Library / Laws / 113th / s / S. 3009 / Introduced in Senate
II
113th CONGRESS
2d Session
S. 3009
IN THE SENATE OF THE UNITED STATES
December 12, 2014Mr. Blumenthal (for himself and Mr. Rockefeller) introduced the following bill; which was read twice and referred to the Committee on Finance
A BILL
To improve end-of-life care.
1.
Short
title; table of contents
(a)
Short
title
This Act may be cited
as the Advance Planning and Compassionate Care Act of 2014.
(b)
Table of
contents
The table of contents of this Act is as follows:
Sec. 1. Short title; table of
contents.Sec. 2. Definitions.TITLE I—Advance Care PlanningSubtitle A—Consumer and Provider EducationPart I—Consumer EducationSUBPART A—National initiativesSec. 101. Advance care planning telephone hotline.Sec. 102. Advance care planning information
clearinghouses.Sec. 103. Advance care planning toolkit.Sec. 104. National public education campaign.Sec. 105. Update of Medicare and Social Security
handbooks.Sec. 106. Authorization of appropriations.SUBPART B—State and local initiativesSec. 111. Financial assistance for advance care
planning.Sec. 112. Grants for programs for orders regarding life
sustaining treatment.Part II—Provider EducationSec. 121. Public provider advance care planning
website.Sec. 122. Continuing education for physicians and
nurses.Subtitle B—Portability of Advance Directives; Health
Information TechnologySec. 131. Portability of advance directives.Sec. 132. State advance directive registries; driver's license
advance directive notation.Sec. 133. GAO study and report on establishment of national
advance directive registry.Subtitle C—National Uniform Policy on Advance Care
PlanningSec. 141. Study and report by the Secretary regarding the
establishment and implementation of a national uniform policy on
advance
directives.TITLE II—Compassionate CareSubtitle A—Workforce developmentPart I—Education and trainingSec. 201. National Geriatric and Palliative Care Services
Corps.Sec. 202. Exemption of palliative medicine fellowship training
from Medicare graduate medical education caps.Sec. 203. Medical school curricula.Subtitle B—Coverage under Medicare, Medicaid, and CHIP
Part I—Coverage of advance care planningSec. 211. Medicare, Medicaid, and CHIP coverage.Part II—HospiceSec. 221. Adoption of MedPAC hospice payment methodology
recommendations.Sec. 222. Removing hospice inpatient days in setting per diem
rates for critical access hospitals.Sec. 223. Hospice payments for dual eligible individuals
residing in long-term care facilities.Sec. 224. Delineation of respective care responsibilities of
hospice programs and long-term care facilities.Sec. 225. Adoption of MedPAC hospice program eligibility
certification and recertification recommendations.Sec. 226. Concurrent care for children.Sec. 227. Making hospice a required benefit under Medicaid and
CHIP.Sec. 228. Medicare Hospice payment model demonstration
projects.Sec. 229. MedPAC studies and reports.Sec. 230. HHS Evaluations.Subtitle C—Quality ImprovementSec. 241. Patient satisfaction surveys.Sec. 242. Development of core end-of-life care quality measures
across each relevant provider setting.Sec. 243. Accreditation of hospital-based palliative care
programs.Sec. 244. Survey and data requirements for all Medicare
participating hospice programs.Subtitle D—Additional reports, research, and
evaluationsSec. 251. National Center On Palliative and End-of-Life
Care.Sec. 252. National Mortality Followback Survey.Sec. 253. Demonstration projects for use of telemedicine
services in advance care planning.Sec. 254. Inspector General investigation of fraud and
abuse.Sec. 255. GAO study and report on provider adherence to advance
directives.
2.
Definitions
In this Act:
(1)
Advance care
planning
The term advance care planning means the
process of—
(A) determining an
individual’s priorities, values and goals for care in the future when the
individual is no longer able to express his or her wishes;
(B) engaging family
members, health care proxies, and health care providers in an ongoing
dialogue
about—
(i) the
individual’s wishes for care;
(ii) what the future
may hold for people with serious illnesses or injuries;
(iii) how
individuals, their health care proxies, and family members want their
beliefs
and preferences to guide care decisions; and
(iv) the steps that
individuals and family members can take regarding, and the resources
available
to help with, finances, family matters, spiritual questions, and other
issues
that impact seriously ill or dying patients and their families; and
(C) executing and
updating advance directives and appointing a health care proxy.
(2)
Advance
directive
The term advance directive means a living
will, medical directive, health care power of attorney, durable power of
attorney, or other written statement by a competent individual that is
recognized under State law and indicates the individual's wishes regarding
medical treatment in the event of future incompetence. Such term includes
an
advance health care directive and a health care directive recognized under
State law.
(3)
CHIP
The
term CHIP means the program established under title XXI of the
Social Security Act (42 U.S.C. 1397aa et seq.).
(4)
End-of-life-care
The
term end-of-life care means all aspects of care of a patient with
a potentially fatal condition, and includes care that is focused on
specific
preparations for an impending death.
(5)
Health care
power of attorney
The term health care power of
attorney means a legal document that identifies a health care proxy or
decisionmaker for a patient who has the authority to act on the patient’s
behalf when the patient is unable to communicate his or her wishes for
medical
care on matters that the patient specifies when he or she is competent.
Such
term includes a durable power of attorney that relates to medical care.
(6)
Living
will
The term living will means a legal
document—
(A) used to specify
the type of medical care (including any type of medical treatment,
including
life-sustaining procedures if that person becomes permanently unconscious
or is
otherwise dying) that an individual wants provided or withheld in the
event the
individual cannot speak for himself or herself and cannot express his or
her
wishes; and
(B) that requires a
physician to honor the provisions of upon receipt or to transfer the care
of
the individual covered by the document to another physician that will
honor
such provisions.
(7)
Medicaid
The
term Medicaid means the program established under title XIX of the
Social Security Act (42 U.S.C. 1396 et seq.).
(8)
Medicare
The
term Medicare means the program established under title XVIII of
the Social Security Act (42 U.S.C. 1395 et seq.).
(9)
Orders for
life-sustaining treatment
The term orders for
life-sustaining treatment means a process for focusing a patients'
values, goals, and preferences on current medical circumstances and to
translate such into visible and portable medical orders applicable across
care
settings, including home, long-term care, emergency medical services, and
hospitals.
(10)
Palliative
care
The term palliative care means
interdisciplinary care for individuals with a life-threatening illness or
injury relating to pain and symptom management and psychological, social,
and
spiritual needs and that seeks to improve the quality of life for the
individual and the individual's family.
(11)
Secretary
The
term Secretary means the Secretary of Health and Human
Services.
I
Advance Care
Planning
A
Consumer and
Provider Education
I
Consumer
Education
A
National
initiatives
101.
Advance care
planning telephone hotline
(a)
In
general
Not later than January 1, 2016, the Secretary, acting
through the Director of the Centers for Disease Control and Prevention,
shall
establish and operate directly, or by grant, contract, or interagency
agreement, a 24-hour toll-free telephone hotline to provide consumer
information regarding advance care planning, including—
(1) an explanation of
advanced care planning and its importance;
(2) issues to be
considered when developing an individual's advance care plan;
(3) how to establish
an advance directive;
(4) procedures to
help ensure that an individual's directives for end-of-life care are
followed;
(5) Federal and
State-specific resources for assistance with advance care planning; and
(6) hospice and
palliative care (including their respective purposes and services).
(b)
Establishment
In
carrying out the requirements under subsection (a), the Director of the
Centers
for Disease Control and Prevention may designate an existing 24-hour
toll-free
telephone hotline or, if no such service is available or appropriate,
establish
a new 24-hour toll-free telephone hotline.
102.
Advance care
planning information clearinghouses
(a)
Expansion of
National Clearinghouse for Long-Term Care Information
(1)
Development
Not
later than January 1, 2015, the Secretary shall develop an online
clearinghouse
to provide comprehensive information regarding advance care planning.
(2)
Maintenance
The
advance care planning clearinghouse, which shall be clearly identifiable
and
available on the homepage of the Department of Health and Human Service's
National Clearinghouse for Long-Term Care Information website, shall be
maintained and publicized by the Secretary on an ongoing basis.
(3)
Content
The
advance care planning clearinghouse shall include—
(A) any relevant
content contained in the national public education campaign required under
section 104;
(B) content
addressing—
(i) an
explanation of advanced care planning and its importance;
(ii) issues to be
considered when developing an individual's advance care plan;
(iii) how to
establish an advance directive;
(iv) procedures to
help ensure that an individual's directives for end-of-life care are
followed;
and
(v) hospice and
palliative care (including their respective purposes and services);
(C) available Federal
and State-specific resources for assistance with advance care planning,
including—
(i) contact
information for any State public health departments that are responsible
for
issues regarding end-of-life care;
(ii) contact
information for relevant legal service organizations, including those
funded
under the Older Americans Act of 1965 (42 U.S.C. 3001 et seq.); and
(iii) advance
directive forms for each State; and
(D) any additional
information, as determined by the Secretary.
(b)
Establishment
of pediatric advance care planning clearinghouse
(1)
Development
Not
later than January 1, 2016, the Secretary, in consultation with the
Assistant
Secretary for Children and Families of the Department of Health and Human
Services, shall develop an online clearinghouse to provide comprehensive
information regarding pediatric advance care planning.
(2)
Maintenance
The
pediatric advance care planning clearinghouse, which shall be clearly
identifiable on the homepage of the Administration for Children and
Families
website, shall be maintained and publicized by the Secretary on an ongoing
basis.
(3)
Content
The
pediatric advance care planning clearinghouse shall provide advance care
planning information specific to children with life-threatening illnesses
or
injuries and their families.
103.
Advance care
planning toolkit
(a)
Development
Not
later than July 1, 2015, the Secretary, in consultation with the Director
of
the Centers for Disease Control and Prevention, shall develop an online
advance
care planning toolkit.
