by a State to
provide the covered medical services
and supplies, or is otherwise certified
by an appropriate national or
professional association that sets
standards for the specific medical
provider. This requirement for State
licensure or other certification would be
similar to TRICARE, which requires that
its providers be either licensed or
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certified by a State, or, where States do
not offer licensure or certification, be
otherwise certified by an appropriate
national or professional association that
sets standards for the specific medical
provider. See TRICARE Policy Manual
6010.60–M, Chapter 11 (‘‘Providers’’),
section 3.2 (‘‘State Licensure And
Certification’’). (For general operationaltype information, one can also refer to
TRICARE Operations Manual 6010.59–
M, Chapter 4, (‘‘Provider Certification
And Credentialing’’) (April 1, 2015).)
We would define ‘‘calendar year’’ as
the period of time between and
including January 1 through December
31. This is plain language and is
consistent with the generally
understood meaning of the phrase
‘‘calendar year.’’
The term ‘‘CHAMPVA beneficiary’’
would be defined as a person enrolled
for CHAMPVA under § 17.271. This
would be a program-specific definition,
but it is in plain language and is
consistent with the generally
understood meaning of the word
‘‘beneficiary.’’ To clarify, an individual
is enrolled in CHAMPVA only after the
individual has successfully completed
the application process (i.e., where the
individual submits a completed VA
Form 10–10d to VA, and VA has
confirmed the individual’s eligibility).
We would define ‘‘CHAMPVAcovered services and supplies’’ to mean
those medical services and supplies that
are medically necessary and appropriate
for the treatment of a condition and that
are not specifically excluded from
coverage under proposed § 17.272(a)(1)
through (84) (current § 17.272(a)(1)
through (86)).
We would define ‘‘CHAMPVA
determined allowable amount’’ by
referencing the proposed paragraph that
would relate to this term, proposed
§ 17.272(b)(1).
We would define ‘‘CHAMPVA Inhouse Treatment Initiative (CITI)’’ to
mean the initiative under section
1781(b) under which participating VA
medical facilities provide medical
services and supplies to CHAMPVA
beneficiaries who are not also eligible
for Medicare, subject to availability of
space and resources.
We would define the term ‘‘child’’
consistent with 38 U.S.C. 101, as we do
in the current regulation at § 17.270(b).
We would define the term ‘‘claim’’
consistent with the current use and
understanding of the term in the context
of CHAMPVA, as a request by an
authorized non-VA provider or
CHAMPVA beneficiary for payment or
reimbursement for medical services and
supplies provided to a CHAMPVA
beneficiary.
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We would define ‘‘fiscal year’’ as the
period of time starting on October 1 and
ending on September 30. This is plain
language and is consistent with the
generally understood meaning of the
phrase ‘‘fiscal year’’ as used within the
Federal Government.
We would define ‘‘Medications by
Mail (MbM)’’ to mean the initiative
under which VA provides outpatient
prescription medications through the
mail to CHAMPVA beneficiaries.
We would define ‘‘other health
insurance’’ (OHI) as a health insurance
plan or program (to include Medicare)
or third-party coverage that provides
coverage to a CHAMPVA beneficiary for
expenses incurred for medical services
and supplies. The inclusion of Medicare
is consistent with the TRICARE
regulation related to double coverage.
See 32 CFR 199.8(d)(1).
We would define the term ‘‘payer’’ to
mean OHI, as defined in this
rulemaking, that is obligated to pay for
CHAMPVA-covered medical services
and supplies. In a situation in which
more than one insurer is responsible to
pay for such services and supplies (e.g.,
a ‘‘double coverage’’ situation), there
would be a primary payer (i.e., the payer
obligated to pay first), a secondary payer
(i.e., the payer obligated to pay after the
primary payer), etc. In double coverage
situations, CHAMPVA would be the last
payer, after payment by the primary
payer and all other secondary payers.
Defining a ‘‘payer’’ and designating
different payer types would not affect
the administration of CHAMPVA
because these concepts of relative
payment responsibility are all accepted
and understood by the insurance
industry and current CHAMPVA
beneficiaries and are an essential part of
current CHAMPVA billing practices. For
instance, Medicare would be the
primary payer in situations governed by
current § 17.271(b) (which remains
unchanged by this proposed
rulemaking). See 38 U.S.C. 1781(d)(2).
The definition of ‘‘service-connected’’
in current § 17.270(b) would be
unchanged and given the same meaning
as that term in 38 U.S.C. 101. However,
the terms ‘‘spouse’’ and ‘‘surviving
spouse’’ would no longer have the
definitions of these same terms in 38
U.S.C. 101(31) and (3), respectively, as
those definitions are outdated; instead,
these terms would both be determined
by operation of 38 U.S.C. 103(c).
Consistent with the waiver provisions
of TRICARE, see 32 CFR 199.1(n), new
proposed paragraph (c) would establish
the discretionary authority of VA to
waive, when it is deemed to be in the
best interest of VA, any regulatory
requirement of this part that is not
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required by 38 U.S.C. 1781 or otherwise
imposed by statute. This discretionary
waiver authority would be limited to
very unusual and limited circumstances
and would not set a precedent for future
decisions. In addition, it would not be
used to deny any individual any right,
benefit, or privilege provided by statute
or these regulations. This new provision
would enable VA to allow payment
under CHAMPVA in cases, for example,
where, by operation of CHAMPVA
rules, the claim is subject to complex
administrative or accounting procedures
that ultimately result in determination
of the claim’s technical noncompliance
when the underlying claim is otherwise
appropriate. Where a claimant’s noncompliance with a purely policy or
administrative-based technical
requirement is both unintentional and
harmless, we believe it would be in
VA’s best interest to have the authority
to waive the regulatory requirement and
allow payment.
17.271 Eligibility
Current § 17.271 identifies persons
who may be eligible for CHAMPVA
benefits. We would revise § 17.271(a) to
recognize as CHAMPVA beneficiaries
those individuals designated as Primary
Family Caregivers under 38 CFR
71.25(f). This substantive addition to the
eligibility criterion would be made
pursuant to the Caregivers and Veterans
Omnibus Health Services Act of 2010,
Public Law 111–163, section 102, which
amended 38 U.S.C. 1781(a) by adding a
new subsection (a)(4) authorizing VA to
provide CHAMPVA benefits to ‘‘an
individual designated as a primary
provider of personal care services under
[38 U.S.C. 1720G(a)(7)(A)] who is not
entitled to care or services under a
health-plan contract (as defined in [38
U.S.C. 1725(f)]).’’ We amend CHAMPVA
eligibility criteria to recognize these
Primary Family Caregivers as
CHAMPVA beneficiaries but not to
establish substantive eligibility rules in
the CHAMPVA regulations to determine
whether an individual is a Primary
Family Caregiver. (VA’s regulations
governing the Caregivers Benefits
Program established by 38 U.S.C. 1720G
are codified at 38 CFR part 71, and the
specific rules governing the
identification of such individuals are
found at 38 CFR 71.15 through 71.25.)
We would redesignate current
§ 17.271(a)(4) as § 17.271(a)(5) and add
a new proposed § 17.271(a)(4) to state
that a Primary Family Caregiver is
eligible for CHAMPVA benefits if they
are not entitled to care or services under
a health-plan contract (as defined in 38
U.S.C. 1725(f)(2)). We note that VA is
already providing CHAMPVA services
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and supplies to these individuals
pursuant to the statutory mandate in
section 1720G(a)(3)(A)(ii)(IV) and under
the Caregivers Benefits Program
regulations. This revision would simply
update the CHAMPVA regulations to
conform to these laws.
17.272 Benefits Limitations/Exclusions
Current § 17.272 provides general
information about what medical
services and supplies are covered by
CHAMPVA and lists coverage
limitations along with the exclusions.
The general information concerning
coverage in current § 17.272(a)
continues to be accurate, and we do not
propose any changes to paragraph (a).
Some of the coverage limitations and
exclusions listed in the numbered
paragraphs under § 17.272(a) require
revision due to either changed standards
in clinical practice or changes in
TRICARE coverage.
Current § 17.272(a)(2) excludes the
provision of services and supplies
required as a result of an occupational
disease or injury for which benefits are
payable under workers’ compensation
or a similar protection plan. We propose
to update the verbiage to clarify the
exclusion for the reader.
Current § 17.272(a)(3) excludes the
provision of services and supplies that
are paid directly or indirectly by local,
State, or Federal government agencies,
with certain exceptions listed in
§ 17.272(a)(3)(i) and (ii) where
CHAMPVA assumes primary payer
status. We propose to add Indian Health
Service and CHAMPVA supplemental
policies as exceptions where
CHAMPVA assumes primary payer
status. This would be consistent with
current CHAMPVA practice as well as
the TRICARE regulation related to
double coverage. See 32 CFR
199.8(b)(4)(ii) and (iv). We also propose
to remove the ‘‘(Medicaid excluded)’’
parenthetical language in current
§ 17.272(a)(3), because § 17.272(a)(3)(i)
already expressly excepts ‘‘Medicaid’’
from the general exclusion in
§ 17.272(a)(3).
Current § 17.272(a)(21) excludes
dental care generally, with exceptions to
such exclusion listed in paragraphs
(a)(21)(i) through (xii). We would amend
paragraph (a)(21)(ix) to clarify that the
provision of initial imaging services for
the treatment of temporomandibular
joint disorder (TMD) could specifically
include Computed Tomography (CT)
and Magnetic Resonance Imaging (MRI)
services. We believe the sole reference
to ‘‘initial radiographs’’ in current
§ 17.272(a)(21)(ix) is outdated and that
modern industry standards include the
use of CT scans as well as MRIs for
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diagnosing TMD. A CT scan provides a
more detailed image of the bones in the
joint, and an MRI provides a more
detailed image of the soft tissue to
determine proper positioning as the jaw
moves. We would also update
§ 17.272(a)(21)(ix) to refer to the more
updated and clinically appropriate
terminology ‘‘temporomandibular joint
disorder (TMD).’’ These revisions would
update CHAMPVA regulations with
current standards of clinical practice for
the benefit of CHAMPVA beneficiaries.
A majority of the remaining proposed
changes to CHAMPVA coverage
exclusions in proposed § 17.272(a)(1)
through (82) are based on changes to
TRICARE coverage and policy. Virtually
all coverage limitations and exclusions
in current § 17.272(a)(1)–(86), as shown
in the chart below, are substantially
identical to services and supplies
excluded from, or limited under,
TRICARE coverage under 32 CFR
199.4(g), or as otherwise noted in the
chart.
LIST OF COMPARABLE CHAMPVA AND
TRICARE EXCLUSIONS
CHAMPVA provision (identified
paragraphs are
from 38 CFR
17.272(a))
(1) .........................
(2) .........................
(3) .........................
(4) .........................
(5) .........................
(6) .........................
(7) .........................
(8) .........................
(9) .........................
(10) .......................
(11) .......................
(12) .......................
(13) .......................
(14), (81) ...............
(15) .......................
(16) .......................
(17) .......................
(18) .......................
(19), (82) ...............
(20) .......................
(21) .......................
(22) .......................
(23) .......................
(24) .......................
(25) .......................
(27) .......................
(28) .......................
(29) .......................
(30) .......................
(31) .......................
(32) .......................
(33) .......................
(34) .......................
(35) .......................
(36) .......................
(37) .......................
(38) .......................
(40) .......................
(41) .......................
(42) .......................
(43) .......................
(44) .......................
(45) .......................
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Frm 00028
TRICARE provision (identified
paragraphs are from 32 CFR
199.4(g), or as otherwise
noted)
(11).
(23).
(13).
(1).
(2).
(3).
(4).
(5).
(6).
(7).
(8).
(9).
(14).
(15).
(16).
(17).
(19).
(21).
(24).
(26).
(27).
(28).
(29).
(30).
(31).
(33).
(34).
(35).
(36).
(37).
(38).
(39).
(40).
(41).
(20), (42).
(43).
(44).
(46).
(47).
(50).
(51).
(48).
(49).
Fmt 4702
Sfmt 4702
LIST OF COMPARABLE CHAMPVA AND
TRICARE EXCLUSIONS—Continued
CHAMPVA provision (identified
paragraphs are
from 38 CFR
17.272(a))
TRICARE provision (identified
paragraphs are from 32 CFR
199.4(g), or as otherwise
noted)
(46) .......................
(47) .......................
(48) .......................
(49) .......................
(50) .......................
(51) .......................
(52) .......................
(53) .......................
(54) .......................
(55), (57) ...............
(56) .......................
(57) .......................
(58) .......................
(59) .......................
(60) .......................
(62) .......................
(52).
(53).
(54).
(55).
(56).
(57).
(58).
(60).
(61).
(62).
(64).
(65).
(66).
(67).
(72).
32 CFR 199.4(a)(12) and
(b)(10)(iv).
32 CFR 199.4(e)(4) and (h).
(73).
32 CFR 199.2(b) and
199.4(e)(2).
32 CFR 199.4(c)(3)(ix) and
199.4(e)(4).
32 CFR 199.4(e)(17).
32 CFR 199.4(g)(15)(iv).
(69).
32 CFR 199.4(a)(1).
32 CFR 199.4(g)(74).
(39), (42).
(25).
32 CFR 199.4(g)(15).
32 CFR 199.2(b) and
199.4(b)(2)(v), (b)(3)(iii),
(b)(5)(v), (d)(3)(vi), (e)(11)(i).
32 CFR 199.4(c)(2), (c)(3),
(e)(8)(i)(E).
32 CFR 199.4(e)(8).
32 CFR 199.2(b), 199.4(e)(8),
(g)(24).
(63) through (65) ..
(66) .......................
(67), (68) ...............
(69) .......................
(70), (71) ...............
(73) .......................
(74) .......................
(75) .......................
(76) .......................
(77) .......................
(78) .......................
(79) .......................
(80) .......................
(83) .......................
(84) .......................
(85), (86) ...............
We note that even where our current
provisions are not identical to a
TRICARE provision, our intent has
consistently been to apply CHAMPVA
comparable exclusions or limitations in
the same or similar manner to their
TRICARE counterpart in accordance
with 38 U.S.C. 1781(b). The same is true
for our proposed revisions below, which
are consistent with changes in DoD’s
administration of TRICARE.
The first change we would make to
our limitations and exclusions based on
TRICARE regulatory and policy changes
concerns current § 17.272(a)(26), which
is not addressed in the chart above
because it correlates with a provision
that has been removed from TRICARE
regulations. See 60 FR 12419 (March 7,
1995). Therefore, we propose to remove
this exclusion from our regulations as
well. Paragraph (a)(26) in current
§ 17.272 excludes coverage for services
and supplies, including psychological
testing, provided in connection with a
specific developmental disorder. By
removing this exclusion, CHAMPVA
would now cover this service, and we
would redesignate current
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§ 17.272(a)(27) through (38) as
§ 17.272(a)(26) through (37),
respectively.
Under section 711 of the 2009 NDAA,
TRICARE must waive all beneficiary
costs associated with certain preventive
services, unless the beneficiary is also
Medicare-eligible. TRICARE regulations
were revised to delete from 32 CFR
199.4(g)(37) the list of preventive
services not excluded from coverage,
and these services were moved to new
§ 199.4(e)(28) so that they instead would
be reflected as preventive services under
TRICARE for which out-of-pocket costs
are eliminated. See 76 FR 81368
(December 28, 2011). We would revise
our current exclusion of preventive care
in § 17.272(a)(31) (proposed to be
redesignated as § 17.272(a)(30)) to
except the same preventive services
identified in paragraphs (d)(1)(A)
through (F) of section 711 of the 2009
NDAA and, further, do so in a manner
that, on the whole, reflects the manner
in which these services are provided
under TRICARE. Section 711 of the
2009 NDAA sets forth the following
preventive services for which
beneficiaries shall pay no associated
costs: Colorectal cancer screening;
breast cancer screening; cervical cancer
screening; prostate cancer screening;
annual physical exam; vaccinations.
Current § 17.272(a)(31)(i) through (x) set
forth exceptions to the general exclusion
of certain specific preventive care.
Respectively, the terms of current
paragraphs (a)(31)(v) and (vi) already
except ‘‘[p]ap smears’’ and
‘‘[m]ammography tests’’ and so
effectively capture ‘‘cervical cancer
screening’’ and ‘‘breast cancer
screening’’ as referred to in the 2009
NDAA. However, because the singular
terms ‘‘mammography test’’ and ‘‘pap
smear’’ are outdated, we are updating to
‘‘breast cancer screening’’ and ‘‘cervical
cancer screening.’’ Therefore, proposed
§ 17.272(a)(30) would revise the
exceptions to the general exclusion of
preventive care to include the four
remaining preventive services specified
in the 2009 NDAA, namely colorectal
cancer screening; prostate cancer
screening; annual physical examination;
and vaccinations/immunizations.
We note that the TRICARE final rule
that implemented the amendments
made by section 711 of the 2009 NDAA
does not include an annual physical
exam benefit for all TRICARE
beneficiaries; instead, such benefit is
limited to certain dependents of Active
Duty military personnel who are
traveling outside the United States and
for beneficiaries ages 5 through 11 who
require such exams for school
enrollment. This benefit is also not
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exempt from cost sharing requirements.
See 76 FR 81368, and 32 CFR
199.4(e)(29). Broadly interpreting our
mandate in section 1781(b), VA
proposes to modify the current
exclusion of preventive care in current
§ 17.272(a)(31) insofar as it defines that
term to include annual physical
examinations and create an exception
permitting such exams. Despite the
limited availability of such
examinations under TRICARE, it is
noteworthy that TRICARE nonetheless
covers some preventive services that are
typically provided as part of an annual
physical examination such as blood
pressure screening, cholesterol testing,
and body measurements. See TRICARE
Policy Manual 6010.60–M
(‘‘Medicine’’), Chapter 7, section 2.1
(‘‘Clinical Preventive Services-TRICARE
Standard’’) (April 1, 2015). To be paid
for by TRICARE, however, these types of
health promotion and disease
prevention services must be billed in
connection with another preventive
service delineated in TRICARE’s policy
manual. Id. We do not believe limiting
the provision of annual physical
examinations to only a few select groups
is appropriate from a clinical
perspective. Further, in the exercise of
our discretion, when broadly
interpreting the mandate of section
1781(b), we conclude it lies within our
discretion to determine that this benefit
should be made available to all
CHAMPVA beneficiaries. This is
particularly the case given that some
individual health promotion and
disease prevention services that are
typically provided as part of an annual
physical examination would eventually
be approved by TRICARE as long as
they are coupled or associated with
billing submitted for a covered service.
(The nature and delivery of those
services remains the same whether
delivered as part of an annual
examination or under the umbrella of
another service for which TRICARE
billing is permitted.) Furthermore, VA
finds that annual physical examinations
are beneficial for both CHAMPVA
beneficiaries and VA, by serving to
identify serious medical issues before
they progress and their clinical
management becomes more difficult and
resource-intensive. Even though our
proposed approach would include
elements of an annual physical
examination not otherwise included as
an adjunct service provided under a
covered benefit as described above, we
believe our approach is sufficiently
‘‘similar’’ to TRICARE. Therefore, we
propose to create an exception to the
exclusion of preventive care, permitting
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2401
an annual physical examination to be
among the benefits available to all
CHAMPVA beneficiaries.
We also note that we would except
‘‘[v]accinations/immunizations’’ from
the general exclusion of preventive
services. Although subsection (d)(1)(F)
of section 711 of the 2009 NDAA
exempts ‘‘vaccination’’ only, TRICARE’s
guidance on this issue additionally
exempts immunizations. See TRICARE
Reimbursement Manual 6010.61–M
Chapter 2 (‘‘Beneficiary Liability’’),
section 1 (‘‘Cost-Shares And
Deductibles’’) (April 1, 2015). We
believe these terms have identical
meanings and would use both terms just
to be clear that this preventive service
is covered regardless of whether it is
called an ‘‘immunization’’ or a
‘‘vaccination.’’
Current § 17.272(a)(39) excludes
coverage for audiological services or
speech therapy, except when prescribed
by a physician and rendered as part of
a treatment addressing a physical defect,
which correlates with a provision not
addressed in the chart above because it
has been removed from TRICARE
regulations. See 75 FR 50880 (August
18, 2010). Therefore, we propose to
remove this exclusion from our
regulations as well. By removing this
exclusion, CHAMPVA would now cover
this service, and we would redesignate
current § 17.272(a)(40) through (56) as
§ 17.272(a)(38) through (54),
respectively.
As stated earlier in this rulemaking,
pursuant to section 713 of the 2009
NDAA, TRICARE must make available
smoking cessation benefits, as specified
in the law, to beneficiaries who are not
also eligible for Medicare. The four
categories of smoking cessation benefits
available to these beneficiaries are set
forth in TRICARE’s regulations under 32
CFR 199.4(e)(30)(ii)(A)–(D). Hence, we
would revise our regulations by
removing our correlate restriction on
smoking cessation services and supplies
in current § 17.272(a)(57). In removing
current § 17.272(a)(57), current
paragraphs (a)(58) through (71) would
be redesignated as paragraphs (a)(55)
through (68), respectively.
Redesignated paragraphs (a)(57)
through (59) would be revised to
reference coverage of mental health
benefits in a ‘‘calendar year’’ versus the
current reference to ‘‘fiscal year.’’ We
propose to change the yearly basis of
this coverage because our beneficiaries
and providers are more familiar with
calendar year events, and the impact of
the change from fiscal to calendar on the
functioning of CHAMPVA would be
minimal.
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With the proposed removal of
§ 17.272(a)(57) and subsequent
redesignations of paragraphs noted
above, current paragraph (a)(67) would
be redesignated as paragraph (a)(64).
CHAMPVA would continue to exclude
the performance of abortions, except
when a physician certifies that the life
of the mother would be endangered if
the fetus were carried to term. This is
the same restriction in current TRICARE
regulations (see 32 CFR 199.4(e)(2)),
although statute and TRICARE policy
statements recently established an
additional exception to the general ban
on abortions. Specifically, section 704 of
the National Defense Authorization Act
for Fiscal Year 2013, Public Law 112–
239 (2013 NDAA), amended 10 U.S.C.
1093(a) and (b) to expand the
circumstances under which funds
available to DoD and MTFs may be used
to provide and perform abortions in
cases of pregnancy resulting from an act
of rape or incest. Despite the recent
amendments to section 1093 of title 10
and TRICARE policy, we do not propose
same or similar changes to CHAMPVA’s
current exclusion at this time because
TRICARE regulations do not provide for
it. Additionally, such changes would
create an even greater disparity between
the women’s health care benefits
afforded veterans and CHAMPVA
beneficiaries.
Current § 17.272(a)(72) excludes from
coverage drug maintenance programs
where one addictive drug is substituted
for another such as methadone
substituted for heroin. A TRICARE final
rule published on October 22, 2013, and
effective November 21, 2013, removes a
correlate restriction from TRICARE
regulations, and so we propose to
similarly remove § 17.272(a)(72). See 78
FR 62427 (October 22, 2013); 32 CFR
199.4(e)(4)(ii). We agree with the stated
rationale in the related TRICARE
proposed rule that the current
restriction fails to recognize the
accumulated medical evidence
supporting certain maintenance
programs as one component of the
continuum of care necessary for the
effective treatment of substance use
disorders. See 76 FR 81899 (December
29, 2011). In removing current
§ 17.272(a)(72), current paragraphs
(a)(73) through (86) would be
redesignated as paragraphs (a)(69)
through (82), respectively.
Current § 17.272(a)(80), as proposed
to be redesignated as paragraph (a)(76),
excludes from CHAMPVA benefits
medications not requiring a
prescription, except for insulin and
related diabetic testing supplies and
syringes. We would revise redesignated
paragraph (a)(76) to instead exclude
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‘‘over-the-counter products’’ and would
additionally expand the exception to
this exclusion to cover over-the-counter
smoking cessation pharmaceutical
supplies that are approved by the U.S.
Food and Drug Administration (FDA),
prescribed, and provided through MbM.
These changes would be consistent with
TRICARE regulations, which require a
prescription from an authorized
provider for smoking cessation
pharmaceutical agents (even for FDAapproved over-the-counter smoking
cessation agents). See 32 CFR
199.4(e)(30)(ii)(A).
