Medicare Program; FY 2018 Hospice Wage Index and Payment Rate Update and Hospice Quality Reporting Requirements, 20750-20792 [2017-08563]
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Federal Register / Vol. 82, No. 84 / Wednesday, May 3, 2017 / Proposed Rules
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Part 418
[CMS–1675–P]
RIN 0938–AT00
Medicare Program; FY 2018 Hospice
Wage Index and Payment Rate Update
and Hospice Quality Reporting
Requirements
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
AGENCY:
This proposed rule would
update the hospice wage index,
payment rates, and cap amount for fiscal
year (FY) 2018. Additionally, this rule
proposes changes to the hospice quality
reporting program, including proposing
new quality measures, soliciting
feedback on an enhanced data collection
instrument, and describing plans to
publicly display quality measures and
other hospice data.
DATES: To be assured consideration,
comments must be received at one of
the addresses provided below, no later
than 5 p.m. on June 26, 2017.
ADDRESSES: In commenting, please refer
to file code CMS–1675–P. Because of
staff and resource limitations, we cannot
accept comments by facsimile (FAX)
transmission.
You may submit comments in one of
four ways (please choose only one of the
ways listed):
1. Electronically. You may submit
electronic comments on this regulation
to https://www.regulations.gov. Follow
the ‘‘Submit a comment’’ instructions.
2. By regular mail. You may mail
written comments to the following
address ONLY: Centers for Medicare &
Medicaid Services, Department of
Health and Human Services, Attention:
CMS–1675–P, P.O. Box 8010, Baltimore,
MD 21244–1850.
Please allow sufficient time for mailed
comments to be received before the
close of the comment period.
3. By express or overnight mail. You
may send written comments to the
following address ONLY: Centers for
Medicare & Medicaid Services,
Department of Health and Human
Services, Attention: CMS–1675–P, Mail
Stop C4–26–05, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
4. By hand or courier. Alternatively,
you may deliver (by hand or courier)
your written comments ONLY to the
following addresses prior to the close of
the comment period:
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SUMMARY:
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a. For delivery in Washington, DC—
Centers for Medicare & Medicaid
Services, Department of Health and
Human Services, Room 445–G, Hubert
H. Humphrey Building, 200
Independence Avenue SW.,
Washington, DC 20201.
(Because access to the interior of the
Hubert H. Humphrey Building is not
readily available to persons without
Federal government identification,
commenters are encouraged to leave
their comments in the CMS drop slots
located in the main lobby of the
building. A stamp-in clock is available
for persons wishing to retain a proof of
filing by stamping in and retaining an
extra copy of the comments being filed.)
b. For delivery in Baltimore, MD—
Centers for Medicare & Medicaid
Services, Department of Health and
Human Services, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
If you intend to deliver your
comments to the Baltimore address, call
telephone number (410) 786–9994 in
advance to schedule your arrival with
one of our staff members.
Comments erroneously mailed to the
addresses indicated as appropriate for
hand or courier delivery may be delayed
and received after the comment period.
For information on viewing public
comments, see the beginning of the
SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT:
Debra Dean-Whittaker, (410) 786–
0848 for questions regarding the
CAHPS® Hospice Survey.
Cindy Massuda, (410) 786–0652 for
questions regarding the hospice quality
reporting program.
For general questions about hospice
payment policy, please send your
inquiry via email to: hospicepolicy@
cms.hhs.gov.
Wage
index addenda will be available only
through the internet on our Web site at:
(https://www.cms.gov/Medicare/
Medicare-Fee-for-Service-Payment/
Hospice/.)
Inspection of Public Comments: All
comments received before the close of
the comment period are available for
viewing by the public, including any
personally identifiable or confidential
business information that is included in
a comment. We post all comments
received before the close of the
comment period on the following Web
site as soon as possible after they have
been received: https://
www.regulations.gov. Follow the search
instructions on that Web site to view
public comments.
Comments received timely will also
be available for public inspection as
SUPPLEMENTARY INFORMATION:
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they are received, generally beginning
approximately 3 weeks after publication
of a document, at the headquarters of
the Centers for Medicare & Medicaid
Services, 7500 Security Boulevard,
Baltimore, Maryland 21244, Monday
through Friday of each week from 8:30
a.m. to 4 p.m. To schedule an
appointment to view public comments,
phone 1–800–743–3951.
Table of Contents
I. Executive Summary
A. Purpose
B. Summary of the Major Provisions
C. Summary of Impacts
II. Background
A. Hospice Care
B. History of the Medicare Hospice Benefit
C. Services Covered by the Medicare
Hospice Benefit
D. Medicare Payment for Hospice Care
1. Omnibus Budget Reconciliation Act of
1989
2. Balanced Budget Act of 1997
3. FY 1998 Hospice Wage Index Final Rule
4. FY 2010 Hospice Wage Index Final Rule
5. The Affordable Care Act
6. FY 2012 Hospice Wage Index Final Rule
7. FY 2015 Hospice Wage Index and
Payment Rate Update Final Rule
8. IMPACT Act of 2014
9. FY 2016 Hospice Wage Index and
Payment Rate Update Final Rule
10. FY 2017 Hospice Wage Index and
Payment Rate Update Final Rule
E. Trends in Medicare Hospice Utilization
III. Provisions of the Proposed Rule
A. Monitoring for Potential Impacts—
Affordable Care Act Hospice Reform
1. Hospice Payment Reform: Research and
Analyses
a. Length of Stay and Live Discharges
b. Skilled Visits in the Last Days of Life
c. Non-Hospice Spending
2. Initial Analysis of Revised Hospice Cost
Report Data
a. Background
b. Methodology
c. Overall Payments and Costs and Costs by
Level of Care
B. Proposed FY 2018 Hospice Wage Index
and Rate Update
1. Proposed FY 2018 Hospice Wage Index
2. Proposed FY 2018 Hospice Payment
Update Percentage
3. Proposed FY 2018 Hospice Payment
Rates
4. Hospice Cap Amount for FY 2018
C. Discussion and Solicitation of
Comments Regarding Sources of Clinical
Information for Certifying Terminal
Illness
D. Proposed Updates to the Hospice
Quality Reporting Program
1. Background and Statutory Authority
2. General Considerations Used for
Selection of Quality Measures for the
HQRP
3. Policy for Retention of HQRP Measures
Adopted for Previous Payment
Determination
4. Policy for Adopting Changes to
Previously Adopted Measures
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5. Previously Adopted Quality Measures
for FY 2018 Payment Determination and
Future Years
6. Proposed Removal of Previously
Adopted Measures
7. Measure Concepts Under Consideration
for Future Years
8. Form, Manner, and Timing of Quality
Data Submission
9. Previously Adopted APU Determination
and Compliance Criteria for the HQRP
10. HQRP Submission Exemption and
Extension Requirements for the FY 2019
Payment Determination and Subsequent
Years
11. CAHPS® Hospice Survey Participation
Requirements for the FY 2020 APU and
Subsequent Years
12. HQRP Reconsideration and Appeals
Procedures for the FY 2018 Payment
Determination and Subsequent Years
13. Confidential Feedback Reports
14. Public Display of Quality Measures and
Other Hospice Data for the HQRP
IV. Collection of Information Requirements
A. Hospice Item Set
B. Summary of CAHPS® Hospice Survey
Information Collection Requirements
(OMB Control Number 0938–1257)
V. Response to Comments
VI. Request for Information on Medicare
Flexibilities and Efficiencies
VII. Regulatory Impact Analysis
A. Statement of Need
B. Overall Impacts
C. Anticipated Effects
D. Detailed Economic Analysis
E. Alternatives Considered
F. Accounting Statement
G. Reducing Regulation and Controlling
Regulatory Costs
H. Conclusion
Acronyms
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Because of the many terms to which
we refer by acronym in this proposed
rule, we are listing the acronyms used
and their corresponding meanings in
alphabetical order:
APU Annual Payment Update
ASPE Assistant Secretary of Planning and
Evaluation
BBA Balanced Budget Act of 1997
BIPA Benefits Improvement and Protection
Act of 2000
BNAF Budget Neutrality Adjustment Factor
BLS Bureau of Labor Statistics
CAHPS® Consumer Assessment of
Healthcare Providers and Systems
CASPER Certification and Survey Provider
Enhanced Reports
CBSA Core-Based Statistical Area
CCN CMS Certification Number
CCW Chronic Conditions Data Warehouse
CFR Code of Federal Regulations
CHC Continuous Home Care
CHF Congestive Heart Failure
CMS Centers for Medicare & Medicaid
Services
COPD Chronic Obstructive Pulmonary
Disease
CoPs Conditions of Participation
CPI–U Consumer Price Index-Urban
Consumers
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CVA Cerebral Vascular Accident
CWF Common Working File
CY Calendar Year
DME Durable Medical Equipment
DRG Diagnostic Related Group
FEHC Family Evaluation of Hospice Care
FR Federal Register
FY Fiscal Year
GAO Government Accountability Office
GIP General Inpatient Care
HCFA Healthcare Financing Administration
HHS Health and Human Services
HIS Hospice Item Set
HQRP Hospice Quality Reporting Program
ICD–9–CM International Classification of
Diseases, Ninth Revision, Clinical
Modification
ICD–10–CM International Classification of
Diseases, Tenth Revision, Clinical
Modification
ICR Information Collection Requirement
IDG Interdisciplinary Group
IMPACT Act Improving Medicare PostAcute Care Transformation Act of 2014
IPPS Inpatient Prospective Payment System
IRC Inpatient Respite Care
LCD Local Coverage Determination
MAC Medicare Administrative Contractor
MACRA Medicare Access and CHIP
Reauthorization Act of 2015
MAP Measure Applications Partnership
MedPAC Medicare Payment Advisory
Commission
MFP Multifactor Productivity
MSA Metropolitan Statistical Area
NF Long Term Care Nursing Facility
NOE Notice of Election
NOTR Notice of Termination/Revocation
NP Nurse Practitioner
NPI National Provider Identifier
NQF National Quality Forum
OIG Office of the Inspector General
OACT Office of the Actuary
OMB Office of Management and Budget
PEPPER Program for Evaluating Payment
Patterns Electronic Report
PRRB Provider Reimbursement Review
Board
PS&R Provider Statistical and
Reimbursement Report
Pub. L. Public Law
POC Plan of Care
QAPI Quality Assessment and Performance
Improvement
QIO Quality Improvement Organization
RHC Routine Home Care
RN Registered Nurse
SBA Small Business Administration
SEC Securities and Exchange Commission
SIA Service Intensity Add-on
SNF Skilled Nursing Facility
TEFRA Tax Equity and Fiscal
Responsibility Act of 1982
TEP Technical Expert Panel
UHDDS Uniform Hospital Discharge Data
Set
U.S.C. United States Code
I. Executive Summary
A. Purpose
This rule proposes updates to the
hospice payment rates for fiscal year
(FY) 2018, as required under section
1814(i) of the Social Security Act (the
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20751
Act). This rule also discusses and
solicits comments on the source of the
clinical information used to certify an
individual as terminally ill (that is,
having a life expectancy of 6 months or
less as defined in section
1861(dd)(3)(A)) as required by section
1814(a)(7)(A) of the Act. Finally, this
rule also proposes new quality measures
and provides an update on the hospice
quality reporting program (HQRP)
consistent with the requirements of
section 1814(i)(5) of the Act. In
accordance with section 1814(i)(5)(A) of
the Act, starting in FY 2014, hospices
that fail to meet quality reporting
requirements receive a 2 percentage
point reduction to their payments.
B. Summary of the Major Provisions
Section III.A of this proposed rule
describes monitoring activities intended
to identify potential impacts related to
the hospice reform policies finalized in
the FY 2016 Hospice Wage Index and
Payment Rate Update final rule and
analyzes current trends in hospice
utilization and expenditures. Section
III.B.1 updates the hospice wage index
with updated wage data and makes the
application of the updated wage data
budget neutral for all four levels of
hospice care. In section III.B.2, we
discuss the FY 2018 hospice payment
update percentage of 1.0 percent.
Sections III.B.3 and III.B.4 update the
hospice payment rates and hospice cap
amount for FY 2018 by the hospice
payment update percentage discussed in
section III.B.2.
In section III.C of this proposed rule,
we discuss and solicit comments on the
appropriate source(s) of the required
clinical information for certification of a
medical prognosis of a life expectancy
of 6 months or less.
Finally, in section III.D of this
proposed rule, we discuss updates to
HQRP, including proposed changes to
the CAHPS® Hospice Survey measures
as well as the possibility of utilizing a
new assessment instrument to collect
quality data. In section III.D, we will
also discuss proposed enhancements to
the current Hospice Item Set (HIS) data
collection instrument to be more in line
with other post-acute care settings. The
new data collection instrument would
be a comprehensive patient assessment
instrument, rather than the current chart
abstraction tool. Additionally, in this
section we discuss our plans for sharing
HQRP data publicly later in Calendar
Year (CY) 2017, as well as plans to
provide public reporting via a Compare
Site in CY 2017 and future years.
C. Summary of Impacts
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TABLE 1—IMPACT SUMMARY TABLE
Provision description
Transfers
FY 2018 Hospice Wage Index and Payment Rate Update
The overall economic impact of this proposed rule is estimated to be an estimated
$180 million in increased payments to hospices during FY 2018.
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II. Background
A. Hospice Care
Hospice care is a comprehensive,
holistic approach to treatment that
recognizes that the impending death of
an individual, upon his or her choice,
warrants a change in the focus from
curative care to palliative care for relief
of pain and for symptom management.
The goal of hospice care is to help
terminally ill individuals continue life
with minimal disruption to normal
activities while remaining primarily in
the home environment. A hospice uses
an interdisciplinary approach to deliver
medical, nursing, social, psychological,
emotional, and spiritual services
through a collaboration of professionals
and other caregivers, with the goal of
making the beneficiary as physically
and emotionally comfortable as
possible. Hospice is compassionate
beneficiary and family/caregivercentered care for those who are
terminally ill.
Medicare regulations define
‘‘palliative care’’ as patient and familycentered care that optimizes quality of
life by anticipating, preventing, and
treating suffering. Palliative care
throughout the continuum of illness
involves addressing physical,
intellectual, emotional, social, and
spiritual needs and to facilitate patient
autonomy, access to information, and
choice (§ 418.3). Palliative care is at the
core of hospice philosophy and care
practices, and is a critical component of
the Medicare hospice benefit. See also
‘‘Medicare and Medicaid Programs:
Hospice Conditions of Participation’’
final rule (73 FR 32088, June 5, 2008).
The goal of palliative care in hospice is
to improve the quality of life of
beneficiaries and their families and
caregivers through early identification
and management of pain and other
issues associated with a life limiting
condition. The hospice interdisciplinary
group works with the beneficiary,
family, and caregivers to develop a
coordinated, comprehensive care plan;
reduce unnecessary diagnostics or
ineffective therapies; and maintain
ongoing communication with
individuals and their families about
changes in their condition. The
beneficiary’s care plan will shift over
time to meet the changing needs of the
individual, family, and caregiver(s) as
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the individual approaches the end of
life.
Medicare hospice care is palliative
care for individuals with a prognosis of
living 6 months or less if the terminal
illness runs its normal course. When a
beneficiary is terminally ill, many
health problems are related to the
underlying condition(s), as bodily
systems are interdependent. In the 2008
Hospice Conditions of Participation
final rule, we stated that ‘‘the [hospice]
medical director must consider the
primary terminal condition, related
diagnoses, current subjective and
objective medical findings, current
medication and treatment orders, and
information about unrelated conditions
when considering the initial
certification of the terminal illness’’ (73
FR 32176). As referenced in our
regulations at § 418.22(b)(1), to be
eligible for Medicare hospice services,
the patient’s attending physician (if any)
and the hospice medical director must
certify that the individual is ‘‘terminally
ill,’’ as defined in section 1861(dd)(3)(A)
of the Act and our regulations at § 418.3;
that is, the individual’s prognosis is for
a life expectancy of 6 months or less if
the terminal illness runs its normal
course. The regulations at § 418.22(b)(3)
require that the certification and
recertification forms include a brief
narrative explanation of the clinical
findings that support a life expectancy
of 6 months or less.
While the goal of hospice care is to
allow the beneficiary to remain in his or
her home, circumstances during the
end-of-life may necessitate short-term
inpatient admission to a hospital,
skilled nursing facility (SNF), or hospice
facility for necessary pain control or
acute or chronic symptom management
that cannot be managed in any other
setting. These acute hospice care
services ensure that any new or
worsening symptoms are intensively
addressed so that the beneficiary can
return to his or her home. Limited,
short-term, intermittent, inpatient
respite care (IRC) is also available
because of the absence or need for relief
of the family or other caregivers.
Additionally, an individual can receive
continuous home care (CHC) during a
period of crisis in which an individual
requires continuous care to achieve
palliation or management of acute
medical symptoms so that the
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individual can remain at home.
Continuous home care may be covered
for as much as 24 hours a day, and these
periods must be predominantly nursing
care, in accordance with our regulations
at § 418.204. A minimum of 8 hours of
nursing care, or nursing and aide care,
must be furnished on a particular day to
qualify for the continuous home care
rate (§ 418.302(e)(4)).
Hospices are expected to comply with
all civil rights laws, including the
provision of auxiliary aids and services
to ensure effective communication with
patients and patient care representatives
with disabilities consistent with section
504 of the Rehabilitation Act of 1973
and the Americans with Disabilities Act.
Additionally, they must provide
language access for such persons who
are limited in English proficiency,
consistent with Title VI of the Civil
Rights Act of 1964. Further information
about these requirements may be found
at https://www.hhs.gov/ocr/civilrights.
B. History of the Medicare Hospice
Benefit
Before the creation of the Medicare
hospice benefit, hospice programs were
originally operated by volunteers who
cared for the dying. During the early
development stages of the Medicare
hospice benefit, hospice advocates were
clear that they wanted a Medicare
benefit that provided all-inclusive care
for terminally-ill individuals, provided
pain relief and symptom management,
and offered the opportunity to die with
dignity in the comfort of one’s home
rather than in an institutional setting.1
As stated in the August 22, 1983
proposed rule entitled ‘‘Medicare
Program; Hospice Care’’ (48 FR 38146),
‘‘the hospice experience in the United
States has placed emphasis on home
care. It offers physician services,
specialized nursing services, and other
forms of care in the home to enable the
terminally ill individual to remain at
home in the company of family and
friends as long as possible.’’ The
concept of a beneficiary ‘‘electing’’ the
hospice benefit and being certified as
terminally ill were two key components
of the legislation responsible for the
creation of the Medicare Hospice
1 Connor, Stephen. (2007). Development of
Hospice and Palliative Care in the United States.
OMEGA. 56(1), p. 89–99.
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Benefit (section 122 of the Tax Equity
and Fiscal Responsibility Act of 1982
(TEFRA), (Pub. L. 97–248)). Section 122
of TEFRA created the Medicare Hospice
benefit, which was implemented on
November 1, 1983. Under sections
1812(d) and 1861(dd) of the Act, we
provide coverage of hospice care for
terminally ill Medicare beneficiaries
who elect to receive care from a
Medicare-certified hospice. Our
regulations at § 418.54(c) stipulate that
the comprehensive hospice assessment
must identify the beneficiary’s physical,
psychosocial, emotional, and spiritual
needs related to the terminal illness and
related conditions, and address those
needs in order to promote the
beneficiary’s well-being, comfort, and
dignity throughout the dying process.
The comprehensive assessment must
take into consideration the following
factors: The nature and condition
causing admission (including the
presence or lack of objective data and
subjective complaints); complications
and risk factors that affect care
planning; functional status; imminence
of death; and severity of symptoms
(§ 418.54(c)). The Medicare hospice
benefit requires the hospice to cover all
reasonable and necessary palliative care
related to the terminal prognosis, as
well as, care for interventions to manage
pain and symptoms, as described in the
beneficiary’s plan of care. Additionally,
the hospice Conditions of Participation
(CoPs) at § 418.56(c) require that the
hospice must provide all reasonable and
necessary services for the palliation and
management of the terminal illness,
related conditions, and interventions to
manage pain and symptoms. Therapy
and interventions must be assessed and
managed in terms of providing
palliation and comfort without undue
symptom burden for the hospice patient
or family.2 In the December 16, 1983
Hospice final rule (48 FR 56010),
regarding what is related versus
unrelated to the terminal illness, we
stated: ‘‘. . . we believe that the unique
physical condition of each terminally ill
individual makes it necessary for these
decisions to be made on a case by case
basis. It is our general view that
hospices are required to provide
virtually all the care that is needed by
terminally ill patients.’’ Therefore,
unless there is clear evidence that a
condition is unrelated to the terminal
prognosis, all conditions are considered
to be related to the terminal prognosis
2 Paolini,
DO, Charlotte. (2001). Symptoms
Management at End of Life. JAOA. 101(10). p. 609–
615.
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and the responsibility of the hospice to
address and treat.
As stated in the December 16, 1983
Hospice final rule, the fundamental
premise upon which the hospice benefit
was designed was the ‘‘revocation’’ of
traditional curative care and the
‘‘election’’ of hospice care for end-of-life
symptom management and
maximization of quality of life (48 FR
56008). After electing hospice care, the
beneficiary typically returns home from
an institutional setting or remains in the
home, to be surrounded by family and
friends, and to prepare emotionally and
spiritually, if requested, for death while
receiving expert symptom management
and other supportive services. Election
of hospice care also requires waiving the
right to Medicare payment for curative
treatment for the terminal prognosis,
and instead receiving palliative care to
manage pain or other symptoms.
The benefit was originally designed to
cover hospice care for a finite period of
time that roughly corresponded to a life
expectancy of 6 months or less. Initially,
beneficiaries could receive three
election periods: Two 90-day periods
and one 30-day period. Currently,
Medicare beneficiaries can elect hospice
care for two 90-day periods and an
unlimited number of subsequent 60-day
periods; however, at the beginning of
each period, a physician must certify
that the beneficiary has a life
expectancy of 6 months or less if the
terminal illness runs its normal course.
C. Services Covered by the Medicare
Hospice Benefit
One requirement for coverage under
the Medicare Hospice benefit is that
hospice services must be reasonable and
necessary for the palliation and
management of the terminal illness and
related conditions. Section 1861(dd)(1)
of the Act establishes the services that
are to be rendered by a Medicarecertified hospice program. These
covered services include: Nursing care;
physical therapy; occupational therapy;
speech-language pathology therapy;
medical social services; home health
aide services (now called hospice aide
services); physician services;
homemaker services; medical supplies
(including drugs and biologicals);
medical appliances; counseling services
(including dietary counseling); shortterm inpatient care in a hospital,
nursing facility, or hospice inpatient
facility (including both respite care and
procedures necessary for pain control
and acute or chronic symptom
management); continuous home care
during periods of crisis, and only as
necessary to maintain the terminally ill
individual at home; and any other item
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or service which is specified in the plan
of care and for which payment may
otherwise be made under Medicare, in
accordance with Title XVIII of the Act.
Section 1814(a)(7)(B) of the Act
requires that a written plan for
providing hospice care to a beneficiary
who is a hospice patient be established
before care is provided by, or under
arrangements made by, that hospice
program and that the written plan be
periodically reviewed by the
beneficiary’s attending physician (if
any), the hospice medical director, and
an interdisciplinary group (described in
section 1861(dd)(2)(B) of the Act). The
services offered under the Medicare
hospice benefit must be available to
beneficiaries as needed, 24 hours a day,
7 days a week (section 1861(dd)(2)(A)(i)
of the Act). Upon the implementation of
the hospice benefit, the Congress
expected hospices to continue to use
volunteer services, though these
services are not reimbursed by Medicare
(see section 1861(dd)(2)(E) of the Act).
As stated in the August 22, 1983
Hospice proposed rule, the hospice
interdisciplinary group should comprise
paid hospice employees as well as
hospice volunteers (48 FR 38149). This
expectation supports the hospice
philosophy of community based,
holistic, comprehensive, and
compassionate end-of-life care.
Before the Medicare hospice benefit
was established, the Congress requested
a demonstration project to test the
feasibility of covering hospice care
under Medicare.3 The National Hospice
Study was initiated in 1980 through a
grant sponsored by the Robert Wood
Johnson and John A. Hartford
Foundations and CMS (then, the Health
Care Financing Administration (HCFA)).
The demonstration project was
conducted between October 1980 and
March 1983. The project summarized
the hospice care philosophy and
principles as the following:
• Patient and family know of the
terminal condition.
• Further medical treatment and
intervention are indicated only on a
supportive basis.
• Pain control should be available to
patients as needed to prevent rather
than to just ameliorate pain.
• Interdisciplinary teamwork is
essential in caring for patient and
family.
• Family members and friends should
be active in providing support during
the death and bereavement process.
3 Greer, D., Mor, V., Sherwood, S. (1983) National
hospice study analysis plan. Journal of Chronic
Diseases, Vol 36, 11, 737–780. https://doi.org/
10.1016/0021-9681(83)90069-3.
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• Trained volunteers should provide
additional support as needed.
The cost data and the findings on
what services hospices provided in the
demonstration project were used to
design the Medicare hospice benefit.
The identified hospice services were
incorporated into the service
requirements under the Medicare
hospice benefit. Importantly, in the
August 22, 1983 Hospice proposed rule,
we stated ‘‘the hospice benefit and the
resulting Medicare reimbursement is not
intended to diminish the voluntary
spirit of hospices’’ (48 FR 38149).
D. Medicare Payment for Hospice Care
Sections 1812(d), 1813(a)(4),
1814(a)(7), 1814(i), and 1861(dd) of the
Act, and our regulations in part 418,
establish eligibility requirements,
payment standards and procedures;
define covered services; and delineate
the conditions a hospice must meet to
be approved for participation in the
Medicare program. Part 418, subpart G,
provides for a per diem payment in one
of four prospectively-determined rate
categories of hospice care (Routine
Home Care (RHC), Continuous Home
Care (CHC), inpatient respite care, and
general inpatient care), based on each
day a qualified Medicare beneficiary is
under hospice care (once the individual
has elected). This per diem payment is
to include all of the hospice services
needed to manage the beneficiary’s care,
as required by section 1861(dd)(1) of the
Act. There has been little change in the
hospice payment structure since the
benefit’s inception. The per diem rate
based on level of care was established
in 1983, and this payment structure
remains today with some adjustments,
as noted below:
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1. Omnibus Budget Reconciliation Act
of 1989
Section 6005(a) of the Omnibus
Budget Reconciliation Act of 1989 (Pub.
L. 101–239) amended section
1814(i)(1)(C) of the Act and provided for
the following two changes in the
methodology concerning updating the
daily payment rates: (1) Effective
January 1, 1990, the daily payment rates
for RHC and other services included in
hospice care were increased to equal
120 percent of the rates in effect on
September 30, 1989; and (2) the daily
payment rate for RHC and other services
included in hospice care for fiscal years
(FYs) beginning on or after October 1,
1990, were the payment rates in effect
during the previous federal fiscal year
increased by the hospital market basket
percentage increase.
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2. Balanced Budget Act of 1997
Section 4441(a) of the Balanced
Budget Act of 1997 (BBA) (Pub. L. 105–
33) amended section 1814(i)(1)(C)(ii)(VI)
of the Act to establish updates to
hospice rates for FYs 1998 through
2002. Hospice rates were updated by a
factor equal to the hospital market
basket percentage increase, minus 1
percentage point. Payment rates for FYs
from 2002 have been updated according
to section 1814(i)(1)(C)(ii)(VII) of the
Act, which states that the update to the
payment rates for subsequent FYs will
be the hospital market basket percentage
increase for the FY. The Act requires us
to use the inpatient hospital market
basket to determine hospice payment
rates.
3. FY 1998 Hospice Wage Index Final
Rule
In the August 8, 1997 FY 1998
Hospice Wage Index final rule (62 FR
42860), we implemented a new
methodology for calculating the hospice
wage index based on the
recommendations of a negotiated
rulemaking committee. The original
hospice wage index was based on 1981
Bureau of Labor Statistics hospital data
and had not been updated since 1983.
In 1994, because of disparity in wages
from one geographical location to
another, the Hospice Wage Index
Negotiated Rulemaking Committee was
formed to negotiate a new wage index
methodology that could be accepted by
the industry and the government. This
Committee was composed of
representatives from national hospice
associations; rural, urban, large and
small hospices, and multi-site hospices;
consumer groups; and a government
representative. The Committee decided
that in updating the hospice wage
index, aggregate Medicare payments to
hospices would remain budget neutral
to payments calculated using the 1983
wage index, to cushion the impact of
using a new wage index methodology.
To implement this policy, a Budget
Neutrality Adjustment Factor (BNAF)
was computed and applied annually to
the pre-floor, pre-reclassified hospital
wage index when deriving the hospice
wage index, subject to a wage index
floor.
4. FY 2010 Hospice Wage Index Final
Rule
Inpatient hospital pre-floor and prereclassified wage index values, as
described in the August 8, 1997 Hospice
Wage Index final rule, were subject to
either a budget neutrality adjustment or
application of the wage index floor.
Wage index values of 0.8 or greater were
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adjusted by the BNAF. Starting in FY
2010, a 7-year phase-out of the BNAF
began (FY 2010 Hospice Wage Index
final rule, (74 FR 39384, August 6,
2009)), with a 10 percent reduction in
FY 2010, an additional 15 percent
reduction for a total of 25 percent in FY
2011, an additional 15 percent
reduction for a total 40 percent
reduction in FY 2012, an additional 15
percent reduction for a total of 55
percent in FY 2013, and an additional
15 percent reduction for a total 70
percent reduction in FY 2014. The
phase-out continued with an additional
15 percent reduction for a total
reduction of 85 percent in FY 2015, and
an additional, and final, 15 percent
reduction for complete elimination in
FY 2016. We note that the BNAF was an
adjustment which increased the hospice
wage index value. Therefore, the BNAF
phase-out reduced the amount of the
BNAF increase applied to the hospice
wage index value. It was not a reduction
in the hospice wage index value itself or
in the hospice payment rates.
5. The Affordable Care Act
Starting with FY 2013 (and in
subsequent FYs), the market basket
percentage update under the hospice
payment system referenced in sections
1814(i)(1)(C)(ii)(VII) and
1814(i)(1)(C)(iii) of the Act is subject to
annual reductions related to changes in
economy-wide productivity, as
specified in section 1814(i)(1)(C)(iv) of
the Act. In FY 2013 through FY 2019,
the market basket percentage update
under the hospice payment system will
be reduced by an additional 0.3
percentage point (although for FY 2014
to FY 2019, the potential 0.3 percentage
point reduction is subject to suspension
under conditions specified in section
1814(i)(1)(C)(v) of the Act).
In addition, sections 1814(i)(5)(A)
through (C) of the Act, as added by
section 3132(a) of the Affordable Care
Act, require hospices to begin
submitting quality data, based on
measures to be specified by the
Secretary of the Department of Health
and Human Services (the Secretary), for
FY 2014 and subsequent FYs. Beginning
in FY 2014, hospices that fail to report
quality data will have their market
basket percentage increase reduced by 2
percentage points.
Section 1814(a)(7)(D)(i) of the Act, as
added by section 3132(b)(2) of the
Affordable Care Act, requires, effective
January 1, 2011, that a hospice
physician or nurse practitioner have a
face-to-face encounter with the
beneficiary to determine continued
eligibility of the beneficiary’s hospice
care prior to the 180th-day
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recertification and each subsequent
recertification, and to attest that such
visit took place. When implementing
this provision, we finalized in the CY
2011 Home Health Prospective Payment
System final rule (75 FR 70435) that the
180th-day recertification and
subsequent recertifications would
correspond to the beneficiary’s third or
subsequent benefit periods. Further,
section 1814(i)(6) of the Act, as added
by section 3132(a)(1)(B) of the
Affordable Care Act, authorizes the
Secretary to collect additional data and
information determined appropriate to
revise payments for hospice care and
other purposes. The types of data and
information suggested in the Affordable
Care Act could capture accurate
resource utilization, which could be
collected on claims, cost reports, and
possibly other mechanisms, as the
Secretary determined to be appropriate.
The data collected could be used to
revise the methodology for determining
the payment rates for RHC and other
services included in hospice care, no
earlier than October 1, 2013, as
described in section 1814(i)(6)(D) of the
Act. In addition, we were required to
consult with hospice programs and the
Medicare Payment Advisory
Commission (MedPAC) regarding
additional data collection and payment
revision options.
6. FY 2012 Hospice Wage Index Final
Rule
When the Medicare Hospice benefit
was implemented, the Congress
included an aggregate cap on hospice
payments, which limits the total
aggregate payments any individual
hospice can receive in a year. The
Congress stipulated that a ‘‘cap amount’’
be computed each year. The cap amount
was set at $6,500 per beneficiary when
first enacted in 1983 and has been
adjusted annually by the change in the
medical care expenditure category of the
consumer price index for urban
consumers from March 1984 to March of
the cap year (section 1814(i)(2)(B) of the
Act). The cap year was defined as the
period from November 1st to October
31st. In the August 4, 2011 FY 2012
Hospice Wage Index final rule (76 FR
47308 through 47314) for the 2012 cap
year and subsequent cap years, we
announced that subsequently, the
hospice aggregate cap would be
calculated using the patient-by-patient
proportional methodology, within
certain limits. We allowed existing
hospices the option of having their cap
calculated via the original streamlined
methodology, also within certain limits.
As of FY 2012, new hospices have their
cap determinations calculated using the
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patient-by-patient proportional
methodology. The patient-by-patient
proportional methodology and the
streamlined methodology are two
different methodologies for counting
beneficiaries when calculating the
hospice aggregate cap. A detailed
explanation of these methods is found
in the August 4, 2011 FY 2012 Hospice
Wage Index final rule (76 FR 47308
through 47314). If a hospice’s total
Medicare payments for the cap year
exceed the hospice aggregate cap, then
the hospice must repay the excess back
to Medicare.
7. FY 2015 Hospice Wage Index and
Payment Rate Update Final Rule
When electing hospice, a beneficiary
waives Medicare coverage for any care
for the terminal illness and related
conditions except for services provided
by the designated hospice and attending
physician. The FY 2015 Hospice Wage
Index and Payment Rate Update final
rule (79 FR 50452) finalized a
requirement that requires the Notice of
Election (NOE) be filed within 5
calendar days after the effective date of
hospice election. If the NOE is filed
beyond this 5 day period, hospice
providers are liable for the services
furnished during the days from the
effective date of hospice election to the
date of NOE filing (79 FR 50474).
Similar to the NOE, the claims
processing system must be notified of a
beneficiary’s discharge from hospice or
hospice benefit revocation. This update
to the beneficiary’s status allows claims
from non-hospice providers to be
processed and paid. Late filing of the
NOE can result in inaccurate benefit
period data and leaves Medicare
vulnerable to paying non-hospice claims
related to the terminal illness and
related conditions and beneficiaries
possibly liable for any cost-sharing of
associated costs. Upon live discharge or
revocation, the beneficiary immediately
resumes the Medicare coverage that had
been waived when he or she elected
hospice. The FY 2015 Hospice Wage
Index and Payment Rate Update final
rule also finalized a requirement that
requires hospices to file a notice of
termination/revocation within 5
calendar days of a beneficiary’s live
discharge or revocation, unless the
hospices have already filed a final
claim. This requirement helps to protect
beneficiaries from delays in accessing
needed care (§ 418.26(e)).
A hospice ‘‘attending physician’’ is
described by the statutory and
regulatory definitions as a medical
doctor, osteopath, or nurse practitioner
whom the beneficiary identifies, at the
time of hospice election, as having the
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20755
most significant role in the
determination and delivery of his or her
medical care. Over time, we have
received reports of problems with the
identification of the person’s designated
attending physician and a third of
hospice patients had multiple providers
submit Part B claims as the ‘‘attending
physician,’’ using a claim modifier. The
FY 2015 Hospice Wage Index and
Payment Rate Update final rule
finalized a requirement that the election
form include the beneficiary’s choice of
attending physician and that the
beneficiary provide the hospice with a
signed document when he or she
chooses to change attending physicians
(79 FR 50479).
Hospice providers are required to
begin using a Hospice Experience of
Care Survey for informal caregivers of
hospice patients as of 2015. The FY
2015 Hospice Wage Index and Payment
Rate Update final rule provided
background and a description of the
development of the Hospice Experience
of Care Survey, including the model of
survey implementation, the survey
respondents, eligibility criteria for the
sample, and the languages in which the
survey is offered. The FY 2015 Hospice
Rate Update final rule also set out
participation requirements for CY 2015
and discussed vendor oversight
activities and the reconsideration and
appeals process for entities that failed to
win CMS approval as vendors (79 FR
50496).
Finally, the FY 2015 Hospice Wage
Index and Payment Rate Update final
rule required providers to complete
their aggregate cap determination not
sooner than 3 months after the end of
the cap year, and not later than 5
months after, and remit any
overpayments. Those hospices that fail
to timely submit their aggregate cap
determinations will have their payments
suspended until the determination is
completed and received by the Medicare
Administrative Contractor (MAC) (79 FR
50503).
8. IMPACT Act of 2014
The Improving Medicare Post-Acute
Care Transformation Act of 2014 (Pub.
L. 113–185) (IMPACT Act) became law
on October 6, 2014. Section 3(a) of the
IMPACT Act mandated that all
Medicare certified hospices be surveyed
every 3 years beginning April 6, 2015
and ending September 30, 2025. In
addition, section 3(c) of the IMPACT
Act requires medical review of hospice
cases involving beneficiaries receiving
more than 180 days care in select
hospices that show a preponderance of
such patients; section 3(d) of the
IMPACT Act contains a new provision
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well as admission requirements for
hospice certifications.
mandating that the cap amount for
accounting years that end after
September 30, 2016, and before October
1, 2025 be updated by the hospice
payment update rather than using the
consumer price index for urban
consumers (CPI–U) for medical care
expenditures.
9. FY 2016 Hospice Wage Index and
Payment Rate Update Final Rule
In the FY 2016 Hospice Rate Update
final rule, we created two different
payment rates for RHC that resulted in
a higher base payment rate for the first
60 days of hospice care and a reduced
base payment rate for subsequent days
of hospice care (80 FR 47172). We also
created a Service Intensity Add-on (SIA)
payment payable for services during the
last 7 days of the beneficiary’s life, equal
to the CHC hourly payment rate
multiplied by the amount of direct
patient care provided by a registered
nurse (RN) or social worker that occurs
during the last 7 days (80 FR 47177).
In addition to the hospice payment
reform changes discussed, the FY 2016
Hospice Wage Index and Payment Rate
Update final rule implemented changes
mandated by the IMPACT Act, in which
the cap amount for accounting years
that end after September 30, 2016 and
before October 1, 2025 is updated by the
hospice payment update percentage
rather than using the CPI–U. This was
applied to the 2016 cap year, starting on
November 1, 2015 and ending on
October 31, 2016. In addition, we
finalized a provision to align the cap
accounting year for both the inpatient
cap and the hospice aggregate cap with
the fiscal year for FY 2017 and later (80
FR 47186). This allows for the timely
implementation of the IMPACT Act
changes while better aligning the cap
accounting year with the timeframe
described in the IMPACT Act.
Finally, the FY 2016 Hospice Wage
Index and Payment Rate Update final
rule clarified that hospices must report
all diagnoses of the beneficiary on the
hospice claim as a part of the ongoing
data collection efforts for possible future
hospice payment refinements. Reporting
of all diagnoses on the hospice claim
aligns with current coding guidelines as
10. FY 2017 Hospice Wage Index and
Payment Rate Update Final Rule
In the FY 2017 Hospice Wage Index
and Payment Rate Update final rule, we
finalized several new policies and
requirements related to the HQRP. First,
we codified our policy that if the
National Quality Forum (NQF) makes
non-substantive changes to
specifications for HQRP measures as
part of the NQF’s re-endorsement
process, we will continue to utilize the
measure in its new endorsed status,
without going through new notice-andcomment rulemaking (81 FR 52160). We
will continue to use rulemaking to
adopt substantive updates made by the
NQF to the endorsed measures we have
adopted for the HQRP; determinations
about what constitutes a substantive
versus non-substantive change will be
made on a measure-by-measure basis.
Second, we finalized two new quality
measures for the HQRP for the FY 2019
payment determination and subsequent
years: Hospice Visits when Death is
Imminent Measure Pair and Hospice
and Palliative Care Composite Process
Measure-Comprehensive Assessment at
Admission (81 FR 52173). The data
collection mechanism for both of these
measures is the HIS, and the measures
are effective April 1, 2017. Regarding
the CAHPS® Hospice Survey, we
finalized a policy that hospices that
receive their CMS Certification Number
(CCN) after January 1, 2017 for the FY
2019 Annual Payment Update (APU)
and January 1, 2018 for the FY 2020
APU will be exempted from the Hospice
CAHPS® requirements due to newness
(81 FR 52182). The exemption is
determined by CMS and is for 1 year
only.
E. Trends in Medicare Hospice
Utilization
Since the implementation of the
hospice benefit in 1983, and especially
within the last decade, there has been
substantial growth in hospice benefit
utilization. The number of Medicare
beneficiaries receiving hospice services
has grown from 513,000 in FY 2000 to
nearly 1.4 million in FY 2016. Similarly,
Medicare hospice expenditures have
risen from $2.8 billion in FY 2000 to
approximately $16.5 billion in FY 2016.
Our Office of the Actuary (OACT)
projects that hospice expenditures are
expected to continue to increase, by
approximately 7 percent annually,
reflecting an increase in the number of
Medicare beneficiaries, more beneficiary
awareness of the Medicare Hospice
Benefit for end-of-life care, and a
growing preference for care provided in
home and community-based settings.
There have also been changes in the
diagnosis patterns among Medicare
hospice enrollees. Specifically, as
described in Table 2, there have been
notable increases between 2002 and
2016 in neurologically-based diagnoses,
including diagnoses of Alzheimer’s
disease. Additionally, there have been
significant increases in the use of nonspecific, symptom-classified diagnoses,
such as ‘‘debility’’ and ‘‘adult failure to
thrive.’’ In FY 2013, ‘‘debility’’ and
‘‘adult failure to thrive’’ were the first
and sixth most common hospice claimsreported diagnoses, respectively,
accounting for approximately 14 percent
of all diagnoses. Effective October 1,
2014, hospice claims are returned to the
provider if ‘‘debility’’ and ‘‘adult failure
to thrive’’ are coded as the principal
hospice diagnosis as well as other ICD–
9–CM (and as of October 1, 2015, ICD–
10–CM) codes that are not permissible
as principal diagnosis codes per ICD–9–
CM (or ICD–10–CM) coding guidelines.
In the FY 2015 Hospice Wage Index and
Payment Rate Update final rule (79 FR
50452), we reminded the hospice
industry that this policy would go into
effect and claims would start to be
returned to the provider effective
October 1, 2014. As a result of this,
there has been a shift in coding patterns
on hospice claims. For FY 2016, the
most common hospice principal
diagnoses were Alzheimer’s disease,
Heart Failure, Chronic Obstructive
Pulmonary Disease, Lung Cancer, and
Senile Degeneration of the Brain, which
constituted approximately 30 percent of
all claims-reported principal diagnosis
codes reported in FY 2016 (see Table 2).
nlaroche on DSK30NT082PROD with PROPOSALS3
TABLE 2—THE TOP TWENTY PRINCIPAL HOSPICE DIAGNOSES, FY 2002, FY 2007, FY 2013, FY 2016
Rank
ICD–9/Reported Principal Diagnosis
Count
Percentage
Year: FY 2002
1
2
3
4
5
.....................
.....................
.....................
.....................
.....................
VerDate Sep<11>2014
162.9
428.0
799.3
496
331.0
Lung Cancer ...........................................................................................................
Congestive Heart Failure .......................................................................................
Debility Unspecified ................................................................................................
COPD .....................................................................................................................
Alzheimer’s Disease ...............................................................................................
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Fmt 4701
Sfmt 4702
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03MYP3
73,769
45,951
36,999
35,197
28,787
11
7
6
5
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TABLE 2—THE TOP TWENTY PRINCIPAL HOSPICE DIAGNOSES, FY 2002, FY 2007, FY 2013, FY 2016—Continued
6 .....................
7 .....................
8 .....................
9 .....................
10 ...................
11 ...................
12 ...................
13 ...................
14 ...................
15 ...................
16 ...................
17 ...................
18 ...................
19 ...................
20 ...................
436
185
783.7
174.9
290.0
153.0
157.9
294.8
429.9
154.0
332.0
586
585
183.0
188.9
CVA/Stroke .............................................................................................................
Prostate Cancer .....................................................................................................
Adult Failure To Thrive ...........................................................................................
Breast Cancer ........................................................................................................
Senile Dementia, Uncomp. ....................................................................................
Colon Cancer .........................................................................................................
Pancreatic Cancer ..................................................................................................
Organic Brain Synd Nec ........................................................................................
Heart Disease Unspecified .....................................................................................
Rectosigmoid Colon Cancer ..................................................................................
Parkinson’s Disease ...............................................................................................
Renal Failure Unspecified ......................................................................................
Chronic Renal Failure (End 2005) .........................................................................
Ovarian Cancer ......................................................................................................
Bladder Cancer ......................................................................................................
26,897
20,262
18,304
17,812
16,999
16,379
15,427
10,394
10,332
8,956
8,865
8,764
8,599
7,432
6,916
4
3
3
3
3
2
2
2
2
1
1
1
1
1
1
90,150
86,954
77,836
60,815
58,303
58,200
37,667
31,800
22,170
22,086
20,378
19,082
19,080
17,697
16,524
15,777
12,188
11,196
8,806
8,434
9
8
7
6
6
6
4
3
2
2
2
2
2
2
2
2
1
1
1
1
127,415
96,171
91,598
82,184
79,626
71,122
60,579
36,914
34,459
30,963
25,396
23,228
23,224
23,059
22,341
21,769
19,309
15,965
14,372
13,687
9
7
6
6
6
5
4
3
2
2
2
2
2
2
2
2
1
1
1
1
162,845
84,088
74,131
57,077
55,305
37,245
33,647
32,851
29,223
27,629
24,576
11
6
5
4
4
2
2
2
2
2
2
Year: FY 2007
1 .....................
2 .....................
3 .....................
4 .....................
5 .....................
6 .....................
7 .....................
8 .....................
9 .....................
10 ...................
11 ...................
12 ...................
13 ...................
14 ...................
15 ...................
16 ...................
17 ...................
18 ...................
19 ...................
20 ...................
799.3
162.9
428.0
496
783.7
331.0
290.0
436
429.9
185
174.9
157.9
153.9
294.8
332.0
294.10
586
585.6
188.9
183.0
Debility Unspecified ................................................................................................
Lung Cancer ...........................................................................................................
Congestive Heart Failure .......................................................................................
COPD .....................................................................................................................
Adult Failure To Thrive ...........................................................................................
Alzheimer’s Disease ...............................................................................................
Senile Dementia Uncomp. .....................................................................................
CVA/Stroke .............................................................................................................
Heart Disease Unspecified .....................................................................................
Prostate Cancer .....................................................................................................
Breast Cancer ........................................................................................................
Pancreas Unspecified ............................................................................................
Colon Cancer .........................................................................................................
Organic Brain Syndrome NEC ...............................................................................
Parkinson’s Disease ...............................................................................................
Dementia in Other Diseases w/o Behavior Dist. ...................................................
Renal Failure Unspecified ......................................................................................
End Stage Renal Disease ......................................................................................
Bladder Cancer ......................................................................................................
Ovarian Cancer ......................................................................................................
Year: FY 2013
1 .....................
2 .....................
3 .....................
4 .....................
5 .....................
6 .....................
7 .....................
8 .....................
9 .....................
10 ...................
11 ...................
12 ...................
13 ...................
14 ...................
15 ...................
16 ...................
17 ...................
18 ...................
19 ...................
20 ...................
799.3
428.0
162.9
496
331.0
783.7
290.0
429.9
436
294.10
332.0
153.9
294.20
174.9
157.9
185
585.6
518.81
294.8
294.11
Debility Unspecified ................................................................................................
Congestive Heart Failure .......................................................................................
Lung Cancer ...........................................................................................................
COPD .....................................................................................................................
Alzheimer’s Disease ...............................................................................................
Adult Failure to Thrive ............................................................................................
Senile Dementia, Uncomp. ....................................................................................
Heart Disease Unspecified .....................................................................................
CVA/Stroke .............................................................................................................
Dementia in Other Diseases w/o Behavioral Dist. .................................................
Parkinson’s Disease ...............................................................................................
Colon Cancer .........................................................................................................
Dementia Unspecified w/o Behavioral Dist. ...........................................................
Breast Cancer ........................................................................................................
Pancreatic Cancer ..................................................................................................
Prostate Cancer .....................................................................................................
End-Stage Renal Disease ......................................................................................
Acute Respiratory Failure .......................................................................................
Other Persistent Mental Dis.—classified elsewhere ..............................................
Dementia In Other Diseases w/Behavioral Dist. ....................................................
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Year: FY 2016
1 .....................
2 .....................
3 .....................
4 .....................
5 .....................
6 .....................
7 .....................
8 .....................
9 .....................
10 ...................
11 ...................
VerDate Sep<11>2014
G30.9
I50.9
J44.9
C34.90
G31.1
G20
I25.10
J44.1
G30.1
I67.2
C61
Alzheimer’s disease, unspecified ...........................................................................
Heart failure, unspecified .......................................................................................
Chronic obstructive pulmonary disease, unspecified .............................................
Malignant Neoplasm of Unsp Part of Unsp Bronchus or Lung .............................
Senile degeneration of brain, not elsewhere classified .........................................
Parkinson’s disease ...............................................................................................
Atherosclerotic heart disease of native coronary art without angina pectoris .......
Chronic obstructive pulmonary disease with (acute) exacerbation .......................
Alzheimer’s disease with late onset .......................................................................
Cerebral atherosclerosis ........................................................................................
Malignant neoplasm of prostate .............................................................................
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TABLE 2—THE TOP TWENTY PRINCIPAL HOSPICE DIAGNOSES, FY 2002, FY 2007, FY 2013, FY 2016—Continued
12
13
14
15
16
17
18
19
20
...................
...................
...................
...................
...................
...................
...................
...................
...................
N18.6
C18.9
I51.9
C25.9
I63.9
I67.9
C50.919
A41.9
I50.22
End stage renal disease ........................................................................................
Malignant neoplasm of colon, unspecified .............................................................
Heart disease, unspecified .....................................................................................
Malignant neoplasm of pancreas, unspecified .......................................................
Cerebral infarction, unspecified ..............................................................................
Cerebrovascular disease, unspecified ...................................................................
Malignant neoplasm of unspecified site of unspecified female breast ..................
Sepsis, unspecified organism ................................................................................
Chronic systolic (congestive) heart failure .............................................................
22,261
22,203
21,868
20,400
18,546
14,879
14,022
12,723
12,083
1
1
1
1
1
1
1
1
1
Note(s): The frequencies shown represent beneficiaries that had at least one claim with the specific ICD–9–CM/ICD–10 code reported as the
principal diagnosis. Beneficiaries could be represented multiple times in the results if they have multiple claims during that time period with different principal diagnoses.
Source: FY 2002 and 2007 hospice claims data from the Chronic Conditions Data Warehouse (CCW), accessed on February 14 and February
20, 2013. FY 2013 hospice claims data from the CCW, accessed on June 26, 2014, and FY 2016 hospice claims data from the CCW, accessed
and merged with ICD–10 codes on January 9, 2017.
While there has been a shift in the
reporting of the principal diagnosis as a
result of diagnosis clarifications, a
significant proportion of hospice claims
(49 percent) in FY 2014 only reported a
single principal diagnosis, which may
not fully explain the characteristics of
Medicare beneficiaries who are
approaching the end of life. To address
this pattern of single diagnosis
reporting, the FY 2015 Hospice Wage
Index and Payment Rate Update final
rule (79 FR 50498) reiterated ICD–9–CM
coding guidelines for the reporting of
the principal and additional diagnoses
on the hospice claim. We reminded
providers to report all diagnoses on the
hospice claim for the terminal illness
and related conditions, including those
that affect the care and clinical
management for the beneficiary.
Additionally, in the FY 2016 Hospice
Wage Index and Payment Rate Update
final rule (80 FR 47201), we provided
further clarification regarding diagnosis
reporting on hospice claims. We
clarified that hospices will report all
diagnoses identified in the initial and
comprehensive assessments on hospice
claims, whether related or unrelated to
the terminal prognosis of the individual,
effective October 1, 2015. Analysis of
FY 2016 hospice claims shows that 100
percent of hospices reported more than
one diagnosis, with 86 percent
submitting at least two diagnoses and 77
percent including at least three
diagnoses.
