Center for Innovation for Care and Payment, 36507-36516 [2019-15891]
Download as PDF
Federal Register / Vol. 84, No. 145 / Monday, July 29, 2019 / Proposed Rules
conduct their projects in Qualified
Opportunity Zones, thus directing
additional resources to some small
entities in our Nation’s most
economically distressed communities.
Intergovernmental Review: Some of
the programs affected by this proposed
priority are subject to Executive Order
12372 and the regulations in 34 CFR
part 79. One of the objectives of the
Executive order is to foster an
intergovernmental partnership and a
strengthened federalism. The Executive
order relies on processes developed by
State and local governments for
coordination and review of proposed
Federal financial assistance.
This document provides early
notification of our specific plans and
actions for this program.
Accessible Format: Individuals with
disabilities can obtain this document in
an accessible format (e.g., braille, large
print, audiotape, or compact disc) on
request to the program contact person
listed under FOR FURTHER INFORMATION
CONTACT.
Electronic Access to This Document:
The official version of this document is
the document published in the Federal
Register. You may access the official
edition of the Federal Register and the
Code of Federal Regulations at
www.govinfo.gov. At this site you can
view this document, as well as all other
documents of this Department
published in the Federal Register, in
text or Portable Document Format
(PDF). To use PDF you must have
Adobe Acrobat Reader, which is
available free at the site.
You may also access documents of the
Department published in the Federal
Register by using the article search
feature at www.federalregister.gov.
Specifically, through the advanced
search feature at this site, you can limit
your search to documents published by
the Department.
Dated: July 24, 2019.
Betsy DeVos,
Secretary of Education.
[FR Doc. 2019–16062 Filed 7–26–19; 8:45 am]
BILLING CODE 4000–01–P
khammond on DSKBBV9HB2PROD with PROPOSALS
DEPARTMENT OF VETERANS
AFFAIRS
38 CFR Part 17
RIN 2900–AQ56
Center for Innovation for Care and
Payment
Department of Veterans Affairs.
Proposed rule.
AGENCY:
ACTION:
VerDate Sep<11>2014
16:18 Jul 26, 2019
Jkt 247001
The Department of Veterans
Affairs (VA) is proposing to amend its
regulations that govern VA health care.
This rule would establish parameters
and authority for the new Center for
Innovation for Care and Payment in its
conduct of pilot programs designed to
develop innovative approaches to
testing payment and service delivery
models to reduce expenditures while
preserving or enhancing the quality of
care furnished by VA.
DATES: Comments must be received on
or before August 28, 2019.
ADDRESSES: Written comments may be
submitted through https://
www.Regulations.gov; by mail or handdelivery to: Director, Office of
Regulation Policy and Management
(00REG), Department of Veterans
Affairs, 810 Vermont Avenue North
West, Room 1064, Washington, DC
20420; or by fax to (202) 273–9026.
(This is not a toll-free telephone
number.) Comments should indicate
that they are submitted in response to
‘‘RIN 2900–AQ56 Center for Innovation
for Care and Payment.’’ Copies of
comments received will be available for
public inspection in the Office of
Regulation Policy and Management,
Room 1064, between the hours of 8 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 telephone number.) In addition,
during the comment period, comments
may be viewed online through the
Federal Docket Management System
(FDMS) at https://www.Regulations.gov.
FOR FURTHER INFORMATION CONTACT:
Michael Akinyele, VA Chief Innovation
Officer and Executive Director (Acting),
VA Innovation Center (VIC) (008E), 810
Vermont Ave. NW, Washington, DC
20420. Michael.Akinyele@va.gov. (202)
461–7271. (This is not a toll-free
number.)
SUPPLEMENTARY INFORMATION: On June 6,
2018, section 152 of Public Law 115–
182, the John S. McCain III, Daniel K.
Akaka, and Samuel R. Johnson VA
Maintaining Internal Systems and
Strengthening Integrated Outside
Networks Act of 2018, or the VA
MISSION Act of 2018, amended title 38
of the United States Code (U.S.C.) by
adding a new section 1703E, Center for
Innovation for Care and Payment.
Section 1703E(a)(1) establishes the
Center for Innovation for Care and
Payment (the Center). Section
1703E(a)(2) authorizes the conduct of
pilot programs to develop innovative
approaches to testing payment and
service delivery models to reduce
expenditures while preserving or
enhancing the quality of care furnished
SUMMARY:
PO 00000
Frm 00028
Fmt 4702
Sfmt 4702
36507
by VA, and subsection (a)(3) requires
VA to determine whether such models
improve access to, and quality,
timeliness, and patient satisfaction of
care and services, and create cost
savings for VA. Section 1703E(a)(4)
requires that VA test a model in a
location where VA determines that the
model will address deficits in care
(including poor clinical outcomes or
potentially avoidable expenditures) for a
defined population; it further directs VA
to focus on models VA expects to
reduce program costs while preserving
or enhancing the quality of care
received by individuals receiving
benefits under chapter 17 of title 38,
United States Code. Under section
1703E(a)(4)(C), VA could select those
models described in 42 U.S.C.
1315a(b)(2)(B), the authority for the
Center for Medicare and Medicaid
Innovation. In selecting models for
testing, section 1703E(a)(5) permits VA
to consider a number of different
factors, including whether the model
includes a regular process for
monitoring and updating patient care
plans in a manner that is consistent
with the needs and preferences of
individuals receiving benefits under
chapter 17; whether the model places
the individual receiving benefits under
chapter 17 (including family members
and other caregivers of such individual)
at the center of the care team of such
individual; whether the model uses
technology or new systems to
coordinate care over time and across
settings; and whether the model
demonstrates effective linkage with
other public sector payers, private sector
payers, or statewide payment models.
Section 1703E(a)(6) states that VA may
not design models in such a way that
would allow the United States to
recover or collect reasonable charges
from other Federal health care
programs, such as Medicare, Medicaid,
or TRICARE.
Section 1703E(b) provides that pilot
programs must be terminated no later
than five (5) years after they begin.
Section 1703E(c) directs VA to ensure
that each pilot program carried out
under this section occurs in an area or
areas appropriate for the intended
purposes of the pilot program; to the
extent practicable, VA should ensure
that pilot programs are located in
geographically diverse areas. Section
1703E(d) states that funding for each
pilot program must come from
appropriations provided in advance in
appropriations acts for the Veterans
Health Administration (VHA) and
information technology systems. Section
1703E(e) requires VA publish
E:\FR\FM\29JYP1.SGM
29JYP1
khammond on DSKBBV9HB2PROD with PROPOSALS
36508
Federal Register / Vol. 84, No. 145 / Monday, July 29, 2019 / Proposed Rules
information about each pilot program in
the Federal Register and to take
reasonable actions to provide direct
notice to veterans eligible to participate
in such pilot programs.
Section 1703E(f) allows VA to waive
requirements in subchapters I, II, and III
of chapter 17, title 38, U.S.C., as VA
determines necessary for the purposes
of carrying out pilot programs under
this section. Before waiving any such
authority, VA will submit to Congress a
report on a request for a waiver that
describes the specific authorities to be
waived, the standard or standards to be
used in lieu of the waived authorities,
the reasons for such waiver or waivers,
and other matters including metrics,
cost estimates (both budgets and
savings), and schedules.
Section 1703E(g) imposes several
restrictions on VA’s authority under this
section, notably limiting the number of
pilot programs (10) that can be carried
out concurrently, requiring VA to
submit the first pilot program proposal
to Congress within 18 months of the
enactment of the Caring for Our
Veterans Act of 2018 (June 6, 2018), and
requiring VA to either modify or
terminate a pilot program if VA
determines it is not improving the
quality of care or producing cost
savings. Section 1703E(h) requires VA
to conduct an evaluation of each pilot
program, and section 1703E(i) requires
VA to obtain advice from the Under
Secretary for Health and the Special
Medical Advisory Group in the
development and implementation of
any pilot program. VA must also consult
representatives of relevant Federal
agencies, and clinical and analytical
experts with expertise in medicine and
health care management. Finally,
section 1703E(j) authorizes VA to
expand, through rulemaking, successful
pilot programs in duration or scope.
This proposed rule would implement
the mandates and authorities of section
1703E, as added by the VA MISSION
Act of 2018, by establishing a new
§ 17.450.
Proposed paragraph (a) would
establish the purpose for this section
and the organization of the Center.
Proposed paragraph (a)(1) would
explain that the Center for Innovation
for Care and Payment will carry out
pilot programs to develop innovative
approaches to testing payment and
service delivery models to reduce
expenditures while preserving or
enhancing the quality of care furnished
by VA. This would be consistent with
section 1703E(a)(2). We would further
state that the Center for Innovation for
Care and Payment will be operationally
independent from any of VA’s three
VerDate Sep<11>2014
16:18 Jul 26, 2019
Jkt 247001
administrations and will be responsible
for collaborating across VA to develop
and implement pilot programs under
this section. As further explained in
proposed paragraphs (a)(2)–(3), being
operationally independent refers to the
decision-making authority of the Center
regarding the strategic, procedural, and
tactical aspects of managing the pilot
programs under this section. To ensure
the limited number (10) of concurrent
pilot programs under this section are
not redundant of or conflicted by
ongoing innovation efforts within any
specific administration, the Center for
Innovation for Care and Payment will
not operate within any specific VA
administration but will operate in VA’s
corporate portfolio.
We are strategically positioning the
Center as operationally independent to
focus on envisioning veteran care and
payment requirements in the distant
future and preparing VA to meet the
needs of veterans today, as well as in
the future; in 2045, for example, the
population of veterans in the United
States is projected to decline to 12
million. Of the approximately 20
million veterans alive today, VA
provides health care for approximately
7 million unique patients each year,
including approximately 1 million
unique non-veterans. If current trends
hold, we anticipate that by 2045, VA
would be providing health care to
approximately 3.6 million unique
veteran patients each year. As such, we
anticipate VA would need to re-imagine
its current approach to furnishing
services and payments for the veterans
it hopes to serve in 2045. For the Center
to be positioned for success in its
mission to re-imagine VA’s current
approach to furnishing services and
payments for veterans, it must enjoy
strategic and operational independence
from existing processes. In the
commercial market, innovation efforts
led by incumbents or large enterprises
are rarely responsible for creating
sustainably disruptive solutions that
revolutionize the products or services of
the incumbent. This is to be expected,
because any new solution that threatens
the viability or market position of
established products or services is
ultimately stifled by the enterprise focus
on the near-term objectives of sustaining
current products and services in lieu of
investing additional time and resources
in emerging solutions that could
revolutionize product and service
offerings to significantly benefit the
organization’s customers. We believe
that creating an autonomous,
independent organization with its own
brand is the best way to enable
PO 00000
Frm 00029
Fmt 4702
Sfmt 4702
corporate innovation to thrive.
Autonomy does not mean the Center
would work in isolation. The Center
will report through the Office of the
Secretary of Veterans Affairs and
ultimately the President of the United
States and does not have the unilateral
authority to execute pilot programs.
Proposed paragraph (b) would define
the terms for this section.
Proposed paragraph (b) would define
the term access. Section 1703E(a)(3)(A)
directs VA to test payment and service
delivery models to determine whether
such models improve access to, and
quality, timeliness, and patient
satisfaction of care and services.
Because VA will be testing models to
determine whether they improve access,
it is important to define the term. We
propose to define access as entry into or
use of VA services. Entry into would
refer to basic eligibility and enrollment,
while use of services would refer to the
actual receipt of care and services.
Access to care is dependent on both
availability and adequacy of services as
well as barriers (e.g., financial, cultural,
etc.) that may interfere with utilization
of available services. See Gulliford, M.
et al., What Does ‘‘Access to Care’’
Mean? Journal of Health Services
Research and Policy (2002), available at
https://www.ncbi.nlm.nih.gov/pubmed/
12171751.
We recognize that our beneficiaries
face various issues affecting access,
including lack of availability of VA
services in a specific geographic area or
barriers to obtaining care for specific
populations. As such, we believe this
comprehensive interpretation of access
would be of greatest benefit to veterans
affected by pilot programs conducted by
the Center.
Proposed paragraph (b) would define
the term patient satisfaction of care and
services to mean the patients’ rating of
their experiences of care and services
and as further defined in a pilot
program proposal. In addition to
requiring that we test payment and
service delivery models to determine
whether they improve access and
timeliness, section 1703E(a)(3)(A) also
requires that we assess whether the
models improve patient satisfaction,
which is a critical indicator of service
quality and patient-centric care. The
health care industry standard is to
assess patients’ perception of their
health care experience using the
Consumer Assessment of Health
Providers and Systems (CAHPS) survey,
which has been in use since the mid1990s. For example, the Centers for
Medicare and Medicaid Services (CMS)
has adopted CAHPS for care delivered
in multiple care settings. Each CAHPS
E:\FR\FM\29JYP1.SGM
29JYP1
khammond on DSKBBV9HB2PROD with PROPOSALS
Federal Register / Vol. 84, No. 145 / Monday, July 29, 2019 / Proposed Rules
survey produces several measures of
patient experience. These measures
include composite measures, which
combine two or more related survey
items; rating measures, which reflect
respondents’ ratings on a scale of 0 to
10; and single-item measures.
Measuring patient experience measures
what is important to the patient: access,
service, and communication. For years
VA has been measuring patient
satisfaction by focusing on patient
experience. VA uses CAHPS to measure
veterans’ experience of care for
outpatient care and VA’s Survey of
Healthcare Experience of Patients
(SHEP) to measure inpatient experience
of care. SHEP has been in use for many
years and uses the same questions as the
Hospital Consumer Assessment of
Healthcare Providers and Systems
(HCAHPS), a standardized, nationallyused, public survey that measures
inpatient experience of care.