Section 702 of the 2013 NDAA grants
the Secretary of Defense the authority to
add certain over-the-counter
medications to the TRICARE formulary
so that such medications may be
administered as if they were
prescription medications. CHAMPVA
does not have a same or similar uniform
formulary as DoD that could be altered
to include certain over-the-counter
medications, and we do not interpret
section 702 as granting authority to alter
VA’s uniform formulary. Therefore, we
would not amend our regulations in
response to section 702 of the 2013
NDAA. Our regulation as revised and
redesignated § 17.272(a)(76) would
permit CHAMPVA to provide the same
over-the-counter smoking cessation
supplies as permitted in TRICARE
policy.
Lastly, we would add two new
exclusions to § 17.272. Proposed
paragraph (a)(83) would exclude
medications that are not approved by
the FDA, excluding FDA exceptions to
the approval requirement. Current
CHAMPVA regulations are silent
regarding the need for medications to
meet FDA approval requirements;
however, this has not been a problem as
a matter of practice because applicable
standards of care generally require
prescribed medications to be FDAapproved or excluded as an exception
from the approval requirement. Still, we
wish to formally and expressly exclude
medications that do not meet these
requirements. In addition, to provide
benefits in the same or similar manner
and subject to the same or similar
limitations as TRICARE, paragraph
(a)(84) would establish exclusions for
services and supplies related to the
treatment of dyslexia. See 38 CFR
199.4(g)(32). This change merely reflects
in regulation current CHAMPVA
practice and policy.
Due to the multiple proposed
deletions and additions in
§ 17.272(a)(1)–(86), we reiterate that we
would redesignate most of the current
paragraphs under § 17.272(a). With the
proposed removal of current paragraph
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(a)(26), current paragraphs (a)(27)
through (38) would be redesignated as
(a)(26) through (37), respectively, with
the substantive changes to redesignated
(a)(30) as noted above. With the
proposed removal of current paragraph
(a)(39), current paragraphs (a)(40)
through (56) would be redesignated as
(a)(38) through (54), respectively, with
no substantive changes. With the
deletion of the current paragraphs
(a)(57) and (72), current paragraphs
(a)(58) through (86) would be
redesignated as (a)(55) through (82),
respectively, with the minor substantive
changes as noted above to redesignated
paragraphs (a)(57) through (59) and
(a)(76). Lastly, we would add new
paragraphs (a)(83) and (84).
Current § 17.272(b) establishes the
‘‘CHAMPVA determined allowable
amount,’’ and paragraph (b)(1) states
that the term ‘‘allowable amount’’ is the
maximum amount that CHAMPVA will
pay an authorized provider for a
covered benefit, which is determined
prior to cost sharing and the application
of deductibles or OHI. (This means, for
instance, that the cost-share would be a
percentage of the entire CHAMPVA
determined allowable amount.)
However, this is merely a definition and
not a statement of coverage limitation or
exclusions. We would revise paragraph
(b) to clearly indicate that amounts
above the CHAMPVA determined
allowable amount are excluded from
CHAMPVA coverage. The actual
payment methodology—the amount to
which cost sharing and deductibles will
be applied—is addressed in proposed
§ 17.274(e) and is discussed below.
Proposed § 17.272(b)(1) would
explain that the CHAMPVA determined
allowable amount is the maximum level
of payment to an authorized non-VA
provider for CHAMPVA-covered
services and supplies and that this
allowable amount is determined before
cost sharing and the application of
deductibles or OHI is considered. This
is a restatement of current
§ 17.272(b)(1), except that we would use
the term ‘‘authorized non-VA provider’’
to encompass all those providers listed
in current § 17.272(b)(1) and include the
term ‘‘supplies’’ after ‘‘covered services’’
to underscore they too can be covered.
See current 38 CFR 17.272(b)(1)
(referencing ‘‘a hospital or other
authorized institutional provider, a
physician or other authorized
individual professional provider, or
other authorized provider for covered
services’’). We believe use of the one
term ‘‘authorized non-VA provider’’ as
defined in proposed § 17.270(b)
properly captures all provider types
now listed in § 17.272(b)(1) and
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simplifies the regulatory reference to
providers for the benefit of CHAMPVA
beneficiaries. Proposed § 17.272(b)(1)
would also clearly state that the
CHAMPVA determined allowable
amount is payment made by VA to an
authorized non-VA provider for the
provision of CHAMPVA-covered
services and supplies to a CHAMPVA
beneficiary.
Current § 17.272(b)(2) states that a
Medicare-participating hospital must
accept the CHAMPVA determined
allowable amount for inpatient services
as payment in full and references 42
CFR parts 489 and 1003. While this is
a true statement of law under 42 CFR
489.25, the references to 42 CFR parts
489 and 1003 are vague, and part 1003
is not relevant to the issue of what
amounts Medicare-participating
hospitals must accept as payment in full
from CHAMPVA. See 42 CFR part 1003
(describing civil money penalties,
assessments, and exclusions generally
for individuals who violate provisions
of or agreements with Federal health
care programs). Proposed § 17.272(b)(2)
would state that inpatient services are
‘‘provided to a CHAMPVA beneficiary’’
and use a single, clarifying reference to
42 CFR 489.25.
Section 503 of The Caregivers and
Veterans Omnibus Health Services Act
of 2010, Public Law 111–163, revised 38
U.S.C. 1781 by adding new subsection
(e), which states: ‘‘Payment by the
Secretary under this section on behalf of
a covered beneficiary for medical care
shall constitute payment in full and
extinguish any liability on the part of
the beneficiary for that care.’’ Current
§ 17.272(b)(3) states that: ‘‘An
authorized provider of covered medical
services or supplies must accept the
CHAMPVA determined allowable
amount as payment in full.’’ Proposed
§ 17.272(b)(3) would state more clearly
that ‘‘accepted assignment’’ refers to the
action of an authorized non-VA
provider who accepts responsibility for
the care of a CHAMPVA beneficiary and
thereby agrees to accept the CHAMPVA
determined allowable amount as full
payment for services and supplies
rendered to the beneficiary. The
provider’s acceptance of the CHAMPVA
determined allowable amount
extinguishes the beneficiary’s payment
liability to the provider with the
exception of applicable cost shares and
deductibles. Proposed § 17.272(b)(3)
would not be substantively different
than current paragraph (b)(3) but would
clarify that the action of accepting
payment is the equivalent of accepting
assignment. The term ‘‘accepted
assignment’’ is used currently in the
administration of CHAMPVA payments,
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and we believe using it in this
regulation as described would increase
clarity in payment practices for both
CHAMPVA beneficiaries and authorized
non-VA providers.
Current § 17.272(b)(4) provides that a
provider who has collected and not
made an appropriate refund, or attempts
to collect from the beneficiary any
amount in excess of the CHAMPVA
determined allowable amount may be
subject to exclusion from Federal
benefit programs. The underlying
authority for this rule is 42 CFR
1003.105, which establishes the terms
for a health care provider’s permissive
or mandatory exclusion from
participation in the Medicare program
and other Federal health care programs.
Exclusion may result, for instance, if a
provider files false claims under these
programs. We would move this
information to proposed § 17.272(b)(3)
for increased clarity and would remove
mention of providers not making an
appropriate refund of amounts collected
from beneficiaries, as the purpose of 38
U.S.C. 1781(e) and proposed
§ 17.272(b)(3) is for these amounts to
never be collected by the provider. By
moving this information to proposed
paragraph (b)(3), we would also remove
current paragraph (b)(4).
17.273 Preauthorization
CHAMPVA preauthorization
requirements for certain medical care
and services are based on CHAMPVA
needs and are substantially the same or
similar as those required by TRICARE.
See 32 CFR 199.4 passim. We propose
to revise the preauthorization
requirements by adding language to
indicate when a beneficiary has ‘‘other
health insurance’’ that provides primary
coverage for the benefit,
preauthorization requirements will not
apply. TRICARE waives
preauthorization requirements in all
instances when OHI, to include
Medicare, is the primary payer. See
TRICARE Policy Manual 6010.60–M,
Chapter 1 (‘‘Administration’’), section
6.1 (‘‘Special Authorization
Requirements’’) (April 1, 2015). To
provide benefits in a similar fashion, we
would waive any requirement for
preauthorization where OHI (as defined
by this rulemaking) covers the benefit.
We would also revise current
§ 17.273(d) to refer to dental coverage
limitations in § 17.272(a)(21)(i)–(xii) to
avoid a potential misconception that
preauthorization is generally required
for dental services. CHAMPVA clearly
excludes all dental services, except for
those listed in current § 17.272(a)(21)(i)–
(xii). We would remove current
§ 17.273(e) and not require
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preauthorization for durable medical
equipment as a covered service or
supply. Removal of § 17.273(e) would be
consistent with TRICARE policy. See
TRICARE Policy Manual 6010.60–M,
Chapter 8 (‘‘Other Services’’), section
2.1 (‘‘Durable Medical Equipment: Basic
Program’’) (April 1, 2015). Based on this
removal, we would redesignate current
§ 17.273(f) as § 17.273(e).
Finally, we would add new proposed
§ 17.273(f) to detail the reviews of
medical necessity. Since CHAMPVA is
a secondary payer, VA would be
required to perform reviews of medical
necessity on a retrospective basis. If
during the coordination of benefits
process it is determined that CHAMPVA
would be the responsible payer for the
services and supplies but CHAMPVA
preauthorization was not obtained prior
to delivery of the services or supplies,
we would obtain the necessary
information and perform a retrospective
medical necessity review. We would
also propose that any claims, where a
retrospective review occurs, are filed
within the appropriate one-year period.
17.274 Cost Sharing
Current § 17.274(a) provides in
general that CHAMPVA is a cost sharing
program in which the cost of
CHAMPVA-covered services and
supplies is shared with the beneficiary,
with the exception of services obtained
through VA medical facilities. This
provision would remain substantively
the same, but we would add new
paragraphs (a)(1)(i) and (ii) to explicate,
respectively, that the former language
‘‘services obtained through VA
facilities’’ refers to services and supplies
provided both through MbM and
through CITI. That is, the exception to
this cost-share requirement would
extend specifically to each of these
initiatives (as these initiatives would be
defined by this proposed rulemaking).
Subsections (d)(1)(A) through (d)(1)(F)
of section 711 of the 2009 NDAA, as
discussed earlier, set forth certain
preventive services for which TRICARE
waives all out-of-pocket costs, even if
the beneficiary has not paid the amount
necessary to cover the beneficiary’s
deductible requirement for the year. We
propose to revise § 17.274(a) to make
clear that there will be no associated
cost share for CHAMPVA beneficiaries
for such services. (We address waiving
the associated deductible requirement
later in the discussion of proposed
§ 17.274(b)). We would add new
paragraphs (a)(1)(iii)(A)–(G) to § 17.274
to waive CHAMPVA beneficiary costshare requirements for the same
preventive services identified in
paragraphs (d)(1)(A) through (F) of
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section 711 of the 2009 NDAA. Section
711 also authorizes, but does not
require, the Secretary of Defense to
extend the waiver of beneficiary costs to
other preventive services. As such, we
state in regulation that the list of
services is not all-inclusive, enabling us
to add supplemental items to the list in
the future if needed, while enabling us
to be sufficiently similar to TRICARE.
See Public Law 110–417, section
711(d)(1)(G). TRICARE regulations and
policy guidance extend this waiver to
well-child visits for children under 6
years of age. See 32 CFR 199.4(e)(28)(iv),
(f); TRICARE Reimbursement Manual
6010.61–M, Chapter 2 (‘‘Beneficiary
Liability’’), section 1 (‘‘Cost-Shares and
Deductibles), 1.3.3.10.1.6 (Preventive
Services’’). We would include this same
waiver in proposed paragraph
(a)(1)(iii)(G) of § 17.274. We would
waive any cost-share requirement for
hospice services in proposed
§ 17.274(a)(1)(iv). This waiver is similar
to the cost-share waiver for hospice
services in TRICARE regulation. See 32
CFR 199.14(g)(9). Lastly, to remain
similar to TRICARE, in § 17.274(a)(1)(v),
we would add a waiver for other
services as determined by the Secretary
of Veterans Affairs.
For TRICARE, the waiver of
beneficiary costs associated with
preventive services in proposed
§ 17.274(a)(1)(iii)(A) through (G) do not
apply to any TRICARE beneficiary who
is also Medicare-eligible. See Public
Law 110–417, section 711(b). We would
not exclude Medicare-eligible
beneficiaries from cost sharing waivers
for preventive services as this would
unfairly disadvantage them as compared
to other CHAMPVA beneficiaries with
OHI. By not including this waiver,
CHAMPVA will treat all beneficiaries
with OHI the same. Additionally, we
believe most preventive services
provided to Medicare-eligible
beneficiaries will be paid in full by
Medicare, and, therefore, CHAMPVA
will not assume any payment
responsibility. In the event a cost share
or deductible is applied for preventive
services, CHAMPVA will treat those
claims as it would the claims for any
other beneficiary with OHI.
The general provisions in current
§ 17.274(b) related to establishing an
annual deductible requirement (in
addition to beneficiary cost share)
would remain substantively the same.
We would move the exception to this
general requirement in current
§ 17.274(b) (last sentence) for services
obtained through VA facilities to a new
§ 17.274(b)(1) and also explain that it
refers to services and supplies provided
through MbM or CITI under the same
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rationale as expressed above for
proposed new § 17.274(a)(1)(i) and (ii),
respectively. We would also move the
exception to the deductible requirement
in current § 17.274(b) (last sentence) for
any inpatient services to a new
§ 17.274(b)(2). Proposed § 17.274(b)(3)
would except the listed preventive
services in proposed
§ 17.274(a)(1)(iii)(A)–(G) from the
general deductible requirement in
current and proposed § 17.274(b), in
accordance with the mandate in section
711 of the 2009 NDAA. See Public Law
110–417, section 711(a)(2) (mandating
that a beneficiary not be charged for
preventive services during a year even
if the beneficiary has not paid the
amount necessary to cover the
beneficiary’s deductible for the year. See
32 CFR 199.4(f)(12)). Proposed
§ 17.274(b)(4) would waive the
CHAMPVA beneficiary deductible
requirement for hospice services, as is
done similarly under TRICARE
regulations. See 32 CFR 199.14(g)(9).
Lastly, to remain similar to TRICARE, in
§ 17.274(b)(5), we would add a waiver
for other services as determined by the
Secretary of Veterans Affairs.
Current § 17.274(c) establishes a
calendar year limit on the ‘‘cost-share
amount’’ incurred by a CHAMPVA
beneficiary through the payment of both
cost-shares and deductible amounts (See
current 38 CFR 17.274(c), indicating
that the cap is ‘‘limited to the applied
annual deductible(s) and the beneficiary
cost-share amount.’’). Proposed
§ 17.274(c) would retain this basic
information but would refer instead to
a cap on ‘‘out-of-pocket costs’’ instead of
‘‘cost-share amounts’’ so that it is clear
that both cost share and deductible
amounts apply to this cap. Current
§ 17.274(c)(i) establishes an annual cap
of cost sharing of $7,500 per CHAMPVA
eligible family ‘‘through December 31,
2001’’, which is an outdated provision.
Current § 17.274(c)(ii) further
establishes a current cap of $3000 per
CHAMPVA eligible family, which was
‘‘[e]ffective January 1, 2002.’’ Under
proposed § 17.274(c), we would
establish an annual (calendar year) cap
on out-of-pocket costs of $3,000 per
CHAMPVA eligible family. The annual
cap amount would be unchanged from
what currently exists but would use the
new terminology proposed above for the
sake of clarity. We would also remove
current § 17.274(c)(i) and (ii).
We do not propose any substantive
changes to current § 17.274(d) as this
provision is legally adequate, and we
are not proposing to revise policies
related to it. However, we are adding a
subject heading in an effort to mirror the
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cost share calculation in proposed
paragraph (e) to § 17.274.
We propose to add a new paragraph
(e) to § 17.274 which would set forth the
principles found in current policy
manuals that VA uses to establish
CHAMPVA beneficiary cost-share
amounts. The calculation methodologies
that would be described in proposed
§ 17.274(e) represent current CHAMPVA
practice and therefore would not
increase or decrease the out-of-pocket
costs for CHAMPVA beneficiaries. The
methodologies described in proposed
§ 17.274(e) are also consistent with
TRICARE cost-share calculation
methodologies for the same or similar
types of care, except as indicated below.
In accordance with current practice,
and as proposed in § 17.274(e), the
CHAMPVA beneficiary’s cost-share
amount, if applicable, is 25 percent of
the CHAMPVA determined allowable
amount in excess of the annual calendar
year deductible for most CHAMPVAcovered services and supplies. This
calculation is similar to that used in
TRICARE to determine cost-share
amounts for a majority of TRICARE
covered services. See 32 CFR
199.4(f)(3)(ii)(C) and (f)(3)(iii). Proposed
§ 17.274(e)(1) and (2) would establish
the services for which the general rule
of a 25 percent cost share does not
always apply. Proposed paragraph (e)(1)
would establish in regulation the
current calculation VA uses to
determine CHAMPVA beneficiary cost
share for inpatient facility services and
supplies that are subject to the
CHAMPVA Diagnosis Related Group
(DRG) payment system. The CHAMPVA
DRG system, like that used by TRICARE
under 32 CFR 199.14, is based on the
Centers for Medicare and Medicaid
Services (CMS) prospective payment
system for hospital services, as set forth
in 42 CFR part 412. For services based
on the CHAMPVA DRG system, the
CHAMPVA beneficiary cost share
would be the lesser of the per diem rate
multiplied by the number of inpatient
days; or, 25 percent of the hospital’s
billed amount; or, the base CHAMPVA
DRG rate. This calculation is similar to
that used in TRICARE regulation. See 32
CFR 199.4(f)(3)(ii)(A) and (f)(8)(ii).
Proposed § 17.274(e)(2) would
establish the CHAMPVA beneficiary
cost share for covered inpatient facility
services and supplies that are subject to
the CHAMPVA mental health low
volume per diem reimbursement
methodology. This methodology covers
mental health inpatient services for
lower volume hospitals and units (less
than 25 mental health discharges per
federal fiscal year). For these services,
the CHAMPVA beneficiary cost share
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would be the lesser of a fixed per diem
amount multiplied by the number of
inpatient days or 25 percent of the
hospital’s billed charges. This
calculation is similar to that used in
TRICARE regulations. See 32 CFR
199.4(f)(3)(ii)(B) and (f)(8)(ii).
Although, as noted above, a majority
of the CHAMPVA cost-share
methodologies are the same or similar as
TRICARE’s, we would not adopt a
recent TRICARE exception to its general
25 percent cost-share rule for
prescription medications. Section 712 of
the 2013 NDAA requires the Secretary
of DoD, through regulations, to establish
specified fixed dollar amounts for cost
shares for pharmacy benefits (e.g.,
generic, formulary, and non-formulary
agents or medications). We would not
establish similar fixed cost-share
amounts because CHAMPVA does not
have an established uniform formulary
and, therefore, is unable to identify all
medications which may be prescribed or
approximate their standard retail
pricing to determine, with certainty,
that a fixed dollar amount would satisfy
beneficiaries’ cost-share liability.
Generally, CHAMPVA coverage of
medications depends upon whether
medications are approved by the FDA
for the indications for which they are
prescribed (as explained above in
connection with new proposed
§ 17.272(a)(83)). Additionally, the fixed
cost-share amounts required by section
712 of the 2013 NDAA would apply
even to medications administered
through TRICARE’s mail order service;
whereas, under proposed § 17.274(a)(1),
as revised for clarity, cost-sharing
requirements would not apply to
services and supplies provided through
VA’s MbM. As a matter of policy, VA
does not wish to apply a cost share for
mail order pharmacy supplies provided
to CHAMPVA beneficiaries. We believe
that this departure from TRICARE is
necessary to ensure the most
appropriate care for CHAMPVA
beneficiaries. Although we would not
establish fixed cost-share amounts for
medications similar to those set forth in
section 712 of the 2013 NDAA, we
would revise our regulations to clarify
the methodology CHAMPVA uses to
determine allowable amounts paid for
outpatient medications obtained in the
community (explained later in the
discussion of proposed § 17.275(f)),
upon which the 25 percent CHAMPVA
beneficiary cost share is based. We
believe these clarifications would
provide more transparency related to
pharmacy costs and subsequent
CHAMPVA beneficiary cost-share
amounts for pharmaceutical supplies
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obtained in the community, which we
believe is a reasonable interpretation of
the goals of section 712 of the 2013
NDAA in establishing fixed cost-share
amounts.
17.275 CHAMPVA Determined
Allowable Amount Calculation
We propose to add a new § 17.275 to
describe the various payment
methodologies used by CHAMPVA to
calculate the CHAMPVA determined
allowable amount for covered services
and supplies. CHAMPVA uses the same
or similar payment methodologies to
establish allowable reimbursement
amounts for providers as TRICARE. See
32 CFR 199.14. As with the cost-share
methodologies that would be described
in § 17.274(e), proposed § 17.275
represents current practice except as
noted below and would not cause
changes for CHAMPVA beneficiaries.
The reason that § 17.274(e) (regarding
cost share) and § 17.275 (regarding
CHAMPVA determined allowable
amount) would be separated is to clarify
for CHAMPVA beneficiaries how much
of the CHAMPVA determined allowable
amount they are responsible for as a cost
share (e.g., 25 percent) and additionally
to provide beneficiaries and providers
with an idea of how such allowable
amounts are calculated.
Proposed § 17.275(a) would establish
in regulation the CHAMPVA
determined allowable amount for
reimbursement of inpatient hospital
services based on the CHAMPVA DRGbased payment system. Proposed
paragraph (a) would explain that, unless
exempt or subject to a methodology in
proposed paragraph (b) or (c), hospital
services provided in the 50 States, the
District of Columbia, and Puerto Rico
are subject to the CHAMPVA DRG-based
payment system. The CHAMPVA DRG
system, similar to that used by TRICARE
under 32 CFR 199.14, is also based on
the CMS prospective payment system as
set forth in 42 CFR part 412. Certain
services provided in a DRG reimbursed
facility will be reimbursed under the
CHAMPVA Cost-to-Charge (CTC)
payment method. See, e.g., 32 CFR
199.14(c). However, we will not list
these specifically in regulations as the
list of services may change more often
than regulations can be updated.
Proposed § 17.275(b) would establish
in regulation the current CHAMPVA
inpatient mental health per diem
payment system used to calculate
reimbursement for inpatient mental
health hospital care in specialty
psychiatric hospitals and psychiatric
units of general acute hospitals that are
exempt from the CHAMPVA DRG-based
payment system. The per diem rate
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would be calculated based on the daily
rate times the number of days (length of
stay). CHAMPVA’s mental health per
diem rates are updated each fiscal year
for both high volume hospitals (25 or
more discharges per fiscal year) and low
volume hospitals (less than 25
discharges per fiscal year). The per diem
rates used by CHAMPVA are
determined by TRICARE per diem rates.
See 32 CFR 199.14(a).
Proposed § 17.275(c) would establish
in regulation the CHAMPVA CTC
payment system that is used to calculate
the CHAMPVA determined allowable
amount for inpatient services furnished
by hospitals or facilities that are exempt
from the CHAMPVA DRG-based
payment system or the CHAMPVA
inpatient mental health per diem
payment system. TRICARE establishes
an alternate methodology to calculate
payments for inpatient services that are
exempt from its DRG and inpatient
mental health per diem payment
systems. See 32 CFR 199.14(a)(4).
Proposed § 17.275(c)(1) would establish
the CHAMPVA CTC methodology used
to calculate costs for hospitals or
facilities by multiplying a CTC ratio by
billed charges. We would further
propose that the billed charges from the
applicable hospitals and facilities must
be customary and not in excess of rates
or fees the hospital or facility charges
the general public for similar services in
a community. This requirement that the
applicable billed charges not be in
excess of what is charged of the general
public is similar to TRICARE’s
requirements. See 32 CFR
199.14(a)(4)(i). Proposed
§ 17.275(c)(2)(i) through (x) would
establish the types of hospitals and
services subject to the CHAMPVA CTC
methodology, similar to TRICARE at 32
CFR 199.14(a)(1)(ii)(D)(1) through (10)
and (a)(1)(ii)(E). We would also add in
proposed § 17.275(c)(2)(xi) that
hospitals and services as determined by
the Secretary of Veterans Affairs may be
subject to the CHAMPVA CTC
methodology.