III. Provisions of the Proposed Rule
nlaroche on DSK30NT082PROD with PROPOSALS3
A. Monitoring for Potential Impacts—
Affordable Care Act Hospice Reform
1. Hospice Payment Reform: Research
and Analyses
This section of the proposed rule
describes current trends in hospice
utilization and provider behavior, such
as lengths of stay, live discharge rates,
skilled visits during the last days of life,
and non-hospice spending. Utilization
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data on these metrics were examined to
determine the potential impacts related
to the hospice reform policies finalized
in the FY 2016 Hospice Wage Index and
Payment Rate Update final rule (80 FR
47142), if any. Moreover, in response to
Office of Inspector General (OIG) report
‘‘Hospice Inappropriately Billed
Medicare Over $250 Million for General
Inpatient Care’’ (OEI–02–10–00491)
released in March 2016, which
identified the drugs paid for by Part D
and provided to beneficiaries during
general inpatient care (GIP) stays, we
have also continued to monitor nonhospice spending during a hospice
election as described in this section.
Additionally, we have included
preliminary information on the costs of
hospice care using data from the new
hospice Medicare cost report, effective
for cost reporting periods that began on
or after October 1, 2014 (FY 2015).
Section 1814(i)(6) of the Act, as
amended by section 3132(a)(1)(B) of the
Affordable Care Act, authorized the
Secretary to collect additional data and
information determined appropriate to
revise payments for hospice care and
other purposes, including such data
sources as the Medicare cost reports.
These preliminary analyses may inform
future work that could include such
refinements to hospice payment rates.
a. Length of Stay and Live Discharges
Hospice Length of Stay
Eligibility under the Medicare hospice
benefit is predicated on the individual
being certified as terminally ill.
Medicare regulations at § 418.3 define
‘‘terminally ill’’ to mean that the
individual has a medical prognosis that
his or her life expectancy is 6 months
or less if the illness runs its normal
course. However, we have recognized in
previous rules that prognostication is
not an exact science (79 FR 50470), and
thus, a beneficiary may be under a
hospice election longer than 6 months,
as long as there remains a reasonable
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expectation that the individual has a life
expectancy of 6 months or less.
The number of days that a hospice
beneficiary receives care under a
hospice election is referred to as the
hospice length of stay. Hospice length of
stay can be influenced by a number of
factors including disease course, timing
of referral, decision to resume curative
treatment, and/or stabilization or
improvement where the individual is no
longer certified as terminally ill. Longer
lengths of stay in hospice may reflect
admission to hospice earlier in the
disease trajectory or miscalculation of
prognosis, among other situations.
Shorter lengths of stay in hospice may
reflect hospice election late in the
disease trajectory or a rapidly
progressing acute condition. This also
may be due to individual reluctance to
accept that his or her condition is
terminal and choose the hospice benefit;
inadequate knowledge regarding the
breadth of services available under
hospice care; cultural, ethnic, and/or
religious backgrounds inhibiting or even
precluding the use of hospice services;
and other reasons.4 As such, hospice
lengths of stay are variable.
We examined length of stay, meaning
the number of hospice days during a
single hospice election at the date of
live discharge or death. We also
examined total lifetime length of stay,
which would include the sum of all
days of hospice care across all hospice
elections. This would mean if a
beneficiary had one hospice election,
was discharged alive, and then reelected the benefit at a later date, the
sum of both elections would count
towards their lifetime length of stay. In
FY 2016, the average length of stay in
hospice was 79 days and the average
lifetime length of stay in hospice was
4 Vig, E., Starks, H., Taylor, J., Hopley, E., FryerEdwards, K. (2010). ‘‘Why Don’t Patients Enroll in
Hospice? Can We Do Anything About It?’’ Journal
of General Internal Medicine. 25(10): 1009–19. Doi:
10.1007/s11606–010–1423–9.
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96.1 days. The average length of stay
remained virtually the same between FY
2015 and FY 2016, 78 days compared to
79 days, respectively. The average
lifetime length of stay similarly
remained virtually the same between FY
2015 and FY 2016, 95.2 and 96.1 days,
respectively.
The median (50th percentile) length
of stay in FY 2016 was 18 days. This
means that half of hospice beneficiaries
received care for fewer than 18 days and
half received care for more than 18 days.
While the median length of stay has
remained relatively constant over the
past several years, the average length of
stay has typically increased from year to
year.
The Medicare hospice benefit
provides four levels of care: Routine
home care (RHC), general inpatient care
(GIP), continuous home care (CHC), and
inpatient respite care (IRC). The
majority of hospice patient care is
provided at the RHC level of care and
can be provided wherever the patient
calls ‘‘home,’’ including nursing homes
and assisted living facilities. As
indicated in Table 3 below, most
hospice care (98 percent) provided is
routine home care (RHC).
Approximately 56 percent of all hospice
days are provided at the RHC level of
care in the patient’s residence whereas
41 percent is provided at the RHC level
of care to patients that reside in a
nursing home or assisted living facility.
TABLE 3—SHARE OF HOSPICE DAYS BY LEVEL OF CARE AND SITE OF SERVICE, FOR BENEFICIARIES DISCHARGED ALIVE
OR DECEASED IN FY 2016
Number of
hospice days
% of all
hospice days
Level of care
Site of service
RHC ..................
Home + Hospice Residential Facility ........................................................................................
SNF/NF .....................................................................................................................................
Assisted Living Facility .............................................................................................................
Other .........................................................................................................................................
59,818,337
25,953,198
18,182,931
1,224,979
55.75
24.19
16.95
1.14
Total ...................................................................................................................................
105,179,445
98.02
Inpatient Hospital ......................................................................................................................
Inpatient Hospice Facility ..........................................................................................................
Skilled Nursing Facility .............................................................................................................
Other .........................................................................................................................................
378,792
1,060,487
59,158
5,571
0.35
0.99
0.06
0.01
Total ...................................................................................................................................
1,504,008
1.40
Home + Hospice Residential Facility ........................................................................................
SNF/NF .....................................................................................................................................
Assisted Living Facility .............................................................................................................
Other .........................................................................................................................................
180,206
42,224
69,849
484
0.17
0.04
0.07
0.00
Total ...................................................................................................................................
292,763
0.27
Inpatient Hospital ......................................................................................................................
Inpatient Hospice Facility ..........................................................................................................
SNF/NF .....................................................................................................................................
Other .........................................................................................................................................
29,895
111,004
185,351
1,490
0.03
0.10
0.17
0.00
Total ...................................................................................................................................
327,740
0.31
...................................................................................................................................................
107,303,956
100
GIP ...................
CHC ..................
IRC ...................
Total ..........
Source: Common Working File (CWF). All hospice claims from 2006 to 2016 were included, for beneficiaries whose final claim in FY 2016, according to through date, for a hospice discharge (excluded status code ‘‘30’’, indicating a continuing patient). Hospice days with invalid or missing
site of service HCPCS code are excluded.
nlaroche on DSK30NT082PROD with PROPOSALS3
In addition to analyzing the hospice
average and average lifetime lengths of
stay, we examined the average lifetime
lengths of stay associated with hospice
principal diagnoses by site of service at
admission in FY 2015 (see Table 4
below). We limited our analysis to those
beneficiaries that were receiving RHC at
admission. As noted in Table 3 above,
RHC was the level of care for 98 percent
of all hospice days. We found that
beneficiaries with chronic, progressive
neurological diseases such as
Alzheimer’s disease and related
dementias, and Parkinson’s disease had
the longest average lifetime lengths of
stay at 165.3 days in FY 2015.
Beneficiaries with Chronic Kidney
Disease and cancer had shorter average
lifetime lengths of stay, 57 and 63.7
days, respectively. For all diagnoses, the
average lifetime length of stay was 113.5
days in FY 2015 when level of care at
admission is RHC.
TABLE 4—AVERAGE LIFETIME LENGTH OF STAY BY DIAGNOSIS AND SITE OF SERVICE ON THE DAY OF ADMISSION IN FY
2015, WHEN LEVEL OF CARE AT ADMISSION IS RHC
Home + hospice
residential facility
Primary hospice diagnosis at admission
All Diagnoses ............................................
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Number
of
benes
Average
lifetime
length
of stay
576,657
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106.75
Assisted living facility
Number
of
benes
Average
lifetime
length
of stay
101,085
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SNF + LTC or nonskilled nursing facility
Number
of
benes
208,747
Average
lifetime
length
of stay
106.21
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Number
of
benes
9,530
03MYP3
All sites of service
Average
lifetime
length
of stay
90.90
Number
of
benes
897,298
Average
lifetime
length
of stay
113.51
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TABLE 4—AVERAGE LIFETIME LENGTH OF STAY BY DIAGNOSIS AND SITE OF SERVICE ON THE DAY OF ADMISSION IN FY
2015, WHEN LEVEL OF CARE AT ADMISSION IS RHC—Continued
Home + hospice
residential facility
Primary hospice diagnosis at admission
Alzheimer’s, Dementia, and Parkinson’s ..
CVA/Stroke ................................................
Cancers .....................................................
Chronic Kidney Disease ............................
Heart (CHF and Other Heart Disease) .....
Lung (COPD and Pneumonias) ................
All Other Diagnoses ..................................
Number
of
benes
Average
lifetime
length
of stay
83,527
32,329
233,771
14,328
101,243
58,183
53,276
Assisted living facility
Number
of
benes
172.45
95.82
62.04
58.41
121.77
131.97
163.47
Average
lifetime
length
of stay
39,019
9,359
11,773
1,655
19,784
6,866
12,629
186.89
98.97
93.90
82.34
131.11
127.83
254.83
SNF + LTC or nonskilled nursing facility
Number
of
benes
Average
lifetime
length
of stay
67,438
23,927
30,437
6,644
35,052
16,631
28,618
Other
Average
lifetime
length
of stay
Number
of
benes
140.34
77.17
63.23
47.60
83.54
82.42
150.98
All sites of service
2,314
971
1,964
273
1,771
870
1,367
Number
of
benes
143.33
53.56
46.41
48.84
84.69
65.42
125.28
Average
lifetime
length
of stay
192,593
66,668
278,047
22,907
158,167
82,656
96,260
165.32
90.06
63.69
57.01
115.14
122.11
173.36
Source: Common Working File (CWF). All hospice claims from 2006 to 2015 were included, for beneficiaries whose final claim in FY 2015, according to through
date, for a hospice discharge (excluded status code ‘‘30’’, indicating a continuing patient). Diagnosis code and site of service were determined by the first hospice
claim for a beneficiary. Diagnosis categories are consistent with those outlined in Abt’s 2015 technical report (https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/Hospice/Downloads/December-2015-Technical-Report.pdf).
Note 1: ‘‘Other’’ category includes inpatient hospital, inpatient hospice facility, LTCH, IPF, and places not otherwise specified. Although dementia was no longer a
valid primary diagnosis for the hospice benefit, our study time period examines primary diagnoses dating back to 2006.
Note 2: The data used for this table spans multiple years (2006 and forward). We were not able to convert ICD–9–CM diagnosis codes to ICD–10–CM codes,
given the inherent complexities with appropriately mapping ICD–9–CM codes to ICD–10–CM codes, in time for this proposed rule. Therefore, we limited this analysis
to those hospice patients that were discharged (alive or deceased) in FY 2015.
As we indicated above, the average
lifetime length of stay across all levels
of care at admission was 96.1 days in FY
2016. However, the average lifetime
length of stay was 114 days in FY 2016
when the level of care was RHC at
admission (see Table 5 below). This
suggests that beneficiaries not receiving
RHC level of care at admission had
shorter lifetime lengths of stay
compared to the beneficiaries whose
level of care was RHC at admission. In
particular, those beneficiaries who are
admitted to hospice at the GIP level of
care typically are more acute and often
die without transitioning to RHC and
thus, have overall shorter lengths of
stay. Therefore, the shorter lengths of
stay for those admitted at the GIP level
of care affect the overall average lifetime
length of stay across all levels of care.
TABLE 5—AVERAGE LIFETIME LENGTH OF STAY LEVEL OF CARE TO RHC AT ADMISSION, FY 2015–FY 2016
FY 2015
Number of
benes
Any Level of Care at Admission ..............................................................
RHC at Admission ...................................................................................
FY 2016
Average
lifetime
length of stay
1,111,967
897,298
Number of
benes
95.16
113.51
1,117,643
909,961
Average
lifetime
length of stay
96.14
114.02
Source: Common Working File (CWF). All hospice claims from 2006 to 2016 were included, for beneficiaries whose final claim in FY 2016, according to through date, for a hospice discharge (excluded status code ‘‘30’’, indicating a continuing patient).
nlaroche on DSK30NT082PROD with PROPOSALS3
Live Discharges
A beneficiary who has elected hospice
may revoke his or her hospice election
at any time and for any reason. The
regulations state that if the hospice
beneficiary (or his or her representative)
revokes the hospice election, the
beneficiary may, at any time, re-elect to
receive hospice coverage for any other
hospice election period that he or she is
eligible to receive (§ 418.24(e) and
§ 418.28(c)(3)). Immediately upon
hospice revocation, Medicare coverage
resumes for those Medicare benefits
previously waived with the hospice
election. A revocation can only be made
by the beneficiary, in writing, and must
specify the effective date of the
revocation. A hospice cannot ‘‘revoke’’
a beneficiary’s hospice election, nor is it
appropriate for hospices to encourage,
request, or demand that the beneficiary
or his or her representative revoke his
or her hospice election. Like the hospice
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election, a hospice revocation is to be an
informed choice based on the
beneficiary’s goals, values and
preferences for the services the person
wishes to receive through Medicare.
Federal regulations limit the
circumstances in which a Medicare
hospice provider may discharge a
patient from its care. In accordance with
§ 418.26, discharge from hospice care is
permissible when the patient moves out
of the provider’s service area, is
determined to be no longer terminally
ill, or for cause. Hospices may not
discharge the patient at their discretion,
even if the care may be costly or
inconvenient for the hospice program.
As we indicated in the FY 2015 Hospice
Wage Index and Payment Rate Update
proposed and final rules, we understand
that the rate of live discharges should
not be zero, given the uncertainties of
prognostication and the ability of
beneficiaries and their families to
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revoke the hospice election at any time
(79 FR 26549 and 79 FR 50463). On July
1, 2012, we began collecting discharge
information on the claim to capture the
reason for all types of discharges which
includes, death, revocation, transfer to
another hospice, moving out of the
hospice’s service area, discharge for
cause, or due to the beneficiary no
longer being considered terminally ill
(that is, no longer qualifying for hospice
services). In FY 2016, approximately 17
percent of hospice beneficiaries were
discharged alive (see Figure 1 below).
Beneficiary revocations represented 38
percent of all live discharges whereas 51
percent of live discharges were
instances where the beneficiary was
discharged because the beneficiary was
considered no longer terminally ill, and
11 percent of live discharges were
instances where beneficiaries
transferred to other hospices. In
analyzing hospice live discharge rates
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over time, Figure 1 demonstrates an
incremental decrease in average annual
rates of live discharge rates from FY
2007 to FY 2015, but an increase in the
live discharge rate between FY 2015 and
FY 2016. Between FY 2007 and FY
2016, there has been a reduction in the
live discharge rate of 22.8 percent over
this time period.
As part of our ongoing monitoring
efforts, we analyzed the distribution of
live discharge rates among hospices
with 50 or more discharges (discharged
alive or deceased). Table 6 shows that
there is significant variation in the rate
of live discharge between the 10th and
90th percentiles. Most notably, hospices
at the 95th percentile discharged 49.1
percent of their patients alive in FY
2016. While the live discharge rate in
FY 2016 for every percentile has
decreased compared to FY 2014, the
median live discharge rate remains
around 17 percent.
TABLE 6—DISTRIBUTION OF LIVE DISCHARGE RATES FOR HOSPICES WITH 50 OR MORE LIVE DISCHARGES, FY 2014 TO
FY 2016
Live discharge rate
Statistics
FY 2014
5th Percentile ...............................................................................................................................
10th Percentile .............................................................................................................................
25th Percentile .............................................................................................................................
Median .........................................................................................................................................
75th Percentile .............................................................................................................................
90th Percentile .............................................................................................................................
95th Percentile .............................................................................................................................
# Providers ...................................................................................................................................
7.5%
9.0%
12.4%
17.6%
26.5%
39.4%
50.0%
3,160
FY 2015
6.9%
8.5%
11.6%
16.8%
24.6%
35.9%
45.6%
3,215
FY 2016
6.8%
8.4%
11.6%
16.9%
25.4%
37.2%
49.1%
3,232
Finally, we looked at the distribution
of live discharges by length of stay
intervals. In looking at the length of stay
intervals, 26 percent of the live
discharges occurred within 30 days of
the start of hospice care, 13 percent
between 31 to 60 days, 14 percent
between 61 to 90 days, 19 percent
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between 91 to 180 days, and 28 percent
of live discharges occurred after a length
of stay over 180 days of hospice care
(see Figure 2 below). The proportion of
live discharges occurring between the
length of stay intervals was relatively
constant from FY 2013 to FY 2016.
Overall, our analyses do not reveal any
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anomalies in trends in lengths of stay
and rates of live discharge at this time.
However, we will continue to monitor
the data available so as to identify any
concerning behavior in response to
recent payment policy reforms.
E:\FR\FM\03MYP3.SGM
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nlaroche on DSK30NT082PROD with PROPOSALS3
Source: FY 2014, FY 2015, and FY 2016 hospice claims data from Common Working File (CWF) that list a discharge status code (meaning
claims were excluded if they listed status code 30, indicating a continuing patient). Live discharges were defined as hospice claims with a status
code of ‘‘01’’.
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nlaroche on DSK30NT082PROD with PROPOSALS3
b. Skilled Visits in the Last Days of Life
As we noted in both the FY 2016 and
FY 2017 Hospice Wage Index and
Payment Rate Update final rules (80 FR
47164 and 81 FR 52143, respectively),
we are concerned that many hospice
beneficiaries may not be receiving
skilled visits during the last days of life.
In the period of time immediately
preceding death, patient needs typically
surge and more intensive services are
warranted, so we expect that the
provision of care would proportionately
escalate in order to meet the increased
clinical, emotional, and other needs of
the hospice beneficiary and his or her
family and caregiver(s). The last week of
life is typically the period within the
terminal illness trajectory that is
associated with the highest symptom
burden, typically marked by impactful
physical and emotional symptoms,
necessitating attentive care and
engagement from the integrated hospice
team.
In the FY 2016 Hospice Wage Index
and Payment Rate Update final rule (80
FR 47164 through 47177), the Service
Intensity Add-on (SIA) payment policy
was finalized with an implementation
date of January 1, 2016. This payment
was developed in part with the objective
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of encouraging visits during the last
days of life. Additionally, in the FY
2017 Hospice Wage Index and Payment
Rate Update final rule (81 FR 52143) we
finalized two new hospice quality
reporting program (HQRP) measures,
effective April 1, 2017: (1) Hospice
Visits When Death is Imminent,
assessing hospice staff visits to patients
and caregivers in the last week of life;
and (2) Hospice and Palliative Care
Composite Process Measure, assessing
the percentage of hospice patients who
received care processes consistent with
existing guidelines. These efforts
represent meaningful advances in
encouraging visits to hospice
beneficiaries during the time period
preceding death.
In the FY 2016 Hospice Wage Index
and Payment Rate Update final rule (80
FR 47164), commenters expressed
concern regarding potential impacts of
the new payment policies. Some noted
that the new payment structures could
potentially impact patient access to
hospice care and articulated concerns
around provider jettisoning of hospice
beneficiaries, specifically around the 60day mark of a hospice stay. In response
to these concerns, we pledged to
monitor real-time hospice data,
evaluating for any shifts in utilization or
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Sfmt 4702
provision of services to Medicare
beneficiaries.
As part of our monitoring efforts, we
assessed the delivery of hospice care
during the period of time preceding
death. Analysis of FY 2016 claims data,
which encompasses hospice claims
from October 1, 2015 through
September 30, 2016, shows that on any
given day during the last 7 days of a
hospice election, nearly 44 percent of
the time the patient has not received a
skilled visit (skilled nursing or social
worker visit) (see Table 7 below). This
figure represents an incremental
improvement when compared to the
figures presented in our FY 2017
Hospice Wage Index and Payment Rate
Update proposed rule (81 FR 25515),
where FY 2014 claims showed
approximately 46 percent for this
metric. Additionally, Table 7 shows that
approximately 21 percent of
beneficiaries did not receive a skilled
visit (skilled nursing or social work
visit) on the day of death in FY 2016.
This value also indicates an
improvement compared to the FY 2014
claims data, in which nearly 26 percent
of hospice beneficiaries did not receive
a skilled visit on the day of death (81
FR 25515).
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TABLE 7—FREQUENCY AND LENGTH OF SKILLED NURSING AND SOCIAL WORK VISITS (COMBINED) DURING THE LAST 7
DAYS OF A HOSPICE ELECTION ENDING IN DEATH, FY 2016
Days Before Death
Visit length
0 days (day
of death)
(%)
No Visit .............................
15 Minutes to 1 Hour .......
1 Hour, 15 Minutes to 2
Hours ............................
2 Hours, 15 Minutes to 3
Hours ............................
3 Hours, 15 Minutes to 3
Hours, 45 Minutes ........
4 or More Hours ...............
1 day
(%)
2 days
(%)
3 days
(%)
4 days
(%)
5 days
(%)
6 days
(%)
All 7 days
combined
(%)
21.2
25.6
36.7
30.0
43.7
28.2
48.9
26.7
53.1
25.2
55.8
24.4
58.0
23.7
43.6
26.5
26.8
20.0
17.8
15.9
14.5
13.5
12.6
17.9
13.8
7.1
5.8
4.9
4.3
3.9
3.5
6.6
4.8
7.8
2.3
3.9
1.8
2.7
1.5
2.1
1.2
1.7
1.1
1.4
1.0
1.2
2.1
3.3
Source: FY 2016 hospice claims data from Common Working File (CWF) (as of December 9, 2016).
While Table 7 above shows the
frequency and length of skilled nursing
and social work visits combined during
the last 7 days of a hospice election in
FY 2016, Tables 8 and 9 below show the
frequency and length of visits for skilled
nursing and social work separately.
(see Tables 8 and 9, respectively). We
believe it is important to ensure that
beneficiaries and their families and
caregivers are, in fact, receiving the
level of care necessary during critical
periods such as the very end of life.
Analysis of FY 2016 claims data shows
that on any given day during the last 7
days of a hospice election, almost 47
percent of the time the patient had not
received a visit by a skilled nurse, and
90 percent of the time the patient had
not received a visit by a social worker
TABLE 8—FREQUENCY AND LENGTH OF SKILLED NURSING VISITS DURING THE LAST 7 DAYS OF A HOSPICE ELECTION
ENDING IN DEATH, FY 2016
Days Before Death
Visit length
0 days (day
of death)
(%)
No Visit .............................
15 Minutes to 1 Hour .......
1 Hour, 15 Minutes to 2
Hours ............................
2 Hours, 15 Minutes to 3
Hours ............................
3 Hours, 15 Minutes to 3
Hours, 45 Minutes ........
4 or More Hours ...............
1 day
(%)
2 days
(%)
3 days
(%)
4 days
(%)
5 days
(%)
6 days
(%)
All 7 days
combined
(%)
22.7
26.4
39.6
31.5
46.9
29.1
52.2
27.0
56.5
25.2
59.2
24.1
61.5
23.2
46.5
27.0
27.3
19.0
16.8
14.9
13.4
12.5
11.5
17.2
13.2
5.4
4.2
3.5
3.0
2.7
2.4
5.4
4.1
6.2
1.6
2.9
1.2
1.9
0.9
1.4
0.7
1.2
0.7
1.0
0.6
0.8
1.5
2.4
Source: FY 2016 hospice claims data from Common Working File (CWF) (as of December 9, 2016).
TABLE 9—FREQUENCY AND LENGTH OF SOCIAL WORK VISITS DURING THE LAST 7 DAYS OF A HOSPICE ELECTION
ENDING IN DEATH, FY 2016
Days Before Death
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Visit length
0 days (day
of death)
(%)
No Visit .............................
15 Minutes to 1 Hour .......
1 Hour, 15 Minutes to 2
Hours ............................
2 Hours, 15 Minutes to 3
Hours ............................
3 Hours, 15 Minutes to 3
Hours, 45 Minutes ........
4 or More Hours ...............
1 day
(%)
2 days
(%)
3 days
(%)
4 days
(%)
5 days
(%)
6 days
(%)
All 7 days
combined
89.9
6.3
87.1
8.8
88.6
7.8
89.7
7.1
90.5
6.6
91.1
6.3
91.4
6.1
89.6
7.1
2.7
3.4
3.0
2.7
2.5
2.3
2.2
2.7
0.7
0.5
0.4
0.4
0.3
0.3
0.3
0.4
0.2
0.2
0.1
0.1
0.1
0.1
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0.1
0.1
Source: FY 2016 hospice claims data from Common Working File (CWF) (as of December 9, 2016).
Additionally, we have analyzed the
overall levels of nursing and medical
social services provided during the 7
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days prior to death. In an assessment of
FY 2015 claims, we estimate that the
total number of hours of skilled
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reported with code G0154) and medical
social services visits, provided to
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averaging around 1.6 hours per day. For
the period spanning January 1, 2016
through December 31, 2016, our
analysis shows that approximately 1.24
hours of services were provided by RNs,
0.18 hours were provided by LPNs, and
0.18 hours were provided by social
workers per day. We note that for
purposes of the SIA payment, only those
hours of service provided by an RN,
which became separately categorized as
G0299 beginning January 1, 2016, and
medical social worker count toward the
calculation of the SIA payment.
Additionally, we note that G0154 was
retired as of January 1, 2016; however,
this code was still reported by some
providers in the months of January and
February 2016, and thus was included
in Figure 3.
Given this evaluation of the initial
wave of data, which now encompasses
the payment policy changes that began
on January 1, 2016, we do not believe
that the results highlight any immediate
concerns regarding behavior changes
among hospices, and it appears that
beneficiaries are receiving similar levels
of care when compared to time periods
prior to the implementation of the
payment policy reforms. As more
complete data become available, we will
continue to monitor the provision of
services at end-of-life and impacts of the
SIA payment and other policies.
for services related to the treatment of
the individual’s condition with respect
to which a diagnosis of terminal illness
has been made, except for services
provided by the designated hospice and
the attending physician. Hospice
services are comprehensive and we have
reiterated since 1983 that ‘‘virtually all’’
care needed by the terminally ill
individual would be provided by
hospice. We believe that it would be
unusual and exceptional to see services
provided outside of hospice for those
individuals who are approaching the
end of life. However, we continue to
conduct ongoing analysis of nonhospice spending during a hospice
election and the results of our analysis
seems to suggest the unbundling of
items and services that perhaps should
have been provided and covered under
the Medicare hospice benefit.
We first reported findings on 2012
non-hospice spending during a hospice
election in the FY 2015 Hospice Wage
Index and Payment Rate Update final
rule (79 FR 50452). This proposed rule
updates our analysis of non-hospice
spending during a hospice election
using FY 2016 data. We found that in
FY 2016, Medicare paid over $900
million for items and services under
Parts A, B, and D for beneficiaries
during a hospice election. Medicare
payments for non-hospice Part A and
Part B items and services received by
hospice beneficiaries during hospice
election were $748 million in FY 2012,
$712 million in FY 2013, $624 million
in FY 2014, $593 million in FY 2015,
c. Non-Hospice Spending
When a beneficiary elects the
Medicare hospice benefit, he or she
waives the right to Medicare payment
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Medicare hospice beneficiaries in the
RHC level of care in the 7 days
preceding death was approximately 1.61
hours per day. As depicted in Figure 3
below, from our analysis of FY 2016
hospice claims data that begins January
1, 2016 and spans through December 31,
2016, a relatively consistent level of
nursing and medical social services
visits are being provided among RHC
days in the 7 days prior to death,
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20765
However, there continues to be a nontrivial amount of non-hospice Parts A
and B spending on beneficiaries under
a hospice election, and we will continue
to monitor data regarding this issue
Recent analyses of Part D prescription
drug event (PDE) data suggest that the
current prior authorization (PA) has
reduced Part D program payments for
drugs in four targeted categories
(analgesics, anti-nauseants, anti-anxiety,
and laxatives). However, under
Medicare Part D there has been an
increase in hospice beneficiaries filling
prescriptions for a separate category of
drugs we refer to as maintenance drugs,
as recently analyzed by CMS.5
Currently, maintenance drugs for
beneficiaries under a hospice election
are not subject to the Part D PA process.
After a hospice election, many
maintenance drugs as well as drugs
used to treat or cure a condition are
typically discontinued as the focus of
care shifts to palliation and comfort
measures. However, there are
maintenance drugs that are appropriate
to continue as they may offer symptom
relief for the palliation and management
of the terminal illness and related
conditions, and therefore should be
covered under the hospice benefit, not
Part D. Examples of maintenance drugs
are those used to treat high blood
pressure, heart disease, asthma and
diabetes. These categories include beta
blockers, calcium channel blockers,
corticosteroids, and insulin.
5 https://www.cms.gov/Medicare/Medicare-Feefor-Service-Payment/Hospice/Downloads/2016-1115-Part-D-Hospice-Guidance.pdf.
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EP03MY17.003
each year since we began reporting
these findings. Overall, from FY 2012 to
FY 2016 non-hospice Medicare
spending for Parts A and B during
hospice election declined 25 percent.
We also examined Part D spending from
FY 2012 to FY 2016 for those
beneficiaries under a hospice election.
The data shows Medicare payments for
non-hospice Part D drugs received by
hospice beneficiaries during a hospice
election were $331.3 million in FY
2012, $348 million in FY 2013, $294
million in FY 2014, $315.2 million in
FY 2015, and $347.5 million in FY 2016
(see Figure 5). In contrast to nonhospice spending during a hospice
election for Medicare Parts A and B
items and services, non-hospice
spending for Part D drugs increased in
FY 2016 compared to FY 2012.
nlaroche on DSK30NT082PROD with PROPOSALS3
and $534 million in FY 2016 (see Figure
4 below). The beneficiary cost sharing
amount in FY 2016 was $129.6 million.
Non-hospice spending for Part A and
Part B items and services has decreased
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prognosis.5 In our ongoing analysis of
non-hospice spending, we remain
concerned that common palliative and
other disease-specific drugs for hospice
beneficiaries that should be covered
under the Part A Medicare hospice
FY 2016
Component
benefit are instead being covered and
expenditures
paid for through Part D. Based on our
Gross Total Drug Costs,
own analysis as demonstrated in the
Reported ........................
436,130,318 data provided above and similar
analyses conducted by the Office of the
Source: Analysis of 100% FY 2016 Medicare Claim Files. For more information on the Inspector General (OIG) regarding Part D
components above and on Part D data, go to drug expenditures for Medicare hospice
the Research Data Assistance Center’s beneficiaries, we believe that Medicare
(ResDAC’s)
Web
site
at:
https:// could be paying twice for drugs that are
www.resdac.org/.
already covered under the hospice per
diem payment by also paying for them
Hospices are responsible for covering
under Part D.6
TABLE 10—DRUG COST SOURCES FOR drugs and biologicals related to the
We continue to expect that hospices
HOSPICE BENEFICIARIES’ FY 2016 palliation and management of the
should be providing virtually all of the
DRUGS RECEIVED THROUGH PART D terminal illness and while the patient is care needed by terminally ill
under hospice care. For a prescription
individuals, including related
FY 2016
drug to be covered under Part D for an
Component
prescription drugs. The comprehensive
expenditures
individual enrolled in hospice, the drug nature of the services covered under the
Medicare hospice benefit is structured
Patient Pay Amount ..............
$47,289,374 must be for treatment unrelated to the
terminal illness or related conditions.
such that hospice beneficiaries should
Low Income Cost-Sharing
Subsidy .............................
103,715,821 After a hospice election, many
not have to routinely seek items,
maintenance drugs or drugs used to
Other True Out-of-Pocket
services, and/or medications beyond
Amount ..............................
1,749,182 treat or cure a condition are typically
those provided by hospice. The hospice
Patient Liability Reduction
discontinued as the focus of care shifts
medical director, the attending
due to Other Payer
to palliation and comfort measures.
physician (if any), and the hospice IDG
Amount ..............................
15,868,623
However, those same drugs may be
Covered Drug Plan Paid
5 https://www.cms.gov/Medicare/Medicare-FeeAmount ..............................
243,791,919 appropriate to continue as they may
for-Service-Payment/Hospice/Downloads/2016-11offer symptom relief for the palliation
Non-Covered Plan Paid
15-Part-D-Hospice-Guidance.pdf.
Amount ..............................
7,878,966 and management of the terminal
6 https://oig.hhs.gov/oas/reports/region6/
Six Payment Amount Totals
Unknown/Unreconciled .........
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TABLE 10—DRUG COST SOURCES FOR
HOSPICE BENEFICIARIES’ FY 2016
DRUGS RECEIVED THROUGH PART
D—Continued
420,293,884
15,836,435
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for Prescriptions for Beneficiaries in Hospice.’’
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Table 10 below details the various
components of Part D spending for
patients receiving hospice care for FY
2016. The portion of the $436.1 million
total Part D spending that was paid by
Medicare is the sum of the Low Income
Cost-Sharing Subsidy (row 2 in Table
10) and the Covered Drug Plan Paid
Amount (row 5), or approximately
$347.5 million. The beneficiary cost
sharing amount was approximately
$64.9 million, including patient pay
amount (row 1), other true out-of-pocket
amount (row 3), and patient liability
reduction due to other payer amount
(row 4).
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determine, on a case-by-case basis, what
items and services are related and
unrelated to the palliation and
management of the terminal illness and
related conditions during the admission
process, the initial and comprehensive
assessments, and in the development of
the hospice plan of care (§§ 418.25,
418.54, and 418.56).
To the extent that individuals receive
services outside of the Medicare hospice
benefit, Medicare coverage is
determined by whether or not the
services are for the treatment of a
condition completely unrelated to the
individual’s terminal illness and related
conditions (48 FR 38148). However, we
have presented hospice monitoring data
from the past several years, as seen
above, that continue to show a nontrivial amount of items, services, and
medications being furnished outside of
the Medicare hospice benefit to
beneficiaries under a hospice election.
We encourage hospices to educate
beneficiaries regarding the
comprehensive nature of the hospice
benefit. Although it should be rare, if
any conditions are identified by the
hospice as unrelated to the terminal
illness and related conditions, we
further encourage hospices to inform the
beneficiary (or representative) at or near
the time of election and provide the
clinical rationale for such
determinations. The regulations at
§ 476.78 state that providers must
inform Medicare beneficiaries at the
time of admission, in writing, that the
care for which Medicare payment is
sought will be subject to Quality
Improvement Organization (QIO)
review. If a beneficiary disagrees with
the hospice determination of what
conditions are unrelated to the terminal
illness and related conditions (and thus
arguably not provided as part of the
hospice benefit), we strongly encourage
hospices to work to resolve the
disagreement with the beneficiary (or
representative), taking into
consideration his or her wishes,
treatment preferences and goals. If a
resolution cannot be reached, the
beneficiary and the hospice can agree to
participate in a flexible, dialogue-based
resolution process, called immediate
advocacy, which is coordinated by the
QIO. We will continue to monitor nonhospice spending during a hospice
election and consider ways to address
this issue through future regulatory and/
or program integrity efforts, if needed.
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2. Initial Analysis of Revised Hospice
Cost Report Data
a. Background
As mentioned in section II.B of this
proposed rule, the Medicare hospice per
diem payment amounts were developed
to cover all services needed for the
palliation and management of the
terminal illness and related conditions,
as described in section 1861(dd)(1) of
the Act. Services provided under a
written plan of care could include:
Nursing care provided by or under the
supervision of a registered professional
nurse; physical therapy, occupational
therapy, speech-language pathology
services; counseling (including dietary
counseling); medical social services
under the direction of a physician;
services of a home health aide;
homemaker services; medical supplies
(including drugs and biologicals) and
the use of durable medical equipment;
physician services; short-term inpatient
care (including both respite care and
care necessary for pain control and
acute and chronic symptom
management) in a qualified inpatient
facility; or any other item or service
which has been specified in the plan of
care for which payment may be made
under Medicare. Under the current
payment system, hospices are paid for
each day that a beneficiary is enrolled
in hospice care, regardless of whether
services are rendered on any given day.
As described in the FY 2016 Hospice
Wage Index and Payment Rate Update
final rule, we finalized changes to the
hospice cost report form in order to
broaden the scope and detail of data we
collect regarding the costs of providing
hospice care (80 FR 47150).7 We
believed that changes were needed to
the hospice cost report in order to
collect data on the costs of services
provided at each level of care, rather
than by costs per day, regardless of the
level of care. The revisions to the cost
report form for freestanding hospices
became effective for cost reporting
periods beginning on or after October 1,
2014. The instructions for completing
the revised freestanding hospice cost
report form are found in the Medicare
Provider Reimbursement Manual—Part
2, chapter 43.8 Medicare-certified
institutional providers are required to
submit an annual cost report to a
Medicare Administrative Contractor
7 CMS Transmittal 2864. ‘‘Additional Data
Reporting Requirements for Hospice Claims’’,
Available at: https://www.cms.gov/Regulations-andGuidance/Guidance/Transmittals/Downloads/
R2864CP.pdf.
8 https://www.cms.gov/Regulations-andGuidance/Guidance/Transmittals/Downloads/
R1P243.pdf.
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20767
(MAC). The cost report contains
provider information such as facility
characteristics, utilization data, costs by
cost center (for all payers as well as
Medicare), Medicare settlement data,
and financial statement data.
b. Methodology
Section 1814(i)(6) of the Act, as
amended by section 3132(a)(1)(B) of the
Affordable Care Act, authorized the
Secretary to collect additional data and
information determined appropriate to
revise payments for hospice care and
other purposes. The data collected may
be used to revise the methodology for
determining the payment rates for RHC
and other services included in hospice
care. Effective October 1, 2014, we
finalized changes to the hospice cost
report to improve data collection on the
costs of providing hospice care. We
conducted a preliminary analysis of the
new cost report data (CMS Form 1984–
14) for freestanding hospices with cost
reporting periods in FY 2015, which
totaled 2,675 reports. Using this data we
calculated preliminary estimates of total
costs per day by level of care. It is
important to note that the values we
computed for cost per day include all
payer sources, both Medicare and nonMedicare; however, we believe that the
total cost figures represent a reasonable
proxy for estimating costs related to the
provision of care for Medicare
beneficiaries. In order to compute total
Medicare-related costs by level of care,
we multiplied the computed cost per
day by level of care (as reported on
Worksheet C) for each hospice by the
number of Medicare days by level of
care. We then calculated total payments
by level of care for each hospice by
multiplying the FY 2015 Medicare
hospice payments by level of care by the
number of Medicare days by level of
care. Total costs, payments, and days by
level of care were summed for each
unique hospice. In order to more
accurately account for the hourly CHC
cost per day, we used data from
Medicare claims in order to quantify the
hours of CHC provided by summing the
hours of CHC reported in revenue center
0652, which tallies the units of CHC
care. We then divided the CHC costs by
the number of CHC hours as reported in
revenue center 0652 to calculate a CHC
per-hour value. In order to mitigate the
impact of statistical outliers, we applied
trims on the outer bounds of cost per
day by level of care, set at the 1st and
99th percentile of the distribution.
c. Overall Payments and Costs and Costs
by Level of Care
For the purposes of evaluating
calculated costs per day by level of care
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compared to Medicare payment
amounts, we compared the reported
costs on the Medicare cost report to the
FY 2015 per diem payment rates by
level of care, as follows (79 FR 50485).
We note that these amounts were not
adjusted by geographic differences in
wage rates and are meant to serve as a
general benchmark:
• $159.34 for RHC
• $929.91 for 24 hours of CHC (hourly
rate of $38.75)
• $164.81 for IRC
• $708.77 for GIP
Table 11 shows the distribution of the
calculated Average Cost Per Day by
Level of Care, using data from
Worksheet C—Rows 3, 8, 13, 18—
Column 3.
TABLE 11—SUMMARY STATISTICS: MEDICARE COSTS PER DAY BY LEVEL OF CARE, FY 2015
Level of care
Number of
cost
reports
Mean
Weighted
mean
Minimum
value
25th
Percentile
Median
75th
Percentile
Maximum
value
CHC cost per day,
per hour.
1,088
$91
$49
$4
$18
$51
$95
$1,853
RHC cost per day ..
IRC cost per day ...
GIP cost per day ...
2,578
1,930
1,782
133
632
1,079
123
467
792
50
38
64
105
221
564
125
343
879
150
549
1,251
399
17,813
10,858
FY2015
per diem
payment
amounts
$929.91
for 24
hours
($38.75
hourly
rate).
159.34.
164.81.
708.77.
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Source: Medicare hospice cost report data for FY 2015.
As mentioned above, the data
analyzed were trimmed to minimize the
effect of statistical anomalies.
Nevertheless, there is substantial
variation in the reported cost per day by
hospices. Total cost per day values in
the four levels of care span from a
minimum of $4 to maximum values in
the tens of thousands. Because of this
wide range of values in the distribution,
we used the median as well as the mean
values weighted by the number of days
by level of care as reference points in
these preliminary analyses. When
compared with the FY 2015 per diem
payment rates, the calculated median
and weighted mean costs associated
with providing RHC are lower than the
base payment rates. As noted in section
III.A of this proposed rule, the RHC
level of care accounts for over 98
percent of all hospice days based on our
analysis of claims for FY 2016. The
median and weighted mean costs for the
provision of RHC are estimated at $125
and $123 respectively, with both figures
presenting lower values than the FY
2015 per diem payment rate of $159.34,
a difference of approximately $35 per
day.
Conversely, for CHC the estimated
median and weighted mean costs per
day, per hour are $51 and $49,
respectively. The FY 2015 payment rate
for CHC was $38.75 per hour. The CHC
level of care accounts for approximately
0.27 percent of all hospice days in FY
2016, as noted in section III.A of this
proposed rule. Similarly, the median
and weighted mean costs per day
associated with the provision of GIP
care is estimated at $879 and $792,
respectively, while the FY 2015 per
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diem payment amount for GIP was
$708.77. As noted in section III.A of this
proposed rule, the GIP level of care
accounts for approximately 1.40 percent
of all hospice days based on our
analysis of FY 2016 claims. Likewise,
the median and weighted mean costs
per day associated with the IRC level of
care are estimated at $343 and $467,
respectively, while the per diem
payment amount for FY 2015 was
$164.81, and we estimate that IRC days
represent approximately 0.31 percent of
all hospice days in FY 2016 claims as
described in section III.A above.
We recognize that this is the first
period in which hospices have supplied
cost information on the revised cost
report that became effective for cost
reporting periods beginning on or after
October 1, 2014 and expect that some of
the early trends may be the result of
hospices learning how to accurately
report this information. Therefore, any
interpretations regarding the overall
alignment between costs and payment
would likely be premature given the
newness of the data. Moreover, this
preliminary analysis did not incorporate
factors that merit consideration in future
analyses, such as the exclusion of
providers surpassing the hospice
inpatient and aggregate caps as well as
the application of a more robust
trimming process to the cost report
dataset. As we continue to gather more
cost report data, we plan to conduct
more thorough analyses of the cost
report data and fully assess Medicarerelated hospice costs as compared with
Medicare hospice payments by level of
care. We encourage hospices to continue
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to submit the most accurate data
possible on Medicare cost reports.
B. Proposed FY 2018 Hospice Wage
Index and Rate Update
1. Proposed FY 2018 Hospice Wage
Index
The hospice wage index is used to
adjust payment rates for hospice
agencies under the Medicare program to
reflect local differences in area wage
levels, based on the location where
services are furnished. The hospice
wage index utilizes the wage adjustment
factors used by the Secretary for
purposes of section 1886(d)(3)(E) of the
Act for hospital wage adjustments. Our
regulations at § 418.306(c) require each
labor market to be established using the
most current hospital wage data
available, including any changes made
by OMB to the Metropolitan Statistical
Areas (MSAs) definitions.
We use the previous FY’s hospital
wage index data to calculate the hospice
wage index values. For FY 2018, the
hospice wage index will be based on the
FY 2017 hospital pre-floor, prereclassified wage index. This means that
the hospital wage data used for the
hospice wage index is not adjusted to
take into account any geographic
reclassification of hospitals including
those in accordance with section
1886(d)(8)(B) or 1886(d)(10) of the Act.
The appropriate wage index value is
applied to the labor portion of the
payment rate based on the geographic
area in which the beneficiary resides
when receiving routine home care
(RHC) or continuous home care (CHC).
The appropriate wage index value is
applied to the labor portion of the
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payment rate based on the geographic
location of the facility for beneficiaries
receiving general inpatient care (GIP) or
Inpatient Respite Care (IRC).
There exist some geographic areas
where there were no hospitals, and thus,
no hospital wage index data on which
to base the calculation of the hospice
wage index. In the FY 2008 Hospice
Wage Index final rule (72 FR 50214), we
implemented a methodology to update
the hospice wage index for such areas.
In cases where there was a rural area
without rural hospital wage data, we use
the average pre-floor, pre-reclassified
hospital wage index data from all
contiguous Core-Based Statistical Areas
(CBSAs), to represent a reasonable
proxy for the rural area. The term
‘‘contiguous’’ means sharing a border
(72 FR 50217). Currently, the only rural
area without a hospital from which
hospital wage data could be derived is
Puerto Rico. However, for rural Puerto
Rico, we would not apply this
methodology due to the distinct
economic circumstances that exist there
(for example, due to the close proximity
to one another of almost all of Puerto
Rico’s various urban and non-urban
areas, this methodology would produce
a wage index for rural Puerto Rico that
is higher than that in half of its urban
areas); instead, we would continue to
use the most recent wage index
previously available for that area. For
FY 2018, we propose to continue to use
the most recent pre-floor, prereclassified hospital wage index value
available for Puerto Rico, which is
0.4047.
In the FY 2010 Hospice Wage Index
final rule (74 FR 39386), we adopted the
policy that for urban labor markets
without a hospital from which hospital
wage index data could be derived, all of
the CBSAs within the state would be
used to calculate a statewide urban
average pre-floor, pre-reclassified
hospital wage index value to use as a
reasonable proxy for these areas. For FY
2018, the only CBSA without a hospital
from which hospital wage data can be
derived is 25980, Hinesville-Fort
Stewart, Georgia.
As described in the August 8, 1997
Hospice Wage Index final rule (62 FR
42860), the pre-floor and prereclassified hospital wage index is used
as the raw wage index for the hospice
benefit. These raw wage index values
are subject to application of the hospice
floor to compute the hospice wage index
used to determine payments to
hospices. Pre-floor, pre-reclassified
hospital wage index values below 0.8
are adjusted by a 15 percent increase
subject to a maximum wage index value
of 0.8. For example, if County A has a
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pre-floor, pre-reclassified hospital wage
index value of 0.3994, we would
multiply 0.3994 by 1.15, which equals
0.4593. Since 0.4593 is not greater than
0.8, then County A’s hospice wage
index would be 0.4593. In another
example, if County B has a pre-floor,
pre-reclassified hospital wage index
value of 0.7440, we would multiply
0.7440 by 1.15 which equals 0.8556.
Because 0.8556 is greater than 0.8,
County B’s hospice wage index would
be 0.8.
On February 28, 2013, OMB issued
OMB Bulletin No. 13–01, announcing
revisions to the delineation of MSAs,
Micropolitan Statistical Areas, and
Combines Statistical Areas, and
guidance on uses of the delineation in
these areas. In the FY 2016 Hospice
Wage Index final rule (80 FR 47178), we
adopted the OMB’s new area
delineations using a 1-year transition. In
the FY 2016 Hospice Wage Index and
Payment Rate Update final rule (80 FR
47178), we stated that beginning
October 1, 2016, the wage index for all
hospice payments would be fully based
on the new OMB delineations. The most
recent bulletin (No. 15–01) concerning
the revised delineations was published
by the OMB on July 15, 2015.
The proposed hospice wage index
applicable for FY 2018 (October 1, 2017
through September 30, 2018) is
available on the Web site at: https://
www.cms.gov/Medicare/Medicare-Feefor-Service-Payment/Hospice/
index.html.
2. Proposed Hospice Payment Update
Percentage
Section 4441(a) of the Balanced
Budget Act of 1997 (BBA) (Pub. L. 105–
33) amended section 1814(i)(1)(C)(ii)(VI)
of the Act to establish updates to
hospice rates for FYs 1998 through
2002. Hospice rates were to be updated
by a factor equal to the inpatient
hospital market basket percentage
increase set out under section
1886(b)(3)(B)(iii) of the Act, minus 1
percentage point. Payment rates for FYs
since 2002 have been updated according
to section 1814(i)(1)(C)(ii)(VII) of the
Act, which states that the update to the
payment rates for subsequent FYs must
be the inpatient market basket
percentage increase for that FY. The Act
historically required us to use the
inpatient hospital market basket as the
basis for the hospice payment rate
update.
Section 3401(g) of the Affordable Care
Act mandated that, starting with FY
2013 (and in subsequent FYs), the
hospice payment update percentage
would be annually reduced by changes
in economy-wide productivity as
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specified in section 1886(b)(3)(B)(xi)(II)
of the Act. The statute defines the
productivity adjustment to be equal to
the 10-year moving average of changes
in annual economy-wide private
nonfarm business multifactor
productivity (MFP). In addition to the
MFP adjustment, section 3401(g) of the
Affordable Care Act also mandated that
in FY 2013 through FY 2019, the
hospice payment update percentage
would be reduced by an additional 0.3
percentage point (although for FY 2014
to FY 2019, the potential 0.3 percentage
point reduction is subject to suspension
under conditions specified in section
1814(i)(1)(C)(v) of the Act).
Normally, the proposed hospice
payment update percentage for FY 2018
would have been based on the estimated
inpatient hospital market basket update
of 2.9 percent (based on IHS Global
Insight, Inc.’s fourth quarter 2016
forecast with historical data through the
third quarter of 2016 of the proposed
2014-based IPPS market basket). Due to
the requirements at section
1886(b)(3)(B)(xi)(II) of the Act, the
estimated FY 2018 inpatient hospital
market basket update of 2.9 percent
would have been reduced by a MFP
adjustment as mandated by Affordable
Care Act (currently estimated to be 0.4
percentage point for FY 2018). Section
1814(i)(1)(C)(v) of the Act requires that
the estimated inpatient hospital market
basket update for FY 2018 would be
reduced further by 0.3 percentage point.
In effect, the proposed hospice payment
update percentage for FY 2018 would be
2.2 percent. However, section 411(d) of
the Medicare Access and CHIP
Reauthorization Act of 2015, Public Law
114–10 (April 16, 2015) (MACRA)
amended section 1814(i)(1)(C) of the Act
such that for hospice payments for FY
2018, the market basket percentage
increase, after application of the
productivity adjustment and the 0.3
percent reduction, if applicable, shall be
1 percent. Therefore, for FY 2018, the
hospice payment update percentage will
be 1 percent.
Currently, the labor portion of the
hospice payment rates is as follows: For
RHC, 68.71 percent; for CHC, 68.71
percent; for General Inpatient Care,
64.01 percent; and for Respite Care,
54.13 percent. The non-labor portion is
equal to 100 percent minus the labor
portion for each level of care. Therefore,
the non-labor portion of the payment
rates is as follows: For RHC, 31.29
percent; for CHC, 31.29 percent; for
General Inpatient Care, 35.99 percent;
and for Respite Care, 45.87 percent.
Beginning with cost reporting periods
starting on or after October 1, 2014,
freestanding hospice providers are
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required to submit cost data using CMS
Form 1984–14 (https://www.cms.gov/
Research-Statistics-Data-and-Systems/
Downloadable-Public-Use-Files/CostReports/Hospice-2014.html). We are
currently analyzing this data for
possible use in updating the labor
portion of the hospice payment rates.
Any changes to the labor portions will
be proposed in future rulemaking and
will be subject to public comments.
3. Proposed FY 2018 Hospice Payment
Rates
There are four payment categories that
are distinguished by the location and
intensity of the services provided. The
base payments are adjusted for
geographic differences in wages by
multiplying the labor share, which
varies by category, of each base rate by
the applicable hospice wage index. A
hospice is paid the RHC rate for each
day the beneficiary is enrolled in
hospice, unless the hospice provides
CHC, IRC, or GIP. CHC is provided
during a period of patient crisis to
maintain the patient at home; IRC is
short-term care to allow the usual
caregiver to rest and be relieved from
caregiving; and GIP is to treat symptoms
that cannot be managed in another
setting.