We believe that using these types of
patient experience of care measures
would be in line with health care
industry standards and VA existing
practices and would ensure that
veterans and providers alike are not
burdened with new types of
assessments or surveys. In addition,
measuring patient perceptions by using
the industry-accepted patient
experience of care would allow veterans
to better understand how the care
provided by VA compares to that
provided outside of VA by having
equivalent data to make comparisons, as
well as how care furnished through the
pilot compares with care furnished
outside the pilot.
Proposed paragraph (b) would define
the term payment models. Section
1703E(a)(2) authorizes VA to carry out
innovative approaches to testing
payment and service delivery models to
reduce expenditures while preserving or
enhancing the quality of care furnished
by VA. Innovative payment models
incorporate different types of
arrangements that help lower cost while
maintaining or improving the quality of
services. We therefore propose to state
that the term payment models refers to
the types of payment, reimbursement, or
incentives that VA deems appropriate
for advancing the health and well-being
of beneficiaries. Use of the term
incentive indicates anything that is
intended to motivate service providers
to perform better or deliver services in
a more favorable manner, which is
consistent with the usual dictionary
definition. While the term payment
models is specifically applicable to
service providers, we note that VA
could use incentives for patients or
other beneficiaries; such an approach
VerDate Sep<11>2014
16:18 Jul 26, 2019
Jkt 247001
would need to be developed through a
pilot program proposal.
Proposed paragraph (b) would define
the term pilot program to refer to a pilot
program conducted under proposed
§ 17.450. VA operates programs on a
pilot or temporary basis under
authorities other than section 1703E, but
because these regulations only
implement that authority and place
requirements or restrictions, or
authorize certain functions under
section 1703E, we propose to define the
term here to avoid any impression that
the proposed § 17.450 extends those
requirements, restrictions, or authorities
to other VA initiatives operated under
separate legal authorities.
We aim, through testing innovative
payment and service delivery models, to
discover novel and innovative ways to
deliver services that enhance the quality
of care for beneficiaries. Section
1703E(a)(2) refers to testing payment
and service delivery models to reduce
expenditures while preserving or
enhancing the quality of care. We
propose to use the term quality
enhancement to refer to enhancing the
quality of care. We propose in paragraph
(b) to state that quality enhancement
refers to improvement or improvements
in such factors as clinical quality,
beneficiary-level outcomes (for example,
symptom burden), and functional status,
which is indicative of an individual’s
ability to perform normal daily activities
required to meet basic needs, fulfill
usual roles, and maintain health and
well-being as documented by
improvements in measurement data
from a reliable and valid source, such as
the electronic health record, and as
further defined in a pilot program
proposal. Quality enhancements are
multi-faceted, and measurements on
such enhancements would be tailored to
the specific area tested by a pilot
program and would be defined in VA’s
proposal, as required by section
1703E(f)(2)(D).
Similarly, we propose to define
quality preservation in paragraph (b) to
refer to the maintenance of such factors
as clinical quality, beneficiary-level
outcomes, and functional status as
documented through measurement data
from an evidence-based source, and as
further defined in a pilot program
proposal. Maintenance in this sense
would mean continued, sustained, or
improved performance by the patient
along several dimensions of care as
demonstrated by the types of factors
described above and as documented
through an evidence-based source. Like
quality enhancement, specific
measurements would be defined in VA’s
proposal.
PO 00000
Frm 00030
Fmt 4702
Sfmt 4702
36509
We propose to define in paragraph (b)
reduction in expenditure. Section
1703E(a)(2) authorizes VA to test
payment and service delivery models
that lead to a reduction in expenditures
while enhancing or preserving the
quality of care furnished by VA. Some
innovative models will require upfront
investment and additional resources
that might increase associated
expenditures in the near term, but we
anticipate the rise in expenditures will
be mitigated by corresponding
improvements in outcomes and value
creation over time. Value creation could
occur in multiple scenarios such as
through cost reduction, cost avoidance,
or reallocation of resources to
alternative, higher-value activities. For
example, investing in a system that
reduces unnecessary or duplicative
testing could lead to long term cost
avoidance. For these reasons, we
propose to state that reduction in
expenditure refers to, but is not limited
to, cost stabilization, cost avoidance,
and/or decreases in long- or short-term
spending and as further defined in a
pilot program proposal. We would not
limit reduction in expenditures to cost
stabilization, cost avoidance, and/or
decreases in long- or short-term
spending in case there are other
methods for determining that VA’s
expenditures have been reduced that do
not fit within any of the descriptions
above. In considering the impact of a
pilot program on expenditures, VA will
estimate how the proposal is anticipated
to impact VA expenditures and also
consider the proposal’s potential impact
on expenditures for other related
Federal programs.
In proposed paragraph (b), we would
state that the term service delivery
models refers to all methods or
programs for furnishing care and
services. Section 1703E(a)(2) authorizes
VA to develop innovative approaches to
testing payment and service delivery
models to reduce expenditures while
preserving or enhancing the quality of
care. Health care services can be
delivered by either VA staff or by nonVA entities or providers, as well as
through different modalities (like
telehealth) or different models (like
VA’s Patient-Aligned Care Teams) and
the definition proposed here would
capture all potential modalities and
models for furnishing services and
would be the common understanding of
this phrase. The term service delivery
model generally includes any method
for furnishing services, and we believe
this is intended to apply broadly given
the range of services and support that
VA provides to different beneficiaries.
E:\FR\FM\29JYP1.SGM
29JYP1
khammond on DSKBBV9HB2PROD with PROPOSALS
36510
Federal Register / Vol. 84, No. 145 / Monday, July 29, 2019 / Proposed Rules
In proposed paragraph (c), we would
establish the procedures VA would use
to determine the geographic locations
where pilot programs would be
conducted. Sections 1703E(a)(4)(A) and
1703E(c) require VA to test models and
pilot programs in locations where there
are deficits in care while ensuring that
pilot programs are in geographically
diverse areas of the United States.
Because different beneficiary
populations may have different needs
depending on where they live, we
believe that geographic location will
play a critical role in the design of any
pilot program. However, VA cannot yet
define the specific factors that we would
use to select geographic locations for
specific pilot programs. We anticipate
the basis for these decisions will vary
based upon the goals and objectives of
each specific pilot program. For
example, if VA were to test a new
payment methodology, it may be more
appropriate to test it in a portion of the
country where providers are already
accustomed to being paid in alignment
with that model. While market
readiness would not serve as the sole
reason for geographic location selection,
it could be a key factor in selecting
specific markets in which to test
specific pilot programs. Consequently,
we would state in proposed paragraph
(c) that VA would make decisions
regarding the location of each pilot
program based upon the
appropriateness of testing a specific
model in a specific area while taking
efforts to ensure that pilot programs are
operated in geographically diverse areas
of the country. We would identify the
proposed geographic locations for each
pilot program, the rationale for those
decisions, and how we believe the
selected locations would address
deficits in care for a defined population
in VA’s proposal to Congress to operate
the pilot program and a document in the
Federal Register.
Proposed paragraph (d) would define
limitations on the authority of the
Center. These limitations would only
apply to pilot programs under this
section. Again, VA operates pilot
programs under different authorities,
and these limits would not affect such
other pilot programs, nor would these
other pilot programs affect the activities
of the Center. Section 1703E(g)
establishes several of VA’s limitations in
carrying out pilot programs through the
Center. Section 1703E(g)(1) states that
VA may not carry out more than 10 pilot
programs concurrently. We propose to
interpret this in paragraph (d)(1) to
mean that VA cannot actively operate
more than 10 pilot programs at one
VerDate Sep<11>2014
16:18 Jul 26, 2019
Jkt 247001
time. Conducting pilot programs
requires advance preparation, as well as
data analysis following the completion
of a pilot program. VA proposes to
exclude the time involved with this
preparatory and post-program analysis
by considering the operation of a pilot
program as only the time of active
operation. This would ensure that VA is
able to operate the maximum number of
pilot programs at any one time and
mitigate potential delays to launching
new pilot programs that could improve
quality and reduce cost during the
preparatory and post-pilot analysis
effort of other pilot programs.
In proposed paragraph (d)(2), we
would state that, unless VA determines
it to be necessary and informs the
appropriate Committees of Congress, VA
would not obligate more than $50
million in any fiscal year to operate all
the pilot programs under this section.
This is consistent with section 1703E(d)
and section 1703E(g)(2), which state
that, subject to notification and approval
conditions, VA may not expend more
than $50 million in any fiscal year in
the conduct of the pilot programs
operated under this section. Funding
required to operate the pilot programs
includes all administrative and
overhead costs, including measurement
and evaluation, as well as the funding
required to implement the specific
payment or service delivery models
being tested. We propose to interpret the
term ‘‘expend’’ under section
1703E(g)(2) to mean ‘‘obligate.’’ This
interpretation accounts for the legal
requirement to record obligations that
may result in immediate or future
expenditures (outlays). An ‘‘obligation’’
is a definite commitment that creates a
legal liability for payment. At the time
that VA incurs a liability (e.g., signing
a contract) it records the full amount of
its legal liability against currentlyavailable funds pursuant to the
recording statute, 31 U.S.C. 1501(a)(1).
The timing of the incurrence of an
obligation is generally within the
agency’s control, while the timing of the
liquidation of the obligation is largely
outside of the agency’s control, due to
factors such as contractor performance
and billing. Thus, interpreting ‘‘expend’’
to mean ‘‘outlay’’ rather than ‘‘obligate’’
would frustrate the legislative intent of
authorizing up to $50 million per fiscal
year to carry out the pilot programs. We
note that paragraph (d)(2) would not
condition VA’s obligation of more than
$50 million upon approval of the
Chairmen of the Committees on
Veterans’ Affairs of the House of
Representatives and the Senate, as is
contemplated in section
PO 00000
Frm 00031
Fmt 4702
Sfmt 4702
1703E(g)(2)(B)(iii). As noted in the
President’s Signing Statement, issued
upon enactment of the VA MISSION Act
of 2018, under the separation of powers,
the Congress may not make the approval
of Members of Congress a precondition
to the execution of the law. See
Statement of the President, June 6, 2018,
available online: https://
www.whitehouse.gov/briefingsstatements/statement-by-the-president3/. VA, accordingly, treats the section
1703E(g)(2)(B)(iii) approval requirement
as advisory and non-binding, but may
submit the required report to the
appropriate Congressional Committees
before exceeding the spending cap, if
VA determines that the additional
expenditure is necessary to carry out the
pilot programs. For the public’s
awareness, coordination and approval of
funding sources under section 1703E(d)
for pilot programs will occur prior to
public notice.
In proposed paragraph (e), we would
define VA’s waiver authority to conduct
pilot programs. Section 1703E provides
a unique ability for VA, temporarily and
in certain locations, to amend
effectively its statutory authority when
carrying out pilot programs under this
section. Specifically, section 1703E(f)(1)
allows VA to waive any provisions of
law in subchapters I, II, and III of
chapter 17, title 38 U.S.C., i.e., sections
1701 through 1730C, as VA determines
necessary solely for the purposes of
carrying out this section with respect to
testing models. However, VA cannot
unilaterally waive these authorities; it
must propose a waiver and describe a
proposed pilot program in a report to
Congressional leadership, and only
upon Congress’ approval may VA carry
out the pilot program. VA must submit
the first request for a waiver by
December 6, 2019, as required by
section 1703E(g)(3).
Proposed paragraph (e) would clarify
VA’s authority regarding the waiver
provisions in section 1703E(f). In
proposed paragraph (e), we would state
that VA’s waiver authority includes
both the authority to propose the
removal of provisions of law or the
addition of provisions of law. VA is a
creature of law, and thus only has the
authority granted to it by statute. Some
statutes are restrictive, in that they
provide a general authority and then
place conditions upon the use of that
authority. For example, section 1705 of
title 38, U.S.C., defines VA’s patient
enrollment system and identifies those
veterans who are eligible to enroll and
in which priority group such veterans
will be enrolled. Under this authority,
VA could propose to waive some
specific provision of law by proposing
E:\FR\FM\29JYP1.SGM
29JYP1
khammond on DSKBBV9HB2PROD with PROPOSALS
Federal Register / Vol. 84, No. 145 / Monday, July 29, 2019 / Proposed Rules
to act as though such language that is in
the statute were not there. At the same
time, because VA is limited by its legal
authority to only carry out those
functions authorized by law, we
propose to include in VA’s waiver
authority the ability to include
additional language creating new
authority for VA to act, or restricting
language currently authorizing or
requiring VA to act. For example,
section 1708 of title 38, U.S.C.,
authorizes VA to provide temporary
lodging in certain situations and for
certain persons. VA could use this
waiver authority to propose to include
additional groups of eligible
beneficiaries under this regulation.
We propose to allow VA to propose
new or different standards under the
waiver authority of section 1703E(f). We
believe this is authorized by section
1703E(f)(1), which authorizes VA to
waive such requirements in subchapters
I, II, or III of chapter 17 of title 38, U.S.C.
These requirements, as explained above,
may either be explicit, which would
require their removal, or implicit, which
would require the addition of further
language. Moreover, we believe this
interpretation is further supported by
section 1703E(f)(2)(B), which requires
VA, in proposing the waiver of authority
for a pilot program, to identify the
standard or standards to be used in the
pilot program in lieu of the waived
authorities. We believe this language
authorizes VA both to suggest additional
standards or the removal of standards as
well. We believe that if Congress or the
public disagreed with the scope of this
authority, Congress could simply choose
to not approve VA’s waiver request, so
there is little to no risk associated with
this interpretation.