Proposed § 17.275(d) would establish
in regulation the CHAMPVA outpatient
prospective payment system (OPPS)
used to calculate the allowable amount
for outpatient services provided in a
hospital subject to Medicare OPPS. This
will include the utilization of
TRICARE’s reimbursement methodology
to include specific coding requirements,
ambulatory payment classifications
(APCs), nationally established APC
amounts, and associated adjustments
(e.g., discounting for multiple surgery
procedures, wage adjustments for
variations in labor-related costs across
geographical regions, and outlier
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calculations). The CHAMPVA OPPS is
the same as that utilized by TRICARE
under 32 CFR 199.14, which is similar
to Medicare’s basic OPPS methodology.
There are differences between
TRICARE’s OPPS methodology and
Medicare’s basic OPPS methodology
due to variations in benefit structure
and beneficiary population. CHAMPVA
is adopting TRICARE’s OPPS because
the CHAMPVA beneficiary population
is more similar to the TRICARE
beneficiary population than to the
Medicare beneficiary population. See 32
CFR 199.14(a)(6)(ii).
Proposed § 17.275(e) would establish
in regulation the reimbursement
methodology for services and supplies
provided by authorized non-VA
providers on an outpatient or inpatient
basis where the services are distinct
from facility-type charges in proposed
§ 17.275(a) through (d). Proposed
§ 17.275(e) would explain that the
CHAMPVA determined allowable
amount paid to authorized non-VA
providers (not hospitals) for services
and supplies provided on an outpatient
or inpatient basis is the lesser of: The
CHAMPVA maximum allowable charge
(equivalent to the maximum allowable
charge for similar services provided by
other than hospitals and skilled nursing
facilities under TRICARE, see 32 CFR
199.14(c)); the prevailing amount,
which is the amount equal to the
maximum reasonable amount allowed
providers for a specific procedure in a
specific locality; or the billed amount.
Certain services that typically may be
provided within a hospital setting, but
not billed as a facility-type charge under
proposed paragraphs (a) through (d),
would be included as examples in
proposed paragraph (e), namely
anesthesia services; laboratory services;
and other professional services
associated with individual authorized
non-VA providers. These examples are
not all-inclusive.
Proposed § 17.275(f) would establish
in regulation the current payment
methodology for outpatient CHAMPVA
pharmacy points of service. CHAMPVA
negotiates rates with retail pharmacies
through its contract with the pharmacy
benefit manager. For services and
supplies obtained from a retail ‘‘innetwork’’ pharmacy, proposed
§ 17.275(f)(1) would establish that VA
pays the lesser of the billed amount or
the contracted rate. For supplies from a
retail ‘‘out-of-network’’ pharmacy,
proposed § 17.275(f)(2) would establish
that VA pays the lesser of the billed
amount plus a dispensing fee or the
average wholesale price plus a
dispensing fee.
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Proposed § 17.275(g) would set forth
in regulation the current CHAMPVA
reimbursement methodology for the
provision of services in a Skilled
Nursing Facility (SNF). This
methodology is based on the CMS
prospective payment system for SNFs
under 42 CFR part 413, subpart J
(Medicare Resource Utilization Group
(RUG) rates), which is the same
methodology used in TRICARE
regulations to calculate SNF payments.
See 32 CFR 199.14(b).
Proposed § 17.275(h) would set forth
in regulation the current reimbursement
methodology for durable medical
equipment, prosthetics, orthotics, and
supplies (DMEPOS). Reimbursement of
DMEPOS would be based on the same
amounts established under the CMS
DMEPOS fee schedule under 42 CFR
part 414, subpart D, which is the same
methodology used in TRICARE
regulations to calculate DMEPOS
payments. See 32 CFR 199.14(k). The
allowed amount would be that which is
in effect in the specific geographic
location at the time CHAMPVA-covered
services and supplies are provided to a
CHAMPVA beneficiary.
Proposed § 17.275(i) would establish
in regulation the current payment
methodology for all ambulance services.
CHAMPVA adopts Medicare’s
Ambulance Fee Schedule (AFS) for
ambulance services, which is based on
the same methodology used by
TRICARE. See TRICARE
Reimbursement Manual 6010.61–M,
Chapter 1 (‘‘General’’), section 14
(‘‘Ambulance Services’’) (April 1, 2015).
Ambulance services are paid based on
the lesser of the Medicare AFS or the
billed amount. Payments for ambulance
services furnished by a Critical Access
Hospital (CAH) are paid on the same
basis as the CTC method under
paragraph (c) of this section.
Proposed § 17.275(j) would establish
in regulation the current reimbursement
methodology for hospice care. This
methodology uses rates in the CMS
hospice per diem rate payment system,
which is the same methodology used in
TRICARE regulations to calculate
hospice payments. See 32 CFR
199.14(g)(9).
Proposed § 17.275(k) would establish
in regulation a reimbursement
methodology for intermittent or parttime home health services similar to the
methodology used in TRICARE, which
is based on Medicare’s payment
methods and rates. See 32 CFR
199.14(h). Under this methodology, a
fixed case-mix and wage-adjusted
national 60-day episode payment
amount will act as payment in full for
costs associated with furnishing home
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health services with exceptions
allowing for additional payment to be
established. This would be a new
limitation in payments for services but
is in line with the 60-day episode
amount specified in the TRICARE
regulation. See 32 CFR 199.14(h).
Proposed § 17.275(l) would establish
in regulation the current reimbursement
methodology for facility charges
associated with procedures performed
in a freestanding surgery center, which
is the basis of a prospectively
determined amount, similar to that used
by TRICARE. See 32 CFR 199.14(d).
These facility charges would not
include physician fees, anesthesiologist
fees, or fees of other authorized non-VA
providers; such independent
professional fees would be submitted
separately from facility fees and
calculated under the methodology in
proposed § 17.275(e). Ambulatory
surgery procedures performed in CAHs
or in hospital outpatient departments
are to be reimbursed in accordance with
the provisions of paragraph (c) or (d)
respectively of this section.
Proposed § 17.275(m) states that VA
shall determine the appropriate
reimbursement method or methods to be
used in the extension of CHAMPVA
benefits for otherwise covered medical
services and supplies provided by
hospitals or other institutional
providers, physicians or other
individual professional providers, or
other providers outside the United
States. The authority to establish these
reimbursement methods is similar to
that in TRICARE regulation. See 32 CFR
199.14(n).
Proposed § 17.275(n) would establish
in regulation the reimbursement
methodology for inpatient services
provided in a Sole Community Hospital
(SCH). TRICARE reimbursement
approximates Medicare reimbursement
for SCHs. TRICARE reimburses on a
two-step process. TRICARE makes an
initial payment based upon multiplying
the billed amount by the applicable
TRICARE percentage, which is the
greater of the SCH’s most recently
available cost-to-charge ratio from the
CMS inpatient Provider Specific File or
the TRICARE allowed-to-billed ratio.
The second step is a year-end
adjustment to compare the aggregate
allowable cost under the first method to
the aggregate amount that would have
been allowed for the same care using the
DRG method. In the event that the DRG
method amount is the greater, the yearend adjustment will be the amount by
which it exceeds the aggregate allowable
costs. See 32 CFR 199.14(a)(7). Due to
certain limitations, CHAMPVA cannot
be the same as TRICARE but can be
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similar. CHAMPVA would compare the
cost-to-charge ratio reimbursement
amount versus the DRG reimbursement
amount and then pay the higher of the
two methods.
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17.276 Claim-Filing Deadlines
Proposed § 17.276 is a revision and
renumbering of current § 17.275. First,
we propose to remove the reference to
‘‘the Center’’ and ‘‘[t]he Director, Health
Administration Center, or his or her
designee’’ in § 17.276(a) and (b), as
renumbered by this rulemaking. Our
intent is to indicate that VA is
responsible for administering
CHAMPVA and has discretion to assign
claims processing responsibility within
the Department.
Proposed § 17.276(c) would clarify
that claims for services and supplies
provided to an individual before the
date of the event that qualifies the
individual as eligible under § 17.271 are
not reimbursable.
We further propose to add new
paragraph (d) to proposed § 17.276 to
clarify CHAMPVA policy concerning
double coverage situations. We would
clearly state that CHAMPVA is the last
payer to all OHI, with the exceptions
noted previously, which would mean
that in cases of double coverage, any
CHAMPVA benefits would generally not
be paid until the claim has first been
filed with the OHI and a final payment
determination or explanation of benefits
has been issued by the other insurer or
payer. This is consistent with the
purpose of TRICARE’s double coverage
provisions in 32 CFR 199.8, which
address double coverage situations with
OHI. Once CHAMPVA, as the last payer,
makes its payment to the authorized
non-VA provider, the CHAMPVA
beneficiary’s personal liability for the
cost of care is then fully extinguished,
as discussed earlier. However, TRICARE
has special rules for double coverage
situations involving TRICARE
beneficiaries who also have Medicare
benefits. See 32 CFR 199.8(e)(1). In the
case of double coverage based on the
availability of both CHAMPVA and
Medicare benefits, the provisions of
current § 17.271(b) would still apply
and be unchanged by this proposed
rulemaking. Under current § 17.271(b),
VA is the secondary payer to Medicare,
as required under 38 U.S.C. 1781(d)(2).
17.277 Appeals
Proposed § 17.277 is a revision and
renumbering of current § 17.276. We
would make two minor revisions to
current § 17.276. First, we would
remove references to ‘‘Director, Health
Administration Center, or his or her
designee’’ (an outdated reference within
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the current Office of Community Care)
and replace it with a reference to ‘‘VA.’’
This is necessary to ensure that VA is
effectively put forth as the general
administrator of CHAMPVA. In
addition, we would clarify when a
beneficiary has OHI, an appeal must
first be filed with the OHI, and a
determination made, before submitting
an appeal to CHAMPVA. We would also
like to note that there may be instances
where we would not require a
beneficiary to appeal with their OHI
first, such as when the OHI deems the
issue non-appealable. Neither of these
revisions are substantive changes. We
will also keep the note located in
current § 17.276, relocating it to the
body of new § 17.277.
We propose to renumber current
§§ 17.277–17.278 to §§ 17.278–17.279.
Additionally, as with proposed § 17.277,
we would remove reference to ‘‘the
Center’’ in current § 17.277 and in its
place insert ‘‘VA.’’ This revision would
clarify that it is VA, and not HAC
independently, that has the authority to
pursue medical care cost recovery in
accordance with applicable law. We
would also remove the reference to
third-party liability in proposed
§ 17.278 because it is unnecessary. VA’s
specific authority to recover for medical
care costs applies to responsible third
parties. We would not make any
substantive changes to proposed
§ 17.279.
Effect of Rulemaking
The Code of Federal Regulations, as
proposed to be revised by this proposed
rulemaking, would represent the
exclusive legal authority on this subject.
No contrary rules or procedures would
be authorized. All VA guidance would
be read to conform with this proposed
rulemaking if possible or, if not
possible, such guidance would be
superseded by this rulemaking.
Paperwork Reduction Act
This proposed rule contains no
provisions constituting a collection of
information under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501–
3521).
Regulatory Flexibility Act
The Secretary hereby certifies that
this proposed rule would not have a
significant economic impact on a
substantial number of small entities as
they are defined in the Regulatory
Flexibility Act, 5 U.S.C. 601–612. The
new proposed payment methods in this
rulemaking will include new
reimbursement rates for the Outpatient
Prospective Payment System (OPPS),
Home Health Prospective Payment
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2407
System (HH PPS), and Sole Community
Hospitals (SCHs) reimbursement
methodologies. These revised
methodologies would not significantly
affect small businesses due to the
following reasons: (1) The health care
industry, to include Medicare and
TRICARE, is currently using these
payment methods and most providers
are used to these reimbursement rates,
if not expecting to receive them; (2)
CHAMPVA’s beneficiary population is
relatively small compared to these other
health care payers. Further support and
data can also be found in VA’s impact
analysis as a supporting document at
https://www.regulations.gov, usually
within 48 hours after the rulemaking
document is published. Additionally, a
copy of this rulemaking and its impact
analysis are available on VA’s website at
https://www.va.gov/orpm/, by following
the link for ‘‘VA Regulations Published
from FY 2004 Through Fiscal Year to
Date.’’ Therefore, pursuant to 5 U.S.C.
605(b), this amendment would be
exempt from the initial and final
regulatory flexibility analysis
requirements of 5 U.S.C. 603 and 604.
Executive Orders 12866, 13563 and
13771
Executive Orders 12866 and 13563
direct agencies to assess the costs and
benefits of available regulatory
alternatives and, when regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
environmental, public health and safety
effects, and other advantages;
distributive impacts; and equity).
Executive Order 13563 (Improving
Regulation and Regulatory Review)
emphasizes the importance of
quantifying both costs and benefits,
reducing costs, harmonizing rules, and
promoting flexibility. Executive Order
12866 (Regulatory Planning and
Review) defines a ‘‘significant
regulatory action,’’ which requires
review by the Office of Management and
Budget (OMB), as ‘‘any regulatory action
that is likely to result in a rule that may:
(1) Have an annual effect on the
economy of $100 million or more or
adversely affect in a material way the
economy, a sector of the economy,
productivity, competition, jobs, the
environment, public health or safety, or
State, local, or tribal governments or
communities; (2) Create a serious
inconsistency or otherwise interfere
with an action taken or planned by
another agency; (3) Materially alter the
budgetary impact of entitlements,
grants, user fees, or loan programs or the
rights and obligations of recipients
thereof; or (4) Raise novel legal or policy
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issues arising out of legal mandates, the
President’s priorities, or the principles
set forth in this Executive Order.’’
The economic, interagency,
budgetary, legal, and policy
implications of this regulatory action
have been examined and OMB has
determined the regulatory action to be
economically significant, because it will
have an annual effect on the economy
of $100 million or more. As noted
above, VA’s impact analysis is available
as a supporting document at https://
www.regulations.gov, usually within 48
hours after the rulemaking document is
published. Additionally, a copy of this
rulemaking and its impact analysis are
available on VA’s website at https://
www.va.gov/orpm/, by following the
link for ‘‘VA Regulations Published
from FY 2004 Through Fiscal Year to
Date.’’
This proposed rule is not expected to
be subject to the requirements of
EO13771 because this proposed rule is
expected to result in no more than de
minimis costs.
The Unfunded Mandates Reform Act
of 1995 requires, at 2 U.S.C. 1532, that
agencies prepare an assessment of
anticipated costs and benefits before
issuing any rule that may result in the
expenditure by State, local, or tribal
governments, in the aggregate, or by the
private sector, of $100 million or more
(adjusted annually for inflation) in any
one year. This proposed rule would
have no such effect on State, local, or
tribal governments, or on the private
sector.
Catalog of Federal Domestic Assistance
The Catalog of Federal Domestic
Assistance numbers and titles for the
programs affected by this document are
64.009, Veterans Medical Care Benefits;
64.010, Veterans Nursing Home Care;
and 64.011, Veterans Dental Care;
64.012, Veterans Prescription Service;
64.013, Veterans Prosthetic Appliances;
and 64.019, Veterans Rehabilitation
Alcohol and Drug Dependence.
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Signing Authority
The Secretary of Veterans Affairs, or
designee, approved this document and
authorized the undersigned to sign and
submit the document to the Office of the
Federal Register for publication
electronically as an official document of
the Department of Veterans Affairs. Gina
S. Farrisee, Deputy Chief of Staff,
Department of Veterans Affairs,
approved this document on October 2,
2017, for publication.
16:35 Jan 16, 2018
Dated: January 5, 2018.
Michael Shores,
Director, Office of Regulation Policy &
Management, Office of the Secretary,
Department of Veterans Affairs.
For the reasons stated in the
preamble, The Department of Veterans
Affairs (VA) proposes to amend 38 CFR
part 17 as follows:
PART 17—MEDICAL
1. The authority citation for part 17
continues to read in part as follows:
■
Authority: 38 U.S.C. 501, and as noted in
specific sections.
*
■
*
*
*
*
2. Revise § 17.270 to read as follows:
§ 17.270 General provisions and
definitions.
Unfunded Mandates
VerDate Sep<11>2014
List of Subjects in 38 CFR Part 17
Administrative practice and
procedure, Archives and records,
Claims, Dental health, Drug abuse,
Health care, Health facilities, Health
professions, Health records, Medical
devices, Mental health programs,
Nursing homes, Veterans.
Jkt 244001
(a) Overview of CHAMPVA.
CHAMPVA is the Civilian Health and
Medical Program of the Department of
Veterans Affairs (VA). Generally,
CHAMPVA furnishes medical care in
the same or similar manner, and subject
to the same or similar limitations, as
medical care furnished to certain
dependents and survivors of active duty
and retired members of the Armed
Forces under chapter 55 of title 10,
United States Code (CHAMPUS),
commonly referred to as the TRICARE
Standard plan. Under CHAMPVA, VA
shares the cost of medically necessary
services and supplies with eligible
beneficiaries within the 50 United
States, the District of Columbia, the U.S.
territories, and abroad. Under
CHAMPVA, medical services and
supplies may be provided as follows:
(1) By an authorized non-VA
provider.
(2) By a VA provider at a VA facility,
on a resource-available basis through
the CHAMPVA In-house Treatment
Initiative (CITI) only to CHAMPVA
beneficiaries who are not also eligible
for Medicare.
(3) Through VA Medications by Mail
(MbM).
(i) Only CHAMPVA beneficiaries who
do not have any other type of health
insurance that pays for prescriptions,
including Medicare Part D, may use
MbM.
(ii) Smoking cessation pharmaceutical
supplies will only be provided through
MbM and only to CHAMPVA
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Fmt 4702
Sfmt 4702
beneficiaries that are not also eligible for
Medicare.
(b) Definitions. The following
definitions apply to CHAMPVA
(§§ 17.270 through 17.278):
Accepted assignment refers to the
action of an authorized non-VA
provider who accepts responsibility for
the care of a CHAMPVA beneficiary and
thereby agrees to accept the CHAMPVA
determined allowable amount as full
payment for services and supplies
rendered to the beneficiary. (The
provider’s acceptance of the CHAMPVA
determined allowable amount
extinguishes the beneficiary’s payment
liability to the provider with the
exception of applicable cost shares and
deductibles.)
Authorized non-VA provider means
an individual or institutional non-VA
provider of CHAMPVA-covered medical
services and supplies that meets any of
the following criteria:
(i) Is licensed or certified by a State
to provide the medical services and
supplies; or
(ii) Where a State does not offer
licensure or certification, is otherwise
certified by an appropriate national or
professional association that sets
standards for the specific medical
provider.
Calendar year means January 1
through December 31.
CHAMPVA beneficiary means a
person enrolled under § 17.271.
CHAMPVA-covered services and
supplies mean those medical services
and supplies that are medically
necessary and appropriate for the
treatment of a condition and that are not
specifically excluded under
§ 17.272(a)(1) through (84).
CHAMPVA determined allowable
amount has the meaning set forth in
§ 17.272(b)(1).
CHAMPVA In-house Treatment
Initiative (CITI) means the initiative
under 38 U.S.C. 1781(b) under which
participating VA medical facilities
provide medical services and supplies
to CHAMPVA beneficiaries who are not
also eligible for Medicare, subject to
availability of space and resources.
Child has the definition established in
38 U.S.C. 101.
Claim means a request by an
authorized non-VA provider or by a
CHAMPVA beneficiary for payment or
reimbursement for medical services and
supplies provided to a CHAMPVA
beneficiary.
Fiscal year means October 1 through
September 30.
Medications by Mail (MbM) means the
initiative under which VA provides
outpatient prescription medications
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through the mail to CHAMPVA
beneficiaries.
Other health insurance (OHI) means
health insurance plans or programs
(including Medicare) or third-party
coverage that provide coverage to a
CHAMPVA beneficiary for expenses
incurred for medical services and
supplies.
Payer refers to OHI, as defined in this
section, that is obligated to pay for
CHAMPVA-covered medical services
and supplies. In a situation in which, in
addition to CHAMPVA, one or more
payers is/are responsible to pay for such
services and supplies (i.e., a ‘‘double
coverage’’ situation), there would be a
primary payer (i.e., the payer obligated
to pay first), secondary payer (i.e., the
payer obligated to pay after the primary
payer), etc. In double coverage
situations, CHAMPVA would be the last
payer.
Service-connected has the definition
established in 38 U.S.C. 101.
Spouse refers to a person who is
married to a veteran and whose
marriage is valid as determined under
38 U.S.C. 103(c).
Surviving spouse refers to a person
who was married to and is the
widow(er) of a veteran as determined
under 38 U.S.C. 103(c).
(c) Discretionary authority. When it is
determined to be in the best interest of
VA, VA may waive any requirement in
§§ 17.270 through 17.278, except any
requirement specifically set forth in 38
U.S.C. 1781, or otherwise imposed by
statute. It is VA’s intent that such
discretionary authority would be used
only under very unusual and limited
circumstances and not to deny any
individual any right, benefit, or
privilege provided to him or her by
statute or these regulations. Any such
waiver shall apply only to the
individual circumstance or case
involved and will in no way be
construed to be precedent-setting.
(Authority: 38 U.S.C. 501, 1781)
3. Amend § 17.271 by:
a. Removing the word ‘‘and’’ at the
end of paragraph (a)(3).
■ b. Redesignating paragraph (a)(4) as
paragraph (a)(5).
■ c. Adding a new paragraph (a)(4).
■ d. Revising the authority citation
following paragraph (a).
The addition and revision read as
follows:
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■
■
§ 17.271
Eligibility.
(a) * * *
(4) An individual designated as a
Primary Family Caregiver, under 38 CFR
71.25(f), who is not entitled to care or
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16:35 Jan 16, 2018
Jkt 244001
services under a health-plan contract (as
defined in 38 U.S.C. 1725(f)(2)); and
*
*
*
*
*
(Authority: 38 U.S.C. 501, 1720G(a)(7)(A),
1781)
*
*
*
*
*
4. Amend § 17.272 by:
a. Revising paragraph (a)(2).
b. In paragraph (a)(3) introductory
text, removing the phrase ‘‘(Medicaid
excluded)’’.
■ c. Adding paragraphs (a)(3)(iii) and
(iv).
■ d. Revising paragraph (a)(21)(ix).
■ e. Removing paragraph (a)(26).
■ f. Redesignating paragraphs (a)(27)
through (38) as paragraphs (a)(26)
through (37), respectively.
■ g. In newly redesignated paragraph
(a)(30), revising the introductory text
and paragraphs (a)(30)(v) and (vi) and
adding paragraphs (a)(30)(xi) through
(xiv).
■ h. Removing paragraph (a)(39).
■ i. Redesignating paragraphs (a)(40)
through (56) as paragraphs (a)(38)
through (54), respectively.
■ j. In newly redesiganted paragraph
(a)(40)(iv), removing ‘‘(a)(42)(iii)(A)’’
and adding in its place ‘‘(a)(40)(iii)(A).’’
■ k. Removing paragraph (a)(57).
■ l. Redesignating paragraphs (a)(58)
through (71) as paragraphs (a)(55)
through (68), respectively.
■ m. Revising newly redesignated
paragraphs (a)(57) through (59).
■ n. Removing paragraph (a)(72).
■ o. Redesignating paragraphs (a)(73)
through (86) as paragraphs (a)(69)
through (82), respectively.
■ p. Revising newly redesignated
paragraph (a)(76).
■ q. Adding paragraphs (a)(83) and (84).
■ r. Revising paragraph (b).
The revisions and additions read as
follows:
■
■
■
§ 17.272
Benefits limitations/exclusions.
(a) * * *
(2) Services and supplies required as
a result of an occupational disease or
injury for which benefits are payable
under workers’ compensation or similar
protection plan (whether or not such
benefits have been applied for or paid)
except when such benefits are
exhausted and the services and supplies
are otherwise not excluded from
CHAMPVA coverage.
(3) * * *
(iii) Indian Health Service.
(iv) CHAMPVA supplemental
policies.
*
*
*
*
*
(21) * * *
(ix) Treatment for stabilization of
myofascial pain dysfunction syndrome,
also referred to as temporomandibular
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2409
joint disorder (TMD). Authorization is
limited to initial imaging such as
radiographs, Computed Tomography, or
Magnetic Resonance Imaging; up to four
office visits; and the construction of an
occlusal splint.
*
*
*
*
*
(30) Preventive care (such as
employment-requested physical
examinations and routine screening
procedures). The following exceptions
apply, including but not limited to:
*
*
*
*
*
(v) Cervical cancer screening.
(vi) Breast cancer screening.
*
*
*
*
*
(xi) Colorectal cancer screening.