(b)
Maintenance
The
advance care planning toolkit, which shall be available in English,
Spanish,
and any other languages that the Secretary deems appropriate, shall be
maintained and publicized by the Secretary on an ongoing basis and made
available on the websites of the following agencies:
(1) The Centers for
Disease Control and Prevention.
(2) The Department of
Health and Human Service's National Clearinghouse for Long-Term Care
Information.
(3) The
Administration for Children and Families.
(c)
Content
The
advance care planning toolkit shall include content addressing—
(1) common issues and
questions regarding advance care planning, including individuals and
resources
to contact for further inquiries;
(2) advance
directives and their uses, including living wills and durable powers of
attorney;
(3) the roles and
responsibilities of a health care proxy;
(4) Federal and
State-specific resources to assist individuals and their families with
advance
care planning, including—
(A) the advance care
planning toll-free telephone hotline established under section 101;
(B) the advance care
planning clearinghouses established under section 102;
(C) the advance care
planning toolkit established under this section;
(D) available State
legal service organizations to assist individuals with advance care
planning,
including those organizations that receive funding pursuant to the Older
Americans Act of 1965 (42 U.S.C. 3001 et seq.); and
(E) website links or
addresses for State-specific advance directive forms; and
(5) any additional
information, as determined by the Secretary.
104.
National
public education campaign
(a)
National public education campaign
(1)
In
general
Not later than
January 1, 2016, the Secretary, acting through the Director of the Centers
for
Disease Control and Prevention, shall, directly or through grants,
contracts,
or interagency agreements, develop and implement a national campaign to
inform
the public of the importance of advance care planning and of an
individual's
right to direct and participate in their health care decisions.
(2)
Content of
Educational Campaign
The national public education campaign
established under paragraph (1) shall—
(A) employ the use of
various media, including regularly televised public service
announcements;
(B) provide
culturally and linguistically appropriate information;
(C) be conducted
continuously over a period of not less than 5 years;
(D) identify and
promote the advance care planning information available on the Department
of
Health and Human Service's National Clearinghouse for Long-Term Care
Information website and Administration for Children and Families website,
as
well as any other relevant Federal or State-specific advance care planning
resources;
(E) raise public
awareness of the consequences that may result if an individual is no
longer
able to express or communicate their health care decisions;
(F) address the
importance of individuals speaking to family members, health care proxies,
and
health care providers as part of an ongoing dialogue regarding their
health
care choices;
(G) address the need
for individuals to obtain readily available legal documents that express
their
health care decisions through advance directives (including living wills,
comfort care orders, and durable powers of attorney for health care);
(H) raise public
awareness regarding the availability of hospice and palliative care; and
(I) encourage
individuals to speak with their physicians about their options and
intentions
for end-of-life care.
(3)
Evaluation
(A)
In
General
Not later than July 1, 2018, the Secretary, acting
through the Director of the Centers for Disease Control and Prevention,
shall
conduct a nationwide survey to evaluate whether the national campaign
conducted
under this subsection has achieved its goal of changing public awareness,
attitudes, and behaviors regarding advance care planning.
(B)
Baseline
Survey
In order to evaluate the effectiveness of the national
campaign, the Secretary shall conduct a baseline survey prior to
implementation
of the campaign.
(C)
Reporting
Requirement
Not later than December 31, 2018, the Secretary shall
report the findings of such survey, as well as any recommendations that
the
Secretary determines appropriate regarding the need for continuation or
legislative or administrative changes to facilitate changing public
awareness,
attitudes, and behaviors regarding advance care planning, to the
appropriate
committees of the Congress.
(b)
Repeal
Section 4751(d) of the Omnibus Budget
Reconciliation Act of 1990 (42 U.S.C. 1396a note; Public Law 101–508) is
repealed.
105.
Update of
Medicare and Social Security handbooks
(a)
Medicare &
You handbook
(1)
In
general
Not later than 60 days after the date of enactment of
this Act, the Secretary shall update the online version of the Plan
Ahead for Long-Term Care section of the Medicare & You Handbook to include—
(A) an explanation of
advance care planning and advance directives, including—
(i) living
wills;
(ii) health care
proxies; and
(iii) after-death
directives;
(B) Federal and
State-specific resources to assist individuals and their families with
advance
care planning, including—
(i) the
advance care planning toll-free telephone hotline established under
section
101;
(ii) the advance care
planning clearinghouses established under section 102;
(iii) the advance
care planning toolkit established under section 103;
(iv) available State
legal service organizations to assist individuals with advance care
planning,
including those organizations that receive funding pursuant to the Older
Americans Act of 1965 (42 U.S.C. 3001 et seq.); and
(v) website links or
addresses for State-specific advance directive forms; and
(C) any additional
information, as determined by the Secretary.
(2)
Update of paper
and subsequent versions
The Secretary shall include the
information described in paragraph (1) in all paper and electronic
versions of
the Medicare & You Handbook that are published on or after the date that is
60 days after the date of enactment of this Act.
(b)
Social Security
handbook
The Commissioner of Social Security shall—
(1) not later than 60
days after the date of enactment of this Act, update the online version of
the
Social Security Handbook for beneficiaries to include the information
described
in subsection (a)(1); and
(2) include such
information in all paper and online versions of such handbook that are
published on or after the date that is 60 days after the date of enactment
of
this Act.
106.
Authorization
of appropriations
There is
authorized to be appropriated for the period of fiscal years 2015 through
2019—
(1) $195,000,000 to the Secretary to carry out
sections 101, 102, 103, 104 and 105(a); and
(2) $5,000,000 to the Commissioner of Social
Security to carry out section 105(b).
B
State and local
initiatives
111.
Financial
assistance for advance care planning
(a)
Legal
assistance for advance care planning
(1)
Definition of
recipient
Section 1002(6) of the Legal Services Corporation Act
(42 U.S.C. 2996a(6)) is amended by striking clause (A) of and
inserting subparagraph (A) or (B) of.
(2)
Advance care
planning
Section 1006 of the Legal Services Corporation Act (42
U.S.C. 2996e) is amended—
(A) in subsection
(a)(1)—
(i) by
striking title, and (B) to make and inserting the following:
“title;
(C) to
make
;
and
(ii) by
inserting after subparagraph (A) the following:
(B) to provide financial assistance, and
make grants and contracts, as described in subparagraph (A), on a
competitive
basis for the purpose of providing legal assistance in the form of
advance care
planning (as defined in section 3 of the Advance Planning and Compassionate Care Act of 2014, and including providing information about State-specific
advance directives, as defined in that section) for eligible
clients under this
title, including providing such planning to the family members of
eligible
clients and persons with power of attorney to make health care
decisions for
the clients; and
;
and
(B) in subsection
(b), by adding at the end the following:
(2) Advance care planning provided in
accordance with subsection (a)(1)(B) shall not be construed to
violate the
Assisted Suicide Funding Restriction Act of 1997 (42 U.S.C. 14401
et
seq.).
.
(3)
Reports
Section
1008(a) of the Legal Services Corporation Act (42 U.S.C. 2996g(a)) is
amended
by adding at the end the following: The Corporation shall require such a
report, on an annual basis, from each grantee, contractor, or other
recipient
of financial assistance under section 1006(a)(1)(B)..
(4)
Authorization
of appropriations
Section 1010 of the Legal Services Corporation
Act (42 U.S.C. 2996i) is amended—
(A) in subsection
(a)—
(i) by
striking (a) and inserting (a)(1);
(ii) in
the last sentence, by striking Appropriations for that purpose
and inserting the following:
(3) Appropriations for a purpose
described in paragraph (1) or (2)
;
and
(iii) by inserting
before paragraph (3) (as designated by clause (ii)) the following:
(2) There are authorized to be
appropriated to carry out section 1006(a)(1)(B), $10,000,000 for
each of fiscal
years 2015, 2016, 2017, 2018, and 2019.
;
and
(B) in subsection
(d), by striking subsection (a) and inserting subsection
(a)(1).
(5)
Effective
date
This subsection and the amendments made by this subsection
take effect July 1, 2015.
(b)
State health
insurance assistance programs
(1)
In
general
The Secretary shall use amounts made available under
paragraph (3) to award grants to States for State health insurance
assistance
programs receiving assistance under section 4360 of the Omnibus Budget
Reconciliation Act of 1990 to provide advance care planning services to
Medicare beneficiaries, personal representatives of such beneficiaries,
and the
families of such beneficiaries. Such services shall include information
regarding State-specific advance directives and ways to discuss individual
care
wishes with health care providers.
(2)
Requirements
(A)
Award of
grants
In making grants under this subsection for a fiscal year,
the Secretary shall satisfy the following requirements:
(i) Two-thirds of the
total amount of funds available under paragraph (3) for a fiscal year
shall be
allocated among those States approved for a grant under this section that
have
adopted the Uniform Health-Care Decisions Act drafted by the National
Conference of Commissioners on Uniform State Laws and approved and
recommended
for enactment by all States at the annual conference of such commissioners
in
1993.
(ii) One-third of the
total amount of funds available under paragraph (3) for a fiscal year
shall be
allocated among those States approved for a grant under this section that
have
adopted a uniform form for orders regarding life sustaining treatment as
defined in section 1861(hhh)(5) of the Social Security Act (as amended by
section 211 of this Act) or a comparable approach to advance care
planning.
(B)
Work plan;
report
As a condition of being awarded a grant under this
subsection, a State shall submit the following to the Secretary:
(i) An
approved plan for expending grant funds.
(ii) For each fiscal
year for which the State is paid grant funds under this subsection, an
annual
report regarding the use of the funds, including the number of Medicare
beneficiaries served and their satisfaction with the services provided.
(C)
Limitation
No
State shall be paid funds from a grant made under this subsection prior to
July
1, 2015.