We also would state that VA may
propose to waive any provision of law
in any provision codified in or included
as a note to any section in subchapters
I through III of chapter 17, title 38,
U.S.C. Some laws are codified in a title
of the United States Code. For example,
section 1710 of title 38, U.S.C., defines
eligibility for hospital, nursing home,
and domiciliary care. Other laws are not
codified but are included as notes to
codified provisions when they deal with
similar or general subject matters. For
example, section 205 of Public Law
111–163 established a pilot program on
assistance for child care for certain
veterans receiving health care. Section
205 of Public Law 111–163 is included
as a note to section 1710 of title 38,
U.S.C. Proposed paragraph (e) would
allow VA to propose to waive
provisions in either the text of section
1710 (for example, relating to eligibility
for hospital, nursing home, or
VerDate Sep<11>2014
16:18 Jul 26, 2019
Jkt 247001
domiciliary care) or a note to section
1710 (for example, relating to the pilot
program on assistance for child care for
certain veterans receiving health care).
We believe this is authorized by section
1703E(f)(1), which authorizes VA to
waive such requirements in subchapters
I, II, and III of this chapter. When citing
to a public law that appears as a note
to a codified provision of law, we
include the U.S.C. section and identify
this as a note; public laws are assigned
as notes to codified provisions of law by
the Office of the Law Revision Counsel
in the U.S. House of Representatives.
This recognizes that these public laws
are requirements in, or at least related
to, the section of law. We also believe
that if Congress or the public disagreed
with the scope of this authority,
Congress could simply choose to not
approve VA’s waiver request, so the risk
associated with this interpretation is
limited. In other words, if VA proposed
to modify a note to a section of law and
Congress did not think we had the
authority to do that, or disagreed with
VA on policy grounds, it would simply
not approve the waiver request and the
provision would not be waived.
Finally, in paragraph (e)(1), we
propose, upon Congressional approval
of a waiver of a provision of law under
this section, that VA will also deem
waived any applicable provision of
regulation implementing such law as
identified in VA’s pilot program
proposal. We believe this would be a
necessary component to exercising the
statutory authority granted by section
1703E(f)(1), which allows VA to waive
‘‘such requirements’’ in subchapters I,
II, and III of chapter 17 as the Secretary
determines necessary solely for the
purposes of carrying out this section
with respect to testing models. We
believe regulations interpreting and
implementing specific statutory
provisions in subchapters I, II, and III
are ‘‘requirements’’ within the context
of this authority. It would be
paradoxical for VA to test innovative
approaches to payment and service
delivery if VA could waive provisions of
statute but not corresponding, and
potentially more limiting, regulations
promulgated by VA. For example, if VA
proposed to waive a provision in section
1712 concerning dental care, and
Congress approved such a proposal, VA
could also waive any regulatory
requirements (such as those found in 38
CFR 17.160) that implemented the
provision of law waived by VA through
the pilot program.
Under proposed paragraph (e)(2), VA
would publish a document in the
Federal Register with information
about, and soliciting public comment
PO 00000
Frm 00032
Fmt 4702
Sfmt 4702
36511
on, each proposed pilot program so that
the public has an opportunity to
comment on VA’s proposals while
Congressional approval is pending. VA
would then publish a document in the
Federal Register to inform the public of
any approved pilot programs, as
required by section 1703E(e)(1). While
this is not required by law, we believe
this would be prudent practice to ensure
that the public also has an opportunity
to submit comments directly to VA
regarding pending pilot program
proposals and to inform their Members
of Congress if they have any issues or
concerns so that Congress can
appropriately decide whether or not to
approve a requested waiver of authority
for the Center.
Under proposed paragraph (f), VA
would establish procedures regarding
notice of eligibility requirements.
Specifically, we would state that VA
would take reasonable actions to
provide direct notice to veterans eligible
to participate in pilot programs operated
under this section and would provide
general notice to other individuals
eligible to participate in a pilot program.
We would further state that VA also
would announce methods of notice in
the Federal Register document
published by VA for each proposed and
approved pilot program. While section
1703E(e)(2) directs VA to take
reasonable actions to provide direct
notice to veterans eligible to participate
in such pilot programs, we note that
other provisions in section 1703E refer
more broadly to individuals that are
eligible for benefits. See, e.g.,
1703E(a)(4)(B), (a)(5)(A)–(B), (j)(2).
Consequently, we read the requirement
in section 1703E(e)(2) to create an
obligation to take reasonable actions to
provide direct notice to veterans eligible
to participate in pilot programs on the
assumption that VA would have more
information about veterans, while VA
would provide general information to
notify any other individuals eligible to
participate in a pilot program. For
example, one pilot program could
expand access to benefits for family
members or caregivers of veterans; in
this case, VA would provide notice to
the veterans in the area where the pilot
program is operating and would provide
other general information as well to
reach the caregivers or family members.
Another example would be a pilot
program involving certain community
providers or other private entities; VA
would provide general information to
the community so that interested parties
could inquire or participate. The exact
nature of the notice will vary depending
upon the type of pilot program
E:\FR\FM\29JYP1.SGM
29JYP1
khammond on DSKBBV9HB2PROD with PROPOSALS
36512
Federal Register / Vol. 84, No. 145 / Monday, July 29, 2019 / Proposed Rules
involved, and so VA will announce how
it intends to inform the public, in
particular, other eligible individuals and
entities, through the document it
publishes in the Federal Register for
each pilot program. Other forms of more
direct communication could include
mailed letters, emails, announcements
to local Veterans Service Organizations,
and posting of information on the
websites of VA medical centers, the VA
Innovation Center website, and other
online sources.
In proposed paragraph (g), VA would
describe generally how it would
evaluate and report on the pilot
programs. Specifically, VA would
evaluate each pilot program operated
under this section and report its
findings. Section 1703E(h) requires VA
to conduct an evaluation of each model
tested, including at a minimum an
analysis of the quality of care furnished
and the changes in spending because of
that model. VA is required to make the
results of the tested model available to
the public in a timely fashion. Once
again, because each pilot program will
vary in terms of the specific outcomes
involved and how it will achieve those
outcomes, VA is not proposing a
discrete list of measures, but will
include more specific information with
each proposal for a pilot program. VA
proposes to base its evaluation of pilot
programs on quantitative data,
qualitative data, or both, depending
upon the nature of the pilot program.
Different types of data may be more
appropriate for different pilot program
models, but each type of data is
instructive and could help VA
determine if VA is improving access to,
and the quality, timeliness and patient
satisfaction of care and services, as well
as creating cost savings for VA.
Whenever appropriate, such evaluation
will also include a survey of
participants or beneficiaries to
determine their satisfaction with the
pilot program; this participant feedback
likely would be subject to the
Paperwork Reduction Act and would
provide direct input regarding the
effects of the pilot program. We propose
to make the evaluation results available
to the public on the VA Innovation
Center website at https://
www.innovation.va.gov/. The schedule
of the release will be indicated in the
proposal for each pilot program. By law,
VA is required to make the results of the
tested model available to the public in
a timely fashion, but we again note that
each model will naturally have different
lengths of time for data collection and
analysis. Some pilot programs may
allow for real-time, or close to real-time
VerDate Sep<11>2014
16:18 Jul 26, 2019
Jkt 247001
reporting of information (for example,
costs or number of appointments), while
others may experience lags between an
action under the pilot program and
health outcomes (for example, 6-month
or 12-month morbidity or mortality
data). VA will identify the measures and
timelines for public reporting in its pilot
program proposal submission to
Congress and its document in the
Federal Register.
In proposed paragraph (h), VA would
establish a process in regulation for the
expansion of pilot programs. Section
1703E(j) authorizes VA through
rulemaking to expand in scope or
duration, including nationwide
implementation, pilot programs if the
expansion is expected to reduce
spending without reducing the quality
of care, or to improve the quality of
patient care without increasing
spending. Furthermore, VA is only
permitted to expand a pilot program if
the pilot program does not deny or limit
the coverage or provision of benefits for
individuals under chapter 17. We
propose to establish through regulation
a general process for expanding the
scope or duration of pilot programs
instead of requiring separate
rulemakings for each expansion for
several reasons. First, the promulgation
of regulations is a lengthy process,
taking on average 18–22 months for a
proposed and final rule to be published
and effective. Given the limitations on
the length of time a pilot program could
operate under this authority of only 5
years, this would effectively require VA
to decide at the halfway point of a pilot
program, and possibly before that, as to
whether or not to expand. This may not
be enough time for VA as a practical
matter, which could either lead to the
expansion of pilot programs that
ultimately prove unsuccessful or the
inability to expand pilot programs that
do prove to be successful. Second, if VA
were required to publish new
regulations for each pilot program it
wished to expand, VA’s regulations
would become cluttered with rules that
would only be applicable for limited
periods of time and locations. This
would likely result in confusion
regarding these provisions. Finally, we
believe that by regulating the process we
would use to expand pilot programs, we
are meeting the requirements of the law,
which does not expressly require VA
proceed through notice and comment
rulemaking for each expansion, but
merely states that VA may expand pilot
programs ‘‘through rulemaking’’. This
requirement merely obligates VA to
allow the public to comment on how
expansion would occur, which this
PO 00000
Frm 00033
Fmt 4702
Sfmt 4702
proposal would do. Moreover, and as
further discussed below, VA is taking
other measures to provide the public
and Congress an opportunity to review
and comment on VA’s proposal for
expansion, which we believe would
result in an opportunity for feedback
similar to a subsequent notice and
comment rulemaking.
Initially, we propose in paragraph
(h)(1) that VA would only meet the
statutory requirement of expecting a
pilot program to reduce spending
without reducing the quality of care or
to improve the quality of patient care
without increasing spending based upon
an analysis of the data collected for the
specific pilot and developed pursuant to
proposed paragraph (g). VA also would
have to provide such results to Congress
through an interim report and to the
public through a document in the
Federal Register. This would be
consistent with the general structure of
the Center’s authority, as any decisions
regarding expansion would have to be
based on publicly available data.
Similarly, VA would have to decide that
expansion would not deny or limit the
coverage or provision of benefits for
individuals under chapter 17. This is a
statutory requirement, and VA’s basis
for making this determination would be
available for public scrutiny prior to any
expansion taking place. VA would
propose that it would not expand a pilot
program until 60 days after submitting
an interim report to Congress and
publishing a document in the Federal
Register regarding its intent to expand
a pilot program. This would provide
Congress and the public 60 days to
evaluate the data VA would be using as
the basis for such an expansion. In the
event the public or Congress do not
believe the data support expansion, they
would have this time to inform VA of
such views. Upon the completion of the
60-day period, if VA still finds that the
statutory prerequisites for expansion
have been met, VA could expand a pilot
program in either scope or duration, as
noted below.
Proposed paragraph (h)(2) would
define how VA could expand a pilot
program in scope. Proposed paragraph
(h)(2) would authorize VA to expand the
scope of a pilot program by modifying,
among other elements of a pilot
program, the range of services provided,
the qualifying conditions covered, the
geographic location of the pilot
program, or the population of eligible
participants in a manner that increases
participation in or benefits under a pilot
program. These are the general
dimensions that we believe could be
expanded, as that term is used in
section 1703E(j). Expansion is generally
E:\FR\FM\29JYP1.SGM
29JYP1
khammond on DSKBBV9HB2PROD with PROPOSALS
Federal Register / Vol. 84, No. 145 / Monday, July 29, 2019 / Proposed Rules
defined to mean becoming larger or
more extensive, and these are the likely
areas of a pilot program that could
become larger or more extensive. For
example, if VA were conducting a pilot
program related to mental health
services in Alaska for homeless
veterans, and VA proposed to expand
the pilot under paragraph (h)(1), VA
could expand to include new
beneficiary populations (e.g., nonhomeless veterans), conditions (e.g.,
additional health services), or
geographic locations (e.g., outside
Alaska), among others. We would
permit some flexibility in the forms that
expansion could occur in case there are
features of a pilot program that could be
made larger or more extensive that do
not fall within one of these categories.
Again, without knowing exactly what
pilot programs will be proposed, we are
unable now to state definitively in what
ways we could expand such a pilot
program.
In proposed paragraph (h)(3), we
propose the conditions under which VA
could extend the duration of a pilot
program. In general, section 1703E(b)
limits pilot programs to 5 years of
operation. Section 1703E(j)(1), however,
authorizes VA to extend the duration of
a pilot program if the conditions for
expansion discussed above are also met.
We propose to authorize VA to extend
the duration of a pilot program for up
to an additional 5 years. Such extension
would be subject to the same
requirements related to the evaluation
and reporting of data that would apply
to a pilot program within the first 5
years of operation under proposed
paragraph (g). We propose limiting the
expansion of a pilot program to an
additional 5 years because Congress
recognized the potential for making
successful pilots permanent in section
1703E(f)(2)(G) when it required VA to
report on the feasibility and advisability
of making a pilot program permanent,
but there is no indication Congress
intended to allow for pilot programs to
run in perpetuity. Moreover, the very
nature of a pilot program is that it has
a beginning and an end date. Finally, on
a practical and legal level, because pilot
programs under this section would
involve the waiver of one or more
provisions of law, we believe it would
create confusion over time if a pilot
program were operated indefinitely
without express statutory authority. We
believe the balance of powers is best
preserved when Congress affirmatively
establishes VA’s parameters through
law.
In proposed paragraph (i), VA would
establish its authority to make minor
modifications to pilot programs
VerDate Sep<11>2014
16:18 Jul 26, 2019
Jkt 247001
approved by Congress. Section
1703E(g)(5)(A) establishes VA’s options
(proposing a modification to Congress
for approval or terminating the pilot
program) when the Secretary determines
that a pilot program is not improving
the quality of care or producing cost
savings, but it and the rest of section
1703E are silent in terms of VA’s
authority to modify pilot programs
when VA has not made a determination
regarding whether the pilot program is
improving the quality of care or
producing cost savings. We anticipate
there may be pilot programs that we
operationalize in a way that becomes
administratively difficult to continue;
alternatively, some pilot programs may
be operationalized in a way that does
not produce clear data that would allow
VA to determine if the pilot program is
improving the quality of care or
producing cost savings. Under proposed
paragraph (i), VA could modify the pilot
program in a manner that is consistent
with the parameters of Congressional
approval without seeking further
Congressional approval for the change.