(xii) Prostate cancer screening.
(xiii) Annual physical examination.
(xiv) Vaccinations/immunizations.
*
*
*
*
*
(57) Unless a waiver for extended
coverage is granted in advance:
Inpatient mental health services in
excess of 30 days in any calendar year
(or in an admission), in the case of a
patient 19 years of age or older; 45 days
in any calendar year (or in an
admission), in the case of a patient
under 19 years of age; or 150 days of
residential treatment care in any
calendar year (or in an admission).
(58) Outpatient mental health services
in excess of 23 visits in a calendar year
unless a waiver for extended coverage is
granted in advance.
(59) Institutional services for partial
hospitalization in excess of 60 treatment
days in any calendar year (or in an
admission) unless a waiver for extended
coverage is granted in advance.
*
*
*
*
*
(76) Over-the-counter products except
for pharmaceutical smoking cessation
supplies that are approved by the U.S.
Food and Drug Administration,
prescribed, and provided through MbM,
and insulin and related diabetic testing
supplies and syringes.
*
*
*
*
*
(83) Medications not approved by the
U.S. Food and Drug Administration
(FDA), excluding FDA exceptions to the
approval requirement.
(84) Services and supplies related to
the treatment of dyslexia.
(b) Costs of services and supplies to
the extent such amounts are billed over
the CHAMPVA determined allowable
amount are specifically excluded from
coverage.
(1) The CHAMPVA determined
allowable amount is the maximum level
of payment by CHAMPVA to an
authorized non-VA provider for the
provision of CHAMPVA-covered
services and supplies to a CHAMPVA
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beneficiary. The CHAMPVA determined
allowable amount is determined before
consideration of cost sharing and the
application of deductibles or OHI.
(2) A Medicare-participating hospital
must accept the CHAMPVA determined
allowable amount for inpatient services
provided to a CHAMPVA beneficiary as
payment in full. See 42 CFR 489.25.
(3) An authorized non-VA provider
who accepts responsibility for the care
of a CHAMPVA beneficiary thereby
agrees to accept the CHAMPVA
determined allowable amount as full
payment for services and supplies
rendered to the beneficiary (i.e.,
accepted assignment). The provider’s
acceptance of the CHAMPVA
determined allowable amount
extinguishes the beneficiary’s payment
liability to the provider. Any attempts to
collect any additional amount from the
CHAMPVA beneficiary may result in
the provider being excluded from
Federal benefits programs. See 42 CFR
1003.105.
*
*
*
*
*
■ 5. Amend § 17.273 by:
■ a. Revising the introductory text and
paragraph (d).
■ b. Removing paragraph (e).
■ c. Redesignating paragraph (f) as
paragraph (e).
■ d. Adding new paragraph (f).
The revisions and addition read as
follows:
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§ 17.273
Preauthorization.
Preauthorization or advance approval
is required for any of the following,
except when the benefit is covered by
the CHAMPVA beneficiary’s other
health insurance (OHI):
*
*
*
*
*
(d) Dental care. For limitations on
dental care, see § 17.272(a)(21)(i)
through (xii).
*
*
*
*
*
(f) CHAMPVA will perform a
retrospective medical necessity review
during the coordination of benefits
process if:
(1) It is determined that CHAMPVA is
the responsible payer for services and
supplies but CHAMPVA
preauthorization was not obtained prior
to delivery of the services or supplies;
and,
(2) The claim for payment is filed
within the appropriate one-year period.
*
*
*
*
*
■ 6. Amend § 17.274 by:
■ a. Revising paragraphs (a), (b), and (c).
■ b. Adding a heading for paragraph (d).
■ c. Adding paragraph (e).
The revisions and additions read as
follows:
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Jkt 244001
§ 17.274
Cost sharing.
(a) Cost sharing generally. CHAMPVA
is a cost sharing program in which the
cost of covered services is shared with
the CHAMPVA beneficiary. CHAMPVA
pays the CHAMPVA determined
allowable amount less the CHAMPVA
deductible, if applicable, and less the
CHAMPVA beneficiary cost share.
(1) CHAMPVA beneficiary cost-share
requirements do not apply to the
following:
(i) Supplies provided through VA
MbM.
(ii) Any medical services and supplies
provided to a CHAMPVA beneficiary
through CITI.
(iii) The following services, even if
not provided through CITI:
(A) Colorectal cancer screening.
(B) Breast cancer screening.
(C) Cervical cancer screening.
(D) Prostate cancer screening.
(E) Annual physical exams.
(F) Vaccinations/immunizations.
(G) Well child care from birth to age
six, as described in § 17.272(a)(30)(i).
(iv) Hospice services.
(v) Or other services as determined by
the Secretary of Veterans Affairs.
(2) [Reserved]
(b) Deductibles. In addition to the
CHAMPVA beneficiary cost share, an
annual (calendar year) outpatient
deductible requirement ($50 per
beneficiary or $100 per family) must be
satisfied prior to VA payment of
outpatient benefits. The deductible
requirement is waived for:
(1) CHAMPVA-covered services and
supplies provided through VA MbM or
through CITI.
(2) Inpatient services.
(3) Preventive services listed in
paragraph (a)(1)(iii) of this section.
(4) Hospice services.
(5) Or other services as determined by
the Secretary of Veterans Affairs.
(c) Cost sharing limitations. To
provide financial protection against the
impact of a long-term illness or injury,
there is a $3,000 calendar year limit or
‘‘catastrophic cap’’ per CHAMPVA
eligible family on the CHAMPVA
beneficiary’s out-of-pocket costs for
allowable services and supplies. After a
family has paid $3,000 in out-of-pocket
costs, to include both cost share and
deductible amounts, in a calendar year,
CHAMPVA will pay the full allowable
amounts for the remaining CHAMPVAcovered services and supplies through
the end of that calendar year. Credits to
the annual catastrophic cap are limited
to the applied annual deductible(s) and
the CHAMPVA beneficiary cost-share
amount. Costs above the CHAMPVA
determined allowable amount, as well
as costs associated with non-covered
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medical services and supplies, are not
credited toward the catastrophic cap
calculation.
(d) Non-payment. * * *
(e) Cost share calculation. The
CHAMPVA beneficiary’s cost-share
amount, if not waived under paragraph
(a)(1) of this section, is 25 percent of the
CHAMPVA determined allowable
amount in excess of the annual calendar
year deductible (see § 17.275 for
procedures related to the calculation of
the allowable amount for CHAMPVAcovered services and supplies), except
for the following:
(1) For inpatient services subject to
the CHAMPVA Diagnosis Related Group
(DRG) payment system, the cost share is
the lesser of:
(i) The per diem rate multiplied by
the number of inpatient days;
(ii) 25 percent of the hospital’s billed
amount; or
(iii) The base CHAMPVA DRG rate.
(2) For inpatient mental health low
volume hospitals and units (less than 25
mental health discharges per federal
fiscal year), the cost share is the lesser
of:
(i) The fixed per diem rate multiplied
by the number of inpatient days; or
(ii) 25 percent of the hospital’s billed
charges.
*
*
*
*
*
§§ 17.275 through 17.278 [Redesignated as
§§ 17.276 through 17.279]
7. Redesignate §§ 17.275 through
17.278 as §§ 17.276 through 17.279.
■ 8. Add new § 17.275 to read as
follows:
■
§ 17.275 CHAMPVA determined allowable
amount calculation.
CHAMPVA calculates the allowable
amount in the following ways, for the
following covered services and supplies:
(a) Inpatient hospital services (nonmental health). Unless exempt or
subject to a methodology under
paragraph (b) or (c) of this section,
inpatient hospital services provided in
the 50 States, the District of Columbia,
and Puerto Rico are subject to the
CHAMPVA Diagnosis Related Group
(DRG)-based reimbursement
methodology. Under the CHAMPVA
DRG-based payment system, hospitals
are paid a predetermined amount per
discharge for inpatient hospital services,
which will not exceed the billed
amount. Certain inpatient services will
be reimbursed under the CHAMPVA
Cost-to-Charge (CTC) reimbursement
methodology.
(b) Inpatient hospital services (mental
health). The CHAMPVA inpatient
mental health per diem reimbursement
methodology is used to calculate
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reimbursement for inpatient mental
health hospital care in specialty
psychiatric hospitals and psychiatric
units of general acute hospitals that are
exempt from the CHAMPVA DRG-based
payment system. The per diem rate is
calculated by multiplying the daily rate
by the number of days (length of stay).
The daily rate is updated each fiscal
year for both high volume hospitals (25
or more discharges per fiscal year) and
low volume hospitals (fewer than 25
discharges per fiscal year).
(c) Other inpatient hospital services.
(1) The CHAMPVA CTC reimbursement
methodology is used to calculate
reimbursement for inpatient care
furnished by hospitals or facilities that
are exempt from either of the
methodologies in paragraph (a) or (b) of
this section. Such hospitals or facilities
will be paid at the CHAMPVA CTC ratio
times the billed charges that are
customary and not in excess of rates or
fees the hospital or facility charges the
general public for similar services in a
community.
(2) The following hospitals and
services are subject to the CHAMPVA
CTC payment methodology:
(i) Any hospital that qualifies as a
cancer hospital under Medicare
standards and has elected to be exempt
from the Centers for Medicare and
Medicaid Services (CMS) prospective
payment system.
(ii) Christian Science sanatoriums.
(iii) Critical Access Hospitals.
(iv) Any hospital outside the 50
States, the District of Columbia, or
Puerto Rico.
(v) Hospitals within hospitals.
(vi) Long-term care hospitals.
(vii) Non-Medicare participating
hospitals.
(viii) Non-VA Federal Health Care
Facilities (e.g., military treatment
facilities, Indian Health Service).
(ix) Rehabilitation hospitals.
(x) Hospital or hospital-based services
subject to State waiver in any State that
has implemented a separate DRG-based
payment system or similar payment
system in order to control costs.
(xi) Hospitals and services as
determined by the Secretary of Veterans
Affairs.
(d) Outpatient hospital services. The
CHAMPVA outpatient prospective
payment system (OPPS) is used to
calculate the allowable amount for
outpatient services provided in
hospitals subject to Medicare OPPS.
This will include the utilization of
TRICARE’s reimbursement methodology
to include specific coding requirements,
ambulatory payment classifications
(APCs), nationally established APC
amounts, and associated adjustments.
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(e) Outpatient and inpatient nonhospital services. Payments to
individual authorized non-VA providers
(not hospitals) for CHAMPVA-covered
medical services and supplies provided
on an outpatient or inpatient basis,
including but not limited to, anesthesia
services, laboratory services, and other
professional fees associated with
individual authorized non-VA
providers, are reimbursed based on the
lesser of:
(1) The CHAMPVA Maximum
Allowable Charge;
(2) The prevailing amount, which is
the amount equal to the maximum
reasonable amount allowed providers
for a specific procedure in a specific
locality; or,
(3) The billed amount.
(f) Pharmacy services and supplies.
The CHAMPVA pharmacy services and
supplies payment methodology is based
on specific CHAMPVA pharmacy points
of service, which dictate the amounts
paid by VA. VA pays:
(1) For services and supplies obtained
from a retail in-network pharmacy, the
lesser of the billed amount or the
contracted rate; or
(2) For supplies obtained from a retail
out-of-network pharmacy, the lesser of
the billed amount plus a dispensing fee
or the average wholesale price plus a
dispensing fee.
(g) Skilled Nursing Facility (SNF)
care. The CHAMPVA SNF
reimbursement methodology is based on
the CMS prospective payment system
for SNFs under 42 CFR part 413, subpart
J (Medicare Resource Utilization Group
(RUG) rates).
(h) Durable medical equipment,
prosthetics, orthotics, and supplies
(DMEPOS). The CHAMPVA DMEPOS
reimbursement methodology is based on
the same amounts established under the
CMS DMEPOS fee schedule under 42
CFR part 414, subpart D. The
CHAMPVA determined allowable
amount for DMEPOS is the amount in
effect in the specific geographic location
at the time CHAMPVA-covered medical
services and supplies are provided to a
CHAMPVA beneficiary.
(i) Ambulance services. CHAMPVA
adopts Medicare’s Ambulance Fee
Schedule (AFS) for ambulance services,
with the exception of services furnished
by a Critical Access Hospital (CAH).
Ambulance services are paid based on
the lesser of the Medicare AFS or the
billed amount. Ambulance services
provided by a CAH are paid on the same
bases as the CTC method under
paragraph (c) of this section.
(j) Hospice care. CHAMPVA hospice
reimbursement methodology uses
Medicare per diem hospice rates.
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2411
(k) Home health care (intermittent or
part-time). CHAMPVA home health care
reimbursement methodology, based on
Medicare’s home health prospective
payment system, uses a fixed case-mix
and wage-adjusted national 60-day
episode payment amount to act as
payment in full for costs associated with
furnishing home health services with
exceptions allowing for additional
payment to be established.
(l) Ambulatory surgery. The
CHAMPVA reimbursement
methodology for facility charges
associated with procedures performed
in a freestanding ambulatory surgery
center is based on a prospectively
determined amount, similar to that used
by TRICARE. These facility charges do
not include physician fees,
anesthesiologist fees, or fees of other
authorized non-VA providers; such
independent professional fees must be
submitted separately from facility fees
and are calculated under the
methodology in paragraph (e) of this
section.
(m) CHAMPVA-covered medical
services and supplies provided outside
the United States. VA shall determine
the appropriate reimbursement
method(s) for CHAMPVA-covered
medical services and supplies provided
by authorized non-VA providers outside
the United States.
(n) Sole Community Hospitals. The
CHAMPVA reimbursement
methodology for inpatient services
provided in a Sole Community Hospital
(SCH) will be the greater of: The
allowable amount determined by
multiplying the billed charges by the
SCH’s most recently available cost-tocharge ratio from the CMS Inpatient
Provider Specific File or the DRG
reimbursement rate.
(Authority: 38 U.S.C. 501, 1781)
9. Amend newly redesignated
§ 17.276 by:
■ b. Revising paragraphs (a)
introductory text and (b).
■ c. Adding paragraphs (c) and (d).
The revisions and additions read as
follows:
■
§ 17.276
Claim-filing deadlines.
(a) Unless an exception is granted
under paragraph (b) of this section,
claims for medical services and supplies
must be filed no later than:
*
*
*
*
*
(b) Requests for an exception to the
claim filing deadline must be submitted
in writing and include a complete
explanation of the circumstances
resulting in late filing along with all
available supporting documentation.
Each request for an exception to the
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claim filing deadline will be reviewed
individually and considered on its own
merit. VA may grant exceptions to the
requirements in paragraph (a) of this
section if it determines that there was
good cause for missing the filing
deadline. For example, when dual
coverage exists, CHAMPVA payment, if
any, cannot be determined until after
the primary insurance carrier has
adjudicated the claim. In such
circumstances an exception may be
granted provided that the delay on the
part of the primary insurance carrier is
not attributable to the beneficiary.
Delays due to provider billing
procedures do not constitute a valid
basis for an exception.
(c) Claims for CHAMPVA-covered
services and supplies provided before
the date of the event that qualifies an
individual under § 17.271 are not
reimbursable.
(d) CHAMPVA is the last payer to
OHI, as that term is defined in
§ 17.270(b). CHAMPVA benefits will
generally not be paid until the claim has
been filed with the OHI and the OHI has
issued a final payment determination or
explanation of benefits. CHAMPVA is
secondary payer to Medicare per the
terms of § 17.271(b).
*
*
*
*
*
■ 10. Revise newly redesignated
§ 17.277 to read as follows:
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§ 17.277
Appeals.
Notice of the initial determination
regarding payment of CHAMPVA
benefits will be provided to the
CHAMPVA beneficiary on a CHAMPVA
Explanation of Benefits (EOB) form. The
EOB form is generated by the
CHAMPVA automated payment
processing system. If a CHAMPVA
beneficiary or provider disagrees with
the determination concerning
CHAMPVA-covered services and
supplies or calculation of benefits, he or
she may request reconsideration. Such
requests must be submitted to VA in
writing within one year of the date of
the initial determination. The request
must state why the CHAMPVA claimant
believes the decision is in error and
must include any new and relevant
information not previously considered.
Any request for reconsideration that
does not identify the reason for dispute
will be returned to the claimant without
further consideration. After reviewing
the claim and any relevant supporting
documentation, VA will issue a written
determination to the claimant that
affirms, reverses, or modifies the
previous decision. If the claimant is still
dissatisfied, within 90 days of the date
of the decision he or she may make a
written request for review by VA. After
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reviewing the claim and any relevant
supporting documentation, VA will
issue a written determination to the
claimant that affirms, reverses, or
modifies the previous decision. The
decision of VA with respect to benefit
coverage and computation of benefits is
final. When a CHAMPVA beneficiary
has other health insurance (OHI), an
appeal must first be filed with the OHI,
and a determination made, before
submitting the appeal to CHAMPVA
with limited exceptions such as if the
OHI deems the issue non-appealable.
Denial of CHAMPVA benefits based on
legal eligibility requirements may be
appealed to the Board of Veterans’
Appeals in accordance with 38 CFR part
20. Medical determinations are not
appealable to the Board. 38 CFR 20.101.
(Authority: 38 U.S.C. 501, 1781)
11. Revise newly redesignated
§ 17.278 to read as follows:
■
§ 17.278
Medical care cost recovery.
VA will actively pursue medical care
cost recovery in accordance with
applicable law.
(Authority: 42 U.S.C. 2651; 38 U.S.C. 501,
1781)
[FR Doc. 2018–00332 Filed 1–16–18; 8:45 am]
are due on or before March 5, 2018. If
you anticipate that you will be
submitting comments, but find it
difficult to do so within the period of
time allowed by this document, you
should advise the contact listed below
as soon as possible.
Federal Communications Commission.
Katura Jackson,
Federal Register Liaison Officer.
[FR Doc. 2018–00451 Filed 1–16–18; 8:45 am]
BILLING CODE 6712–01–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
50 CFR Part 300
[Docket No. 161228999–7867–01]
RIN 0648–BG51
Commerce Trusted Trader Program
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Proposed rule; request for
comments.
AGENCY:
BILLING CODE 8320–01–P
The National Marine
Fisheries Service is proposing this
Commerce Trusted Trader Program
(CTTP) as part of an effective seafood
traceability process to combat Illegal,
Unreported, and Unregulated (IUU)
fishing and seafood fraud. The
voluntary CTTP supplements the
Seafood Import Monitoring Program
(SIMP), recently implemented under the
Magnuson-Stevens Fishery
Conservation and Management Act.
Qualified importers who choose to
participate in the CTTP would benefit
from reduced reporting and
recordkeeping requirements, and
streamlined entry into U.S. commerce
for seafood imports subject to the SIMP.
DATES: Written comments must be
received by March 19, 2018.
ADDRESSES: Written comments on this
action, identified by NOAA–NMFS–
2016–0165, may be submitted by either
of the following methods:
• Federal eRulemaking Portal: Go to
https://www.regulations.gov/#!
docketDetail;D=NOAA-NMFS-20160165, click the ‘‘Comment Now!’’ icon,
complete the required fields, and enter
or attach your comments.
• Mail: Melissa Beaudry, Office of
International Affairs and Seafood
Inspection, NOAA Fisheries, 1315 EastWest Highway, Silver Spring, MD
20910.
SUMMARY:
FEDERAL COMMUNICATIONS
COMMISSION
47 CFR Part 54
[WC Docket No. 17–310; FCC 17–164]
Promoting Telehealth in Rural
America; Correction
Federal Communications
Commission.
ACTION: Notice; correction.
AGENCY:
The Federal Communications
Commission (Commission) published a
document in the Federal Register of
January 3, 2018 seeking comment on
how to strengthen the Rural Health Care
Program and improve access to
telehealth in rural America. The
document contained an incorrect reply
comment date.
FOR FURTHER INFORMATION CONTACT:
Radhika Karmarkar, Wireline
Competition Bureau, (202) 418–7400 or
TTY: (202) 418–0484.
SUMMARY:
Correction
In the Federal Register of January 3,
2018, in FR Doc. 2017–28298, on page
303, in the first column, correct the
DATES caption to read:
DATES: Comments are due on or before
February 2, 2018, and reply comments
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Agencies
[Federal Register Volume 83, Number 11 (Wednesday, January 17, 2018)]
[Proposed Rules]
[Pages 2396-2412]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-00332]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF VETERANS AFFAIRS
38 CFR Part 17
RIN 2900-AP02
Civilian Health and Medical Program of the Department of Veterans
Affairs
AGENCY: Department of Veterans Affairs.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: The Department of Veterans Affairs (VA) proposes to amend its
regulations governing the Civilian Health and Medical Program of the
Department of Veterans Affairs (CHAMPVA). The proposed revisions would
clarify and update these regulations to conform to changes in law and
policy that control the administration of CHAMPVA and would include
details concerning the administration of CHAMPVA that are not reflected
in current regulations. The proposed revisions would also expand
covered services and supplies to include certain preventive services
and eliminate cost-share amounts and deductibles for certain covered
services.
DATES: Written comments must be received on or before March 19, 2018.
ADDRESSES: Written comments may be submitted through https://www.Regulations.gov; by mail or hand-delivery to the Director,
Regulation and Policy Management (00REG), Department of Veterans
Affairs, 810 Vermont Avenue NW, Room 1068, Washington, DC 20420; or by
fax to (202) 273-9026. Comments should indicate that they are submitted
in
[[Page 2397]]
response to ``RIN 2900-AP02, Civilian Health and Medical Program of the
Department of Veterans Affairs.'' Copies of comments received will be
available for public inspection in the Office of Regulation Policy and
Management, Room 1063B, between the hours of 8:00 a.m. and 4:30 p.m.
Monday through Friday (except holidays). Please call (202) 461-4902 for
an appointment. (This is not a toll-free number.) In addition, during
the comment period, comments may be viewed online through the Federal
Docket Management System at https://www.Regulations.gov.
FOR FURTHER INFORMATION CONTACT: Joseph Duran, Director, Policy and
Planning, Office of Community Care (OCC), 3773 Cherry Creek North
Drive, Denver, Colorado 80209, [email protected], (303) 370-1637.
(This is not a toll-free number.)
SUPPLEMENTARY INFORMATION: The Civilian Health and Medical Program of
the Department of Veterans Affairs (CHAMPVA) is a health benefits
program in which the Department of Veterans Affairs (VA) shares the
cost of covered medical care services and supplies with spouses,
children, survivors, and certain caregivers of veterans who meet
eligibility criteria under 38 U.S.C. 1781. CHAMPVA beneficiaries must
not be eligible for TRICARE, a health care program administered by the
Department of Defense (DoD) that is also authorized to provide health
care to certain family members of veterans. Certain Primary Family
Caregivers designated under 38 U.S.C. 1720G(a)(7)(A) are eligible under
section 1781 as long as they are not entitled to services under a
health-plan contract as that term is defined in 38 U.S.C. 1725(f).
Under section 1781, VA ``shall provide for medical care in the same
or similar manner and subject to the same or similar limitations as
medical care is furnished to certain dependents and survivors of active
duty and retired members of the Armed Forces under chapter 55 of title
10 [United States Code] (CHAMPUS).'' 38 U.S.C. 1781(b). CHAMPUS was the
original program administered by DoD to provide civilian health
benefits for active duty military personnel, military retirees, and
their dependents. 32 CFR 199.1. Although the CHAMPUS program is still
referenced in DoD regulations, DoD effectively replaced the CHAMPUS
program with what is commonly known as the ``TRICARE Standard'' plan
(``TRICARE''). See 32 CFR 199.1(r), 199.17(a)(6)(ii)(C) (identifying
``TRICARE Standard'' as the basic CHAMPUS program). TRICARE's current
benefit structure offers varying degrees of medical benefits under
multiple plan options beyond its Standard plan, but we administer
CHAMPVA in the same or similar manner as TRICARE Standard only, because
that basic program is the one that is referenced by the CHAMPUS
authority. Thus, all references in this rulemaking to ``TRICARE'' are
to the TRICARE Standard plan, which we refer to simply as ``TRICARE''
throughout most of this rulemaking for ease of reference.
VA interprets the mandate in 38 U.S.C. 1781(b) to administer
CHAMPVA in the ``same or similar manner . . . as medical care is
furnished . . . under title 10 chapter 55 (CHAMPUS)'' to mean that we
must generally administer CHAMPVA in a ``same or similar manner'' as
the TRICARE Standard plan. The phrase ``same or similar manner'' does
not require the programs to be administered in an identical manner.