As discussed in the FY 2016 Hospice
Wage Index and Payment Rate Update
final rule (80 FR 47172), we
implemented two different RHC
payment rates, one RHC rate for the first
60 days and a second RHC rate for days
61 and beyond. In addition, in the final
rule, we adopted a Service Intensity
Add-on (SIA) payment for RHC for
when direct patient care is provided by
a RN or social worker during the last 7
days of the beneficiary’s life. The SIA
payment is equal to the CHC hourly rate
multiplied by the hours of nursing or
social work provided (up to 4 hours
total) that occurred on the day of
service, if certain criteria are met. In
order to maintain budget neutrality, as
required under section 1814(i)(6)(D)(ii)
of the Act, the new RHC rates were
adjusted by a SIA budget neutrality
factor.
As discussed in the FY 2016 Hospice
Wage Index and Payment Rate Update
final rule (80 FR 47177), we will
continue to make the SIA payments
budget neutral through an annual
determination of the SIA budget
neutrality factor (SBNF), which will
then be applied to the RHC payment
rates. The SBNF will be calculated for
each FY using the most current and
complete FY utilization data available at
the time of rulemaking. For FY 2018, we
calculated the SBNF using FY 2016
utilization data. We examined skilled
nursing and social work visit data for
the last 7 days of life where RHC was
billed and found that, from January 1
through September 30, 2016,
approximately 86 percent of nursing
visits were identified as RN visits (using
G0299) and 14 percent of nursing visits
were identified as LPN visits (using
G0300). For skilled nursing visits during
the last 7 days of life where RHC was
billed and that occurred between
October 1 and December 31, 2015, we
assumed that 86 percent of the line item
visits reported using G0154 were RN
and 14 percent were LPN. For FY 2018,
the budget neutrality adjustment that
would apply to days 1 through 60 is
calculated to be 1.0018. The budget
neutrality adjustment that would apply
to days 61 and beyond is calculated to
be 1.0005.
In the FY 2017 Hospice Wage Index
and Payment Rate Update final rule (82
FR 52156), we initiated a policy of
applying a wage index standardization
factor to hospice payments in order to
eliminate the aggregate effect of annual
variations in hospital wage data. In
order to calculate the wage index
standardization factor, we simulate total
payments using the proposed FY 2018
hospice wage index and compare it to
our simulation of total payments using
the FY 2017 hospice wage index. By
dividing payments for each level of care
using the proposed FY 2018 wage index
by payments for each level of care using
the FY 2017 wage index, we obtain a
wage index standardization factor for
each level of care (RHC days 1–60, RHC
days 61+, CHC, IRC, and GIP). The wage
index standardization factors for each
level of care are shown in the tables
below.
Lastly, the hospice payment rates for
hospices that submit the required
quality data would be increased by the
proposed FY 2018 hospice payment
update percentage of 1.0 percent as
discussed in section III.B.2. The
proposed FY 2018 RHC rates are shown
in Table 12. The proposed FY 2018
payment rates for CHC, IRC, and GIP are
shown in Table 13.
TABLE 12—PROPOSED FY 2018 HOSPICE RHC PAYMENT RATES
FY 2017
payment
rates
Code
Description
651 ....................
651 ....................
Routine Home Care (days 1–60) .....
Routine Home Care (days 61+) .......
$190.55
$149.82
SBNF
× 1.0018
× 1.0005
Wage index
standardization
factor
FY 2018
proposed
hospice
payment
update
× 1.0000
× 1.0001
× 1.01
× 1.01
FY 2018
Proposed
payment
rates
$192.80
$151.41
TABLE 13—PROPOSED FY 2018 HOSPICE CHC, IRC, AND GIP PAYMENT RATES
FY 2017
payment
rates
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Code
Description
652 ....................
Continuous Home Care ................................................
Full Rate = 24 hours of care
$40.68 = FY 2018 hourly rate
Inpatient Respite Care ..................................................
General Inpatient Care .................................................
655 ....................
656 ....................
Sections 1814(i)(5)(A) through (C) of
the Act require that hospices submit
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FY 2018
proposed
hospice
payment
update
FY 2018
proposed
payment
rates
$964.63
× 1.0022
× 1.01
$976.42
170.97
734.94
× 1.0006
× 1.0017
× 1.01
× 1.01
172.78
743.55
quality data, based on measures to be
specified by the Secretary. In the FY
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factor
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2012 Hospice Wage Index final rule (76
FR 47320 through 47324), we
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implemented a Hospice Quality
Reporting Program (HQRP) as required
by section 3004 of the Affordable Care
Act. Hospices were required to begin
collecting quality data in October 2012,
and submit that quality data in 2013.
Section 1814(i)(5)(A)(i) of the Act
20771
2018 rates for hospices that do not
submit the required quality data would
be updated by the proposed FY 2018
hospice payment update percentage of 1
percent minus 2 percentage points.
These rates are shown in Tables 14 and
15.
requires that beginning with FY 2014
and each subsequent FY, the Secretary
shall reduce the market basket update
by 2 percentage points for any hospice
that does not comply with the quality
data submission requirements with
respect to that FY. The proposed FY
TABLE 14—PROPOSED FY 2018 HOSPICE RHC PAYMENT RATES FOR HOSPICES THAT DO NOT SUBMIT THE REQUIRED
QUALITY DATA
FY 2017
payment
rates
Code
Description
651 ....................
651 ....................
Routine Home Care (days 1–60) .....
Routine Home Care (days 61+) .......
$190.55
$149.82
SBNF
Wage index
standardization
factor
× 1.0018
× 1.0005
FY 2018
proposed
hospice
payment
update of 1%
minus 2
percentage
points = -0.1%
× 1.0000
× 1.0001
× 0.99
× 0.99
FY 2018
proposed
payment
rates
$188.98
148.41
TABLE 15—PROPOSED FY 2018 HOSPICE CHC, IRC, AND GIP PAYMENT RATES FOR HOSPICES THAT DO NOT SUBMIT
THE REQUIRED QUALITY DATA
FY 2017
payment
rates
Code
Description
652 ....................
Continuous Home Care ................................................
Full Rate = 24 hours of care
$39.88 = FY 2018 hourly rate
Inpatient Respite Care ..................................................
General Inpatient Care .................................................
655 ....................
656 ....................
4. Hospice Cap Amount for FY 2018
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As discussed in the FY 2016 Hospice
Wage Index and Payment Rate Update
final rule (80 FR 47183), we
implemented changes mandated by the
Improving Medicare Post-Acute Care
Transformation Act of 2014 (IMPACT
Act). Specifically, for accounting years
that end after September 30, 2016 and
before October 1, 2025, the hospice cap
is updated by the hospice payment
update percentage rather than using the
consumer price index for urban
consumers (CPI–U). The hospice cap
amount for the 2018 cap year will be
$28,689.04, which is equal to the 2017
cap amount ($28,404.99) updated by the
FY 2018 hospice payment update
percentage of 1.0 percent.
C. Discussion and Solicitation of
Comments Regarding Sources of
Clinical Information for Certifying
Terminal Illness
Hospice provides relief from pain and
symptoms, provides psychosocial and
spiritual comfort, and allows an
individual to die with dignity and
surrounded by family and friends.
Despite the invaluable support hospices
offer, it is not an easy decision and not
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Wage index
standardization
factor
× 1.0022
× 0.99
$957.08
$170.97
734.94
× 1.0006
× 1.0017
× 0.99
× 0.99
$169.36
728.83
9 Michelle T. Weckmann, MD, MS, University of
Iowa Hospitals and Clinics, Iowa The Role of the
Family Physician in the Referral and Management
of Hospice Patients. Am Fam Physician, 2008 Mar
15;77(6):807–812.
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Proposed
payment
rates
$964.63
one individuals generally arrive at on
their own. Election of hospice is a
significant decision and one which
patients and their physicians do not
take lightly, as it involves a shift in
traditional health care philosophy from
curative to palliative care. In general,
the majority of hospice referrals do
come from family physicians who have
often cared for patients with chronic
illnesses for long periods of time.9
These providers are in the unique
position of understanding and
identifying the individualized
progression of the patient’s illness and
recognizing when the condition
becomes terminal. To be eligible to elect
the Medicare hospice benefit, the
individual must have Medicare Part A
and be certified as terminally ill as
articulated at § 418.20. The regulations
define ‘‘terminally ill’’ to mean that the
individual has a medical prognosis that
his or her life expectancy is 6 months
or less if the illness runs its normal
course (§ 418.3). The regulations at
§ 418.22(c) require that for the initial 90-
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update
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day period of hospice care, the hospice
must obtain written certification
statements from the medical director of
the hospice or the physician member of
the hospice interdisciplinary group, and
the individual’s attending physician, if
the individual has an attending
physician. The current regulations at
§ 418.25(b) state that in reaching a
decision to certify, the hospice medical
director, or hospice physician designee
reviews the clinical information for each
hospice patient and provides written
certification that it is anticipated that
the patient’s life expectancy is 6 months
or less if the illness runs its normal
course. These regulations require that
the hospice medical director consider at
least the following information:
1. Diagnosis of the terminal condition
of the patient.
2. Other health conditions, whether
related or unrelated to the terminal
condition.
3. Current clinically relevant
information supporting all diagnoses.
The admission requirements at
§ 418.22(b)(2) require that this clinical
information and other documentation
that supports the medical prognosis
must accompany the certification and be
filed in the medical record with the
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written certification. Whereas the
regulations at § 418.25(b) provide the
type of clinical information the hospice
medical director or hospice physician
designee must consider in the
certification of terminal illness, the
source of this clinical information is not
clearly identified. This raises the
question as to what clinical information
the hospice medical director (or hospice
physician designee) is relying on to
support his or her certification that the
individual is terminally ill and from
where this information was obtained.
Multiple clinical tools and guidelines,
and more specifically the Medicare
Administrative Contractor (MAC) Local
Coverage Determinations (LCDs), exist
to assist the patient-designated
attending physician and hospice
medical director/hospice physician
designee in determining the patient’s
terminal prognosis. These guidelines
provide indicators that support a
decline in clinical status, including, but
not limited to: History of recurrent
infections, worsening symptoms that are
non- responsive to treatment, increasing
emergency department and clinician
visits, laboratory results supporting
progression of disease, and change in
functional status.10 However,
documentation of these indicators
would likely not exist without some
degree of long-term monitoring and
evaluation by a physician separate from
the hospice medical director/hospice
physician designee. As such, this
information would typically be found in
the referring physician’s and/or acute/
post- acute care facility’s medical
records.
Understandably, many family
physicians typically take on the role of
the attending physician once the patient
chooses to elect hospice. They have
played an invaluable role in
coordinating care throughout the
spectrum of the patient’s life, and as
such, have in depth ‘‘knowledge of the
patient’s values, family issues, and
communication style.’’ 11 However, in
accordance with our regulation at
§ 418.22(c)(1)(ii), only the initial
certification has to involve the attending
physician and only IF the patient has
designated one. There is currently no
requirement that a patient must
designate an attending physician and
therefore the responsibility for
certification can solely reside with the
hospice medical director or the
10 https://www.cms.gov/medicare-coveragedatabase/details/lcd-details.aspx.
11 Michelle T. Weckmann, MD, MS, University of
Iowa Hospitals and Clinics, Iowa City, Iowa The
Role of the Family Physician in the Referral and
Management of Hospice Patients. Am Fam
Physician, 2008 Mar 15;77(6):807–812.
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physician member of the hospice
interdisciplinary group. Furthermore,
this regulation does not require that the
hospice medical director or physician
member of the hospice interdisciplinary
group designee has a face-to-face
encounter with the patient when
initially certifying the patient as
terminally ill. Rather, a face-to-face
encounter with a hospice physician or
allowed non-physician practitioner is
not required until the third election
period and each subsequent
recertification thereafter. Consequently,
a patient may never be seen by the
hospice physician who is certifying that
he or she is terminally ill.
No visits to the patient are covered
under the Medicare hospice benefit
until the individual has been certified as
terminally ill, an election statement has
been signed, and a plan of care has been
established (§ 418.200). Therefore, any
information regarding the patient’s
health status from hospice staff (for
example, registered nurses) should not
be the sole documentation used to
support the initial certification
requirement as the patient has yet to
meet the eligibility requirement.
Because Medicare hospice coverage
depends on being certified as terminally
ill and requires an individual to waive
rights to Medicare payment for services
for the terminal illness and related
conditions, except when provided by
the designated hospice or attending
physician, the expectation is that the
hospice physician certifying terminal
illness will be thorough and accountable
in his review of clinical information. As
discussed in the 1983 final rule
‘‘Medicare Program; Hospice Care’’,
‘‘written certification is the only true
assurance that the patient’s condition
has been assessed at or before the time
of admission to a hospice program’’ (48
FR 56010). This is important to both the
hospice who will be assuming virtually
all of the care needs of the terminally ill
individual and to the patient, who must
have a thorough basis for his or her
decision to elect hospice rather than
continue curative care.
There are ongoing concerns that some
hospice patients may be inappropriately
certified as terminally ill. Operation
Restore Trust (ORT), an anti-fraud and
abuse initiative by the Department of
Health and Human Services Office of
Inspector General (OIG) to identify
vulnerabilities in the Medicare program
and to pursue ways to reduce
Medicare’s exposure to fraud and abuse,
identified several areas of weakness in
the hospice benefit, primarily in the
area of hospice eligibility. Specifically,
it uncovered instances of insufficient
hospice documentation and
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inappropriately reported diagnoses.4 In
1995, in response to ORT’s initial
report, CMS issued program memoranda
requiring submission of clinical
information and other documentation
that supports the medical prognosis.
The Medicare, Medicaid, and SCHIP
Benefits Improvement and Protection
Act of 2000 amended section 1814(a) of
the Social Security Act (The Act)
clarifying that certification is based on
the physician or medical director’s
clinical judgment. Regardless,
subsequent ORT reports and CMS
Regional Offices and Regional Home
Health Intermediary (now called
Medicare Administrative Contractors)
reviews continued to raise concerns
regarding inappropriate certifications,
specifically, certifications made for
patients who are chronically ill, but
who are without complications or other
circumstances that indicate a life
expectancy of 6 months or less.12
In response to those concerns, the
‘‘Medicare Program; Hospice Care
Amendments’’ proposed rule (67 FR
70363, November 22, 2002), which
proposed the implementation of
revisions required by the Balanced
Budget Act of 1997, the Medicare,
Medicaid, and SCHIP Balanced Budget
Refinement Act of 1999, and the
Medicare, Medicaid, and SCHIP
Benefits Improvement and Protection
Act of 2000 to the existing regulations
at the time governing coverage and
payment for hospice care under the
Medicare program, proposed revisions
to § 418.22, Certification of Terminal
Illness, requiring that specific clinical
findings and other documentation
supporting the medical prognosis
accompany the written certification and
be filed in the hospice medical record.
Additionally, the 2002 rule proposed
adding § 418.25 Admission to Hospice
Care, which established general
guidance on hospice admission
procedures. These changes
acknowledged that ‘‘the amendment
regarding the physician’s clinical
judgment does not negate the fact that
there must be a basis for certification’’
and that ‘‘a mere signed certification,
absent a medically sound basis that
supports the clinical judgment, is not
sufficient for application of the hospice
benefit under Medicare.’’ Ultimately,
the final rule, ‘‘Medicare Program;
Hospice Care Amendments’’ (70 FR
70532, November 22, 2005) codified the
requirements and the expectations about
the clinical information needed to
12 Department of Health and Human Services:
Office of the Inspector General. Operation Restore
Trust Activities by June Gibbs Brown, IG. November
1995.
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support the certification of a medical
prognosis of 6 months or less at § 418.22
(70 FR 70538). The final rule also set out
the specific admission requirements
indicating that the hospice medical
director along with the patient’s
attending physician, if any, is
responsible for admitting the patient,
and identifies what information he or
she must consider when certifying a
patient as terminally ill (§ 418.25).
Additionally, the Medicare Payment
Advisory Commission’s (MedPAC)
March 2009 report entitled ‘‘Report to
the Congress: Medicare’s Payment
Policy’’ noted specific concerns
regarding trends towards an increasing
proportion of hospice patients with
stays exceeding 180 days.13 An analysis
of this trend by a hospice expert panel
illuminated limited medical director
engagement in the certification or
recertification process as a possible
cause of this utilization pattern, reviving
concerns that patients were again being
inappropriately certified as terminally
ill and were not actually eligible to elect
the benefit. The panel determined that
‘‘physicians responsible for certifying
and recertifying a patient’s eligibility for
hospice may inappropriately delegate
much of this responsibility to other
parties.’’ In response to these concerns,
we finalized a policy requiring that
certifications and recertifications
include a brief narrative describing the
clinical basis for the patient’s prognosis.
The FY 2010 Hospice Wage Index final
rule (74 FR 39398) codified this
narrative requirement for the
certification of terminal illness at
§ 418.22(b)(3), in order to increase
accountability and add oversight to the
physician certification/recertification
process
In the ‘‘Medicare Program; Hospice
Wage Index and Payment Rate Update
FY 2015’’ final rule (79 FR 50470), we
again provided guidance on determining
beneficiaries’ eligibility for hospice,
reiterating that the hospice ‘‘is required
to make certain that the physician’s
clinical judgment can be supported by
clinical information and other
documentation that provide a basis for
the certification of a life expectancy of
6 months or less if the illness runs its
normal course.’’ This discussion
reinforced the importance of ensuring
that hospices are thorough in their
eligibility determinations so that
hospice beneficiaries are able to access
all of their Medicare benefits
13 Medicare Payment Advisory Commission.
Report to the Congress: Medicare’s Payment Policy.
Washington, DC, March 2009_Accessed on March
31, 2017 at: https://www.medpac.gov/docs/defaultsource/reports/march-2009-report-to-congressmedicare-payment-policy.pdf?sfvrsn=0.
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appropriately and added additional
oversight to the physician certification
and recertification process. The inherent
challenges in prognostication make it
critical for a hospice to obtain, and the
certifying hospice medical director or
hospice physician designee to
comprehensively review, the patient’s
clinical information when making the
determination that the patient is
terminally ill, and thus eligible for the
Medicare hospice benefit. By increasing
physician engagement and
accountability, patients can be assured
they are making the most informed
decision possible, without limiting their
treatment choices. In the FY 2006
Hospice Wage Index final rule (70 FR
70538), we received comments stating
that it is common practice for hospices
to obtain clinical information from the
referring physician, which is then
documented in the patient’s hospice
medical record.
Accordingly, we are soliciting
comments for possible future
rulemaking, on amending the
regulations at § 418.25 to specify that
the referring physician’s and/or the
acute/post-acute care facility’s medical
record would serve as the basis for
initial hospice eligibility
determinations. Clinical information
from the referring physician and/or
acute/post-acute care facility supporting
a terminal prognosis would be obtained
by the hospice prior to election of the
benefit, when determining certification
and subsequent eligibility. This
potential clarifying regulatory text
change would be in alignment with
benefit eligibility criteria that the
individual must be certified as
terminally ill prior to receiving hospice
services, and fundamentally could not
be determined by hospice
documentation obtained after
admission. We are also soliciting
comments on amending the regulations
text at § 418.25 to specify that
documentation of an in-person visit
from the hospice Medical Director or the
hospice physician member of the
interdisciplinary group could be used as
documentation to support initial
hospice eligibility determinations, only
if needed to augment the clinical
information from the referring
physician/facility’s medical records.
Comments on current processes used by
hospices to ensure comprehensive
clinical review to support certification
and any alternate suggestions for
supporting clinical documentation
sources are also encouraged.
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D. Proposed Updates to the Hospice
Quality Reporting Program (HQRP)
1. Background and Statutory Authority
Section 3004(c) of the Affordable Care
Act amended section 1814(i)(5) of the
Act to authorize a quality reporting
program for hospices. Section
1814(i)(5)(A)(i) of the Act requires that
beginning with FY 2014 and each
subsequent FY, the Secretary shall
reduce the market basket update by 2
percentage points for any hospice that
does not comply with the quality data
submission requirements for that FY.
Depending on the amount of the annual
update for a particular year, a reduction
of 2 percentage points could result in
the annual market basket update being
less than 0 percent for a FY and may
result in payment rates that are less than
payment rates for the preceding FY. Any
reduction based on failure to comply
with the reporting requirements, as
required by section 1814(i)(5)(B) of the
Act, would apply only for the particular
year involved. Any such reduction
would not be cumulative or be taken
into account in computing the payment
amount for subsequent FYs. Section
1814(i)(5)(C) of the Act requires that
each hospice submit data to the
Secretary on quality measures specified
by the Secretary. The data must be
submitted in a form, manner, and at a
time specified by the Secretary.
2. General Considerations Used for
Selection of Quality Measures for the
HQRP
Any measures selected by the
Secretary must be endorsed by the
consensus-based entity, which holds a
contract regarding performance
measurement, including the
endorsement of quality measures, with
the Secretary under section 1890(a) of
the Act. This contract is currently held
by the National Quality Forum (NQF).
However, section 1814(i)(5)(D)(ii) of the
Act provides that in the case of a
specified area or medical topic
determined appropriate by the Secretary
for which a feasible and practical
measure has not been endorsed by the
consensus-based entity, the Secretary
may specify measures that are not so
endorsed as long as due consideration is
given to measures that have been
endorsed or adopted by a consensusbased organization identified by the
Secretary. Our paramount concern is the
successful development of a HQRP that
promotes the delivery of high quality
healthcare services. We seek to adopt
measures for the HQRP that promote
person-centered, high quality, and safe
care. Our measure selection activities
for the HQRP take into consideration
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input from the Measure Applications
Partnership (MAP), convened by the
NQF, as part of the established CMS
pre-rulemaking process required under
section 1890A of the Act. The MAP is
a public-private partnership comprised
of multi-stakeholder groups convened
by the NQF for the primary purpose of
providing input to CMS on the selection
of certain categories of quality and
efficiency measures, as required by
section 1890A(a)(3) of the Act. By
February 1st of each year, the NQF must
provide that input to CMS. Input from
the MAP is located at: https://
www.qualityforum.org/Setting_
Priorities/Partnership/Measure_
Applications_Partnership.aspx. We also
take into account national priorities,
such as those established by the HHS
Strategic Plan (https://www.hhs.gov/
secretary/about/priorities/
priorities.html), the National Strategy
for Quality Improvement in Healthcare,
(https://www.ahrq.gov/
workingforquality/reports/annualreports/nqs2015annlrpt.htm) and the
CMS Quality Strategy (https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/QualityInitiativesGenInfo/
CMS-Quality-Strategy.html). To the
extent practicable, we have sought to
adopt measures endorsed by member
organizations of the National Consensus
Project (NCP) (https://
www.nationalconsensusproject.org/
Default.aspx), recommended by multistakeholder organizations, and
developed with the input of providers,
purchasers/payers, and other
stakeholders.
We consider related factors that may
affect measures in the HQRP. We
understand that social risk factors such
as income, education, race and
ethnicity, employment, disability,
community resources, and social
support (certain factors of which are
also sometimes referred to as
socioeconomic status (SES) factors or
socio-demographic status (SDS) factors)
play a major role in health. One of our
core objectives is to improve beneficiary
outcomes including reducing health
disparities, and we want to ensure that
all beneficiaries, including those with
social risk factors, receive high quality
care. In addition, we seek to ensure that
the quality of care furnished by
providers and suppliers is assessed as
fairly as possible under our programs
while ensuring that beneficiaries have
adequate access to excellent care.
We have been reviewing reports
prepared by the Office of the Assistant
Secretary for Planning and Evaluation
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(ASPE) 14 and the National Academies
of Sciences, Engineering, and Medicine
on the issue of measuring and
accounting for social risk factors in
CMS’ value-based purchasing and
quality reporting programs, and
considering options on how to address
the issue in these programs. On
December 21, 2016, ASPE submitted a
Report to Congress on a study it was
required to conduct under section 2(d)
of the Improving Medicare Post-Acute
Care Transformation (IMPACT) Act of
2014. The study analyzed the effects of
certain social risk factors of Medicare
beneficiaries on quality measures and
measures of resource use used in one or
more of nine Medicare value-based
purchasing programs.15 The report also
included considerations for strategies to
account for social risk factors in these
programs. In a January 10, 2017 report
released by The National Academies of
Sciences, Engineering, and Medicine,
that body provided various potential
methods for measuring and accounting
for social risk factors, including
stratified public reporting.16
In addition, the NQF has undertaken
a 2-year trial period in which new
measures, measures undergoing
maintenance review, and measures
endorsed with the condition that they
enter the trial period can be assessed to
determine whether risk adjustment for
selected social risk factors is appropriate
for these measures. This trial entails
temporarily allowing inclusion of social
risk factors in the risk-adjustment
approach for these measures. At the
conclusion of the trial, NQF will issue
recommendations on the future
inclusion of social risk factors in risk
adjustment for quality measures.
As we continue to consider the
analyses and recommendations from
these reports and await the results of the
NQF trial on risk adjustment for quality
measures, we are continuing to work
with stakeholders in this process. As we
have previously communicated, we are
concerned about holding providers to
different standards for the outcomes of
their patients with social risk factors
because we do not want to mask
potential disparities or minimize
incentives to improve the outcomes for
disadvantaged populations. Keeping
this concern in mind, while we sought
input on this topic previously, we
continue to seek public comment on
whether we should account for social
risk factors in measures in the HQRP,
and if so, what method or combination
of methods would be most appropriate
for accounting for social risk factors.
Examples of methods include:
Confidential reporting to providers of
measure rates stratified by social risk
factors, public reporting of stratified
measure rates, and potential risk
adjustment of a particular measure as
appropriate based on data and evidence.
In addition, we are also seeking
public comment on which social risk
factors might be most appropriate for
reporting stratified measure scores and/
or potential risk adjustment of a
particular measure. Examples of social
risk factors include, but are not limited
to, dual eligibility/low-income subsidy,
race and ethnicity, and geographic area
of residence. We are seeking comments
on which of these factors, including
current data sources where this
information would be available, could
be used alone or in combination, and
whether other data should be collected
to better capture the effects of social
risk. We will take commenters’ input
into consideration as we continue to
assess the appropriateness and
feasibility of accounting for social risk
factors in the HQRP. We note that any
such changes would be proposed
through future notice and comment
rulemaking.
We look forward to working with
stakeholders as we consider the issue of
accounting for social risk factors and
reducing health disparities in our
programs. Of note, implementing any of
the above methods would be taken into
consideration in the context of how this
and our other programs operate (for
example, data submission methods,
availability of data, statistical
considerations relating to reliability of
data calculations, among others), so we
also welcome comment on operational
considerations. We are committed to
ensuring that its beneficiaries have
access to and receive excellent care, and
that the quality of care furnished by
providers and suppliers is assessed
fairly in our programs.
14 https://aspe.hhs.gov/pdf-report/reportcongress-social-risk-factors-and-performanceunder-medicares-value-based-purchasingprograms.
15 https://aspe.hhs.gov/pdf-report/reportcongress-social-risk-factors-and-performanceunder-medicares-value-based-purchasingprograms.
16 National Academies of Sciences, Engineering,
and Medicine. 2017. Accounting for social risk
factors in Medicare payment. Washington, DC: The
National Academies Press.
3. Policy for Retention of HQRP
Measures Adopted for Previous
Payment Determinations
For the purpose of streamlining the
rulemaking process, we finalized our
policy in the FY 2016 Hospice Wage
Index final rule (80 FR 47187) that when
we adopt measures for the HQRP
beginning with a payment
determination year, these measures
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would automatically be adopted for all
subsequent years’ payment
determinations, unless we proposed to
remove, suspend, or replace the
measures. Quality measures would be
considered for removal by us for reasons
including, but not limited to:
• Measure performance among
hospices was so high and unvarying that
meaningful distinction in improvements
in performance could no longer be
made;
• Performance or improvement on a
measure did not result in better patient
outcomes;
• A measure did not align with
current clinical guidelines or practice;
• A more broadly applicable measure
(across settings, populations, or
conditions) for the particular topic was
available;
• A measure that was more proximal
in time to desired patient outcomes for
the particular topic was available;
• A measure that was more strongly
associated with desired patient
outcomes for the particular topic was
available; or
• Collection or public reporting of a
measure led to negative unintended
consequences.
For any such removal, the public
would be given an opportunity to
comment through the annual
rulemaking process. However, if there
was reason to believe continued
inclusion of a measure in the HQRP
would encourage delivery of care that
raised potential safety concerns, we
would take immediate action to remove
the measure from the HQRP and not
wait for the annual rulemaking cycle.
The measures would be promptly
removed and we would immediately
notify hospices and the public of such
a decision through the CMS HQRP Web
site, listserv messages via the Post-Acute
Care QRP listserv,17 MLN Connects®
National Provider Calls & Events, MLN
Connects® Provider eNews. Following
immediate removal of the measures, we
would also notify the public of any such
removal in the next annual rulemaking
cycle. CMS expects immediate removal
of a measure due to safety concerns to
be an unlikely event, given the rigorous
testing and analysis all measures
undergo prior to adoption in the HQRP.
4. Policy for Adopting Changes to
Previously Adopted Measures
To further streamline the rulemaking
process, we finalized in the FY 2017
Hospice Wage Index final rule that if
measures in the HQRP undergo non17 CMS,
Post-Acute Care QRP listerv, available at:
https://public-dc2.govdelivery.com/accounts/
USCMS/subscriber/new?topic_id=USCMS_12265.
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substantive changes in specifications as
part of their NQF re-endorsement
process, we would subsequently utilize
the measure with their new endorsed
status in the HQRP without going
through new notice-and-comment
rulemaking (81 FR 52159). As
mentioned previously, quality measures
selected for the HQRP must be endorsed
by the NQF unless they meet the
statutory criteria for exception under
section 1814(i)(5)(D)(ii) of the Act. The
NQF is a voluntary consensus standardsetting organization with a diverse
representation of consumer, purchaser,
provider, academic, clinical, and other
healthcare stakeholder organizations.
The NQF was established to standardize
healthcare quality measurement and
reporting through its consensus measure
development process (https://
www.qualityforum.org/About_NQF/
Mission_and_Vision.aspx). The NQF
undertakes review of: (a) New quality
measures and national consensus
standards for measuring and publicly
reporting on performance, (b) regular
maintenance processes for endorsed
quality measures, (c) measures with
time-limited endorsement for
consideration of full endorsement, and
(d) ad hoc review of endorsed quality
measures, practices, consensus
standards, or events with adequate
justification to substantiate the review.
Through NQF’s or the measure
steward’s measure maintenance process,
measures are sometimes updated to
incorporate changes that we believe do
not substantively change the intent of
the measure. Examples of such changes
may include updated diagnosis or
procedure codes or changes to
exclusions to the patient population or
definitions. While we address such
changes on a case-by case basis, we
generally believe these types of
maintenance changes are distinct from
substantive changes to measures that
result in what are considered new or
different measures. Additionally, since
the NQF endorsement and measure
maintenance process is one that ensures
transparency, public input, and
discussion among representatives across
the healthcare enterprise,18 we believe
that the NQF measure endorsement and
maintenance process itself is
transparent, scientifically rigorous, and
provides opportunity for public input.
Thus, we finalized our proposal to
codify at § 418.312 that if the NQF
makes only non-substantive changes to
specifications for HQRP measures in the
18 ‘‘NQF: How Endorsement Happens—National
Quality Forum.’’ 2010. 26 Jan. 2016 https://
www.qualityforum.org/Measuring_Performance/
ABCs/How_Endorsement_Happens.aspx.
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20775
NQF’s re-endorsement process, we
would continue to utilize the measure
in its new endorsed status (81 FR 52159
through 52160). If NQF-endorsed
specifications change and we do not
adopt those changes, then we would
propose the measure as a modification.
A modification of a NQF-endorsed
quality measure is utilized in instances
when we have identified a need to use
a NQF-endorsed measure in a QRP but
need to use it with one or more
modifications to the quality measure’s
specifications. These modifications
pertain to, but are not limited to, one or
more of the following aspects of a NQFendorsed quality measure: (a)
Numerator, (b) denominator, (c) setting,
(d) look-back period, (e) calculation
period, (f) risk adjustment, and (g)
revisions to data elements used to
collect the data required for the
measure, etc. CMS may adopt a quality
measure for the HQRP under section
1814(i)(5)(D)(ii) of the Act, which states,
‘‘[i]n the case of a specified area or
medical topic determined appropriate
by the Secretary for which a feasible and
practical measure has not been endorsed
by [the NQF], the Secretary may specify
a measure that is not so endorsed as
long as due consideration is given to
measures that have been endorsed or
adopted by a consensus organization
identified by the Secretary.’’ Reasons for
not adopting changes in measure
specifications to a measure may include
any of the aforementioned criteria in the
prior section, including that the new
specification does not align with
clinical guidelines or practice or that the
new specification leads to negative
unintended consequences.
Finally, we will continue to use
rulemaking to adopt substantive updates
made by the NQF to the endorsed
measures we have adopted for the
HQRP. We continue to make these
determinations about what constitutes a
substantive versus non-substantive
change on a measure-by-measure basis.
A change would be deemed substantive
if the intent of the measure changes, the
facility/setting changes, the data sources
changes, the level of analysis changes,
and/or the measure is removed. We will
continue to provide updates about
changes to measure specifications as a
result of NQF endorsement or
maintenance processes through the CMS
HQRP Web site, listserv messages on the
Post-Acute Care QRP listserv, MLN
Connects® National Provider Calls &
Events, MLN Connects® Provider eNews
and announcements on Open Door
Forums and Special Open Door Forums.
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5. Previously Adopted Quality Measures
for FY 2018 Payment Determination and
Future Years
In the FY 2014 Hospice Wage Index
final rule (78 FR 48257), and in
compliance with section 1814(i)(5)(C) of
the Act, we finalized the specific
collection of data items that support the
following 7 NQF-endorsed measures for
hospice:
• NQF #1617 Patients Treated with
an Opioid who are Given a Bowel
Regimen,
• NQF #1634 Pain Screening,
• NQF #1637 Pain Assessment,
• NQF #1638 Dyspnea Treatment,
• NQF #1639 Dyspnea Screening,
• NQF #1641 Treatment Preferences,
• NQF #1647 Beliefs/Values
Addressed (if desired by the patient).19
We finalized the following two
additional measures in the FY 2017
Hospice Wage Index final rule effective
April 1, 2017. Data collected will, if not
reported, affect payments for FY 2019
and subsequent years. (81 FR 52163
through 52173):
• Hospice Visits when Death is
Imminent
• Hospice and Palliative Care
Composite Process Measure—
Comprehensive Assessment at
Admission
We finalized the HIS effective July 1,
2014 (78 FR 48258). The HIS is the data
collection mechanism for all of the
aforementioned measures. To meet the
quality reporting requirements for
hospices for the FY 2016 payment
determination and each subsequent
year, we require regular and ongoing
electronic submission of the HIS data
for each patient admission to hospice
after July 1, 2014, regardless of payer or
patient age (78 FR 48234 through
48258). For the two measures finalized
in the FY 2017 Hospice Wage Index
final rule, we require regular and
ongoing electronic submission for each
patient admission to hospice after April
1, 2017. We finalized a requirement in
the FY 2014 Hospice Wage Index final
rule (78 FR 48258) that hospice
providers collect data on all patients to
ensure that all patients regardless of
payer or patient age are receiving the
same care and that provider metrics
measure performance across the
spectrum of patients. Table 16 below
provides a summary of measures
previously finalized affecting the FY
2019 APU, data collection mechanism,
and data submission deadline.
Hospices are required to complete and
submit a HIS-Admission and a HISDischarge record for each patient
admission. Hospices failing to report
quality data via the HIS for patient
admissions occurring in 2017 will have
their market basket update reduced by
2 percentage points in FY 2019
(beginning in October 1, 2018). In the
FY 2015 Hospice Wage Index final rule
(79 FR 50485 through 50487), we
finalized the proposal to codify the HIS
submission requirement at § 418.312.
The System of Record (SOR) Notice
titled ‘‘Hospice Item Set (HIS) System,’’
SOR number 09–70–0548, was
published in the Federal Register on
April 8, 2014 (79 FR 19341).
The 7 NQF endorsed HIS measures
adopted in FY 2014 Hospice Wage
Index final rule successfully underwent
NQF Endorsement Maintenance in
2016.20 We recognize that the NQF
endorsement process is an important
part of measure development and plan
to submit the two measures finalized in
the FY 2017 Hospice Wage Index final
rule for NQF endorsement once
sufficient measure data are available
and we conduct the analyses necessary
to support NQF submission for
endorsement (for example, reliability
and validity analyses). Typically, we
need at least 4 quarters worth of data to
conduct the necessary analyses and
establish measure reliability and
validity. Because the Hospice and
Palliative Care Composite Process
Measure—Comprehensive Assessment
at Admission did not require any new
data collection and can be calculated
using existing data, CMS’s measure
development contractor, RTI
International, has already conducted the
analyses necessary to support
submission of the measure for NQF
endorsement. We have already
submitted the Hospice and Palliative
Care Composite Process Measure for
consideration for endorsement at NQF
(NQF #3235); the measure is currently
under review. Data for the Hospice
Visits when Death is Imminent measure
pair will be collected using new items
added to the HIS V2.00.0, effective April
1, 2017. Once data collection for the
measure pair begins, we will need at
least 4 quarters of reliable data to
conduct the necessary analyses to
support submission to NQF. We will
also need to assess the quality of data
submitted in the first quarter of item
implementation to determine whether
they can be used in the analyses.
Pending analysis, we will submit the
Hospice Visits when Death is Imminent
measure pair to NQF for endorsement
review in accordance with NQF project
timelines and call for measures. In the
FY 2015 Hospice Wage Index final rule
(79 FR 50491 through 50496), we also
finalized the Consumer Assessment of
Healthcare Providers and Systems
(CAHPS®) Hospice Survey to support
quality measures based on patient and
family experience of care. We refer
readers to section III.D.11 of this notice
of proposed rulemaking for details
regarding the CAHPS® Hospice Survey,
including public reporting of selected
survey measures.
TABLE 16—PREVIOUSLY FINALIZED QUALITY MEASURES AFFECTING THE FY 2019 PAYMENT DETERMINATION AND
SUBSEQUENT YEARS
Measure name
1641 .....
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NQF No.
Payment
determination
(APU) year for
which the quality
measure was first
adopted
Treatment Preferences .............................
FY 2016 ...................
1647 .....
Beliefs/Values Addressed (if desired by
the patient).
Pain Screening ..........................................
Pain Assessment ......................................
FY 2016.
1634 .....
1637 .....
19 Previously finalized as a ‘‘modified measure’’
in the FY17 and prior rules (81 FR 52160).
Following NQF maintenance endorsement, NQF
#1647 measure specifications where updated and
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Data
collection
mechanism
Data submission
deadline
Hospice Item Set .....
Rolling—within 30 days of patient admission or discharge (event date).
FY 2016.
FY 2016.
now aligns with the measure data lookback period
for this program.
20 National Quality Forum, NQF Palliative and
End-of-Life Care 2015–2016 Report, available at:
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TABLE 16—PREVIOUSLY FINALIZED QUALITY MEASURES AFFECTING THE FY 2019 PAYMENT DETERMINATION AND
SUBSEQUENT YEARS—Continued
Payment
determination
(APU) year for
which the quality
measure was first
adopted
NQF No.
Measure name
1639 .....
1638 .....
1617 .....
Dyspnea Screening ...................................
Dyspnea Treatment ...................................
Patients Treated with an Opioid Who Are
Given a Bowel Regimen.
Hospice and Palliative Care Composite
Process Measure—Comprehensive Assessment at Admission.
FY 2019.
N/A .......
N/A .......
6. Proposed Removal of Previously
Adopted Measures
We are not proposing to remove any
of the current HQRP measures at this
time. Any future proposals regarding
removal, suspension, or replacement of
measures will be proposed in this
section of future rules. As stated in
section III.D.3, a quality measure that is
adopted and implemented in the HQRP
will be retained for all subsequent years,
unless the measure is proposed for
removal, suspension, or replacement by
CMS. Policies and criteria for removing
a measure include those identified in
section III.D.3 of this proposed rule.
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Data submission
deadline
FY 2016.
FY 2016.
FY 2016.
Hospice Visits When Death is Imminent
Measure Pair.
Data
collection
mechanism
7. Measure Concepts Under
Consideration for Future Years
Although we are not proposing any
HIS-based measures in this proposed
rule, we have measure concepts under
consideration for future years.
Our paramount concern is to develop
quality measures that promote care that
is person-centered, high quality, and
safe. We continue to work with our
measure development contractor, RTI
International, to identify measure
concepts for future implementation in
the HQRP. In identifying priority areas
for future measure enhancement and
development, we take into
consideration input from numerous
stakeholders, including the MAP, the
MedPAC, Technical Expert Panels
(TEP), and national priorities, such as
those established by the HHS Strategic
Plan, the National Strategy for Quality
Improvement in Healthcare, and the
CMS Quality Strategy. In addition, we
take into consideration vital feedback
and input from research published by
our payment reform contractor. The
current HQRP measure set is also an
important consideration for future
measure development areas; future
measure development areas should
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FY 2019 ...................
.............................
complement the current HQRP measure
set, including current HIS measures and
CAHPS® Hospice Survey measures,
without creating unnecessary burden or
redundant reporting. Based on input
from stakeholders, we identified two
high priority areas that will be
addressed by claims-based measure
development. Developing quality
measures using claims does not require
new data collection, thus minimizing
provider burden and expediting
implementation.
• Priority Area 1: Potentially Avoidable
Hospice Care Transitions
The concept of a claims-based
measure focusing on transitions of care
was first introduced in the FY 2016
Hospice Wage Index final rule (80 FR
47188 through 47189). Comments
received during this rule were overall
supportive of our efforts to develop
more robust quality measures that
capture hospice performance and show
links to patient and family outcomes.
We refer readers to the FY 2016 Hospice
Wage Index final rule (80 FR 47188
through 47189) for additional detail:
https://www.gpo.gov/fdsys/pkg/FR2015-08-06/pdf/2015-19033.pdf.
Potentially avoidable hospice care
transitions at end of life are burdensome
to patients, families, and the health care
system at large, because they are
associated with adverse health
outcomes, lower patient and family
satisfaction, higher health care costs,
and fragmentation of care
delivery.21 22 23 24 25 By encouraging
21 Aldridge MDP, MBA; Epstein, Andrew J. Ph.D.;
Brody, Abraham A. RN, Ph.D.; Lee, Eric J. MPH;
Cherlin, Emily Ph.D., MSW; Bradley, Elizabeth H.
Ph.D. The Impact of Reported Hospice Preferred
Practices on Hospital Utilization at the End of Life
Medical Care. 2016;54(7):657–663.
22 Wang S-Y, Aldridge MD, Gross CP, et al.
Transitions Between Healthcare Settings of Hospice
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Rolling—within 30 days of patient admission or discharge (event date) for patient admissions to hospice on 04/01/
2017 and onward.
hospice providers to assess and manage
patients’ risk of care transitions, this
measure concept has the potential to
improve quality care at the end of life
by reducing potentially avoidable
hospice care transitions.
• Priority Area 2: Access to Levels of
Hospice Care
The Medicare Hospice Benefit covers
four levels of care to meet patients’ and
families’ clinical needs: Routine home
care (RHC), continuous home care
(CHC), general inpatient care (GIP), and
inpatient respite care. The goal of this
measure concept is to assess the rates at
which hospices provide different levels
of hospice care. The measure has the
potential to improve access to various
levels of care for patients and caregivers.
Appropriate use of CHC and GIP
increases the likelihood of a hospice
patient dying in his or her location of
choice, decreases health resource
utilization resulting in potential cost
savings, and increases patient and
caregiver satisfaction.26 27 Measuring use
of levels of care will incentivize hospice
providers to continuously assess patient
Enrollees at the End of Life. Journal of the American
Geriatrics Society. 2016;64(2):314–322.
23 Carlson MDA, Herrin J, Du Q, et al. Impact of
Hospice Disenrollment on Health Care Use and
Medicare Expenditures for Patients With Cancer.
Journal of Clinical Oncology. 2010;28(28):4371–
4375.
24 Teno JM, Bowman J, Plotzke M, et al.
Characteristics of Hospice Programs With
Problematic Live Discharges. Journal of Pain and
Symptom Management. 2015;50(4):548–552.
25 Prsic E, Plotzke M, Christian TJ, Gozalo P, Teno
JM. A National Study of Live Hospice Discharges
between 2000 and 2012. Journal of Palliative
Medicine. 2016;19(9):987–990.
26 Barclay, J., et al., Association of hospice
patients’ income and care level with place of death.
JAMA Internal Medicine, 2013. 173(6): p. 450–456.
27 Casarett, D., et al., Does Continuous Hospice
Care Help Patients Remain at Home? Journal of Pain
and Symptom Management, 2015. 50(3): p. 297–
304.
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and caregiver needs and provide the
appropriate level of care to meet these
needs.
These two measure concepts are
under development, and details
regarding measure definitions,
specifications and timeline for
implementation will be communicated
in future rulemaking. We are soliciting
comments regarding high priority
concept areas for future measure
development.
8. Form, Manner, and Timing of Quality
Data Submission
a. Background
Section 1814(i)(5)(C) of the Act
requires that each hospice submit data
to the Secretary on quality measures
specified by the Secretary. Such data
must be submitted in a form and
manner, and at a time specified by the
Secretary. Section 1814(i)(5)(A)(i) of the
Act requires that beginning with the FY
2014 and for each subsequent FY, the
Secretary shall reduce the market basket
update by 2 percentage points for any
hospice that does not comply with the
quality data submission requirements
for that FY.
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b. Policy for New Facilities To Begin
Submitting Quality Data
In the FY 2015 Hospice Wage Index
final rule (79 FR 50488), we finalized a
policy stating that any hospice that
receives its CMS Certification Number
(CCN) (also known as the Medicare
Provider Number) notification letter
dated on or after November 1 of the
preceding year involved is excluded
from any payment penalty for quality
reporting purposes for the following FY.
This requirement was codified at
§ 418.312.
In the FY 2016 Hospice Wage Index
final rule (80 FR 47189), we further
clarified and finalized our policy for the
timing of new providers to begin
reporting data to CMS. The clarified
policy finalized in the FY 2016 Hospice
Wage Index final rule (80 FR 47189)
distinguished between when new
hospice providers are required to begin
submitting HIS data and when providers
will be subject to the potential 2
percentage point annual payment
update (APU) reduction for failure to
comply with HQRP requirements. In
summary, the policy finalized in the FY
2016 Hospice Wage Index final rule (80
FR 47189 through 47190) clarified that
providers must begin submitting HIS
data on the date listed in the letterhead
of the CCN Notification letter received
from CMS but will be subject to the
APU reduction based on whether the
CCN Notification letter was dated before
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or after November 1 of the reporting
year involved. Thus, beginning with the
FY 2018 payment determination and for
each subsequent payment
determination, we finalized our policy
that a new hospice be responsible for
HQRP quality data submission
beginning on the date of the CCN
notification letter; we retained our prior
policy that hospices not be subject to
the APU reduction if the CCN
notification letter was dated after
November 1 of the year involved. For
example, if a provider receives their
CCN notification letter and the date in
the letterhead is November 5, 2017, that
provider will begin submitting HIS data
for patient admissions occurring after
November 5, 2017. However, since the
CCN notification letter was dated after
November 1st, they would not be
evaluated for, or subject to any payment
penalties for, the relevant FY APU
update (which in this instance is the FY
2019 APU, which is associated with
patient admissions occurring January 1,
2017 through December 31, 2017).
This policy allows us to receive HIS
data on all patient admissions on or
after the date a hospice receives their
CCN notification letter, while at the
same time allowing hospices flexibility
and time to establish the necessary
accounts for data submission before
they are subject to the potential APU
reduction for a given reporting year.
Currently, new hospices may experience
a lag between Medicare certification and
receipt of their actual CCN Number.
Since hospices cannot submit data to
the QIES ASAP system without a valid
CCN Number, we finalized that new
hospices begin collecting HIS quality
data beginning on the date noted on the
CCN notification letter. We believe this
policy provides sufficient time for new
hospices to establish appropriate
collection and reporting mechanisms to
submit the required quality data to
CMS. Requiring quality data reporting
beginning on the date listed in the
letterhead of the CCN notification letter
aligns our policy requirements for new
providers with the functionality of the
HIS data submission system (QIES
ASAP).
c. Previously Finalized Data Submission
Mechanisms, Timelines, and Deadlines
In the FY 2015 Hospice Wage Index
final rule (79 FR 50486), we finalized
our policy requiring that hospices
complete and submit HIS records for all
patient admissions to hospice after July
1, 2014. For each HQRP program year,
we require that hospices submit data on
each of the adopted measures in
accordance with the reporting
requirements specified in sections
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III.C.9.b through III.C.9.c of the FY 2015
rule for the designated reporting period.
This requirement applies to previously
finalized and adopted measures, as well
as new measures proposed through the
rulemaking process. Electronic
submission is required for all HIS
records. Although electronic submission
of HIS records is required, hospices do
not need to have an electronic medical
record to complete or submit HIS data.
In the FY 2014 Hospice Wage Index
final rule (78 FR 48258), we finalized a
provision requiring that providers use
either the Hospice Abstraction
Reporting Tool (HART) (which is free to
download and use) or vendor-designed
software to complete HIS records. HART
provides an alternative option for
hospice providers to collect and
maintain facility, patient, and HIS
Record information for subsequent
submission to the QIES ASAP system.
Once HIS records are complete,
electronic HIS files must be submitted
to CMS via the QIES ASAP system.
Electronic data submission via the QIES
ASAP system is required for all HIS
submissions; there are no other data
submission methods available. Hospices
have 30 days from a patient admission
or discharge to submit the appropriate
HIS record for that patient through the
QIES ASAP system. We will continue to
make HIS completion and submission
software available to hospices at no cost.
We provided details on data collection
and submission timing under the
downloads section of the HIS Web page
on the CMS.gov Web site at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/Hospice-Quality-Reporting/
Hospice-Item-Set-HIS.html.
The QIES ASAP system provides
reports upon successful submission and
processing of the HIS records. The final
validation report may serve as evidence
of submission. This is the same data
submission system used by nursing
homes, inpatient rehabilitation
facilities, home health agencies, and
long-term care hospitals for the
submission of Minimum Data Set
Version 3.0 (MDS 3.0), Inpatient
Rehabilitation Facility-patient
assessment instrument (IRF–PAI),
Outcome Assessment Information Set
(OASIS), and Long-Term Care Hospital
Continuity Assessment Record &
Evaluation Data Set (LTCH CARE),
respectively. We have provided
hospices with information and details
about use of the HIS through postings
on the HQRP Web site, Open Door
Forums, announcements in the CMS
MLN Connects® Provider e-News (ENews), and provider training.
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Hospices are evaluated for purposes
of the quality reporting program based
on whether or not they submit data, not
on their substantive performance level
for the required quality measures. In
order for us to appropriately evaluate
the quality reporting data received by
hospice providers, it is essential HIS
data be received in a timely manner.
The submission date is the date on
which the completed record is
submitted and accepted by the QIES
ASAP system. In the FY 2016 Hospice
Wage Index final rule (80 FR 47191), we
finalized our policy that beginning with
the FY 2018 payment determination,
hospices must submit all HIS records
within 30 days of the event date, which
is the patient’s admission date for HISAdmission records or discharge date for
HIS-Discharge records.
For HIS-Admission records, the
submission date must be no later than
the admission date plus 30 calendar
days. The submission date can be equal
to the admission date, or no greater than
30 days later. The QIES ASAP system
will issue a warning on the Final
Validation Report if the submission date
is more than 30 days after the patient’s
admission date.
For HIS-Discharge records, the
submission date must be no later than
the discharge date plus 30 calendar
days. The submission date can be equal
to the discharge date, or no greater than
30 days later. The QIES ASAP system
will issue a warning on the Final
Validation Report if the submission date
is more than 30 days after the patient’s
discharge date.
The QIES ASAP system validation
edits are designed to monitor the
timeliness of submission and ensure
that providers’ submitted records
conform to the HIS data submission
specifications. Providers are notified
when timing criteria have not been met
by warnings that appear on their Final
Validation Reports. A standardized data
collection approach that coincides with
timely submission of data is essential to
establish a robust quality reporting
program and ensure the scientific
reliability of the data received. In the FY
2016 Hospice Wage Index final rule (80
FR 47191), we also clarified the
difference between the completion
deadlines and the submission deadlines.