Modifications that would be consistent
with the parameters of Congressional
approval would vary based on each
pilot program, but we offer a few
examples for the public’s
understanding. For example, VA may
plan to operate a pilot program in a
particular location, but later determine
that this location is unsuitable for
reasons beyond VA’s control. For
example, an anticipated pilot site may
be unavailable due to a natural disaster,
or interest in participation in the pilot
program may be inadequate to support
valid results. In these cases, it would
seem a poor use of government
resources to continue attempting to
operate the pilot program while waiting
for a subsequent Act of Congress to
allow VA to select another location. As
another example, VA may want to
conduct a pilot program offering a
particular service, but VA may later
determine this service is not appropriate
while another similar service would be.
VA plans to submit proposals to
Congress that provide it enough
information to know what it is
authorizing, while still providing some
flexibility for VA to address potential
minor corrections without further
Congressional approval. In identifying
geographic locations for the pilot
program under paragraph (c) of this
section, for example, rather than
identifying specifically the VA medical
centers or facilities that would
participate, we anticipate providing the
general criteria VA will use to identify
locations (e.g., urban areas, rural areas,
PO 00000
Frm 00034
Fmt 4702
Sfmt 4702
36513
highly rural areas; areas near military
bases; facilities with academic affiliates,
etc.) and possibly a list of facilities that
could meet those requirements. This
would allow VA to select another
suitable location if needed. Similarly,
for services that VA might provide, or
populations of beneficiaries that might
be included, we would attempt to
describe these generally enough to allow
for further modification as needed to
either specify another service or another
population. We are sensitive to
Congress’ need to conduct oversight and
to understand clearly what it is
authorizing when it approves a waiver,
and so we limit VA’s ability to modify
a pilot program to changes that are
consistent with the parameters of
Congress’ initial approval. VA could
not, for example, modify a
Congressionally approved pilot program
on beneficiary travel to become a pilot
program on the provision of care to
beneficiaries otherwise ineligible for VA
care. Such a change would clearly be
outside the parameters of Congress’
initial approval.
In proposed paragraph (j), we would
define the conditions for termination of
pilot programs. As noted before, section
1703E(g)(5)(A) establishes that, when
the Secretary determines that a pilot
program is not improving the quality of
care or producing cost savings, VA’s
options include proposing a
modification to Congress for approval or
terminating the pilot program. In
proposed paragraph (j), we would use
the terms quality enhancement and
quality preservation to reflect the
statutory language related to improving
the quality of care, and we would use
the term reduction in expenditures to
reflect the statutory language related to
producing cost savings. These
substitutions would be consistent with
the terms as they would be defined
through paragraph (b) of this section.
We would also clarify that a
modification that can only be achieved
through submission of a new waiver
request to Congress would be distinct
from a modification under paragraph (i)
of this section, as just discussed.
Congress specifically recognized that
not all pilot programs will meet or
exceed their primary goals of enhancing
or preserving care while reducing costs.
Under proposed paragraph (j), VA
would, upon determining that a pilot
program is not producing quality
enhancement or quality preservation, or
is not resulting in the reduction of
expenditures, and that it is not possible
or advisable to modify the pilot program
either through submission of a new
waiver request under paragraph (e) or
E:\FR\FM\29JYP1.SGM
29JYP1
36514
Federal Register / Vol. 84, No. 145 / Monday, July 29, 2019 / Proposed Rules
through modification under paragraph
(i), terminate the pilot program within
30 days of submitting an interim report
to Congress stating such determination.
VA also would publish a document in
the Federal Register regarding the pilot
program’s termination, and we would
notify participants in the same manner
that we notified them under paragraph
(f) of their initial eligibility for the pilot
program. This would ensure
determinations regarding expansion and
termination are made using the same
methodology. This 30-day period is the
maximum amount of time permitted by
section 1703E(g)(5)(A)(ii).
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 rulemaking does not contain any
provisions constituting collections of
information under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501–
3521).
khammond on DSKBBV9HB2PROD with PROPOSALS
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. This
proposed rule would not have a
significant economic impact on
qualifying non-VA entities or providers.
Therefore, pursuant to 5 U.S.C. 605(b),
this rulemaking is 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
VerDate Sep<11>2014
16:18 Jul 26, 2019
Jkt 247001
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
issues arising out of legal mandates, the
President’s priorities, or the principles
set forth in this Executive Order.’’
The Office of Information and
Regulatory Affairs has determined that
this rulemaking is a significant
regulatory action under Executive Order
12866. VA’s impact analysis can be
found as a supporting document at
https://www.regulations.gov, usually
within 48 hours after the rulemaking
document is published. Additionally, a
copy of the 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 FYTD. This
proposed rule is not expected to be
subject to the requirements of Executive
Order 13771 because this proposed rule
is expected to result in no more than de
minimis costs.
Executive Order 12866 also directs
agencies to ‘‘in most cases . . . include
a comment period of not less than 60
days.’’ This regulation aims to test
innovative payment and service
delivery models that will maintain or
enhance the quality of care for
beneficiaries while reducing cost.
Providing a 30-day comment period will
allow VA to begin pilot programs more
quickly, thereby increasing
opportunities for access to quality, costeffective care to participating
beneficiaries. The regulations proposed
here are largely procedural, and will
not, without Congressional approval of
a pilot program proposal from VA,
result in any change in benefits or
services by themselves. Moreover, we
believe that the requirement to receive
Congressional approval for any waiver
of authority, and VA’s proposal to
publish specific pilot program proposals
in the Federal Register for public
comment while Congressional approval
PO 00000
Frm 00035
Fmt 4702
Sfmt 4702
is pending, should provide the public a
more meaningful opportunity to
comment on the actual pilot programs
implemented under section 1703E. For
these reasons, we believe that 30 days
would be a sufficient period of time for
the public to comment on this
rulemaking. In sum, providing a 60-day
public comment period instead of a 30day public comment period would be
against public interest. For the above
reasons, VA issues this rule with a 30day public comment period. VA will
consider and address comments that are
received within 30 days of the date this
proposed rule is published in the
Federal Register.
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, and 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, and
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
as follows: 64.007, Blind Rehabilitation
Centers; 64.008, Veterans Domiciliary
Care; 64.009, Veterans Medical Care
Benefits; 64.010, Veterans Nursing
Home Care; 64.011, Veterans Dental
Care; 64.012, Veterans Prescription
Service; 64.013, Veterans Prosthetic
Appliances; 64.014, Veterans State
Domiciliary Care; 64.015, Veterans State
Nursing Home Care; 64.016, Veterans
State Hospital Care; 64.018, Sharing
Specialized Medical Resources; 64.019,
Veterans Rehabilitation Alcohol and
Drug Dependence; and 64.022, Veterans
Home Based Primary Care
List of Subjects in 38 CFR Part 17
Administrative practice and
procedure, Alcohol abuse, Alcoholism,
Claims, Day care, Dental health, Drug
abuse, Foreign relations, Government
contracts, Grant programs—health,
Grant programs—veterans, Health care,
Health facilities, Health professions,
Health records, Homeless, Medical and
dental schools, Medical devices,
Medical research, Mental health
programs, Nursing homes, Philippines,
Reporting and recordkeeping
requirements, Scholarships and
fellowships, Travel and transportation
expenses, Veterans.
E:\FR\FM\29JYP1.SGM
29JYP1
Federal Register / Vol. 84, No. 145 / Monday, July 29, 2019 / Proposed Rules
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.
Robert L. Wilkie, Secretary, Department
of Veterans Affairs, approved this
document on April 10, 2019, for
publication.
Dated: July 23, 2019.
Consuela Benjamin,
Regulations Development Coordinator, Office
of Regulation Policy & Management, Office
of the Secretary, Department of Veterans
Affairs
For the reasons set forth in the
preamble, we propose to amend 38 CFR
part 17 as follows:
PART 17—MEDICAL
1. The authority citation for part 17 is
amended by adding an entry for
§ 17.450 to read in part as follows:
■
Authority: 38 U.S.C. 501, and as noted in
specific sections.
*
*
*
*
*
Section 17.450 is also issued under 38
U.S.C. 1703E.
*
*
*
*
*
2. Add an undesignated center
heading immediately following § 17.417
to read as follows:
■
Center for Innovation for Care and
Payment
3. Add a new § 17.450 to read as
follows.
■
khammond on DSKBBV9HB2PROD with PROPOSALS
§ 17.450 Center for Innovation for Care
and Payment.
(a) Purpose and organization. The
purpose of this section is to establish
procedures for the Center for Innovation
for Care and Payment.
(1) The Center for Innovation for Care
and Payment will be operationally
independent from any of VA’s
administrations and will be responsible
for working across VA to carry out pilot
programs to develop innovative
approaches to testing payment and
service delivery models to reduce
expenditures while preserving or
enhancing the quality of care furnished
by VA.
(2) For purposes of this paragraph (a),
operational independence refers to the
strategic, procedural, and tactical
aspects of managing the pilot programs
under this section.
(3) The Center for Innovation for Care
and Payment will not operate within
any specific administration but will
operate in VA’s corporate portfolio to
VerDate Sep<11>2014
16:18 Jul 26, 2019
Jkt 247001
ensure the limited number of concurrent
pilot programs under this section are
not redundant of or conflicted by
ongoing innovation efforts within any
specific administration.
(b) Definitions. The following
definitions apply to this section.
Access refers to entry into or use of
VA services.
Patient satisfaction of care and
services refers to patients’ rating of their
experiences of care and services and as
further defined in a pilot program
proposal.
Payment models refer to the types of
payment, reimbursement, or incentives
that VA deems appropriate for
advancing the health and well-being of
beneficiaries.
Pilot program refers to a pilot program
conducted under this section.
Quality enhancement refers to
improvement or improvements in such
factors as clinical quality, beneficiarylevel outcomes, and functional status as
documented through improvements in
measurement data from a reliable and
valid source, and as further defined in
a pilot program proposal.
Quality preservation refers to the
maintenance of such factors as clinical
quality, beneficiary-level outcomes, and
functional status as documented
through maintenance of measurement
data from an evidence-based source, and
as further defined in a pilot program
proposal.
Reduction in expenditure refers to,
but is not limited to, cost stabilization,
cost avoidance, or decreases in long- or
short-term spending, and as further
defined in a pilot program proposal.
Note: VA will also consider the
proposal’s potential impact on
expenditures for other related Federal
programs; however, this potential
impact will not count against the
limitation in paragraph (d)(2) of this
section.
Service delivery models refer to all
methods or programs for furnishing care
or services.
(c) Geographic Locations. VA will
make decisions regarding the location of
each pilot program based upon the
appropriateness of testing a specific
model in a specific area while taking
efforts to ensure that pilot programs are
operated in geographically diverse areas
of the country. VA will include in its
proposal to Congress and publish a
document in the Federal Register
identifying the geographic locations
proposed for each pilot program, the
rationale for those selections, and how
VA believes the selected locations will
address deficits in care for a defined
population.
PO 00000
Frm 00036
Fmt 4702
Sfmt 4702
36515
(d) Limitations. In carrying out pilot
programs under this section, VA will
not:
(1) Actively operate more than 10
pilot programs at the same time; and
(2) Consistent with section 1703E(d),
obligate more than $50 million in any
fiscal year in the conduct of the pilot
programs (including all administrative
and overhead costs, such as
measurement, evaluation, and expenses
to implement the pilot programs
themselves) operated under this section,
unless VA determines it to be necessary
and submits a report to the appropriate
Committees of Congress that sets forth
the amount of, and justification for, the
additional expenditure.
(e) Waiver of authorities. In carrying
out pilot programs under this section,
VA may waive statutory provisions by
adding to or removing from statutory
text in subchapters I, II, and III of
chapter 17, title 38, upon Congressional
approval, including waiving any
provisions of law in any provision
codified in or included as a note to any
section in subchapters I, II, or III of
chapter 17, title 38, U.S.C.
(1) Upon Congressional approval of
the waiver of a provision of law under
this section, VA will also deem waived
any applicable provision of regulation
implementing such law as identified in
VA’s pilot program proposal.
(2) VA will publish a document in the
Federal Register providing information
about, and seeking comment on, each
proposed pilot program upon its
submission of a proposal to Congress for
approval. VA will publish a document
in the Federal Register to inform the
public of any pilot programs that have
been approved by Congress.
(f) Notice of eligibility. VA will take
reasonable actions to provide direct
notice to veterans eligible to participate
in a pilot program operated under this
section and will provide general notice
to other individuals eligible to
participate in a pilot program. VA will
announce its methods of providing
notice to veterans, the public, and other
individuals eligible to participate
through the document it publishes in
the Federal Register for each proposed
and approved pilot program.
(g) Evaluation and reporting. VA will
evaluate each pilot program operated
under this section and report its
findings. Evaluations may be based on
quantitative data, qualitative data, or
both. Whenever appropriate,
evaluations will include a survey of
participants or beneficiaries to
determine their satisfaction with the
pilot program. VA will make the
evaluation results available to the public
on the VA Innovation Center website on
E:\FR\FM\29JYP1.SGM
29JYP1
khammond on DSKBBV9HB2PROD with PROPOSALS
36516
Federal Register / Vol. 84, No. 145 / Monday, July 29, 2019 / Proposed Rules
the schedule identified in VA’s proposal
for the pilot program.
(h) Expansion of pilot programs. VA
may expand a pilot program consistent
with this paragraph (h).
(1) VA may expand the scope or
duration of a pilot program if, based on
an analysis of the data developed
pursuant to paragraph (g) of this section
for the pilot program, VA expects the
pilot program to reduce spending
without reducing the quality of care or
improve the quality of patient care
without increasing spending. Expansion
may only occur if VA determines that
expansion would not deny or limit the
coverage or provision of benefits for
individuals under chapter 17.
Expansion of a pilot program may not
occur until 60 days after VA has
published a document in the Federal
Register and submitted an interim
report to Congress stating its intent to
expand a pilot program.