Rather, we broadly interpret this language as affording us needed
flexibility to administer the program for CHAMPVA beneficiaries. For
this reason, not every aspect of CHAMPVA will find a corollary in the
TRICARE Standard Plan.
TRICARE has undergone changes in legal authority and policy that
have prompted these proposed revisions to our CHAMPVA regulations. This
rulemaking is intended to ensure that our regulations continue to be,
again broadly speaking, the same or similar to the regulations and
policies governing TRICARE. As noted throughout this proposed rule,
there are necessary variations from TRICARE, particularly due to
TRICARE's current benefit structure with varying degrees of medical
benefits under multiple plan options, but we believe these variations
satisfy the same or similar requirement in 38 U.S.C. 1781(b).
This rulemaking also proposes clarifications and revisions that
will improve our ability to effectively administer CHAMPVA, as well as
technical revisions to make our regulations more understandable.
17.270 General Provisions and Definitions
Current Sec. 17.270(a) broadly discusses general administrative
provisions of CHAMPVA, and current Sec. 17.270(b) establishes certain
definitions for the CHAMPVA regulations. We would revise the title of
Sec. 17.270 to clearly indicate that it contains both general
provisions as well as definitions and would revise and reorganize the
current definitions as well as add new definitions. Finally, we would
add a new paragraph (c) to permit VA to waive, under certain
circumstances, any requirements in the CHAMPVA regulations that are not
otherwise required by statute, as is allowed under TRICARE. See 32 CFR
199.1(n). Waiver would be limited to very unusual and limited
circumstances when waiver was determined to be in the best interests of
VA; would not set a precedent for future decisions; and would not be
used to deny any individual any right, benefit, or privilege provided
to him or her by statute or these regulations.
Proposed Sec. 17.270(a) would continue to provide an overview of
CHAMPVA, including a general summary of the manner in which CHAMPVA is
administered. We would refer to CHAMPUS, as we do in the current
regulation, but would also reference TRICARE because the reference to
CHAMPUS is outdated, as explained above, and may be misunderstood by
CHAMPVA beneficiaries. Current Sec. 17.270(a) states that CHAMPVA is
administered by the ``Health Administration Center'' (HAC) (referred to
now as the Office of Community Care (OCC)), which is located in Denver,
Colorado. We propose to delete this statement because that fact is not
substantively relevant to the regulations. These revisions are not
substantively different from current Sec. 17.270(a).
Proposed Sec. 17.270(a)(1) would state that an authorized non-VA
provider may provide medical services and supplies that are covered by
CHAMPVA. This is current practice and would reflect in regulation VA's
authority to provide CHAMPVA-covered services and supplies under 38
U.S.C. 1781(b)(2). As explained in greater detail below in connection
with proposed Sec. 17.272(b)(3), CHAMPVA-covered services and supplies
are those provided by authorized non-VA providers who agree to provide
covered services and supplies to CHAMPVA beneficiaries in exchange for
payment of the CHAMPVA determined allowable amount. Proposed Sec.
17.270(a)(2) would also reference VA's alternate authority under
section 1781(b) to provide medical care to CHAMPVA beneficiaries
through VA medical facilities equipped to provide the care and services
if such resources are not being used for the care of eligible veterans.
This initiative is called the CHAMPVA In-house Treatment Initiative
(CITI) and would be referenced as such in proposed Sec. 17.270(a)(2).
CITI affords beneficiaries the same medical services available to
veterans. CITI claims submitted to OCC are processed in the same manner
as all other CHAMPVA claims. However, a monthly transfer of funds, or
Transfer
[[Page 2398]]
Dispersing Authority (TDA), from OCC to the providing VA facility is
used to reimburse CITI claims whereas electronic funds transfer or
paper checks are used to reimburse beneficiaries and providers for non-
CITI claims.
With regards to CHAMPVA beneficiaries receiving care in VA medical
facilities through CITI, we have historically interpreted section
1781(b) to mean that such care may be provided only if the CHAMPVA
beneficiary is not also eligible for Medicare benefits. We base this
interpretation on the fact that CHAMPVA has always been the last payer
for CHAMPVA-covered medical services and supplies when a CHAMPVA
beneficiary has Medicare (included in this rulemaking's definition of
``other health insurance'' (OHI), see 38 U.S.C. 1781(d)(2)). The
mandated coordination of benefits found in section 1781(d)(2) is
essentially the same as the requirement in TRICARE codified at 32 CFR
199.8, which provides that if a TRICARE beneficiary is eligible for
both Medicare and TRICARE, Medicare is the primary payer and TRICARE is
the secondary payer. In addition, this policy limitation for CITI is
reasonable because VA is a publicly funded health care system that
cannot bill Medicare (see section 1814(c) and section 1835(d) of the
Social Security Act, codified at 42 U.S.C. 1395f(c) and 1395n(d)).
Moreover, Medicare is an entitlement program, whereas the provision of
CHAMPVA medical benefits is subject to the availability of
appropriations which, for any given time period, might or might not be
sufficient to cover all CHAMPVA-covered medical services and supplies
in a VA medical facility. Requiring beneficiaries to use their Medicare
benefits first accomplishes our goal of protecting all patients' access
to care. Therefore, we would further clarify in proposed Sec.
17.270(a)(2) that any CHAMPVA beneficiary who is also eligible for
Medicare benefits may not receive medical services and supplies through
CITI.
Proposed Sec. 17.270(a)(3) would newly indicate in regulation that
outpatient prescription medications may be provided to certain CHAMPVA
beneficiaries through Medications by Mail (MbM), administered by VA.
Proposed paragraph (a)(3)(i) would further provide that VA's MbM
provides prescription medications through the mail to CHAMPVA
beneficiaries who do not have any OHI that pays for prescriptions,
including Medicare Part D. This restriction largely is consistent with
TRICARE policy on the provision of medications by mail, except that
TRICARE covers prescribed medications for beneficiaries with OHI in two
instances: When the prescribed medication is not covered by the OHI or
when the beneficiary's OHI prescription benefit has been exhausted. See
TRICARE Pharmacy Program Handbook (October 2015), pages 18-19. CHAMPVA
is unable to duplicate these two exceptions due to system limitations,
meaning that CHAMPVA will only provide prescription medications through
the mail to beneficiaries who do not have any OHI prescription
coverage. Despite this, CHAMPVA's inclusion of prescription medications
is, broadly speaking, sufficiently similar to TRICARE that VA remains
in substantial compliance with the requirements of section 1781(b).
Proposed paragraph (a)(3)(ii) would provide that smoking cessation
pharmaceutical supplies are available only through MbM. Section 713 of
the Duncan Hunter National Defense Authorization Act for Fiscal Year
2009, Public Law 110-417 (October 14, 2008) (``2009 NDAA'') required
DoD to establish a smoking cessation program under TRICARE under which
specified smoking cessation benefits are to be made available to
beneficiaries who are not also eligible for Medicare. This TRICARE
benefit is codified at 32 CFR 199.4(e)(30). As to the pharmaceutical
component of this TRICARE benefit, smoking cessation pharmaceutical
agents (which VA refers to as pharmaceutical supplies) are available
only through Military Treatment Facility (MTF) pharmacies or the
TRICARE Mail Order Program. See 32 CFR 199.4(e)(30)(ii)(A) and
199.21(h)(2)(iii). Similar to 32 CFR 199.4(e)(30)(i), proposed Sec.
17.270(a)(3)(ii) would provide that the same smoking cessation supplies
will be made available to CHAMPVA beneficiaries who are not eligible
for Medicare. Additionally, smoking cessation pharmaceutical supplies
would be available only through MbM. For purposes of CITI, we would not
provide smoking cessation pharmaceutical supplies through VA facility
pharmacies because it is administratively more efficient for CHAMPVA to
provide these through MbM, and because, in complying with the
requirements of section 1781(b), as discussed above, VA facility
pharmacies would be required to administer any needed smoking cessation
pharmaceutical supplies first to veterans before providing them to
CHAMPVA beneficiaries. We would also remove the restriction on smoking
cessation services and supplies in current Sec. 17.272(a)(57), as
discussed later in this proposed rule.
For clarity, we would establish abbreviations for the Civilian
Health and Medical Program of the Department of Veterans Affairs as
``CHAMPVA'' and the Department of Veterans Affairs as ``VA.'' The
current regulations refer to the part of VA that administratively
handles CHAMPVA claims as the ``Center'' in several places (see current
Sec. Sec. 17.275-17.277), and to the ``Health Administration Center''
in other places (see current Sec. Sec. 17.270, 17.275-17.276), and we
believe that referring to ``VA'' is more appropriately descriptive and
would eliminate ambiguity.
Proposed Sec. 17.270(b) would establish definitions for the
CHAMPVA regulations. We would define ``accepted assignment'' as the
action of an authorized non-VA provider who accepts responsibility for
the care of a CHAMPVA beneficiary and thereby agrees to accept the
CHAMPVA determined allowable amount as full payment for services and
supplies rendered to the beneficiary. This extinguishes the
beneficiary's payment liability to the provider with the exception of
applicable cost shares and deductibles. This definition is consistent
with our explanation for proposed Sec. 17.272(b)(3), which further
outlines the necessity for defining ``accepted assignment.'' Our
current regulations do not define the term ``authorized provider,'' but
the term ``authorized provider'' (and variations thereof) is used
throughout current Sec. 17.272 to refer to an institutional or
individual provider of CHAMPVA-covered services and supplies. The term
is used to describe persons or institutions that are considered
appropriately licensed or credentialed to competently provide medical
services and supplies to CHAMPVA beneficiaries and that VA will pay to
provide such services and supplies. In addition, an ``authorized
provider'' has historically been interpreted in CHAMPVA to be a non-VA
medical provider. To capture this historical interpretation in full, we
would define an ``authorized non-VA provider'' to mean an individual or
institutional non-VA provider of CHAMPVA-covered medical services and
supplies who is licensed or certified by a State to provide the covered
medical services and supplies, or is otherwise certified by an
appropriate national or professional association that sets standards
for the specific medical provider. This requirement for State licensure
or other certification would be similar to TRICARE, which requires that
its providers be either licensed or
[[Page 2399]]
certified by a State, or, where States do not offer licensure or
certification, be otherwise certified by an appropriate national or
professional association that sets standards for the specific medical
provider. See TRICARE Policy Manual 6010.60-M, Chapter 11
(``Providers''), section 3.2 (``State Licensure And Certification'').
(For general operational-type information, one can also refer to
TRICARE Operations Manual 6010.59-M, Chapter 4, (``Provider
Certification And Credentialing'') (April 1, 2015).)
We would define ``calendar year'' as the period of time between and
including January 1 through December 31. This is plain language and is
consistent with the generally understood meaning of the phrase
``calendar year.''
The term ``CHAMPVA beneficiary'' would be defined as a person
enrolled for CHAMPVA under Sec. 17.271. This would be a program-
specific definition, but it is in plain language and is consistent with
the generally understood meaning of the word ``beneficiary.'' To
clarify, an individual is enrolled in CHAMPVA only after the individual
has successfully completed the application process (i.e., where the
individual submits a completed VA Form 10-10d to VA, and VA has
confirmed the individual's eligibility).
We would define ``CHAMPVA-covered services and supplies'' to mean
those medical services and supplies that are medically necessary and
appropriate for the treatment of a condition and that are not
specifically excluded from coverage under proposed Sec. 17.272(a)(1)
through (84) (current Sec. 17.272(a)(1) through (86)).
We would define ``CHAMPVA determined allowable amount'' by
referencing the proposed paragraph that would relate to this term,
proposed Sec. 17.272(b)(1).
We would define ``CHAMPVA In-house Treatment Initiative (CITI)'' to
mean the initiative under section 1781(b) under which participating VA
medical facilities provide medical services and supplies to CHAMPVA
beneficiaries who are not also eligible for Medicare, subject to
availability of space and resources.
We would define the term ``child'' consistent with 38 U.S.C. 101,
as we do in the current regulation at Sec. 17.270(b).
We would define the term ``claim'' consistent with the current use
and understanding of the term in the context of CHAMPVA, as a request
by an authorized non-VA provider or CHAMPVA beneficiary for payment or
reimbursement for medical services and supplies provided to a CHAMPVA
beneficiary.
We would define ``fiscal year'' as the period of time starting on
October 1 and ending on September 30. This is plain language and is
consistent with the generally understood meaning of the phrase ``fiscal
year'' as used within the Federal Government.
We would define ``Medications by Mail (MbM)'' to mean the
initiative under which VA provides outpatient prescription medications
through the mail to CHAMPVA beneficiaries.
We would define ``other health insurance'' (OHI) as a health
insurance plan or program (to include Medicare) or third-party coverage
that provides coverage to a CHAMPVA beneficiary for expenses incurred
for medical services and supplies. The inclusion of Medicare is
consistent with the TRICARE regulation related to double coverage. See
32 CFR 199.8(d)(1).
We would define the term ``payer'' to mean OHI, as defined in this
rulemaking, that is obligated to pay for CHAMPVA-covered medical
services and supplies. In a situation in which more than one insurer is
responsible to pay for such services and supplies (e.g., a ``double
coverage'' situation), there would be a primary payer (i.e., the payer
obligated to pay first), a secondary payer (i.e., the payer obligated
to pay after the primary payer), etc. In double coverage situations,
CHAMPVA would be the last payer, after payment by the primary payer and
all other secondary payers.
Defining a ``payer'' and designating different payer types would
not affect the administration of CHAMPVA because these concepts of
relative payment responsibility are all accepted and understood by the
insurance industry and current CHAMPVA beneficiaries and are an
essential part of current CHAMPVA billing practices. For instance,
Medicare would be the primary payer in situations governed by current
Sec. 17.271(b) (which remains unchanged by this proposed rulemaking).
See 38 U.S.C. 1781(d)(2).
The definition of ``service-connected'' in current Sec. 17.270(b)
would be unchanged and given the same meaning as that term in 38 U.S.C.
101. However, the terms ``spouse'' and ``surviving spouse'' would no
longer have the definitions of these same terms in 38 U.S.C. 101(31)
and (3), respectively, as those definitions are outdated; instead,
these terms would both be determined by operation of 38 U.S.C. 103(c).
Consistent with the waiver provisions of TRICARE, see 32 CFR
199.1(n), new proposed paragraph (c) would establish the discretionary
authority of VA to waive, when it is deemed to be in the best interest
of VA, any regulatory requirement of this part that is not required by
38 U.S.C. 1781 or otherwise imposed by statute. This discretionary
waiver authority would be limited to very unusual and limited
circumstances and would not set a precedent for future decisions. In
addition, it would not be used to deny any individual any right,
benefit, or privilege provided by statute or these regulations. This
new provision would enable VA to allow payment under CHAMPVA in cases,
for example, where, by operation of CHAMPVA rules, the claim is subject
to complex administrative or accounting procedures that ultimately
result in determination of the claim's technical noncompliance when the
underlying claim is otherwise appropriate. Where a claimant's non-
compliance with a purely policy or administrative-based technical
requirement is both unintentional and harmless, we believe it would be
in VA's best interest to have the authority to waive the regulatory
requirement and allow payment.
17.271 Eligibility
Current Sec. 17.271 identifies persons who may be eligible for
CHAMPVA benefits. We would revise Sec. 17.271(a) to recognize as
CHAMPVA beneficiaries those individuals designated as Primary Family
Caregivers under 38 CFR 71.25(f). This substantive addition to the
eligibility criterion would be made pursuant to the Caregivers and
Veterans Omnibus Health Services Act of 2010, Public Law 111-163,
section 102, which amended 38 U.S.C. 1781(a) by adding a new subsection
(a)(4) authorizing VA to provide CHAMPVA benefits to ``an individual
designated as a primary provider of personal care services under [38
U.S.C. 1720G(a)(7)(A)] who is not entitled to care or services under a
health-plan contract (as defined in [38 U.S.C. 1725(f)]).'' We amend
CHAMPVA eligibility criteria to recognize these Primary Family
Caregivers as CHAMPVA beneficiaries but not to establish substantive
eligibility rules in the CHAMPVA regulations to determine whether an
individual is a Primary Family Caregiver. (VA's regulations governing
the Caregivers Benefits Program established by 38 U.S.C. 1720G are
codified at 38 CFR part 71, and the specific rules governing the
identification of such individuals are found at 38 CFR 71.15 through
71.25.) We would redesignate current Sec. 17.271(a)(4) as Sec.
17.271(a)(5) and add a new proposed Sec. 17.271(a)(4) to state that a
Primary Family Caregiver is eligible for CHAMPVA benefits if they are
not entitled to care or services under a health-plan contract (as
defined in 38 U.S.C. 1725(f)(2)). We note that VA is already providing
CHAMPVA services
[[Page 2400]]
and supplies to these individuals pursuant to the statutory mandate in
section 1720G(a)(3)(A)(ii)(IV) and under the Caregivers Benefits
Program regulations. This revision would simply update the CHAMPVA
regulations to conform to these laws.
17.272 Benefits Limitations/Exclusions
Current Sec. 17.272 provides general information about what
medical services and supplies are covered by CHAMPVA and lists coverage
limitations along with the exclusions. The general information
concerning coverage in current Sec. 17.272(a) continues to be
accurate, and we do not propose any changes to paragraph (a). Some of
the coverage limitations and exclusions listed in the numbered
paragraphs under Sec. 17.272(a) require revision due to either changed
standards in clinical practice or changes in TRICARE coverage.
Current Sec. 17.272(a)(2) excludes the provision of services and
supplies required as a result of an occupational disease or injury for
which benefits are payable under workers' compensation or a similar
protection plan. We propose to update the verbiage to clarify the
exclusion for the reader.
Current Sec. 17.272(a)(3) excludes the provision of services and
supplies that are paid directly or indirectly by local, State, or
Federal government agencies, with certain exceptions listed in Sec.
17.272(a)(3)(i) and (ii) where CHAMPVA assumes primary payer status. We
propose to add Indian Health Service and CHAMPVA supplemental policies
as exceptions where CHAMPVA assumes primary payer status. This would be
consistent with current CHAMPVA practice as well as the TRICARE
regulation related to double coverage. See 32 CFR 199.8(b)(4)(ii) and
(iv). We also propose to remove the ``(Medicaid excluded)''
parenthetical language in current Sec. 17.272(a)(3), because Sec.
17.272(a)(3)(i) already expressly excepts ``Medicaid'' from the general
exclusion in Sec. 17.272(a)(3).
Current Sec. 17.272(a)(21) excludes dental care generally, with
exceptions to such exclusion listed in paragraphs (a)(21)(i) through
(xii). We would amend paragraph (a)(21)(ix) to clarify that the
provision of initial imaging services for the treatment of
temporomandibular joint disorder (TMD) could specifically include
Computed Tomography (CT) and Magnetic Resonance Imaging (MRI) services.
We believe the sole reference to ``initial radiographs'' in current
Sec. 17.272(a)(21)(ix) is outdated and that modern industry standards
include the use of CT scans as well as MRIs for diagnosing TMD. A CT
scan provides a more detailed image of the bones in the joint, and an
MRI provides a more detailed image of the soft tissue to determine
proper positioning as the jaw moves. We would also update Sec.
17.272(a)(21)(ix) to refer to the more updated and clinically
appropriate terminology ``temporomandibular joint disorder (TMD).''
These revisions would update CHAMPVA regulations with current standards
of clinical practice for the benefit of CHAMPVA beneficiaries.
A majority of the remaining proposed changes to CHAMPVA coverage
exclusions in proposed Sec. 17.272(a)(1) through (82) are based on
changes to TRICARE coverage and policy. Virtually all coverage
limitations and exclusions in current Sec. 17.272(a)(1)-(86), as shown
in the chart below, are substantially identical to services and
supplies excluded from, or limited under, TRICARE coverage under 32 CFR
199.4(g), or as otherwise noted in the chart.
List of Comparable CHAMPVA and TRICARE Exclusions
------------------------------------------------------------------------
TRICARE provision (identified
CHAMPVA provision (identified paragraphs are from 32 CFR
paragraphs are from 38 CFR 17.272(a)) 199.4(g), or as otherwise noted)
------------------------------------------------------------------------
(1)................................... (11).
(2)................................... (23).
(3)................................... (13).
(4)................................... (1).
(5)................................... (2).
(6)................................... (3).
(7)................................... (4).
(8)................................... (5).
(9)................................... (6).
(10).................................. (7).
(11).................................. (8).
(12).................................. (9).
(13).................................. (14).
(14), (81)............................ (15).
(15).................................. (16).
(16).................................. (17).
(17).................................. (19).
(18).................................. (21).
(19), (82)............................ (24).
(20).................................. (26).
(21).................................. (27).
(22).................................. (28).
(23).................................. (29).
(24).................................. (30).
(25).................................. (31).
(27).................................. (33).
(28).................................. (34).
(29).................................. (35).
(30).................................. (36).
(31).................................. (37).
(32).................................. (38).
(33).................................. (39).
(34).................................. (40).
(35).................................. (41).
(36).................................. (20), (42).
(37).................................. (43).
(38).................................. (44).
(40).................................. (46).
(41).................................. (47).
(42).................................. (50).
(43).................................. (51).
(44).................................. (48).
(45).................................. (49).
(46).................................. (52).
(47).................................. (53).
(48).................................. (54).
(49).................................. (55).
(50).................................. (56).
(51).................................. (57).
(52).................................. (58).
(53).................................. (60).
(54).................................. (61).
(55), (57)............................ (62).
(56).................................. (64).
(57).................................. (65).
(58).................................. (66).
(59).................................. (67).
(60).................................. (72).
(62).................................. 32 CFR 199.4(a)(12) and
(b)(10)(iv).
(63) through (65)..................... 32 CFR 199.4(e)(4) and (h).
(66).................................. (73).
(67), (68)............................ 32 CFR 199.2(b) and 199.4(e)(2).
(69).................................. 32 CFR 199.4(c)(3)(ix) and
199.4(e)(4).
(70), (71)............................ 32 CFR 199.4(e)(17).
(73).................................. 32 CFR 199.4(g)(15)(iv).
(74).................................. (69).
(75).................................. 32 CFR 199.4(a)(1).
(76).................................. 32 CFR 199.4(g)(74).
(77).................................. (39), (42).
(78).................................. (25).
(79).................................. 32 CFR 199.4(g)(15).
(80).................................. 32 CFR 199.2(b) and
199.4(b)(2)(v), (b)(3)(iii),
(b)(5)(v), (d)(3)(vi),
(e)(11)(i).
(83).................................. 32 CFR 199.4(c)(2), (c)(3),
(e)(8)(i)(E).
(84).................................. 32 CFR 199.4(e)(8).
(85), (86)............................ 32 CFR 199.2(b), 199.4(e)(8),
(g)(24).
------------------------------------------------------------------------
We note that even where our current provisions are not identical to
a TRICARE provision, our intent has consistently been to apply CHAMPVA
comparable exclusions or limitations in the same or similar manner to
their TRICARE counterpart in accordance with 38 U.S.C. 1781(b). The
same is true for our proposed revisions below, which are consistent
with changes in DoD's administration of TRICARE.
The first change we would make to our limitations and exclusions
based on TRICARE regulatory and policy changes concerns current Sec.
17.272(a)(26), which is not addressed in the chart above because it
correlates with a provision that has been removed from TRICARE
regulations. See 60 FR 12419 (March 7, 1995). Therefore, we propose to
remove this exclusion from our regulations as well. Paragraph (a)(26)
in current Sec. 17.272 excludes coverage for services and supplies,
including psychological testing, provided in connection with a specific
developmental disorder. By removing this exclusion, CHAMPVA would now
cover this service, and we would redesignate current
[[Page 2401]]
Sec. 17.272(a)(27) through (38) as Sec. 17.272(a)(26) through (37),
respectively.