(3)
Authorization
of appropriations
There is authorized to be appropriated to the
Secretary to the Centers for Medicare & Medicaid Services Program
Management Account, $12,000,000 for each of fiscal years 2015 through 2019
for
purposes of awarding grants to States under paragraph (1).
(c)
Medicaid
transformation grants for advance care planning
Section 1903(z)
of the Social Security Act (42 U.S.C. 1396b(z)) is amended—
(1) in paragraph (2),
by adding at the end the following new subparagraph:
(G) Methods for
improving the effectiveness and efficiency of medical assistance
provided under
this title by making available to individuals enrolled in the State
plan or
under a waiver of such plan information regarding advance care
planning (as
defined in section 3 of the Advance Planning and Compassionate Care Act of 2014), including at time of
enrollment or renewal of enrollment in the plan or waiver, through
providers,
and through such other innovative means as the State determines
appropriate.
;
(2) in paragraph (3),
by adding at the end the following new subparagraph:
(D)
Work plan
required for award of advance care planning grants
Payment to a
State under this subsection to adopt the innovative methods
described in
paragraph (2)(G) is conditioned on the State submitting to the
Secretary an
approved plan for expending the funds awarded to the State under
this
subsection.
;
and
(3) in paragraph
(4)—
(A) in subparagraph
(A)—
(i) in
clause (i), by striking and at the end;
(ii) in
clause (ii), by striking the period at the end and inserting ;
and; and
(iii) by
inserting after clause (ii), the following new clause:
(iii) $20,000,000 for
each of fiscal years 2015 through 2019.
;
and
(B) by striking
subparagraph (B), and inserting the following:
(B)
Allocation of funds
The Secretary shall specify a method for
allocating the funds made available under this subsection among
States awarded
a grant for fiscal year 2015, 2016, 2017, 2018, or 2019. Such
method shall
provide that—
(i) 100 percent of such funds for each of
fiscal years 2015 through 2019 shall be awarded to States that
design programs
to adopt the innovative methods described in paragraph (2)(G); and
(ii) in no event
shall a payment to a State awarded a grant under this subsection
for fiscal
year 2015 be made prior to July 1,
2015.
.
(d)
Advance care
planning community training grants
(1)
In
general
The Secretary shall use amounts made available under
paragraph (3) to award grants to area agencies on aging (as defined in
section
102 of the Older Americans Act of 1965 (42 U.S.C. 3002)).
(2)
Requirements
(A)
Use of
funds
Funds awarded to an area agency on aging under this
subsection shall be used to provide advance care planning education and
training opportunities for local aging service providers and
organizations.
(B)
Work plan;
report
As a condition of being awarded a grant under this
subsection, an area agency on aging shall submit the following to the
Secretary:
(i) An approved plan
for expending grant funds.
(ii) For each fiscal
year for which the agency is paid grant funds under this subsection, an
annual
report regarding the use of the funds, including the number of Medicare
beneficiaries served and their satisfaction with the services provided.
(C)
Limitation
No
area agency on aging shall be paid funds from a grant made under this
subsection prior to July 1, 2015.
(3)
Authorization
of appropriations
There is authorized to be appropriated to the
Secretary to the Centers for Medicare & Medicaid Services Program
Management Account, $12,000,000 for each of fiscal years 2015 through 2019
for
purposes of awarding grants to area agencies on aging under paragraph
(1).
(e)
Nonduplication
of activities
The Secretary shall establish procedures to ensure
that funds made available under grants awarded under this section or
pursuant
to amendments made by this section supplement, not supplant, existing
Federal
funding, and that such funds are not used to duplicate activities carried
out
under such grants or under other Federally funded programs.
112.
Grants for
programs for orders regarding life sustaining treatment
(a)
In
general
The Secretary shall make grants to eligible entities for
the purpose of—
(1) establishing new programs for orders
regarding life sustaining treatment in States or localities;
(2) expanding or
enhancing an existing program for orders regarding life sustaining
treatment in
States or localities; or
(3) providing a
clearinghouse of information on programs for orders for life sustaining
treatment and consultative services for the development or enhancement of
such
programs.
(b)
Authorized
activities
Activities funded through a grant under this section
for an area may include—
(1) developing such a
program for the area that includes home care, hospice, long-term care,
community and assisted living residences, skilled nursing facilities,
inpatient
rehabilitation facilities, hospitals, and emergency medical services
within the
area;
(2) securing
consultative services and advice from institutions with experience in
developing and managing such programs; and
(3) expanding an
existing program for orders regarding life sustaining treatment to serve
more
patients or enhance the quality of services, including educational
services for
patients and patients' families or training of health care
professionals.
(c)
Distribution of
funds
In funding grants under this section, the Secretary shall
ensure that, of the funds appropriated to carry out this section for each
fiscal year—
(1) at least two-thirds are used for
establishing or developing new programs for orders regarding life
sustaining
treatment; and
(2) one-third is used for expanding or
enhancing existing programs for orders regarding life sustaining
treatment.
(d)
Definitions
In
this section:
(1) The term
eligible entity includes—
(A) an academic medical center, a medical
school, a State health department, a State medical association, a
multi-State
taskforce, a hospital, or a health system capable of administering a
program
for orders regarding life sustaining treatment for a State or locality;
or
(B) any other health
care agency or entity as the Secretary determines appropriate.
(2) The term
order regarding life sustaining treatment has the meaning given
such term in section 1861(hhh)(5) of the Social Security Act, as added by
section 211.
(3) The term
program for orders regarding life sustaining treatment means, with
respect to an area, a program that supports the active use of orders
regarding
life sustaining treatment in the area.
(e)
Authorization of
appropriations
To carry out this section, there are authorized to
be appropriated such sums as may be necessary for each of the fiscal years
2014
through 2019.
II
Provider
Education
121.
Public
provider advance care planning website
(a)
Development
Not
later than January 1, 2015, the Secretary, acting through the
Administrator of
the Centers for Medicare & Medicaid Services and the Director of the Agency
for Healthcare Research and Quality, shall establish a website for
providers
under Medicare, Medicaid, the Children's Health Insurance Program, the
Indian
Health Service (include contract providers) and other public health
providers
on each individual's right to make decisions concerning medical care,
including
the right to accept or refuse medical or surgical treatment, and the
existence
of advance directives.
(b)
Maintenance
The
website, shall be maintained and publicized by the Secretary on an ongoing
basis.
(c)
Content
The
website shall include content, tools, and resources necessary to do the
following:
(1) Inform providers
about the advance directive requirements under the health care programs
described in subsection (a) and other State and Federal laws and
regulations
related to advance care planning.
(2) Educate providers
about advance care planning quality improvement activities.
(3) Provide
assistance to providers to—
(A) integrate advance
directives into electronic health records, including oral directives;
and
(B) develop and
disseminate advance care planning informational materials for their
patients.
(4) Inform providers
about advance care planning continuing education requirements and
opportunities.
(5) Encourage
providers to discuss advance care planning with their patients of all
ages.
(6) Assist providers'
understanding of the continuum of end-of-life care services and supports
available to patients, including palliative care and hospice.
(7) Inform providers
of best practices for discussing end-of-life care with dying patients and
their
loved ones.
122.
Continuing
education for physicians and nurses
(a)
In
general
Not later than
January 1, 2017, the Secretary, acting through the Director of Health
Resources
and Services Administration, shall develop, in consultation with health
care
providers and State boards of medicine and nursing, a curriculum for
continuing
education that States may adopt for physicians and nurses on advance care
planning and end-of-life care.
(b)
Content
(1)
In
general
The continuing education curriculum developed under
subsection (a) for physicians and nurses shall, at a minimum, include—
(A) a description of
the meaning and importance of advance care planning;
(B) a description of
advance directives, including living wills and durable powers of attorney,
and
the use of such directives;
(C) palliative care
principles and approaches to care; and
(D) the continuum of
end-of-life services and supports, including palliative care and
hospice.
(2)
Additional
content for physicians
The continuing education curriculum for
physicians developed under subsection (a) shall include instruction on how
to
conduct advance care planning with patients and their loved ones.
B
Portability of
Advance Directives; Health Information Technology
131.
Portability of
advance directives
(a)
Medicare
Section 1866(f) of the
Social Security Act (42 U.S.C.
1395cc(f)) is amended—
(1) in paragraph (1)—
(A) in subparagraph (B), by inserting
and if presented by the individual, to include the content of such
advance directive in a prominent part of such record before the
semicolon at the end;
(B) in subparagraph (D), by striking
and after the semicolon at the end;
(C) in subparagraph (E), by striking the period
at the end and inserting ; and; and
(D) by inserting after subparagraph (E) the
following new subparagraph:
(F) to
provide each individual with the opportunity to discuss issues
relating to the
information provided to that individual pursuant to subparagraph
(A) with an
appropriately trained
professional.
; and
(2) by adding at the end the following new
paragraph:
(5)
(A) An advance directive validly executed
outside of the State in which such advance directive is presented
by an adult
individual to a provider of services, a Medicare Advantage
organization, or a
prepaid or eligible organization shall be given the same effect by
that
provider or organization as an advance directive validly executed
under the law
of the State in which it is presented would be given effect.
(B)
(i) The definition of an advanced directive
shall also include actual knowledge of instructions made while an
individual
was able to express the wishes of such individual with regard to
health
care.
(ii) For purposes of clause (i), the term
actual knowledge means the possession of information of an
individual’s wishes communicated to the health care provider orally
or in
writing by the individual, the individual’s medical power of
attorney
representative, the individual’s health care surrogate, or other
individuals
resulting in the health care provider’s personal cognizance of
these wishes.
Other forms of imputed knowledge are not actual knowledge.