(2) VA may expand the scope of a
pilot program by modifying, among
other elements of a pilot program, the
range of services provided, the
qualifying conditions covered, the
geographic location of the pilot
program, or the population of eligible
participants in a manner that increases
participation in or benefits under a pilot
program.
(3) In general, pilot programs are
limited to 5 years of operation. VA may
extend the duration of a pilot program
by up to an additional 5 years of
operation. Any pilot program extended
beyond its initial 5-year period must
continue to comply with the provisions
of this section regarding evaluation and
reporting under paragraph (g) of this
section.
(i) Modification of pilot programs. The
Secretary may modify elements of a
pilot program in a manner that is
consistent with the parameters of the
Congressional approval of the waiver
described in paragraph (e) of this
section. Such modification does not
require a submission to Congress for
approval under paragraph (e) of this
section.
(j) Termination of pilot programs. If
VA determines that a pilot program is
not producing quality enhancement or
quality preservation, or is not resulting
in the reduction of expenditures, and
that it is not possible or advisable to
modify the pilot program either through
submission of a new waiver request
under paragraph (e) of this section or
through modification under paragraph
(i) of this section, VA will terminate the
pilot program within 30 days of
submitting an interim report to Congress
that states such determination. VA will
also publish a document in the Federal
VerDate Sep<11>2014
16:18 Jul 26, 2019
Jkt 247001
Register regarding the pilot program’s
termination.
[FR Doc. 2019–15891 Filed 7–26–19; 8:45 am]
BILLING CODE 8320–01–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 52
[EPA–R08–OAR–2019–0140; FRL–9996–89–
Region 8]
Promulgation of State Implementation
Plan Revisions; Infrastructure
Requirements for the 2015 Ozone
National Ambient Air Quality
Standards; Colorado and North Dakota
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
AGENCY:
On October 1, 2015, the
Environmental Protection Agency (EPA)
promulgated the 2015 ozone NAAQS,
revising the standard to 0.070 parts per
million. Whenever a new or revised
National Ambient Air Quality Standard
(NAAQS) is promulgated, the Clean Air
Act (CAA or Act) requires each state to
submit a State Implementation Plan
(SIP) revision for the implementation,
maintenance, and enforcement of the
new standard. This submission is
commonly referred to as an
infrastructure SIP. In this action we are
proposing to approve multiple elements
and disapprove a single element of the
following infrastructure SIP
submissions with respect to
infrastructure requirements for the 2015
ozone NAAQS: Colorado, submitted to
the EPA on September 17, 2018; and
North Dakota, submitted to the EPA on
November 6, 2018. We are also
proposing to approve a portion of North
Dakota’s May 2, 2019 submission of
chapter 33.1–15–15, the air pollution
control rules of the State of North
Dakota, that updates the date of
incorporation by reference (IBR) of
Federal rules.
DATES: Written comments must be
received on or before August 28, 2019.
ADDRESSES: Submit your comments,
identified by Docket ID No. EPA–R08–
OAR–2019–0140, to the Federal
Rulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Once submitted, comments cannot be
edited or removed from
www.regulations.gov. The EPA may
publish any comment received to its
public docket. Do not submit
electronically any information you
consider to be Confidential Business
SUMMARY:
PO 00000
Frm 00037
Fmt 4702
Sfmt 4702
Information (CBI) or other information
whose disclosure is restricted by statute.
Multimedia submissions (audio, video,
etc.) must be accompanied by a written
comment. The written comment is
considered the official comment and
should include discussion of all points
you wish to make. The EPA will
generally not consider comments or
comment contents located outside of the
primary submission (i.e., on the web,
cloud, or other file sharing system). For
additional submission methods, the full
EPA public comment policy,
information about CBI or multimedia
submissions, and general guidance on
making effective comments, please visit
https://www2.epa.gov/dockets/
commenting-epa-dockets.
Docket: All documents in the docket
are listed in the www.regulations.gov
index. Although listed in the index,
some information is not publicly
available, e.g., CBI or other information
whose disclosure is restricted by statute.
Certain other material, such as
copyrighted material, will be publicly
available only in hard copy. Publicly
available docket materials are available
either electronically in
www.regulations.gov or in hard copy at
the Air and Radiation Division,
Environmental Protection Agency
(EPA), Region 8, 1595 Wynkoop Street,
Denver, Colorado 80202–1129. The EPA
requests that if at all possible, you
contact the individual listed in the FOR
FURTHER INFORMATION CONTACT section to
view the hard copy of the docket. You
may view the hard copy of the docket
Monday through Friday, 8:00 a.m. to
4:00 p.m., excluding Federal holidays.
FOR FURTHER INFORMATION CONTACT:
Amrita Singh, (303) 312–6103,
singh.amrita@epa.gov; or Clayton Bean,
(303) 312–6143, bean.clayton@epa.gov.
Mail can be directed to the Air and
Radiation Division, U.S. EPA, Region 8,
Mail-code 8ARD–QP, 1595 Wynkoop
Street, Denver, Colorado 80202–1129.
SUPPLEMENTARY INFORMATION:
Throughout this document, ‘‘reviewing
authority,’’ ‘‘we,’’ ‘‘us,’’ and ‘‘our’’ refer
to the EPA.
Table of Contents
I. Background
A. What infrastructure elements are
required under sections 110(a)(1) and
(2)?
B. How did the states address the
infrastructure elements of sections
110(a)(1) and (2)?
1. Colorado
2. North Dakota
II. What is the scope of this proposed rule?
III. The EPA’s Evaluation of the State
Submittals
A. CAA Section 110(a)(2)(A): Emission
Limits and Other Control Measures
E:\FR\FM\29JYP1.SGM
29JYP1
Agencies
[Federal Register Volume 84, Number 145 (Monday, July 29, 2019)]
[Proposed Rules]
[Pages 36507-36516]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-15891]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF VETERANS AFFAIRS
38 CFR Part 17
RIN 2900-AQ56
Center for Innovation for Care and Payment
AGENCY: Department of Veterans Affairs.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: The Department of Veterans Affairs (VA) is proposing to amend
its regulations that govern VA health care. This rule would establish
parameters and authority for the new Center for Innovation for Care and
Payment in its conduct of pilot programs designed to develop innovative
approaches to testing payment and service delivery models to reduce
expenditures while preserving or enhancing the quality of care
furnished by VA.
DATES: Comments must be received on or before August 28, 2019.
ADDRESSES: Written comments may be submitted through https://www.Regulations.gov; by mail or hand-delivery to: Director, Office of
Regulation Policy and Management (00REG), Department of Veterans
Affairs, 810 Vermont Avenue North West, Room 1064, Washington, DC
20420; or by fax to (202) 273-9026. (This is not a toll-free telephone
number.) Comments should indicate that they are submitted in response
to ``RIN 2900-AQ56 Center for Innovation for Care and Payment.'' Copies
of comments received will be available for public inspection in the
Office of Regulation Policy and Management, Room 1064, between the
hours of 8 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
telephone number.) In addition, during the comment period, comments may
be viewed online through the Federal Docket Management System (FDMS) at
https://www.Regulations.gov.
FOR FURTHER INFORMATION CONTACT: Michael Akinyele, VA Chief Innovation
Officer and Executive Director (Acting), VA Innovation Center (VIC)
(008E), 810 Vermont Ave. NW, Washington, DC 20420.
[email protected]. (202) 461-7271. (This is not a toll-free
number.)
SUPPLEMENTARY INFORMATION: On June 6, 2018, section 152 of Public Law
115-182, the John S. McCain III, Daniel K. Akaka, and Samuel R. Johnson
VA Maintaining Internal Systems and Strengthening Integrated Outside
Networks Act of 2018, or the VA MISSION Act of 2018, amended title 38
of the United States Code (U.S.C.) by adding a new section 1703E,
Center for Innovation for Care and Payment. Section 1703E(a)(1)
establishes the Center for Innovation for Care and Payment (the
Center). Section 1703E(a)(2) authorizes the conduct of pilot programs
to develop innovative approaches to testing payment and service
delivery models to reduce expenditures while preserving or enhancing
the quality of care furnished by VA, and subsection (a)(3) requires VA
to determine whether such models improve access to, and quality,
timeliness, and patient satisfaction of care and services, and create
cost savings for VA. Section 1703E(a)(4) requires that VA test a model
in a location where VA determines that the model will address deficits
in care (including poor clinical outcomes or potentially avoidable
expenditures) for a defined population; it further directs VA to focus
on models VA expects to reduce program costs while preserving or
enhancing the quality of care received by individuals receiving
benefits under chapter 17 of title 38, United States Code. Under
section 1703E(a)(4)(C), VA could select those models described in 42
U.S.C. 1315a(b)(2)(B), the authority for the Center for Medicare and
Medicaid Innovation. In selecting models for testing, section
1703E(a)(5) permits VA to consider a number of different factors,
including whether the model includes a regular process for monitoring
and updating patient care plans in a manner that is consistent with the
needs and preferences of individuals receiving benefits under chapter
17; whether the model places the individual receiving benefits under
chapter 17 (including family members and other caregivers of such
individual) at the center of the care team of such individual; whether
the model uses technology or new systems to coordinate care over time
and across settings; and whether the model demonstrates effective
linkage with other public sector payers, private sector payers, or
statewide payment models. Section 1703E(a)(6) states that VA may not
design models in such a way that would allow the United States to
recover or collect reasonable charges from other Federal health care
programs, such as Medicare, Medicaid, or TRICARE.
Section 1703E(b) provides that pilot programs must be terminated no
later than five (5) years after they begin. Section 1703E(c) directs VA
to ensure that each pilot program carried out under this section occurs
in an area or areas appropriate for the intended purposes of the pilot
program; to the extent practicable, VA should ensure that pilot
programs are located in geographically diverse areas. Section 1703E(d)
states that funding for each pilot program must come from
appropriations provided in advance in appropriations acts for the
Veterans Health Administration (VHA) and information technology
systems. Section 1703E(e) requires VA publish
[[Page 36508]]
information about each pilot program in the Federal Register and to
take reasonable actions to provide direct notice to veterans eligible
to participate in such pilot programs.
Section 1703E(f) allows VA to waive requirements in subchapters I,
II, and III of chapter 17, title 38, U.S.C., as VA determines necessary
for the purposes of carrying out pilot programs under this section.
Before waiving any such authority, VA will submit to Congress a report
on a request for a waiver that describes the specific authorities to be
waived, the standard or standards to be used in lieu of the waived
authorities, the reasons for such waiver or waivers, and other matters
including metrics, cost estimates (both budgets and savings), and
schedules.
Section 1703E(g) imposes several restrictions on VA's authority
under this section, notably limiting the number of pilot programs (10)
that can be carried out concurrently, requiring VA to submit the first
pilot program proposal to Congress within 18 months of the enactment of
the Caring for Our Veterans Act of 2018 (June 6, 2018), and requiring
VA to either modify or terminate a pilot program if VA determines it is
not improving the quality of care or producing cost savings. Section
1703E(h) requires VA to conduct an evaluation of each pilot program,
and section 1703E(i) requires VA to obtain advice from the Under
Secretary for Health and the Special Medical Advisory Group in the
development and implementation of any pilot program. VA must also
consult representatives of relevant Federal agencies, and clinical and
analytical experts with expertise in medicine and health care
management. Finally, section 1703E(j) authorizes VA to expand, through
rulemaking, successful pilot programs in duration or scope.
This proposed rule would implement the mandates and authorities of
section 1703E, as added by the VA MISSION Act of 2018, by establishing
a new Sec. 17.450.
Proposed paragraph (a) would establish the purpose for this section
and the organization of the Center. Proposed paragraph (a)(1) would
explain that the Center for Innovation for Care and Payment will carry
out pilot programs to develop innovative approaches to testing payment
and service delivery models to reduce expenditures while preserving or
enhancing the quality of care furnished by VA. This would be consistent
with section 1703E(a)(2). We would further state that the Center for
Innovation for Care and Payment will be operationally independent from
any of VA's three administrations and will be responsible for
collaborating across VA to develop and implement pilot programs under
this section. As further explained in proposed paragraphs (a)(2)-(3),
being operationally independent refers to the decision-making authority
of the Center regarding the strategic, procedural, and tactical aspects
of managing the pilot programs under this section. To ensure the
limited number (10) of concurrent pilot programs under this section are
not redundant of or conflicted by ongoing innovation efforts within any
specific administration, the Center for Innovation for Care and Payment
will not operate within any specific VA administration but will operate
in VA's corporate portfolio.
We are strategically positioning the Center as operationally
independent to focus on envisioning veteran care and payment
requirements in the distant future and preparing VA to meet the needs
of veterans today, as well as in the future; in 2045, for example, the
population of veterans in the United States is projected to decline to
12 million. Of the approximately 20 million veterans alive today, VA
provides health care for approximately 7 million unique patients each
year, including approximately 1 million unique non-veterans. If current
trends hold, we anticipate that by 2045, VA would be providing health
care to approximately 3.6 million unique veteran patients each year. As
such, we anticipate VA would need to re-imagine its current approach to
furnishing services and payments for the veterans it hopes to serve in
2045. For the Center to be positioned for success in its mission to re-
imagine VA's current approach to furnishing services and payments for
veterans, it must enjoy strategic and operational independence from
existing processes. In the commercial market, innovation efforts led by
incumbents or large enterprises are rarely responsible for creating
sustainably disruptive solutions that revolutionize the products or
services of the incumbent. This is to be expected, because any new
solution that threatens the viability or market position of established
products or services is ultimately stifled by the enterprise focus on
the near-term objectives of sustaining current products and services in
lieu of investing additional time and resources in emerging solutions
that could revolutionize product and service offerings to significantly
benefit the organization's customers. We believe that creating an
autonomous, independent organization with its own brand is the best way
to enable corporate innovation to thrive. Autonomy does not mean the
Center would work in isolation. The Center will report through the
Office of the Secretary of Veterans Affairs and ultimately the
President of the United States and does not have the unilateral
authority to execute pilot programs.