Under section 711 of the 2009 NDAA, TRICARE must waive all
beneficiary costs associated with certain preventive services, unless
the beneficiary is also Medicare-eligible. TRICARE regulations were
revised to delete from 32 CFR 199.4(g)(37) the list of preventive
services not excluded from coverage, and these services were moved to
new Sec. 199.4(e)(28) so that they instead would be reflected as
preventive services under TRICARE for which out-of-pocket costs are
eliminated. See 76 FR 81368 (December 28, 2011). We would revise our
current exclusion of preventive care in Sec. 17.272(a)(31) (proposed
to be redesignated as Sec. 17.272(a)(30)) to except the same
preventive services identified in paragraphs (d)(1)(A) through (F) of
section 711 of the 2009 NDAA and, further, do so in a manner that, on
the whole, reflects the manner in which these services are provided
under TRICARE. Section 711 of the 2009 NDAA sets forth the following
preventive services for which beneficiaries shall pay no associated
costs: Colorectal cancer screening; breast cancer screening; cervical
cancer screening; prostate cancer screening; annual physical exam;
vaccinations. Current Sec. 17.272(a)(31)(i) through (x) set forth
exceptions to the general exclusion of certain specific preventive
care. Respectively, the terms of current paragraphs (a)(31)(v) and (vi)
already except ``[p]ap smears'' and ``[m]ammography tests'' and so
effectively capture ``cervical cancer screening'' and ``breast cancer
screening'' as referred to in the 2009 NDAA. However, because the
singular terms ``mammography test'' and ``pap smear'' are outdated, we
are updating to ``breast cancer screening'' and ``cervical cancer
screening.'' Therefore, proposed Sec. 17.272(a)(30) would revise the
exceptions to the general exclusion of preventive care to include the
four remaining preventive services specified in the 2009 NDAA, namely
colorectal cancer screening; prostate cancer screening; annual physical
examination; and vaccinations/immunizations.
We note that the TRICARE final rule that implemented the amendments
made by section 711 of the 2009 NDAA does not include an annual
physical exam benefit for all TRICARE beneficiaries; instead, such
benefit is limited to certain dependents of Active Duty military
personnel who are traveling outside the United States and for
beneficiaries ages 5 through 11 who require such exams for school
enrollment. This benefit is also not exempt from cost sharing
requirements. See 76 FR 81368, and 32 CFR 199.4(e)(29). Broadly
interpreting our mandate in section 1781(b), VA proposes to modify the
current exclusion of preventive care in current Sec. 17.272(a)(31)
insofar as it defines that term to include annual physical examinations
and create an exception permitting such exams. Despite the limited
availability of such examinations under TRICARE, it is noteworthy that
TRICARE nonetheless covers some preventive services that are typically
provided as part of an annual physical examination such as blood
pressure screening, cholesterol testing, and body measurements. See
TRICARE Policy Manual 6010.60-M (``Medicine''), Chapter 7, section 2.1
(``Clinical Preventive Services-TRICARE Standard'') (April 1, 2015). To
be paid for by TRICARE, however, these types of health promotion and
disease prevention services must be billed in connection with another
preventive service delineated in TRICARE's policy manual. Id. We do not
believe limiting the provision of annual physical examinations to only
a few select groups is appropriate from a clinical perspective.
Further, in the exercise of our discretion, when broadly interpreting
the mandate of section 1781(b), we conclude it lies within our
discretion to determine that this benefit should be made available to
all CHAMPVA beneficiaries. This is particularly the case given that
some individual health promotion and disease prevention services that
are typically provided as part of an annual physical examination would
eventually be approved by TRICARE as long as they are coupled or
associated with billing submitted for a covered service. (The nature
and delivery of those services remains the same whether delivered as
part of an annual examination or under the umbrella of another service
for which TRICARE billing is permitted.) Furthermore, VA finds that
annual physical examinations are beneficial for both CHAMPVA
beneficiaries and VA, by serving to identify serious medical issues
before they progress and their clinical management becomes more
difficult and resource-intensive. Even though our proposed approach
would include elements of an annual physical examination not otherwise
included as an adjunct service provided under a covered benefit as
described above, we believe our approach is sufficiently ``similar'' to
TRICARE. Therefore, we propose to create an exception to the exclusion
of preventive care, permitting an annual physical examination to be
among the benefits available to all CHAMPVA beneficiaries.
We also note that we would except ``[v]accinations/immunizations''
from the general exclusion of preventive services. Although subsection
(d)(1)(F) of section 711 of the 2009 NDAA exempts ``vaccination'' only,
TRICARE's guidance on this issue additionally exempts immunizations.
See TRICARE Reimbursement Manual 6010.61-M Chapter 2 (``Beneficiary
Liability''), section 1 (``Cost-Shares And Deductibles'') (April 1,
2015). We believe these terms have identical meanings and would use
both terms just to be clear that this preventive service is covered
regardless of whether it is called an ``immunization'' or a
``vaccination.''
Current Sec. 17.272(a)(39) excludes coverage for audiological
services or speech therapy, except when prescribed by a physician and
rendered as part of a treatment addressing a physical defect, which
correlates with a provision not addressed in the chart above because it
has been removed from TRICARE regulations. See 75 FR 50880 (August 18,
2010). Therefore, we propose to remove this exclusion from our
regulations as well. By removing this exclusion, CHAMPVA would now
cover this service, and we would redesignate current Sec.
17.272(a)(40) through (56) as Sec. 17.272(a)(38) through (54),
respectively.
As stated earlier in this rulemaking, pursuant to section 713 of
the 2009 NDAA, TRICARE must make available smoking cessation benefits,
as specified in the law, to beneficiaries who are not also eligible for
Medicare. The four categories of smoking cessation benefits available
to these beneficiaries are set forth in TRICARE's regulations under 32
CFR 199.4(e)(30)(ii)(A)-(D). Hence, we would revise our regulations by
removing our correlate restriction on smoking cessation services and
supplies in current Sec. 17.272(a)(57). In removing current Sec.
17.272(a)(57), current paragraphs (a)(58) through (71) would be
redesignated as paragraphs (a)(55) through (68), respectively.
Redesignated paragraphs (a)(57) through (59) would be revised to
reference coverage of mental health benefits in a ``calendar year''
versus the current reference to ``fiscal year.'' We propose to change
the yearly basis of this coverage because our beneficiaries and
providers are more familiar with calendar year events, and the impact
of the change from fiscal to calendar on the functioning of CHAMPVA
would be minimal.
[[Page 2402]]
With the proposed removal of Sec. 17.272(a)(57) and subsequent
redesignations of paragraphs noted above, current paragraph (a)(67)
would be redesignated as paragraph (a)(64). CHAMPVA would continue to
exclude the performance of abortions, except when a physician certifies
that the life of the mother would be endangered if the fetus were
carried to term. This is the same restriction in current TRICARE
regulations (see 32 CFR 199.4(e)(2)), although statute and TRICARE
policy statements recently established an additional exception to the
general ban on abortions. Specifically, section 704 of the National
Defense Authorization Act for Fiscal Year 2013, Public Law 112-239
(2013 NDAA), amended 10 U.S.C. 1093(a) and (b) to expand the
circumstances under which funds available to DoD and MTFs may be used
to provide and perform abortions in cases of pregnancy resulting from
an act of rape or incest. Despite the recent amendments to section 1093
of title 10 and TRICARE policy, we do not propose same or similar
changes to CHAMPVA's current exclusion at this time because TRICARE
regulations do not provide for it. Additionally, such changes would
create an even greater disparity between the women's health care
benefits afforded veterans and CHAMPVA beneficiaries.
Current Sec. 17.272(a)(72) excludes from coverage drug maintenance
programs where one addictive drug is substituted for another such as
methadone substituted for heroin. A TRICARE final rule published on
October 22, 2013, and effective November 21, 2013, removes a correlate
restriction from TRICARE regulations, and so we propose to similarly
remove Sec. 17.272(a)(72). See 78 FR 62427 (October 22, 2013); 32 CFR
199.4(e)(4)(ii). We agree with the stated rationale in the related
TRICARE proposed rule that the current restriction fails to recognize
the accumulated medical evidence supporting certain maintenance
programs as one component of the continuum of care necessary for the
effective treatment of substance use disorders. See 76 FR 81899
(December 29, 2011). In removing current Sec. 17.272(a)(72), current
paragraphs (a)(73) through (86) would be redesignated as paragraphs
(a)(69) through (82), respectively.
Current Sec. 17.272(a)(80), as proposed to be redesignated as
paragraph (a)(76), excludes from CHAMPVA benefits medications not
requiring a prescription, except for insulin and related diabetic
testing supplies and syringes. We would revise redesignated paragraph
(a)(76) to instead exclude ``over-the-counter products'' and would
additionally expand the exception to this exclusion to cover over-the-
counter smoking cessation pharmaceutical supplies that are approved by
the U.S. Food and Drug Administration (FDA), prescribed, and provided
through MbM. These changes would be consistent with TRICARE
regulations, which require a prescription from an authorized provider
for smoking cessation pharmaceutical agents (even for FDA-approved
over-the-counter smoking cessation agents). See 32 CFR
199.4(e)(30)(ii)(A).
Section 702 of the 2013 NDAA grants the Secretary of Defense the
authority to add certain over-the-counter medications to the TRICARE
formulary so that such medications may be administered as if they were
prescription medications. CHAMPVA does not have a same or similar
uniform formulary as DoD that could be altered to include certain over-
the-counter medications, and we do not interpret section 702 as
granting authority to alter VA's uniform formulary. Therefore, we would
not amend our regulations in response to section 702 of the 2013 NDAA.
Our regulation as revised and redesignated Sec. 17.272(a)(76) would
permit CHAMPVA to provide the same over-the-counter smoking cessation
supplies as permitted in TRICARE policy.
Lastly, we would add two new exclusions to Sec. 17.272. Proposed
paragraph (a)(83) would exclude medications that are not approved by
the FDA, excluding FDA exceptions to the approval requirement. Current
CHAMPVA regulations are silent regarding the need for medications to
meet FDA approval requirements; however, this has not been a problem as
a matter of practice because applicable standards of care generally
require prescribed medications to be FDA-approved or excluded as an
exception from the approval requirement. Still, we wish to formally and
expressly exclude medications that do not meet these requirements. In
addition, to provide benefits in the same or similar manner and subject
to the same or similar limitations as TRICARE, paragraph (a)(84) would
establish exclusions for services and supplies related to the treatment
of dyslexia. See 38 CFR 199.4(g)(32). This change merely reflects in
regulation current CHAMPVA practice and policy.
Due to the multiple proposed deletions and additions in Sec.
17.272(a)(1)-(86), we reiterate that we would redesignate most of the
current paragraphs under Sec. 17.272(a). With the proposed removal of
current paragraph (a)(26), current paragraphs (a)(27) through (38)
would be redesignated as (a)(26) through (37), respectively, with the
substantive changes to redesignated (a)(30) as noted above. With the
proposed removal of current paragraph (a)(39), current paragraphs
(a)(40) through (56) would be redesignated as (a)(38) through (54),
respectively, with no substantive changes. With the deletion of the
current paragraphs (a)(57) and (72), current paragraphs (a)(58) through
(86) would be redesignated as (a)(55) through (82), respectively, with
the minor substantive changes as noted above to redesignated paragraphs
(a)(57) through (59) and (a)(76). Lastly, we would add new paragraphs
(a)(83) and (84).
Current Sec. 17.272(b) establishes the ``CHAMPVA determined
allowable amount,'' and paragraph (b)(1) states that the term
``allowable amount'' is the maximum amount that CHAMPVA will pay an
authorized provider for a covered benefit, which is determined prior to
cost sharing and the application of deductibles or OHI. (This means,
for instance, that the cost-share would be a percentage of the entire
CHAMPVA determined allowable amount.) However, this is merely a
definition and not a statement of coverage limitation or exclusions. We
would revise paragraph (b) to clearly indicate that amounts above the
CHAMPVA determined allowable amount are excluded from CHAMPVA coverage.
The actual payment methodology--the amount to which cost sharing and
deductibles will be applied--is addressed in proposed Sec. 17.274(e)
and is discussed below.
Proposed Sec. 17.272(b)(1) would explain that the CHAMPVA
determined allowable amount is the maximum level of payment to an
authorized non-VA provider for CHAMPVA-covered services and supplies
and that this allowable amount is determined before cost sharing and
the application of deductibles or OHI is considered. This is a
restatement of current Sec. 17.272(b)(1), except that we would use the
term ``authorized non-VA provider'' to encompass all those providers
listed in current Sec. 17.272(b)(1) and include the term ``supplies''
after ``covered services'' to underscore they too can be covered. See
current 38 CFR 17.272(b)(1) (referencing ``a hospital or other
authorized institutional provider, a physician or other authorized
individual professional provider, or other authorized provider for
covered services''). We believe use of the one term ``authorized non-VA
provider'' as defined in proposed Sec. 17.270(b) properly captures all
provider types now listed in Sec. 17.272(b)(1) and
[[Page 2403]]
simplifies the regulatory reference to providers for the benefit of
CHAMPVA beneficiaries. Proposed Sec. 17.272(b)(1) would also clearly
state that the CHAMPVA determined allowable amount is payment made by
VA to an authorized non-VA provider for the provision of CHAMPVA-
covered services and supplies to a CHAMPVA beneficiary.
Current Sec. 17.272(b)(2) states that a Medicare-participating
hospital must accept the CHAMPVA determined allowable amount for
inpatient services as payment in full and references 42 CFR parts 489
and 1003. While this is a true statement of law under 42 CFR 489.25,
the references to 42 CFR parts 489 and 1003 are vague, and part 1003 is
not relevant to the issue of what amounts Medicare-participating
hospitals must accept as payment in full from CHAMPVA. See 42 CFR part
1003 (describing civil money penalties, assessments, and exclusions
generally for individuals who violate provisions of or agreements with
Federal health care programs). Proposed Sec. 17.272(b)(2) would state
that inpatient services are ``provided to a CHAMPVA beneficiary'' and
use a single, clarifying reference to 42 CFR 489.25.
Section 503 of The Caregivers and Veterans Omnibus Health Services
Act of 2010, Public Law 111-163, revised 38 U.S.C. 1781 by adding new
subsection (e), which states: ``Payment by the Secretary under this
section on behalf of a covered beneficiary for medical care shall
constitute payment in full and extinguish any liability on the part of
the beneficiary for that care.'' Current Sec. 17.272(b)(3) states
that: ``An authorized provider of covered medical services or supplies
must accept the CHAMPVA determined allowable amount as payment in
full.'' Proposed Sec. 17.272(b)(3) would state more clearly that
``accepted assignment'' refers to the action of an authorized non-VA
provider who accepts responsibility for the care of a CHAMPVA
beneficiary and thereby agrees to accept the CHAMPVA determined
allowable amount as full payment for services and supplies rendered to
the beneficiary. The provider's acceptance of the CHAMPVA determined
allowable amount extinguishes the beneficiary's payment liability to
the provider with the exception of applicable cost shares and
deductibles. Proposed Sec. 17.272(b)(3) would not be substantively
different than current paragraph (b)(3) but would clarify that the
action of accepting payment is the equivalent of accepting assignment.
The term ``accepted assignment'' is used currently in the
administration of CHAMPVA payments, and we believe using it in this
regulation as described would increase clarity in payment practices for
both CHAMPVA beneficiaries and authorized non-VA providers.
Current Sec. 17.272(b)(4) provides that a provider who has
collected and not made an appropriate refund, or attempts to collect
from the beneficiary any amount in excess of the CHAMPVA determined
allowable amount may be subject to exclusion from Federal benefit
programs. The underlying authority for this rule is 42 CFR 1003.105,
which establishes the terms for a health care provider's permissive or
mandatory exclusion from participation in the Medicare program and
other Federal health care programs. Exclusion may result, for instance,
if a provider files false claims under these programs. We would move
this information to proposed Sec. 17.272(b)(3) for increased clarity
and would remove mention of providers not making an appropriate refund
of amounts collected from beneficiaries, as the purpose of 38 U.S.C.
1781(e) and proposed Sec. 17.272(b)(3) is for these amounts to never
be collected by the provider. By moving this information to proposed
paragraph (b)(3), we would also remove current paragraph (b)(4).
17.273 Preauthorization
CHAMPVA preauthorization requirements for certain medical care and
services are based on CHAMPVA needs and are substantially the same or
similar as those required by TRICARE. See 32 CFR 199.4 passim. We
propose to revise the preauthorization requirements by adding language
to indicate when a beneficiary has ``other health insurance'' that
provides primary coverage for the benefit, preauthorization
requirements will not apply. TRICARE waives preauthorization
requirements in all instances when OHI, to include Medicare, is the
primary payer. See TRICARE Policy Manual 6010.60-M, Chapter 1
(``Administration''), section 6.1 (``Special Authorization
Requirements'') (April 1, 2015). To provide benefits in a similar
fashion, we would waive any requirement for preauthorization where OHI
(as defined by this rulemaking) covers the benefit. We would also
revise current Sec. 17.273(d) to refer to dental coverage limitations
in Sec. 17.272(a)(21)(i)-(xii) to avoid a potential misconception that
preauthorization is generally required for dental services. CHAMPVA
clearly excludes all dental services, except for those listed in
current Sec. 17.272(a)(21)(i)-(xii). We would remove current Sec.
17.273(e) and not require preauthorization for durable medical
equipment as a covered service or supply. Removal of Sec. 17.273(e)
would be consistent with TRICARE policy. See TRICARE Policy Manual
6010.60-M, Chapter 8 (``Other Services''), section 2.1 (``Durable
Medical Equipment: Basic Program'') (April 1, 2015). Based on this
removal, we would redesignate current Sec. 17.273(f) as Sec.
17.273(e).
Finally, we would add new proposed Sec. 17.273(f) to detail the
reviews of medical necessity. Since CHAMPVA is a secondary payer, VA
would be required to perform reviews of medical necessity on a
retrospective basis. If during the coordination of benefits process it
is determined that CHAMPVA would be the responsible payer for the
services and supplies but CHAMPVA preauthorization was not obtained
prior to delivery of the services or supplies, we would obtain the
necessary information and perform a retrospective medical necessity
review. We would also propose that any claims, where a retrospective
review occurs, are filed within the appropriate one-year period.
17.274 Cost Sharing
Current Sec. 17.274(a) provides in general that CHAMPVA is a cost
sharing program in which the cost of CHAMPVA-covered services and
supplies is shared with the beneficiary, with the exception of services
obtained through VA medical facilities. This provision would remain
substantively the same, but we would add new paragraphs (a)(1)(i) and
(ii) to explicate, respectively, that the former language ``services
obtained through VA facilities'' refers to services and supplies
provided both through MbM and through CITI. That is, the exception to
this cost-share requirement would extend specifically to each of these
initiatives (as these initiatives would be defined by this proposed
rulemaking).
Subsections (d)(1)(A) through (d)(1)(F) of section 711 of the 2009
NDAA, as discussed earlier, set forth certain preventive services for
which TRICARE waives all out-of-pocket costs, even if the beneficiary
has not paid the amount necessary to cover the beneficiary's deductible
requirement for the year. We propose to revise Sec. 17.274(a) to make
clear that there will be no associated cost share for CHAMPVA
beneficiaries for such services. (We address waiving the associated
deductible requirement later in the discussion of proposed Sec.
17.274(b)). We would add new paragraphs (a)(1)(iii)(A)-(G) to Sec.
17.274 to waive CHAMPVA beneficiary cost-share requirements for the
same preventive services identified in paragraphs (d)(1)(A) through (F)
of
[[Page 2404]]
section 711 of the 2009 NDAA. Section 711 also authorizes, but does not
require, the Secretary of Defense to extend the waiver of beneficiary
costs to other preventive services. As such, we state in regulation
that the list of services is not all-inclusive, enabling us to add
supplemental items to the list in the future if needed, while enabling
us to be sufficiently similar to TRICARE. See Public Law 110-417,
section 711(d)(1)(G). TRICARE regulations and policy guidance extend
this waiver to well-child visits for children under 6 years of age. See
32 CFR 199.4(e)(28)(iv), (f); TRICARE Reimbursement Manual 6010.61-M,
Chapter 2 (``Beneficiary Liability''), section 1 (``Cost-Shares and
Deductibles), 1.3.3.10.1.6 (Preventive Services''). We would include
this same waiver in proposed paragraph (a)(1)(iii)(G) of Sec. 17.274.
We would waive any cost-share requirement for hospice services in
proposed Sec. 17.274(a)(1)(iv). This waiver is similar to the cost-
share waiver for hospice services in TRICARE regulation. See 32 CFR
199.14(g)(9). Lastly, to remain similar to TRICARE, in Sec.
17.274(a)(1)(v), we would add a waiver for other services as determined
by the Secretary of Veterans Affairs.
For TRICARE, the waiver of beneficiary costs associated with
preventive services in proposed Sec. 17.274(a)(1)(iii)(A) through (G)
do not apply to any TRICARE beneficiary who is also Medicare-eligible.
See Public Law 110-417, section 711(b). We would not exclude Medicare-
eligible beneficiaries from cost sharing waivers for preventive
services as this would unfairly disadvantage them as compared to other
CHAMPVA beneficiaries with OHI. By not including this waiver, CHAMPVA
will treat all beneficiaries with OHI the same. Additionally, we
believe most preventive services provided to Medicare-eligible
beneficiaries will be paid in full by Medicare, and, therefore, CHAMPVA
will not assume any payment responsibility. In the event a cost share
or deductible is applied for preventive services, CHAMPVA will treat
those claims as it would the claims for any other beneficiary with OHI.
The general provisions in current Sec. 17.274(b) related to
establishing an annual deductible requirement (in addition to
beneficiary cost share) would remain substantively the same. We would
move the exception to this general requirement in current Sec.
17.274(b) (last sentence) for services obtained through VA facilities
to a new Sec. 17.274(b)(1) and also explain that it refers to services
and supplies provided through MbM or CITI under the same rationale as
expressed above for proposed new Sec. 17.274(a)(1)(i) and (ii),
respectively. We would also move the exception to the deductible
requirement in current Sec. 17.274(b) (last sentence) for any
inpatient services to a new Sec. 17.274(b)(2). Proposed Sec.
17.274(b)(3) would except the listed preventive services in proposed
Sec. 17.274(a)(1)(iii)(A)-(G) from the general deductible requirement
in current and proposed Sec. 17.274(b), in accordance with the mandate
in section 711 of the 2009 NDAA. See Public Law 110-417, section
711(a)(2) (mandating that a beneficiary not be charged for preventive
services during a year even if the beneficiary has not paid the amount
necessary to cover the beneficiary's deductible for the year. See 32
CFR 199.4(f)(12)). Proposed Sec. 17.274(b)(4) would waive the CHAMPVA
beneficiary deductible requirement for hospice services, as is done
similarly under TRICARE regulations. See 32 CFR 199.14(g)(9). Lastly,
to remain similar to TRICARE, in Sec. 17.274(b)(5), we would add a
waiver for other services as determined by the Secretary of Veterans
Affairs.
Current Sec. 17.274(c) establishes a calendar year limit on the
``cost-share amount'' incurred by a CHAMPVA beneficiary through the
payment of both cost-shares and deductible amounts (See current 38 CFR
17.274(c), indicating that the cap is ``limited to the applied annual
deductible(s) and the beneficiary cost-share amount.''). Proposed Sec.
17.274(c) would retain this basic information but would refer instead
to a cap on ``out-of-pocket costs'' instead of ``cost-share amounts''
so that it is clear that both cost share and deductible amounts apply
to this cap. Current Sec. 17.274(c)(i) establishes an annual cap of
cost sharing of $7,500 per CHAMPVA eligible family ``through December
31, 2001'', which is an outdated provision. Current Sec. 17.274(c)(ii)
further establishes a current cap of $3000 per CHAMPVA eligible family,
which was ``[e]ffective January 1, 2002.'' Under proposed Sec.
17.274(c), we would establish an annual (calendar year) cap on out-of-
pocket costs of $3,000 per CHAMPVA eligible family. The annual cap
amount would be unchanged from what currently exists but would use the
new terminology proposed above for the sake of clarity. We would also
remove current Sec. 17.274(c)(i) and (ii).
We do not propose any substantive changes to current Sec.
17.274(d) as this provision is legally adequate, and we are not
proposing to revise policies related to it. However, we are adding a
subject heading in an effort to mirror the cost share calculation in
proposed paragraph (e) to Sec. 17.274.
We propose to add a new paragraph (e) to Sec. 17.274 which would
set forth the principles found in current policy manuals that VA uses
to establish CHAMPVA beneficiary cost-share amounts. The calculation
methodologies that would be described in proposed Sec. 17.274(e)
represent current CHAMPVA practice and therefore would not increase or
decrease the out-of-pocket costs for CHAMPVA beneficiaries. The
methodologies described in proposed Sec. 17.274(e) are also consistent
with TRICARE cost-share calculation methodologies for the same or
similar types of care, except as indicated below.