(C) The provisions of this paragraph shall
preempt any State law to the extent such law is inconsistent with
such
provisions. The provisions of this paragraph shall not preempt any
State law
that provides for greater portability, more deference to a
patient’s wishes, or
more latitude in determining a patient’s
wishes.
.
(b)
Medicaid
Section 1902(w) of the
Social Security Act (42 U.S.C.
1396a(w)) is amended—
(1) in paragraph (1)—
(A) in subparagraph (B)—
(i) by striking in the individual’s
medical record and inserting in a prominent part of the
individual’s current medical record; and
(ii) by inserting and if presented by the
individual, to include the content of such advance directive in a
prominent
part of such record before the semicolon at the end;
(B) in subparagraph (D), by striking
and after the semicolon at the end;
(C) in subparagraph (E), by striking the period
at the end and inserting ; and; and
(D) by inserting after subparagraph (E) the
following new subparagraph:
(F) to
provide each individual with the opportunity to discuss issues
relating to the
information provided to that individual pursuant to subparagraph
(A) with an
appropriately trained
professional.
; and
(2) by adding at the end the following
paragraph:
(6)
(A) An advance directive validly executed
outside of the State in which such advance directive is presented
by an adult
individual to a provider or organization shall be given the same
effect by that
provider or organization as an advance directive validly executed
under the law
of the State in which it is presented would be given effect.
(B)
(i) The definition of an advance directive
shall also include actual knowledge of instructions made while an
individual
was able to express the wishes of such individual with regard to
health
care.
(ii) For purposes of clause (i), the term
actual knowledge means the possession of information of an
individual’s wishes communicated to the health care provider orally
or in
writing by the individual, the individual’s medical power of
attorney
representative, the individual’s health care surrogate, or other
individuals
resulting in the health care provider’s personal cognizance of
these wishes.
Other forms of imputed knowledge are not actual knowledge.
(C) The provisions of this paragraph shall
preempt any State law to the extent such law is inconsistent with
such
provisions. The provisions of this paragraph shall not preempt any
State law
that provides for greater portability, more deference to a
patient’s wishes, or
more latitude in determining a patient’s
wishes.
.
(c)
CHIP
Section
2107(e)(1) of the Social Security Act (42 U.S.C. 1397gg(e)(1)) is
amended—
(1) by redesignating
subparagraphs (G) through (O) as subparagraphs (H) through (P),
respectively;
and
(2) by inserting
after subparagraph (F) the following:
(G) Section 1902(w)
(relating to advance
directives).
.
(d)
Study and report regarding
implementation
(1)
Study
The Secretary shall conduct a study
regarding the implementation of the amendments made by subsections (a) and
(b).
(2)
Report
Not later than 18 months after the date of
enactment of this Act, the Secretary shall submit to Congress a report on
the
study conducted under paragraph (1), together with recommendations for
such
legislation and administrative actions as the Secretary considers
appropriate.
(e)
Effective dates
(1)
In general
Subject to paragraph (2), the amendments
made by subsections (a), (b), and (c) shall apply to provider agreements
and
contracts entered into, renewed, or extended under title XVIII of the
Social Security Act (42 U.S.C. 1395 et
seq.), and to State plans under title XIX of such Act (42 U.S.C. 1396 et seq.) and State
child health plans under title XXI of such Act (42 U.S.C. 1397aa et seq.),
on
or after such date as the Secretary specifies, but in no case may such
date be
later than 1 year after the date of enactment of this Act.
(2)
Extension of effective date for state law
amendment
In the case of a
State plan under title XIX of the Social Security
Act or a State child health plan under title XXI of such Act which
the Secretary determines requires State legislation in order for the plan
to
meet the additional requirements imposed by the amendments made by
subsections
(b) and (c), the State plan shall not be regarded as failing to comply
with the
requirements of such title solely on the basis of its failure to meet
these
additional requirements before the first day of the first calendar quarter
beginning after the close of the first regular session of the State
legislature
that begins after the date of enactment of this Act. For purposes of the
previous sentence, in the case of a State that has a 2-year legislative
session, each year of the session is considered to be a separate regular
session of the State legislature.
132.
State advance
directive registries; Driver's license advance directive notation
Part P of title III of the Public Health
Service Act (42 U.S.C. 280g) is amended by inserting after section 399S
the following new sections:
399S–1.
State advance
directive registries
(a)
State advance
directive registry
In this section, the term State advance
directive registry means a secure, electronic database that—
(1) is available free
of charge to residents of a State; and
(2) stores advance
directive documents and makes such documents accessible to medical
service
providers in accordance with Federal and State privacy laws.
(b)
Grant
program
Beginning on July 1, 2015, the Secretary, acting through
the Director of the Centers for Disease Control and Prevention,
shall award
grants on a competitive basis to eligible entities to establish and
operate,
directly or indirectly (by competitive grant or competitive
contract), State
advance directive registries.
(c)
Eligible
entities
(1)
In
general
To be eligible to receive a grant under this section, an
entity shall—
(A) be a State
department of health; and
(B) submit to the
Director an application at such time, in such manner, and
containing—
(i) a
plan for the establishment and operation of a State advance
directive registry;
and
(ii) such other
information as the Director may require.
(2)
No requirement
of notation mechanism
The Secretary shall not require that an
entity establish and operate a driver's license advance directive
notation
mechanism for State residents under section 399V to be eligible to
receive a
grant under this section.
(d)
Annual
report
For each year for which an entity receives an award under
this section, such entity shall submit an annual report to the
Director on the
use of the funds received pursuant to such award, including the
number of State
residents served through the registry.
(e)
Authorization
There
is authorized to be appropriated to carry out this section
$20,000,000 for
fiscal year 2015 and each fiscal year thereafter.
399S–2.
Driver's
license advance directive notation
(a)
In
general
Beginning July 1, 2015, the Secretary, acting through the
Director of the Centers for Disease Control and Prevention, shall
award grants
on a competitive basis to States to establish and operate a
mechanism for a
State resident with a driver's license to include a notice of the
existence of
an advance directive for such resident on such license.
(b)
Eligibility
To
be eligible to receive a grant under this section, a State shall—
(1) establish and
operate a State advance directive registry under section 399S–1;
and
(2) submit to the
Director an application at such time, in such manner, and
containing—
(A) a plan that
includes a description of how the State will—
(i) disseminate
information about advance directives at the time of driver’s
license
application or renewal;
(ii) enable each
State resident with a driver's license to include a notice of the
existence of
an advance directive for such resident on such license in a manner
consistent
with the notice on such a license indicating a driver's intent to
be an organ
donor; and
(iii) coordinate with
the State department of health to ensure that, if a State resident
has an
advance directive notice on his or her driver's license, the
existence of such
advance directive is included in the State registry established
under section
399S–1; and
(B) any other
information as the Director may require.
(c)
Annual
report
For each year for which a State receives an award under
this section, such State shall submit an annual report to the
Director on the
use of the funds received pursuant to such award, including the
number of State
residents served through the mechanism.
(d)
Authorization
There
is authorized to be appropriated to carry out this section
$50,000,000 for
fiscal year 2015 and each fiscal year
thereafter.
.
133.
GAO Study and
Report on Establishment of National Advance Directive Registry
(a)
Study
The
Comptroller General of the United States shall conduct a study on the
feasibility of a national registry for advance directives, taking into
consideration the constraints created by the privacy provisions enacted as
a
result of the Health Insurance Portability and Accountability Act of 1996
(Public Law 104–191).
(b)
Report
Not
later than 18 months after the date of enactment of this Act, the
Comptroller
General of the United States shall submit to Congress a report on the
study
conducted under subsection (a) together with recommendations for such
legislation and administrative action as the Comptroller General of the
United
States determines to be appropriate.
C
National Uniform
Policy on Advance Care Planning
141.
Study and report by the Secretary regarding
the establishment and implementation of a national uniform policy on
advance
directives
(a)
Study
(1)
In general
The Secretary, acting through the Office of
the Assistant Secretary for Planning and Evaluation, shall conduct a
thorough
study of all matters relating to the establishment and implementation of a
national uniform policy on advance directives for individuals receiving
items
and services under titles XVIII, XIX, or XXI of the
Social Security Act (42 U.S.C. 1395 et
seq., 1396 et seq., or 1397aa et seq.).
(2)
Matters studied
The matters studied by the Secretary under
paragraph (1) shall include issues concerning—
(A) family satisfaction that a patient’s
wishes, as stated in the patient’s advance directive, were carried out;
(B) the portability of advance directives,
including cases involving the transfer of an individual from 1 health care
setting to another;
(C) immunity from civil liability and criminal
responsibility for health care providers that follow the instructions in
an
individual’s advance directive that was validly executed in, and
consistent
with the laws of, the State in which it was executed;
(D) conditions under which an advance directive
is operative;
(E) revocation of an advance directive by an
individual;
(F) the criteria used by States for determining
that an individual has a terminal condition;
(G) surrogate decisionmaking regarding
end-of-life care;
(H) the provision of adequate palliative care
(as defined in paragraph (3)), including pain management;
(I) adequate and timely referrals to hospice
care programs; and
(J) the end-of-life
care needs of children and their families.
(3)
Palliative care
For purposes of paragraph (2)(H), the term
palliative care means interdisciplinary care for individuals with
a life-threatening illness or injury relating to pain and symptom
management
and psychological, social, and spiritual needs and that seeks to improve
the
quality of life for the individual and the individual’s family.
(b)
Report to congress
Not later than 18 months after the date of
enactment of this Act, the Secretary shall submit to Congress a report on
the
study conducted under subsection (a), together with recommendations for
such
legislation and administrative actions as the Secretary considers
appropriate.
(c)
Consultation
In conducting the study and developing the
report under this section, the Secretary shall consult with the Uniform
Law
Commissioners, and other interested parties.
II
Compassionate
Care
A
Workforce
development
I
Education and
training
201.