Proposed paragraph (b) would define the terms for this section.
Proposed paragraph (b) would define the term access. Section
1703E(a)(3)(A) directs VA to test payment and service delivery models
to determine whether such models improve access to, and quality,
timeliness, and patient satisfaction of care and services. Because VA
will be testing models to determine whether they improve access, it is
important to define the term. We propose to define access as entry into
or use of VA services. Entry into would refer to basic eligibility and
enrollment, while use of services would refer to the actual receipt of
care and services. Access to care is dependent on both availability and
adequacy of services as well as barriers (e.g., financial, cultural,
etc.) that may interfere with utilization of available services. See
Gulliford, M. et al., What Does ``Access to Care'' Mean? Journal of
Health Services Research and Policy (2002), available at https://www.ncbi.nlm.nih.gov/pubmed/12171751.
We recognize that our beneficiaries face various issues affecting
access, including lack of availability of VA services in a specific
geographic area or barriers to obtaining care for specific populations.
As such, we believe this comprehensive interpretation of access would
be of greatest benefit to veterans affected by pilot programs conducted
by the Center.
Proposed paragraph (b) would define the term patient satisfaction
of care and services to mean the patients' rating of their experiences
of care and services and as further defined in a pilot program
proposal. In addition to requiring that we test payment and service
delivery models to determine whether they improve access and
timeliness, section 1703E(a)(3)(A) also requires that we assess whether
the models improve patient satisfaction, which is a critical indicator
of service quality and patient-centric care. The health care industry
standard is to assess patients' perception of their health care
experience using the Consumer Assessment of Health Providers and
Systems (CAHPS) survey, which has been in use since the mid-1990s. For
example, the Centers for Medicare and Medicaid Services (CMS) has
adopted CAHPS for care delivered in multiple care settings. Each CAHPS
[[Page 36509]]
survey produces several measures of patient experience. These measures
include composite measures, which combine two or more related survey
items; rating measures, which reflect respondents' ratings on a scale
of 0 to 10; and single-item measures. Measuring patient experience
measures what is important to the patient: access, service, and
communication. For years VA has been measuring patient satisfaction by
focusing on patient experience. VA uses CAHPS to measure veterans'
experience of care for outpatient care and VA's Survey of Healthcare
Experience of Patients (SHEP) to measure inpatient experience of care.
SHEP has been in use for many years and uses the same questions as the
Hospital Consumer Assessment of Healthcare Providers and Systems
(HCAHPS), a standardized, nationally-used, public survey that measures
inpatient experience of care.
We believe that using these types of patient experience of care
measures would be in line with health care industry standards and VA
existing practices and would ensure that veterans and providers alike
are not burdened with new types of assessments or surveys. In addition,
measuring patient perceptions by using the industry-accepted patient
experience of care would allow veterans to better understand how the
care provided by VA compares to that provided outside of VA by having
equivalent data to make comparisons, as well as how care furnished
through the pilot compares with care furnished outside the pilot.
Proposed paragraph (b) would define the term payment models.
Section 1703E(a)(2) authorizes VA to carry out innovative approaches to
testing payment and service delivery models to reduce expenditures
while preserving or enhancing the quality of care furnished by VA.
Innovative payment models incorporate different types of arrangements
that help lower cost while maintaining or improving the quality of
services. We therefore propose to state that the term payment models
refers to the types of payment, reimbursement, or incentives that VA
deems appropriate for advancing the health and well-being of
beneficiaries. Use of the term incentive indicates anything that is
intended to motivate service providers to perform better or deliver
services in a more favorable manner, which is consistent with the usual
dictionary definition. While the term payment models is specifically
applicable to service providers, we note that VA could use incentives
for patients or other beneficiaries; such an approach would need to be
developed through a pilot program proposal.
Proposed paragraph (b) would define the term pilot program to refer
to a pilot program conducted under proposed Sec. 17.450. VA operates
programs on a pilot or temporary basis under authorities other than
section 1703E, but because these regulations only implement that
authority and place requirements or restrictions, or authorize certain
functions under section 1703E, we propose to define the term here to
avoid any impression that the proposed Sec. 17.450 extends those
requirements, restrictions, or authorities to other VA initiatives
operated under separate legal authorities.
We aim, through testing innovative payment and service delivery
models, to discover novel and innovative ways to deliver services that
enhance the quality of care for beneficiaries. Section 1703E(a)(2)
refers to testing payment and service delivery models to reduce
expenditures while preserving or enhancing the quality of care. We
propose to use the term quality enhancement to refer to enhancing the
quality of care. We propose in paragraph (b) to state that quality
enhancement refers to improvement or improvements in such factors as
clinical quality, beneficiary-level outcomes (for example, symptom
burden), and functional status, which is indicative of an individual's
ability to perform normal daily activities required to meet basic
needs, fulfill usual roles, and maintain health and well-being as
documented by improvements in measurement data from a reliable and
valid source, such as the electronic health record, and as further
defined in a pilot program proposal. Quality enhancements are multi-
faceted, and measurements on such enhancements would be tailored to the
specific area tested by a pilot program and would be defined in VA's
proposal, as required by section 1703E(f)(2)(D).
Similarly, we propose to define quality preservation in paragraph
(b) to refer to the maintenance of such factors as clinical quality,
beneficiary-level outcomes, and functional status as documented through
measurement data from an evidence-based source, and as further defined
in a pilot program proposal. Maintenance in this sense would mean
continued, sustained, or improved performance by the patient along
several dimensions of care as demonstrated by the types of factors
described above and as documented through an evidence-based source.
Like quality enhancement, specific measurements would be defined in
VA's proposal.
We propose to define in paragraph (b) reduction in expenditure.
Section 1703E(a)(2) authorizes VA to test payment and service delivery
models that lead to a reduction in expenditures while enhancing or
preserving the quality of care furnished by VA. Some innovative models
will require upfront investment and additional resources that might
increase associated expenditures in the near term, but we anticipate
the rise in expenditures will be mitigated by corresponding
improvements in outcomes and value creation over time. Value creation
could occur in multiple scenarios such as through cost reduction, cost
avoidance, or reallocation of resources to alternative, higher-value
activities. For example, investing in a system that reduces unnecessary
or duplicative testing could lead to long term cost avoidance. For
these reasons, we propose to state that reduction in expenditure refers
to, but is not limited to, cost stabilization, cost avoidance, and/or
decreases in long- or short-term spending and as further defined in a
pilot program proposal. We would not limit reduction in expenditures to
cost stabilization, cost avoidance, and/or decreases in long- or short-
term spending in case there are other methods for determining that VA's
expenditures have been reduced that do not fit within any of the
descriptions above. In considering the impact of a pilot program on
expenditures, VA will estimate how the proposal is anticipated to
impact VA expenditures and also consider the proposal's potential
impact on expenditures for other related Federal programs.
In proposed paragraph (b), we would state that the term service
delivery models refers to all methods or programs for furnishing care
and services. Section 1703E(a)(2) authorizes VA to develop innovative
approaches to testing payment and service delivery models to reduce
expenditures while preserving or enhancing the quality of care. Health
care services can be delivered by either VA staff or by non-VA entities
or providers, as well as through different modalities (like telehealth)
or different models (like VA's Patient-Aligned Care Teams) and the
definition proposed here would capture all potential modalities and
models for furnishing services and would be the common understanding of
this phrase. The term service delivery model generally includes any
method for furnishing services, and we believe this is intended to
apply broadly given the range of services and support that VA provides
to different beneficiaries.
[[Page 36510]]
In proposed paragraph (c), we would establish the procedures VA
would use to determine the geographic locations where pilot programs
would be conducted. Sections 1703E(a)(4)(A) and 1703E(c) require VA to
test models and pilot programs in locations where there are deficits in
care while ensuring that pilot programs are in geographically diverse
areas of the United States. Because different beneficiary populations
may have different needs depending on where they live, we believe that
geographic location will play a critical role in the design of any
pilot program. However, VA cannot yet define the specific factors that
we would use to select geographic locations for specific pilot
programs. We anticipate the basis for these decisions will vary based
upon the goals and objectives of each specific pilot program. For
example, if VA were to test a new payment methodology, it may be more
appropriate to test it in a portion of the country where providers are
already accustomed to being paid in alignment with that model. While
market readiness would not serve as the sole reason for geographic
location selection, it could be a key factor in selecting specific
markets in which to test specific pilot programs. Consequently, we
would state in proposed paragraph (c) that VA would make decisions
regarding the location of each pilot program based upon the
appropriateness of testing a specific model in a specific area while
taking efforts to ensure that pilot programs are operated in
geographically diverse areas of the country. We would identify the
proposed geographic locations for each pilot program, the rationale for
those decisions, and how we believe the selected locations would
address deficits in care for a defined population in VA's proposal to
Congress to operate the pilot program and a document in the Federal
Register.
Proposed paragraph (d) would define limitations on the authority of
the Center. These limitations would only apply to pilot programs under
this section. Again, VA operates pilot programs under different
authorities, and these limits would not affect such other pilot
programs, nor would these other pilot programs affect the activities of
the Center. Section 1703E(g) establishes several of VA's limitations in
carrying out pilot programs through the Center. Section 1703E(g)(1)
states that VA may not carry out more than 10 pilot programs
concurrently. We propose to interpret this in paragraph (d)(1) to mean
that VA cannot actively operate more than 10 pilot programs at one
time. Conducting pilot programs requires advance preparation, as well
as data analysis following the completion of a pilot program. VA
proposes to exclude the time involved with this preparatory and post-
program analysis by considering the operation of a pilot program as
only the time of active operation. This would ensure that VA is able to
operate the maximum number of pilot programs at any one time and
mitigate potential delays to launching new pilot programs that could
improve quality and reduce cost during the preparatory and post-pilot
analysis effort of other pilot programs.
In proposed paragraph (d)(2), we would state that, unless VA
determines it to be necessary and informs the appropriate Committees of
Congress, VA would not obligate more than $50 million in any fiscal
year to operate all the pilot programs under this section. This is
consistent with section 1703E(d) and section 1703E(g)(2), which state
that, subject to notification and approval conditions, VA may not
expend more than $50 million in any fiscal year in the conduct of the
pilot programs operated under this section. Funding required to operate
the pilot programs includes all administrative and overhead costs,
including measurement and evaluation, as well as the funding required
to implement the specific payment or service delivery models being
tested. We propose to interpret the term ``expend'' under section
1703E(g)(2) to mean ``obligate.'' This interpretation accounts for the
legal requirement to record obligations that may result in immediate or
future expenditures (outlays). An ``obligation'' is a definite
commitment that creates a legal liability for payment. At the time that
VA incurs a liability (e.g., signing a contract) it records the full
amount of its legal liability against currently-available funds
pursuant to the recording statute, 31 U.S.C. 1501(a)(1). The timing of
the incurrence of an obligation is generally within the agency's
control, while the timing of the liquidation of the obligation is
largely outside of the agency's control, due to factors such as
contractor performance and billing. Thus, interpreting ``expend'' to
mean ``outlay'' rather than ``obligate'' would frustrate the
legislative intent of authorizing up to $50 million per fiscal year to
carry out the pilot programs. We note that paragraph (d)(2) would not
condition VA's obligation of more than $50 million upon approval of the
Chairmen of the Committees on Veterans' Affairs of the House of
Representatives and the Senate, as is contemplated in section
1703E(g)(2)(B)(iii). As noted in the President's Signing Statement,
issued upon enactment of the VA MISSION Act of 2018, under the
separation of powers, the Congress may not make the approval of Members
of Congress a precondition to the execution of the law. See Statement
of the President, June 6, 2018, available online: https://www.whitehouse.gov/briefings-statements/statement-by-the-president-3/.
VA, accordingly, treats the section 1703E(g)(2)(B)(iii) approval
requirement as advisory and non-binding, but may submit the required
report to the appropriate Congressional Committees before exceeding the
spending cap, if VA determines that the additional expenditure is
necessary to carry out the pilot programs. For the public's awareness,
coordination and approval of funding sources under section 1703E(d) for
pilot programs will occur prior to public notice.
In proposed paragraph (e), we would define VA's waiver authority to
conduct pilot programs. Section 1703E provides a unique ability for VA,
temporarily and in certain locations, to amend effectively its
statutory authority when carrying out pilot programs under this
section. Specifically, section 1703E(f)(1) allows VA to waive any
provisions of law in subchapters I, II, and III of chapter 17, title 38
U.S.C., i.e., sections 1701 through 1730C, as VA determines necessary
solely for the purposes of carrying out this section with respect to
testing models. However, VA cannot unilaterally waive these
authorities; it must propose a waiver and describe a proposed pilot
program in a report to Congressional leadership, and only upon
Congress' approval may VA carry out the pilot program. VA must submit
the first request for a waiver by December 6, 2019, as required by
section 1703E(g)(3).
Proposed paragraph (e) would clarify VA's authority regarding the
waiver provisions in section 1703E(f). In proposed paragraph (e), we
would state that VA's waiver authority includes both the authority to
propose the removal of provisions of law or the addition of provisions
of law. VA is a creature of law, and thus only has the authority
granted to it by statute. Some statutes are restrictive, in that they
provide a general authority and then place conditions upon the use of
that authority. For example, section 1705 of title 38, U.S.C., defines
VA's patient enrollment system and identifies those veterans who are
eligible to enroll and in which priority group such veterans will be
enrolled. Under this authority, VA could propose to waive some specific
provision of law by proposing
[[Page 36511]]
to act as though such language that is in the statute were not there.