Current sub-regulatory guidance
produced by CMS (for example, HIS
Manual, HIS trainings) states that the
completion deadlines for HIS records
are 14 days after the Event Date for HISAdmission records and 7 days after the
Event Date for HIS-Discharge records.
Completion deadlines continue to
reflect CMS guidance only; these
guidelines are not statutorily specified
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and are not designated through
regulation. These guidelines are
intended to offer clear direction to
hospice agencies in regards to the timely
completion of HIS-Admission and HISDischarge records. The completion
deadlines define only the latest possible
date on which a hospice should
complete each HIS record. This
guidance is meant to better align HIS
completion processes with clinical
workflow processes; however, hospices
may develop alternative internal
policies to complete HIS records.
Although it is at the discretion of the
hospice to develop internal policies for
completing HIS records, we will
continue to recommend that providers
complete and attempt to submit HIS
records early, prior to the previously
finalized submission deadline of 30
days, beginning in FY 2018. Completing
and attempting to submit records early
allows providers ample time to address
any technical issues encountered in the
QIES ASAP submission process, such as
correcting fatal error messages.
Completing and attempting to submit
records early will ensure that providers
are able to comply with the 30 day
submission deadline. HQRP guidance
documents, including the CMS HQRP
Web site, HIS Manual, HIS trainings,
Frequently Asked Questions, and Fact
Sheets, continue to offer the most up-todate CMS guidance to assist providers
in the successful completion and
submission of HIS records. Availability
of updated guidance will be
communicated to providers through the
CMS HQRP Web site, listserv messages
via the Post-Acute Care QRP listserv,
MLN Connects® National Provider Calls
& Events, MLN Connects® Provider
eNews and announcements on Open
Door Forums and Special Open Door
Forums.
d. New Data Collection and Submission
Mechanisms Under Consideration:
Hospice Evaluation & Assessment
Reporting Tool (HEART)
We have made great progress in
implementing the objectives set forth in
the quality reporting and data collection
activities required by sections 3004 of
the Affordable Care Act. To date, we
have established the HQRP, which
includes clinical quality measures from
the HIS and patient experience of care
measures from the CAHPS® Hospice
Survey. We have also finalized payment
reform measures, including changes to
the RHC payment rate and the
implementation of a Service Intensity
Add-On (SIA) payment, effective
January 1st, 2016.
As discussed in the FY 2017 final rule
(81 FR 52177), to facilitate continued
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progress towards the requirements set
forth in section 3004 of the Affordable
Care Act, we are in the early stages of
the development of a new data
collection mechanism for use by
hospices. This new data collection
mechanism would be a hospice patient
assessment tool, which would serve two
primary objectives concordant with the
Affordable Care Act legislation: (1) To
provide the quality data necessary for
HQRP requirements and the current
function of the HIS; and (2) provide
additional clinical data that could
inform future payment refinements. In
the FY 2017 final rule (81 FR 52176
through 52179), we solicited input from
the public on the development of a
hospice patient assessment tool that
would collect quality, clinical, and
other data with the ability to be used to
inform future payment refinement
efforts. Overall, feedback from the
public was supportive of the move
towards a standardized patient
assessment instrument, and commenters
offered some guiding principles for CMS
to keep in mind in the development of
a patient assessment tool, given the
unique nature of hospice care. For a
detailed discussion of the public
comments and responses, as well as
CMS’s guiding principles and
motivation behind the development of a
hospice patient assessment tool, we
refer readers to the FY 2017 final rule
(81 FR 52177 through 52179).
As noted in the FY 2017 final rule, we
envision the hospice patient assessment
tool itself as an expanded HIS. The
hospice patient assessment tool would
include current HIS items, as well as
additional clinical items that could also
be used for payment refinement
purposes or to develop new quality
measures. The hospice patient
assessment tool would not replace
existing requirements set forth in the
Medicare Hospice CoPs (such as the
initial and comprehensive assessment),
but would be designed to complement
data that are collected as part of highquality clinical care. The new data
collection effort would replace the
current HIS, but would not replace other
HQRP data collection efforts (that is, the
CAHPS® Hospice Survey), nor would it
replace regular submission of claims
data. We envision that patient
assessment data would be collected
upon a patient’s admission to and
discharge from any Medicare-certified
hospice provider; additional interim
data collection efforts are also possible.
We are not proposing a hospice
patient assessment tool at this time; we
are still in the early stages of
development of an assessment tool to
determine the appropriate content and
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feasibility of such a tool. As such, we
have made progress over the past year
in the development of a hospice patient
assessment tool, preliminarily called the
Hospice Evaluation & Assessment
Reporting Tool (HEART). CMS’s
measure development contractor, RTI
International, has begun preliminary
HEART development activities,
including: Conducting environmental
scans and engaging clinical experts to
determine which domains of care are
important to capture in a hospice
patient assessment; posting a national
provider call and forming a Clinical
Committee comprised of hospice
organizations from across the U.S. to
participate in the early development of
an assessment; and collaborating within
CMS to assess various stakeholder needs
and encourage collaboration within
CMS and across other HHS agencies. As
we move forward with the development
of the HEART patient assessment tool,
we will continue to keep the public
informed of our progress and solicit
input as we establish and finalize
domains of care to include in the
assessment, and as we move towards
specific item wording and development.
Once we move past the preliminary
phases of development and
conceptualization, we will
communicate a timeline for the HEART
development, testing, and
implementation in future rulemaking
cycles.
As mentioned in the FY 2017 final
rule, it is important for CMS to develop
a hospice patient assessment tool that is
scientifically rigorous and clinically
appropriate for the hospice population,
thus we believe that continued and
transparent involvement of stakeholders
is critical. We will continue to receive
stakeholder input from MedPAC and
ongoing input from the provider
community, Medicare beneficiaries, and
technical experts. Additionally, it is
important for CMS to minimize data
collection burden on providers; in the
development of HEART. We will ensure
that hospice patient assessment data
items are not duplicative or overly
burdensome to providers, patients,
caregivers, or their families. We will
also work with the public and other
stakeholders to ensure that HEART
takes into account the unique aspects of
hospice care delivery including
symptom burden and psychosocial
needs, patient and family preferences,
care of imminently dying patients, and
the complexity of providing hospice
care in multiple settings and at multiple
intensity levels.
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9. Previously Adopted APU
Determination and Compliance Criteria
for the HQRP
a. Background
The HQRP is currently designed as a
‘‘pay-for-reporting’’ system, meaning
that it is the act of submitting data that
determines compliance with HQRP
requirements. Performance level is not a
consideration when determining market
basket updates/APU. Reporting
compliance is determined by
successfully fulfilling both the Hospice
CAHPS® Survey requirements and the
HIS data submission requirements.
b. Previously Finalized HIS Data
Submission Timelines and Compliance
Thresholds for FY 2018 Payment
Determination and Subsequent Years
To accurately analyze quality
reporting data received by hospice
providers, it is imperative we receive
ongoing and timely submission of all
HIS-Admission and HIS-Discharge
records. In the FY 2016 Hospice Wage
Index final rule (80 FR 47192), we
finalized the timeliness criteria for
submission of HIS-Admission and HISDischarge records. The finalized
timeliness criteria were in response to
input from our stakeholders seeking
additional specificity related to HQRP
compliance affecting FY payment
determinations and, due to the
importance of ensuring the integrity of
quality data submitted.
As stated in that rule, beginning with
the FY 2018 payment determination and
subsequent FY payment determinations,
all HIS records would have to be
submitted within 30 days of the event
date, which is the patient’s admission
date or discharge date.
In conjunction with the timeliness
criteria for submission of HISAdmission and HIS-Discharge records,
in the FY 2016 Hospice Wage Index
final rule (80 FR 47192) we also
finalized a policy to establish an
incremental threshold for compliance
over a 3-year period. To be compliant
for the FY 2018 APU determination,
hospices must submit no less than 70
percent of their total number of HISAdmission and HIS-Discharge records
by no later than 30 days from the event
date. The timeliness threshold is set at
80 percent for the FY 2019 APU
determination and at 90 percent for the
FY 2020 APU determination and
subsequent years. The threshold
corresponds with the overall amount of
HIS records received from each provider
that fall within the established 30 day
submission timeframes. Our ultimate
goal is to require all hospices to achieve
a compliance rate of 90 percent or more.
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To summarize, in the FY 2016
Hospice Wage Index final rule (80 FR
47193), we finalized our policy to
implement the timeliness threshold
requirement beginning with all HISAdmission and HIS-Discharge records
that occur after January 1, 2016, in
accordance with the following schedule:
• Beginning January 1, 2016 to
December 31, 2016, hospices must
submit at least 70 percent of all required
HIS records within the 30 day
submission timeframe for the year or be
subject to a 2 percentage point reduction
to their market basket update for FY
2018.
• Beginning January 1, 2017 to
December 31, 2017, hospices must
submit at least 80 percent of all required
HIS records within the 30 day
submission timeframe for the year or be
subject to a 2 percentage point reduction
to their market basket update for FY
2019.
• Beginning January 1, 2018 to
December 31, 2018, hospices must
submit at least 90 percent of all required
HIS records within the 30 day
submission timeframe for the year or be
subject to a 2 percentage point reduction
to their market basket update for FY
2020.
In July of 2016, we released the
Hospice Timeliness Compliance
Threshold Report in the Certification
and Survey Provider Enhanced Reports
(CASPER) system. This report allows
providers with a QIES ASAP User ID to
check their preliminary compliance
with the 70/80/90 timeliness
compliance threshold described above.
For more information on the Hospice
Timeliness Compliance Threshold
Report, we refer readers to the
Timeliness Compliance Threshold Fact
Sheet, available on the HIS portion of
the CMS HQRP Web site: https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/Hospice-Quality-Reporting/
Hospice-Item-Set-HIS.html and Chapter
3 of the CASPER User’s Manual,
available on the QTSO Web site: https://
www.qtso.com/hospicetrain.html.
In the FY 2016 Hospice Wage Index
final rule (80 FR 47192 through 47193),
we provided clarification regarding the
methodology used in calculating the 70
percent/80 percent/90 percent
compliance thresholds. In general, HIS
records submitted for patient
admissions and discharges occurring
during the reporting period (January 1st
to December 31st of the reporting year
involved) will be included in the
denominator for the compliance
threshold calculation. The numerator of
the compliance threshold calculation
would include any records from the
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denominator that were submitted within
the 30 day submission deadline. In the
FY 2016 Hospice Wage Index final rule
(80 FR 47192), we also stated that we
would make allowances in the
calculation methodology for two
circumstances. First, the calculation
methodology will be adjusted following
the applicable reporting period for
records for which a hospice is granted
an extension or exemption by CMS.
Second, adjustments will be made for
instances of modification/inactivation
requests (Item A0050. Type of Record =
2 or 3). Additional helpful resources
regarding the timeliness compliance
threshold for HIS submissions can be
found under the downloads section of
the HIS Web page at CMS.gov at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/Hospice-Quality-Reporting/
Hospice-Item-Set-HIS.html. Lastly, as
further details of the data submission
and compliance threshold are
determined by CMS, we anticipate
communicating these details through
the CMS HQRP Web site, listserv
messages via the Post-Acute Care QRP
listserv, MLN Connects® National
Provider Calls & Events, MLN
Connects® Provider eNews and
announcements on Open Door Forums
and Special Open Door Forums.
c. CAHPS® Participation Requirements
for FY 2018 APU Determination and
Determinations for Subsequent Years
In the FY 2015 Hospice Wage Index
final rule, we added the CAHPS®
Hospice Survey to the Hospice Quality
Reporting Program requirements for the
FY 2017 payment determination and
determinations for subsequent FY APU
years (79 FR 50491).
In the FY 2017 Hospice Wage Index
final rule, we finalized that to meet the
HQRP requirements for the FY 2018, FY
2019 and FY 2020 APU payment
determinations, hospices would collect
survey data on a monthly basis for the
months of January 1, 2016 through
December 31, 2016 to qualify for the full
FY 2018 APU; hospices would collect
survey data on a monthly basis for the
months of January 1, 2017 through
December 31, 2017, to qualify for the
full FY 2019 APU, and hospices would
collect survey data on a monthly basis
for the months of January 1, 2018
through December 31, 2018 for the full
FY 2020 APU (81 FR 25529–25530). We
are proposing in this FY 2018 proposed
rule, that to meet the HQRP
requirements for the FY 2021 APU
payment determination, hospices would
collect survey data on a monthly basis
for the months of January 1, 2019
through December 31, 2019 to qualify
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for the FY 2021 APU. We are
additionally proposing in this FY 2018
proposed rule, that to meet the HQRP
requirements for the FY 2022 APU
payment determination, hospices would
collect survey data on a monthly basis
for the months of January 1, 2020
through December 31, 2020 to qualify
for the FY 2022 APU.
10. HQRP Submission Exemption and
Extension Requirements for the FY 2019
Payment Determination and Subsequent
Years
a. Extraordinary Circumstances
Exemption and Extension
In the FY 2015 Hospice Wage Index
final rule (79 FR 50488), we finalized
our proposal to allow hospices to
request, and for CMS to grant,
exemptions/extensions for the reporting
of required HIS quality data when there
are extraordinary circumstances beyond
the control of the provider. Such
extraordinary circumstances may
include, but are not limited to, acts of
nature or other systemic issues with our
data systems. We further finalized that
hospices must request such an
exemption or extension within 30 days
of the date that the extraordinary
circumstances occurred.
In certain instances, however, it may
be difficult for hospices to timely
evaluate the impact of extraordinary
circumstances within 30 calendar days.
For other quality reporting programs
such as the Hospital Inpatient Quality
Reporting (81 FR 57182), Inpatient
Rehabilitation Facility Quality
Reporting Program (81 FR 52125) and
the Long-term Care Hospital Quality
Reporting Program (81 FR 25205), we
have reevaluated our policy and
subsequently finalized through
rulemaking an extension of that period
of time to 90 calendar days. We are
therefore proposing to extend the
deadline for submitting an exemption or
extension request to 90 calendar days
from the qualifying event which is
preventing a hospice from submitting
their quality data for the HQRP. We
believe that extending the deadline to
90 calendar days would allow hospices
more time to determine whether it is
necessary and appropriate to submit an
exemption or extension request and to
provide a more comprehensive account
of the qualifying event in their request
form to CMS. For example, if a hospice
has suffered damage due to a hurricane
on January 1st, it would have until
March 31st to submit a request form to
CMS via email to the HQRP mailbox at
HospiceQRPReconsiderations@
cms.hhs.gov.
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Further, while we finalized our policy
in the past for exception/extension for
the submission of the HIS data, we
propose to extend this policy beyond
the submission of the HIS date to
submission of the CAHPS® Hospice
Survey data, given that multiple data
submission processes could be impacted
by the same qualifying event.
Therefore, we are proposing for FY
2019 payment determination and
subsequent payment determinations to
extend the period of time a hospice may
have to submit a request for an
extension or exception for quality
reporting purposes from 30 calendar
days to 90 calendar days after the date
that the extraordinary circumstances
occurred, by submitting a request to
CMS via email to the HQRP mailbox at
HospiceQRPReconsiderations@
cms.hhs.gov. Exemption or extension
requests sent to us through any other
channel will not be considered valid.
The request for an exemption or
extension must contain all of the
finalized requirements as outlined on
our Web site at https://www.cms.gov/
Medicare/Quality-Initiatives-PatientAssessment-Instruments/HospiceQuality-Reporting/Extensions-andExemption-Requests.html.
If a hospice is granted an exemption
or extension, timeframes for which an
exemption or extension is granted will
be applied to the new timeliness
requirement so such hospices are not
penalized. If a hospice is granted an
exemption, we will not require that the
hospice submit HIS and/or CAHPS®
Hospice Survey data for a given period
of time. By contrast, if we grant an
extension to a hospice, the hospice will
still remain responsible for submitting
data collected during the timeframe in
question, although we will specify a
revised deadline by which the hospice
must submit these quality data.
This process does not preclude us
from granting extensions/exemptions to
hospices that have not requested them
when we determine that an
extraordinary circumstance, such as an
act of nature, affects an entire region or
locale. We may grant an extension/
exemption to a hospice if we determine
that a systemic problem with our data
collection systems directly affected the
ability of the hospice to submit data. If
we make the determination to grant an
extension/exemption to hospices in a
region or locale, we will communicate
this decision through the various means,
including the CMS HQRP Web site,
listserv messages via the Post-Acute
Care QRP listserv, MLN Connects®
National Provider Calls & Events, MLN
Connects® Provider eNews and
announcements on Open Door Forums
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and Special Open Door Forums. We are
soliciting comments on these proposals.
b. Volume-Based Exemption for
CAHPS® Hospice Survey Data
Collection and Reporting Requirements
We previously finalized a volumebased exemption for CAHPS® Hospice
Survey Data Collection and Reporting
requirements in the FY 2017 Final Rule
(81 FR 52181). Hospices that have fewer
than 50 survey-eligible decedents/
caregivers in the period from January 1,
2017 through December 31, 2017 are
eligible to apply for an exemption from
CAHPS® Hospice Survey data collection
and reporting requirements for the FY
2020 payment determination
(corresponds to the CY 2018 data
collection period). To qualify, hospices
must submit an exemption request form
for the FY 2020 APU. The exemption
request form is available on the official
CAHPS® Hospice Survey Web site
https://www.hospiceCAHPSsurvey.org.
Hospices that intend to claim the size
exemption are required to submit to
CMS their total unique patient count for
the period of January 1, 2017 through
December 31, 2017. The due date for
submitting the exemption request form
for the FY 2020 APU is December 31,
2018. Small hospices that meet the
exemption for size criteria for FY 2020
must complete an exemption form for
FY 2020. Exemptions for size are active
for 1 year only. If a hospice continues
to meet the eligibility requirements for
this exemption in future FY APU
periods, the organization needs to
request the exemption annually for
every applicable FY APU period.
Hospices that have fewer than 50
survey-eligible decedents/caregivers in
the period from January 1, 2018 through
December 31, 2018 are eligible to apply
for an exemption from CAHPS® Hospice
Survey data collection and reporting
requirements for the FY 2021 payment
determination. Hospices that intend to
claim the size exemption are required to
submit to CMS their total unique patient
count for the period of January 1, 2018
through December 31, 2018. The due
date for submitting the exemption
request form for the FY 2021 APU is
December 31, 2019. Small hospices that
meet the exemption for size criteria for
FY 2021 must complete an exemption
form for FY 2021.
Hospices that have fewer than 50
survey-eligible decedents/caregivers in
the period from January 1, 2019 through
December 31, 2019 are eligible to apply
for an exemption from CAHPS® Hospice
Survey data collection and reporting
requirements for the FY 2022 payment
determination. Hospices that intend to
claim the size exemption are required to
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submit to CMS their total unique patient
count for the period of January 1, 2019
through December 31, 2019. The due
date for submitting the exemption
request form for the FY 2022 APU is
December 31, 2020. If a hospice
continues to meet the eligibility
requirements for this exemption in
future FY APU periods, the organization
should request the exemption annually
for every applicable FY APU period.
c. Newness Exemption for CAHPS®
Hospice Survey Data Collection and
Reporting Requirements
CMS previously finalized a one-time
newness exemption for hospices that
meet the criteria (81 FR 52181).
Accordingly, hospices that are notified
about their Medicare CCN after January
1, 2018 are exempted from the FY 2020
APU CAHPS® Hospice Survey
requirements due to newness. No action
is required on the part of the hospice to
receive this exemption. The newness
exemption is a one-time exemption from
the survey. Likewise, hospices notified
about their Medicare CCN after January
1, 2019 are exempted from the FY 2021
APU CAHPS® Hospice Survey and
hospices notified about their Medicare
CCN after January 1, 2020 are exempted
from the FY 2022 APU CAHPS®
Hospice Survey requirements.
11. CAHPS® Hospice Survey
Participation Requirements for the FY
2020 APU and Subsequent Years
The CAHPS® Hospice Survey of CMS’
Hospice Quality Reporting Program is
used to collect data on the experiences
of hospice patients and the primary
caregivers listed in their hospice
records. Readers who want more
information are referred to our extensive
discussion of the Hospice Experience of
Care prior to our proposal for the public
reporting of measures should refer to 79
FR 50452 and 78 FR 48261.
a. Background and Description of the
CAHPS® Hospice Survey
The CAHPS® Hospice Survey is the
first standardized national survey
available to collect information on
patient’s and informal caregiver’s
experience of hospice care. Patientcentered experience measures are a key
component of the CMS Quality Strategy,
emphasizing patient-centered care by
rating experience as a means to
empower patients and their caregivers
and improving the quality of their
care.28 In addition, the survey
28 CMS National Quality Strategy 2016. Available
at: https://www.cms.gov/medicare/qualityinitiatives-patient-assessment-instruments/
qualityinitiativesgeninfo/downloads/cms-qualitystrategy.pdf.
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introduces standard survey
administration protocols that allow for
fair comparisons across hospices.
Details regarding CAHPS® Hospice
Survey national implementation, survey
administration, participation
requirements, exemptions from the
survey’s requirements, hospice patient
and caregiver eligibility criteria, fielding
schedules, sampling requirements,
survey instruments, and the languages
that are available for the survey, are all
available on the official CAHPS®
Hospice Survey Web site,
www.HospiceCAHPSsurvey.org and in
the CAHPS® Hospice Survey Quality
Assurance Guidelines (QAG), which is
posted on the Web site.
b. Overview of Proposed Measures
The CAHPS Hospice Survey was
developed in line with the U.S.
Department of Health and Human
Services’ Transparency Initiative to
measure patient experience. Unlike the
Hospital CAHPS® Survey deployed in
2006 (71 FR 48037 through 48039) and
other subsequent CAHPS® surveys, the
CAHPS® Hospice Survey is
administered after the patient is
deceased and queries the decedent’s
primary caregiver regarding the patient
and family experience of care. National
implementation of the CAHPS® Hospice
Survey commenced January 1, 2015 as
stated in the FY 2015 Hospice Wage
Index and Payment Rate Update final
rule (79 FR 50452).
The survey consists of 47 questions
and is available (using the mailed
version) in English, Spanish, Chinese,
Russian, Portuguese, Vietnamese,
Polish, and Korean. It covers topics such
as access to care, communications,
experience at hospice facilities, and
interactions with hospice staff. The
survey also contains two global rating
questions and asks for self-reported
demographic information (race/
ethnicity, educational attainment level,
languages spoken at home, among
others).
The CAHPS® Hospice Survey
measures received NQF endorsement on
October 26th, 2016 (NQF number 2651).
Measures derived from the CAHPS®
Hospice Survey include six multi-item
(composite) measures and two global
ratings measures under NQF 2651. We
are proposing to adopt these eight
survey-based measures for the CY 2018
data collection period and for
subsequent years. We believe these
survey-based measures will be useful in
assessing aspects of hospice care where
the family/primary caregiver is the most
useful or only source of information,
and to allow meaningful and objective
comparisons between hospice
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providers. The six CAHPS® Hospice
Survey composite survey-based
measures are:
• Hospice Team Communication;
• Getting Timely Care;
• Treating Family Member with
Respect;
• Getting Emotional and Religious
Support;
• Getting Help for Symptoms; and
• Getting Hospice Care Training.
Each of the six composite surveybased measures consists of two or more
questions. The two global survey-based
measures are:
• Rating of Hospice; and
• Willingness to Recommend
Hospice.
The two global survey-based measures
are comprised of a single question each
and ask the primary caregiver of the
decedent to rate the care provided by
the hospice facility and his or her
willingness to recommend the hospice
to family and friends. More information
about these measures can be found on
the official CAHPS® Hospice Survey
Web site,
www.HospiceCAHPSsurvey.org and in
the CAHPS® Hospice Survey Quality
Assurance Guidelines (QAG), which is
posted on the Web site.
The eight survey-based measures we
are proposing were included on the CY
2016 MUC 29 list, and reviewed by the
MAP.30
• CAHPS® Hospice Survey: Rating of
Hospice (MUC ID: MUC16–31)
• CAHPS® Hospice Survey: Hospice
Team Communications (MUC16–32)
• CAHPS® Hospice Survey:
Willingness to Recommend (MUC16–
33)
• CAHPS® Hospice Survey: Getting
Hospice Care Training (MUC16–35)
• CAHPS® Hospice Survey: Getting
Timely Care (MUC16–36)
• CAHPS® Hospice Survey: Getting
Emotional and Religious Support
(MUC16–37)
• CAHPS® Hospice Survey: Getting
Help for Symptoms (MUC16–39)
• CAHPS® Hospice Survey: Treating
Family Member with Respect (MUC16–
40)
The MAP supported rulemaking for
all eight ‘‘patient-reported’’ measures
derived from the CAHPS® Hospice
Survey. The MAP noted that the
29 CMS, List of Measures Under Consideration for
December 1, 2016. Available at: https://
www.cms.gov/Medicare/Quality-Initiatives-PatientAssessment-Instruments/QualityMeasures/
Downloads/Measures-under-Consideration-List-for2016.pdf.
30 The National Quality Forum. MAP 2016–2017
Preliminary Recommendations. National Quality
Forum, 2016 Recommendations for Measures Under
Consideration, Jan. 2017. Available at: https://
www.qualityforum.org/map/.
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CAHPS® Hospice Survey measures may
offer an indication of global quality of
care by including the perspective of
both patients and their caregivers.
c. Data Sources
As discussed in the CAHPS® Hospice
Survey Quality Assurance Guidelines
V3.0 (QAG V3.0) (https://
www.hospicecahpssurvey.org/en/
quality-assurance-guidelines/), the
survey has three administration
methods: Mail-only, telephone only,
and mixed mode (mail with telephone
follow-up of non-respondents). We
previously finalized the participation
requirements for the FY 2018 and FY
2019 Annual Payment Updates (80 FR
47194). To summarize, to meet the
CAHPS® Hospice Survey requirements
for the HQRP, we are proposing that
hospice facilities must contract with a
CMS-approved vendor to collect survey
data for eligible patients on a monthly
basis and report that data to CMS on the
hospice’s behalf by the quarterly
deadlines established for each data
collection period. The list of approved
vendors is available at: https://
www.hospicecahpssurvey.org/en/
approved-vendor-list.
Hospices are required to provide lists
of the patients who died under their
care, along with the associated primary
caregiver information, to their
respective survey vendors to form the
samples for the CAHPS® Hospice
Survey. We emphasize the importance
of hospices providing complete and
accurate information to their respective
survey vendors in a timely manner.
Hospices must contract with an
approved CAHPS® Hospice Survey
vendor to conduct the survey on their
behalf. Hospices are responsible for
making sure their respective survey
vendors meet all data submission
deadlines. Vendor failures to submit
data on time are the responsibility of the
hospices.
i. Requirements for the FY 2020 Annual
Payment Update
To meet participation requirements
for the FY 2020 annual payment update
(APU), Medicare-certified hospices must
collect CAHPS® Hospice Survey data on
an ongoing monthly basis from January
2018 through December 2018 (all 12
months) in order to receive their full
payment for the FY 2020 APU. All data
submission deadlines for the FY 2020
APU are in Table 17. CAHPS® Hospice
Survey vendors must submit data by the
deadlines listed in Table 17 for all APU
periods listed in the table and moving
forward. There are no late submissions
permitted after the deadlines, except for
extraordinary circumstances beyond the
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control of the provider as discussed
above.
TABLE 17—CAHPS® HOSPICE SURVEY DATA SUBMISSION DATES FOR
THE APU IN FY 2020, FY 2021,
AND FY 2022
Sample months
(that is, month of
death) 1
Quarterly data submission deadlines 2
FY 2020 APU
January–March 2018
(Q1).
April–June 2018 (Q2)
July–September 2018
(Q3).
October–December
2018 (Q4).
August 8, 2018.
November 14, 2018.
February 13, 2019.
May 8, 2019.
FY 2021 APU
January–March 2019
(Q1).
April–June 2019 (Q2)
July–September 2019
(Q3).
October–December
2019 (Q4).
August 14, 2019.
November 13, 2019.
February 12, 2020.
May 13, 2020.
FY 2022 APU
January–March 2020
(Q1).
April–June 2020 (Q2)
July–September 2020
(Q3).
October–December
2020 (Q4).
August 12, 2020.
November 12, 2020.3
February 10, 2021.
May 12, 2021.
1 Data collection for each sample month initiates 2 months following the month of patient
death (for example, in April for deaths occurring in January).
2 Data submission deadlines are the second
Wednesday of the submission months, which
are the months August, November, February,
and May.
3 Second
Wednesday is Veterans Day
Holiday.
ii. Requirements for the FY 2021 Annual
Payment Update
To meet participation requirements
for the FY 2021 APU, Medicare-certified
hospices must collect CAHPS® Hospice
Survey data on an ongoing monthly
basis from January 2019 through
December 2019 (all 12 months) in order
to receive their full payment for the FY
2021 APU. All data submission
deadlines for the FY 2021 APU are in
Table 17. CAHPS® Hospice Survey
vendors must submit data by the
deadlines listed in Table 17 for all APU
periods listed in the table and moving
forward. There are no late submissions
permitted after the deadlines, except for
extraordinary circumstances beyond the
control of the provider as discussed
above.
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iii. Requirements for the FY 2022
Annual Payment Update
To meet participation requirements
for the FY 2022 APU, Medicare-certified
hospices must collect CAHPS® Hospice
Survey data on an ongoing monthly
basis from January 2020 through
December 2020 (all 12 months) in order
to receive their full payment for the FY
2022 APU. All data submission
deadlines for the FY 2022 APU are in
Table 17. CAHPS® Hospice Survey
vendors must submit data by the
deadlines listed in Table 17 for all APU
periods listed in the table and moving
forward. There are no late submissions
permitted after the deadlines, except for
extraordinary circumstances beyond the
control of the provider as discussed
above.
d. Measure Calculations
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As noted above, we are proposing to
adopt six composite CAHPS® Hospice
Survey-based measures and two global
survey-based measures. As with other
measures adopted for HQRP, a hospice’s
performance for a given payment
determination year will be based upon
the successful submission of data
required in accordance with the
administrative, form, manner and
timing requirements established for the
program. Therefore, hospices’ scores on
the CAHPS® Hospice Survey-based
measures will not affect whether they
are subject to the 2.0 percentage point
This calculation would give this
example hospice an unadjusted score of
0.78 or 78 percent for the Hospice Team
Communication measure for purposes of
public reporting. We note that an
adjusted hospice score would be
calculated by adjusting the score for
each question for differences in the
characteristics of decedents and
caregivers across hospices and for mode
as described in section 11.e, and then
averaging across questions within the
measure as described here. Further
detailed information regarding scoring
and risk adjustment can be found at the
CAHPS® Hospice Survey Web site
(https://www.hospicecahpssurvey.org/
en/technical-specifications/).
ii. Global Survey-Based Measures
We are proposing to adopt two global
CAHPS® Hospice Survey measures.
CAHPS® Hospice Survey—Rating of
Hospice asks the primary caregiver of
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payment reduction for hospices that fail
to report data required to be submitted.
We propose that CAHPS Hospice
Survey scores for a given hospice be
displayed as ‘‘top-box’’ scores, with the
national average top-box score for
participating hospices provided for
comparison. Top-box scores reflect the
proportion of caregiver respondents that
endorse the most positive response(s) to
a given measure, such as the proportion
that rate the hospice a 9 or 10 out of 10
on a 0 to 10 scale, or the proportion that
report that they ‘‘always’’ received
timely care. The top-box numerator for
each question within a measure is the
number of respondents that endorse the
most positive response(s) to the
question. The denominator includes all
respondents eligible to respond to the
question, with one exception. The
exception is the Getting Hospice Care
Training measure; for this measure, the
measure score is calculated only among
those respondents who indicated that
their family member received hospice
care at home or in an assisted living
facility.
For additional information on the
specifications of these measures,
including details regarding top-box
scoring methodology and mode and
case-mix adjustment, please refer to the
CAHPS® Hospice Survey Web page at
https://www.hospicecahpssurvey.org/en/.
i. Composite Survey-Based Measures
Unadjusted hospice scores on each
composite CAHPS® Hospice Survey-
the decedent to rate the care provided
by the hospice on a scale of 0 to 10, and
CAHPS® Hospice Survey—Willingness
to Recommend asks about the
caregiver’s willingness to recommend
the hospice to family and friends on a
scale of ‘‘Definitely No’’ to ‘‘Definitely
Yes’’. Unadjusted hospice performance
on each of the two global CAHPS®
Hospice Survey-based measures would
be calculated by the proportion of
respondents providing high-value
responses (that is, a 9 to 10 rating or
‘‘Definitely Yes’’) to the survey
questions over the total number of
respondents. For example, if a hospice
received 45 9- and 10-point ratings out
of 50 responses, this hospital would
receive a 0.9 or 90 percent unadjusted
score, which would then be adjusted for
differences in the characteristics of
decedents and caregivers across
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based measure would be calculated by
determining the proportion of ‘‘top-box’’
responses for each question within the
composite and averaging these
proportions over all the questions in the
composite measure. For example, to
assess hospice performance on the
composite measure CAHPS® Hospice
Survey—Hospice Team
Communication, we would calculate the
proportion of top-box responses for each
of the measure’s six questions, add
those proportions together, and divide
by the number of questions in the
composite measure (in this case, six).
As a specific example, we take a
theoretical hospice facility that had 50
surveys completed and received the
proportions of ‘‘top-box’’ responses
through sample calculations:
• 25 ‘‘top-box’’ responses out of 50 total
responses on Question One
• 40 ‘‘top-box’’ responses out of 50 total
responses on Question Two
• 50 ‘‘top-box’’ responses out of 50 total
responses on Question Three
• 35 ‘‘top-box’’ responses out of 50 total
responses on Question Four
• 45 ‘‘top-box’’ responses out of 50 total
responses on Question Five
• 40 ‘‘top-box’’ responses out of 50 total
responses on Question Six
Based on the above responses, we
would calculate that hospice’s
unadjusted measure score for public
reporting as follows:
hospices and modes, as described in
section 12.E.
iii. Cohort
The CAHPS® Hospice Survey is
administered to all eligible patients/
caregivers—or a random sample
thereof—who meet the eligibility
criteria. Eligible patients, regardless of
insurance or payment, can participate.
For purposes of each survey-based
measure captured in the CAHPS®
Hospice Survey, an ‘‘eligible patient’’ is
a decedent 18 years or older:
• With death at least 48 hours following
last admission to hospice care
• for whom there is a caregiver of
record
• whose caregiver is someone other
than a non-familial legal guardian
• for whom the caregiver has a U.S. or
U.S. Territory home address
Patients who are still alive or whose
admission to the hospice resulted in a
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live discharge, are not eligible to
participate in the survey. In addition,
decedents/caregivers who initiate or
voluntarily request that the hospice not
reveal the patient’s identity; and/or not
survey the patient/caregiver (‘‘no
publicity patients/caregivers’’) are
excluded from the sample.
e. Risk Adjustment
The CAHPS® Hospice Survey
measures assess activities that are fully
under the control of hospice care
professionals and/or hospice
organizations. In order to ensure fair
comparisons in public reporting, we
believe it is necessary and appropriate
to adjust for factors that are not directly
related to hospice performance, such as
patient mix, for these CAHPS® Hospice
Survey measures. The survey based
measures are adjusted for decedent and
caregiver characteristics (including the
lag time between patient death and
survey response; decedent’s age, payer
for hospice care, decedent’s primary
diagnosis, decedent’s length of final
episode of hospice care, caregiver’s
education, decedent’s relationship to
caregiver, caregiver’s preferred language
and language in which the survey was
completed, and caregiver’s age) known
to be associated with systematic
difference in survey responses.
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i. Patient Mix Adjustment
Previous research, on both CAHPS®
surveys and other types of surveys, has
identified respondent characteristics
that are not under the control of the
entities being assessed but tend to be
related to survey responses. Hence,
variations in the proportion of
respondents with such characteristics
will be associated with variations in
survey responses that are unrelated to
the actual quality of hospice care. To
ensure that comparisons between
hospices reflect differences in
performance rather than differences in
patient and/or caregiver characteristics,
publicly reported hospice scores will be
adjusted for variations of such
characteristics across hospices. This
adjustment is performed using a linear
regression model applied to all data
within a quarter, with indicator
variables for each hospice and each
characteristic as an independent
variable in the model.
ii. Mode Adjustment
We conducted an experiment to
determine whether survey mode
adjustments were needed to fairly
compare CAHPS® Hospice Survey
scores. The experiment found that mode
adjustments are needed. Publicly
reported CAHPS® Hospice Survey
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scores will be adjusted for the mode of
survey administration, which affects
scores but is not related to quality of
hospice care. (Authorized survey modes
are: Mail-only, telephone-only, and mail
with telephone follow up, also called
mixed mode.) Mode adjustment is
performed prior to patient-mix
adjustment; a mode adjustment value is
added/subtracted (depending on the
mode) to each response to the survey by
mail-only mode or mixed mode.
Responses obtained using telephoneonly mode are not adjusted since this is
the reference mode.
As a result of the risk adjustment
methodologies proposed here, the final
percentages may vary from the
unadjusted percentage as calculated in
the examples provided above.
f. For Further Information About the
CAHPS® Hospice Survey
We encourage hospices and other
entities to learn more about the survey
on www.hospicecahpssurvey.org. For
direct questions, please contact the
CAHPS® Hospice Survey Team at
hospicecahpssurvey@HCQIS.org or
telephone 1–844–472–4621.
12. HQRP Reconsideration and Appeals
Procedures for the FY 2018 Payment
Determination and Subsequent Years
In the FY 2015 Hospice Wage Index
final rule (79 FR 50496), we notified
hospice providers on how to seek
reconsideration if they received a
noncompliance decision for the FY 2016
payment determination and subsequent
years. A hospice may request
reconsideration of a decision by CMS
that the hospice has not met the
requirements of the HQRP for a
particular period.
We clarified that any hospice that
wishes to submit a reconsideration
request must do so by submitting an
email to CMS containing all of the
requirements listed on the HQRP Web
site at https://www.cms.gov/Medicare/
Quality-Initiatives-Patient-AssessmentInstruments/Hospice-Quality-Reporting/
Reconsideration-Requests.html.
Electronic email sent to
HospiceQRPReconsiderations@
cms.hhs.gov is the only form of
submission that will be accepted. Any
reconsideration requests received
through any other channel including the
United States Postal Service (USPS) or
phone will not be considered as a valid
reconsideration request. In the FY 2017
final rule we further clarified that
providers should submit
reconsideration requests of decision by
CMS that the hospice has not met the
CAHPS® Hospice Survey requirements
using the same process (81 FR 52181)
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(Details about the reports and emails
received after data submission are in the
CAHPS® Hospice Quality Assurance
Guidelines, which is available on the
official CAHPS® Hospice Survey Web
site, www.hospicecahpssurvey.org). We
codified this process at § 418.312(h). In
addition, we codified at § 418.306(b)(2)
that beginning with FY 2014 and each
subsequent FY, the Secretary shall
reduce the market basket update by 2
percentage points for any hospice that
does not comply with the quality data
submission requirements for that FY
and solicited comments on all of the
proposals and the associated regulations
text at § 418.312 and in § 418.306 in
section VI. Official instructions
regarding the payment reduction
reconsideration process can be located
under the Regulations and Guidance,
Transmittals, 2015 Transmittals Web
site at https://www.cms.gov/
Regulations-and-Guidance/Guidance/
Transmittals/2017-Transmittals.html.
In the past, only hospices found to be
non-compliant with the reporting
requirements set forth for a given
payment determination received a
notification from CMS of this finding
along with instructions for requesting
reconsideration in the form of a USPS
letter. In the FY 2016 Hospice Wage
Index final rule (80 FR 47198), we stated
that we would use the QIES CASPER
reporting system as an additional
mechanism to communicate to hospices
regarding their compliance with the
reporting requirements for the given
reporting cycle. We have implemented
this additional communication
mechanism via the CASPER Hospice
Timeliness Compliance Threshold
Report previously discussed in the FY
2017 Hospice Wage Index rule at 81 FR
25527 and 25528. We will continue to
send notification of noncompliance via
delivery of a letter via the USPS. We
previously finalized our proposal (80 FR
47198) to publish a list of hospices who
successfully meet the reporting
requirements for the applicable payment
determination on the CMS HQRP Web
site. The list of providers found to be
compliant with the FY 2017 APU
requirements can be found on the CMS
HQRP Web site here: https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/Hospice-Quality-Reporting/
HQRP-Requirements-and-BestPractices.html.
13. Confidential Feedback Reports
As part of our effort to promote use
of standardized quality data to improve
quality of care, in December 2016, we
made available two new provider
feedback reports: The Hospice-Level
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Quality Measure Report and the Patient
Stay-Level Quality Measure Report.
These confidential feedback reports are
available to each hospice using the
CASPER system, and are part of the
class of CASPER reports known as
Quality Measure (QM) Reports. These
reports are separate from public
reporting and are for provider viewing
only, for the purposes of internal
provider quality improvement. These
reports are on-demand and thus enable
hospice providers to view and compare
their performance to the national
average for a reporting period of their
choice.
Providers are able to view their data
and information at both the hospice and
patient stay levels for it’s HIS based
quality measures. The CASPER hospicelevel QM Reports contain information
such as the numerator, denominator,
hospice-level QM score, and national
average. The CASPER patient stay-level
QM Reports show whether each patient
stay is counted toward each quality
measure. The HIS based QMs reported
in both reports include:
• NQF #1641 Treatment Preferences
• NQF #1647 Beliefs/Values
• NQF #1634 Pain Screening
• NQF #1637 Pain Assessment
• NQF #1639 Dyspnea Screening
• NQF #1638 Dyspnea Treatment
• NQF #1617 Bowel Regimen
For more information on the CASPER
QM Reports, we refer readers to the
CASPER QM Factsheet on the HQRP
Web site at https://www.cms.gov/
Medicare/Quality-Initiatives-PatientAssessment-Instruments/HospiceQuality-Reporting/HQRP-Requirementsand-Best-Practices.html. This fact sheet
contains detailed information about
each CASPER QM report currently
available, the data included in the
reports, and how providers can use the
reports as part of their Quality
Assessment and Performance
Improvement (QAPI) efforts. For
technical information on the reports and
how to access the CASPER QM Reports,
we refer readers to: https://
www.qtso.com/hospicetrain.html.
As new HIS measures are
implemented in the HQRP, we will
continue to expand the functionality of
the QM reports to allow providers to
view data on additional HIS measures.
We will announce refinements and
additions to the QM reports through
sub-regulatory communication channels
and in future rulemaking cycles.
We also propose to provide hospices
with preview reports of their data prior
to the quarterly publication of CAHPS®
Hospice Survey data on the Compare
site. The reports will be provided
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through the CASPER reporting system.
Each hospice will receive only its own,
individual reports.
14. Public Display of Quality Measures
and Other Hospice Data for the HQRP
Under section 1814(i)(5)(E) of the Act,
the Secretary is required to establish
procedures for making any quality data
submitted by hospices available to the
public. These procedures shall ensure
that a hospice has the opportunity to
review the data that is to be made public
for the hospice prior to such data being
made public. The Secretary shall report
quality measures that relate to hospice
care provided by hospice programs on a
publicly available CMS Web site.
In the FY 2017 rule, we discussed our
analysis of HIS data to inform which
measures were eligible for public
reporting and reportability analysis to
determine data selection period and
minimum denominator size for
measures to be publicly reported. Based
on analysis results, we determined that
all 7 HIS quality measures adopted for
the FY 2016 and beyond (NQF #1634,
NQF #1637, NQF #1639, NQF #1638,
NQF #1641, NQF #1647, NQF #1617),
calculated based on a rolling 12 month
data selection period, to be eligible for
public reporting with a minimum
denominator size of 20 patient stays. For
additional details on these analyses, we
refer readers to the FY 2017 final rule
(81 FR 52183 through 52184).
In the FY 2017 final rule we also
clarified policies for reportability
analyses for new measures. As stated in
the FY 2017 final rule, new measures
will undergo reportability analysis to
determine (1) appropriateness for public
reporting and (2) appropriate data
selection period. In accordance with
discussion in the prior year’s rule, we
will use the same analytic approach
used in previous reportability analyses
to determine data selection period and
minimum denominator size for the
Hospice and Palliative Care Composite
Process Measure—Comprehensive
Assessment at Admission. We will
begin reportability analyses for the
Hospice Visits When Death is Imminent
Measure Pair once data for the measure
are available. Results of reportability
analyses conducted for these new
measures will be communicated
through future rulemaking.
To meet the Affordable Care Act’s
requirement for making quality measure
data public, we are developing a CMS
Hospice Compare Web site, which will
allow consumers, providers and
stakeholders to search for all Medicarecertified hospice providers and view
their information and quality measure
scores. We anticipate that public
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reporting of HQRP data on the CMS
Compare Web site will begin sometime
in the summer of CY 2017. To help
providers prepare for public reporting,
we will offer opportunities for
stakeholder engagement and education
prior to the rollout of a CMS Hospice
Compare site. We will offer outreach
opportunities for providers through
CMS HQRP Public reporting Web page:
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/Hospice-Quality-Reporting/
Hospice-Quality-Public-Reporting.html,
listserv messages via the Post-Acute
Care QRP listserv, MLN Connects®
National Provider Calls & Events, MLN
Connects® Provider eNews and
announcements on Open Door Forums
and Special Open Door Forums. Finally,
we will offer educational support and
outreach to all hospice providers on the
systems and processes for reviewing
their data prior to public reporting;
availability of educational support and
outreach opportunities will be
communicated through the listed
channels above.
We will provide hospices an
opportunity to preview their quality
measure data prior to publicly reporting
information. These quality measure data
reports or ‘‘preview reports’’ will be
made available in the CASPER system
prior to public reporting and will offer
providers the opportunity to preview
their quality measure data prior to
public reporting on the CMS Hospice
Compare Web site. We will provide
hospices 30 days to review the preview
report beginning from the date on which
they can access the report. Hospices will
have an opportunity to request review of
their data by CMS during the 30-day
preview period if they believe that
errors in data submitted to CMS may
have resulted in incorrect measure
scores and can submit proof along with
a plan describing how the errors will be
corrected. We will review these requests
and if we confirm that the errors have
affected the measures and agree to
correct the measure, we will suppress
the measure on the Hospice Compare
Web site for one time only and display
the corrected measure during the
subsequent quarterly refresh of the
Compare Web site. When the preview
reports are ready for providers to access,
anticipated summer of CY 2017 prior to
the release of Hospice Compare, we will
post the policies and procedures for
providers to submit requests for
reviewing of their data by CMS on the
CMS HQRP Web site: https://
www.cms.gov/Medicare/QualityInitiatives-Patient-Assessment-
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Instruments/Hospice-Quality-Reporting/
Hospice-Quality-Public-Reporting.html.
CMS encourages hospices to use
CASPER QM Reports (see section
III.D.14 of this proposed rule) to review
their HIS quality measures after they
submit the HIS data to CMS. If hospices
determine that erroneous data have been
submitted, they should submit either of
these two types of HIS records: Modify
existing record or inactivate existing
record to correct their data. HIS data
corrected before the data are frozen for
the creation of the preview reports will
be reflected in the preview reports.
We propose to begin public reporting
of CAHPS® Hospice Survey measures in
2018. Specifically, we are proposing to
publicly report data in winter CY 2018
on all eight CAHPS® Hospice Survey
measures. Scores would be displayed
based on eight rolling quarters of data
and would initially use CAHPS®
Hospice Survey data collected from
caregivers of patients who died while
receiving hospice care between April 1,
2015 and March 31, 2017. We are
proposing that the display of these
scores be updated quarterly, and that
scores be displayed only for those
hospices for which there are 30 or more
completed questionnaires during the
reporting period. Scores will not be
displayed for hospices with fewer than
30 completed questionnaires during the
reporting period.
Like other CMS Compare Web sites,
the Hospice Compare Web site will, in
time, feature a quality rating system that
gives each hospice a rating of between
1 and 5 stars. Hospices will have
prepublication access to their own
agency’s quality data, which enables
each agency to know how it is
performing before public posting of data
on the Hospice Compare Web site.
Public comments regarding how the
rating system would determine a
hospice’s star rating and the methods
used for calculations, as well as a
proposed timeline for implementation
will be announced via the CMS HQRP
Web page, listserv messages via the
Post-Acute Care QRP listserv, MLN
Connects® National Provider Calls &
Events, MLN Connects® Provider eNews
and announcements on Open Door
Forums and Special Open Door Forums.
We will announce the timeline for
development and implementation of the
star rating system in future rulemaking.
Lastly, as part of our ongoing efforts
to make healthcare more transparent,
affordable, and accountable for all
hospice stakeholders, we have posted a
hospice directory and quality data on a
public data set located at https://
data.medicare.gov. This data will serve
as a helpful resource regarding
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information on Medicare-certified
hospice agencies throughout the nation.
In an effort to move toward public
reporting of hospice data, we have
initially posted demographic data of
hospice agencies that have been
registered with Medicare. This list
includes high-level demographic data
for each agency, including provider
name, address, phone numbers,
ownership type, CCN, profit status, and
date of original CMS certification. The
posting of this hospice data directory
occurred on June 14, 2016 and will be
refreshed quarterly. Information can be
located at https://data.medicare.gov/
data/hospice-directory. Additionally,
we have posted two hospice data files
containing national level aggregate
quality data regarding seven HIS quality
measures and CAHPS® Hospice Survey
measures in December 2016. These data
file are a one-time release with a goal to
make quality data available prior to the
release of the Hospice Compare in
summer of CY 2017. Additional details
regarding hospice datasets will be
announced via the CMS HQRP Web
page, listserv messages via the PostAcute Care QRP listserv, MLN
Connects® National Provider Calls &
Events, MLN Connects® Provider eNews
and announcements on Open Door
Forums and Special Open Door Forums.
In addition, we have provided the list of
CASPER/ASPEN contacts, Regional
Office and State coordinators in the
event that a Medicare-certified agency is
either not listed in the database or the
characteristics/administrative data
(name, address, phone number, services,
or type of ownership) are incorrect or
have changed. To continue to meet
Medicare enrollment requirements, all
Medicare providers are required to
report changes to their information in
their enrollment application as outlined
in the Provider-Supplier Enrollment
Fact Sheet Series located at https://
www.cms.gov/Outreach-and-Education/
Medicare-Learning-Network-MLN/
MLNProducts/downloads/
MedEnroll_InstProv_FactSheet_ICN903
783.pdf. Once the Hospice Compare
Web site is released in the summer of
CY 2017, https://data.medicare.gov will
post the official datasets used on the
Medicare.gov Compare Web sites
provided by CM.
IV. Collection of Information
Requirements
Under the Paperwork Reduction Act
of 1995, we are required to provide 60day notice in the Federal Register and
solicit public comment before a
collection of information requirement is
submitted to the Office of Management
and Budget (OMB) for review and
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approval. In order to fairly evaluate
whether an information collection
should be approved by OMB, section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires that we
solicit comment on the following issues:
• The need for the information
collection and its usefulness in carrying
out the proper functions of our agency.
• The accuracy of our estimate of the
information collection burden.
• The quality, utility, and clarity of
the information to be collected.
• Recommendations to minimize the
information collection burden on the
affected public, including automated
collection techniques.
Unless noted otherwise, all salary
information is from the Bureau of Labor
Statistics (BLS) Web site at https://
www.bls.gov/oes and includes a fringe
benefits package worth 100 percent of
the base salary. The mean hourly wage
rates are based on May, 2015 BLS data
for each discipline.
Section 1814(i)(5)(C) of the Act
requires that each hospice submit data
to the Secretary on quality measures
specified by the Secretary. This data
must be submitted in a form and
manner, and at a time specified by the
Secretary.
We are soliciting public comment on
each of these issues for the following
sections of this document that contain
information collection requirements
(ICRs):
A. Hospice Item Set
In the FY 2014 Hospice Wage Index
final rule (78 FR 48257), and in
compliance with section 1814(i)(5)(C) of
the Act, we finalized the specific
collection of data items that support the
following 7 NQF endorsed measures for
hospice:
• NQF #1617 Patients Treated with
an Opioid who are Given a Bowel
Regimen,
• NQF #1634 Pain Screening,
• NQF #1637 Pain Assessment,
• NQF #1638 Dyspnea Treatment,
• NQF #1639 Dyspnea Screening,
• NQF #1641 Treatment Preferences,
• NQF #1647 Beliefs/Values
Addressed (if desired by the patient).