National
Geriatric and Palliative Care Services Corps
Section 331 of the Public Health Service Act
(42 U.S.C. 254d) is amended—
(1) by redesignating subsection (j) as
subsection (k); and
(2) by inserting
after subsection (i), the following:
(j)
National
Geriatric and Palliative Care Services Corps
(1)
Establishment
Not
later than January 1, 2017, the Secretary shall establish within
the National
Health Service Corps a National Geriatric and Palliative Care
Services Corps
(referred to in this subsection as the Corps) which shall
consist of—
(A) such officers of
the Regular and Reserve Corps of the Service as the Secretary may
designate;
(B) such civilian
employees of the United States as the Secretary may appoint; and
(C) such other
individuals who are not employees of the United States.
(2)
Duties
The
Corps shall be utilized by the Secretary to provide geriatric and
palliative
care services within health professional shortage areas.
(3)
Application of
provisions
The loan-forgiveness, scholarship, and direct
financial incentives programs provided for under this section shall
apply to
physicians, nurses, and other health professionals (as identified
by the
Secretary) with respect to the training necessary to enable such
individuals to
become geriatric or palliative care specialists and provide
geriatric and
palliative care services in health professional shortage areas.
(4)
Report
Not
later than 6 months prior to the date on which the Secretary
establishes the
Corps under paragraph (1), the Secretary shall submit to Congress a
report
concerning the organization of the Corps, the application process
for
membership in the Corps, and the funding necessary for the Corps
(targeted by
profession and by
specialization).
.
202.
Exemption of
palliative medicine fellowship training from Medicare graduate medical
education caps
(a)
Direct graduate
medical education
Section 1886(h)(4)(F) of the
Social Security Act (42 U.S.C.
1395ww(h)(4)(F)) is amended—
(1) in clause (i), by
inserting clause (iii) and after subject to;
and
(2) by adding at the
end the following new clause:
(iii)
Increase
allowed for palliative medicine fellowship training
For cost
reporting periods beginning on or after January 1, 2016, in
applying clause
(i), there shall not be taken into account full-time equivalent
residents in
the field of allopathic or osteopathic medicine who are in
palliative medicine
fellowship training that is approved by the Accreditation Council
for Graduate
Medical
Education.
.
(b)
Indirect
Medical Education
Section 1886(d)(5)(B) of the
Social Security Act (42 U.S.C.
1395ww(d)(5)(B)) is amended—
(1) by redesignating the second clause (x), as added by section 5505(b) of the Patient Protection and
Affordable Care Act (Public Law 111–148), as clause (xi) and moving such
clause 4 ems to the left, and realigning the left margins of subclauses
(II) and (III) of such clause and items (aa), (bb), (cc), and (dd) of
subclause (II) of such clause appropriately; and
(2) by adding at the end the following new clause:
(xii) Clause (iii) of subsection (h)(4)(F)
shall apply to clause (v) in the same manner and for the same
period as such
clause (iii) applies to clause (i) of such
subsection.
.
203.
Medical school
curricula
(a)
In
general
The Secretary, in consultation with the Association of
American Medical Colleges, shall establish guidelines for the imposition
by
medical schools of a minimum amount of end-of-life training as a
requirement
for obtaining a Doctor of Medicine degree in the field of allopathic or
osteopathic medicine.
(b)
Training
Under
the guidelines established under subsection (a), minimum training shall
include—
(1) training in how
to discuss and help patients and their loved ones with advance care
planning;
(2) with respect to
students and trainees who will work with children, specialized pediatric
training;
(3) training in the
continuum of end-of-life services and supports, including palliative care
and
hospice;
(4) training in how
to discuss end-of-life care with dying patients and their loved ones;
and
(5) medical and legal
issues training.
(c)
Distribution
Not
later than January 1, 2016, the Secretary shall disseminate the guidelines
established under subsection (a) to medical schools.
(d)
Compliance
Effective
beginning not later than July 1, 2017, a medical school that is receiving
Federal assistance shall be required to implement the guidelines
established
under subsection (a). A medical school that the Secretary determines is
not
implementing such guidelines shall not be eligible for Federal
assistance.
B
Coverage under
Medicare, Medicaid, and CHIP
I
Coverage of
advance care planning
211.
Medicare,
Medicaid, and CHIP coverage
(a)
Medicare
(1)
In
general
Section 1861 of the Social
Security Act (42 U.S.C. 1395x) is amended—
(A) in subsection
(s)(2)—
(i) by
striking and at the end of subparagraph (EE);
(ii) by
adding and at the end of subparagraph (FF); and
(iii) by adding at
the end the following new subparagraph:
(GG) advance care
planning consultation (as defined in subsection
(iii)(1));
;
and
(B) by adding at the
end the following new subsection:
(iii)
Advance care planning consultation
(1) Subject to paragraphs (3) and (4), the term
advance care planning consultation means a consultation between
the individual and a practitioner described in paragraph (2)
regarding advance
care planning, if, subject to subparagraphs (A) and (B) of
paragraph (3), the
individual involved has not had such a consultation within the last
5 years.
Such consultation shall include the following:
(A) An explanation by the practitioner of
advance care planning, including key questions and considerations,
important
steps, and suggested people to talk to.
(B) An explanation by the practitioner of
advance directives, including living wills and durable powers of
attorney, and
their uses.
(C) An explanation by the practitioner of
the role and responsibilities of a health care proxy.
(D) The provision by the practitioner of a
list of national and State-specific resources to assist consumers
and their
families with advance care planning, including the national
toll-free hotline,
the advance care planning clearinghouses, and State legal service
organizations
(including those funded through the Older Americans Act).
(E) An explanation by the practitioner of
the continuum of end-of-life services and supports available,
including
palliative care and hospice, and benefits for such services and
supports that
are available under this title.
(F)
(i) Subject to clause (ii),
an explanation of orders regarding life sustaining treatment or
similar orders,
which shall include—
(I) the reasons why the development of
such an order is beneficial to the individual and the individual’s
family and
the reasons why such an order should be updated periodically as the
health of
the individual changes;
(II) the information needed for an individual or
legal surrogate to make informed decisions regarding the completion
of such an
order; and
(III) the identification of resources
that an individual may use to determine the requirements of the
State in which
such individual resides so that the treatment wishes of that
individual will be
carried out if the individual is unable to communicate those
wishes, including
requirements regarding the designation of a surrogate decisionmaker
(also known
as a health care proxy).
(ii) The Secretary may limit the
requirement for explanations under clause (i) to consultations
furnished in
States, localities, or other geographic areas in which orders
described in such
clause have been widely adopted.
(2) A practitioner described in this
paragraph is—
(A) a physician (as defined in subsection
(r)(1)); and
(B) a nurse practitioner or physician's
assistant who has the authority under State law to sign orders for
life
sustaining treatments.
(3)
(A) An initial preventive
physical examination under subsection (ww), including any related
discussion
during such examination, shall not be considered an advance care
planning
consultation for purposes of applying the 5-year limitation under
paragraph
(1).
(B) An advance care planning consultation
with respect to an individual shall be conducted more frequently
than provided
under paragraph (1) if there is a significant change in the health
condition of
the individual, including diagnosis of a chronic, progressive,
life-limiting
disease, a life-threatening or terminal diagnosis or
life-threatening injury,
or upon admission to a skilled nursing facility, a long-term care
facility (as
defined by the Secretary), or a hospice program.
(4) A consultation under this subsection
may include the formulation of an order regarding life sustaining
treatment or
a similar order.
(5)
(A) For purposes of this
section, the term order regarding life sustaining treatment means,
with respect to an individual, an actionable medical order relating
to the
treatment of that individual that—
(i) is signed and dated by a physician (as
defined in subsection (r)(1)) or another health care professional
(as specified
by the Secretary and who is acting within the scope of the
professional’s
authority under State law in signing such an order) and is in a
form that
permits it to stay with the patient and be followed by health care
professionals and providers across the continuum of care, including
home care,
hospice, long-term care, community and assisted living residences,
skilled
nursing facilities, inpatient rehabilitation facilities, hospitals,
and
emergency medical services;
(ii) effectively communicates the individual’s
preferences regarding life sustaining treatment, including an
indication of the
treatment and care desired by the individual;
(iii) is uniquely identifiable and standardized
within a given locality, region, or State (as identified by the
Secretary);
(iv) is portable across care settings;
and
(v) may incorporate any advance directive
(as defined in section 1866(f)(3)) if executed by the individual.
(B) The level of treatment indicated
under subparagraph (A)(ii) may range from an indication for full
treatment to
an indication to limit some or all or specified interventions. Such
indicated
levels of treatment may include indications respecting, among other
items—
(i) the intensity of medical intervention
if the patient is pulseless, apneic, or has serious cardiac or
pulmonary
problems;
(ii) the individual’s desire regarding
transfer to a hospital or remaining at the current care setting;
(iii) the use of antibiotics; and
(iv) the use of artificially administered
nutrition and
hydration.
.
(2)
Payment
Section 1848(j)(3) of the Social Security
Act (42 U.S.C. 1395w–4(j)(3)) is amended by inserting (2)(GG),
after (including administration of the health risk assessment),.
(3)
Frequency
Limitation
Section 1862(a) of the Social Security Act (42 U.S.C. 1395y(a)) is
amended—
(A) in paragraph
(1)—
(i) in
subparagraph (O), by striking and at the end;
(ii) in
subparagraph (P), by striking the semicolon at the end and inserting ,
and; and
(iii) by adding at
the end the following new subparagraph:
(Q) in the case of advance care planning
consultations (as defined in section 1861(iii)(1)), which are
performed more
frequently than is covered under such
section;
;
and
(B) in paragraph (7),
by striking or (P) and inserting (P), or
(Q).
(4)
Effective
Date
The amendments made by this subsection shall apply to
consultations furnished on or after January 1, 2016.