At the same time, because VA is limited by its legal authority to only
carry out those functions authorized by law, we propose to include in
VA's waiver authority the ability to include additional language
creating new authority for VA to act, or restricting language currently
authorizing or requiring VA to act. For example, section 1708 of title
38, U.S.C., authorizes VA to provide temporary lodging in certain
situations and for certain persons. VA could use this waiver authority
to propose to include additional groups of eligible beneficiaries under
this regulation.
We propose to allow VA to propose new or different standards under
the waiver authority of section 1703E(f). We believe this is authorized
by section 1703E(f)(1), which authorizes VA to waive such requirements
in subchapters I, II, or III of chapter 17 of title 38, U.S.C. These
requirements, as explained above, may either be explicit, which would
require their removal, or implicit, which would require the addition of
further language. Moreover, we believe this interpretation is further
supported by section 1703E(f)(2)(B), which requires VA, in proposing
the waiver of authority for a pilot program, to identify the standard
or standards to be used in the pilot program in lieu of the waived
authorities. We believe this language authorizes VA both to suggest
additional standards or the removal of standards as well. We believe
that if Congress or the public disagreed with the scope of this
authority, Congress could simply choose to not approve VA's waiver
request, so there is little to no risk associated with this
interpretation.
We also would state that VA may propose to waive any provision of
law in any provision codified in or included as a note to any section
in subchapters I through III of chapter 17, title 38, U.S.C. Some laws
are codified in a title of the United States Code. For example, section
1710 of title 38, U.S.C., defines eligibility for hospital, nursing
home, and domiciliary care. Other laws are not codified but are
included as notes to codified provisions when they deal with similar or
general subject matters. For example, section 205 of Public Law 111-163
established a pilot program on assistance for child care for certain
veterans receiving health care. Section 205 of Public Law 111-163 is
included as a note to section 1710 of title 38, U.S.C. Proposed
paragraph (e) would allow VA to propose to waive provisions in either
the text of section 1710 (for example, relating to eligibility for
hospital, nursing home, or domiciliary care) or a note to section 1710
(for example, relating to the pilot program on assistance for child
care for certain veterans receiving health care). We believe this is
authorized by section 1703E(f)(1), which authorizes VA to waive such
requirements in subchapters I, II, and III of this chapter. When citing
to a public law that appears as a note to a codified provision of law,
we include the U.S.C. section and identify this as a note; public laws
are assigned as notes to codified provisions of law by the Office of
the Law Revision Counsel in the U.S. House of Representatives. This
recognizes that these public laws are requirements in, or at least
related to, the section of law. We also believe that if Congress or the
public disagreed with the scope of this authority, Congress could
simply choose to not approve VA's waiver request, so the risk
associated with this interpretation is limited. In other words, if VA
proposed to modify a note to a section of law and Congress did not
think we had the authority to do that, or disagreed with VA on policy
grounds, it would simply not approve the waiver request and the
provision would not be waived.
Finally, in paragraph (e)(1), we propose, upon Congressional
approval of a waiver of a provision of law under this section, that VA
will also deem waived any applicable provision of regulation
implementing such law as identified in VA's pilot program proposal. We
believe this would be a necessary component to exercising the statutory
authority granted by section 1703E(f)(1), which allows VA to waive
``such requirements'' in subchapters I, II, and III of chapter 17 as
the Secretary determines necessary solely for the purposes of carrying
out this section with respect to testing models. We believe regulations
interpreting and implementing specific statutory provisions in
subchapters I, II, and III are ``requirements'' within the context of
this authority. It would be paradoxical for VA to test innovative
approaches to payment and service delivery if VA could waive provisions
of statute but not corresponding, and potentially more limiting,
regulations promulgated by VA. For example, if VA proposed to waive a
provision in section 1712 concerning dental care, and Congress approved
such a proposal, VA could also waive any regulatory requirements (such
as those found in 38 CFR 17.160) that implemented the provision of law
waived by VA through the pilot program.
Under proposed paragraph (e)(2), VA would publish a document in the
Federal Register with information about, and soliciting public comment
on, each proposed pilot program so that the public has an opportunity
to comment on VA's proposals while Congressional approval is pending.
VA would then publish a document in the Federal Register to inform the
public of any approved pilot programs, as required by section
1703E(e)(1). While this is not required by law, we believe this would
be prudent practice to ensure that the public also has an opportunity
to submit comments directly to VA regarding pending pilot program
proposals and to inform their Members of Congress if they have any
issues or concerns so that Congress can appropriately decide whether or
not to approve a requested waiver of authority for the Center.
Under proposed paragraph (f), VA would establish procedures
regarding notice of eligibility requirements. Specifically, we would
state that VA would take reasonable actions to provide direct notice to
veterans eligible to participate in pilot programs operated under this
section and would provide general notice to other individuals eligible
to participate in a pilot program. We would further state that VA also
would announce methods of notice in the Federal Register document
published by VA for each proposed and approved pilot program. While
section 1703E(e)(2) directs VA to take reasonable actions to provide
direct notice to veterans eligible to participate in such pilot
programs, we note that other provisions in section 1703E refer more
broadly to individuals that are eligible for benefits. See, e.g.,
1703E(a)(4)(B), (a)(5)(A)-(B), (j)(2). Consequently, we read the
requirement in section 1703E(e)(2) to create an obligation to take
reasonable actions to provide direct notice to veterans eligible to
participate in pilot programs on the assumption that VA would have more
information about veterans, while VA would provide general information
to notify any other individuals eligible to participate in a pilot
program. For example, one pilot program could expand access to benefits
for family members or caregivers of veterans; in this case, VA would
provide notice to the veterans in the area where the pilot program is
operating and would provide other general information as well to reach
the caregivers or family members. Another example would be a pilot
program involving certain community providers or other private
entities; VA would provide general information to the community so that
interested parties could inquire or participate. The exact nature of
the notice will vary depending upon the type of pilot program
[[Page 36512]]
involved, and so VA will announce how it intends to inform the public,
in particular, other eligible individuals and entities, through the
document it publishes in the Federal Register for each pilot program.
Other forms of more direct communication could include mailed letters,
emails, announcements to local Veterans Service Organizations, and
posting of information on the websites of VA medical centers, the VA
Innovation Center website, and other online sources.
In proposed paragraph (g), VA would describe generally how it would
evaluate and report on the pilot programs. Specifically, VA would
evaluate each pilot program operated under this section and report its
findings. Section 1703E(h) requires VA to conduct an evaluation of each
model tested, including at a minimum an analysis of the quality of care
furnished and the changes in spending because of that model. VA is
required to make the results of the tested model available to the
public in a timely fashion. Once again, because each pilot program will
vary in terms of the specific outcomes involved and how it will achieve
those outcomes, VA is not proposing a discrete list of measures, but
will include more specific information with each proposal for a pilot
program. VA proposes to base its evaluation of pilot programs on
quantitative data, qualitative data, or both, depending upon the nature
of the pilot program. Different types of data may be more appropriate
for different pilot program models, but each type of data is
instructive and could help VA determine if VA is improving access to,
and the quality, timeliness and patient satisfaction of care and
services, as well as creating cost savings for VA. Whenever
appropriate, such evaluation will also include a survey of participants
or beneficiaries to determine their satisfaction with the pilot
program; this participant feedback likely would be subject to the
Paperwork Reduction Act and would provide direct input regarding the
effects of the pilot program. We propose to make the evaluation results
available to the public on the VA Innovation Center website at https://www.innovation.va.gov/. The schedule of the release will be indicated
in the proposal for each pilot program. By law, VA is required to make
the results of the tested model available to the public in a timely
fashion, but we again note that each model will naturally have
different lengths of time for data collection and analysis. Some pilot
programs may allow for real-time, or close to real-time reporting of
information (for example, costs or number of appointments), while
others may experience lags between an action under the pilot program
and health outcomes (for example, 6-month or 12-month morbidity or
mortality data). VA will identify the measures and timelines for public
reporting in its pilot program proposal submission to Congress and its
document in the Federal Register.
In proposed paragraph (h), VA would establish a process in
regulation for the expansion of pilot programs. Section 1703E(j)
authorizes VA through rulemaking to expand in scope or duration,
including nationwide implementation, pilot programs if the expansion is
expected to reduce spending without reducing the quality of care, or to
improve the quality of patient care without increasing spending.
Furthermore, VA is only permitted to expand a pilot program if the
pilot program does not deny or limit the coverage or provision of
benefits for individuals under chapter 17. We propose to establish
through regulation a general process for expanding the scope or
duration of pilot programs instead of requiring separate rulemakings
for each expansion for several reasons. First, the promulgation of
regulations is a lengthy process, taking on average 18-22 months for a
proposed and final rule to be published and effective. Given the
limitations on the length of time a pilot program could operate under
this authority of only 5 years, this would effectively require VA to
decide at the halfway point of a pilot program, and possibly before
that, as to whether or not to expand. This may not be enough time for
VA as a practical matter, which could either lead to the expansion of
pilot programs that ultimately prove unsuccessful or the inability to
expand pilot programs that do prove to be successful. Second, if VA
were required to publish new regulations for each pilot program it
wished to expand, VA's regulations would become cluttered with rules
that would only be applicable for limited periods of time and
locations. This would likely result in confusion regarding these
provisions. Finally, we believe that by regulating the process we would
use to expand pilot programs, we are meeting the requirements of the
law, which does not expressly require VA proceed through notice and
comment rulemaking for each expansion, but merely states that VA may
expand pilot programs ``through rulemaking''. This requirement merely
obligates VA to allow the public to comment on how expansion would
occur, which this proposal would do. Moreover, and as further discussed
below, VA is taking other measures to provide the public and Congress
an opportunity to review and comment on VA's proposal for expansion,
which we believe would result in an opportunity for feedback similar to
a subsequent notice and comment rulemaking.
Initially, we propose in paragraph (h)(1) that VA would only meet
the statutory requirement of expecting a pilot program to reduce
spending without reducing the quality of care or to improve the quality
of patient care without increasing spending based upon an analysis of
the data collected for the specific pilot and developed pursuant to
proposed paragraph (g). VA also would have to provide such results to
Congress through an interim report and to the public through a document
in the Federal Register. This would be consistent with the general
structure of the Center's authority, as any decisions regarding
expansion would have to be based on publicly available data. Similarly,
VA would have to decide that expansion would not deny or limit the
coverage or provision of benefits for individuals under chapter 17.
This is a statutory requirement, and VA's basis for making this
determination would be available for public scrutiny prior to any
expansion taking place. VA would propose that it would not expand a
pilot program until 60 days after submitting an interim report to
Congress and publishing a document in the Federal Register regarding
its intent to expand a pilot program. This would provide Congress and
the public 60 days to evaluate the data VA would be using as the basis
for such an expansion. In the event the public or Congress do not
believe the data support expansion, they would have this time to inform
VA of such views. Upon the completion of the 60-day period, if VA still
finds that the statutory prerequisites for expansion have been met, VA
could expand a pilot program in either scope or duration, as noted
below.
Proposed paragraph (h)(2) would define how VA could expand a pilot
program in scope. Proposed paragraph (h)(2) would authorize VA to
expand the scope of a pilot program by modifying, among other elements
of a pilot program, the range of services provided, the qualifying
conditions covered, the geographic location of the pilot program, or
the population of eligible participants in a manner that increases
participation in or benefits under a pilot program. These are the
general dimensions that we believe could be expanded, as that term is
used in section 1703E(j). Expansion is generally
[[Page 36513]]
defined to mean becoming larger or more extensive, and these are the
likely areas of a pilot program that could become larger or more
extensive. For example, if VA were conducting a pilot program related
to mental health services in Alaska for homeless veterans, and VA
proposed to expand the pilot under paragraph (h)(1), VA could expand to
include new beneficiary populations (e.g., non-homeless veterans),
conditions (e.g., additional health services), or geographic locations
(e.g., outside Alaska), among others. We would permit some flexibility
in the forms that expansion could occur in case there are features of a
pilot program that could be made larger or more extensive that do not
fall within one of these categories. Again, without knowing exactly
what pilot programs will be proposed, we are unable now to state
definitively in what ways we could expand such a pilot program.
In proposed paragraph (h)(3), we propose the conditions under which
VA could extend the duration of a pilot program. In general, section
1703E(b) limits pilot programs to 5 years of operation. Section
1703E(j)(1), however, authorizes VA to extend the duration of a pilot
program if the conditions for expansion discussed above are also met.
We propose to authorize VA to extend the duration of a pilot program
for up to an additional 5 years. Such extension would be subject to the
same requirements related to the evaluation and reporting of data that
would apply to a pilot program within the first 5 years of operation
under proposed paragraph (g). We propose limiting the expansion of a
pilot program to an additional 5 years because Congress recognized the
potential for making successful pilots permanent in section
1703E(f)(2)(G) when it required VA to report on the feasibility and
advisability of making a pilot program permanent, but there is no
indication Congress intended to allow for pilot programs to run in
perpetuity. Moreover, the very nature of a pilot program is that it has
a beginning and an end date. Finally, on a practical and legal level,
because pilot programs under this section would involve the waiver of
one or more provisions of law, we believe it would create confusion
over time if a pilot program were operated indefinitely without express
statutory authority. We believe the balance of powers is best preserved
when Congress affirmatively establishes VA's parameters through law.