In accordance with current practice, and as proposed in Sec.
17.274(e), the CHAMPVA beneficiary's cost-share amount, if applicable,
is 25 percent of the CHAMPVA determined allowable amount in excess of
the annual calendar year deductible for most CHAMPVA-covered services
and supplies. This calculation is similar to that used in TRICARE to
determine cost-share amounts for a majority of TRICARE covered
services. See 32 CFR 199.4(f)(3)(ii)(C) and (f)(3)(iii). Proposed Sec.
17.274(e)(1) and (2) would establish the services for which the general
rule of a 25 percent cost share does not always apply. Proposed
paragraph (e)(1) would establish in regulation the current calculation
VA uses to determine CHAMPVA beneficiary cost share for inpatient
facility services and supplies that are subject to the CHAMPVA
Diagnosis Related Group (DRG) payment system. The CHAMPVA DRG system,
like that used by TRICARE under 32 CFR 199.14, is based on the Centers
for Medicare and Medicaid Services (CMS) prospective payment system for
hospital services, as set forth in 42 CFR part 412. For services based
on the CHAMPVA DRG system, the CHAMPVA beneficiary cost share would be
the lesser of the per diem rate multiplied by the number of inpatient
days; or, 25 percent of the hospital's billed amount; or, the base
CHAMPVA DRG rate. This calculation is similar to that used in TRICARE
regulation. See 32 CFR 199.4(f)(3)(ii)(A) and (f)(8)(ii).
Proposed Sec. 17.274(e)(2) would establish the CHAMPVA beneficiary
cost share for covered inpatient facility services and supplies that
are subject to the CHAMPVA mental health low volume per diem
reimbursement methodology. This methodology covers mental health
inpatient services for lower volume hospitals and units (less than 25
mental health discharges per federal fiscal year). For these services,
the CHAMPVA beneficiary cost share
[[Page 2405]]
would be the lesser of a fixed per diem amount multiplied by the number
of inpatient days or 25 percent of the hospital's billed charges. This
calculation is similar to that used in TRICARE regulations. See 32 CFR
199.4(f)(3)(ii)(B) and (f)(8)(ii).
Although, as noted above, a majority of the CHAMPVA cost-share
methodologies are the same or similar as TRICARE's, we would not adopt
a recent TRICARE exception to its general 25 percent cost-share rule
for prescription medications. Section 712 of the 2013 NDAA requires the
Secretary of DoD, through regulations, to establish specified fixed
dollar amounts for cost shares for pharmacy benefits (e.g., generic,
formulary, and non-formulary agents or medications). We would not
establish similar fixed cost-share amounts because CHAMPVA does not
have an established uniform formulary and, therefore, is unable to
identify all medications which may be prescribed or approximate their
standard retail pricing to determine, with certainty, that a fixed
dollar amount would satisfy beneficiaries' cost-share liability.
Generally, CHAMPVA coverage of medications depends upon whether
medications are approved by the FDA for the indications for which they
are prescribed (as explained above in connection with new proposed
Sec. 17.272(a)(83)). Additionally, the fixed cost-share amounts
required by section 712 of the 2013 NDAA would apply even to
medications administered through TRICARE's mail order service; whereas,
under proposed Sec. 17.274(a)(1), as revised for clarity, cost-sharing
requirements would not apply to services and supplies provided through
VA's MbM. As a matter of policy, VA does not wish to apply a cost share
for mail order pharmacy supplies provided to CHAMPVA beneficiaries. We
believe that this departure from TRICARE is necessary to ensure the
most appropriate care for CHAMPVA beneficiaries. Although we would not
establish fixed cost-share amounts for medications similar to those set
forth in section 712 of the 2013 NDAA, we would revise our regulations
to clarify the methodology CHAMPVA uses to determine allowable amounts
paid for outpatient medications obtained in the community (explained
later in the discussion of proposed Sec. 17.275(f)), upon which the 25
percent CHAMPVA beneficiary cost share is based. We believe these
clarifications would provide more transparency related to pharmacy
costs and subsequent CHAMPVA beneficiary cost-share amounts for
pharmaceutical supplies obtained in the community, which we believe is
a reasonable interpretation of the goals of section 712 of the 2013
NDAA in establishing fixed cost-share amounts.
17.275 CHAMPVA Determined Allowable Amount Calculation
We propose to add a new Sec. 17.275 to describe the various
payment methodologies used by CHAMPVA to calculate the CHAMPVA
determined allowable amount for covered services and supplies. CHAMPVA
uses the same or similar payment methodologies to establish allowable
reimbursement amounts for providers as TRICARE. See 32 CFR 199.14. As
with the cost-share methodologies that would be described in Sec.
17.274(e), proposed Sec. 17.275 represents current practice except as
noted below and would not cause changes for CHAMPVA beneficiaries. The
reason that Sec. 17.274(e) (regarding cost share) and Sec. 17.275
(regarding CHAMPVA determined allowable amount) would be separated is
to clarify for CHAMPVA beneficiaries how much of the CHAMPVA determined
allowable amount they are responsible for as a cost share (e.g., 25
percent) and additionally to provide beneficiaries and providers with
an idea of how such allowable amounts are calculated.
Proposed Sec. 17.275(a) would establish in regulation the CHAMPVA
determined allowable amount for reimbursement of inpatient hospital
services based on the CHAMPVA DRG-based payment system. Proposed
paragraph (a) would explain that, unless exempt or subject to a
methodology in proposed paragraph (b) or (c), hospital services
provided in the 50 States, the District of Columbia, and Puerto Rico
are subject to the CHAMPVA DRG-based payment system. The CHAMPVA DRG
system, similar to that used by TRICARE under 32 CFR 199.14, is also
based on the CMS prospective payment system as set forth in 42 CFR part
412. Certain services provided in a DRG reimbursed facility will be
reimbursed under the CHAMPVA Cost-to-Charge (CTC) payment method. See,
e.g., 32 CFR 199.14(c). However, we will not list these specifically in
regulations as the list of services may change more often than
regulations can be updated.
Proposed Sec. 17.275(b) would establish in regulation the current
CHAMPVA inpatient mental health per diem payment system used to
calculate reimbursement for inpatient mental health hospital care in
specialty psychiatric hospitals and psychiatric units of general acute
hospitals that are exempt from the CHAMPVA DRG-based payment system.
The per diem rate would be calculated based on the daily rate times the
number of days (length of stay). CHAMPVA's mental health per diem rates
are updated each fiscal year for both high volume hospitals (25 or more
discharges per fiscal year) and low volume hospitals (less than 25
discharges per fiscal year). The per diem rates used by CHAMPVA are
determined by TRICARE per diem rates. See 32 CFR 199.14(a).
Proposed Sec. 17.275(c) would establish in regulation the CHAMPVA
CTC payment system that is used to calculate the CHAMPVA determined
allowable amount for inpatient services furnished by hospitals or
facilities that are exempt from the CHAMPVA DRG-based payment system or
the CHAMPVA inpatient mental health per diem payment system. TRICARE
establishes an alternate methodology to calculate payments for
inpatient services that are exempt from its DRG and inpatient mental
health per diem payment systems. See 32 CFR 199.14(a)(4). Proposed
Sec. 17.275(c)(1) would establish the CHAMPVA CTC methodology used to
calculate costs for hospitals or facilities by multiplying a CTC ratio
by billed charges. We would further propose that the billed charges
from the applicable hospitals and facilities must be customary and not
in excess of rates or fees the hospital or facility charges the general
public for similar services in a community. This requirement that the
applicable billed charges not be in excess of what is charged of the
general public is similar to TRICARE's requirements. See 32 CFR
199.14(a)(4)(i). Proposed Sec. 17.275(c)(2)(i) through (x) would
establish the types of hospitals and services subject to the CHAMPVA
CTC methodology, similar to TRICARE at 32 CFR 199.14(a)(1)(ii)(D)(1)
through (10) and (a)(1)(ii)(E). We would also add in proposed Sec.
17.275(c)(2)(xi) that hospitals and services as determined by the
Secretary of Veterans Affairs may be subject to the CHAMPVA CTC
methodology.
Proposed Sec. 17.275(d) would establish in regulation the CHAMPVA
outpatient prospective payment system (OPPS) used to calculate the
allowable amount for outpatient services provided in a hospital subject
to Medicare OPPS. This will include the utilization of TRICARE's
reimbursement methodology to include specific coding requirements,
ambulatory payment classifications (APCs), nationally established APC
amounts, and associated adjustments (e.g., discounting for multiple
surgery procedures, wage adjustments for variations in labor-related
costs across geographical regions, and outlier
[[Page 2406]]
calculations). The CHAMPVA OPPS is the same as that utilized by TRICARE
under 32 CFR 199.14, which is similar to Medicare's basic OPPS
methodology. There are differences between TRICARE's OPPS methodology
and Medicare's basic OPPS methodology due to variations in benefit
structure and beneficiary population. CHAMPVA is adopting TRICARE's
OPPS because the CHAMPVA beneficiary population is more similar to the
TRICARE beneficiary population than to the Medicare beneficiary
population. See 32 CFR 199.14(a)(6)(ii).
Proposed Sec. 17.275(e) would establish in regulation the
reimbursement methodology for services and supplies provided by
authorized non-VA providers on an outpatient or inpatient basis where
the services are distinct from facility-type charges in proposed Sec.
17.275(a) through (d). Proposed Sec. 17.275(e) would explain that the
CHAMPVA determined allowable amount paid to authorized non-VA providers
(not hospitals) for services and supplies provided on an outpatient or
inpatient basis is the lesser of: The CHAMPVA maximum allowable charge
(equivalent to the maximum allowable charge for similar services
provided by other than hospitals and skilled nursing facilities under
TRICARE, see 32 CFR 199.14(c)); the prevailing amount, which is the
amount equal to the maximum reasonable amount allowed providers for a
specific procedure in a specific locality; or the billed amount.
Certain services that typically may be provided within a hospital
setting, but not billed as a facility-type charge under proposed
paragraphs (a) through (d), would be included as examples in proposed
paragraph (e), namely anesthesia services; laboratory services; and
other professional services associated with individual authorized non-
VA providers. These examples are not all-inclusive.
Proposed Sec. 17.275(f) would establish in regulation the current
payment methodology for outpatient CHAMPVA pharmacy points of service.
CHAMPVA negotiates rates with retail pharmacies through its contract
with the pharmacy benefit manager. For services and supplies obtained
from a retail ``in-network'' pharmacy, proposed Sec. 17.275(f)(1)
would establish that VA pays the lesser of the billed amount or the
contracted rate. For supplies from a retail ``out-of-network''
pharmacy, proposed Sec. 17.275(f)(2) would establish that VA pays the
lesser of the billed amount plus a dispensing fee or the average
wholesale price plus a dispensing fee.
Proposed Sec. 17.275(g) would set forth in regulation the current
CHAMPVA reimbursement methodology for the provision of services in a
Skilled Nursing Facility (SNF). This methodology is based on the CMS
prospective payment system for SNFs under 42 CFR part 413, subpart J
(Medicare Resource Utilization Group (RUG) rates), which is the same
methodology used in TRICARE regulations to calculate SNF payments. See
32 CFR 199.14(b).
Proposed Sec. 17.275(h) would set forth in regulation the current
reimbursement methodology for durable medical equipment, prosthetics,
orthotics, and supplies (DMEPOS). Reimbursement of DMEPOS would be
based on the same amounts established under the CMS DMEPOS fee schedule
under 42 CFR part 414, subpart D, which is the same methodology used in
TRICARE regulations to calculate DMEPOS payments. See 32 CFR 199.14(k).
The allowed amount would be that which is in effect in the specific
geographic location at the time CHAMPVA-covered services and supplies
are provided to a CHAMPVA beneficiary.
Proposed Sec. 17.275(i) would establish in regulation the current
payment methodology for all ambulance services. CHAMPVA adopts
Medicare's Ambulance Fee Schedule (AFS) for ambulance services, which
is based on the same methodology used by TRICARE. See TRICARE
Reimbursement Manual 6010.61-M, Chapter 1 (``General''), section 14
(``Ambulance Services'') (April 1, 2015). Ambulance services are paid
based on the lesser of the Medicare AFS or the billed amount. Payments
for ambulance services furnished by a Critical Access Hospital (CAH)
are paid on the same basis as the CTC method under paragraph (c) of
this section.
Proposed Sec. 17.275(j) would establish in regulation the current
reimbursement methodology for hospice care. This methodology uses rates
in the CMS hospice per diem rate payment system, which is the same
methodology used in TRICARE regulations to calculate hospice payments.
See 32 CFR 199.14(g)(9).
Proposed Sec. 17.275(k) would establish in regulation a
reimbursement methodology for intermittent or part-time home health
services similar to the methodology used in TRICARE, which is based on
Medicare's payment methods and rates. See 32 CFR 199.14(h). Under this
methodology, a fixed case-mix and wage-adjusted national 60-day episode
payment amount will act as payment in full for costs associated with
furnishing home health services with exceptions allowing for additional
payment to be established. This would be a new limitation in payments
for services but is in line with the 60-day episode amount specified in
the TRICARE regulation. See 32 CFR 199.14(h).
Proposed Sec. 17.275(l) would establish in regulation the current
reimbursement methodology for facility charges associated with
procedures performed in a freestanding surgery center, which is the
basis of a prospectively determined amount, similar to that used by
TRICARE. See 32 CFR 199.14(d). These facility charges would not include
physician fees, anesthesiologist fees, or fees of other authorized non-
VA providers; such independent professional fees would be submitted
separately from facility fees and calculated under the methodology in
proposed Sec. 17.275(e). Ambulatory surgery procedures performed in
CAHs or in hospital outpatient departments are to be reimbursed in
accordance with the provisions of paragraph (c) or (d) respectively of
this section.
Proposed Sec. 17.275(m) states that VA shall determine the
appropriate reimbursement method or methods to be used in the extension
of CHAMPVA benefits for otherwise covered medical services and supplies
provided by hospitals or other institutional providers, physicians or
other individual professional providers, or other providers outside the
United States. The authority to establish these reimbursement methods
is similar to that in TRICARE regulation. See 32 CFR 199.14(n).
Proposed Sec. 17.275(n) would establish in regulation the
reimbursement methodology for inpatient services provided in a Sole
Community Hospital (SCH). TRICARE reimbursement approximates Medicare
reimbursement for SCHs. TRICARE reimburses on a two-step process.
TRICARE makes an initial payment based upon multiplying the billed
amount by the applicable TRICARE percentage, which is the greater of
the SCH's most recently available cost-to-charge ratio from the CMS
inpatient Provider Specific File or the TRICARE allowed-to-billed
ratio. The second step is a year-end adjustment to compare the
aggregate allowable cost under the first method to the aggregate amount
that would have been allowed for the same care using the DRG method. In
the event that the DRG method amount is the greater, the year-end
adjustment will be the amount by which it exceeds the aggregate
allowable costs. See 32 CFR 199.14(a)(7). Due to certain limitations,
CHAMPVA cannot be the same as TRICARE but can be
[[Page 2407]]
similar. CHAMPVA would compare the cost-to-charge ratio reimbursement
amount versus the DRG reimbursement amount and then pay the higher of
the two methods.
17.276 Claim-Filing Deadlines
Proposed Sec. 17.276 is a revision and renumbering of current
Sec. 17.275. First, we propose to remove the reference to ``the
Center'' and ``[t]he Director, Health Administration Center, or his or
her designee'' in Sec. 17.276(a) and (b), as renumbered by this
rulemaking. Our intent is to indicate that VA is responsible for
administering CHAMPVA and has discretion to assign claims processing
responsibility within the Department.
Proposed Sec. 17.276(c) would clarify that claims for services and
supplies provided to an individual before the date of the event that
qualifies the individual as eligible under Sec. 17.271 are not
reimbursable.
We further propose to add new paragraph (d) to proposed Sec.
17.276 to clarify CHAMPVA policy concerning double coverage situations.
We would clearly state that CHAMPVA is the last payer to all OHI, with
the exceptions noted previously, which would mean that in cases of
double coverage, any CHAMPVA benefits would generally not be paid until
the claim has first been filed with the OHI and a final payment
determination or explanation of benefits has been issued by the other
insurer or payer. This is consistent with the purpose of TRICARE's
double coverage provisions in 32 CFR 199.8, which address double
coverage situations with OHI. Once CHAMPVA, as the last payer, makes
its payment to the authorized non-VA provider, the CHAMPVA
beneficiary's personal liability for the cost of care is then fully
extinguished, as discussed earlier. However, TRICARE has special rules
for double coverage situations involving TRICARE beneficiaries who also
have Medicare benefits. See 32 CFR 199.8(e)(1). In the case of double
coverage based on the availability of both CHAMPVA and Medicare
benefits, the provisions of current Sec. 17.271(b) would still apply
and be unchanged by this proposed rulemaking. Under current Sec.
17.271(b), VA is the secondary payer to Medicare, as required under 38
U.S.C. 1781(d)(2).
17.277 Appeals
Proposed Sec. 17.277 is a revision and renumbering of current
Sec. 17.276. We would make two minor revisions to current Sec.
17.276. First, we would remove references to ``Director, Health
Administration Center, or his or her designee'' (an outdated reference
within the current Office of Community Care) and replace it with a
reference to ``VA.'' This is necessary to ensure that VA is effectively
put forth as the general administrator of CHAMPVA. In addition, we
would clarify when a beneficiary has OHI, an appeal must first be filed
with the OHI, and a determination made, before submitting an appeal to
CHAMPVA. We would also like to note that there may be instances where
we would not require a beneficiary to appeal with their OHI first, such
as when the OHI deems the issue non-appealable. Neither of these
revisions are substantive changes. We will also keep the note located
in current Sec. 17.276, relocating it to the body of new Sec. 17.277.
We propose to renumber current Sec. Sec. 17.277-17.278 to
Sec. Sec. 17.278-17.279. Additionally, as with proposed Sec. 17.277,
we would remove reference to ``the Center'' in current Sec. 17.277 and
in its place insert ``VA.'' This revision would clarify that it is VA,
and not HAC independently, that has the authority to pursue medical
care cost recovery in accordance with applicable law. We would also
remove the reference to third-party liability in proposed Sec. 17.278
because it is unnecessary. VA's specific authority to recover for
medical care costs applies to responsible third parties. We would not
make any substantive changes to proposed Sec. 17.279.
Effect of Rulemaking
The Code of Federal Regulations, as proposed to be revised by this
proposed rulemaking, would represent the exclusive legal authority on
this subject. No contrary rules or procedures would be authorized. All
VA guidance would be read to conform with this proposed rulemaking if
possible or, if not possible, such guidance would be superseded by this
rulemaking.
Paperwork Reduction Act
This proposed rule contains no provisions constituting a collection
of information under the Paperwork Reduction Act of 1995 (44 U.S.C.
3501-3521).
Regulatory Flexibility Act
The Secretary hereby certifies that this proposed rule would not
have a significant economic impact on a substantial number of small
entities as they are defined in the Regulatory Flexibility Act, 5
U.S.C. 601-612. The new proposed payment methods in this rulemaking
will include new reimbursement rates for the Outpatient Prospective
Payment System (OPPS), Home Health Prospective Payment System (HH PPS),
and Sole Community Hospitals (SCHs) reimbursement methodologies. These
revised methodologies would not significantly affect small businesses
due to the following reasons: (1) The health care industry, to include
Medicare and TRICARE, is currently using these payment methods and most
providers are used to these reimbursement rates, if not expecting to
receive them; (2) CHAMPVA's beneficiary population is relatively small
compared to these other health care payers. Further support and data
can also be found in VA's impact analysis as a supporting document at
https://www.regulations.gov, usually within 48 hours after the
rulemaking document is published. Additionally, a copy of this
rulemaking and its impact analysis are available on VA's website at
https://www.va.gov/orpm/, by following the link for ``VA Regulations
Published from FY 2004 Through Fiscal Year to Date.'' Therefore,
pursuant to 5 U.S.C. 605(b), this amendment would be exempt from the
initial and final regulatory flexibility analysis requirements of 5
U.S.C. 603 and 604.
Executive Orders 12866, 13563 and 13771
Executive Orders 12866 and 13563 direct agencies to assess the
costs and benefits of available regulatory alternatives and, when
regulation is necessary, to select regulatory approaches that maximize
net benefits (including potential economic, environmental, public
health and safety effects, and other advantages; distributive impacts;
and equity). Executive Order 13563 (Improving Regulation and Regulatory
Review) emphasizes the importance of quantifying both costs and
benefits, reducing costs, harmonizing rules, and promoting flexibility.
Executive Order 12866 (Regulatory Planning and Review) defines a
``significant regulatory action,'' which requires review by the Office
of Management and Budget (OMB), as ``any regulatory action that is
likely to result in a rule that may: (1) Have an annual effect on the
economy of $100 million or more or adversely affect in a material way
the economy, a sector of the economy, productivity, competition, jobs,
the environment, public health or safety, or State, local, or tribal
governments or communities; (2) Create a serious inconsistency or
otherwise interfere with an action taken or planned by another agency;
(3) Materially alter the budgetary impact of entitlements, grants, user
fees, or loan programs or the rights and obligations of recipients
thereof; or (4) Raise novel legal or policy
[[Page 2408]]
issues arising out of legal mandates, the President's priorities, or
the principles set forth in this Executive Order.''
The economic, interagency, budgetary, legal, and policy
implications of this regulatory action have been examined and OMB has
determined the regulatory action to be economically significant,
because it will have an annual effect on the economy of $100 million or
more. As noted above, VA's impact analysis is available as a supporting
document at https://www.regulations.gov, usually within 48 hours after
the rulemaking document is published. Additionally, a copy of this
rulemaking and its impact analysis are available on VA's website at
https://www.va.gov/orpm/, by following the link for ``VA Regulations
Published from FY 2004 Through Fiscal Year to Date.''
This proposed rule is not expected to be subject to the
requirements of EO13771 because this proposed rule is expected to
result in no more than de minimis costs.
Unfunded Mandates
The Unfunded Mandates Reform Act of 1995 requires, at 2 U.S.C.
1532, that agencies prepare an assessment of anticipated costs and
benefits before issuing any rule that may result in the expenditure by
State, local, or tribal governments, in the aggregate, or by the
private sector, of $100 million or more (adjusted annually for
inflation) in any one year. This proposed rule would have no such
effect on State, local, or tribal governments, or on the private
sector.
Catalog of Federal Domestic Assistance
The Catalog of Federal Domestic Assistance numbers and titles for
the programs affected by this document are 64.009, Veterans Medical
Care Benefits; 64.010, Veterans Nursing Home Care; and 64.011, Veterans
Dental Care; 64.012, Veterans Prescription Service; 64.013, Veterans
Prosthetic Appliances; and 64.019, Veterans Rehabilitation Alcohol and
Drug Dependence.
Signing Authority
The Secretary of Veterans Affairs, or designee, approved this
document and authorized the undersigned to sign and submit the document
to the Office of the Federal Register for publication electronically as
an official document of the Department of Veterans Affairs. Gina S.
Farrisee, Deputy Chief of Staff, Department of Veterans Affairs,
approved this document on October 2, 2017, for publication.
List of Subjects in 38 CFR Part 17
Administrative practice and procedure, Archives and records,
Claims, Dental health, Drug abuse, Health care, Health facilities,
Health professions, Health records, Medical devices, Mental health
programs, Nursing homes, Veterans.
Dated: January 5, 2018.
Michael Shores,
Director, Office of Regulation Policy & Management, Office of the
Secretary, Department of Veterans Affairs.
For the reasons stated in the preamble, The Department of Veterans
Affairs (VA) proposes to amend 38 CFR part 17 as follows:
PART 17--MEDICAL
0
1. The authority citation for part 17 continues to read in part as
follows:
Authority: 38 U.S.C. 501, and as noted in specific sections.
* * * * *
0
2. Revise Sec. 17.270 to read as follows:
Sec. 17.270 General provisions and definitions.
(a) Overview of CHAMPVA. CHAMPVA is the Civilian Health and Medical
Program of the Department of Veterans Affairs (VA). Generally, CHAMPVA
furnishes medical care in the same or similar manner, and subject to
the same or similar limitations, as medical care furnished to certain
dependents and survivors of active duty and retired members of the
Armed Forces under chapter 55 of title 10, United States Code
(CHAMPUS), commonly referred to as the TRICARE Standard plan. Under
CHAMPVA, VA shares the cost of medically necessary services and
supplies with eligible beneficiaries within the 50 United States, the
District of Columbia, the U.S. territories, and abroad. Under CHAMPVA,
medical services and supplies may be provided as follows:
(1) By an authorized non-VA provider.