We finalized the following two
additional measures in the FY 2017
Hospice Wage Index final rule affecting
FY 2019 payment determinations (81 FR
52163 through 52173):
• Hospice Visits when Death is
Imminent
• Hospice and Palliative Care
Composite Process Measure—
Comprehensive Assessment at
Admission
Data for the aforementioned 9
measures is collected via the HIS as
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discussed in the FY 2017 Hospice Wage
Index final rule (81 FR 52189) and
covered under OMB control number
0938–1153. The HIS V2.00.0 was
approved by the Office of Management
and Budget on April 17, 2017 under
control number 0938–1153. We are not
proposing any new updates or
additional collections of information in
this proposed rule in regards to the
Hospice Item Set or its constituent
quality measures.
B. Summary of CAHPS® Hospice Survey
Information Collection Requirements
(OMB Control Number 0938–1257)
National Implementation of the
Hospice Experience of Care Survey
(CAHPs Hospice Survey) data measures
are covered under OMB control number
0938–1257 and is summarized here for
convenience. We have implemented
patient experience surveys in a number
of settings including Medicare,
Medicare Advantage, and Part D
Prescription Drug Plans, hospitals, and
home health agencies. Other CAHPS®
surveys exist for hemodialysis facilities,
nursing homes, and physician practices.
The hospice survey differs from most
other CMS patient experience surveys
because its target population is bereaved
family members or close friends of
patients who died in hospice care.
Family members and friends are the best
source of information regarding the
entire trajectory of hospice care. In
addition, many hospice patients are
very ill and unable to answer survey
questions.
Surveys are administered by CMSapproved survey vendors hired by
hospice providers to conduct the survey
on their behalf. The survey vendor may
collect data in one of three modes: Mailonly, telephone-only, or mixed mode
(mail with telephone follow-up). The
sample consists of bereaved family
members or close friends of patients
who died while receiving hospice care
(1) at home, (2) in a nursing home, or
(3) an inpatient setting (that is,
freestanding inpatient unit or acute care
hospital). The questionnaire is
composed of 47 items.
The estimated annualized burden
hours and costs to respondents for the
national implementation of the CAHPS®
Hospice Survey are shown in Tables 18
and 19. Based on participation in
national implementation in the CAHPS®
Hospice Survey from Quarter 2 2015
through Quarter 1 2016, we assume that
3,414 hospices will administer the
survey to an average of 278.7 cases.
Thus, we estimate that the CAHPS®
Hospice Survey will be administered to
a maximum of 951,482 individuals each
year for the duration of the collection
period covered by this application for
the purposes of national
implementation. As not all sampled
cases will complete the survey, this
estimate reflects the maximum burden
possible. The estimated number of
responses is based on actual hospice
participation in national
implementation of the CAHPS® Hospice
Survey.
Table 18 shows the estimated
annualized burden for the respondents’
time to participate in the national
implementation data collection. The
survey contains 47 items and is
estimated to require an average
administration time of 10.4 minutes in
English (at a pace of 4.5 items per
minute) and 12.5 minutes in Spanish
(assuming 20 percent more words in the
Spanish translation), for an average
response time of 10.47 minutes or 0.174
hours (assuming that 1 percent of survey
respondents complete the survey in
Spanish). These burden and pace
estimates are based on CMS’ experience
with the CAHPS® Hospice Survey and
surveys of similar length that were
fielded with Medicare beneficiaries. As
indicated below, the annual total
burden hours for survey participants are
estimated to be 165,959.57 for the
continued national implementation of
the survey.
TABLE 18—ESTIMATED ANNUALIZED BURDEN HOURS FOR RESPONDENTS: NATIONAL IMPLEMENTATION OF THE CAHPS®
HOSPICE SURVEY
Number of
respondents
Survey version
Number of
responses per
respondent
Hours per
response
Total burden
hours
CAHPS® Hospice Survey ................................................................................
951,482
1
0.174
165,959.57
Total ..........................................................................................................
951,482
1
0.174
165,959.57
Table 19 shows the cost burden to
respondents associated with their time
to complete a survey as part of national
implementation. The annual total cost
burden is estimated to be $7,710,481.60.
This estimate is higher than the
$3,034,789.70 estimated in the prior
OMB filing, due to the increased
number of hospices participating (and
correspondingly, the increased number
of respondents), as well as an increase
in the average hourly rate.
TABLE 19—ESTIMATED ANNUALIZED COST BURDEN FOR RESPONDENTS: NATIONAL IMPLEMENTATION
Number of
respondents
Form name
Total burden
hours
Average
hourly wage
rate*
Total cost
burden
951,482
165,959.57
* $46.46
$7,710,481.60
Total ..........................................................................................................
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CAHPS® Hospice Survey ................................................................................
951,482
165,959.57
* $46.46
$7,710,481.60
* Source: Data from the U.S. Bureau of Labor Statistics’ May 2015 National Occupational Employment and Wage Estimates for all salary estimates (https://www.bls.gov/oes). This figure includes a 100% fringe benefit on an average wage of $23.23. Retrieved April 10, 2017.
If you comment on these information
collection, that is, reporting,
recordkeeping or third-party disclosure
requirements, please submit your
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comments electronically as specified in
the ADDRESSES section of this proposed
rule.
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Comments must be received by 5 p.m.
June 26, 2017.
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V. Response to Comments
Because of the large number of public
comments we normally receive on
Federal Register documents, we are not
able to acknowledge or respond to them
individually. We will consider all
comments we receive by the date and
time specified in the DATES section of
this preamble, and, when we proceed
with a subsequent document, we will
respond to the comments in the
preamble to that document.
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VI. Request for Information on CMS
Flexibilities and Efficiencies
CMS is committed to transforming the
health care delivery system—and the
Medicare program—by putting an
additional focus on patient-centered
care and working with providers,
physicians, and patients to improve
outcomes. We seek to reduce burdens
for hospitals, physicians, and patients,
improve the quality of care, decrease
costs, and ensure that patients and their
providers and physicians are making the
best health care choices possible. These
are the reasons we are including this
Request for Information in this proposed
rule.
As we work to maintain flexibility
and efficiency throughout the Medicare
program, we would like to start a
national conversation about
improvements that can be made to the
health care delivery system that reduce
unnecessary burdens for clinicians,
other providers, and patients and their
families. We aim to increase quality of
care, lower costs improve program
integrity, and make the health care
system more effective, simple and
accessible.
We would like to take this
opportunity to invite the public to
submit their ideas for regulatory,
subregulatory, policy, practice, and
procedural changes to better accomplish
these goals. Ideas could include
payment system redesign, elimination
or streamlining of reporting, monitoring
and documentation requirements,
aligning Medicare requirements and
processes with those from Medicaid and
other payers, operational flexibility,
feedback mechanisms and data sharing
that would enhance patient care,
support of the physician-patient
relationship in care delivery, and
facilitation of individual preferences.
Responses to this Request for
Information could also include
recommendations regarding when and
how CMS issues regulations and
policies and how CMS can simplify
rules and policies for beneficiaries,
clinicians, physicians, providers, and
suppliers. Where practicable, data and
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specific examples would be helpful. If
the proposals involve novel legal
questions, analysis regarding CMS’
authority is welcome for CMS’
consideration. We are particularly
interested in ideas for incentivizing
organizations and the full range of
relevant professionals and
paraprofessionals to provide screening,
assessment and evidence-based
treatment for individuals with opioid
use disorder and other substance use
disorders, including reimbursement
methodologies, care coordination,
systems and services integration, use of
paraprofessionals including community
paramedics and other strategies. We are
requesting commenters to provide clear
and concise proposals that include data
and specific examples that could be
implemented within the law.
We note that this is a Request for
Information only. Respondents are
encouraged to provide complete but
concise responses. This Request for
Information is issued solely for
information and planning purposes; it
does not constitute a Request for
Proposal (RFP), applications, proposal
abstracts, or quotations. This Request for
Information does not commit the U.S.
Government to contract for any supplies
or services or make a grant award.
Further, CMS is not seeking proposals
through this Request for Information
and will not accept unsolicited
proposals. Responders are advised that
the U.S. Government will not pay for
any information or administrative costs
incurred in response to this Request for
Information; all costs associated with
responding to this Request for
Information will be solely at the
interested party’s expense. We note that
not responding to this Request for
Information does not preclude
participation in any future procurement,
if conducted. It is the responsibility of
the potential responders to monitor this
Request for Information announcement
for additional information pertaining to
this request. In addition, we note that
CMS will not respond to questions
about the policy issues raised in this
Request for Information. CMS will not
respond to comment submissions in
response to this Request for Information
in the FY 2018 Hospice Wage Index and
Payment Rate Update and Hospice
Quality Reporting Requirements final
rule. Rather, CMS will actively consider
all input as we develop future
regulatory proposals or future
subregulatory policy guidance. CMS
may or may not choose to contact
individual responders. Such
communications would be for the sole
purpose of clarifying statements in the
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responders’ written responses.
Contractor support personnel may be
used to review responses to this Request
for Information. Responses to this notice
are not offers and cannot be accepted by
the Government to form a binding
contract or issue a grant. Information
obtained as a result of this Request for
Information may be used by the
Government for program planning on a
nonattribution basis. Respondents
should not include any information that
might be considered proprietary or
confidential. This Request for
Information should not be construed as
a commitment or authorization to incur
cost for which reimbursement would be
required or sought. All submissions
become U.S. Government property and
will not be returned. CMS may publicly
post the public comments received, or a
summary of those public comments.
VII. Regulatory Impact Analyses
A. Statement of Need
This proposed rule meets the
requirements of our regulations at
§ 418.306(c), which requires annual
issuance, in the Federal Register, of the
hospice wage index based on the most
current available CMS hospital wage
data, including any changes to the
definitions of Core-Based Statistical
Areas (CBSAs), or previously used
Metropolitan Statistical Areas (MSAs).
This proposed rule would also update
payment rates for each of the categories
of hospice care, described in
§ 418.302(b), for FY 2018 as required
under section 1814(i)(1)(C)(ii)(VII) of the
Act. Section 411(d) of the Medicare
Access and CHIP Reauthorization Act of
2015 (MACRA) amended section
1814(i)(1)(C) of the Act such that for
hospice payments for FY 2018, the
market basket percentage increase shall
be 1 percent. Finally, section 3004 of the
Affordable Care Act amended the Act to
authorize a quality reporting program
for hospices and this rule discusses
changes in the requirements for the
hospice quality reporting program in
accordance with section 1814(i)(5) of
the Act.
B. Overall Impacts
We estimate that the aggregate impact
of the payment provisions in this
proposed rule would result in an
increase of $180 million in payments to
hospices, resulting from the hospice
payment update percentage of 1.0
percent. The impact analysis of this
proposed rule represents the projected
effects of the changes in hospice
payments from FY 2017 to FY 2018.
Using the most recent data available at
the time of rulemaking, in this case FY
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2016 hospice claims data, we apply the
current FY 2017 wage index and laborrelated share values to the level of care
per diem payments and SIA payments
for each day of hospice care to simulate
FY 2017 payments. Then, using the
same FY 2016 data, we apply the
proposed FY 2018 wage index and
labor-related share values to simulate
FY 2018 payments. Certain events may
limit the scope or accuracy of our
impact analysis, because such an
analysis is susceptible to forecasting
errors due to other changes in the
forecasted impact time period. The
nature of the Medicare program is such
that the changes may interact, and the
complexity of the interaction of these
changes could make it difficult to
predict accurately the full scope of the
impact upon hospices.
We have examined the impacts of this
rule as required by Executive Order
12866 on Regulatory Planning and
Review (September 30, 1993), Executive
Order 13563 on Improving Regulation
and Regulatory Review (January 18,
2011), the Regulatory Flexibility Act
(RFA) (September 19, 1980, Pub. L. 96–
354), section 1102(b) of the Social
Security Act, section 202 of the
Unfunded Mandates Reform Act of 1995
(March 22, 1995; Pub. L. 104–4),
Executive Order 13132 on Federalism
(August 4, 1999), the Congressional
Review Act (5 U.S.C. 804(2) and
Executive Order 13771 on Reducing
Regulation and Controlling Regulatory
Costs (January 30, 2017).
Executive Orders 12866 and 13563
direct agencies to assess all costs and
benefits of available regulatory
alternatives and, if regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
environmental, public health and safety
effects, distributive impacts, and
equity). Section 3(f) of Executive Order
12866 defines a ‘‘significant regulatory
action’’ as an action that is likely to
result in a rule: (1) Having an annual
effect on the economy of $100 million
or more in any 1 year, or adversely and
materially affecting a sector of the
economy, productivity, competition,
jobs, the environment, public health or
safety, or state, local or tribal
governments or communities (also
referred to as ‘‘economically
significant’’); (2) creating a serious
inconsistency or otherwise interfering
with an action taken or planned by
another agency; (3) materially altering
the budgetary impacts of entitlement
grants, user fees, or loan programs or the
rights and obligations of recipients
thereof; or (4) raising novel legal or
policy issues arising out of legal
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mandates, the President’s priorities, or
the principles set forth in the Executive
Order.
A regulatory impact analysis (RIA)
must be prepared for major rules with
economically significant effects ($100
million or more in any 1 year). We
estimate that this rulemaking is
‘‘economically significant’’ as measured
by the $100 million threshold, and
hence also a major rule under the
Congressional Review Act. Accordingly,
we have prepared a RIA that, to the best
of our ability presents the costs and
benefits of the rulemaking.
C. Anticipated Effects
The RFA requires agencies to analyze
options for regulatory relief of small
businesses if a rule has a significant
impact on a substantial number of small
entities. The great majority of hospitals
and most other health care providers
and suppliers are small entities by
meeting the Small Business
Administration (SBA) definition of a
small business (in the service sector,
having revenues of less than $7.5
million to $38.5 million in any 1 year),
or being nonprofit organizations. For
purposes of the RFA, we consider all
hospices as small entities as that term is
used in the RFA. HHS’s practice in
interpreting the RFA is to consider
effects economically ‘‘significant’’ only
if they reach a threshold of 3 to 5
percent or more of total revenue or total
costs. The effect of the proposed FY
2018 hospice payment update
percentage results in an overall increase
in estimated hospice payments of 1.0
percent, or $180 million. Therefore, the
Secretary has determined that this
proposed rule will not create a
significant economic impact on a
substantial number of small entities.
In addition, section 1102(b) of the Act
requires us to prepare a regulatory
impact analysis if a rule may have a
significant impact on the operations of
a substantial number of small rural
hospitals. This analysis must conform to
the provisions of section 604 of the
RFA. For purposes of section 1102(b) of
the Act, we define a small rural hospital
as a hospital that is located outside of
a metropolitan statistical area and has
fewer than 100 beds. This proposed rule
only affects hospices. Therefore, the
Secretary has determined that this
proposed rule would not have a
significant impact on the operations of
a substantial number of small rural
hospitals.
Section 202 of the Unfunded
Mandates Reform Act of 1995 (UMRA)
also requires that agencies assess
anticipated costs and benefits before
issuing any rule whose mandates
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require spending in any 1 year of $100
million in 1995 dollars, updated
annually for inflation. In 2017, that
threshold is approximately $148
million. This proposed rule is not
anticipated to have an effect on state,
local, or tribal governments, in the
aggregate, or on the private sector of
$148 million or more.
Executive Order 13132 establishes
certain requirements that an agency
must meet when it promulgates a
proposed rule (and subsequent final
rule) that imposes substantial direct
requirement costs on state and local
governments, preempts State law, or
otherwise has Federalism implications.
We have reviewed this proposed rule
under these criteria of Executive Order
13132, and have determined that it will
not impose substantial direct costs on
state or local governments.
If regulations impose administrative
costs on private entities, such as the
time needed to read and interpret this
proposed rule, we should estimate the
cost associated with regulatory review.
Due to the uncertainty involved with
accurately quantifying the number of
entities that will review the rule, we
assume that the total number of unique
commenters on last year’s proposed rule
will be the number of reviewers of this
proposed rule. We acknowledge that
this assumption may understate or
overstate the costs of reviewing this
rule. It is possible that not all
commenters reviewed last year’s rule in
detail, and it is also possible that some
reviewers chose not to comment on the
proposed rule. For these reasons we
thought that the number of past
commenters would be a fair estimate of
the number of reviewers of this rule. We
welcome any comments on the
approach in estimating the number of
entities which will review this proposed
rule.
We also recognize that different types
of entities are in many cases affected by
mutually exclusive sections of this
proposed rule, and therefore for the
purposes of our estimate we assume that
each reviewer reads approximately 50
percent of the rule. We seek comments
on this assumption.
Using the wage information from the
BLS for medical and health service
managers (Code 11–9111), we estimate
that the cost of reviewing this rule is
$90.16 per hour, including overhead
and fringe benefits (https://www.bls.gov/
oes/2015/may/naics4_621100.htm).
Assuming an average reading speed, we
estimate that it would take
approximately 1.3 hours for the staff to
review half of this proposed rule. For
each hospice that reviews the rule, the
estimated cost is $117.21 (1.3 hours ×
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$90.16). Therefore, we estimate that the
total cost of reviewing this regulation is
$7, 032.60 ($117.21 × 60 reviewers).
D. Detailed Economic Analysis
The proposed FY 2018 hospice
payment impacts appear in Table 20.
We tabulate the resulting payments
according to the classifications in Table
20 (for example, facility type,
geographic region, facility ownership),
and compare the difference between
current and proposed payments to
determine the overall impact.
The first column shows the
breakdown of all hospices by urban or
rural status, census region, hospitalbased or freestanding status, size, and
type of ownership, and hospice base.
The second column shows the number
of hospices in each of the categories in
the first column.
The third column shows the effect of
the annual update to the wage index.
This represents the effect of using the
proposed FY 2018 hospice wage index.
The aggregate impact of this change is
zero percent, due to the proposed
hospice wage index standardization
factor. However, there are distributional
effects of the proposed FY 2018 hospice
wage index.
The fourth column shows the effect of
the proposed hospice payment update
percentage for FY 2018. The proposed
FY 2018 hospice payment update
percentage of 1 percent is mandated by
section 1814(i)(1)(C) of the Act, as
amended by section 411(d) of the
MACRA.
The fifth column shows the effect of
all the proposed changes on FY 2018
hospice payments. It is projected that
aggregate payments will increase by 1.0
percent, assuming hospices do not
change their service and billing
practices in response.
As illustrated in Table 20, the
combined effects of all the proposals
vary by specific types of providers and
by location. For example, due to the
changes proposed in this rule, the
estimated impacts on FY 2018 payments
range from a 0.9 percent decrease for
hospices providing care in the rural
outlying region to a 1.7 percent increase
for hospices providing care in the urban
Pacific region.
TABLE 20—PROJECTED IMPACT TO HOSPICES FOR FY 2018
Number of
providers
Updated
wage data
(%)
Proposed FY
2018 hospice
payment
update
(%)
FY 2018
total change
(%)
(2)
(3)
(4)
(5)
(1)
nlaroche on DSK30NT082PROD with PROPOSALS3
All Hospices .....................................................................................................
Urban Hospices ...............................................................................................
Rural Hospices ................................................................................................
Urban Hospices—New England ......................................................................
Urban Hospices—Middle Atlantic ....................................................................
Urban Hospices—South Atlantic .....................................................................
Urban Hospices—East North Central ..............................................................
Urban Hospices—East South Central .............................................................
Urban Hospices—West North Central .............................................................
Urban Hospices—West South Central ............................................................
Urban Hospices—Mountain .............................................................................
Urban Hospices—Pacific .................................................................................
Urban Hospices—Outlying ..............................................................................
Rural Hospices—New England .......................................................................
Rural Hospices—Middle Atlantic .....................................................................
Rural Hospices—South Atlantic .......................................................................
Rural Hospices—East North Central ...............................................................
Rural Hospices—East South Central ..............................................................
Rural Hospices—West North Central ..............................................................
Rural Hospices—West South Central .............................................................
Rural Hospices—Mountain ..............................................................................
Rural Hospices—Pacific ..................................................................................
Rural Hospices—Outlying ................................................................................
0—3,499 RHC Days (Small) ............................................................................
3,500–19,999 RHC Days (Medium) ................................................................
20,000+ RHC Days (Large) .............................................................................
Non-Profit Ownership ......................................................................................
For Profit Ownership ........................................................................................
Government Ownership ...................................................................................
Other Ownership ..............................................................................................
Freestanding Facility Type ..............................................................................
HHA/Facility-Based Facility Type ....................................................................
4,295
3,323
972
134
249
429
405
159
229
648
315
716
39
23
40
134
140
124
181
180
101
46
3
960
2,001
1,334
1,058
2,682
155
400
3,323
972
0.0
0.0
0.1
¥0.7
0.1
¥0.3
¥0.1
0.0
¥0.2
0.0
¥0.1
0.7
¥0.6
0.0
0.6
0.1
0.2
¥0.1
0.2
0.1
0.2
0.3
¥1.9
0.2
0.1
0.0
0.0
0.1
¥0.3
¥0.2
0.0
0.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.1
0.3
1.1
0.7
0.9
1.0
0.8
1.0
0.9
1.7
0.4
1.0
1.6
1.1
1.2
0.9
1.2
1.1
1.2
1.3
¥0.9
1.2
1.1
1.0
1.0
1.1
0.7
0.8
1.0
1.0
Source: FY 2016 hospice claims from the Chronic Condition Data Warehouse (CCW) Research Identifiable File (RIF) in January 2017.
Region Key: New England=Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont; Middle Atlantic=Pennsylvania, New
Jersey, New York; South Atlantic=Delaware, District of Columbia, Florida, Georgia, Maryland, North Carolina, South Carolina, Virginia, West Virginia; East North Central=Illinois, Indiana, Michigan, Ohio, Wisconsin; East South Central=Alabama, Kentucky, Mississippi, Tennessee; West
North Central=Iowa, Kansas, Minnesota, Missouri, Nebraska, North Dakota, South Dakota; West South Central=Arkansas, Louisiana, Oklahoma,
Texas; Mountain=Arizona, Colorado, Idaho, Montana, Nevada, New Mexico, Utah, Wyoming; Pacific=Alaska, California, Hawaii, Oregon, Washington; Outlying=Guam, Puerto Rico, Virgin Islands
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E. Alternatives Considered
Since the hospice payment update
percentage is determined based on
statutory requirements, we did not
consider not updating hospice payment
rates by the payment update percentage.
Payment rates since FY 2002 have been
updated according to section
1814(i)(1)(C)(ii)(VII) of the Act, which
states that the update to the payment
rates for subsequent years must be the
market basket percentage for that FY.
Section 3401(g) of the Affordable Care
Act also mandates that, starting with FY
2013 (and in subsequent years), the
hospice payment update percentage will
be annually reduced by changes in
economy-wide productivity as specified
in section 1886(b)(3)(B)(xi)(II) of the
Act. In addition, section 3401(g) of the
Affordable Care Act mandates that in FY
2013 through FY 2019, the hospice
payment update percentage will be
reduced by an additional 0.3 percentage
point (although for FY 2014 to FY 2019,
the potential 0.3 percentage point
reduction is subject to suspension under
conditions specified in section
1814(i)(1)(C)(v) of the Act). For FY 2018,
since the hospice payment update
percentage is determined based on
statutory requirements at section
1814(i)(1)(C) of the Act, as amended by
section 411(d) of the MACRA, we
cannot consider not updating the
hospice payment rates by the hospice
payment update percentage, nor can we
consider updating the hospice payment
rates by the hospice payment update
percentage absent the change to section
1814(i)(1)(C) as amended by MACRA.
F. Accounting Statement
As required by OMB Circular A–4
(available at https://www.whitehouse.gov
/omb/circulars/a004/a-4.pdf), in Table
21, we have prepared an accounting
statement showing the classification of
the expenditures associated with the
provisions of this proposed rule. Table
21 provides our best estimate of the
possible changes in Medicare payments
under the hospice benefit as a result of
the policies in this proposed rule. This
estimate is based on the data for 4,295
hospices in our impact analysis file,
which was constructed using FY 2016
claims available in January 2017. All
expenditures are classified as transfers
to hospices.
TABLE 21—ACCOUNTING STATEMENT: CLASSIFICATION OF ESTIMATED TRANSFERS AND COSTS, FROM FY 2017 TO FY
2018
Category
Transfers
Annualized Monetized Transfers ..............................................................
From Whom to Whom? ............................................................................
$ 180 million.*
Federal Government to Medicare Hospices.
* The net increase of $180 million in transfer payments is a result of the 1.0 percent hospice payment update compared to payments in FY
2017.
G. Reducing Regulation and Controlling
Regulatory Costs
nlaroche on DSK30NT082PROD with PROPOSALS3
Executive Order 13771, titled
‘‘Reducing Regulation and Controlling
Regulatory Costs,’’ was issued on
January 30, 2017 (82 FR 9339, February
3, 2017). Section 2(a) of Executive Order
13771 requires an agency, unless
prohibited by law, to identify at least
two existing regulations to be repealed
when the agency publicly proposes for
notice and comment, or otherwise
promulgates, a new regulation. In
furtherance of this requirement, section
2(c) of Executive Order 13771 requires
that the new incremental costs
associated with new regulations shall, to
the extent permitted by law, be offset by
the elimination of existing costs
associated with at least two prior
regulations. OMB’s implementation
guidance, issued on April 5, 2017,
explains that ‘‘Federal spending
regulatory actions that cause only
income transfers between taxpayers and
program beneficiaries (for example,
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regulations associated with . . .
Medicare spending) are considered
‘transfer rules’ and are not covered by
EO 13771. . . . However . . . such
regulatory actions may impose
requirements apart from transfers . . .
In those cases, the actions would need
to be offset to the extent they impose
more than de minimis costs. Examples
of ancillary requirements that may
require offsets include new reporting or
recordkeeping requirements.’’ It has
been determined that this proposed rule
is a transfer rule that does not impose
more than de minimis costs as described
above and thus is not a regulatory action
for the purposes of EO 13771.
H. Conclusion
We estimate that aggregate payments
to hospices in FY 2018 would increase
by $180 million, or 1.0 percent,
compared to payments in FY 2017. We
estimate that in FY 2018, hospices in
urban and rural areas would experience,
on average, 1.0 percent and 1.1 percent
increases, respectively, in estimated
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payments compared to FY 2017.
Hospices providing services in the
urban Pacific and rural Middle Atlantic
regions would experience the largest
estimated increases in payments of 1.7
percent and 1.6 percent, respectively.
Hospices serving patients in urban areas
in the New England region would
experience, on average, the lowest
estimated increase of 0.3 percent in FY
2018 payments.
In accordance with the provisions of
Executive Order 12866, this regulation
was reviewed by the Office of
Management and Budget.
Dated: April 12, 2017.
Seema Verma,
Administrator, Centers for Medicare &
Medicaid Services.
Dated: April 17, 2017.
Thomas E. Price,
Secretary, Department of Health and Human
Services.
[FR Doc. 2017–08563 Filed 4–27–17; 4:15 pm]
BILLING CODE 4120–01–P
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[Federal Register Volume 82, Number 84 (Wednesday, May 3, 2017)]
[Proposed Rules]
[Pages 20750-20792]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-08563]
[[Page 20749]]
Vol. 82
Wednesday,
No. 84
May 3, 2017
Part III
Department of Health and Human Services
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Centers for Medicare & Medicaid Services
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42 CFR Part 418
Medicare Program; FY 2018 Hospice Wage Index and Payment Rate Update
and Hospice Quality Reporting Requirements; Proposed Rule
Federal Register / Vol. 82 , No. 84 / Wednesday, May 3, 2017 /
Proposed Rules
[[Page 20750]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Part 418
[CMS-1675-P]
RIN 0938-AT00
Medicare Program; FY 2018 Hospice Wage Index and Payment Rate
Update and Hospice Quality Reporting Requirements
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: This proposed rule would update the hospice wage index,
payment rates, and cap amount for fiscal year (FY) 2018. Additionally,
this rule proposes changes to the hospice quality reporting program,
including proposing new quality measures, soliciting feedback on an
enhanced data collection instrument, and describing plans to publicly
display quality measures and other hospice data.
DATES: To be assured consideration, comments must be received at one of
the addresses provided below, no later than 5 p.m. on June 26, 2017.
ADDRESSES: In commenting, please refer to file code CMS-1675-P. Because
of staff and resource limitations, we cannot accept comments by
facsimile (FAX) transmission.
You may submit comments in one of four ways (please choose only one
of the ways listed):
1. Electronically. You may submit electronic comments on this
regulation to https://www.regulations.gov. Follow the ``Submit a
comment'' instructions.
2. By regular mail. You may mail written comments to the following
address ONLY: Centers for Medicare & Medicaid Services, Department of
Health and Human Services, Attention: CMS-1675-P, P.O. Box 8010,
Baltimore, MD 21244-1850.
Please allow sufficient time for mailed comments to be received
before the close of the comment period.
3. By express or overnight mail. You may send written comments to
the following address ONLY: Centers for Medicare & Medicaid Services,
Department of Health and Human Services, Attention: CMS-1675-P, Mail
Stop C4-26-05, 7500 Security Boulevard, Baltimore, MD 21244-1850.
4. By hand or courier. Alternatively, you may deliver (by hand or
courier) your written comments ONLY to the following addresses prior to
the close of the comment period:
a. For delivery in Washington, DC--Centers for Medicare & Medicaid
Services, Department of Health and Human Services, Room 445-G, Hubert
H. Humphrey Building, 200 Independence Avenue SW., Washington, DC
20201.
(Because access to the interior of the Hubert H. Humphrey Building
is not readily available to persons without Federal government
identification, commenters are encouraged to leave their comments in
the CMS drop slots located in the main lobby of the building. A stamp-
in clock is available for persons wishing to retain a proof of filing
by stamping in and retaining an extra copy of the comments being
filed.)
b. For delivery in Baltimore, MD--Centers for Medicare & Medicaid
Services, Department of Health and Human Services, 7500 Security
Boulevard, Baltimore, MD 21244-1850.
If you intend to deliver your comments to the Baltimore address,
call telephone number (410) 786-9994 in advance to schedule your
arrival with one of our staff members.
Comments erroneously mailed to the addresses indicated as
appropriate for hand or courier delivery may be delayed and received
after the comment period.
For information on viewing public comments, see the beginning of
the SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT:
Debra Dean-Whittaker, (410) 786-0848 for questions regarding the
CAHPS[supreg] Hospice Survey.
Cindy Massuda, (410) 786-0652 for questions regarding the hospice
quality reporting program.
For general questions about hospice payment policy, please send
your inquiry via email to: hospicepolicy@cms.hhs.gov.
SUPPLEMENTARY INFORMATION: Wage index addenda will be available only
through the internet on our Web site at: (https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/Hospice/.)
Inspection of Public Comments: All comments received before the
close of the comment period are available for viewing by the public,
including any personally identifiable or confidential business
information that is included in a comment. We post all comments
received before the close of the comment period on the following Web
site as soon as possible after they have been received: https://www.regulations.gov. Follow the search instructions on that Web site to
view public comments.
Comments received timely will also be available for public
inspection as they are received, generally beginning approximately 3
weeks after publication of a document, at the headquarters of the
Centers for Medicare & Medicaid Services, 7500 Security Boulevard,
Baltimore, Maryland 21244, Monday through Friday of each week from 8:30
a.m. to 4 p.m. To schedule an appointment to view public comments,
phone 1-800-743-3951.
Table of Contents
I. Executive Summary
A. Purpose
B. Summary of the Major Provisions
C. Summary of Impacts
II. Background
A. Hospice Care
B. History of the Medicare Hospice Benefit
C. Services Covered by the Medicare Hospice Benefit
D. Medicare Payment for Hospice Care
1. Omnibus Budget Reconciliation Act of 1989
2. Balanced Budget Act of 1997
3. FY 1998 Hospice Wage Index Final Rule
4. FY 2010 Hospice Wage Index Final Rule
5. The Affordable Care Act
6. FY 2012 Hospice Wage Index Final Rule
7. FY 2015 Hospice Wage Index and Payment Rate Update Final Rule
8. IMPACT Act of 2014
9. FY 2016 Hospice Wage Index and Payment Rate Update Final Rule
10. FY 2017 Hospice Wage Index and Payment Rate Update Final
Rule
E. Trends in Medicare Hospice Utilization
III. Provisions of the Proposed Rule
A. Monitoring for Potential Impacts--Affordable Care Act Hospice
Reform
1. Hospice Payment Reform: Research and Analyses
a. Length of Stay and Live Discharges
b. Skilled Visits in the Last Days of Life
c. Non-Hospice Spending
2. Initial Analysis of Revised Hospice Cost Report Data
a. Background
b. Methodology
c. Overall Payments and Costs and Costs by Level of Care
B. Proposed FY 2018 Hospice Wage Index and Rate Update
1. Proposed FY 2018 Hospice Wage Index
2. Proposed FY 2018 Hospice Payment Update Percentage
3. Proposed FY 2018 Hospice Payment Rates
4. Hospice Cap Amount for FY 2018
C. Discussion and Solicitation of Comments Regarding Sources of
Clinical Information for Certifying Terminal Illness
D. Proposed Updates to the Hospice Quality Reporting Program
1. Background and Statutory Authority
2. General Considerations Used for Selection of Quality Measures
for the HQRP
3. Policy for Retention of HQRP Measures Adopted for Previous
Payment Determination
4. Policy for Adopting Changes to Previously Adopted Measures
[[Page 20751]]
5. Previously Adopted Quality Measures for FY 2018 Payment
Determination and Future Years
6. Proposed Removal of Previously Adopted Measures
7. Measure Concepts Under Consideration for Future Years
8. Form, Manner, and Timing of Quality Data Submission
9. Previously Adopted APU Determination and Compliance Criteria
for the HQRP
10. HQRP Submission Exemption and Extension Requirements for the
FY 2019 Payment Determination and Subsequent Years
11. CAHPS[supreg] Hospice Survey Participation Requirements for
the FY 2020 APU and Subsequent Years
12. HQRP Reconsideration and Appeals Procedures for the FY 2018
Payment Determination and Subsequent Years
13. Confidential Feedback Reports
14. Public Display of Quality Measures and Other Hospice Data
for the HQRP
IV. Collection of Information Requirements
A. Hospice Item Set
B. Summary of CAHPS[supreg] Hospice Survey Information
Collection Requirements (OMB Control Number 0938-1257)
V. Response to Comments
VI. Request for Information on Medicare Flexibilities and
Efficiencies
VII. Regulatory Impact Analysis
A. Statement of Need
B. Overall Impacts
C. Anticipated Effects
D. Detailed Economic Analysis
E. Alternatives Considered
F. Accounting Statement
G. Reducing Regulation and Controlling Regulatory Costs
H. Conclusion
Acronyms
Because of the many terms to which we refer by acronym in this
proposed rule, we are listing the acronyms used and their corresponding
meanings in alphabetical order:
APU Annual Payment Update
ASPE Assistant Secretary of Planning and Evaluation
BBA Balanced Budget Act of 1997
BIPA Benefits Improvement and Protection Act of 2000
BNAF Budget Neutrality Adjustment Factor
BLS Bureau of Labor Statistics
CAHPS[supreg] Consumer Assessment of Healthcare Providers and
Systems
CASPER Certification and Survey Provider Enhanced Reports
CBSA Core-Based Statistical Area
CCN CMS Certification Number
CCW Chronic Conditions Data Warehouse
CFR Code of Federal Regulations
CHC Continuous Home Care
CHF Congestive Heart Failure
CMS Centers for Medicare & Medicaid Services
COPD Chronic Obstructive Pulmonary Disease
CoPs Conditions of Participation
CPI-U Consumer Price Index-Urban Consumers
CVA Cerebral Vascular Accident
CWF Common Working File
CY Calendar Year
DME Durable Medical Equipment
DRG Diagnostic Related Group
FEHC Family Evaluation of Hospice Care
FR Federal Register
FY Fiscal Year
GAO Government Accountability Office
GIP General Inpatient Care
HCFA Healthcare Financing Administration
HHS Health and Human Services
HIS Hospice Item Set
HQRP Hospice Quality Reporting Program
ICD-9-CM International Classification of Diseases, Ninth Revision,
Clinical Modification
ICD-10-CM International Classification of Diseases, Tenth Revision,
Clinical Modification
ICR Information Collection Requirement
IDG Interdisciplinary Group
IMPACT Act Improving Medicare Post-Acute Care Transformation Act of
2014
IPPS Inpatient Prospective Payment System
IRC Inpatient Respite Care
LCD Local Coverage Determination
MAC Medicare Administrative Contractor
MACRA Medicare Access and CHIP Reauthorization Act of 2015
MAP Measure Applications Partnership
MedPAC Medicare Payment Advisory Commission
MFP Multifactor Productivity
MSA Metropolitan Statistical Area
NF Long Term Care Nursing Facility
NOE Notice of Election
NOTR Notice of Termination/Revocation
NP Nurse Practitioner
NPI National Provider Identifier
NQF National Quality Forum
OIG Office of the Inspector General
OACT Office of the Actuary
OMB Office of Management and Budget
PEPPER Program for Evaluating Payment Patterns Electronic Report
PRRB Provider Reimbursement Review Board
PS&R Provider Statistical and Reimbursement Report
Pub. L. Public Law
POC Plan of Care
QAPI Quality Assessment and Performance Improvement
QIO Quality Improvement Organization
RHC Routine Home Care
RN Registered Nurse
SBA Small Business Administration
SEC Securities and Exchange Commission
SIA Service Intensity Add-on
SNF Skilled Nursing Facility
TEFRA Tax Equity and Fiscal Responsibility Act of 1982
TEP Technical Expert Panel
UHDDS Uniform Hospital Discharge Data Set
U.S.C. United States Code
I. Executive Summary
A. Purpose
This rule proposes updates to the hospice payment rates for fiscal
year (FY) 2018, as required under section 1814(i) of the Social
Security Act (the Act). This rule also discusses and solicits comments
on the source of the clinical information used to certify an individual
as terminally ill (that is, having a life expectancy of 6 months or
less as defined in section 1861(dd)(3)(A)) as required by section
1814(a)(7)(A) of the Act. Finally, this rule also proposes new quality
measures and provides an update on the hospice quality reporting
program (HQRP) consistent with the requirements of section 1814(i)(5)
of the Act. In accordance with section 1814(i)(5)(A) of the Act,
starting in FY 2014, hospices that fail to meet quality reporting
requirements receive a 2 percentage point reduction to their payments.
B. Summary of the Major Provisions
Section III.A of this proposed rule describes monitoring activities
intended to identify potential impacts related to the hospice reform
policies finalized in the FY 2016 Hospice Wage Index and Payment Rate
Update final rule and analyzes current trends in hospice utilization
and expenditures. Section III.B.1 updates the hospice wage index with
updated wage data and makes the application of the updated wage data
budget neutral for all four levels of hospice care. In section III.B.2,
we discuss the FY 2018 hospice payment update percentage of 1.0
percent. Sections III.B.3 and III.B.4 update the hospice payment rates
and hospice cap amount for FY 2018 by the hospice payment update
percentage discussed in section III.B.2.
In section III.C of this proposed rule, we discuss and solicit
comments on the appropriate source(s) of the required clinical
information for certification of a medical prognosis of a life
expectancy of 6 months or less.
Finally, in section III.D of this proposed rule, we discuss updates
to HQRP, including proposed changes to the CAHPS[supreg] Hospice Survey
measures as well as the possibility of utilizing a new assessment
instrument to collect quality data. In section III.D, we will also
discuss proposed enhancements to the current Hospice Item Set (HIS)
data collection instrument to be more in line with other post-acute
care settings. The new data collection instrument would be a
comprehensive patient assessment instrument, rather than the current
chart abstraction tool. Additionally, in this section we discuss our
plans for sharing HQRP data publicly later in Calendar Year (CY) 2017,
as well as plans to provide public reporting via a Compare Site in CY
2017 and future years.
C. Summary of Impacts
[[Page 20752]]
Table 1--Impact Summary Table
------------------------------------------------------------------------
Provision description Transfers
------------------------------------------------------------------------
FY 2018 Hospice Wage Index and The overall economic impact of this
Payment Rate Update. proposed rule is estimated to be an
estimated $180 million in increased
payments to hospices during FY
2018.
------------------------------------------------------------------------
II. Background
A. Hospice Care
Hospice care is a comprehensive, holistic approach to treatment
that recognizes that the impending death of an individual, upon his or
her choice, warrants a change in the focus from curative care to
palliative care for relief of pain and for symptom management. The goal
of hospice care is to help terminally ill individuals continue life
with minimal disruption to normal activities while remaining primarily
in the home environment. A hospice uses an interdisciplinary approach
to deliver medical, nursing, social, psychological, emotional, and
spiritual services through a collaboration of professionals and other
caregivers, with the goal of making the beneficiary as physically and
emotionally comfortable as possible. Hospice is compassionate
beneficiary and family/caregiver-centered care for those who are
terminally ill.
Medicare regulations define ``palliative care'' as patient and
family-centered care that optimizes quality of life by anticipating,
preventing, and treating suffering. Palliative care throughout the
continuum of illness involves addressing physical, intellectual,
emotional, social, and spiritual needs and to facilitate patient
autonomy, access to information, and choice (Sec. 418.3). Palliative
care is at the core of hospice philosophy and care practices, and is a
critical component of the Medicare hospice benefit. See also ``Medicare
and Medicaid Programs: Hospice Conditions of Participation'' final rule
(73 FR 32088, June 5, 2008). The goal of palliative care in hospice is
to improve the quality of life of beneficiaries and their families and
caregivers through early identification and management of pain and
other issues associated with a life limiting condition. The hospice
interdisciplinary group works with the beneficiary, family, and
caregivers to develop a coordinated, comprehensive care plan; reduce
unnecessary diagnostics or ineffective therapies; and maintain ongoing
communication with individuals and their families about changes in
their condition. The beneficiary's care plan will shift over time to
meet the changing needs of the individual, family, and caregiver(s) as
the individual approaches the end of life.
Medicare hospice care is palliative care for individuals with a
prognosis of living 6 months or less if the terminal illness runs its
normal course. When a beneficiary is terminally ill, many health
problems are related to the underlying condition(s), as bodily systems
are interdependent. In the 2008 Hospice Conditions of Participation
final rule, we stated that ``the [hospice] medical director must
consider the primary terminal condition, related diagnoses, current
subjective and objective medical findings, current medication and
treatment orders, and information about unrelated conditions when
considering the initial certification of the terminal illness'' (73 FR
32176). As referenced in our regulations at Sec. 418.22(b)(1), to be
eligible for Medicare hospice services, the patient's attending
physician (if any) and the hospice medical director must certify that
the individual is ``terminally ill,'' as defined in section
1861(dd)(3)(A) of the Act and our regulations at Sec. 418.3; that is,
the individual's prognosis is for a life expectancy of 6 months or less
if the terminal illness runs its normal course. The regulations at
Sec. 418.22(b)(3) require that the certification and recertification
forms include a brief narrative explanation of the clinical findings
that support a life expectancy of 6 months or less.
While the goal of hospice care is to allow the beneficiary to
remain in his or her home, circumstances during the end-of-life may
necessitate short-term inpatient admission to a hospital, skilled
nursing facility (SNF), or hospice facility for necessary pain control
or acute or chronic symptom management that cannot be managed in any
other setting. These acute hospice care services ensure that any new or
worsening symptoms are intensively addressed so that the beneficiary
can return to his or her home. Limited, short-term, intermittent,
inpatient respite care (IRC) is also available because of the absence
or need for relief of the family or other caregivers. Additionally, an
individual can receive continuous home care (CHC) during a period of
crisis in which an individual requires continuous care to achieve
palliation or management of acute medical symptoms so that the
individual can remain at home. Continuous home care may be covered for
as much as 24 hours a day, and these periods must be predominantly
nursing care, in accordance with our regulations at Sec. 418.204. A
minimum of 8 hours of nursing care, or nursing and aide care, must be
furnished on a particular day to qualify for the continuous home care
rate (Sec. 418.302(e)(4)).
Hospices are expected to comply with all civil rights laws,
including the provision of auxiliary aids and services to ensure
effective communication with patients and patient care representatives
with disabilities consistent with section 504 of the Rehabilitation Act
of 1973 and the Americans with Disabilities Act. Additionally, they
must provide language access for such persons who are limited in
English proficiency, consistent with Title VI of the Civil Rights Act
of 1964. Further information about these requirements may be found at
https://www.hhs.gov/ocr/civilrights.
B. History of the Medicare Hospice Benefit
Before the creation of the Medicare hospice benefit, hospice
programs were originally operated by volunteers who cared for the
dying. During the early development stages of the Medicare hospice
benefit, hospice advocates were clear that they wanted a Medicare
benefit that provided all-inclusive care for terminally-ill
individuals, provided pain relief and symptom management, and offered
the opportunity to die with dignity in the comfort of one's home rather
than in an institutional setting.\1\ As stated in the August 22, 1983
proposed rule entitled ``Medicare Program; Hospice Care'' (48 FR
38146), ``the hospice experience in the United States has placed
emphasis on home care. It offers physician services, specialized
nursing services, and other forms of care in the home to enable the
terminally ill individual to remain at home in the company of family
and friends as long as possible.'' The concept of a beneficiary
``electing'' the hospice benefit and being certified as terminally ill
were two key components of the legislation responsible for the creation
of the Medicare Hospice
[[Page 20753]]
Benefit (section 122 of the Tax Equity and Fiscal Responsibility Act of
1982 (TEFRA), (Pub. L. 97-248)). Section 122 of TEFRA created the
Medicare Hospice benefit, which was implemented on November 1, 1983.
Under sections 1812(d) and 1861(dd) of the Act, we provide coverage of
hospice care for terminally ill Medicare beneficiaries who elect to
receive care from a Medicare-certified hospice. Our regulations at
Sec. 418.54(c) stipulate that the comprehensive hospice assessment
must identify the beneficiary's physical, psychosocial, emotional, and
spiritual needs related to the terminal illness and related conditions,
and address those needs in order to promote the beneficiary's well-
being, comfort, and dignity throughout the dying process. The
comprehensive assessment must take into consideration the following
factors: The nature and condition causing admission (including the
presence or lack of objective data and subjective complaints);
complications and risk factors that affect care planning; functional
status; imminence of death; and severity of symptoms (Sec. 418.54(c)).
The Medicare hospice benefit requires the hospice to cover all
reasonable and necessary palliative care related to the terminal
prognosis, as well as, care for interventions to manage pain and
symptoms, as described in the beneficiary's plan of care. Additionally,
the hospice Conditions of Participation (CoPs) at Sec. 418.56(c)
require that the hospice must provide all reasonable and necessary
services for the palliation and management of the terminal illness,
related conditions, and interventions to manage pain and symptoms.
Therapy and interventions must be assessed and managed in terms of
providing palliation and comfort without undue symptom burden for the
hospice patient or family.\2\ In the December 16, 1983 Hospice final
rule (48 FR 56010), regarding what is related versus unrelated to the
terminal illness, we stated: ``. . . we believe that the unique
physical condition of each terminally ill individual makes it necessary
for these decisions to be made on a case by case basis. It is our
general view that hospices are required to provide virtually all the
care that is needed by terminally ill patients.'' Therefore, unless
there is clear evidence that a condition is unrelated to the terminal
prognosis, all conditions are considered to be related to the terminal
prognosis and the responsibility of the hospice to address and treat.
---------------------------------------------------------------------------
\1\ Connor, Stephen. (2007). Development of Hospice and
Palliative Care in the United States. OMEGA. 56(1), p. 89-99.
\2\ Paolini, DO, Charlotte. (2001). Symptoms Management at End
of Life. JAOA. 101(10). p. 609-615.
---------------------------------------------------------------------------
As stated in the December 16, 1983 Hospice final rule, the
fundamental premise upon which the hospice benefit was designed was the
``revocation'' of traditional curative care and the ``election'' of
hospice care for end-of-life symptom management and maximization of
quality of life (48 FR 56008). After electing hospice care, the
beneficiary typically returns home from an institutional setting or
remains in the home, to be surrounded by family and friends, and to
prepare emotionally and spiritually, if requested, for death while
receiving expert symptom management and other supportive services.
Election of hospice care also requires waiving the right to Medicare
payment for curative treatment for the terminal prognosis, and instead
receiving palliative care to manage pain or other symptoms.
The benefit was originally designed to cover hospice care for a
finite period of time that roughly corresponded to a life expectancy of
6 months or less. Initially, beneficiaries could receive three election
periods: Two 90-day periods and one 30-day period. Currently, Medicare
beneficiaries can elect hospice care for two 90-day periods and an
unlimited number of subsequent 60-day periods; however, at the
beginning of each period, a physician must certify that the beneficiary
has a life expectancy of 6 months or less if the terminal illness runs
its normal course.
C. Services Covered by the Medicare Hospice Benefit
One requirement for coverage under the Medicare Hospice benefit is
that hospice services must be reasonable and necessary for the
palliation and management of the terminal illness and related
conditions. Section 1861(dd)(1) of the Act establishes the services
that are to be rendered by a Medicare-certified hospice program. These
covered services include: Nursing care; physical therapy; occupational
therapy; speech-language pathology therapy; medical social services;
home health aide services (now called hospice aide services); physician
services; homemaker services; medical supplies (including drugs and
biologicals); medical appliances; counseling services (including
dietary counseling); short-term inpatient care in a hospital, nursing
facility, or hospice inpatient facility (including both respite care
and procedures necessary for pain control and acute or chronic symptom
management); continuous home care during periods of crisis, and only as
necessary to maintain the terminally ill individual at home; and any
other item or service which is specified in the plan of care and for
which payment may otherwise be made under Medicare, in accordance with
Title XVIII of the Act.
Section 1814(a)(7)(B) of the Act requires that a written plan for
providing hospice care to a beneficiary who is a hospice patient be
established before care is provided by, or under arrangements made by,
that hospice program and that the written plan be periodically reviewed
by the beneficiary's attending physician (if any), the hospice medical
director, and an interdisciplinary group (described in section
1861(dd)(2)(B) of the Act). The services offered under the Medicare
hospice benefit must be available to beneficiaries as needed, 24 hours
a day, 7 days a week (section 1861(dd)(2)(A)(i) of the Act). Upon the
implementation of the hospice benefit, the Congress expected hospices
to continue to use volunteer services, though these services are not
reimbursed by Medicare (see section 1861(dd)(2)(E) of the Act). As
stated in the August 22, 1983 Hospice proposed rule, the hospice
interdisciplinary group should comprise paid hospice employees as well
as hospice volunteers (48 FR 38149). This expectation supports the
hospice philosophy of community based, holistic, comprehensive, and
compassionate end-of-life care.
Before the Medicare hospice benefit was established, the Congress
requested a demonstration project to test the feasibility of covering
hospice care under Medicare.\3\ The National Hospice Study was
initiated in 1980 through a grant sponsored by the Robert Wood Johnson
and John A. Hartford Foundations and CMS (then, the Health Care
Financing Administration (HCFA)). The demonstration project was
conducted between October 1980 and March 1983. The project summarized
the hospice care philosophy and principles as the following:
---------------------------------------------------------------------------
\3\ Greer, D., Mor, V., Sherwood, S. (1983) National hospice
study analysis plan. Journal of Chronic Diseases, Vol 36, 11, 737-
780. https://doi.org/10.1016/0021-9681(83)90069-3.
---------------------------------------------------------------------------
Patient and family know of the terminal condition.
Further medical treatment and intervention are indicated
only on a supportive basis.
Pain control should be available to patients as needed to
prevent rather than to just ameliorate pain.
Interdisciplinary teamwork is essential in caring for
patient and family.
Family members and friends should be active in providing
support during the death and bereavement process.
[[Page 20754]]
Trained volunteers should provide additional support as
needed.
The cost data and the findings on what services hospices provided
in the demonstration project were used to design the Medicare hospice
benefit. The identified hospice services were incorporated into the
service requirements under the Medicare hospice benefit. Importantly,
in the August 22, 1983 Hospice proposed rule, we stated ``the hospice
benefit and the resulting Medicare reimbursement is not intended to
diminish the voluntary spirit of hospices'' (48 FR 38149).