(b)
Medicaid
(1)
Mandatory
benefit
Section 1902(a)(10)(A) of the Social Security Act (42
U.S.C. 1396a(a)(10)(A)) is amended in the matter preceding clause (i) by
striking and (28) and inserting (28), and
(29).
(2)
Medical
assistance
Section 1905 of such Act (42 U.S.C. 1396d) is
amended—
(A) in subsection
(a)—
(i) in paragraph
(28), by striking and at the end;
(ii) by redesignating
paragraph (29) as paragraph (30); and
(iii) by inserting
after paragraph (28) the following new paragraph:
(29) advance care
planning consultations (as defined in subsection
(ee));
;
and
(B) by adding at the
end the following:
(ee)
(1) For purposes of
subsection (a)(29), the term advance care planning consultation
means a consultation between the individual and a practitioner
described in
paragraph (2) regarding advance care planning, if, subject to
paragraph (3),
the individual involved has not had such a consultation within the
last 5
years. Such consultation shall include the following:
(A) An explanation by the practitioner of
advance care planning, including key questions and considerations,
important
steps, and suggested people to talk to.
(B) An explanation by the practitioner of
advance directives, including living wills and durable powers of
attorney, and
their uses.
(C) An explanation by the practitioner of
the role and responsibilities of a health care proxy.
(D) The provision by the practitioner of a
list of national and State-specific resources to assist consumers
and their
families with advance care planning, including the national
toll-free hotline,
the advance care planning clearinghouses, and State legal service
organizations
(including those funded through the Older Americans Act).
(E) An explanation by the practitioner of
the continuum of end-of-life services and supports available,
including
palliative care and hospice, and benefits for such services and
supports that
are available under this title.
(F)
(i) Subject to clause (ii),
an explanation of orders for life sustaining treatments or similar
orders,
which shall include—
(I) the reasons why the development of
such an order is beneficial to the individual and the individual’s
family and
the reasons why such an order should be updated periodically as the
health of
the individual changes;
(II) the information needed for an individual or
legal surrogate to make informed decisions regarding the completion
of such an
order; and
(III) the identification of resources
that an individual may use to determine the requirements of the
State in which
such individual resides so that the treatment wishes of that
individual will be
carried out if the individual is unable to communicate those
wishes, including
requirements regarding the designation of a surrogate decisionmaker
(also known
as a health care proxy).
(ii) The Secretary may limit the
requirement for explanations under clause (i) to consultations
furnished in
States, localities, or other geographic areas in which orders
described in such
clause have been widely adopted.
(2) A practitioner described in this
paragraph is—
(A) a physician (as defined in section
1861(r)(1)); and
(B) a nurse practitioner or physician's
assistant who has the authority under State law to sign orders for
life
sustaining treatments.
(3) An advance care planning consultation
with respect to an individual shall be conducted more frequently
than provided
under paragraph (1) if there is a significant change in the health
condition of
the individual including diagnosis of a chronic, progressive,
life-limiting
disease, a life-threatening or terminal diagnosis or
life-threatening injury,
or upon admission to a nursing facility, a long-term care facility
(as defined
by the Secretary), or a hospice program.
(4) A
consultation under this subsection may include the formulation of
an order
regarding life sustaining treatment or a similar order.
(5) For purposes of this subsection, the term
orders regarding life sustaining treatment has the meaning given
that term in section
1861(iii)(5).
.
(c)
CHIP
(1)
Child health
assistance
Section 2110(a) of the Social Security Act (42 U.S.C.
1397jj) is amended—
(A) by redesignating
paragraph (28) as paragraph (29); and
(B) by inserting
after paragraph (27), the following:
(28) Advance care
planning consultations (as defined in section
1905(ee)).
.
(2)
Mandatory
coverage
(A)
In
general
Section 2103 of such Act (42 U.S.C. 1397cc), is
amended—
(i) in
subsection (a), in the matter preceding paragraph (1), by striking and
(7) and inserting (7), and (9); and
(ii) in
subsection (c), by adding at the end the following:
(9)
End-of-life
care
The child health assistance provided to a targeted
low-income child shall include coverage of advance care planning
consultations
(as defined in section 1905(ee) and at the same payment rate as the
rate that
would apply to such a consultation under the State plan under title
XIX).
.
(B)
Conforming
amendment
Section 2102(a)(7)(B) of such Act (42 U.S.C.
1397bb(a)(7)(B)) is amended by striking section 2103(c)(5) and
inserting paragraphs (5) and (9) of section 2103(c).
(d)
Definition of
advance directive under Medicare, Medicaid, and CHIP
(1)
Medicare
Section
1866(f)(3) of the Social Security Act (42 U.S.C. 1395cc(f)(3)) is amended
by
striking means and all that follows through the period and
inserting means a living will, medical directive, health care power of
attorney, durable power of attorney, or other written statement by a
competent
individual that is recognized under State law and indicates the
individual's
wishes regarding medical treatment in the event of future incompetence.
Such
term includes an advance health care directive and a health care directive
recognized under State law..
(2)
Medicaid and
chip
Section 1902(w)(4) of such Act (42 U.S.C. 1396a(w)(4)) is
amended by striking means and all that follows through the
period and inserting means a living will, medical directive, health care
power of attorney, durable power of attorney, or other written statement
by a
competent individual that is recognized under State law and indicates the
individual's wishes regarding medical treatment in the event of future
incompetence. Such term includes an advance health care directive and a
health
care directive recognized under State law..
(e)
Effective
date
The amendments made by this section take effect January 1,
2015.
II
Hospice
221.
Adoption of
MedPAC hospice payment methodology recommendations
Section
1814(i) of the Social Security Act (42 U.S.C. 1395f(i)) is amended by
adding at
the end the following new paragraph:
(8)
(A) The Secretary shall conduct an evaluation
of the recommendations of the Medicare Payment Commission for
reforming the
hospice care benefit under this title that are contained in chapter
6 of the
Commission's report entitled Report to Congress: Medicare Payment Policy
(March 2009), including the impact that such recommendations if
implemented would have on access to care and the quality of care.
In conducting
such evaluation, the Secretary shall take into account data
collected in
accordance with section 263(b) of the Advance Planning and Compassionate Care Act of 2014.
(B) Based on the results of the
examination conducted under subparagraph (A), the Secretary shall
make
appropriate refinements to the recommendations described in
subparagraph (A).
Such refinements shall take into account—
(i) the impact on patient populations
with longer that average lengths of stay;
(ii) the impact on populations with
shorter that average lengths of stay; and
(iii) the utilization patterns of
hospice providers in underserved areas, including rural hospices.
(C) Not later than January 1, 2018, the
Secretary shall submit to Congress a report that contains a
detailed
description of—
(i) the refinements determined
appropriate by the Secretary under subparagraph (B);
(ii) the revisions that the Secretary
will implement through regulation under this title pursuant to
subparagraph
(D); and
(iii) the revisions that the Secretary
determines require additional legislative action by Congress.
(D)
(i) The Secretary shall implement the
recommendations described in subparagraph (A), as refined under
subparagraph
(B).
(ii) Subject to clause (iii), the
implementation of such recommendations shall apply to hospice care
furnished on
or after January 1, 2019.
(iii) The Secretary shall establish an
appropriate transition to the implementation of such
recommendations.
(E) For purposes of carrying out the
provisions of this paragraph, the Secretary shall provide for the
transfer,
from the Federal Hospital Insurance Trust Fund under section 1817,
of such sums
as may be necessary to the Centers for Medicare & Medicaid Services Program
Management
Account.
.
222.
Removing
hospice inpatient days in setting per diem rates for critical access
hospitals
Section 1814(l) of
the Social Security Act (42 U.S.C. 1395f(l)), as amended by section
4102(b)(2)
of the HITECH Act (Public Law 111–5), is amended by adding at the end the
following new paragraph:
(6) For cost reporting periods beginning on or
after January 1, 2016, the Secretary shall remove
Medicare-certified hospice
inpatient days from the calculation of per diem rates for inpatient
critical
access hospital services.
.
223.
Hospice
payments for dual eligible individuals residing in long-term care
facilities
(a)
In
general
Section 1888 of the
Social Security Act (42 U.S.C. 1395yy) is amended by adding at the end the
following new subsection:
(i)
Payments for
Dual Eligible Individuals Residing in Long-Term Care Facilities
For cost reporting periods beginning on or
after January 1, 2016, the Secretary, acting through the
Administrator of the
Centers for Medicare & Medicaid Services, shall establish procedures under
which payments for room and board under the State Medicaid plan
with respect to
an applicable individual are made directly to the long-term care
facility (as
defined by the Secretary for purposes of title XIX) the individual
is a
resident of. For purposes of the preceding sentence, the term applicable
individual means an individual who is entitled to or enrolled for
benefits under part A or enrolled for benefits under part B and is
eligible for
medical assistance for hospice care under a State plan under title
XIX.
.
(b)
State plan
requirement
(1)
In
general
Section 1902(a) of the Social Security Act (42 U.S.C.
1396a(a)) is amended—
(A) in paragraph
(74), by striking and at the end;
(B) in paragraph
(80), by striking and at the end;
(C) in paragraph (81), by striking the period at the end and inserting ; and;
and
(D) by inserting
after paragraph (81) the following new paragraph:
(82) provide that the
State will make payments for room and board with respect to
applicable
individuals in accordance with section
1888(i).
.
(2)
Effective
date
(A)
In
general
Except as provided in subparagraph (B), the amendments
made by paragraph (1) take effect on January 1, 2016.
(B)
Extension of
effective date for state law amendment
In the case of a State
plan under title XIX of the Social Security Act (42 U.S.C. 1396 et seq.)
which
the Secretary determines requires State legislation in order for the plan
to
meet the additional requirements imposed by the amendments made by
paragraph
(1), the State plan shall not be regarded as failing to comply with the
requirements of such title solely on the basis of its failure to meet
these
additional requirements before the first day of the first calendar quarter
beginning after the close of the first regular session of the State
legislature
that begins after the date of enactment of this Act. For purposes of the
previous sentence, in the case of a State that has a 2-year legislative
session, each year of the session is considered to be a separate regular
session of the State legislature.