(2) By a VA provider at a VA facility, on a resource-available
basis through the CHAMPVA In-house Treatment Initiative (CITI) only to
CHAMPVA beneficiaries who are not also eligible for Medicare.
(3) Through VA Medications by Mail (MbM).
(i) Only CHAMPVA beneficiaries who do not have any other type of
health insurance that pays for prescriptions, including Medicare Part
D, may use MbM.
(ii) Smoking cessation pharmaceutical supplies will only be
provided through MbM and only to CHAMPVA beneficiaries that are not
also eligible for Medicare.
(b) Definitions. The following definitions apply to CHAMPVA
(Sec. Sec. 17.270 through 17.278):
Accepted assignment refers to the action of an authorized non-VA
provider who accepts responsibility for the care of a CHAMPVA
beneficiary and thereby agrees to accept the CHAMPVA determined
allowable amount as full payment for services and supplies rendered to
the beneficiary. (The provider's acceptance of the CHAMPVA determined
allowable amount extinguishes the beneficiary's payment liability to
the provider with the exception of applicable cost shares and
deductibles.)
Authorized non-VA provider means an individual or institutional
non-VA provider of CHAMPVA-covered medical services and supplies that
meets any of the following criteria:
(i) Is licensed or certified by a State to provide the medical
services and supplies; or
(ii) Where a State does not offer licensure or certification, is
otherwise certified by an appropriate national or professional
association that sets standards for the specific medical provider.
Calendar year means January 1 through December 31.
CHAMPVA beneficiary means a person enrolled under Sec. 17.271.
CHAMPVA-covered services and supplies mean those medical services
and supplies that are medically necessary and appropriate for the
treatment of a condition and that are not specifically excluded under
Sec. 17.272(a)(1) through (84).
CHAMPVA determined allowable amount has the meaning set forth in
Sec. 17.272(b)(1).
CHAMPVA In-house Treatment Initiative (CITI) means the initiative
under 38 U.S.C. 1781(b) under which participating VA medical facilities
provide medical services and supplies to CHAMPVA beneficiaries who are
not also eligible for Medicare, subject to availability of space and
resources.
Child has the definition established in 38 U.S.C. 101.
Claim means a request by an authorized non-VA provider or by a
CHAMPVA beneficiary for payment or reimbursement for medical services
and supplies provided to a CHAMPVA beneficiary.
Fiscal year means October 1 through September 30.
Medications by Mail (MbM) means the initiative under which VA
provides outpatient prescription medications
[[Page 2409]]
through the mail to CHAMPVA beneficiaries.
Other health insurance (OHI) means health insurance plans or
programs (including Medicare) or third-party coverage that provide
coverage to a CHAMPVA beneficiary for expenses incurred for medical
services and supplies.
Payer refers to OHI, as defined in this section, that is obligated
to pay for CHAMPVA-covered medical services and supplies. In a
situation in which, in addition to CHAMPVA, one or more payers is/are
responsible to pay for such services and supplies (i.e., a ``double
coverage'' situation), there would be a primary payer (i.e., the payer
obligated to pay first), secondary payer (i.e., the payer obligated to
pay after the primary payer), etc. In double coverage situations,
CHAMPVA would be the last payer.
Service-connected has the definition established in 38 U.S.C. 101.
Spouse refers to a person who is married to a veteran and whose
marriage is valid as determined under 38 U.S.C. 103(c).
Surviving spouse refers to a person who was married to and is the
widow(er) of a veteran as determined under 38 U.S.C. 103(c).
(c) Discretionary authority. When it is determined to be in the
best interest of VA, VA may waive any requirement in Sec. Sec. 17.270
through 17.278, except any requirement specifically set forth in 38
U.S.C. 1781, or otherwise imposed by statute. It is VA's intent that
such discretionary authority would be used only under very unusual and
limited circumstances and not to deny any individual any right,
benefit, or privilege provided to him or her by statute or these
regulations. Any such waiver shall apply only to the individual
circumstance or case involved and will in no way be construed to be
precedent-setting.
(Authority: 38 U.S.C. 501, 1781)
0
3. Amend Sec. 17.271 by:
0
a. Removing the word ``and'' at the end of paragraph (a)(3).
0
b. Redesignating paragraph (a)(4) as paragraph (a)(5).
0
c. Adding a new paragraph (a)(4).
0
d. Revising the authority citation following paragraph (a).
The addition and revision read as follows:
Sec. 17.271 Eligibility.
(a) * * *
(4) An individual designated as a Primary Family Caregiver, under
38 CFR 71.25(f), who is not entitled to care or services under a
health-plan contract (as defined in 38 U.S.C. 1725(f)(2)); and
* * * * *
(Authority: 38 U.S.C. 501, 1720G(a)(7)(A), 1781)
* * * * *
0
4. Amend Sec. 17.272 by:
0
a. Revising paragraph (a)(2).
0
b. In paragraph (a)(3) introductory text, removing the phrase
``(Medicaid excluded)''.
0
c. Adding paragraphs (a)(3)(iii) and (iv).
0
d. Revising paragraph (a)(21)(ix).
0
e. Removing paragraph (a)(26).
0
f. Redesignating paragraphs (a)(27) through (38) as paragraphs (a)(26)
through (37), respectively.
0
g. In newly redesignated paragraph (a)(30), revising the introductory
text and paragraphs (a)(30)(v) and (vi) and adding paragraphs
(a)(30)(xi) through (xiv).
0
h. Removing paragraph (a)(39).
0
i. Redesignating paragraphs (a)(40) through (56) as paragraphs (a)(38)
through (54), respectively.
0
j. In newly redesiganted paragraph (a)(40)(iv), removing
``(a)(42)(iii)(A)'' and adding in its place ``(a)(40)(iii)(A).''
0
k. Removing paragraph (a)(57).
0
l. Redesignating paragraphs (a)(58) through (71) as paragraphs (a)(55)
through (68), respectively.
0
m. Revising newly redesignated paragraphs (a)(57) through (59).
0
n. Removing paragraph (a)(72).
0
o. Redesignating paragraphs (a)(73) through (86) as paragraphs (a)(69)
through (82), respectively.
0
p. Revising newly redesignated paragraph (a)(76).
0
q. Adding paragraphs (a)(83) and (84).
0
r. Revising paragraph (b).
The revisions and additions read as follows:
Sec. 17.272 Benefits limitations/exclusions.
(a) * * *
(2) Services and supplies required as a result of an occupational
disease or injury for which benefits are payable under workers'
compensation or similar protection plan (whether or not such benefits
have been applied for or paid) except when such benefits are exhausted
and the services and supplies are otherwise not excluded from CHAMPVA
coverage.
(3) * * *
(iii) Indian Health Service.
(iv) CHAMPVA supplemental policies.
* * * * *
(21) * * *
(ix) Treatment for stabilization of myofascial pain dysfunction
syndrome, also referred to as temporomandibular joint disorder (TMD).
Authorization is limited to initial imaging such as radiographs,
Computed Tomography, or Magnetic Resonance Imaging; up to four office
visits; and the construction of an occlusal splint.
* * * * *
(30) Preventive care (such as employment-requested physical
examinations and routine screening procedures). The following
exceptions apply, including but not limited to:
* * * * *
(v) Cervical cancer screening.
(vi) Breast cancer screening.
* * * * *
(xi) Colorectal cancer screening.
(xii) Prostate cancer screening.
(xiii) Annual physical examination.
(xiv) Vaccinations/immunizations.
* * * * *
(57) Unless a waiver for extended coverage is granted in advance:
Inpatient mental health services in excess of 30 days in any calendar
year (or in an admission), in the case of a patient 19 years of age or
older; 45 days in any calendar year (or in an admission), in the case
of a patient under 19 years of age; or 150 days of residential
treatment care in any calendar year (or in an admission).
(58) Outpatient mental health services in excess of 23 visits in a
calendar year unless a waiver for extended coverage is granted in
advance.
(59) Institutional services for partial hospitalization in excess
of 60 treatment days in any calendar year (or in an admission) unless a
waiver for extended coverage is granted in advance.
* * * * *
(76) Over-the-counter products except for pharmaceutical smoking
cessation supplies that are approved by the U.S. Food and Drug
Administration, prescribed, and provided through MbM, and insulin and
related diabetic testing supplies and syringes.
* * * * *
(83) Medications not approved by the U.S. Food and Drug
Administration (FDA), excluding FDA exceptions to the approval
requirement.
(84) Services and supplies related to the treatment of dyslexia.
(b) Costs of services and supplies to the extent such amounts are
billed over the CHAMPVA determined allowable amount are specifically
excluded from coverage.
(1) The CHAMPVA determined allowable amount is the maximum level of
payment by CHAMPVA to an authorized non-VA provider for the provision
of CHAMPVA-covered services and supplies to a CHAMPVA
[[Page 2410]]
beneficiary. The CHAMPVA determined allowable amount is determined
before consideration of cost sharing and the application of deductibles
or OHI.
(2) A Medicare-participating hospital must accept the CHAMPVA
determined allowable amount for inpatient services provided to a
CHAMPVA beneficiary as payment in full. See 42 CFR 489.25.
(3) An authorized non-VA provider who accepts responsibility for
the care of a CHAMPVA beneficiary thereby agrees to accept the CHAMPVA
determined allowable amount as full payment for services and supplies
rendered to the beneficiary (i.e., accepted assignment). The provider's
acceptance of the CHAMPVA determined allowable amount extinguishes the
beneficiary's payment liability to the provider. Any attempts to
collect any additional amount from the CHAMPVA beneficiary may result
in the provider being excluded from Federal benefits programs. See 42
CFR 1003.105.
* * * * *
0
5. Amend Sec. 17.273 by:
0
a. Revising the introductory text and paragraph (d).
0
b. Removing paragraph (e).
0
c. Redesignating paragraph (f) as paragraph (e).
0
d. Adding new paragraph (f).
The revisions and addition read as follows:
Sec. 17.273 Preauthorization.
Preauthorization or advance approval is required for any of the
following, except when the benefit is covered by the CHAMPVA
beneficiary's other health insurance (OHI):
* * * * *
(d) Dental care. For limitations on dental care, see Sec.
17.272(a)(21)(i) through (xii).
* * * * *
(f) CHAMPVA will perform a retrospective medical necessity review
during the coordination of benefits process if:
(1) It is determined that CHAMPVA is the responsible payer for
services and supplies but CHAMPVA preauthorization was not obtained
prior to delivery of the services or supplies; and,
(2) The claim for payment is filed within the appropriate one-year
period.
* * * * *
0
6. Amend Sec. 17.274 by:
0
a. Revising paragraphs (a), (b), and (c).
0
b. Adding a heading for paragraph (d).
0
c. Adding paragraph (e).
The revisions and additions read as follows:
Sec. 17.274 Cost sharing.
(a) Cost sharing generally. CHAMPVA is a cost sharing program in
which the cost of covered services is shared with the CHAMPVA
beneficiary. CHAMPVA pays the CHAMPVA determined allowable amount less
the CHAMPVA deductible, if applicable, and less the CHAMPVA beneficiary
cost share.
(1) CHAMPVA beneficiary cost-share requirements do not apply to the
following:
(i) Supplies provided through VA MbM.
(ii) Any medical services and supplies provided to a CHAMPVA
beneficiary through CITI.
(iii) The following services, even if not provided through CITI:
(A) Colorectal cancer screening.
(B) Breast cancer screening.
(C) Cervical cancer screening.
(D) Prostate cancer screening.
(E) Annual physical exams.
(F) Vaccinations/immunizations.
(G) Well child care from birth to age six, as described in Sec.
17.272(a)(30)(i).
(iv) Hospice services.
(v) Or other services as determined by the Secretary of Veterans
Affairs.
(2) [Reserved]
(b) Deductibles. In addition to the CHAMPVA beneficiary cost share,
an annual (calendar year) outpatient deductible requirement ($50 per
beneficiary or $100 per family) must be satisfied prior to VA payment
of outpatient benefits. The deductible requirement is waived for:
(1) CHAMPVA-covered services and supplies provided through VA MbM
or through CITI.
(2) Inpatient services.
(3) Preventive services listed in paragraph (a)(1)(iii) of this
section.
(4) Hospice services.
(5) Or other services as determined by the Secretary of Veterans
Affairs.
(c) Cost sharing limitations. To provide financial protection
against the impact of a long-term illness or injury, there is a $3,000
calendar year limit or ``catastrophic cap'' per CHAMPVA eligible family
on the CHAMPVA beneficiary's out-of-pocket costs for allowable services
and supplies. After a family has paid $3,000 in out-of-pocket costs, to
include both cost share and deductible amounts, in a calendar year,
CHAMPVA will pay the full allowable amounts for the remaining CHAMPVA-
covered services and supplies through the end of that calendar year.
Credits to the annual catastrophic cap are limited to the applied
annual deductible(s) and the CHAMPVA beneficiary cost-share amount.
Costs above the CHAMPVA determined allowable amount, as well as costs
associated with non-covered medical services and supplies, are not
credited toward the catastrophic cap calculation.
(d) Non-payment. * * *
(e) Cost share calculation. The CHAMPVA beneficiary's cost-share
amount, if not waived under paragraph (a)(1) of this section, is 25
percent of the CHAMPVA determined allowable amount in excess of the
annual calendar year deductible (see Sec. 17.275 for procedures
related to the calculation of the allowable amount for CHAMPVA-covered
services and supplies), except for the following:
(1) For inpatient services subject to the CHAMPVA Diagnosis Related
Group (DRG) payment system, the cost share is the lesser of:
(i) The per diem rate multiplied by the number of inpatient days;
(ii) 25 percent of the hospital's billed amount; or
(iii) The base CHAMPVA DRG rate.
(2) For inpatient mental health low volume hospitals and units
(less than 25 mental health discharges per federal fiscal year), the
cost share is the lesser of:
(i) The fixed per diem rate multiplied by the number of inpatient
days; or
(ii) 25 percent of the hospital's billed charges.
* * * * *
Sec. Sec. 17.275 through 17.278 [Redesignated as Sec. Sec. 17.276
through 17.279]
0
7. Redesignate Sec. Sec. 17.275 through 17.278 as Sec. Sec. 17.276
through 17.279.
0
8. Add new Sec. 17.275 to read as follows:
Sec. 17.275 CHAMPVA determined allowable amount calculation.
CHAMPVA calculates the allowable amount in the following ways, for
the following covered services and supplies:
(a) Inpatient hospital services (non-mental health). Unless exempt
or subject to a methodology under paragraph (b) or (c) of this section,
inpatient hospital services provided in the 50 States, the District of
Columbia, and Puerto Rico are subject to the CHAMPVA Diagnosis Related
Group (DRG)-based reimbursement methodology. Under the CHAMPVA DRG-
based payment system, hospitals are paid a predetermined amount per
discharge for inpatient hospital services, which will not exceed the
billed amount. Certain inpatient services will be reimbursed under the
CHAMPVA Cost-to-Charge (CTC) reimbursement methodology.
(b) Inpatient hospital services (mental health). The CHAMPVA
inpatient mental health per diem reimbursement methodology is used to
calculate
[[Page 2411]]
reimbursement for inpatient mental health hospital care in specialty
psychiatric hospitals and psychiatric units of general acute hospitals
that are exempt from the CHAMPVA DRG-based payment system. The per diem
rate is calculated by multiplying the daily rate by the number of days
(length of stay). The daily rate is updated each fiscal year for both
high volume hospitals (25 or more discharges per fiscal year) and low
volume hospitals (fewer than 25 discharges per fiscal year).
(c) Other inpatient hospital services. (1) The CHAMPVA CTC
reimbursement methodology is used to calculate reimbursement for
inpatient care furnished by hospitals or facilities that are exempt
from either of the methodologies in paragraph (a) or (b) of this
section. Such hospitals or facilities will be paid at the CHAMPVA CTC
ratio times the billed charges that are customary and not in excess of
rates or fees the hospital or facility charges the general public for
similar services in a community.
(2) The following hospitals and services are subject to the CHAMPVA
CTC payment methodology:
(i) Any hospital that qualifies as a cancer hospital under Medicare
standards and has elected to be exempt from the Centers for Medicare
and Medicaid Services (CMS) prospective payment system.
(ii) Christian Science sanatoriums.
(iii) Critical Access Hospitals.
(iv) Any hospital outside the 50 States, the District of Columbia,
or Puerto Rico.
(v) Hospitals within hospitals.
(vi) Long-term care hospitals.
(vii) Non-Medicare participating hospitals.
(viii) Non-VA Federal Health Care Facilities (e.g., military
treatment facilities, Indian Health Service).
(ix) Rehabilitation hospitals.
(x) Hospital or hospital-based services subject to State waiver in
any State that has implemented a separate DRG-based payment system or
similar payment system in order to control costs.
(xi) Hospitals and services as determined by the Secretary of
Veterans Affairs.
(d) Outpatient hospital services. The CHAMPVA outpatient
prospective payment system (OPPS) is used to calculate the allowable
amount for outpatient services provided in hospitals subject to
Medicare OPPS. This will include the utilization of TRICARE's
reimbursement methodology to include specific coding requirements,
ambulatory payment classifications (APCs), nationally established APC
amounts, and associated adjustments.
(e) Outpatient and inpatient non-hospital services. Payments to
individual authorized non-VA providers (not hospitals) for CHAMPVA-
covered medical services and supplies provided on an outpatient or
inpatient basis, including but not limited to, anesthesia services,
laboratory services, and other professional fees associated with
individual authorized non-VA providers, are reimbursed based on the
lesser of:
(1) The CHAMPVA Maximum Allowable Charge;
(2) The prevailing amount, which is the amount equal to the maximum
reasonable amount allowed providers for a specific procedure in a
specific locality; or,
(3) The billed amount.
(f) Pharmacy services and supplies. The CHAMPVA pharmacy services
and supplies payment methodology is based on specific CHAMPVA pharmacy
points of service, which dictate the amounts paid by VA. VA pays:
(1) For services and supplies obtained from a retail in-network
pharmacy, the lesser of the billed amount or the contracted rate; or
(2) For supplies obtained from a retail out-of-network pharmacy,
the lesser of the billed amount plus a dispensing fee or the average
wholesale price plus a dispensing fee.
(g) Skilled Nursing Facility (SNF) care. The CHAMPVA SNF
reimbursement methodology is based on the CMS prospective payment
system for SNFs under 42 CFR part 413, subpart J (Medicare Resource
Utilization Group (RUG) rates).
(h) Durable medical equipment, prosthetics, orthotics, and supplies
(DMEPOS). The CHAMPVA DMEPOS reimbursement methodology is based on the
same amounts established under the CMS DMEPOS fee schedule under 42 CFR
part 414, subpart D. The CHAMPVA determined allowable amount for DMEPOS
is the amount in effect in the specific geographic location at the time
CHAMPVA-covered medical services and supplies are provided to a CHAMPVA
beneficiary.
(i) Ambulance services. CHAMPVA adopts Medicare's Ambulance Fee
Schedule (AFS) for ambulance services, with the exception of services
furnished by a Critical Access Hospital (CAH). Ambulance services are
paid based on the lesser of the Medicare AFS or the billed amount.
Ambulance services provided by a CAH are paid on the same bases as the
CTC method under paragraph (c) of this section.
(j) Hospice care. CHAMPVA hospice reimbursement methodology uses
Medicare per diem hospice rates.
(k) Home health care (intermittent or part-time). CHAMPVA home
health care reimbursement methodology, based on Medicare's home health
prospective payment system, uses a fixed case-mix and wage-adjusted
national 60-day episode payment amount to act as payment in full for
costs associated with furnishing home health services with exceptions
allowing for additional payment to be established.
(l) Ambulatory surgery. The CHAMPVA reimbursement methodology for
facility charges associated with procedures performed in a freestanding
ambulatory surgery center is based on a prospectively determined
amount, similar to that used by TRICARE. These facility charges do not
include physician fees, anesthesiologist fees, or fees of other
authorized non-VA providers; such independent professional fees must be
submitted separately from facility fees and are calculated under the
methodology in paragraph (e) of this section.
(m) CHAMPVA-covered medical services and supplies provided outside
the United States. VA shall determine the appropriate reimbursement
method(s) for CHAMPVA-covered medical services and supplies provided by
authorized non-VA providers outside the United States.
(n) Sole Community Hospitals. The CHAMPVA reimbursement methodology
for inpatient services provided in a Sole Community Hospital (SCH) will
be the greater of: The allowable amount determined by multiplying the
billed charges by the SCH's most recently available cost-to-charge
ratio from the CMS Inpatient Provider Specific File or the DRG
reimbursement rate.
(Authority: 38 U.S.C. 501, 1781)
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9. Amend newly redesignated Sec. 17.276 by:
0
b. Revising paragraphs (a) introductory text and (b).
0
c. Adding paragraphs (c) and (d).
The revisions and additions read as follows:
Sec. 17.276 Claim-filing deadlines.
(a) Unless an exception is granted under paragraph (b) of this
section, claims for medical services and supplies must be filed no
later than:
* * * * *
(b) Requests for an exception to the claim filing deadline must be
submitted in writing and include a complete explanation of the
circumstances resulting in late filing along with all available
supporting documentation. Each request for an exception to the
[[Page 2412]]
claim filing deadline will be reviewed individually and considered on
its own merit. VA may grant exceptions to the requirements in paragraph
(a) of this section if it determines that there was good cause for
missing the filing deadline. For example, when dual coverage exists,
CHAMPVA payment, if any, cannot be determined until after the primary
insurance carrier has adjudicated the claim. In such circumstances an
exception may be granted provided that the delay on the part of the
primary insurance carrier is not attributable to the beneficiary.
Delays due to provider billing procedures do not constitute a valid
basis for an exception.
(c) Claims for CHAMPVA-covered services and supplies provided
before the date of the event that qualifies an individual under Sec.
17.271 are not reimbursable.
(d) CHAMPVA is the last payer to OHI, as that term is defined in
Sec. 17.270(b). CHAMPVA benefits will generally not be paid until the
claim has been filed with the OHI and the OHI has issued a final
payment determination or explanation of benefits. CHAMPVA is secondary
payer to Medicare per the terms of Sec. 17.271(b).
* * * * *
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10. Revise newly redesignated Sec. 17.277 to read as follows:
Sec. 17.277 Appeals.
Notice of the initial determination regarding payment of CHAMPVA
benefits will be provided to the CHAMPVA beneficiary on a CHAMPVA
Explanation of Benefits (EOB) form. The EOB form is generated by the
CHAMPVA automated payment processing system. If a CHAMPVA beneficiary
or provider disagrees with the determination concerning CHAMPVA-covered
services and supplies or calculation of benefits, he or she may request
reconsideration. Such requests must be submitted to VA in writing
within one year of the date of the initial determination. The request
must state why the CHAMPVA claimant believes the decision is in error
and must include any new and relevant information not previously
considered. Any request for reconsideration that does not identify the
reason for dispute will be returned to the claimant without further
consideration. After reviewing the claim and any relevant supporting
documentation, VA will issue a written determination to the claimant
that affirms, reverses, or modifies the previous decision. If the
claimant is still dissatisfied, within 90 days of the date of the
decision he or she may make a written request for review by VA. After
reviewing the claim and any relevant supporting documentation, VA will
issue a written determination to the claimant that affirms, reverses,
or modifies the previous decision. The decision of VA with respect to
benefit coverage and computation of benefits is final. When a CHAMPVA
beneficiary has other health insurance (OHI), an appeal must first be
filed with the OHI, and a determination made, before submitting the
appeal to CHAMPVA with limited exceptions such as if the OHI deems the
issue non-appealable. Denial of CHAMPVA benefits based on legal
eligibility requirements may be appealed to the Board of Veterans'
Appeals in accordance with 38 CFR part 20. Medical determinations are
not appealable to the Board. 38 CFR 20.101.
(Authority: 38 U.S.C. 501, 1781)
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11. Revise newly redesignated Sec. 17.278 to read as follows:
Sec. 17.278 Medical care cost recovery.
VA will actively pursue medical care cost recovery in accordance
with applicable law.
(Authority: 42 U.S.C. 2651; 38 U.S.C. 501, 1781)
[FR Doc. 2018-00332 Filed 1-16-18; 8:45 am]
BILLING CODE 8320-01-P