D. Medicare Payment for Hospice Care
Sections 1812(d), 1813(a)(4), 1814(a)(7), 1814(i), and 1861(dd) of
the Act, and our regulations in part 418, establish eligibility
requirements, payment standards and procedures; define covered
services; and delineate the conditions a hospice must meet to be
approved for participation in the Medicare program. Part 418, subpart
G, provides for a per diem payment in one of four prospectively-
determined rate categories of hospice care (Routine Home Care (RHC),
Continuous Home Care (CHC), inpatient respite care, and general
inpatient care), based on each day a qualified Medicare beneficiary is
under hospice care (once the individual has elected). This per diem
payment is to include all of the hospice services needed to manage the
beneficiary's care, as required by section 1861(dd)(1) of the Act.
There has been little change in the hospice payment structure since the
benefit's inception. The per diem rate based on level of care was
established in 1983, and this payment structure remains today with some
adjustments, as noted below:
1. Omnibus Budget Reconciliation Act of 1989
Section 6005(a) of the Omnibus Budget Reconciliation Act of 1989
(Pub. L. 101-239) amended section 1814(i)(1)(C) of the Act and provided
for the following two changes in the methodology concerning updating
the daily payment rates: (1) Effective January 1, 1990, the daily
payment rates for RHC and other services included in hospice care were
increased to equal 120 percent of the rates in effect on September 30,
1989; and (2) the daily payment rate for RHC and other services
included in hospice care for fiscal years (FYs) beginning on or after
October 1, 1990, were the payment rates in effect during the previous
federal fiscal year increased by the hospital market basket percentage
increase.
2. Balanced Budget Act of 1997
Section 4441(a) of the Balanced Budget Act of 1997 (BBA) (Pub. L.
105-33) amended section 1814(i)(1)(C)(ii)(VI) of the Act to establish
updates to hospice rates for FYs 1998 through 2002. Hospice rates were
updated by a factor equal to the hospital market basket percentage
increase, minus 1 percentage point. Payment rates for FYs from 2002
have been updated according to section 1814(i)(1)(C)(ii)(VII) of the
Act, which states that the update to the payment rates for subsequent
FYs will be the hospital market basket percentage increase for the FY.
The Act requires us to use the inpatient hospital market basket to
determine hospice payment rates.
3. FY 1998 Hospice Wage Index Final Rule
In the August 8, 1997 FY 1998 Hospice Wage Index final rule (62 FR
42860), we implemented a new methodology for calculating the hospice
wage index based on the recommendations of a negotiated rulemaking
committee. The original hospice wage index was based on 1981 Bureau of
Labor Statistics hospital data and had not been updated since 1983. In
1994, because of disparity in wages from one geographical location to
another, the Hospice Wage Index Negotiated Rulemaking Committee was
formed to negotiate a new wage index methodology that could be accepted
by the industry and the government. This Committee was composed of
representatives from national hospice associations; rural, urban, large
and small hospices, and multi-site hospices; consumer groups; and a
government representative. The Committee decided that in updating the
hospice wage index, aggregate Medicare payments to hospices would
remain budget neutral to payments calculated using the 1983 wage index,
to cushion the impact of using a new wage index methodology. To
implement this policy, a Budget Neutrality Adjustment Factor (BNAF) was
computed and applied annually to the pre-floor, pre-reclassified
hospital wage index when deriving the hospice wage index, subject to a
wage index floor.
4. FY 2010 Hospice Wage Index Final Rule
Inpatient hospital pre-floor and pre-reclassified wage index
values, as described in the August 8, 1997 Hospice Wage Index final
rule, were subject to either a budget neutrality adjustment or
application of the wage index floor. Wage index values of 0.8 or
greater were adjusted by the BNAF. Starting in FY 2010, a 7-year phase-
out of the BNAF began (FY 2010 Hospice Wage Index final rule, (74 FR
39384, August 6, 2009)), with a 10 percent reduction in FY 2010, an
additional 15 percent reduction for a total of 25 percent in FY 2011,
an additional 15 percent reduction for a total 40 percent reduction in
FY 2012, an additional 15 percent reduction for a total of 55 percent
in FY 2013, and an additional 15 percent reduction for a total 70
percent reduction in FY 2014. The phase-out continued with an
additional 15 percent reduction for a total reduction of 85 percent in
FY 2015, and an additional, and final, 15 percent reduction for
complete elimination in FY 2016. We note that the BNAF was an
adjustment which increased the hospice wage index value. Therefore, the
BNAF phase-out reduced the amount of the BNAF increase applied to the
hospice wage index value. It was not a reduction in the hospice wage
index value itself or in the hospice payment rates.
5. The Affordable Care Act
Starting with FY 2013 (and in subsequent FYs), the market basket
percentage update under the hospice payment system referenced in
sections 1814(i)(1)(C)(ii)(VII) and 1814(i)(1)(C)(iii) of the Act is
subject to annual reductions related to changes in economy-wide
productivity, as specified in section 1814(i)(1)(C)(iv) of the Act. In
FY 2013 through FY 2019, the market basket percentage update under the
hospice payment system will be reduced by an additional 0.3 percentage
point (although for FY 2014 to FY 2019, the potential 0.3 percentage
point reduction is subject to suspension under conditions specified in
section 1814(i)(1)(C)(v) of the Act).
In addition, sections 1814(i)(5)(A) through (C) of the Act, as
added by section 3132(a) of the Affordable Care Act, require hospices
to begin submitting quality data, based on measures to be specified by
the Secretary of the Department of Health and Human Services (the
Secretary), for FY 2014 and subsequent FYs. Beginning in FY 2014,
hospices that fail to report quality data will have their market basket
percentage increase reduced by 2 percentage points.
Section 1814(a)(7)(D)(i) of the Act, as added by section 3132(b)(2)
of the Affordable Care Act, requires, effective January 1, 2011, that a
hospice physician or nurse practitioner have a face-to-face encounter
with the beneficiary to determine continued eligibility of the
beneficiary's hospice care prior to the 180th-day
[[Page 20755]]
recertification and each subsequent recertification, and to attest that
such visit took place. When implementing this provision, we finalized
in the CY 2011 Home Health Prospective Payment System final rule (75 FR
70435) that the 180th-day recertification and subsequent
recertifications would correspond to the beneficiary's third or
subsequent benefit periods. Further, section 1814(i)(6) of the Act, as
added by section 3132(a)(1)(B) of the Affordable Care Act, authorizes
the Secretary to collect additional data and information determined
appropriate to revise payments for hospice care and other purposes. The
types of data and information suggested in the Affordable Care Act
could capture accurate resource utilization, which could be collected
on claims, cost reports, and possibly other mechanisms, as the
Secretary determined to be appropriate. The data collected could be
used to revise the methodology for determining the payment rates for
RHC and other services included in hospice care, no earlier than
October 1, 2013, as described in section 1814(i)(6)(D) of the Act. In
addition, we were required to consult with hospice programs and the
Medicare Payment Advisory Commission (MedPAC) regarding additional data
collection and payment revision options.
6. FY 2012 Hospice Wage Index Final Rule
When the Medicare Hospice benefit was implemented, the Congress
included an aggregate cap on hospice payments, which limits the total
aggregate payments any individual hospice can receive in a year. The
Congress stipulated that a ``cap amount'' be computed each year. The
cap amount was set at $6,500 per beneficiary when first enacted in 1983
and has been adjusted annually by the change in the medical care
expenditure category of the consumer price index for urban consumers
from March 1984 to March of the cap year (section 1814(i)(2)(B) of the
Act). The cap year was defined as the period from November 1st to
October 31st. In the August 4, 2011 FY 2012 Hospice Wage Index final
rule (76 FR 47308 through 47314) for the 2012 cap year and subsequent
cap years, we announced that subsequently, the hospice aggregate cap
would be calculated using the patient-by-patient proportional
methodology, within certain limits. We allowed existing hospices the
option of having their cap calculated via the original streamlined
methodology, also within certain limits. As of FY 2012, new hospices
have their cap determinations calculated using the patient-by-patient
proportional methodology. The patient-by-patient proportional
methodology and the streamlined methodology are two different
methodologies for counting beneficiaries when calculating the hospice
aggregate cap. A detailed explanation of these methods is found in the
August 4, 2011 FY 2012 Hospice Wage Index final rule (76 FR 47308
through 47314). If a hospice's total Medicare payments for the cap year
exceed the hospice aggregate cap, then the hospice must repay the
excess back to Medicare.
7. FY 2015 Hospice Wage Index and Payment Rate Update Final Rule
When electing hospice, a beneficiary waives Medicare coverage for
any care for the terminal illness and related conditions except for
services provided by the designated hospice and attending physician.
The FY 2015 Hospice Wage Index and Payment Rate Update final rule (79
FR 50452) finalized a requirement that requires the Notice of Election
(NOE) be filed within 5 calendar days after the effective date of
hospice election. If the NOE is filed beyond this 5 day period, hospice
providers are liable for the services furnished during the days from
the effective date of hospice election to the date of NOE filing (79 FR
50474). Similar to the NOE, the claims processing system must be
notified of a beneficiary's discharge from hospice or hospice benefit
revocation. This update to the beneficiary's status allows claims from
non-hospice providers to be processed and paid. Late filing of the NOE
can result in inaccurate benefit period data and leaves Medicare
vulnerable to paying non-hospice claims related to the terminal illness
and related conditions and beneficiaries possibly liable for any cost-
sharing of associated costs. Upon live discharge or revocation, the
beneficiary immediately resumes the Medicare coverage that had been
waived when he or she elected hospice. The FY 2015 Hospice Wage Index
and Payment Rate Update final rule also finalized a requirement that
requires hospices to file a notice of termination/revocation within 5
calendar days of a beneficiary's live discharge or revocation, unless
the hospices have already filed a final claim. This requirement helps
to protect beneficiaries from delays in accessing needed care (Sec.
418.26(e)).
A hospice ``attending physician'' is described by the statutory and
regulatory definitions as a medical doctor, osteopath, or nurse
practitioner whom the beneficiary identifies, at the time of hospice
election, as having the most significant role in the determination and
delivery of his or her medical care. Over time, we have received
reports of problems with the identification of the person's designated
attending physician and a third of hospice patients had multiple
providers submit Part B claims as the ``attending physician,'' using a
claim modifier. The FY 2015 Hospice Wage Index and Payment Rate Update
final rule finalized a requirement that the election form include the
beneficiary's choice of attending physician and that the beneficiary
provide the hospice with a signed document when he or she chooses to
change attending physicians (79 FR 50479).
Hospice providers are required to begin using a Hospice Experience
of Care Survey for informal caregivers of hospice patients as of 2015.
The FY 2015 Hospice Wage Index and Payment Rate Update final rule
provided background and a description of the development of the Hospice
Experience of Care Survey, including the model of survey
implementation, the survey respondents, eligibility criteria for the
sample, and the languages in which the survey is offered. The FY 2015
Hospice Rate Update final rule also set out participation requirements
for CY 2015 and discussed vendor oversight activities and the
reconsideration and appeals process for entities that failed to win CMS
approval as vendors (79 FR 50496).
Finally, the FY 2015 Hospice Wage Index and Payment Rate Update
final rule required providers to complete their aggregate cap
determination not sooner than 3 months after the end of the cap year,
and not later than 5 months after, and remit any overpayments. Those
hospices that fail to timely submit their aggregate cap determinations
will have their payments suspended until the determination is completed
and received by the Medicare Administrative Contractor (MAC) (79 FR
50503).
8. IMPACT Act of 2014
The Improving Medicare Post-Acute Care Transformation Act of 2014
(Pub. L. 113-185) (IMPACT Act) became law on October 6, 2014. Section
3(a) of the IMPACT Act mandated that all Medicare certified hospices be
surveyed every 3 years beginning April 6, 2015 and ending September 30,
2025. In addition, section 3(c) of the IMPACT Act requires medical
review of hospice cases involving beneficiaries receiving more than 180
days care in select hospices that show a preponderance of such
patients; section 3(d) of the IMPACT Act contains a new provision
[[Page 20756]]
mandating that the cap amount for accounting years that end after
September 30, 2016, and before October 1, 2025 be updated by the
hospice payment update rather than using the consumer price index for
urban consumers (CPI-U) for medical care expenditures.
9. FY 2016 Hospice Wage Index and Payment Rate Update Final Rule
In the FY 2016 Hospice Rate Update final rule, we created two
different payment rates for RHC that resulted in a higher base payment
rate for the first 60 days of hospice care and a reduced base payment
rate for subsequent days of hospice care (80 FR 47172). We also created
a Service Intensity Add-on (SIA) payment payable for services during
the last 7 days of the beneficiary's life, equal to the CHC hourly
payment rate multiplied by the amount of direct patient care provided
by a registered nurse (RN) or social worker that occurs during the last
7 days (80 FR 47177).
In addition to the hospice payment reform changes discussed, the FY
2016 Hospice Wage Index and Payment Rate Update final rule implemented
changes mandated by the IMPACT Act, in which the cap amount for
accounting years that end after September 30, 2016 and before October
1, 2025 is updated by the hospice payment update percentage rather than
using the CPI-U. This was applied to the 2016 cap year, starting on
November 1, 2015 and ending on October 31, 2016. In addition, we
finalized a provision to align the cap accounting year for both the
inpatient cap and the hospice aggregate cap with the fiscal year for FY
2017 and later (80 FR 47186). This allows for the timely implementation
of the IMPACT Act changes while better aligning the cap accounting year
with the timeframe described in the IMPACT Act.
Finally, the FY 2016 Hospice Wage Index and Payment Rate Update
final rule clarified that hospices must report all diagnoses of the
beneficiary on the hospice claim as a part of the ongoing data
collection efforts for possible future hospice payment refinements.
Reporting of all diagnoses on the hospice claim aligns with current
coding guidelines as well as admission requirements for hospice
certifications.
10. FY 2017 Hospice Wage Index and Payment Rate Update Final Rule
In the FY 2017 Hospice Wage Index and Payment Rate Update final
rule, we finalized several new policies and requirements related to the
HQRP. First, we codified our policy that if the National Quality Forum
(NQF) makes non-substantive changes to specifications for HQRP measures
as part of the NQF's re-endorsement process, we will continue to
utilize the measure in its new endorsed status, without going through
new notice-and-comment rulemaking (81 FR 52160). We will continue to
use rulemaking to adopt substantive updates made by the NQF to the
endorsed measures we have adopted for the HQRP; determinations about
what constitutes a substantive versus non-substantive change will be
made on a measure-by-measure basis. Second, we finalized two new
quality measures for the HQRP for the FY 2019 payment determination and
subsequent years: Hospice Visits when Death is Imminent Measure Pair
and Hospice and Palliative Care Composite Process Measure-Comprehensive
Assessment at Admission (81 FR 52173). The data collection mechanism
for both of these measures is the HIS, and the measures are effective
April 1, 2017. Regarding the CAHPS[supreg] Hospice Survey, we finalized
a policy that hospices that receive their CMS Certification Number
(CCN) after January 1, 2017 for the FY 2019 Annual Payment Update (APU)
and January 1, 2018 for the FY 2020 APU will be exempted from the
Hospice CAHPS[supreg] requirements due to newness (81 FR 52182). The
exemption is determined by CMS and is for 1 year only.
E. Trends in Medicare Hospice Utilization
Since the implementation of the hospice benefit in 1983, and
especially within the last decade, there has been substantial growth in
hospice benefit utilization. The number of Medicare beneficiaries
receiving hospice services has grown from 513,000 in FY 2000 to nearly
1.4 million in FY 2016. Similarly, Medicare hospice expenditures have
risen from $2.8 billion in FY 2000 to approximately $16.5 billion in FY
2016. Our Office of the Actuary (OACT) projects that hospice
expenditures are expected to continue to increase, by approximately 7
percent annually, reflecting an increase in the number of Medicare
beneficiaries, more beneficiary awareness of the Medicare Hospice
Benefit for end-of-life care, and a growing preference for care
provided in home and community-based settings.
There have also been changes in the diagnosis patterns among
Medicare hospice enrollees. Specifically, as described in Table 2,
there have been notable increases between 2002 and 2016 in
neurologically-based diagnoses, including diagnoses of Alzheimer's
disease. Additionally, there have been significant increases in the use
of non-specific, symptom-classified diagnoses, such as ``debility'' and
``adult failure to thrive.'' In FY 2013, ``debility'' and ``adult
failure to thrive'' were the first and sixth most common hospice
claims-reported diagnoses, respectively, accounting for approximately
14 percent of all diagnoses. Effective October 1, 2014, hospice claims
are returned to the provider if ``debility'' and ``adult failure to
thrive'' are coded as the principal hospice diagnosis as well as other
ICD-9-CM (and as of October 1, 2015, ICD-10-CM) codes that are not
permissible as principal diagnosis codes per ICD-9-CM (or ICD-10-CM)
coding guidelines. In the FY 2015 Hospice Wage Index and Payment Rate
Update final rule (79 FR 50452), we reminded the hospice industry that
this policy would go into effect and claims would start to be returned
to the provider effective October 1, 2014. As a result of this, there
has been a shift in coding patterns on hospice claims. For FY 2016, the
most common hospice principal diagnoses were Alzheimer's disease, Heart
Failure, Chronic Obstructive Pulmonary Disease, Lung Cancer, and Senile
Degeneration of the Brain, which constituted approximately 30 percent
of all claims-reported principal diagnosis codes reported in FY 2016
(see Table 2).
Table 2--The Top Twenty Principal Hospice Diagnoses, FY 2002, FY 2007, FY 2013, FY 2016
----------------------------------------------------------------------------------------------------------------
----------------------------------------------------------------------------------------------------------------
Rank ICD-9/Reported Principal Diagnosis Count Percentage
----------------------------------------------------------------------------------------------------------------
Year: FY 2002
----------------------------------------------------------------------------------------------------------------
1............................ 162.9 Lung Cancer.............. 73,769 11
2............................ 428.0 Congestive Heart Failure. 45,951 7
3............................ 799.3 Debility Unspecified..... 36,999 6
4............................ 496 COPD..................... 35,197 5
5............................ 331.0 Alzheimer's Disease...... 28,787 4
[[Page 20757]]
6............................ 436 CVA/Stroke............... 26,897 4
7............................ 185 Prostate Cancer.......... 20,262 3
8............................ 783.7 Adult Failure To Thrive.. 18,304 3
9............................ 174.9 Breast Cancer............ 17,812 3
10........................... 290.0 Senile Dementia, Uncomp.. 16,999 3
11........................... 153.0 Colon Cancer............. 16,379 2
12........................... 157.9 Pancreatic Cancer........ 15,427 2
13........................... 294.8 Organic Brain Synd Nec... 10,394 2
14........................... 429.9 Heart Disease Unspecified 10,332 2
15........................... 154.0 Rectosigmoid Colon Cancer 8,956 1
16........................... 332.0 Parkinson's Disease...... 8,865 1
17........................... 586 Renal Failure Unspecified 8,764 1
18........................... 585 Chronic Renal Failure 8,599 1
(End 2005).
19........................... 183.0 Ovarian Cancer........... 7,432 1
20........................... 188.9 Bladder Cancer........... 6,916 1
----------------------------------------------------------------------------------------------------------------
Year: FY 2007
----------------------------------------------------------------------------------------------------------------
1............................ 799.3 Debility Unspecified..... 90,150 9
2............................ 162.9 Lung Cancer.............. 86,954 8
3............................ 428.0 Congestive Heart Failure. 77,836 7
4............................ 496 COPD..................... 60,815 6
5............................ 783.7 Adult Failure To Thrive.. 58,303 6
6............................ 331.0 Alzheimer's Disease...... 58,200 6
7............................ 290.0 Senile Dementia Uncomp... 37,667 4
8............................ 436 CVA/Stroke............... 31,800 3
9............................ 429.9 Heart Disease Unspecified 22,170 2
10........................... 185 Prostate Cancer.......... 22,086 2
11........................... 174.9 Breast Cancer............ 20,378 2
12........................... 157.9 Pancreas Unspecified..... 19,082 2
13........................... 153.9 Colon Cancer............. 19,080 2
14........................... 294.8 Organic Brain Syndrome 17,697 2
NEC.
15........................... 332.0 Parkinson's Disease...... 16,524 2
16........................... 294.10 Dementia in Other 15,777 2
Diseases w/o Behavior
Dist..
17........................... 586 Renal Failure Unspecified 12,188 1
18........................... 585.6 End Stage Renal Disease.. 11,196 1
19........................... 188.9 Bladder Cancer........... 8,806 1
20........................... 183.0 Ovarian Cancer........... 8,434 1
----------------------------------------------------------------------------------------------------------------
Year: FY 2013
----------------------------------------------------------------------------------------------------------------
1............................ 799.3 Debility Unspecified..... 127,415 9
2............................ 428.0 Congestive Heart Failure. 96,171 7
3............................ 162.9 Lung Cancer.............. 91,598 6
4............................ 496 COPD..................... 82,184 6
5............................ 331.0 Alzheimer's Disease...... 79,626 6
6............................ 783.7 Adult Failure to Thrive.. 71,122 5
7............................ 290.0 Senile Dementia, Uncomp.. 60,579 4
8............................ 429.9 Heart Disease Unspecified 36,914 3
9............................ 436 CVA/Stroke............... 34,459 2
10........................... 294.10 Dementia in Other 30,963 2
Diseases w/o Behavioral
Dist..
11........................... 332.0 Parkinson's Disease...... 25,396 2
12........................... 153.9 Colon Cancer............. 23,228 2
13........................... 294.20 Dementia Unspecified w/o 23,224 2
Behavioral Dist..
14........................... 174.9 Breast Cancer............ 23,059 2
15........................... 157.9 Pancreatic Cancer........ 22,341 2
16........................... 185 Prostate Cancer.......... 21,769 2
17........................... 585.6 End-Stage Renal Disease.. 19,309 1
18........................... 518.81 Acute Respiratory Failure 15,965 1
19........................... 294.8 Other Persistent Mental 14,372 1
Dis.--classified
elsewhere.
20........................... 294.11 Dementia In Other 13,687 1
Diseases w/Behavioral
Dist..
----------------------------------------------------------------------------------------------------------------
Year: FY 2016
----------------------------------------------------------------------------------------------------------------
1............................ G30.9 Alzheimer's disease, 162,845 11
unspecified.
2............................ I50.9 Heart failure, 84,088 6
unspecified.
3............................ J44.9 Chronic obstructive 74,131 5
pulmonary disease,
unspecified.
4............................ C34.90 Malignant Neoplasm of 57,077 4
Unsp Part of Unsp
Bronchus or Lung.
5............................ G31.1 Senile degeneration of 55,305 4
brain, not elsewhere
classified.
6............................ G20 Parkinson's disease...... 37,245 2
7............................ I25.10 Atherosclerotic heart 33,647 2
disease of native
coronary art without
angina pectoris.
8............................ J44.1 Chronic obstructive 32,851 2
pulmonary disease with
(acute) exacerbation.
9............................ G30.1 Alzheimer's disease with 29,223 2
late onset.
10........................... I67.2 Cerebral atherosclerosis. 27,629 2
11........................... C61 Malignant neoplasm of 24,576 2
prostate.
[[Page 20758]]
12........................... N18.6 End stage renal disease.. 22,261 1
13........................... C18.9 Malignant neoplasm of 22,203 1
colon, unspecified.
14........................... I51.9 Heart disease, 21,868 1
unspecified.
15........................... C25.9 Malignant neoplasm of 20,400 1
pancreas, unspecified.
16........................... I63.9 Cerebral infarction, 18,546 1
unspecified.
17........................... I67.9 Cerebrovascular disease, 14,879 1
unspecified.
18........................... C50.919 Malignant neoplasm of 14,022 1
unspecified site of
unspecified female
breast.
19........................... A41.9 Sepsis, unspecified 12,723 1
organism.
20........................... I50.22 Chronic systolic 12,083 1
(congestive) heart
failure.
----------------------------------------------------------------------------------------------------------------
Note(s): The frequencies shown represent beneficiaries that had at least one claim with the specific ICD-9-CM/
ICD-10 code reported as the principal diagnosis. Beneficiaries could be represented multiple times in the
results if they have multiple claims during that time period with different principal diagnoses.
Source: FY 2002 and 2007 hospice claims data from the Chronic Conditions Data Warehouse (CCW), accessed on
February 14 and February 20, 2013. FY 2013 hospice claims data from the CCW, accessed on June 26, 2014, and FY
2016 hospice claims data from the CCW, accessed and merged with ICD-10 codes on January 9, 2017.
While there has been a shift in the reporting of the principal
diagnosis as a result of diagnosis clarifications, a significant
proportion of hospice claims (49 percent) in FY 2014 only reported a
single principal diagnosis, which may not fully explain the
characteristics of Medicare beneficiaries who are approaching the end
of life. To address this pattern of single diagnosis reporting, the FY
2015 Hospice Wage Index and Payment Rate Update final rule (79 FR
50498) reiterated ICD-9-CM coding guidelines for the reporting of the
principal and additional diagnoses on the hospice claim. We reminded
providers to report all diagnoses on the hospice claim for the terminal
illness and related conditions, including those that affect the care
and clinical management for the beneficiary. Additionally, in the FY
2016 Hospice Wage Index and Payment Rate Update final rule (80 FR
47201), we provided further clarification regarding diagnosis reporting
on hospice claims. We clarified that hospices will report all diagnoses
identified in the initial and comprehensive assessments on hospice
claims, whether related or unrelated to the terminal prognosis of the
individual, effective October 1, 2015. Analysis of FY 2016 hospice
claims shows that 100 percent of hospices reported more than one
diagnosis, with 86 percent submitting at least two diagnoses and 77
percent including at least three diagnoses.
III. Provisions of the Proposed Rule
A. Monitoring for Potential Impacts--Affordable Care Act Hospice Reform
1. Hospice Payment Reform: Research and Analyses
This section of the proposed rule describes current trends in
hospice utilization and provider behavior, such as lengths of stay,
live discharge rates, skilled visits during the last days of life, and
non-hospice spending. Utilization data on these metrics were examined
to determine the potential impacts related to the hospice reform
policies finalized in the FY 2016 Hospice Wage Index and Payment Rate
Update final rule (80 FR 47142), if any. Moreover, in response to
Office of Inspector General (OIG) report ``Hospice Inappropriately
Billed Medicare Over $250 Million for General Inpatient Care'' (OEI-02-
10-00491) released in March 2016, which identified the drugs paid for
by Part D and provided to beneficiaries during general inpatient care
(GIP) stays, we have also continued to monitor non-hospice spending
during a hospice election as described in this section. Additionally,
we have included preliminary information on the costs of hospice care
using data from the new hospice Medicare cost report, effective for
cost reporting periods that began on or after October 1, 2014 (FY
2015). Section 1814(i)(6) of the Act, as amended by section
3132(a)(1)(B) of the Affordable Care Act, authorized the Secretary to
collect additional data and information determined appropriate to
revise payments for hospice care and other purposes, including such
data sources as the Medicare cost reports. These preliminary analyses
may inform future work that could include such refinements to hospice
payment rates.
a. Length of Stay and Live Discharges
Hospice Length of Stay
Eligibility under the Medicare hospice benefit is predicated on the
individual being certified as terminally ill. Medicare regulations at
Sec. 418.3 define ``terminally ill'' to mean that the individual has a
medical prognosis that his or her life expectancy is 6 months or less
if the illness runs its normal course. However, we have recognized in
previous rules that prognostication is not an exact science (79 FR
50470), and thus, a beneficiary may be under a hospice election longer
than 6 months, as long as there remains a reasonable expectation that
the individual has a life expectancy of 6 months or less.
The number of days that a hospice beneficiary receives care under a
hospice election is referred to as the hospice length of stay. Hospice
length of stay can be influenced by a number of factors including
disease course, timing of referral, decision to resume curative
treatment, and/or stabilization or improvement where the individual is
no longer certified as terminally ill. Longer lengths of stay in
hospice may reflect admission to hospice earlier in the disease
trajectory or miscalculation of prognosis, among other situations.
Shorter lengths of stay in hospice may reflect hospice election late in
the disease trajectory or a rapidly progressing acute condition. This
also may be due to individual reluctance to accept that his or her
condition is terminal and choose the hospice benefit; inadequate
knowledge regarding the breadth of services available under hospice
care; cultural, ethnic, and/or religious backgrounds inhibiting or even
precluding the use of hospice services; and other reasons.\4\ As such,
hospice lengths of stay are variable.
---------------------------------------------------------------------------
\4\ Vig, E., Starks, H., Taylor, J., Hopley, E., Fryer-Edwards,
K. (2010). ``Why Don't Patients Enroll in Hospice? Can We Do
Anything About It?'' Journal of General Internal Medicine. 25(10):
1009-19. Doi: 10.1007/s11606-010-1423-9.
---------------------------------------------------------------------------
We examined length of stay, meaning the number of hospice days
during a single hospice election at the date of live discharge or
death. We also examined total lifetime length of stay, which would
include the sum of all days of hospice care across all hospice
elections. This would mean if a beneficiary had one hospice election,
was discharged alive, and then re-elected the benefit at a later date,
the sum of both elections would count towards their lifetime length of
stay. In FY 2016, the average length of stay in hospice was 79 days and
the average lifetime length of stay in hospice was
[[Page 20759]]
96.1 days. The average length of stay remained virtually the same
between FY 2015 and FY 2016, 78 days compared to 79 days, respectively.
The average lifetime length of stay similarly remained virtually the
same between FY 2015 and FY 2016, 95.2 and 96.1 days, respectively.
The median (50th percentile) length of stay in FY 2016 was 18 days.
This means that half of hospice beneficiaries received care for fewer
than 18 days and half received care for more than 18 days. While the
median length of stay has remained relatively constant over the past
several years, the average length of stay has typically increased from
year to year.
The Medicare hospice benefit provides four levels of care: Routine
home care (RHC), general inpatient care (GIP), continuous home care
(CHC), and inpatient respite care (IRC). The majority of hospice
patient care is provided at the RHC level of care and can be provided
wherever the patient calls ``home,'' including nursing homes and
assisted living facilities. As indicated in Table 3 below, most hospice
care (98 percent) provided is routine home care (RHC). Approximately 56
percent of all hospice days are provided at the RHC level of care in
the patient's residence whereas 41 percent is provided at the RHC level
of care to patients that reside in a nursing home or assisted living
facility.
Table 3--Share of Hospice Days by Level of Care and Site of Service, for Beneficiaries Discharged Alive or
Deceased in FY 2016
----------------------------------------------------------------------------------------------------------------
Number of % of all
Level of care Site of service hospice days hospice days
----------------------------------------------------------------------------------------------------------------
RHC.................................... Home + Hospice Residential Facility.... 59,818,337 55.75
SNF/NF................................. 25,953,198 24.19
Assisted Living Facility............... 18,182,931 16.95
Other.................................. 1,224,979 1.14
-------------------------------
Total............................... 105,179,445 98.02
----------------------------------------------------------------------------------------------------------------
GIP.................................... Inpatient Hospital..................... 378,792 0.35
Inpatient Hospice Facility............. 1,060,487 0.99
Skilled Nursing Facility............... 59,158 0.06
Other.................................. 5,571 0.01
-------------------------------
Total............................... 1,504,008 1.40
----------------------------------------------------------------------------------------------------------------
CHC.................................... Home + Hospice Residential Facility.... 180,206 0.17
SNF/NF................................. 42,224 0.04
Assisted Living Facility............... 69,849 0.07
Other.................................. 484 0.00
-------------------------------
Total............................... 292,763 0.27
----------------------------------------------------------------------------------------------------------------
IRC.................................... Inpatient Hospital..................... 29,895 0.03
Inpatient Hospice Facility............. 111,004 0.10
SNF/NF................................. 185,351 0.17
Other.................................. 1,490 0.00
-------------------------------
Total............................... 327,740 0.31
-------------------------------
Total.............................. ....................................... 107,303,956 100
----------------------------------------------------------------------------------------------------------------
Source: Common Working File (CWF). All hospice claims from 2006 to 2016 were included, for beneficiaries whose
final claim in FY 2016, according to through date, for a hospice discharge (excluded status code ``30'',
indicating a continuing patient). Hospice days with invalid or missing site of service HCPCS code are
excluded.
In addition to analyzing the hospice average and average lifetime
lengths of stay, we examined the average lifetime lengths of stay
associated with hospice principal diagnoses by site of service at
admission in FY 2015 (see Table 4 below). We limited our analysis to
those beneficiaries that were receiving RHC at admission. As noted in
Table 3 above, RHC was the level of care for 98 percent of all hospice
days. We found that beneficiaries with chronic, progressive
neurological diseases such as Alzheimer's disease and related
dementias, and Parkinson's disease had the longest average lifetime
lengths of stay at 165.3 days in FY 2015. Beneficiaries with Chronic
Kidney Disease and cancer had shorter average lifetime lengths of stay,
57 and 63.7 days, respectively. For all diagnoses, the average lifetime
length of stay was 113.5 days in FY 2015 when level of care at
admission is RHC.
Table 4--Average Lifetime Length of Stay by Diagnosis and Site of Service on the Day of Admission in FY 2015, When Level of Care at Admission Is RHC
--------------------------------------------------------------------------------------------------------------------------------------------------------
Home + hospice Assisted living SNF + LTC or non- Other All sites of service
residential facility facility skilled nursing -------------------------------------------
-------------------------------------------- facility
---------------------- Average Average
Primary hospice diagnosis at admission Average Average Average Number of lifetime Number of lifetime
Number of lifetime Number of lifetime Number of lifetime benes length of benes length of
benes length of benes length of benes length of stay stay
stay stay stay
--------------------------------------------------------------------------------------------------------------------------------------------------------
All Diagnoses............................. 576,657 106.75 101,085 159.77 208,747 106.21 9,530 90.90 897,298 113.51
[[Page 20760]]
Alzheimer's, Dementia, and Parkinson's.... 83,527 172.45 39,019 186.89 67,438 140.34 2,314 143.33 192,593 165.32
CVA/Stroke................................ 32,329 95.82 9,359 98.97 23,927 77.17 971 53.56 66,668 90.06
Cancers................................... 233,771 62.04 11,773 93.90 30,437 63.23 1,964 46.41 278,047 63.69
Chronic Kidney Disease.................... 14,328 58.41 1,655 82.34 6,644 47.60 273 48.84 22,907 57.01
Heart (CHF and Other Heart Disease)....... 101,243 121.77 19,784 131.11 35,052 83.54 1,771 84.69 158,167 115.14
Lung (COPD and Pneumonias)................ 58,183 131.97 6,866 127.83 16,631 82.42 870 65.42 82,656 122.11
All Other Diagnoses....................... 53,276 163.47 12,629 254.83 28,618 150.98 1,367 125.28 96,260 173.36
--------------------------------------------------------------------------------------------------------------------------------------------------------
Source: Common Working File (CWF). All hospice claims from 2006 to 2015 were included, for beneficiaries whose final claim in FY 2015, according to
through date, for a hospice discharge (excluded status code ``30'', indicating a continuing patient). Diagnosis code and site of service were
determined by the first hospice claim for a beneficiary. Diagnosis categories are consistent with those outlined in Abt's 2015 technical report
(https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/Hospice/Downloads/December-2015-Technical-Report.pdf).
Note 1: ``Other'' category includes inpatient hospital, inpatient hospice facility, LTCH, IPF, and places not otherwise specified. Although dementia was
no longer a valid primary diagnosis for the hospice benefit, our study time period examines primary diagnoses dating back to 2006.
Note 2: The data used for this table spans multiple years (2006 and forward). We were not able to convert ICD-9-CM diagnosis codes to ICD-10-CM codes,
given the inherent complexities with appropriately mapping ICD-9-CM codes to ICD-10-CM codes, in time for this proposed rule. Therefore, we limited
this analysis to those hospice patients that were discharged (alive or deceased) in FY 2015.
As we indicated above, the average lifetime length of stay across
all levels of care at admission was 96.1 days in FY 2016. However, the
average lifetime length of stay was 114 days in FY 2016 when the level
of care was RHC at admission (see Table 5 below). This suggests that
beneficiaries not receiving RHC level of care at admission had shorter
lifetime lengths of stay compared to the beneficiaries whose level of
care was RHC at admission. In particular, those beneficiaries who are
admitted to hospice at the GIP level of care typically are more acute
and often die without transitioning to RHC and thus, have overall
shorter lengths of stay. Therefore, the shorter lengths of stay for
those admitted at the GIP level of care affect the overall average
lifetime length of stay across all levels of care.
Table 5--Average Lifetime Length of Stay Level of Care to RHC at Admission, FY 2015-FY 2016
----------------------------------------------------------------------------------------------------------------
FY 2015 FY 2016
-------------------------------------------------------------------
Number of Average lifetime Number of Average lifetime
benes length of stay benes length of stay
----------------------------------------------------------------------------------------------------------------
Any Level of Care at Admission.............. 1,111,967 95.16 1,117,643 96.14
RHC at Admission............................ 897,298 113.51 909,961 114.02
----------------------------------------------------------------------------------------------------------------
Source: Common Working File (CWF). All hospice claims from 2006 to 2016 were included, for beneficiaries whose
final claim in FY 2016, according to through date, for a hospice discharge (excluded status code ``30'',
indicating a continuing patient).
Live Discharges
A beneficiary who has elected hospice may revoke his or her hospice
election at any time and for any reason. The regulations state that if
the hospice beneficiary (or his or her representative) revokes the
hospice election, the beneficiary may, at any time, re-elect to receive
hospice coverage for any other hospice election period that he or she
is eligible to receive (Sec. 418.24(e) and Sec. 418.28(c)(3)).
Immediately upon hospice revocation, Medicare coverage resumes for
those Medicare benefits previously waived with the hospice election. A
revocation can only be made by the beneficiary, in writing, and must
specify the effective date of the revocation. A hospice cannot
``revoke'' a beneficiary's hospice election, nor is it appropriate for
hospices to encourage, request, or demand that the beneficiary or his
or her representative revoke his or her hospice election. Like the
hospice election, a hospice revocation is to be an informed choice
based on the beneficiary's goals, values and preferences for the
services the person wishes to receive through Medicare.
Federal regulations limit the circumstances in which a Medicare
hospice provider may discharge a patient from its care. In accordance
with Sec. 418.26, discharge from hospice care is permissible when the
patient moves out of the provider's service area, is determined to be
no longer terminally ill, or for cause. Hospices may not discharge the
patient at their discretion, even if the care may be costly or
inconvenient for the hospice program. As we indicated in the FY 2015
Hospice Wage Index and Payment Rate Update proposed and final rules, we
understand that the rate of live discharges should not be zero, given
the uncertainties of prognostication and the ability of beneficiaries
and their families to revoke the hospice election at any time (79 FR
26549 and 79 FR 50463). On July 1, 2012, we began collecting discharge
information on the claim to capture the reason for all types of
discharges which includes, death, revocation, transfer to another
hospice, moving out of the hospice's service area, discharge for cause,
or due to the beneficiary no longer being considered terminally ill
(that is, no longer qualifying for hospice services). In FY 2016,
approximately 17 percent of hospice beneficiaries were discharged alive
(see Figure 1 below). Beneficiary revocations represented 38 percent of
all live discharges whereas 51 percent of live discharges were
instances where the beneficiary was discharged because the beneficiary
was considered no longer terminally ill, and 11 percent of live
discharges were instances where beneficiaries transferred to other
hospices. In analyzing hospice live discharge rates
[[Page 20761]]
over time, Figure 1 demonstrates an incremental decrease in average
annual rates of live discharge rates from FY 2007 to FY 2015, but an
increase in the live discharge rate between FY 2015 and FY 2016.
Between FY 2007 and FY 2016, there has been a reduction in the live
discharge rate of 22.8 percent over this time period.
[GRAPHIC] [TIFF OMITTED] TP03MY17.000
As part of our ongoing monitoring efforts, we analyzed the
distribution of live discharge rates among hospices with 50 or more
discharges (discharged alive or deceased). Table 6 shows that there is
significant variation in the rate of live discharge between the 10th
and 90th percentiles. Most notably, hospices at the 95th percentile
discharged 49.1 percent of their patients alive in FY 2016. While the
live discharge rate in FY 2016 for every percentile has decreased
compared to FY 2014, the median live discharge rate remains around 17
percent.
Table 6--Distribution of Live Discharge Rates for Hospices With 50 or More Live Discharges, FY 2014 to FY 2016
----------------------------------------------------------------------------------------------------------------
Live discharge rate
Statistics -----------------------------------------------
FY 2014 FY 2015 FY 2016
----------------------------------------------------------------------------------------------------------------
5th Percentile.................................................. 7.5% 6.9% 6.8%
10th Percentile................................................. 9.0% 8.5% 8.4%
25th Percentile................................................. 12.4% 11.6% 11.6%
Median.......................................................... 17.6% 16.8% 16.9%
75th Percentile................................................. 26.5% 24.6% 25.4%
90th Percentile................................................. 39.4% 35.9% 37.2%
95th Percentile................................................. 50.0% 45.6% 49.1%
# Providers..................................................... 3,160 3,215 3,232
----------------------------------------------------------------------------------------------------------------
Source: FY 2014, FY 2015, and FY 2016 hospice claims data from Common Working File (CWF) that list a discharge
status code (meaning claims were excluded if they listed status code 30, indicating a continuing patient).
Live discharges were defined as hospice claims with a status code of ``01''.
Finally, we looked at the distribution of live discharges by length
of stay intervals. In looking at the length of stay intervals, 26
percent of the live discharges occurred within 30 days of the start of
hospice care, 13 percent between 31 to 60 days, 14 percent between 61
to 90 days, 19 percent between 91 to 180 days, and 28 percent of live
discharges occurred after a length of stay over 180 days of hospice
care (see Figure 2 below). The proportion of live discharges occurring
between the length of stay intervals was relatively constant from FY
2013 to FY 2016. Overall, our analyses do not reveal any anomalies in
trends in lengths of stay and rates of live discharge at this time.
However, we will continue to monitor the data available so as to
identify any concerning behavior in response to recent payment policy
reforms.
[[Page 20762]]
[GRAPHIC] [TIFF OMITTED] TP03MY17.001
b. Skilled Visits in the Last Days of Life
As we noted in both the FY 2016 and FY 2017 Hospice Wage Index and
Payment Rate Update final rules (80 FR 47164 and 81 FR 52143,
respectively), we are concerned that many hospice beneficiaries may not
be receiving skilled visits during the last days of life. In the period
of time immediately preceding death, patient needs typically surge and
more intensive services are warranted, so we expect that the provision
of care would proportionately escalate in order to meet the increased
clinical, emotional, and other needs of the hospice beneficiary and his
or her family and caregiver(s). The last week of life is typically the
period within the terminal illness trajectory that is associated with
the highest symptom burden, typically marked by impactful physical and
emotional symptoms, necessitating attentive care and engagement from
the integrated hospice team.
In the FY 2016 Hospice Wage Index and Payment Rate Update final
rule (80 FR 47164 through 47177), the Service Intensity Add-on (SIA)
payment policy was finalized with an implementation date of January 1,
2016. This payment was developed in part with the objective of
encouraging visits during the last days of life. Additionally, in the
FY 2017 Hospice Wage Index and Payment Rate Update final rule (81 FR
52143) we finalized two new hospice quality reporting program (HQRP)
measures, effective April 1, 2017: (1) Hospice Visits When Death is
Imminent, assessing hospice staff visits to patients and caregivers in
the last week of life; and (2) Hospice and Palliative Care Composite
Process Measure, assessing the percentage of hospice patients who
received care processes consistent with existing guidelines. These
efforts represent meaningful advances in encouraging visits to hospice
beneficiaries during the time period preceding death.
In the FY 2016 Hospice Wage Index and Payment Rate Update final
rule (80 FR 47164), commenters expressed concern regarding potential
impacts of the new payment policies. Some noted that the new payment
structures could potentially impact patient access to hospice care and
articulated concerns around provider jettisoning of hospice
beneficiaries, specifically around the 60-day mark of a hospice stay.
In response to these concerns, we pledged to monitor real-time hospice
data, evaluating for any shifts in utilization or provision of services
to Medicare beneficiaries.
As part of our monitoring efforts, we assessed the delivery of
hospice care during the period of time preceding death. Analysis of FY
2016 claims data, which encompasses hospice claims from October 1, 2015
through September 30, 2016, shows that on any given day during the last
7 days of a hospice election, nearly 44 percent of the time the patient
has not received a skilled visit (skilled nursing or social worker
visit) (see Table 7 below). This figure represents an incremental
improvement when compared to the figures presented in our FY 2017
Hospice Wage Index and Payment Rate Update proposed rule (81 FR 25515),
where FY 2014 claims showed approximately 46 percent for this metric.
Additionally, Table 7 shows that approximately 21 percent of
beneficiaries did not receive a skilled visit (skilled nursing or
social work visit) on the day of death in FY 2016. This value also
indicates an improvement compared to the FY 2014 claims data, in which
nearly 26 percent of hospice beneficiaries did not receive a skilled
visit on the day of death (81 FR 25515).
[[Page 20763]]
Table 7--Frequency and Length of Skilled Nursing and Social Work Visits (Combined) During the Last 7 Days of a Hospice Election Ending in Death, FY 2016
--------------------------------------------------------------------------------------------------------------------------------------------------------
Days Before Death
------------------------------------------------------------------------------------------- All 7 days
Visit length 0 days (day combined
of death) 1 day (%) 2 days (%) 3 days (%) 4 days (%) 5 days (%) 6 days (%) (%)
(%)
---------------------------------------------------------------------------------------------------------------------------------------------
No Visit............................. 21.2 36.7 43.7 48.9 53.1 55.8 58.0 43.6
15 Minutes to 1 Hour................. 25.6 30.0 28.2 26.7 25.2 24.4 23.7 26.5
1 Hour, 15 Minutes to 2 Hours........ 26.8 20.0 17.8 15.9 14.5 13.5 12.6 17.9
2 Hours, 15 Minutes to 3 Hours....... 13.8 7.1 5.8 4.9 4.3 3.9 3.5 6.6
3 Hours, 15 Minutes to 3 Hours, 45 4.8 2.3 1.8 1.5 1.2 1.1 1.0 2.1
Minutes.............................
4 or More Hours...................... 7.8 3.9 2.7 2.1 1.7 1.4 1.2 3.3
--------------------------------------------------------------------------------------------------------------------------------------------------------
Source: FY 2016 hospice claims data from Common Working File (CWF) (as of December 9, 2016).
While Table 7 above shows the frequency and length of skilled
nursing and social work visits combined during the last 7 days of a
hospice election in FY 2016, Tables 8 and 9 below show the frequency
and length of visits for skilled nursing and social work separately.
Analysis of FY 2016 claims data shows that on any given day during the
last 7 days of a hospice election, almost 47 percent of the time the
patient had not received a visit by a skilled nurse, and 90 percent of
the time the patient had not received a visit by a social worker (see
Tables 8 and 9, respectively). We believe it is important to ensure
that beneficiaries and their families and caregivers are, in fact,
receiving the level of care necessary during critical periods such as
the very end of life.
Table 8--Frequency and Length of Skilled Nursing Visits During the Last 7 Days of a Hospice Election Ending in Death, FY 2016
--------------------------------------------------------------------------------------------------------------------------------------------------------
Days Before Death
------------------------------------------------------------------------------------------- All 7 days
Visit length 0 days (day combined
of death) 1 day (%) 2 days (%) 3 days (%) 4 days (%) 5 days (%) 6 days (%) (%)
(%)
---------------------------------------------------------------------------------------------------------------------------------------------
No Visit............................. 22.7 39.6 46.9 52.2 56.5 59.2 61.5 46.5
15 Minutes to 1 Hour................. 26.4 31.5 29.1 27.0 25.2 24.1 23.2 27.0
1 Hour, 15 Minutes to 2 Hours........ 27.3 19.0 16.8 14.9 13.4 12.5 11.5 17.2
2 Hours, 15 Minutes to 3 Hours....... 13.2 5.4 4.2 3.5 3.0 2.7 2.4 5.4
3 Hours, 15 Minutes to 3 Hours, 45 4.1 1.6 1.2 0.9 0.7 0.7 0.6 1.5
Minutes.............................
4 or More Hours...................... 6.2 2.9 1.9 1.4 1.2 1.0 0.8 2.4
--------------------------------------------------------------------------------------------------------------------------------------------------------
Source: FY 2016 hospice claims data from Common Working File (CWF) (as of December 9, 2016).
Table 9--Frequency and Length of Social Work Visits During the Last 7 Days of a Hospice Election Ending in Death, FY 2016
--------------------------------------------------------------------------------------------------------------------------------------------------------
Days Before Death
-------------------------------------------------------------------------------------------
Visit length 0 days (day All 7 days
of death) 1 day (%) 2 days (%) 3 days (%) 4 days (%) 5 days (%) 6 days (%) combined
(%)
---------------------------------------------------------------------------------------------------------------------------------------------
No Visit............................. 89.9 87.1 88.6 89.7 90.5 91.1 91.4 89.6
15 Minutes to 1 Hour................. 6.3 8.8 7.8 7.1 6.6 6.3 6.1 7.1
1 Hour, 15 Minutes to 2 Hours........ 2.7 3.4 3.0 2.7 2.5 2.3 2.2 2.7
2 Hours, 15 Minutes to 3 Hours....... 0.7 0.5 0.4 0.4 0.3 0.3 0.3 0.4
3 Hours, 15 Minutes to 3 Hours, 45 0.2 0.1 0.1 0.0 0.0 0.0 0.0 0.1
Minutes.............................
4 or More Hours...................... 0.2 0.1 0.1 0.0 0.0 0.0 0.0 0.1
--------------------------------------------------------------------------------------------------------------------------------------------------------
Source: FY 2016 hospice claims data from Common Working File (CWF) (as of December 9, 2016).
Additionally, we have analyzed the overall levels of nursing and
medical social services provided during the 7 days prior to death. In
an assessment of FY 2015 claims, we estimate that the total number of
hours of skilled services, including skilled nursing (as reported with
code G0154) and medical social services visits, provided to
[[Page 20764]]
Medicare hospice beneficiaries in the RHC level of care in the 7 days
preceding death was approximately 1.61 hours per day. As depicted in
Figure 3 below, from our analysis of FY 2016 hospice claims data that
begins January 1, 2016 and spans through December 31, 2016, a
relatively consistent level of nursing and medical social services
visits are being provided among RHC days in the 7 days prior to death,
averaging around 1.6 hours per day. For the period spanning January 1,
2016 through December 31, 2016, our analysis shows that approximately
1.24 hours of services were provided by RNs, 0.18 hours were provided
by LPNs, and 0.18 hours were provided by social workers per day. We
note that for purposes of the SIA payment, only those hours of service
provided by an RN, which became separately categorized as G0299
beginning January 1, 2016, and medical social worker count toward the
calculation of the SIA payment. Additionally, we note that G0154 was
retired as of January 1, 2016; however, this code was still reported by
some providers in the months of January and February 2016, and thus was
included in Figure 3.
[GRAPHIC] [TIFF OMITTED] TP03MY17.002
Given this evaluation of the initial wave of data, which now
encompasses the payment policy changes that began on January 1, 2016,
we do not believe that the results highlight any immediate concerns
regarding behavior changes among hospices, and it appears that
beneficiaries are receiving similar levels of care when compared to
time periods prior to the implementation of the payment policy reforms.
As more complete data become available, we will continue to monitor the
provision of services at end-of-life and impacts of the SIA payment and
other policies.
c. Non-Hospice Spending
When a beneficiary elects the Medicare hospice benefit, he or she
waives the right to Medicare payment for services related to the
treatment of the individual's condition with respect to which a
diagnosis of terminal illness has been made, except for services
provided by the designated hospice and the attending physician. Hospice
services are comprehensive and we have reiterated since 1983 that
``virtually all'' care needed by the terminally ill individual would be
provided by hospice. We believe that it would be unusual and
exceptional to see services provided outside of hospice for those
individuals who are approaching the end of life. However, we continue
to conduct ongoing analysis of non-hospice spending during a hospice
election and the results of our analysis seems to suggest the
unbundling of items and services that perhaps should have been provided
and covered under the Medicare hospice benefit.
