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II
118TH CONGRESS
1ST SESSION
S. 1845
To amend title XI of the Social Security Act to provide for the testing
of a community-based palliative care model.
IN THE SENATE OF THE UNITED STATES
JUNE 7, 2023
Ms. ROSEN (for herself, Mr. BARRASSO, Ms. BALDWIN, and Mrs. FISCHER)
introduced the following bill; which was read twice and referred to the
Committee on Finance
A BILL
To amend title XI of the Social Security Act to provide
for the testing of a community-based palliative care model.
Be it enacted by the Senate and House of Representa-
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tives of the United States of America in Congress assembled,
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SECTION 1. SHORT TITLE.
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This Act may be cited as the ‘‘Expanding Access to
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Palliative Care Act’’.
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SEC. 2. COMMUNITY-BASED PALLIATIVE CARE MODEL.
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Section 1115A of the Social Security Act (42 U.S.C.
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1315a) is amended—
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(1) in subsection (b)(2)(A), by adding at the
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end the following new sentence: ‘‘The models se-
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lected under this subparagraph shall include the
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testing of the model described in subsection (h).’’;
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and
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(2) by adding at the end the following new sub-
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section:
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‘‘(h)
COMMUNITY-BASED
PALLIATIVE
CARE
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MODEL.—
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‘‘(1) IN GENERAL.—The CMI shall develop and
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implement a model to provide community-based pal-
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liative care and care coordination for high-risk bene-
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ficiaries, in co-management with other providers of
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services and suppliers, aimed at improving outcomes
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and experience of care and reducing unnecessary or
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unwanted emergency department visits and hos-
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pitalizations (in this subsection referred to as the
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‘model’), and that is intended to replace the Medi-
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care Care Choices Model.
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‘‘(2) DURATION.—The model shall be imple-
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mented for a 5-year period, beginning not later than
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one year after the date of the enactment of this sub-
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section.
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‘‘(3) TARGET POPULATION.—
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‘‘(A) IN GENERAL.—The target population
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for the model is an individual—
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‘‘(i) entitled to, or enrolled for, bene-
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fits under part A of title XVIII; and
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‘‘(ii) with a diagnosis of a serious ill-
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ness or injury, which may include a diag-
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nosis of cancer, heart and vascular disease,
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pulmonary
disease,
human
immuno-
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deficiency virus/acquired immunodeficiency,
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Alzheimer’s and dementia, stroke, serious
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injury requiring rehabilitation including
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burns,
kidney
disease,
liver
disease,
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Amyotrophic lateral sclerosis, any neuro
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degenerative disease, or any other serious
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illness or injury the Secretary determines
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appropriate.
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‘‘(B) NO EXCLUSION FOR PRIOR USE OF
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HOSPICE CARE BENEFITS.—An individual shall
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not be excluded from participation in the model
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based on prior use of hospice care benefits dur-
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ing any period prior to such participation, re-
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gardless of the source of coverage for such ben-
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efits.
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‘‘(4) PARTICIPATING PROVIDERS.—Providers el-
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igible to participate under the model may include
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palliative care teams working as an independent
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practice or associated with a hospice program, home
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health agencies, hospitals, integrated health systems,
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and other facilities determined appropriate by the
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Secretary.
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‘‘(5)
TEAM-BASED
APPROACH.—Under
the
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model, at least one member of the multi-disciplinary
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palliative care team shall be certified in hospice and
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palliative care. This is a co-management model with
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palliative care aligning with primary and specialist
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care for a team-based approach. Care must be co-
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ordinated across providers and community services
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for inclusion of all pain, symptom management, dis-
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ease-modifying and curative treatments, and other
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palliative care services.
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‘‘(6) LOCATION.—Care may be furnished under
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the model in any beneficiary ‘home’, including a
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caregiver’s residence, an extended care facility, or a
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community setting as appropriate based on the indi-
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vidual’s ability to access services. The model shall
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include access within an in-patient stay so long as
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the patient begins receiving palliative care services
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prior to admission. Services shall not be disrupted
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solely due to change in location from a residence to
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an in-patient setting, and shall be part of care co-
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ordination and care planning following hospital dis-
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charge.
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‘‘(7) SERVICES.—The model shall include items
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and services based on specific patient needs with re-
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spect to pain, symptom management, education, dis-
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ease modifying treatments, advance care planning
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and shared decision making, goals clarification, men-
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tal health services, family and caregiver support
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services, spiritual support care, personal care assist-
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ance, and stress reduction therapies. This includes a
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comprehensive assessment of symptoms and stress
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factors that impact quality of life.
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‘‘(8) ACCESS.—Care shall be available under
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the model 24 hours a day, 7 days a week, and 365
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days a year, including telehealth services. The CMI
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shall specifically consider the needs of rural and un-
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derserved areas and adjust accordingly to ensure eq-
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uitable access to care. A broad range of providers
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must be included with no geographic limitations.
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‘‘(9) METRICS.—The CMI shall assess the
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model by comparing participants to other members
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of the target population who are receiving care out-
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side of the model, including with respect to the fol-
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lowing:
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‘‘(A) Demographics (including age, diag-
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nosis, residence type, medical encounters in pre-
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ceding 12 months leading to enrollment, geo-
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graphic location (such as urban or rural) and
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others as determined by the CMI).
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‘‘(B) Impact on utilization of items and
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services under title XVIII (such as emergency
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department services, hospital observation serv-
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ices, inpatient admissions, and intensive care
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unit (ICU) stays).
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‘‘(C) Election of hospice care.
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‘‘(D) Duration of hospice care.
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‘‘(E) Care Experience (beneficiary and
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caregiver).’’.
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Æ
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