224.
Delineation of
respective care responsibilities of hospice programs and long-term care
facilities
Section 1888 of the
Social Security Act (42 U.S.C. 1395yy), as amended by section 223(a), is
amended by adding at the end the following new subsection:
(j)
Delineation of
respective care responsibilities of hospice programs and long-term
care
facilities
Not later than July 1, 2016, the Secretary, acting
through the Administrator of the Centers for Medicare & Medicaid Services,
shall delineate and enforce the respective care responsibilities of
hospice
programs and long-term care facilities (as defined by the Secretary
for
purposes of title XIX) with respect to individuals residing in such
facilities
who are furnished hospice
care.
.
225.
Adoption of
MedPAC hospice program eligibility certification and recertification
recommendations
In accordance
with the recommendations of the Medicare Payment Advisory Commission
contained
in the March 2009 report entitled Report to Congress: Medicare Payment
Policy, section 1814(a)(7) of the Social Security Act (42 U.S.C.
1395f(a)(7)) is amended—
(1) in subparagraph (C), by striking
and at the end; and
(2) by adding at the end the following new
subparagraph:
(E) on or after January 1, 2016—
(i) a hospice physician or advance practice
nurse visits the individual to determine continued eligibility of
the
individual for hospice care prior to the 180th-day recertification
and each
subsequent recertification under subparagraph (A)(ii) and attests
that such
visit took place (in accordance with procedures established by the
Secretary,
in consultation with the Administrator of the Centers for Medicare &
Medicaid Services); and
(ii) any
certification or recertification under subparagraph (A) includes a
brief
narrative describing the clinical basis for the individual’s
prognosis (in
accordance with procedures established by the Secretary, in
consultation with
the Administrator of the Centers for Medicare & Medicaid Services);
and
.
226.
Concurrent
care for children
(a)
Permitting
Medicare hospice beneficiaries 18 years of age or younger To receive
curative
care
(1)
In general
Section 1812 of the Social Security Act (42
U.S.C. 1395d) is amended—
(A) in subsection (a)(4), by inserting
(subject to the second sentence of subsection (d)(2)(A)) after
in lieu of certain other benefits; and
(B) in subsection (d)—
(i) in paragraph (1), by inserting ,
subject to the second sentence of paragraph (2)(A), after
instead; and
(ii) in paragraph (2)(A), by adding at the end
the following new sentence: Clause (ii)(I) shall not apply to an
individual who is 18 years of age or younger.
(2)
Conforming amendment
Section 1862(a)(1)(C) of the Social
Security Act (42 U.S.C. 1395y(a)(1)(C)) is amended inserting subject to
the second sentence of section 1812(d)(2)(A), after hospice
care,.
(b)
Application to
Medicaid and CHIP
(1)
Medicaid
Section
1905(o)(1)(A) of the Social Security Act (42 U.S.C. 1395d(o)(1)(A)) is
amended
by inserting (subject, in the case of an individual who is a child, to
the second sentence of such section) after section
1812(d)(2)(A).
(2)
CHIP
Section
2110(a)(23) of the Social Security Act (42 U.S.C. 1397jj(a)(23)) is
amended by
striking (concurrent and all that follows through the period and inserting (concurrent, in the case of an individual who is a child, with
care related to the treatment of the individual's condition with respect
to
which a diagnosis of terminal illness has been made)..
(c)
Effective
date
The amendments made by
this section shall apply to items and services furnished on or after
January 1,
2016.
227.
Making hospice
a required benefit under Medicaid and CHIP
(a)
Mandatory
benefit
(1)
Medicaid
(A)
In
general
Section 1902(a)(10)(A) of the Social Security Act (42
U.S.C. 1396a(a)(10)(A)), as amended by section 211(b)(1), is amended in
the
matter preceding clause (i) by inserting (18), after
(17),.
(B)
Conforming
amendment
Section 1902(a)(10)(C) of such Act (42 U.S.C.
1396a(a)(10)(C)) is amended—
(i) in
clause (iii)—
(I) in subclause (I),
by inserting and hospice care after ambulatory
services; and
(II) in subclause
(II), by inserting and hospice care after delivery
services; and
(ii) in
clause (iv), by inserting and (18) after
(17).
(2)
CHIP
Section
2103(c)(9) of such Act (42 U.S.C. 1397cc(c)(9)), as added by section
211(c)(2)(A), is amended by inserting and hospice care before
the period.
(b)
Effective
date
The amendments made
subsection (a) take effect on January 1, 2016.
228.
Medicare
Hospice payment model demonstration projects
(a)
Establishment
Not
later than July 1, 2017, the Secretary, acting through the Administrator
of the
Centers for Medicare & Medicaid Services and the Director of the Agency for
Healthcare Research and Quality, shall conduct demonstration projects to
examine ways to improve how the Medicare hospice care benefit predicts
disease
trajectory. Projects shall include the following models:
(1) Models that
better and more appropriately care for, and transition as needed, patients
in
their last years of life who need palliative care, but do not qualify for
hospice care under the Medicare hospice eligibility criteria.
(2) Models that
better and more appropriately care for long-term patients who are not
recertified in hospice but still need palliative care.
(3) Any other models
determined appropriate by the Secretary.
(b)
Waiver authority
The Secretary may waive compliance of such
requirements of titles XI and XVIII of the Social
Security Act as the Secretary determines necessary to conduct the
demonstration projects under this section.
(c)
Reports
The Secretary shall submit to Congress
periodic reports on the demonstration projects conducted under this
section.
229.
MedPAC studies
and reports
(a)
Study and
report regarding an alternative payment methodology for hospice care under
the
Medicare program
(1)
Study
The
Medicare Payment Advisory Commission (in this section referred to as the
Commission) shall conduct a study on the establishment of a
reimbursement system for hospice care furnished under the Medicare program
that
is based on diagnoses. In conducting such study, the Commission shall use
data
collected under new provider data requirements. Such study shall include
an
analysis of the following:
(A) Whether such a
reimbursement system better meets patient needs and better corresponds
with
provider resource expenditures than the current system.
(B) Whether such a
reimbursement system improves quality, including facilitating
standardization
of care toward best practices and diagnoses-specific clinical pathways in
hospice.
(C) Whether such a
reimbursement system could address concerns about the blanket 6-month
terminal
prognosis requirement in hospice.
(D) Whether such a
reimbursement system is more cost effective than the current system.
(E) Any other areas
determined appropriate by the Commission.
(2)
Report
Not
later than June 15, 2018, the Commission shall submit to Congress a report
on
the study conducted under subsection (a) together with recommendations for
such
legislation and administrative action as the Commission determines
appropriate.
(b)
Study and
report regarding rural hospice transportation costs under the Medicare
program
(1)
Study
The
Commission shall conduct a study on rural Medicare hospice transportation
mileage to determine potential Medicare reimbursement changes to account
for
potential higher costs.
(2)
Report
Not
later than June 15, 2018, the Commission shall submit to Congress a report
on
the study conducted under subsection (a) together with recommendations for
such
legislation and administrative action as the Commission determines
appropriate.
(c)
Evaluation of
reimbursement disincentives To elect medicare hospice within the medicare
skilled nursing facility benefit
(1)
Study
The
Commission shall conduct a study to determine potential Medicare
reimbursement
changes to remove Medicare reimbursement disincentives for patients in a
skilled nursing facility who want to elect hospice.
(2)
Report
Not
later than June 15, 2018, the Commission shall submit to Congress a report
on
the study conducted under subsection (a) together with recommendations for
such
legislation and administrative action as the Commission determines
appropriate.
230.
HHS
Evaluations
(a)
Evaluation of
Access to Hospice and Hospital-Based Palliative Care
(1)
Evaluation
The Secretary, acting through the
Administrator of the Health Resources and Services Administration, shall
conduct an evaluation of geographic areas and populations underserved by
hospice and hospital-based palliative care to identify potential barriers
to
access.
(2)
Report
Not later than December 31, 2017, the
Secretary shall report to Congress, on the evaluation conducted under
subsection (a) together with recommendations for such legislation and
administrative action as the Secretary determines appropriate to address
barriers to access to hospice and hospital-based palliative care.
(b)
Evaluation of
awareness and use of hospice respite care under Medicare, Medicaid, and
CHIP
(1)
Evaluation
The Secretary, acting through the Director
of the Centers for Medicare and Medicaid Services, shall evaluate the
awareness
and use of hospice respite care by informal caregivers of beneficiaries
under
Medicare, Medicaid, and CHIP.
(2)
Report
Not later than December 31, 2015, the
Secretary shall report to Congress, on the evaluation conducted under
subsection (a) together with recommendations for such legislation and
administrative action as the Secretary determines appropriate to increase
awareness or use of hospice respite care under Medicare, Medicaid, and
CHIP.
C
Quality
Improvement
241.
Patient
satisfaction surveys
Not later
than January 1, 2017, the Secretary, acting through the Administrator of
the
Centers for Medicare & Medicaid Services, shall establish a mechanism
for—
(1) collecting information from patients (or
their health care proxies or families members in the event patients are
unable
to speak for themselves) in relevant provider settings regarding their
care at
the end of life; and
(2) incorporating such information in a timely
manner into mechanisms used by the Administrator to provide quality of
care
information to consumers, including the Hospital Compare and Nursing Home
Compare websites maintained by the Administrator.
242.