We first reported findings on 2012 non-hospice spending during a
hospice election in the FY 2015 Hospice Wage Index and Payment Rate
Update final rule (79 FR 50452). This proposed rule updates our
analysis of non-hospice spending during a hospice election using FY
2016 data. We found that in FY 2016, Medicare paid over $900 million
for items and services under Parts A, B, and D for beneficiaries during
a hospice election. Medicare payments for non-hospice Part A and Part B
items and services received by hospice beneficiaries during hospice
election were $748 million in FY 2012, $712 million in FY 2013, $624
million in FY 2014, $593 million in FY 2015,
[[Page 20765]]
and $534 million in FY 2016 (see Figure 4 below). The beneficiary cost
sharing amount in FY 2016 was $129.6 million. Non-hospice spending for
Part A and Part B items and services has decreased each year since we
began reporting these findings. Overall, from FY 2012 to FY 2016 non-
hospice Medicare spending for Parts A and B during hospice election
declined 25 percent. However, there continues to be a non-trivial
amount of non-hospice Parts A and B spending on beneficiaries under a
hospice election, and we will continue to monitor data regarding this
issue
[GRAPHIC] [TIFF OMITTED] TP03MY17.003
We also examined Part D spending from FY 2012 to FY 2016 for those
beneficiaries under a hospice election. The data shows Medicare
payments for non-hospice Part D drugs received by hospice beneficiaries
during a hospice election were $331.3 million in FY 2012, $348 million
in FY 2013, $294 million in FY 2014, $315.2 million in FY 2015, and
$347.5 million in FY 2016 (see Figure 5). In contrast to non-hospice
spending during a hospice election for Medicare Parts A and B items and
services, non-hospice spending for Part D drugs increased in FY 2016
compared to FY 2012.
Recent analyses of Part D prescription drug event (PDE) data
suggest that the current prior authorization (PA) has reduced Part D
program payments for drugs in four targeted categories (analgesics,
anti-nauseants, anti-anxiety, and laxatives). However, under Medicare
Part D there has been an increase in hospice beneficiaries filling
prescriptions for a separate category of drugs we refer to as
maintenance drugs, as recently analyzed by CMS.\5\ Currently,
maintenance drugs for beneficiaries under a hospice election are not
subject to the Part D PA process. After a hospice election, many
maintenance drugs as well as drugs used to treat or cure a condition
are typically discontinued as the focus of care shifts to palliation
and comfort measures. However, there are maintenance drugs that are
appropriate to continue as they may offer symptom relief for the
palliation and management of the terminal illness and related
conditions, and therefore should be covered under the hospice benefit,
not Part D. Examples of maintenance drugs are those used to treat high
blood pressure, heart disease, asthma and diabetes. These categories
include beta blockers, calcium channel blockers, corticosteroids, and
insulin.
---------------------------------------------------------------------------
\5\ https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/Hospice/Downloads/2016-11-15-Part-D-Hospice-Guidance.pdf.
---------------------------------------------------------------------------
[[Page 20766]]
[GRAPHIC] [TIFF OMITTED] TP03MY17.004
Table 10 below details the various components of Part D spending
for patients receiving hospice care for FY 2016. The portion of the
$436.1 million total Part D spending that was paid by Medicare is the
sum of the Low Income Cost-Sharing Subsidy (row 2 in Table 10) and the
Covered Drug Plan Paid Amount (row 5), or approximately $347.5 million.
The beneficiary cost sharing amount was approximately $64.9 million,
including patient pay amount (row 1), other true out-of-pocket amount
(row 3), and patient liability reduction due to other payer amount (row
4).
Table 10--Drug Cost Sources for Hospice Beneficiaries' FY 2016 Drugs
Received Through Part D
------------------------------------------------------------------------
FY 2016
Component expenditures
------------------------------------------------------------------------
Patient Pay Amount...................................... $47,289,374
Low Income Cost-Sharing Subsidy......................... 103,715,821
Other True Out-of-Pocket Amount......................... 1,749,182
Patient Liability Reduction due to Other Payer Amount... 15,868,623
Covered Drug Plan Paid Amount........................... 243,791,919
Non-Covered Plan Paid Amount............................ 7,878,966
Six Payment Amount Totals............................... 420,293,884
Unknown/Unreconciled.................................... 15,836,435
Gross Total Drug Costs, Reported...................... 436,130,318
------------------------------------------------------------------------
Source: Analysis of 100% FY 2016 Medicare Claim Files. For more
information on the components above and on Part D data, go to the
Research Data Assistance Center's (ResDAC's) Web site at: https://www.resdac.org/.
Hospices are responsible for covering drugs and biologicals related
to the palliation and management of the terminal illness and while the
patient is under hospice care. For a prescription drug to be covered
under Part D for an individual enrolled in hospice, the drug must be
for treatment unrelated to the terminal illness or related conditions.
After a hospice election, many maintenance drugs or drugs used to treat
or cure a condition are typically discontinued as the focus of care
shifts to palliation and comfort measures. However, those same drugs
may be appropriate to continue as they may offer symptom relief for the
palliation and management of the terminal prognosis.\5\ In our ongoing
analysis of non-hospice spending, we remain concerned that common
palliative and other disease-specific drugs for hospice beneficiaries
that should be covered under the Part A Medicare hospice benefit are
instead being covered and paid for through Part D. Based on our own
analysis as demonstrated in the data provided above and similar
analyses conducted by the Office of the Inspector General (OIG)
regarding Part D drug expenditures for Medicare hospice beneficiaries,
we believe that Medicare could be paying twice for drugs that are
already covered under the hospice per diem payment by also paying for
them under Part D.\6\
---------------------------------------------------------------------------
\5\ https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/Hospice/Downloads/2016-11-15-Part-D-Hospice-Guidance.pdf.
\6\ https://oig.hhs.gov/oas/reports/region6/61000059.asp,
``Medicare Could Be Paying Twice for Prescriptions for Beneficiaries
in Hospice.''
---------------------------------------------------------------------------
We continue to expect that hospices should be providing virtually
all of the care needed by terminally ill individuals, including related
prescription drugs. The comprehensive nature of the services covered
under the Medicare hospice benefit is structured such that hospice
beneficiaries should not have to routinely seek items, services, and/or
medications beyond those provided by hospice. The hospice medical
director, the attending physician (if any), and the hospice IDG
[[Page 20767]]
determine, on a case-by-case basis, what items and services are related
and unrelated to the palliation and management of the terminal illness
and related conditions during the admission process, the initial and
comprehensive assessments, and in the development of the hospice plan
of care (Sec. Sec. 418.25, 418.54, and 418.56).
To the extent that individuals receive services outside of the
Medicare hospice benefit, Medicare coverage is determined by whether or
not the services are for the treatment of a condition completely
unrelated to the individual's terminal illness and related conditions
(48 FR 38148). However, we have presented hospice monitoring data from
the past several years, as seen above, that continue to show a non-
trivial amount of items, services, and medications being furnished
outside of the Medicare hospice benefit to beneficiaries under a
hospice election. We encourage hospices to educate beneficiaries
regarding the comprehensive nature of the hospice benefit. Although it
should be rare, if any conditions are identified by the hospice as
unrelated to the terminal illness and related conditions, we further
encourage hospices to inform the beneficiary (or representative) at or
near the time of election and provide the clinical rationale for such
determinations. The regulations at Sec. 476.78 state that providers
must inform Medicare beneficiaries at the time of admission, in
writing, that the care for which Medicare payment is sought will be
subject to Quality Improvement Organization (QIO) review. If a
beneficiary disagrees with the hospice determination of what conditions
are unrelated to the terminal illness and related conditions (and thus
arguably not provided as part of the hospice benefit), we strongly
encourage hospices to work to resolve the disagreement with the
beneficiary (or representative), taking into consideration his or her
wishes, treatment preferences and goals. If a resolution cannot be
reached, the beneficiary and the hospice can agree to participate in a
flexible, dialogue-based resolution process, called immediate advocacy,
which is coordinated by the QIO. We will continue to monitor non-
hospice spending during a hospice election and consider ways to address
this issue through future regulatory and/or program integrity efforts,
if needed.
2. Initial Analysis of Revised Hospice Cost Report Data
a. Background
As mentioned in section II.B of this proposed rule, the Medicare
hospice per diem payment amounts were developed to cover all services
needed for the palliation and management of the terminal illness and
related conditions, as described in section 1861(dd)(1) of the Act.
Services provided under a written plan of care could include: Nursing
care provided by or under the supervision of a registered professional
nurse; physical therapy, occupational therapy, speech-language
pathology services; counseling (including dietary counseling); medical
social services under the direction of a physician; services of a home
health aide; homemaker services; medical supplies (including drugs and
biologicals) and the use of durable medical equipment; physician
services; short-term inpatient care (including both respite care and
care necessary for pain control and acute and chronic symptom
management) in a qualified inpatient facility; or any other item or
service which has been specified in the plan of care for which payment
may be made under Medicare. Under the current payment system, hospices
are paid for each day that a beneficiary is enrolled in hospice care,
regardless of whether services are rendered on any given day.
As described in the FY 2016 Hospice Wage Index and Payment Rate
Update final rule, we finalized changes to the hospice cost report form
in order to broaden the scope and detail of data we collect regarding
the costs of providing hospice care (80 FR 47150).\7\ We believed that
changes were needed to the hospice cost report in order to collect data
on the costs of services provided at each level of care, rather than by
costs per day, regardless of the level of care. The revisions to the
cost report form for freestanding hospices became effective for cost
reporting periods beginning on or after October 1, 2014. The
instructions for completing the revised freestanding hospice cost
report form are found in the Medicare Provider Reimbursement Manual--
Part 2, chapter 43.\8\ Medicare-certified institutional providers are
required to submit an annual cost report to a Medicare Administrative
Contractor (MAC). The cost report contains provider information such as
facility characteristics, utilization data, costs by cost center (for
all payers as well as Medicare), Medicare settlement data, and
financial statement data.
---------------------------------------------------------------------------
\7\ CMS Transmittal 2864. ``Additional Data Reporting
Requirements for Hospice Claims'', Available at: https://www.cms.gov/Regulations-and-Guidance/Guidance/Transmittals/Downloads/R2864CP.pdf.
\8\ https://www.cms.gov/Regulations-and-Guidance/Guidance/Transmittals/Downloads/R1P243.pdf.
---------------------------------------------------------------------------
b. Methodology
Section 1814(i)(6) of the Act, as amended by section 3132(a)(1)(B)
of the Affordable Care Act, authorized the Secretary to collect
additional data and information determined appropriate to revise
payments for hospice care and other purposes. The data collected may be
used to revise the methodology for determining the payment rates for
RHC and other services included in hospice care. Effective October 1,
2014, we finalized changes to the hospice cost report to improve data
collection on the costs of providing hospice care. We conducted a
preliminary analysis of the new cost report data (CMS Form 1984-14) for
freestanding hospices with cost reporting periods in FY 2015, which
totaled 2,675 reports. Using this data we calculated preliminary
estimates of total costs per day by level of care. It is important to
note that the values we computed for cost per day include all payer
sources, both Medicare and non-Medicare; however, we believe that the
total cost figures represent a reasonable proxy for estimating costs
related to the provision of care for Medicare beneficiaries. In order
to compute total Medicare-related costs by level of care, we multiplied
the computed cost per day by level of care (as reported on Worksheet C)
for each hospice by the number of Medicare days by level of care. We
then calculated total payments by level of care for each hospice by
multiplying the FY 2015 Medicare hospice payments by level of care by
the number of Medicare days by level of care. Total costs, payments,
and days by level of care were summed for each unique hospice. In order
to more accurately account for the hourly CHC cost per day, we used
data from Medicare claims in order to quantify the hours of CHC
provided by summing the hours of CHC reported in revenue center 0652,
which tallies the units of CHC care. We then divided the CHC costs by
the number of CHC hours as reported in revenue center 0652 to calculate
a CHC per-hour value. In order to mitigate the impact of statistical
outliers, we applied trims on the outer bounds of cost per day by level
of care, set at the 1st and 99th percentile of the distribution.
c. Overall Payments and Costs and Costs by Level of Care
For the purposes of evaluating calculated costs per day by level of
care
[[Page 20768]]
compared to Medicare payment amounts, we compared the reported costs on
the Medicare cost report to the FY 2015 per diem payment rates by level
of care, as follows (79 FR 50485). We note that these amounts were not
adjusted by geographic differences in wage rates and are meant to serve
as a general benchmark:
$159.34 for RHC
$929.91 for 24 hours of CHC (hourly rate of $38.75)
$164.81 for IRC
$708.77 for GIP
Table 11 shows the distribution of the calculated Average Cost Per
Day by Level of Care, using data from Worksheet C--Rows 3, 8, 13, 18--
Column 3.
Table 11--Summary Statistics: Medicare Costs Per Day By Level of Care, FY 2015
--------------------------------------------------------------------------------------------------------------------------------------------------------
FY2015 per
Number of Weighted Minimum 25th 75th Maximum diem
Level of care cost Mean mean value Percentile Median Percentile value payment
reports amounts
-----------------------------------------------------------------------------------------------------------------------------------------
CHC cost per day, per hour... 1,088 $91 $49 $4 $18 $51 $95 $1,853 $929.91
for 24
hours
($38.75
hourly
rate).
RHC cost per day............. 2,578 133 123 50 105 125 150 399 159.34.
IRC cost per day............. 1,930 632 467 38 221 343 549 17,813 164.81.
GIP cost per day............. 1,782 1,079 792 64 564 879 1,251 10,858 708.77.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Source: Medicare hospice cost report data for FY 2015.
As mentioned above, the data analyzed were trimmed to minimize the
effect of statistical anomalies. Nevertheless, there is substantial
variation in the reported cost per day by hospices. Total cost per day
values in the four levels of care span from a minimum of $4 to maximum
values in the tens of thousands. Because of this wide range of values
in the distribution, we used the median as well as the mean values
weighted by the number of days by level of care as reference points in
these preliminary analyses. When compared with the FY 2015 per diem
payment rates, the calculated median and weighted mean costs associated
with providing RHC are lower than the base payment rates. As noted in
section III.A of this proposed rule, the RHC level of care accounts for
over 98 percent of all hospice days based on our analysis of claims for
FY 2016. The median and weighted mean costs for the provision of RHC
are estimated at $125 and $123 respectively, with both figures
presenting lower values than the FY 2015 per diem payment rate of
$159.34, a difference of approximately $35 per day.
Conversely, for CHC the estimated median and weighted mean costs
per day, per hour are $51 and $49, respectively. The FY 2015 payment
rate for CHC was $38.75 per hour. The CHC level of care accounts for
approximately 0.27 percent of all hospice days in FY 2016, as noted in
section III.A of this proposed rule. Similarly, the median and weighted
mean costs per day associated with the provision of GIP care is
estimated at $879 and $792, respectively, while the FY 2015 per diem
payment amount for GIP was $708.77. As noted in section III.A of this
proposed rule, the GIP level of care accounts for approximately 1.40
percent of all hospice days based on our analysis of FY 2016 claims.
Likewise, the median and weighted mean costs per day associated with
the IRC level of care are estimated at $343 and $467, respectively,
while the per diem payment amount for FY 2015 was $164.81, and we
estimate that IRC days represent approximately 0.31 percent of all
hospice days in FY 2016 claims as described in section III.A above.
We recognize that this is the first period in which hospices have
supplied cost information on the revised cost report that became
effective for cost reporting periods beginning on or after October 1,
2014 and expect that some of the early trends may be the result of
hospices learning how to accurately report this information. Therefore,
any interpretations regarding the overall alignment between costs and
payment would likely be premature given the newness of the data.
Moreover, this preliminary analysis did not incorporate factors that
merit consideration in future analyses, such as the exclusion of
providers surpassing the hospice inpatient and aggregate caps as well
as the application of a more robust trimming process to the cost report
dataset. As we continue to gather more cost report data, we plan to
conduct more thorough analyses of the cost report data and fully assess
Medicare-related hospice costs as compared with Medicare hospice
payments by level of care. We encourage hospices to continue to submit
the most accurate data possible on Medicare cost reports.
B. Proposed FY 2018 Hospice Wage Index and Rate Update
1. Proposed FY 2018 Hospice Wage Index
The hospice wage index is used to adjust payment rates for hospice
agencies under the Medicare program to reflect local differences in
area wage levels, based on the location where services are furnished.
The hospice wage index utilizes the wage adjustment factors used by the
Secretary for purposes of section 1886(d)(3)(E) of the Act for hospital
wage adjustments. Our regulations at Sec. 418.306(c) require each
labor market to be established using the most current hospital wage
data available, including any changes made by OMB to the Metropolitan
Statistical Areas (MSAs) definitions.
We use the previous FY's hospital wage index data to calculate the
hospice wage index values. For FY 2018, the hospice wage index will be
based on the FY 2017 hospital pre-floor, pre-reclassified wage index.
This means that the hospital wage data used for the hospice wage index
is not adjusted to take into account any geographic reclassification of
hospitals including those in accordance with section 1886(d)(8)(B) or
1886(d)(10) of the Act. The appropriate wage index value is applied to
the labor portion of the payment rate based on the geographic area in
which the beneficiary resides when receiving routine home care (RHC) or
continuous home care (CHC). The appropriate wage index value is applied
to the labor portion of the
[[Page 20769]]
payment rate based on the geographic location of the facility for
beneficiaries receiving general inpatient care (GIP) or Inpatient
Respite Care (IRC).
There exist some geographic areas where there were no hospitals,
and thus, no hospital wage index data on which to base the calculation
of the hospice wage index. In the FY 2008 Hospice Wage Index final rule
(72 FR 50214), we implemented a methodology to update the hospice wage
index for such areas. In cases where there was a rural area without
rural hospital wage data, we use the average pre-floor, pre-
reclassified hospital wage index data from all contiguous Core-Based
Statistical Areas (CBSAs), to represent a reasonable proxy for the
rural area. The term ``contiguous'' means sharing a border (72 FR
50217). Currently, the only rural area without a hospital from which
hospital wage data could be derived is Puerto Rico. However, for rural
Puerto Rico, we would not apply this methodology due to the distinct
economic circumstances that exist there (for example, due to the close
proximity to one another of almost all of Puerto Rico's various urban
and non-urban areas, this methodology would produce a wage index for
rural Puerto Rico that is higher than that in half of its urban areas);
instead, we would continue to use the most recent wage index previously
available for that area. For FY 2018, we propose to continue to use the
most recent pre-floor, pre-reclassified hospital wage index value
available for Puerto Rico, which is 0.4047.
In the FY 2010 Hospice Wage Index final rule (74 FR 39386), we
adopted the policy that for urban labor markets without a hospital from
which hospital wage index data could be derived, all of the CBSAs
within the state would be used to calculate a statewide urban average
pre-floor, pre-reclassified hospital wage index value to use as a
reasonable proxy for these areas. For FY 2018, the only CBSA without a
hospital from which hospital wage data can be derived is 25980,
Hinesville-Fort Stewart, Georgia.
As described in the August 8, 1997 Hospice Wage Index final rule
(62 FR 42860), the pre-floor and pre-reclassified hospital wage index
is used as the raw wage index for the hospice benefit. These raw wage
index values are subject to application of the hospice floor to compute
the hospice wage index used to determine payments to hospices. Pre-
floor, pre-reclassified hospital wage index values below 0.8 are
adjusted by a 15 percent increase subject to a maximum wage index value
of 0.8. For example, if County A has a pre-floor, pre-reclassified
hospital wage index value of 0.3994, we would multiply 0.3994 by 1.15,
which equals 0.4593. Since 0.4593 is not greater than 0.8, then County
A's hospice wage index would be 0.4593. In another example, if County B
has a pre-floor, pre-reclassified hospital wage index value of 0.7440,
we would multiply 0.7440 by 1.15 which equals 0.8556. Because 0.8556 is
greater than 0.8, County B's hospice wage index would be 0.8.
On February 28, 2013, OMB issued OMB Bulletin No. 13-01, announcing
revisions to the delineation of MSAs, Micropolitan Statistical Areas,
and Combines Statistical Areas, and guidance on uses of the delineation
in these areas. In the FY 2016 Hospice Wage Index final rule (80 FR
47178), we adopted the OMB's new area delineations using a 1-year
transition. In the FY 2016 Hospice Wage Index and Payment Rate Update
final rule (80 FR 47178), we stated that beginning October 1, 2016, the
wage index for all hospice payments would be fully based on the new OMB
delineations. The most recent bulletin (No. 15-01) concerning the
revised delineations was published by the OMB on July 15, 2015.
The proposed hospice wage index applicable for FY 2018 (October 1,
2017 through September 30, 2018) is available on the Web site at:
https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/Hospice/.
2. Proposed Hospice Payment Update Percentage
Section 4441(a) of the Balanced Budget Act of 1997 (BBA) (Pub. L.
105-33) amended section 1814(i)(1)(C)(ii)(VI) of the Act to establish
updates to hospice rates for FYs 1998 through 2002. Hospice rates were
to be updated by a factor equal to the inpatient hospital market basket
percentage increase set out under section 1886(b)(3)(B)(iii) of the
Act, minus 1 percentage point. Payment rates for FYs since 2002 have
been updated according to section 1814(i)(1)(C)(ii)(VII) of the Act,
which states that the update to the payment rates for subsequent FYs
must be the inpatient market basket percentage increase for that FY.
The Act historically required us to use the inpatient hospital market
basket as the basis for the hospice payment rate update.
Section 3401(g) of the Affordable Care Act mandated that, starting
with FY 2013 (and in subsequent FYs), the hospice payment update
percentage would be annually reduced by changes in economy-wide
productivity as specified in section 1886(b)(3)(B)(xi)(II) of the Act.
The statute defines the productivity adjustment to be equal to the 10-
year moving average of changes in annual economy-wide private nonfarm
business multifactor productivity (MFP). In addition to the MFP
adjustment, section 3401(g) of the Affordable Care Act also mandated
that in FY 2013 through FY 2019, the hospice payment update percentage
would be reduced by an additional 0.3 percentage point (although for FY
2014 to FY 2019, the potential 0.3 percentage point reduction is
subject to suspension under conditions specified in section
1814(i)(1)(C)(v) of the Act).
Normally, the proposed hospice payment update percentage for FY
2018 would have been based on the estimated inpatient hospital market
basket update of 2.9 percent (based on IHS Global Insight, Inc.'s
fourth quarter 2016 forecast with historical data through the third
quarter of 2016 of the proposed 2014-based IPPS market basket). Due to
the requirements at section 1886(b)(3)(B)(xi)(II) of the Act, the
estimated FY 2018 inpatient hospital market basket update of 2.9
percent would have been reduced by a MFP adjustment as mandated by
Affordable Care Act (currently estimated to be 0.4 percentage point for
FY 2018). Section 1814(i)(1)(C)(v) of the Act requires that the
estimated inpatient hospital market basket update for FY 2018 would be
reduced further by 0.3 percentage point. In effect, the proposed
hospice payment update percentage for FY 2018 would be 2.2 percent.
However, section 411(d) of the Medicare Access and CHIP Reauthorization
Act of 2015, Public Law 114-10 (April 16, 2015) (MACRA) amended section
1814(i)(1)(C) of the Act such that for hospice payments for FY 2018,
the market basket percentage increase, after application of the
productivity adjustment and the 0.3 percent reduction, if applicable,
shall be 1 percent. Therefore, for FY 2018, the hospice payment update
percentage will be 1 percent.
Currently, the labor portion of the hospice payment rates is as
follows: For RHC, 68.71 percent; for CHC, 68.71 percent; for General
Inpatient Care, 64.01 percent; and for Respite Care, 54.13 percent. The
non-labor portion is equal to 100 percent minus the labor portion for
each level of care. Therefore, the non-labor portion of the payment
rates is as follows: For RHC, 31.29 percent; for CHC, 31.29 percent;
for General Inpatient Care, 35.99 percent; and for Respite Care, 45.87
percent. Beginning with cost reporting periods starting on or after
October 1, 2014, freestanding hospice providers are
[[Page 20770]]
required to submit cost data using CMS Form 1984-14 (https://www.cms.gov/Research-Statistics-Data-and-Systems/Downloadable-Public-Use-Files/Cost-Reports/Hospice-2014.html). We are currently analyzing
this data for possible use in updating the labor portion of the hospice
payment rates. Any changes to the labor portions will be proposed in
future rulemaking and will be subject to public comments.
3. Proposed FY 2018 Hospice Payment Rates
There are four payment categories that are distinguished by the
location and intensity of the services provided. The base payments are
adjusted for geographic differences in wages by multiplying the labor
share, which varies by category, of each base rate by the applicable
hospice wage index. A hospice is paid the RHC rate for each day the
beneficiary is enrolled in hospice, unless the hospice provides CHC,
IRC, or GIP. CHC is provided during a period of patient crisis to
maintain the patient at home; IRC is short-term care to allow the usual
caregiver to rest and be relieved from caregiving; and GIP is to treat
symptoms that cannot be managed in another setting.
As discussed in the FY 2016 Hospice Wage Index and Payment Rate
Update final rule (80 FR 47172), we implemented two different RHC
payment rates, one RHC rate for the first 60 days and a second RHC rate
for days 61 and beyond. In addition, in the final rule, we adopted a
Service Intensity Add-on (SIA) payment for RHC for when direct patient
care is provided by a RN or social worker during the last 7 days of the
beneficiary's life. The SIA payment is equal to the CHC hourly rate
multiplied by the hours of nursing or social work provided (up to 4
hours total) that occurred on the day of service, if certain criteria
are met. In order to maintain budget neutrality, as required under
section 1814(i)(6)(D)(ii) of the Act, the new RHC rates were adjusted
by a SIA budget neutrality factor.
As discussed in the FY 2016 Hospice Wage Index and Payment Rate
Update final rule (80 FR 47177), we will continue to make the SIA
payments budget neutral through an annual determination of the SIA
budget neutrality factor (SBNF), which will then be applied to the RHC
payment rates. The SBNF will be calculated for each FY using the most
current and complete FY utilization data available at the time of
rulemaking. For FY 2018, we calculated the SBNF using FY 2016
utilization data. We examined skilled nursing and social work visit
data for the last 7 days of life where RHC was billed and found that,
from January 1 through September 30, 2016, approximately 86 percent of
nursing visits were identified as RN visits (using G0299) and 14
percent of nursing visits were identified as LPN visits (using G0300).
For skilled nursing visits during the last 7 days of life where RHC was
billed and that occurred between October 1 and December 31, 2015, we
assumed that 86 percent of the line item visits reported using G0154
were RN and 14 percent were LPN. For FY 2018, the budget neutrality
adjustment that would apply to days 1 through 60 is calculated to be
1.0018. The budget neutrality adjustment that would apply to days 61
and beyond is calculated to be 1.0005.
In the FY 2017 Hospice Wage Index and Payment Rate Update final
rule (82 FR 52156), we initiated a policy of applying a wage index
standardization factor to hospice payments in order to eliminate the
aggregate effect of annual variations in hospital wage data. In order
to calculate the wage index standardization factor, we simulate total
payments using the proposed FY 2018 hospice wage index and compare it
to our simulation of total payments using the FY 2017 hospice wage
index. By dividing payments for each level of care using the proposed
FY 2018 wage index by payments for each level of care using the FY 2017
wage index, we obtain a wage index standardization factor for each
level of care (RHC days 1-60, RHC days 61+, CHC, IRC, and GIP). The
wage index standardization factors for each level of care are shown in
the tables below.
Lastly, the hospice payment rates for hospices that submit the
required quality data would be increased by the proposed FY 2018
hospice payment update percentage of 1.0 percent as discussed in
section III.B.2. The proposed FY 2018 RHC rates are shown in Table 12.
The proposed FY 2018 payment rates for CHC, IRC, and GIP are shown in
Table 13.
Table 12--Proposed FY 2018 Hospice RHC Payment Rates
--------------------------------------------------------------------------------------------------------------------------------------------------------
FY 2018
Wage index proposed FY 2018
Code Description FY 2017 SBNF standardization hospice Proposed
payment rates factor payment payment rates
update
--------------------------------------------------------------------------------------------------------------------------------------------------------
651............................... Routine Home Care (days 1-60)..... $190.55 x 1.0018 x 1.0000 x 1.01 $192.80
651............................... Routine Home Care (days 61+)...... $149.82 x 1.0005 x 1.0001 x 1.01 $151.41
--------------------------------------------------------------------------------------------------------------------------------------------------------
Table 13--Proposed FY 2018 Hospice CHC, IRC, and GIP Payment Rates
----------------------------------------------------------------------------------------------------------------
FY 2018
Wage index proposed FY 2018
Code Description FY 2017 standardization hospice proposed
payment rates factor payment payment rates
update
----------------------------------------------------------------------------------------------------------------
652................... Continuous Home Care.. $964.63 x 1.0022 x 1.01 $976.42
Full Rate = 24 hours
of care.
$40.68 = FY 2018
hourly rate.
655................... Inpatient Respite Care 170.97 x 1.0006 x 1.01 172.78
656................... General Inpatient Care 734.94 x 1.0017 x 1.01 743.55
----------------------------------------------------------------------------------------------------------------
Sections 1814(i)(5)(A) through (C) of the Act require that hospices
submit quality data, based on measures to be specified by the
Secretary. In the FY 2012 Hospice Wage Index final rule (76 FR 47320
through 47324), we
[[Page 20771]]
implemented a Hospice Quality Reporting Program (HQRP) as required by
section 3004 of the Affordable Care Act. Hospices were required to
begin collecting quality data in October 2012, and submit that quality
data in 2013. Section 1814(i)(5)(A)(i) of the Act requires that
beginning with FY 2014 and each subsequent FY, the Secretary shall
reduce the market basket update by 2 percentage points for any hospice
that does not comply with the quality data submission requirements with
respect to that FY. The proposed FY 2018 rates for hospices that do not
submit the required quality data would be updated by the proposed FY
2018 hospice payment update percentage of 1 percent minus 2 percentage
points. These rates are shown in Tables 14 and 15.
Table 14--Proposed FY 2018 Hospice RHC Payment Rates for Hospices That DO NOT Submit the Required Quality Data
--------------------------------------------------------------------------------------------------------------------------------------------------------
FY 2018
proposed
hospice FY 2018
FY 2017 Wage index payment FY 2018 Proposed
Code Description payment rates SBNF standardization update of 1% proposed Payment
factor minus 2 payment rates Rates
percentage
points = -0.1%
------------------------------------------------------------------------------------------------------------------------------------------------ ----------
651........................... Routine Home Care (days 1-60). $190.55 x 1.0018 x 1.0000 x 0.99 $188.98
651........................... Routine Home Care (days 61+).. $149.82 x 1.0005 x 1.0001 x 0.99 148.41
--------------------------------------------------------------------------------------------------------------------------------------------------------
Table 15--Proposed FY 2018 Hospice CHC, IRC, and GIP Payment Rates for Hospices That DO NOT Submit the Required
Quality Data
----------------------------------------------------------------------------------------------------------------
FY 2018
Wage index proposed FY 2018
Code Description FY 2017 standardization hospice Proposed
payment rates factor payment payment rates
update
----------------------------------------------------------------------------------------------------------------
652................... Continuous Home Care.. $964.63 x 1.0022 x 0.99 $957.08
Full Rate = 24 hours
of care.
$39.88 = FY 2018
hourly rate.
655................... Inpatient Respite Care $170.97 x 1.0006 x 0.99 $169.36
656................... General Inpatient Care 734.94 x 1.0017 x 0.99 728.83
----------------------------------------------------------------------------------------------------------------
4. Hospice Cap Amount for FY 2018
As discussed in the FY 2016 Hospice Wage Index and Payment Rate
Update final rule (80 FR 47183), we implemented changes mandated by the
Improving Medicare Post-Acute Care Transformation Act of 2014 (IMPACT
Act). Specifically, for accounting years that end after September 30,
2016 and before October 1, 2025, the hospice cap is updated by the
hospice payment update percentage rather than using the consumer price
index for urban consumers (CPI-U). The hospice cap amount for the 2018
cap year will be $28,689.04, which is equal to the 2017 cap amount
($28,404.99) updated by the FY 2018 hospice payment update percentage
of 1.0 percent.
C. Discussion and Solicitation of Comments Regarding Sources of
Clinical Information for Certifying Terminal Illness
Hospice provides relief from pain and symptoms, provides
psychosocial and spiritual comfort, and allows an individual to die
with dignity and surrounded by family and friends. Despite the
invaluable support hospices offer, it is not an easy decision and not
one individuals generally arrive at on their own. Election of hospice
is a significant decision and one which patients and their physicians
do not take lightly, as it involves a shift in traditional health care
philosophy from curative to palliative care. In general, the majority
of hospice referrals do come from family physicians who have often
cared for patients with chronic illnesses for long periods of time.\9\
These providers are in the unique position of understanding and
identifying the individualized progression of the patient's illness and
recognizing when the condition becomes terminal. To be eligible to
elect the Medicare hospice benefit, the individual must have Medicare
Part A and be certified as terminally ill as articulated at Sec.
418.20. The regulations define ``terminally ill'' to mean that the
individual has a medical prognosis that his or her life expectancy is 6
months or less if the illness runs its normal course (Sec. 418.3). The
regulations at Sec. 418.22(c) require that for the initial 90-day
period of hospice care, the hospice must obtain written certification
statements from the medical director of the hospice or the physician
member of the hospice interdisciplinary group, and the individual's
attending physician, if the individual has an attending physician. The
current regulations at Sec. 418.25(b) state that in reaching a
decision to certify, the hospice medical director, or hospice physician
designee reviews the clinical information for each hospice patient and
provides written certification that it is anticipated that the
patient's life expectancy is 6 months or less if the illness runs its
normal course. These regulations require that the hospice medical
director consider at least the following information:
---------------------------------------------------------------------------
\9\ Michelle T. Weckmann, MD, MS, University of Iowa Hospitals
and Clinics, Iowa The Role of the Family Physician in the Referral
and Management of Hospice Patients. Am Fam Physician, 2008 Mar
15;77(6):807-812.
---------------------------------------------------------------------------
1. Diagnosis of the terminal condition of the patient.
2. Other health conditions, whether related or unrelated to the
terminal condition.
3. Current clinically relevant information supporting all
diagnoses.
The admission requirements at Sec. 418.22(b)(2) require that this
clinical information and other documentation that supports the medical
prognosis must accompany the certification and be filed in the medical
record with the
[[Page 20772]]
written certification. Whereas the regulations at Sec. 418.25(b)
provide the type of clinical information the hospice medical director
or hospice physician designee must consider in the certification of
terminal illness, the source of this clinical information is not
clearly identified. This raises the question as to what clinical
information the hospice medical director (or hospice physician
designee) is relying on to support his or her certification that the
individual is terminally ill and from where this information was
obtained.
Multiple clinical tools and guidelines, and more specifically the
Medicare Administrative Contractor (MAC) Local Coverage Determinations
(LCDs), exist to assist the patient-designated attending physician and
hospice medical director/hospice physician designee in determining the
patient's terminal prognosis. These guidelines provide indicators that
support a decline in clinical status, including, but not limited to:
History of recurrent infections, worsening symptoms that are non-
responsive to treatment, increasing emergency department and clinician
visits, laboratory results supporting progression of disease, and
change in functional status.\10\ However, documentation of these
indicators would likely not exist without some degree of long-term
monitoring and evaluation by a physician separate from the hospice
medical director/hospice physician designee. As such, this information
would typically be found in the referring physician's and/or acute/
post- acute care facility's medical records.
---------------------------------------------------------------------------
\10\ https://www.cms.gov/medicare-coverage-database/details/lcd-details.aspx.
---------------------------------------------------------------------------
Understandably, many family physicians typically take on the role
of the attending physician once the patient chooses to elect hospice.
They have played an invaluable role in coordinating care throughout the
spectrum of the patient's life, and as such, have in depth ``knowledge
of the patient's values, family issues, and communication style.'' \11\
However, in accordance with our regulation at Sec. 418.22(c)(1)(ii),
only the initial certification has to involve the attending physician
and only IF the patient has designated one. There is currently no
requirement that a patient must designate an attending physician and
therefore the responsibility for certification can solely reside with
the hospice medical director or the physician member of the hospice
interdisciplinary group. Furthermore, this regulation does not require
that the hospice medical director or physician member of the hospice
interdisciplinary group designee has a face-to-face encounter with the
patient when initially certifying the patient as terminally ill.
Rather, a face-to-face encounter with a hospice physician or allowed
non-physician practitioner is not required until the third election
period and each subsequent recertification thereafter. Consequently, a
patient may never be seen by the hospice physician who is certifying
that he or she is terminally ill.
---------------------------------------------------------------------------
\11\ Michelle T. Weckmann, MD, MS, University of Iowa Hospitals
and Clinics, Iowa City, Iowa The Role of the Family Physician in the
Referral and Management of Hospice Patients. Am Fam Physician, 2008
Mar 15;77(6):807-812.
---------------------------------------------------------------------------
No visits to the patient are covered under the Medicare hospice
benefit until the individual has been certified as terminally ill, an
election statement has been signed, and a plan of care has been
established (Sec. 418.200). Therefore, any information regarding the
patient's health status from hospice staff (for example, registered
nurses) should not be the sole documentation used to support the
initial certification requirement as the patient has yet to meet the
eligibility requirement. Because Medicare hospice coverage depends on
being certified as terminally ill and requires an individual to waive
rights to Medicare payment for services for the terminal illness and
related conditions, except when provided by the designated hospice or
attending physician, the expectation is that the hospice physician
certifying terminal illness will be thorough and accountable in his
review of clinical information. As discussed in the 1983 final rule
``Medicare Program; Hospice Care'', ``written certification is the only
true assurance that the patient's condition has been assessed at or
before the time of admission to a hospice program'' (48 FR 56010). This
is important to both the hospice who will be assuming virtually all of
the care needs of the terminally ill individual and to the patient, who
must have a thorough basis for his or her decision to elect hospice
rather than continue curative care.
There are ongoing concerns that some hospice patients may be
inappropriately certified as terminally ill. Operation Restore Trust
(ORT), an anti-fraud and abuse initiative by the Department of Health
and Human Services Office of Inspector General (OIG) to identify
vulnerabilities in the Medicare program and to pursue ways to reduce
Medicare's exposure to fraud and abuse, identified several areas of
weakness in the hospice benefit, primarily in the area of hospice
eligibility. Specifically, it uncovered instances of insufficient
hospice documentation and inappropriately reported diagnoses.\4\ In
1995, in response to ORT's initial report, CMS issued program memoranda
requiring submission of clinical information and other documentation
that supports the medical prognosis. The Medicare, Medicaid, and SCHIP
Benefits Improvement and Protection Act of 2000 amended section 1814(a)
of the Social Security Act (The Act) clarifying that certification is
based on the physician or medical director's clinical judgment.
Regardless, subsequent ORT reports and CMS Regional Offices and
Regional Home Health Intermediary (now called Medicare Administrative
Contractors) reviews continued to raise concerns regarding
inappropriate certifications, specifically, certifications made for
patients who are chronically ill, but who are without complications or
other circumstances that indicate a life expectancy of 6 months or
less.\12\
---------------------------------------------------------------------------
\12\ Department of Health and Human Services: Office of the
Inspector General. Operation Restore Trust Activities by June Gibbs
Brown, IG. November 1995.
---------------------------------------------------------------------------
In response to those concerns, the ``Medicare Program; Hospice Care
Amendments'' proposed rule (67 FR 70363, November 22, 2002), which
proposed the implementation of revisions required by the Balanced
Budget Act of 1997, the Medicare, Medicaid, and SCHIP Balanced Budget
Refinement Act of 1999, and the Medicare, Medicaid, and SCHIP Benefits
Improvement and Protection Act of 2000 to the existing regulations at
the time governing coverage and payment for hospice care under the
Medicare program, proposed revisions to Sec. 418.22, Certification of
Terminal Illness, requiring that specific clinical findings and other
documentation supporting the medical prognosis accompany the written
certification and be filed in the hospice medical record. Additionally,
the 2002 rule proposed adding Sec. 418.25 Admission to Hospice Care,
which established general guidance on hospice admission procedures.
These changes acknowledged that ``the amendment regarding the
physician's clinical judgment does not negate the fact that there must
be a basis for certification'' and that ``a mere signed certification,
absent a medically sound basis that supports the clinical judgment, is
not sufficient for application of the hospice benefit under Medicare.''
Ultimately, the final rule, ``Medicare Program; Hospice Care
Amendments'' (70 FR 70532, November 22, 2005) codified the requirements
and the expectations about the clinical information needed to
[[Page 20773]]
support the certification of a medical prognosis of 6 months or less at
Sec. 418.22 (70 FR 70538). The final rule also set out the specific
admission requirements indicating that the hospice medical director
along with the patient's attending physician, if any, is responsible
for admitting the patient, and identifies what information he or she
must consider when certifying a patient as terminally ill (Sec.
418.25).
Additionally, the Medicare Payment Advisory Commission's (MedPAC)
March 2009 report entitled ``Report to the Congress: Medicare's Payment
Policy'' noted specific concerns regarding trends towards an increasing
proportion of hospice patients with stays exceeding 180 days.\13\ An
analysis of this trend by a hospice expert panel illuminated limited
medical director engagement in the certification or recertification
process as a possible cause of this utilization pattern, reviving
concerns that patients were again being inappropriately certified as
terminally ill and were not actually eligible to elect the benefit. The
panel determined that ``physicians responsible for certifying and
recertifying a patient's eligibility for hospice may inappropriately
delegate much of this responsibility to other parties.'' In response to
these concerns, we finalized a policy requiring that certifications and
recertifications include a brief narrative describing the clinical
basis for the patient's prognosis. The FY 2010 Hospice Wage Index final
rule (74 FR 39398) codified this narrative requirement for the
certification of terminal illness at Sec. 418.22(b)(3), in order to
increase accountability and add oversight to the physician
certification/recertification process
---------------------------------------------------------------------------
\13\ Medicare Payment Advisory Commission. Report to the
Congress: Medicare's Payment Policy. Washington, DC, March
2009_Accessed on March 31, 2017 at: https://www.medpac.gov/docs/default-source/reports/march-2009-report-to-congress-medicare-payment-policy.pdf?sfvrsn=0.
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In the ``Medicare Program; Hospice Wage Index and Payment Rate
Update FY 2015'' final rule (79 FR 50470), we again provided guidance
on determining beneficiaries' eligibility for hospice, reiterating that
the hospice ``is required to make certain that the physician's clinical
judgment can be supported by clinical information and other
documentation that provide a basis for the certification of a life
expectancy of 6 months or less if the illness runs its normal course.''
This discussion reinforced the importance of ensuring that hospices are
thorough in their eligibility determinations so that hospice
beneficiaries are able to access all of their Medicare benefits
appropriately and added additional oversight to the physician
certification and recertification process. The inherent challenges in
prognostication make it critical for a hospice to obtain, and the
certifying hospice medical director or hospice physician designee to
comprehensively review, the patient's clinical information when making
the determination that the patient is terminally ill, and thus eligible
for the Medicare hospice benefit. By increasing physician engagement
and accountability, patients can be assured they are making the most
informed decision possible, without limiting their treatment choices.
In the FY 2006 Hospice Wage Index final rule (70 FR 70538), we received
comments stating that it is common practice for hospices to obtain
clinical information from the referring physician, which is then
documented in the patient's hospice medical record.
Accordingly, we are soliciting comments for possible future
rulemaking, on amending the regulations at Sec. 418.25 to specify that
the referring physician's and/or the acute/post-acute care facility's
medical record would serve as the basis for initial hospice eligibility
determinations. Clinical information from the referring physician and/
or acute/post-acute care facility supporting a terminal prognosis would
be obtained by the hospice prior to election of the benefit, when
determining certification and subsequent eligibility. This potential
clarifying regulatory text change would be in alignment with benefit
eligibility criteria that the individual must be certified as
terminally ill prior to receiving hospice services, and fundamentally
could not be determined by hospice documentation obtained after
admission. We are also soliciting comments on amending the regulations
text at Sec. 418.25 to specify that documentation of an in-person
visit from the hospice Medical Director or the hospice physician member
of the interdisciplinary group could be used as documentation to
support initial hospice eligibility determinations, only if needed to
augment the clinical information from the referring physician/
facility's medical records. Comments on current processes used by
hospices to ensure comprehensive clinical review to support
certification and any alternate suggestions for supporting clinical
documentation sources are also encouraged.
D. Proposed Updates to the Hospice Quality Reporting Program (HQRP)
1. Background and Statutory Authority
Section 3004(c) of the Affordable Care Act amended section
1814(i)(5) of the Act to authorize a quality reporting program for
hospices. Section 1814(i)(5)(A)(i) of the Act requires that beginning
with FY 2014 and each subsequent FY, the Secretary shall reduce the
market basket update by 2 percentage points for any hospice that does
not comply with the quality data submission requirements for that FY.
Depending on the amount of the annual update for a particular year, a
reduction of 2 percentage points could result in the annual market
basket update being less than 0 percent for a FY and may result in
payment rates that are less than payment rates for the preceding FY.
Any reduction based on failure to comply with the reporting
requirements, as required by section 1814(i)(5)(B) of the Act, would
apply only for the particular year involved. Any such reduction would
not be cumulative or be taken into account in computing the payment
amount for subsequent FYs. Section 1814(i)(5)(C) of the Act requires
that each hospice submit data to the Secretary on quality measures
specified by the Secretary. The data must be submitted in a form,
manner, and at a time specified by the Secretary.
2. General Considerations Used for Selection of Quality Measures for
the HQRP
Any measures selected by the Secretary must be endorsed by the
consensus-based entity, which holds a contract regarding performance
measurement, including the endorsement of quality measures, with the
Secretary under section 1890(a) of the Act. This contract is currently
held by the National Quality Forum (NQF). However, section
1814(i)(5)(D)(ii) of the Act provides that in the case of a specified
area or medical topic determined appropriate by the Secretary for which
a feasible and practical measure has not been endorsed by the
consensus-based entity, the Secretary may specify measures that are not
so endorsed as long as due consideration is given to measures that have
been endorsed or adopted by a consensus-based organization identified
by the Secretary. Our paramount concern is the successful development
of a HQRP that promotes the delivery of high quality healthcare
services. We seek to adopt measures for the HQRP that promote person-
centered, high quality, and safe care. Our measure selection activities
for the HQRP take into consideration
[[Page 20774]]
input from the Measure Applications Partnership (MAP), convened by the
NQF, as part of the established CMS pre-rulemaking process required
under section 1890A of the Act. The MAP is a public-private partnership
comprised of multi-stakeholder groups convened by the NQF for the
primary purpose of providing input to CMS on the selection of certain
categories of quality and efficiency measures, as required by section
1890A(a)(3) of the Act. By February 1st of each year, the NQF must
provide that input to CMS. Input from the MAP is located at: https://www.qualityforum.org/Setting_Priorities/Partnership/Measure_Applications_Partnership.aspx. We also take into account
national priorities, such as those established by the HHS Strategic
Plan (https://www.hhs.gov/secretary/about/priorities/priorities.html),
the National Strategy for Quality Improvement in Healthcare, (https://www.ahrq.gov/workingforquality/reports/annual-reports/nqs2015annlrpt.htm) and the CMS Quality Strategy (https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/QualityInitiativesGenInfo/CMS-Quality-Strategy.html). To the extent
practicable, we have sought to adopt measures endorsed by member
organizations of the National Consensus Project (NCP) (https://www.nationalconsensusproject.org/Default.aspx), recommended by multi-
stakeholder organizations, and developed with the input of providers,
purchasers/payers, and other stakeholders.
We consider related factors that may affect measures in the HQRP.
We understand that social risk factors such as income, education, race
and ethnicity, employment, disability, community resources, and social
support (certain factors of which are also sometimes referred to as
socioeconomic status (SES) factors or socio-demographic status (SDS)
factors) play a major role in health. One of our core objectives is to
improve beneficiary outcomes including reducing health disparities, and
we want to ensure that all beneficiaries, including those with social
risk factors, receive high quality care. In addition, we seek to ensure
that the quality of care furnished by providers and suppliers is
assessed as fairly as possible under our programs while ensuring that
beneficiaries have adequate access to excellent care.
We have been reviewing reports prepared by the Office of the
Assistant Secretary for Planning and Evaluation (ASPE) \14\ and the
National Academies of Sciences, Engineering, and Medicine on the issue
of measuring and accounting for social risk factors in CMS' value-based
purchasing and quality reporting programs, and considering options on
how to address the issue in these programs. On December 21, 2016, ASPE
submitted a Report to Congress on a study it was required to conduct
under section 2(d) of the Improving Medicare Post-Acute Care
Transformation (IMPACT) Act of 2014. The study analyzed the effects of
certain social risk factors of Medicare beneficiaries on quality
measures and measures of resource use used in one or more of nine
Medicare value-based purchasing programs.\15\ The report also included
considerations for strategies to account for social risk factors in
these programs. In a January 10, 2017 report released by The National
Academies of Sciences, Engineering, and Medicine, that body provided
various potential methods for measuring and accounting for social risk
factors, including stratified public reporting.\16\
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\14\ https://aspe.hhs.gov/pdf-report/report-congress-social-risk-factors-and-performance-under-medicares-value-based-purchasing-programs.
\15\ https://aspe.hhs.gov/pdf-report/report-congress-social-risk-factors-and-performance-under-medicares-value-based-purchasing-programs.
\16\ National Academies of Sciences, Engineering, and Medicine.
2017. Accounting for social risk factors in Medicare payment.
Washington, DC: The National Academies Press.
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In addition, the NQF has undertaken a 2-year trial period in which
new measures, measures undergoing maintenance review, and measures
endorsed with the condition that they enter the trial period can be
assessed to determine whether risk adjustment for selected social risk
factors is appropriate for these measures. This trial entails
temporarily allowing inclusion of social risk factors in the risk-
adjustment approach for these measures. At the conclusion of the trial,
NQF will issue recommendations on the future inclusion of social risk
factors in risk adjustment for quality measures.
As we continue to consider the analyses and recommendations from
these reports and await the results of the NQF trial on risk adjustment
for quality measures, we are continuing to work with stakeholders in
this process. As we have previously communicated, we are concerned
about holding providers to different standards for the outcomes of
their patients with social risk factors because we do not want to mask
potential disparities or minimize incentives to improve the outcomes
for disadvantaged populations. Keeping this concern in mind, while we
sought input on this topic previously, we continue to seek public
comment on whether we should account for social risk factors in
measures in the HQRP, and if so, what method or combination of methods
would be most appropriate for accounting for social risk factors.
Examples of methods include: Confidential reporting to providers of
measure rates stratified by social risk factors, public reporting of
stratified measure rates, and potential risk adjustment of a particular
measure as appropriate based on data and evidence.
In addition, we are also seeking public comment on which social
risk factors might be most appropriate for reporting stratified measure
scores and/or potential risk adjustment of a particular measure.
Examples of social risk factors include, but are not limited to, dual
eligibility/low-income subsidy, race and ethnicity, and geographic area
of residence. We are seeking comments on which of these factors,
including current data sources where this information would be
available, could be used alone or in combination, and whether other
data should be collected to better capture the effects of social risk.
We will take commenters' input into consideration as we continue to
assess the appropriateness and feasibility of accounting for social
risk factors in the HQRP. We note that any such changes would be
proposed through future notice and comment rulemaking.
We look forward to working with stakeholders as we consider the
issue of accounting for social risk factors and reducing health
disparities in our programs. Of note, implementing any of the above
methods would be taken into consideration in the context of how this
and our other programs operate (for example, data submission methods,
availability of data, statistical considerations relating to
reliability of data calculations, among others), so we also welcome
comment on operational considerations. We are committed to ensuring
that its beneficiaries have access to and receive excellent care, and
that the quality of care furnished by providers and suppliers is
assessed fairly in our programs.
3. Policy for Retention of HQRP Measures Adopted for Previous Payment
Determinations
For the purpose of streamlining the rulemaking process, we
finalized our policy in the FY 2016 Hospice Wage Index final rule (80
FR 47187) that when we adopt measures for the HQRP beginning with a
payment determination year, these measures
[[Page 20775]]
would automatically be adopted for all subsequent years' payment
determinations, unless we proposed to remove, suspend, or replace the
measures. Quality measures would be considered for removal by us for
reasons including, but not limited to:
Measure performance among hospices was so high and
unvarying that meaningful distinction in improvements in performance
could no longer be made;
Performance or improvement on a measure did not result in
better patient outcomes;
A measure did not align with current clinical guidelines
or practice;
A more broadly applicable measure (across settings,
populations, or conditions) for the particular topic was available;
A measure that was more proximal in time to desired
patient outcomes for the particular topic was available;
A measure that was more strongly associated with desired
patient outcomes for the particular topic was available; or
Collection or public reporting of a measure led to
negative unintended consequences.