In proposed paragraph (i), VA would establish its authority to make
minor modifications to pilot programs approved by Congress. Section
1703E(g)(5)(A) establishes VA's options (proposing a modification to
Congress for approval or terminating the pilot program) when the
Secretary determines that a pilot program is not improving the quality
of care or producing cost savings, but it and the rest of section 1703E
are silent in terms of VA's authority to modify pilot programs when VA
has not made a determination regarding whether the pilot program is
improving the quality of care or producing cost savings. We anticipate
there may be pilot programs that we operationalize in a way that
becomes administratively difficult to continue; alternatively, some
pilot programs may be operationalized in a way that does not produce
clear data that would allow VA to determine if the pilot program is
improving the quality of care or producing cost savings. Under proposed
paragraph (i), VA could modify the pilot program in a manner that is
consistent with the parameters of Congressional approval without
seeking further Congressional approval for the change. Modifications
that would be consistent with the parameters of Congressional approval
would vary based on each pilot program, but we offer a few examples for
the public's understanding. For example, VA may plan to operate a pilot
program in a particular location, but later determine that this
location is unsuitable for reasons beyond VA's control. For example, an
anticipated pilot site may be unavailable due to a natural disaster, or
interest in participation in the pilot program may be inadequate to
support valid results. In these cases, it would seem a poor use of
government resources to continue attempting to operate the pilot
program while waiting for a subsequent Act of Congress to allow VA to
select another location. As another example, VA may want to conduct a
pilot program offering a particular service, but VA may later determine
this service is not appropriate while another similar service would be.
VA plans to submit proposals to Congress that provide it enough
information to know what it is authorizing, while still providing some
flexibility for VA to address potential minor corrections without
further Congressional approval. In identifying geographic locations for
the pilot program under paragraph (c) of this section, for example,
rather than identifying specifically the VA medical centers or
facilities that would participate, we anticipate providing the general
criteria VA will use to identify locations (e.g., urban areas, rural
areas, highly rural areas; areas near military bases; facilities with
academic affiliates, etc.) and possibly a list of facilities that could
meet those requirements. This would allow VA to select another suitable
location if needed. Similarly, for services that VA might provide, or
populations of beneficiaries that might be included, we would attempt
to describe these generally enough to allow for further modification as
needed to either specify another service or another population. We are
sensitive to Congress' need to conduct oversight and to understand
clearly what it is authorizing when it approves a waiver, and so we
limit VA's ability to modify a pilot program to changes that are
consistent with the parameters of Congress' initial approval. VA could
not, for example, modify a Congressionally approved pilot program on
beneficiary travel to become a pilot program on the provision of care
to beneficiaries otherwise ineligible for VA care. Such a change would
clearly be outside the parameters of Congress' initial approval.
In proposed paragraph (j), we would define the conditions for
termination of pilot programs. As noted before, section 1703E(g)(5)(A)
establishes that, when the Secretary determines that a pilot program is
not improving the quality of care or producing cost savings, VA's
options include proposing a modification to Congress for approval or
terminating the pilot program. In proposed paragraph (j), we would use
the terms quality enhancement and quality preservation to reflect the
statutory language related to improving the quality of care, and we
would use the term reduction in expenditures to reflect the statutory
language related to producing cost savings. These substitutions would
be consistent with the terms as they would be defined through paragraph
(b) of this section. We would also clarify that a modification that can
only be achieved through submission of a new waiver request to Congress
would be distinct from a modification under paragraph (i) of this
section, as just discussed. Congress specifically recognized that not
all pilot programs will meet or exceed their primary goals of enhancing
or preserving care while reducing costs. Under proposed paragraph (j),
VA would, upon determining that a pilot program is not producing
quality enhancement or quality preservation, or is not resulting in the
reduction of expenditures, and that it is not possible or advisable to
modify the pilot program either through submission of a new waiver
request under paragraph (e) or
[[Page 36514]]
through modification under paragraph (i), terminate the pilot program
within 30 days of submitting an interim report to Congress stating such
determination. VA also would publish a document in the Federal Register
regarding the pilot program's termination, and we would notify
participants in the same manner that we notified them under paragraph
(f) of their initial eligibility for the pilot program. This would
ensure determinations regarding expansion and termination are made
using the same methodology. This 30-day period is the maximum amount of
time permitted by section 1703E(g)(5)(A)(ii).
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 rulemaking does not contain any provisions constituting
collections 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. This proposed rule would not have a significant
economic impact on qualifying non-VA entities or providers. Therefore,
pursuant to 5 U.S.C. 605(b), this rulemaking is 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 issues arising out of legal
mandates, the President's priorities, or the principles set forth in
this Executive Order.''
The Office of Information and Regulatory Affairs has determined
that this rulemaking is a significant regulatory action under Executive
Order 12866. VA's impact analysis can be found as a supporting document
at https://www.regulations.gov, usually within 48 hours after the
rulemaking document is published. Additionally, a copy of the
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 FYTD. This proposed rule is not expected
to be subject to the requirements of Executive Order 13771 because this
proposed rule is expected to result in no more than de minimis costs.
Executive Order 12866 also directs agencies to ``in most cases . .
. include a comment period of not less than 60 days.'' This regulation
aims to test innovative payment and service delivery models that will
maintain or enhance the quality of care for beneficiaries while
reducing cost. Providing a 30-day comment period will allow VA to begin
pilot programs more quickly, thereby increasing opportunities for
access to quality, cost-effective care to participating beneficiaries.
The regulations proposed here are largely procedural, and will not,
without Congressional approval of a pilot program proposal from VA,
result in any change in benefits or services by themselves. Moreover,
we believe that the requirement to receive Congressional approval for
any waiver of authority, and VA's proposal to publish specific pilot
program proposals in the Federal Register for public comment while
Congressional approval is pending, should provide the public a more
meaningful opportunity to comment on the actual pilot programs
implemented under section 1703E. For these reasons, we believe that 30
days would be a sufficient period of time for the public to comment on
this rulemaking. In sum, providing a 60-day public comment period
instead of a 30-day public comment period would be against public
interest. For the above reasons, VA issues this rule with a 30-day
public comment period. VA will consider and address comments that are
received within 30 days of the date this proposed rule is published in
the Federal Register.
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, and 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, and 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 as follows: 64.007, Blind
Rehabilitation Centers; 64.008, Veterans Domiciliary Care; 64.009,
Veterans Medical Care Benefits; 64.010, Veterans Nursing Home Care;
64.011, Veterans Dental Care; 64.012, Veterans Prescription Service;
64.013, Veterans Prosthetic Appliances; 64.014, Veterans State
Domiciliary Care; 64.015, Veterans State Nursing Home Care; 64.016,
Veterans State Hospital Care; 64.018, Sharing Specialized Medical
Resources; 64.019, Veterans Rehabilitation Alcohol and Drug Dependence;
and 64.022, Veterans Home Based Primary Care
List of Subjects in 38 CFR Part 17
Administrative practice and procedure, Alcohol abuse, Alcoholism,
Claims, Day care, Dental health, Drug abuse, Foreign relations,
Government contracts, Grant programs--health, Grant programs--veterans,
Health care, Health facilities, Health professions, Health records,
Homeless, Medical and dental schools, Medical devices, Medical
research, Mental health programs, Nursing homes, Philippines, Reporting
and recordkeeping requirements, Scholarships and fellowships, Travel
and transportation expenses, Veterans.
[[Page 36515]]
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. Robert L.
Wilkie, Secretary, Department of Veterans Affairs, approved this
document on April 10, 2019, for publication.
Dated: July 23, 2019.
Consuela Benjamin,
Regulations Development Coordinator, Office of Regulation Policy &
Management, Office of the Secretary, Department of Veterans Affairs
For the reasons set forth in the preamble, we propose to amend 38
CFR part 17 as follows:
PART 17--MEDICAL
0
1. The authority citation for part 17 is amended by adding an entry for
Sec. 17.450 to read in part as follows:
Authority: 38 U.S.C. 501, and as noted in specific sections.
* * * * *
Section 17.450 is also issued under 38 U.S.C. 1703E.
* * * * *
0
2. Add an undesignated center heading immediately following Sec.
17.417 to read as follows:
Center for Innovation for Care and Payment
0
3. Add a new Sec. 17.450 to read as follows.
Sec. 17.450 Center for Innovation for Care and Payment.
(a) Purpose and organization. The purpose of this section is to
establish procedures for the Center for Innovation for Care and
Payment.
(1) The Center for Innovation for Care and Payment will be
operationally independent from any of VA's administrations and will be
responsible for working across VA to carry out pilot programs to
develop innovative approaches to testing payment and service delivery
models to reduce expenditures while preserving or enhancing the quality
of care furnished by VA.
(2) For purposes of this paragraph (a), operational independence
refers to the strategic, procedural, and tactical aspects of managing
the pilot programs under this section.
(3) The Center for Innovation for Care and Payment will not operate
within any specific administration but will operate in VA's corporate
portfolio to ensure the limited number of concurrent pilot programs
under this section are not redundant of or conflicted by ongoing
innovation efforts within any specific administration.
(b) Definitions. The following definitions apply to this section.
Access refers to entry into or use of VA services.
Patient satisfaction of care and services refers to patients'
rating of their experiences of care and services and as further defined
in a pilot program proposal.
Payment models refer to the types of payment, reimbursement, or
incentives that VA deems appropriate for advancing the health and well-
being of beneficiaries.
Pilot program refers to a pilot program conducted under this
section.
Quality enhancement refers to improvement or improvements in such
factors as clinical quality, beneficiary-level outcomes, and functional
status as documented through improvements in measurement data from a
reliable and valid source, and as further defined in a pilot program
proposal.
Quality preservation refers to the maintenance of such factors as
clinical quality, beneficiary-level outcomes, and functional status as
documented through maintenance of measurement data from an evidence-
based source, and as further defined in a pilot program proposal.
Reduction in expenditure refers to, but is not limited to, cost
stabilization, cost avoidance, or decreases in long- or short-term
spending, and as further defined in a pilot program proposal. Note: VA
will also consider the proposal's potential impact on expenditures for
other related Federal programs; however, this potential impact will not
count against the limitation in paragraph (d)(2) of this section.
Service delivery models refer to all methods or programs for
furnishing care or services.
(c) Geographic Locations. VA will make decisions regarding the
location of each pilot program based upon the appropriateness of
testing a specific model in a specific area while taking efforts to
ensure that pilot programs are operated in geographically diverse areas
of the country. VA will include in its proposal to Congress and publish
a document in the Federal Register identifying the geographic locations
proposed for each pilot program, the rationale for those selections,
and how VA believes the selected locations will address deficits in
care for a defined population.
(d) Limitations. In carrying out pilot programs under this section,
VA will not:
(1) Actively operate more than 10 pilot programs at the same time;
and
(2) Consistent with section 1703E(d), obligate more than $50
million in any fiscal year in the conduct of the pilot programs
(including all administrative and overhead costs, such as measurement,
evaluation, and expenses to implement the pilot programs themselves)
operated under this section, unless VA determines it to be necessary
and submits a report to the appropriate Committees of Congress that
sets forth the amount of, and justification for, the additional
expenditure.
(e) Waiver of authorities. In carrying out pilot programs under
this section, VA may waive statutory provisions by adding to or
removing from statutory text in subchapters I, II, and III of chapter
17, title 38, upon Congressional approval, including waiving any
provisions of law in any provision codified in or included as a note to
any section in subchapters I, II, or III of chapter 17, title 38,
U.S.C.
(1) Upon Congressional approval of the waiver of a provision of law
under this section, VA will also deem waived any applicable provision
of regulation implementing such law as identified in VA's pilot program
proposal.
(2) VA will publish a document in the Federal Register providing
information about, and seeking comment on, each proposed pilot program
upon its submission of a proposal to Congress for approval. VA will
publish a document in the Federal Register to inform the public of any
pilot programs that have been approved by Congress.
(f) Notice of eligibility. VA will take reasonable actions to
provide direct notice to veterans eligible to participate in a pilot
program operated under this section and will provide general notice to
other individuals eligible to participate in a pilot program. VA will
announce its methods of providing notice to veterans, the public, and
other individuals eligible to participate through the document it
publishes in the Federal Register for each proposed and approved pilot
program.
(g) Evaluation and reporting. VA will evaluate each pilot program
operated under this section and report its findings. Evaluations may be
based on quantitative data, qualitative data, or both. Whenever
appropriate, evaluations will include a survey of participants or
beneficiaries to determine their satisfaction with the pilot program.
VA will make the evaluation results available to the public on the VA
Innovation Center website on
[[Page 36516]]
the schedule identified in VA's proposal for the pilot program.
(h) Expansion of pilot programs. VA may expand a pilot program
consistent with this paragraph (h).
(1) VA may expand the scope or duration of a pilot program if,
based on an analysis of the data developed pursuant to paragraph (g) of
this section for the pilot program, VA expects the pilot program to
reduce spending without reducing the quality of care or improve the
quality of patient care without increasing spending. Expansion may only
occur if VA determines that expansion would not deny or limit the
coverage or provision of benefits for individuals under chapter 17.
Expansion of a pilot program may not occur until 60 days after VA has
published a document in the Federal Register and submitted an interim
report to Congress stating its intent to expand a pilot program.
(2) VA may expand the scope of a pilot program by modifying, among
other elements of a pilot program, the range of services provided, the
qualifying conditions covered, the geographic location of the pilot
program, or the population of eligible participants in a manner that
increases participation in or benefits under a pilot program.
(3) In general, pilot programs are limited to 5 years of operation.
VA may extend the duration of a pilot program by up to an additional 5
years of operation. Any pilot program extended beyond its initial 5-
year period must continue to comply with the provisions of this section
regarding evaluation and reporting under paragraph (g) of this section.
(i) Modification of pilot programs. The Secretary may modify
elements of a pilot program in a manner that is consistent with the
parameters of the Congressional approval of the waiver described in
paragraph (e) of this section. Such modification does not require a
submission to Congress for approval under paragraph (e) of this
section.
(j) Termination of pilot programs. If VA determines that a pilot
program is not producing quality enhancement or quality preservation,
or is not resulting in the reduction of expenditures, and that it is
not possible or advisable to modify the pilot program either through
submission of a new waiver request under paragraph (e) of this section
or through modification under paragraph (i) of this section, VA will
terminate the pilot program within 30 days of submitting an interim
report to Congress that states such determination. VA will also publish
a document in the Federal Register regarding the pilot program's
termination.
[FR Doc. 2019-15891 Filed 7-26-19; 8:45 am]
BILLING CODE 8320-01-P