Development of
core end-of-life care quality measures across each relevant provider
setting
(a)
In
general
The Secretary, acting
through the Administrator of the Agency for Healthcare Research and
Quality (in
this section referred to as the Administrator) and in
consultation with the Director of the National Institutes of Health, shall
require specific end-of-life quality measures for each relevant provider
setting, as identified by the Administrator, in accordance with the
requirements of subsection (b).
(b)
Requirements
For purposes of subsection (a), the
requirements specified in this subsection are the following:
(1) Selection of the
specific measure or measures for an identified provider setting shall
be—
(A) based on an
assessment of what is likely to have the greatest positive impact on
quality of
end-of-life care in that setting; and
(B) made in
consultation with affected providers and public and private organizations,
that
have developed such measures.
(2) The measures may
be structure-oriented, process-oriented, or outcome-oriented, as
determined
appropriate by the Administrator.
(3) The Administrator
shall ensure that reporting requirements related to such measures are
imposed
consistent with other applicable laws and regulations, and in a manner
that
takes into account existing measures, the needs of patient populations,
and the
specific services provided.
(4) Not later than—
(A) April 1, 2016, the Secretary shall
disseminate the reporting requirements to all affected providers; and
(B) April 1, 2017, initial reporting relating
to the measures shall begin.
243.
Accreditation
of Hospital-Based Palliative Care Programs
(a)
In
General
The Secretary, acting through the Director of the Agency
for Healthcare Research and Quality, shall designate a public or private
agency, entity, or organization to develop requirements, standards, and
procedures for accreditation of hospital-based palliative care programs.
(b)
Reporting
Not
later than January 1, 2017, the Secretary shall prepare and submit a
report to
Congress on the proposed accreditation process for hospital-based
palliative
care programs.
(c)
Accreditation
Not
later than July 1, 2017, the Secretary shall—
(1) establish and
promulgate standards and procedures for accreditation of hospital-based
palliative care programs; and
(2) designate an
agency, entity, or organization that shall be responsible for certifying
such
programs in accordance with the standards established under paragraph
(1).
(d)
Definitions
For
the purposes of this section:
(1) The term
hospital-based palliative care program means a hospital-based
program that is comprised of an interdisciplinary team that specializes in
providing palliative care services and consultations in a variety of
health
care settings, including hospitals, nursing homes, and home and
community-based
services.
(2) The term
interdisciplinary team means a group of health care professionals
(consisting of, at a minimum, a doctor, a nurse, and a social worker) that
have
received specialized training in palliative care.
244.
Survey and
data requirements for all Medicare participating hospice programs
(a)
Hospice
surveys
Section 1861(dd) of
the Social Security Act (42 U.S.C. 1395x(dd)) is amended by adding at the
end
the following new paragraph:
(6) In accordance with the recommendations of
the Medicare Payment Advisory Commission contained in the March
2009 report
entitled Report to Congress: Medicare Payment Policy, the
Secretary shall establish, effective July 1, 2015, the following
survey
requirements for hospice programs:
(A) Any hospice program seeking initial
certification under this title on or after that date shall be
subject to an
initial survey by an appropriate State or local agency, or an
approved
accreditation agency, not later than 6 months after the program
first seeks
such certification.
(B) All hospice programs certified for
participation under this title shall be subject to a standard
survey by an
appropriate State or local agency, or an approved accreditation
agency, at
least every 3 years after initially being so
certified.
.
(b)
Required
hospice resource inputs data
Section 1861(dd) of the Social
Security Act (42 U.S.C. 1395x(dd)), as amended by subsection (a), is
amended—
(1) in paragraph
(2)—
(A) in subparagraph
(F), by striking and at the end;
(B) by redesignating
subparagraph (G) as subparagraph (H); and
(C) by inserting
after subparagraph (F) the following new subparagraph:
(G) complies with the reporting
requirements under paragraph (7); and
;
and
(2) by adding at the
end the following new paragraph:
(7)
(A) In accordance with the recommendations of
the Medicare Payment Advisory Commission for additional data (as
contained in
the March 2009 report entitled Report to Congress: Medicare Payment
Policy), beginning January 1, 2016, a hospice program shall report to
the Secretary, in such form and manner, and at such intervals, as
the Secretary
shall require, the following data with respect to each patient
visit:
(i) Visit type (such as admission, routine,
emergency, education for family, other).
(ii) Visit length.
(iii) Professional or paraprofessional
disciplines involved in the visit, including nurse, social worker,
home health
aide, physician, nurse practitioner, chaplain or spiritual
counselor,
counselor, dietician, physical therapist, occupational therapist,
speech
language pathologist, music or art therapist, and including
bereavement and
support services provided to a family after a patient’s death.
(iv) Drugs and other therapeutic interventions
provided.
(v) Home medical equipment and other medical
supplies provided.
(B) In collecting the data required under
subparagraph (A), the Secretary shall ensure that the data are
reported in a
manner that allows for summarized cross-tabulations of the data by
patients’
terminal diagnoses, lengths of stay, age, sex, and
race.
.
D
Additional
reports, research, and evaluations
251.
National
Center On Palliative and End-of-Life Care
Part E of title IV of the Public Health
Service Act (42 U.S.C. 287 et seq.) is amended by adding at the end the
following:
7
National Center
on Palliative and End-of-Life Care
485J.
National
Center On Palliative and End-of-Life Care
(a)
Establishment
Not
later than July 1, 2016, there shall be established within the
National
Institutes of Health, a National Center on Palliative and
End-of-Life Care
(referred to in this section as the Center).
(b)
Purpose
The
general purpose of the Center is to conduct and support research
relating to
palliative and end-of-life care interventions and approaches.
(c)
Activities
The
Center shall—
(1) develop and
continuously update a research agenda with the goal of—
(A) providing a
better biomedical understanding of the end of life; and
(B) improving the
quality of care and life at the end of life; and
(2) provide funding
for peer-review-selected extra- and intra-mural research that
includes the
evaluation of existing, and the development of new, palliative and
end-of-life
care interventions and
approaches.
.
252.
National
Mortality Followback Survey
(a)
In
general
Not later than December 31, 2015, and annually
thereafter, the Secretary, acting through the Director of the Centers for
Disease Control and Prevention, shall renew and conduct the National
Mortality
Followback Survey (referred to in this section as the Survey) to
collect data on end-of-life care.
(b)
Purpose
The
purpose of the Survey shall be to gain a better understanding of current
end-of-life care in the United States.
(c)
Questions
(1)
In
general
In conducting the Survey, the Director of the Centers for
Disease Control and Prevention shall, at a minimum, include the following
questions with respect to the loved one of a respondent:
(A) Did he or she
have an advance directive, and if so, when it was completed.
(B) Did he or she
have an order for life-sustaining treatment, and if so, when was it
completed.
(C) Did he or she
have a durable power of attorney, and if so, when it was completed.
(D) Had he or she
discussed his or her wishes with loved ones, and if so, when.
(E) Had he or she
discussed his or her wishes with his or her physician, and if so, when.
(F) In the opinion of
the respondent, was he or she satisfied with the care he or she received
in the
last year of life and in the last week of life.
(G) Was he or she
cared for by hospice, and if so, when.
(H) Was he or she
cared for by palliative care specialists, and if so, when.
(I) Did he or she
receive effective pain management (if needed).
(J) What was the
experience of the main caregiver (including if such caregiver was the
respondent), and whether he or she received sufficient support in this
role.
(2)
Additional
questions
Additional questions to be asked during the Survey
shall be determined by the Director of the Centers for Disease Control and
Prevention on an ongoing basis with input from relevant research
entities.
253.
Demonstration
Projects for Use of Telemedicine Services in Advance Care Planning
(a)
In
General
Not later than July 1, 2018, the Secretary shall
establish a demonstration program to reimburse eligible entities for costs
associated with the use of telemedicine services (including equipment and
connection costs) to provide advance care planning consultations with
geographically distant physicians and their patients.
(b)
Duration
The
demonstration project under this section shall be conducted for at least a
3-year period.
(c)
Definitions
For
purposes of this section:
(1) The term
eligible entity means a physician or an advance practice nurse who
provides services pursuant to a hospital-based palliative care program (as
defined in section 262(d)(1)).
(2) The term
geographically distant has the meaning given that term by the
Secretary for purposes of conducting the demonstration program established
under this section.
(3) The term
telemedicine services means a service or consultation provided via
telecommunication equipment that allows an eligible entity to exchange or
discuss medical information with a patient or a health care professional
at a
separate location through real-time videoconferencing, or a similar
format, for
the purpose of providing health care diagnosis and treatment.
(d)
Funding
There
are authorized to be appropriated to the Secretary such sums as may be
necessary to carry out this section.
254.
Inspector
General investigation of fraud and abuse
In accordance with the recommendations of
the Medicare Payment Advisory Commission for additional data (as contained
in
the March 2009 report entitled Report to Congress: Medicare Payment
Policy), the Secretary shall direct the Office of the Inspector General
of the Department of Health and Human Services to investigate, not later
than
January 1, 2017, the following with respect to hospice benefit under
Medicare,
Medicaid, and CHIP:
(1) The prevalence of financial relationships
between hospices and long-term care facilities, such as nursing facilities
and
assisted living facilities, that may represent a conflict of interest and
influence admissions to hospice.
(2) Differences in patterns of nursing home
referrals to hospice.
(3) The appropriateness of enrollment practices
for hospices with unusual utilization patterns (such as high frequency of
very
long stays, very short stays, or enrollment of patients discharged from
other
hospices).
(4) The appropriateness of hospice marketing
materials and other admissions practices and potential correlations
between
length of stay and deficiencies in marketing or admissions practices.
255.
GAO study and report
on provider adherence to advance directives
Not later than January 1, 2017, the
Comptroller General of the United States shall conduct a study of the
extent to
which providers comply with advance directives under the Medicare and
Medicaid
programs and shall submit a report to Congress on the results of such
study,
together with such recommendations for administrative or legislative
changes as
the Comptroller General determines appropriate.