For any such removal, the public would be given an opportunity to
comment through the annual rulemaking process. However, if there was
reason to believe continued inclusion of a measure in the HQRP would
encourage delivery of care that raised potential safety concerns, we
would take immediate action to remove the measure from the HQRP and not
wait for the annual rulemaking cycle. The measures would be promptly
removed and we would immediately notify hospices and the public of such
a decision through the CMS HQRP Web site, listserv messages via the
Post-Acute Care QRP listserv,\17\ MLN Connects[supreg] National
Provider Calls & Events, MLN Connects[supreg] Provider eNews. Following
immediate removal of the measures, we would also notify the public of
any such removal in the next annual rulemaking cycle. CMS expects
immediate removal of a measure due to safety concerns to be an unlikely
event, given the rigorous testing and analysis all measures undergo
prior to adoption in the HQRP.
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\17\ CMS, Post-Acute Care QRP listerv, available at: https://public-dc2.govdelivery.com/accounts/USCMS/subscriber/new?topic_id=USCMS_12265.
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4. Policy for Adopting Changes to Previously Adopted Measures
To further streamline the rulemaking process, we finalized in the
FY 2017 Hospice Wage Index final rule that if measures in the HQRP
undergo non-substantive changes in specifications as part of their NQF
re-endorsement process, we would subsequently utilize the measure with
their new endorsed status in the HQRP without going through new notice-
and-comment rulemaking (81 FR 52159). As mentioned previously, quality
measures selected for the HQRP must be endorsed by the NQF unless they
meet the statutory criteria for exception under section
1814(i)(5)(D)(ii) of the Act. The NQF is a voluntary consensus
standard-setting organization with a diverse representation of
consumer, purchaser, provider, academic, clinical, and other healthcare
stakeholder organizations. The NQF was established to standardize
healthcare quality measurement and reporting through its consensus
measure development process (https://www.qualityforum.org/About_NQF/Mission_and_Vision.aspx). The NQF undertakes review of: (a) New quality
measures and national consensus standards for measuring and publicly
reporting on performance, (b) regular maintenance processes for
endorsed quality measures, (c) measures with time-limited endorsement
for consideration of full endorsement, and (d) ad hoc review of
endorsed quality measures, practices, consensus standards, or events
with adequate justification to substantiate the review. Through NQF's
or the measure steward's measure maintenance process, measures are
sometimes updated to incorporate changes that we believe do not
substantively change the intent of the measure. Examples of such
changes may include updated diagnosis or procedure codes or changes to
exclusions to the patient population or definitions. While we address
such changes on a case-by case basis, we generally believe these types
of maintenance changes are distinct from substantive changes to
measures that result in what are considered new or different measures.
Additionally, since the NQF endorsement and measure maintenance process
is one that ensures transparency, public input, and discussion among
representatives across the healthcare enterprise,\18\ we believe that
the NQF measure endorsement and maintenance process itself is
transparent, scientifically rigorous, and provides opportunity for
public input. Thus, we finalized our proposal to codify at Sec.
418.312 that if the NQF makes only non-substantive changes to
specifications for HQRP measures in the NQF's re-endorsement process,
we would continue to utilize the measure in its new endorsed status (81
FR 52159 through 52160). If NQF-endorsed specifications change and we
do not adopt those changes, then we would propose the measure as a
modification. A modification of a NQF-endorsed quality measure is
utilized in instances when we have identified a need to use a NQF-
endorsed measure in a QRP but need to use it with one or more
modifications to the quality measure's specifications. These
modifications pertain to, but are not limited to, one or more of the
following aspects of a NQF-endorsed quality measure: (a) Numerator, (b)
denominator, (c) setting, (d) look-back period, (e) calculation period,
(f) risk adjustment, and (g) revisions to data elements used to collect
the data required for the measure, etc. CMS may adopt a quality measure
for the HQRP under section 1814(i)(5)(D)(ii) of the Act, which states,
``[i]n the case of a specified area or medical topic determined
appropriate by the Secretary for which a feasible and practical measure
has not been endorsed by [the NQF], the Secretary may specify a measure
that is not so endorsed as long as due consideration is given to
measures that have been endorsed or adopted by a consensus organization
identified by the Secretary.'' Reasons for not adopting changes in
measure specifications to a measure may include any of the
aforementioned criteria in the prior section, including that the new
specification does not align with clinical guidelines or practice or
that the new specification leads to negative unintended consequences.
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\18\ [thinsp]``NQF: How Endorsement Happens--National Quality
Forum.'' 2010. 26 Jan. 2016 https://www.qualityforum.org/Measuring_Performance/ABCs/How_Endorsement_Happens.aspx.
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Finally, we will continue to use rulemaking to adopt substantive
updates made by the NQF to the endorsed measures we have adopted for
the HQRP. We continue to make these determinations about what
constitutes a substantive versus non-substantive change on a measure-
by-measure basis. A change would be deemed substantive if the intent of
the measure changes, the facility/setting changes, the data sources
changes, the level of analysis changes, and/or the measure is removed.
We will continue to provide updates about changes to measure
specifications as a result of NQF endorsement or maintenance processes
through the CMS HQRP Web site, listserv messages on the Post-Acute Care
QRP listserv, MLN Connects[supreg] National Provider Calls & Events,
MLN Connects[supreg] Provider eNews and announcements on Open Door
Forums and Special Open Door Forums.
[[Page 20776]]
5. Previously Adopted Quality Measures for FY 2018 Payment
Determination and Future Years
In the FY 2014 Hospice Wage Index final rule (78 FR 48257), and in
compliance with section 1814(i)(5)(C) of the Act, we finalized the
specific collection of data items that support the following 7 NQF-
endorsed measures for hospice:
NQF #1617 Patients Treated with an Opioid who are Given a
Bowel Regimen,
NQF #1634 Pain Screening,
NQF #1637 Pain Assessment,
NQF #1638 Dyspnea Treatment,
NQF #1639 Dyspnea Screening,
NQF #1641 Treatment Preferences,
NQF #1647 Beliefs/Values Addressed (if desired by the
patient).\19\
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\19\ Previously finalized as a ``modified measure'' in the FY17
and prior rules (81 FR 52160). Following NQF maintenance
endorsement, NQF #1647 measure specifications where updated and now
aligns with the measure data lookback period for this program.
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We finalized the following two additional measures in the FY 2017
Hospice Wage Index final rule effective April 1, 2017. Data collected
will, if not reported, affect payments for FY 2019 and subsequent
years. (81 FR 52163 through 52173):
Hospice Visits when Death is Imminent
Hospice and Palliative Care Composite Process Measure--
Comprehensive Assessment at Admission
We finalized the HIS effective July 1, 2014 (78 FR 48258). The HIS
is the data collection mechanism for all of the aforementioned
measures. To meet the quality reporting requirements for hospices for
the FY 2016 payment determination and each subsequent year, we require
regular and ongoing electronic submission of the HIS data for each
patient admission to hospice after July 1, 2014, regardless of payer or
patient age (78 FR 48234 through 48258). For the two measures finalized
in the FY 2017 Hospice Wage Index final rule, we require regular and
ongoing electronic submission for each patient admission to hospice
after April 1, 2017. We finalized a requirement in the FY 2014 Hospice
Wage Index final rule (78 FR 48258) that hospice providers collect data
on all patients to ensure that all patients regardless of payer or
patient age are receiving the same care and that provider metrics
measure performance across the spectrum of patients. Table 16 below
provides a summary of measures previously finalized affecting the FY
2019 APU, data collection mechanism, and data submission deadline.
Hospices are required to complete and submit a HIS-Admission and a
HIS-Discharge record for each patient admission. Hospices failing to
report quality data via the HIS for patient admissions occurring in
2017 will have their market basket update reduced by 2 percentage
points in FY 2019 (beginning in October 1, 2018). In the FY 2015
Hospice Wage Index final rule (79 FR 50485 through 50487), we finalized
the proposal to codify the HIS submission requirement at Sec. 418.312.
The System of Record (SOR) Notice titled ``Hospice Item Set (HIS)
System,'' SOR number 09-70-0548, was published in the Federal Register
on April 8, 2014 (79 FR 19341).
The 7 NQF endorsed HIS measures adopted in FY 2014 Hospice Wage
Index final rule successfully underwent NQF Endorsement Maintenance in
2016.\20\ We recognize that the NQF endorsement process is an important
part of measure development and plan to submit the two measures
finalized in the FY 2017 Hospice Wage Index final rule for NQF
endorsement once sufficient measure data are available and we conduct
the analyses necessary to support NQF submission for endorsement (for
example, reliability and validity analyses). Typically, we need at
least 4 quarters worth of data to conduct the necessary analyses and
establish measure reliability and validity. Because the Hospice and
Palliative Care Composite Process Measure--Comprehensive Assessment at
Admission did not require any new data collection and can be calculated
using existing data, CMS's measure development contractor, RTI
International, has already conducted the analyses necessary to support
submission of the measure for NQF endorsement. We have already
submitted the Hospice and Palliative Care Composite Process Measure for
consideration for endorsement at NQF (NQF #3235); the measure is
currently under review. Data for the Hospice Visits when Death is
Imminent measure pair will be collected using new items added to the
HIS V2.00.0, effective April 1, 2017. Once data collection for the
measure pair begins, we will need at least 4 quarters of reliable data
to conduct the necessary analyses to support submission to NQF. We will
also need to assess the quality of data submitted in the first quarter
of item implementation to determine whether they can be used in the
analyses. Pending analysis, we will submit the Hospice Visits when
Death is Imminent measure pair to NQF for endorsement review in
accordance with NQF project timelines and call for measures. In the FY
2015 Hospice Wage Index final rule (79 FR 50491 through 50496), we also
finalized the Consumer Assessment of Healthcare Providers and Systems
(CAHPS[supreg]) Hospice Survey to support quality measures based on
patient and family experience of care. We refer readers to section
III.D.11 of this notice of proposed rulemaking for details regarding
the CAHPS[supreg] Hospice Survey, including public reporting of
selected survey measures.
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\20\ National Quality Forum, NQF Palliative and End-of-Life Care
2015-2016 Report, available at: https://www.qualityforum.org/WorkArea/linkit.aspx?LinkIdentifier=id&ItemID=84242.
Table 16--Previously Finalized Quality Measures Affecting the FY 2019 Payment Determination and Subsequent Years
----------------------------------------------------------------------------------------------------------------
Payment determination
(APU) year for which Data collection Data submission
NQF No. Measure name the quality measure mechanism deadline
was first adopted
----------------------------------------------------------------------------------------------------------------
1641............. Treatment Preferences. FY 2016............... Hospice Item Set...... Rolling--within 30
days of patient
admission or
discharge (event
date).
1647............. Beliefs/Values FY 2016...............
Addressed (if desired
by the patient).
1634............. Pain Screening........ FY 2016...............
1637............. Pain Assessment....... FY 2016...............
[[Page 20777]]
1639............. Dyspnea Screening..... FY 2016...............
1638............. Dyspnea Treatment..... FY 2016...............
1617............. Patients Treated with FY 2016...............
an Opioid Who Are
Given a Bowel Regimen.
N/A.............. Hospice and Palliative FY 2019............... ...................... Rolling--within 30
Care Composite days of patient
Process Measure-- admission or
Comprehensive discharge (event
Assessment at date) for patient
Admission. admissions to
hospice on 04/01/
2017 and onward.
N/A.............. Hospice Visits When FY 2019...............
Death is Imminent
Measure Pair.
----------------------------------------------------------------------------------------------------------------
6. Proposed Removal of Previously Adopted Measures
We are not proposing to remove any of the current HQRP measures at
this time. Any future proposals regarding removal, suspension, or
replacement of measures will be proposed in this section of future
rules. As stated in section III.D.3, a quality measure that is adopted
and implemented in the HQRP will be retained for all subsequent years,
unless the measure is proposed for removal, suspension, or replacement
by CMS. Policies and criteria for removing a measure include those
identified in section III.D.3 of this proposed rule.
7. Measure Concepts Under Consideration for Future Years
Although we are not proposing any HIS-based measures in this
proposed rule, we have measure concepts under consideration for future
years.
Our paramount concern is to develop quality measures that promote
care that is person-centered, high quality, and safe. We continue to
work with our measure development contractor, RTI International, to
identify measure concepts for future implementation in the HQRP. In
identifying priority areas for future measure enhancement and
development, we take into consideration input from numerous
stakeholders, including the MAP, the MedPAC, Technical Expert Panels
(TEP), and national priorities, such as those established by the HHS
Strategic Plan, the National Strategy for Quality Improvement in
Healthcare, and the CMS Quality Strategy. In addition, we take into
consideration vital feedback and input from research published by our
payment reform contractor. The current HQRP measure set is also an
important consideration for future measure development areas; future
measure development areas should complement the current HQRP measure
set, including current HIS measures and CAHPS[supreg] Hospice Survey
measures, without creating unnecessary burden or redundant reporting.
Based on input from stakeholders, we identified two high priority areas
that will be addressed by claims-based measure development. Developing
quality measures using claims does not require new data collection,
thus minimizing provider burden and expediting implementation.
Priority Area 1: Potentially Avoidable Hospice Care
Transitions
The concept of a claims-based measure focusing on transitions of
care was first introduced in the FY 2016 Hospice Wage Index final rule
(80 FR 47188 through 47189). Comments received during this rule were
overall supportive of our efforts to develop more robust quality
measures that capture hospice performance and show links to patient and
family outcomes. We refer readers to the FY 2016 Hospice Wage Index
final rule (80 FR 47188 through 47189) for additional detail: https://www.gpo.gov/fdsys/pkg/FR-2015-08-06/pdf/2015-19033.pdf.
Potentially avoidable hospice care transitions at end of life are
burdensome to patients, families, and the health care system at large,
because they are associated with adverse health outcomes, lower patient
and family satisfaction, higher health care costs, and fragmentation of
care delivery.21 22 23 24 25 By encouraging hospice
providers to assess and manage patients' risk of care transitions, this
measure concept has the potential to improve quality care at the end of
life by reducing potentially avoidable hospice care transitions.
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\21\ Aldridge MDP, MBA; Epstein, Andrew J. Ph.D.; Brody, Abraham
A. RN, Ph.D.; Lee, Eric J. MPH; Cherlin, Emily Ph.D., MSW; Bradley,
Elizabeth H. Ph.D. The Impact of Reported Hospice Preferred
Practices on Hospital Utilization at the End of Life Medical Care.
2016;54(7):657-663.
\22\ Wang S-Y, Aldridge MD, Gross CP, et al. Transitions Between
Healthcare Settings of Hospice Enrollees at the End of Life. Journal
of the American Geriatrics Society. 2016;64(2):314-322.
\23\ Carlson MDA, Herrin J, Du Q, et al. Impact of Hospice
Disenrollment on Health Care Use and Medicare Expenditures for
Patients With Cancer. Journal of Clinical Oncology.
2010;28(28):4371-4375.
\24\ Teno JM, Bowman J, Plotzke M, et al. Characteristics of
Hospice Programs With Problematic Live Discharges. Journal of Pain
and Symptom Management. 2015;50(4):548-552.
\25\ Prsic E, Plotzke M, Christian TJ, Gozalo P, Teno JM. A
National Study of Live Hospice Discharges between 2000 and 2012.
Journal of Palliative Medicine. 2016;19(9):987-990.
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Priority Area 2: Access to Levels of Hospice Care
The Medicare Hospice Benefit covers four levels of care to meet
patients' and families' clinical needs: Routine home care (RHC),
continuous home care (CHC), general inpatient care (GIP), and inpatient
respite care. The goal of this measure concept is to assess the rates
at which hospices provide different levels of hospice care. The measure
has the potential to improve access to various levels of care for
patients and caregivers. Appropriate use of CHC and GIP increases the
likelihood of a hospice patient dying in his or her location of choice,
decreases health resource utilization resulting in potential cost
savings, and increases patient and caregiver
satisfaction.26 27 Measuring use of levels of care will
incentivize hospice providers to continuously assess patient
[[Page 20778]]
and caregiver needs and provide the appropriate level of care to meet
these needs.
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\26\ Barclay, J., et al., Association of hospice patients'
income and care level with place of death. JAMA Internal Medicine,
2013. 173(6): p. 450-456.
\27\ Casarett, D., et al., Does Continuous Hospice Care Help
Patients Remain at Home? Journal of Pain and Symptom Management,
2015. 50(3): p. 297-304.
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These two measure concepts are under development, and details
regarding measure definitions, specifications and timeline for
implementation will be communicated in future rulemaking. We are
soliciting comments regarding high priority concept areas for future
measure development.
8. Form, Manner, and Timing of Quality Data Submission
a. Background
Section 1814(i)(5)(C) of the Act requires that each hospice submit
data to the Secretary on quality measures specified by the Secretary.
Such data must be submitted in a form and manner, and at a time
specified by the Secretary. Section 1814(i)(5)(A)(i) of the Act
requires that beginning with the FY 2014 and for each subsequent FY,
the Secretary shall reduce the market basket update by 2 percentage
points for any hospice that does not comply with the quality data
submission requirements for that FY.
b. Policy for New Facilities To Begin Submitting Quality Data
In the FY 2015 Hospice Wage Index final rule (79 FR 50488), we
finalized a policy stating that any hospice that receives its CMS
Certification Number (CCN) (also known as the Medicare Provider Number)
notification letter dated on or after November 1 of the preceding year
involved is excluded from any payment penalty for quality reporting
purposes for the following FY. This requirement was codified at Sec.
418.312.
In the FY 2016 Hospice Wage Index final rule (80 FR 47189), we
further clarified and finalized our policy for the timing of new
providers to begin reporting data to CMS. The clarified policy
finalized in the FY 2016 Hospice Wage Index final rule (80 FR 47189)
distinguished between when new hospice providers are required to begin
submitting HIS data and when providers will be subject to the potential
2 percentage point annual payment update (APU) reduction for failure to
comply with HQRP requirements. In summary, the policy finalized in the
FY 2016 Hospice Wage Index final rule (80 FR 47189 through 47190)
clarified that providers must begin submitting HIS data on the date
listed in the letterhead of the CCN Notification letter received from
CMS but will be subject to the APU reduction based on whether the CCN
Notification letter was dated before or after November 1 of the
reporting year involved. Thus, beginning with the FY 2018 payment
determination and for each subsequent payment determination, we
finalized our policy that a new hospice be responsible for HQRP quality
data submission beginning on the date of the CCN notification letter;
we retained our prior policy that hospices not be subject to the APU
reduction if the CCN notification letter was dated after November 1 of
the year involved. For example, if a provider receives their CCN
notification letter and the date in the letterhead is November 5, 2017,
that provider will begin submitting HIS data for patient admissions
occurring after November 5, 2017. However, since the CCN notification
letter was dated after November 1st, they would not be evaluated for,
or subject to any payment penalties for, the relevant FY APU update
(which in this instance is the FY 2019 APU, which is associated with
patient admissions occurring January 1, 2017 through December 31,
2017).
This policy allows us to receive HIS data on all patient admissions
on or after the date a hospice receives their CCN notification letter,
while at the same time allowing hospices flexibility and time to
establish the necessary accounts for data submission before they are
subject to the potential APU reduction for a given reporting year.
Currently, new hospices may experience a lag between Medicare
certification and receipt of their actual CCN Number. Since hospices
cannot submit data to the QIES ASAP system without a valid CCN Number,
we finalized that new hospices begin collecting HIS quality data
beginning on the date noted on the CCN notification letter. We believe
this policy provides sufficient time for new hospices to establish
appropriate collection and reporting mechanisms to submit the required
quality data to CMS. Requiring quality data reporting beginning on the
date listed in the letterhead of the CCN notification letter aligns our
policy requirements for new providers with the functionality of the HIS
data submission system (QIES ASAP).
c. Previously Finalized Data Submission Mechanisms, Timelines, and
Deadlines
In the FY 2015 Hospice Wage Index final rule (79 FR 50486), we
finalized our policy requiring that hospices complete and submit HIS
records for all patient admissions to hospice after July 1, 2014. For
each HQRP program year, we require that hospices submit data on each of
the adopted measures in accordance with the reporting requirements
specified in sections III.C.9.b through III.C.9.c of the FY 2015 rule
for the designated reporting period. This requirement applies to
previously finalized and adopted measures, as well as new measures
proposed through the rulemaking process. Electronic submission is
required for all HIS records. Although electronic submission of HIS
records is required, hospices do not need to have an electronic medical
record to complete or submit HIS data. In the FY 2014 Hospice Wage
Index final rule (78 FR 48258), we finalized a provision requiring that
providers use either the Hospice Abstraction Reporting Tool (HART)
(which is free to download and use) or vendor-designed software to
complete HIS records. HART provides an alternative option for hospice
providers to collect and maintain facility, patient, and HIS Record
information for subsequent submission to the QIES ASAP system. Once HIS
records are complete, electronic HIS files must be submitted to CMS via
the QIES ASAP system. Electronic data submission via the QIES ASAP
system is required for all HIS submissions; there are no other data
submission methods available. Hospices have 30 days from a patient
admission or discharge to submit the appropriate HIS record for that
patient through the QIES ASAP system. We will continue to make HIS
completion and submission software available to hospices at no cost. We
provided details on data collection and submission timing under the
downloads section of the HIS Web page on the CMS.gov Web site at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Hospice-Quality-Reporting/Hospice-Item-Set-HIS.html.
The QIES ASAP system provides reports upon successful submission
and processing of the HIS records. The final validation report may
serve as evidence of submission. This is the same data submission
system used by nursing homes, inpatient rehabilitation facilities, home
health agencies, and long-term care hospitals for the submission of
Minimum Data Set Version 3.0 (MDS 3.0), Inpatient Rehabilitation
Facility-patient assessment instrument (IRF-PAI), Outcome Assessment
Information Set (OASIS), and Long-Term Care Hospital Continuity
Assessment Record & Evaluation Data Set (LTCH CARE), respectively. We
have provided hospices with information and details about use of the
HIS through postings on the HQRP Web site, Open Door Forums,
announcements in the CMS MLN Connects[supreg] Provider e-News (E-News),
and provider training.
[[Page 20779]]
Hospices are evaluated for purposes of the quality reporting
program based on whether or not they submit data, not on their
substantive performance level for the required quality measures. In
order for us to appropriately evaluate the quality reporting data
received by hospice providers, it is essential HIS data be received in
a timely manner.
The submission date is the date on which the completed record is
submitted and accepted by the QIES ASAP system. In the FY 2016 Hospice
Wage Index final rule (80 FR 47191), we finalized our policy that
beginning with the FY 2018 payment determination, hospices must submit
all HIS records within 30 days of the event date, which is the
patient's admission date for HIS-Admission records or discharge date
for HIS-Discharge records.
For HIS-Admission records, the submission date must be no later
than the admission date plus 30 calendar days. The submission date can
be equal to the admission date, or no greater than 30 days later. The
QIES ASAP system will issue a warning on the Final Validation Report if
the submission date is more than 30 days after the patient's admission
date.
For HIS-Discharge records, the submission date must be no later
than the discharge date plus 30 calendar days. The submission date can
be equal to the discharge date, or no greater than 30 days later. The
QIES ASAP system will issue a warning on the Final Validation Report if
the submission date is more than 30 days after the patient's discharge
date.
The QIES ASAP system validation edits are designed to monitor the
timeliness of submission and ensure that providers' submitted records
conform to the HIS data submission specifications. Providers are
notified when timing criteria have not been met by warnings that appear
on their Final Validation Reports. A standardized data collection
approach that coincides with timely submission of data is essential to
establish a robust quality reporting program and ensure the scientific
reliability of the data received. In the FY 2016 Hospice Wage Index
final rule (80 FR 47191), we also clarified the difference between the
completion deadlines and the submission deadlines. Current sub-
regulatory guidance produced by CMS (for example, HIS Manual, HIS
trainings) states that the completion deadlines for HIS records are 14
days after the Event Date for HIS-Admission records and 7 days after
the Event Date for HIS-Discharge records. Completion deadlines continue
to reflect CMS guidance only; these guidelines are not statutorily
specified and are not designated through regulation. These guidelines
are intended to offer clear direction to hospice agencies in regards to
the timely completion of HIS-Admission and HIS-Discharge records. The
completion deadlines define only the latest possible date on which a
hospice should complete each HIS record. This guidance is meant to
better align HIS completion processes with clinical workflow processes;
however, hospices may develop alternative internal policies to complete
HIS records. Although it is at the discretion of the hospice to develop
internal policies for completing HIS records, we will continue to
recommend that providers complete and attempt to submit HIS records
early, prior to the previously finalized submission deadline of 30
days, beginning in FY 2018. Completing and attempting to submit records
early allows providers ample time to address any technical issues
encountered in the QIES ASAP submission process, such as correcting
fatal error messages. Completing and attempting to submit records early
will ensure that providers are able to comply with the 30 day
submission deadline. HQRP guidance documents, including the CMS HQRP
Web site, HIS Manual, HIS trainings, Frequently Asked Questions, and
Fact Sheets, continue to offer the most up-to-date CMS guidance to
assist providers in the successful completion and submission of HIS
records. Availability of updated guidance will be communicated to
providers through the CMS HQRP Web site, listserv messages via the
Post-Acute Care QRP listserv, MLN Connects[supreg] National Provider
Calls & Events, MLN Connects[supreg] Provider eNews and announcements
on Open Door Forums and Special Open Door Forums.
d. New Data Collection and Submission Mechanisms Under Consideration:
Hospice Evaluation & Assessment Reporting Tool (HEART)
We have made great progress in implementing the objectives set
forth in the quality reporting and data collection activities required
by sections 3004 of the Affordable Care Act. To date, we have
established the HQRP, which includes clinical quality measures from the
HIS and patient experience of care measures from the CAHPS[supreg]
Hospice Survey. We have also finalized payment reform measures,
including changes to the RHC payment rate and the implementation of a
Service Intensity Add-On (SIA) payment, effective January 1st, 2016.
As discussed in the FY 2017 final rule (81 FR 52177), to facilitate
continued progress towards the requirements set forth in section 3004
of the Affordable Care Act, we are in the early stages of the
development of a new data collection mechanism for use by hospices.
This new data collection mechanism would be a hospice patient
assessment tool, which would serve two primary objectives concordant
with the Affordable Care Act legislation: (1) To provide the quality
data necessary for HQRP requirements and the current function of the
HIS; and (2) provide additional clinical data that could inform future
payment refinements. In the FY 2017 final rule (81 FR 52176 through
52179), we solicited input from the public on the development of a
hospice patient assessment tool that would collect quality, clinical,
and other data with the ability to be used to inform future payment
refinement efforts. Overall, feedback from the public was supportive of
the move towards a standardized patient assessment instrument, and
commenters offered some guiding principles for CMS to keep in mind in
the development of a patient assessment tool, given the unique nature
of hospice care. For a detailed discussion of the public comments and
responses, as well as CMS's guiding principles and motivation behind
the development of a hospice patient assessment tool, we refer readers
to the FY 2017 final rule (81 FR 52177 through 52179).
As noted in the FY 2017 final rule, we envision the hospice patient
assessment tool itself as an expanded HIS. The hospice patient
assessment tool would include current HIS items, as well as additional
clinical items that could also be used for payment refinement purposes
or to develop new quality measures. The hospice patient assessment tool
would not replace existing requirements set forth in the Medicare
Hospice CoPs (such as the initial and comprehensive assessment), but
would be designed to complement data that are collected as part of
high-quality clinical care. The new data collection effort would
replace the current HIS, but would not replace other HQRP data
collection efforts (that is, the CAHPS[supreg] Hospice Survey), nor
would it replace regular submission of claims data. We envision that
patient assessment data would be collected upon a patient's admission
to and discharge from any Medicare-certified hospice provider;
additional interim data collection efforts are also possible.
We are not proposing a hospice patient assessment tool at this
time; we are still in the early stages of development of an assessment
tool to determine the appropriate content and
[[Page 20780]]
feasibility of such a tool. As such, we have made progress over the
past year in the development of a hospice patient assessment tool,
preliminarily called the Hospice Evaluation & Assessment Reporting Tool
(HEART). CMS's measure development contractor, RTI International, has
begun preliminary HEART development activities, including: Conducting
environmental scans and engaging clinical experts to determine which
domains of care are important to capture in a hospice patient
assessment; posting a national provider call and forming a Clinical
Committee comprised of hospice organizations from across the U.S. to
participate in the early development of an assessment; and
collaborating within CMS to assess various stakeholder needs and
encourage collaboration within CMS and across other HHS agencies. As we
move forward with the development of the HEART patient assessment tool,
we will continue to keep the public informed of our progress and
solicit input as we establish and finalize domains of care to include
in the assessment, and as we move towards specific item wording and
development. Once we move past the preliminary phases of development
and conceptualization, we will communicate a timeline for the HEART
development, testing, and implementation in future rulemaking cycles.
As mentioned in the FY 2017 final rule, it is important for CMS to
develop a hospice patient assessment tool that is scientifically
rigorous and clinically appropriate for the hospice population, thus we
believe that continued and transparent involvement of stakeholders is
critical. We will continue to receive stakeholder input from MedPAC and
ongoing input from the provider community, Medicare beneficiaries, and
technical experts. Additionally, it is important for CMS to minimize
data collection burden on providers; in the development of HEART. We
will ensure that hospice patient assessment data items are not
duplicative or overly burdensome to providers, patients, caregivers, or
their families. We will also work with the public and other
stakeholders to ensure that HEART takes into account the unique aspects
of hospice care delivery including symptom burden and psychosocial
needs, patient and family preferences, care of imminently dying
patients, and the complexity of providing hospice care in multiple
settings and at multiple intensity levels.
9. Previously Adopted APU Determination and Compliance Criteria for the
HQRP
a. Background
The HQRP is currently designed as a ``pay-for-reporting'' system,
meaning that it is the act of submitting data that determines
compliance with HQRP requirements. Performance level is not a
consideration when determining market basket updates/APU. Reporting
compliance is determined by successfully fulfilling both the Hospice
CAHPS[supreg] Survey requirements and the HIS data submission
requirements.
b. Previously Finalized HIS Data Submission Timelines and Compliance
Thresholds for FY 2018 Payment Determination and Subsequent Years
To accurately analyze quality reporting data received by hospice
providers, it is imperative we receive ongoing and timely submission of
all HIS-Admission and HIS-Discharge records. In the FY 2016 Hospice
Wage Index final rule (80 FR 47192), we finalized the timeliness
criteria for submission of HIS-Admission and HIS-Discharge records. The
finalized timeliness criteria were in response to input from our
stakeholders seeking additional specificity related to HQRP compliance
affecting FY payment determinations and, due to the importance of
ensuring the integrity of quality data submitted.
As stated in that rule, beginning with the FY 2018 payment
determination and subsequent FY payment determinations, all HIS records
would have to be submitted within 30 days of the event date, which is
the patient's admission date or discharge date.
In conjunction with the timeliness criteria for submission of HIS-
Admission and HIS-Discharge records, in the FY 2016 Hospice Wage Index
final rule (80 FR 47192) we also finalized a policy to establish an
incremental threshold for compliance over a 3-year period. To be
compliant for the FY 2018 APU determination, hospices must submit no
less than 70 percent of their total number of HIS-Admission and HIS-
Discharge records by no later than 30 days from the event date. The
timeliness threshold is set at 80 percent for the FY 2019 APU
determination and at 90 percent for the FY 2020 APU determination and
subsequent years. The threshold corresponds with the overall amount of
HIS records received from each provider that fall within the
established 30 day submission timeframes. Our ultimate goal is to
require all hospices to achieve a compliance rate of 90 percent or
more.
To summarize, in the FY 2016 Hospice Wage Index final rule (80 FR
47193), we finalized our policy to implement the timeliness threshold
requirement beginning with all HIS-Admission and HIS-Discharge records
that occur after January 1, 2016, in accordance with the following
schedule:
Beginning January 1, 2016 to December 31, 2016, hospices
must submit at least 70 percent of all required HIS records within the
30 day submission timeframe for the year or be subject to a 2
percentage point reduction to their market basket update for FY 2018.
Beginning January 1, 2017 to December 31, 2017, hospices
must submit at least 80 percent of all required HIS records within the
30 day submission timeframe for the year or be subject to a 2
percentage point reduction to their market basket update for FY 2019.
Beginning January 1, 2018 to December 31, 2018, hospices
must submit at least 90 percent of all required HIS records within the
30 day submission timeframe for the year or be subject to a 2
percentage point reduction to their market basket update for FY 2020.
In July of 2016, we released the Hospice Timeliness Compliance
Threshold Report in the Certification and Survey Provider Enhanced
Reports (CASPER) system. This report allows providers with a QIES ASAP
User ID to check their preliminary compliance with the 70/80/90
timeliness compliance threshold described above. For more information
on the Hospice Timeliness Compliance Threshold Report, we refer readers
to the Timeliness Compliance Threshold Fact Sheet, available on the HIS
portion of the CMS HQRP Web site: https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Hospice-Quality-Reporting/Hospice-Item-Set-HIS.html and Chapter 3 of the CASPER User's Manual,
available on the QTSO Web site: https://www.qtso.com/hospicetrain.html.
In the FY 2016 Hospice Wage Index final rule (80 FR 47192 through
47193), we provided clarification regarding the methodology used in
calculating the 70 percent/80 percent/90 percent compliance thresholds.
In general, HIS records submitted for patient admissions and discharges
occurring during the reporting period (January 1st to December 31st of
the reporting year involved) will be included in the denominator for
the compliance threshold calculation. The numerator of the compliance
threshold calculation would include any records from the
[[Page 20781]]
denominator that were submitted within the 30 day submission deadline.
In the FY 2016 Hospice Wage Index final rule (80 FR 47192), we also
stated that we would make allowances in the calculation methodology for
two circumstances. First, the calculation methodology will be adjusted
following the applicable reporting period for records for which a
hospice is granted an extension or exemption by CMS. Second,
adjustments will be made for instances of modification/inactivation
requests (Item A0050. Type of Record = 2 or 3). Additional helpful
resources regarding the timeliness compliance threshold for HIS
submissions can be found under the downloads section of the HIS Web
page at CMS.gov at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Hospice-Quality-Reporting/Hospice-Item-Set-HIS.html. Lastly, as further details of the data submission and
compliance threshold are determined by CMS, we anticipate communicating
these details through the CMS HQRP Web site, listserv messages via the
Post-Acute Care QRP listserv, MLN Connects[supreg] National Provider
Calls & Events, MLN Connects[supreg] Provider eNews and announcements
on Open Door Forums and Special Open Door Forums.
c. CAHPS[supreg] Participation Requirements for FY 2018 APU
Determination and Determinations for Subsequent Years
In the FY 2015 Hospice Wage Index final rule, we added the
CAHPS[supreg] Hospice Survey to the Hospice Quality Reporting Program
requirements for the FY 2017 payment determination and determinations
for subsequent FY APU years (79 FR 50491).
In the FY 2017 Hospice Wage Index final rule, we finalized that to
meet the HQRP requirements for the FY 2018, FY 2019 and FY 2020 APU
payment determinations, hospices would collect survey data on a monthly
basis for the months of January 1, 2016 through December 31, 2016 to
qualify for the full FY 2018 APU; hospices would collect survey data on
a monthly basis for the months of January 1, 2017 through December 31,
2017, to qualify for the full FY 2019 APU, and hospices would collect
survey data on a monthly basis for the months of January 1, 2018
through December 31, 2018 for the full FY 2020 APU (81 FR 25529-25530).
We are proposing in this FY 2018 proposed rule, that to meet the HQRP
requirements for the FY 2021 APU payment determination, hospices would
collect survey data on a monthly basis for the months of January 1,
2019 through December 31, 2019 to qualify for the FY 2021 APU. We are
additionally proposing in this FY 2018 proposed rule, that to meet the
HQRP requirements for the FY 2022 APU payment determination, hospices
would collect survey data on a monthly basis for the months of January
1, 2020 through December 31, 2020 to qualify for the FY 2022 APU.
10. HQRP Submission Exemption and Extension Requirements for the FY
2019 Payment Determination and Subsequent Years
a. Extraordinary Circumstances Exemption and Extension
In the FY 2015 Hospice Wage Index final rule (79 FR 50488), we
finalized our proposal to allow hospices to request, and for CMS to
grant, exemptions/extensions for the reporting of required HIS quality
data when there are extraordinary circumstances beyond the control of
the provider. Such extraordinary circumstances may include, but are not
limited to, acts of nature or other systemic issues with our data
systems. We further finalized that hospices must request such an
exemption or extension within 30 days of the date that the
extraordinary circumstances occurred.
In certain instances, however, it may be difficult for hospices to
timely evaluate the impact of extraordinary circumstances within 30
calendar days. For other quality reporting programs such as the
Hospital Inpatient Quality Reporting (81 FR 57182), Inpatient
Rehabilitation Facility Quality Reporting Program (81 FR 52125) and the
Long-term Care Hospital Quality Reporting Program (81 FR 25205), we
have reevaluated our policy and subsequently finalized through
rulemaking an extension of that period of time to 90 calendar days. We
are therefore proposing to extend the deadline for submitting an
exemption or extension request to 90 calendar days from the qualifying
event which is preventing a hospice from submitting their quality data
for the HQRP. We believe that extending the deadline to 90 calendar
days would allow hospices more time to determine whether it is
necessary and appropriate to submit an exemption or extension request
and to provide a more comprehensive account of the qualifying event in
their request form to CMS. For example, if a hospice has suffered
damage due to a hurricane on January 1st, it would have until March
31st to submit a request form to CMS via email to the HQRP mailbox at
HospiceQRPReconsiderations@cms.hhs.gov.
Further, while we finalized our policy in the past for exception/
extension for the submission of the HIS data, we propose to extend this
policy beyond the submission of the HIS date to submission of the
CAHPS[supreg] Hospice Survey data, given that multiple data submission
processes could be impacted by the same qualifying event.
Therefore, we are proposing for FY 2019 payment determination and
subsequent payment determinations to extend the period of time a
hospice may have to submit a request for an extension or exception for
quality reporting purposes from 30 calendar days to 90 calendar days
after the date that the extraordinary circumstances occurred, by
submitting a request to CMS via email to the HQRP mailbox at
HospiceQRPReconsiderations@cms.hhs.gov. Exemption or extension requests
sent to us through any other channel will not be considered valid. The
request for an exemption or extension must contain all of the finalized
requirements as outlined on our Web site at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Hospice-Quality-Reporting/Extensions-and-Exemption-Requests.html.
If a hospice is granted an exemption or extension, timeframes for
which an exemption or extension is granted will be applied to the new
timeliness requirement so such hospices are not penalized. If a hospice
is granted an exemption, we will not require that the hospice submit
HIS and/or CAHPS[supreg] Hospice Survey data for a given period of
time. By contrast, if we grant an extension to a hospice, the hospice
will still remain responsible for submitting data collected during the
timeframe in question, although we will specify a revised deadline by
which the hospice must submit these quality data.
This process does not preclude us from granting extensions/
exemptions to hospices that have not requested them when we determine
that an extraordinary circumstance, such as an act of nature, affects
an entire region or locale. We may grant an extension/exemption to a
hospice if we determine that a systemic problem with our data
collection systems directly affected the ability of the hospice to
submit data. If we make the determination to grant an extension/
exemption to hospices in a region or locale, we will communicate this
decision through the various means, including the CMS HQRP Web site,
listserv messages via the Post-Acute Care QRP listserv, MLN
Connects[supreg] National Provider Calls & Events, MLN Connects[supreg]
Provider eNews and announcements on Open Door Forums
[[Page 20782]]
and Special Open Door Forums. We are soliciting comments on these
proposals.
b. Volume-Based Exemption for CAHPS[supreg] Hospice Survey Data
Collection and Reporting Requirements
We previously finalized a volume-based exemption for CAHPS[supreg]
Hospice Survey Data Collection and Reporting requirements in the FY
2017 Final Rule (81 FR 52181). Hospices that have fewer than 50 survey-
eligible decedents/caregivers in the period from January 1, 2017
through December 31, 2017 are eligible to apply for an exemption from
CAHPS[supreg] Hospice Survey data collection and reporting requirements
for the FY 2020 payment determination (corresponds to the CY 2018 data
collection period). To qualify, hospices must submit an exemption
request form for the FY 2020 APU. The exemption request form is
available on the official CAHPS[supreg] Hospice Survey Web site https://www.hospiceCAHPSsurvey.org. Hospices that intend to claim the size
exemption are required to submit to CMS their total unique patient
count for the period of January 1, 2017 through December 31, 2017. The
due date for submitting the exemption request form for the FY 2020 APU
is December 31, 2018. Small hospices that meet the exemption for size
criteria for FY 2020 must complete an exemption form for FY 2020.
Exemptions for size are active for 1 year only. If a hospice continues
to meet the eligibility requirements for this exemption in future FY
APU periods, the organization needs to request the exemption annually
for every applicable FY APU period.
Hospices that have fewer than 50 survey-eligible decedents/
caregivers in the period from January 1, 2018 through December 31, 2018
are eligible to apply for an exemption from CAHPS[supreg] Hospice
Survey data collection and reporting requirements for the FY 2021
payment determination. Hospices that intend to claim the size exemption
are required to submit to CMS their total unique patient count for the
period of January 1, 2018 through December 31, 2018. The due date for
submitting the exemption request form for the FY 2021 APU is December
31, 2019. Small hospices that meet the exemption for size criteria for
FY 2021 must complete an exemption form for FY 2021.
Hospices that have fewer than 50 survey-eligible decedents/
caregivers in the period from January 1, 2019 through December 31, 2019
are eligible to apply for an exemption from CAHPS[supreg] Hospice
Survey data collection and reporting requirements for the FY 2022
payment determination. Hospices that intend to claim the size exemption
are required to submit to CMS their total unique patient count for the
period of January 1, 2019 through December 31, 2019. The due date for
submitting the exemption request form for the FY 2022 APU is December
31, 2020. If a hospice continues to meet the eligibility requirements
for this exemption in future FY APU periods, the organization should
request the exemption annually for every applicable FY APU period.
c. Newness Exemption for CAHPS[supreg] Hospice Survey Data Collection
and Reporting Requirements
CMS previously finalized a one-time newness exemption for hospices
that meet the criteria (81 FR 52181). Accordingly, hospices that are
notified about their Medicare CCN after January 1, 2018 are exempted
from the FY 2020 APU CAHPS[supreg] Hospice Survey requirements due to
newness. No action is required on the part of the hospice to receive
this exemption. The newness exemption is a one-time exemption from the
survey. Likewise, hospices notified about their Medicare CCN after
January 1, 2019 are exempted from the FY 2021 APU CAHPS[supreg] Hospice
Survey and hospices notified about their Medicare CCN after January 1,
2020 are exempted from the FY 2022 APU CAHPS[supreg] Hospice Survey
requirements.
11. CAHPS[supreg] Hospice Survey Participation Requirements for the FY
2020 APU and Subsequent Years
The CAHPS[supreg] Hospice Survey of CMS' Hospice Quality Reporting
Program is used to collect data on the experiences of hospice patients
and the primary caregivers listed in their hospice records. Readers who
want more information are referred to our extensive discussion of the
Hospice Experience of Care prior to our proposal for the public
reporting of measures should refer to 79 FR 50452 and 78 FR 48261.
a. Background and Description of the CAHPS[supreg] Hospice Survey
The CAHPS[supreg] Hospice Survey is the first standardized national
survey available to collect information on patient's and informal
caregiver's experience of hospice care. Patient-centered experience
measures are a key component of the CMS Quality Strategy, emphasizing
patient-centered care by rating experience as a means to empower
patients and their caregivers and improving the quality of their
care.\28\ In addition, the survey introduces standard survey
administration protocols that allow for fair comparisons across
hospices.
---------------------------------------------------------------------------
\28\ CMS National Quality Strategy 2016. Available at: https://www.cms.gov/medicare/quality-initiatives-patient-assessment-instruments/qualityinitiativesgeninfo/downloads/cms-quality-strategy.pdf.
---------------------------------------------------------------------------
Details regarding CAHPS[supreg] Hospice Survey national
implementation, survey administration, participation requirements,
exemptions from the survey's requirements, hospice patient and
caregiver eligibility criteria, fielding schedules, sampling
requirements, survey instruments, and the languages that are available
for the survey, are all available on the official CAHPS[supreg] Hospice
Survey Web site, www.HospiceCAHPSsurvey.org and in the CAHPS[supreg]
Hospice Survey Quality Assurance Guidelines (QAG), which is posted on
the Web site.
b. Overview of Proposed Measures
The CAHPS Hospice Survey was developed in line with the U.S.
Department of Health and Human Services' Transparency Initiative to
measure patient experience. Unlike the Hospital CAHPS[supreg] Survey
deployed in 2006 (71 FR 48037 through 48039) and other subsequent
CAHPS[supreg] surveys, the CAHPS[supreg] Hospice Survey is administered
after the patient is deceased and queries the decedent's primary
caregiver regarding the patient and family experience of care. National
implementation of the CAHPS[supreg] Hospice Survey commenced January 1,
2015 as stated in the FY 2015 Hospice Wage Index and Payment Rate
Update final rule (79 FR 50452).
The survey consists of 47 questions and is available (using the
mailed version) in English, Spanish, Chinese, Russian, Portuguese,
Vietnamese, Polish, and Korean. It covers topics such as access to
care, communications, experience at hospice facilities, and
interactions with hospice staff. The survey also contains two global
rating questions and asks for self-reported demographic information
(race/ethnicity, educational attainment level, languages spoken at
home, among others).
The CAHPS[supreg] Hospice Survey measures received NQF endorsement
on October 26th, 2016 (NQF number 2651). Measures derived from the
CAHPS[supreg] Hospice Survey include six multi-item (composite)
measures and two global ratings measures under NQF 2651. We are
proposing to adopt these eight survey-based measures for the CY 2018
data collection period and for subsequent years. We believe these
survey-based measures will be useful in assessing aspects of hospice
care where the family/primary caregiver is the most useful or only
source of information, and to allow meaningful and objective
comparisons between hospice
[[Page 20783]]
providers. The six CAHPS[supreg] Hospice Survey composite survey-based
measures are:
Hospice Team Communication;
Getting Timely Care;
Treating Family Member with Respect;
Getting Emotional and Religious Support;
Getting Help for Symptoms; and
Getting Hospice Care Training.
Each of the six composite survey-based measures consists of two or
more questions. The two global survey-based measures are:
Rating of Hospice; and
Willingness to Recommend Hospice.
The two global survey-based measures are comprised of a single
question each and ask the primary caregiver of the decedent to rate the
care provided by the hospice facility and his or her willingness to
recommend the hospice to family and friends. More information about
these measures can be found on the official CAHPS[supreg] Hospice
Survey Web site, www.HospiceCAHPSsurvey.org and in the CAHPS[supreg]
Hospice Survey Quality Assurance Guidelines (QAG), which is posted on
the Web site.
The eight survey-based measures we are proposing were included on
the CY 2016 MUC \29\ list, and reviewed by the MAP.\30\
---------------------------------------------------------------------------
\29\ CMS, List of Measures Under Consideration for December 1,
2016. Available at: https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/QualityMeasures/Downloads/Measures-under-Consideration-List-for-2016.pdf.
\30\ The National Quality Forum. MAP 2016-2017 Preliminary
Recommendations. National Quality Forum, 2016 Recommendations for
Measures Under Consideration, Jan. 2017. Available at: https://www.qualityforum.org/map/.
---------------------------------------------------------------------------
CAHPS[supreg] Hospice Survey: Rating of Hospice (MUC ID:
MUC16-31)
CAHPS[supreg] Hospice Survey: Hospice Team Communications
(MUC16-32)
CAHPS[supreg] Hospice Survey: Willingness to Recommend
(MUC16-33)
CAHPS[supreg] Hospice Survey: Getting Hospice Care
Training (MUC16-35)
CAHPS[supreg] Hospice Survey: Getting Timely Care (MUC16-
36)
CAHPS[supreg] Hospice Survey: Getting Emotional and
Religious Support (MUC16-37)
CAHPS[supreg] Hospice Survey: Getting Help for Symptoms
(MUC16-39)
CAHPS[supreg] Hospice Survey: Treating Family Member with
Respect (MUC16-40)
The MAP supported rulemaking for all eight ``patient-reported''
measures derived from the CAHPS[supreg] Hospice Survey. The MAP noted
that the CAHPS[supreg] Hospice Survey measures may offer an indication
of global quality of care by including the perspective of both patients
and their caregivers.
c. Data Sources
As discussed in the CAHPS[supreg] Hospice Survey Quality Assurance
Guidelines V3.0 (QAG V3.0) (https://www.hospicecahpssurvey.org/en/quality-assurance-guidelines/), the survey has three administration
methods: Mail-only, telephone only, and mixed mode (mail with telephone
follow-up of non-respondents). We previously finalized the
participation requirements for the FY 2018 and FY 2019 Annual Payment
Updates (80 FR 47194). To summarize, to meet the CAHPS[supreg] Hospice
Survey requirements for the HQRP, we are proposing that hospice
facilities must contract with a CMS-approved vendor to collect survey
data for eligible patients on a monthly basis and report that data to
CMS on the hospice's behalf by the quarterly deadlines established for
each data collection period. The list of approved vendors is available
at: https://www.hospicecahpssurvey.org/en/approved-vendor-list.
Hospices are required to provide lists of the patients who died
under their care, along with the associated primary caregiver
information, to their respective survey vendors to form the samples for
the CAHPS[supreg] Hospice Survey. We emphasize the importance of
hospices providing complete and accurate information to their
respective survey vendors in a timely manner. Hospices must contract
with an approved CAHPS[supreg] Hospice Survey vendor to conduct the
survey on their behalf. Hospices are responsible for making sure their
respective survey vendors meet all data submission deadlines. Vendor
failures to submit data on time are the responsibility of the hospices.
i. Requirements for the FY 2020 Annual Payment Update
To meet participation requirements for the FY 2020 annual payment
update (APU), Medicare-certified hospices must collect CAHPS[supreg]
Hospice Survey data on an ongoing monthly basis from January 2018
through December 2018 (all 12 months) in order to receive their full
payment for the FY 2020 APU. All data submission deadlines for the FY
2020 APU are in Table 17. CAHPS[supreg] Hospice Survey vendors must
submit data by the deadlines listed in Table 17 for all APU periods
listed in the table and moving forward. There are no late submissions
permitted after the deadlines, except for extraordinary circumstances
beyond the control of the provider as discussed above.
Table 17--CAHPS[supreg] Hospice Survey Data Submission Dates for the APU
in FY 2020, FY 2021, and FY 2022
------------------------------------------------------------------------
Sample months (that is, month of death) Quarterly data submission
\1\ deadlines \2\
------------------------------------------------------------------------
FY 2020 APU
------------------------------------------------------------------------
January-March 2018 (Q1)................... August 8, 2018.
April-June 2018 (Q2)...................... November 14, 2018.
July-September 2018 (Q3).................. February 13, 2019.
October-December 2018 (Q4)................ May 8, 2019.
------------------------------------------------------------------------
FY 2021 APU
------------------------------------------------------------------------
January-March 2019 (Q1)................... August 14, 2019.
April-June 2019 (Q2)...................... November 13, 2019.
July-September 2019 (Q3).................. February 12, 2020.
October-December 2019 (Q4)................ May 13, 2020.
------------------------------------------------------------------------
FY 2022 APU
------------------------------------------------------------------------
January-March 2020 (Q1)................... August 12, 2020.
April-June 2020 (Q2)...................... November 12, 2020.\3\
July-September 2020 (Q3).................. February 10, 2021.
October-December 2020 (Q4)................ May 12, 2021.
------------------------------------------------------------------------
\1\ Data collection for each sample month initiates 2 months following
the month of patient death (for example, in April for deaths occurring
in January).
\2\ Data submission deadlines are the second Wednesday of the submission
months, which are the months August, November, February, and May.
\3\ Second Wednesday is Veterans Day Holiday.
ii. Requirements for the FY 2021 Annual Payment Update
To meet participation requirements for the FY 2021 APU, Medicare-
certified hospices must collect CAHPS[supreg] Hospice Survey data on an
ongoing monthly basis from January 2019 through December 2019 (all 12
months) in order to receive their full payment for the FY 2021 APU. All
data submission deadlines for the FY 2021 APU are in Table 17.
CAHPS[supreg] Hospice Survey vendors must submit data by the deadlines
listed in Table 17 for all APU periods listed in the table and moving
forward. There are no late submissions permitted after the deadlines,
except for extraordinary circumstances beyond the control of the
provider as discussed above.
[[Page 20784]]
iii. Requirements for the FY 2022 Annual Payment Update
To meet participation requirements for the FY 2022 APU, Medicare-
certified hospices must collect CAHPS[supreg] Hospice Survey data on an
ongoing monthly basis from January 2020 through December 2020 (all 12
months) in order to receive their full payment for the FY 2022 APU. All
data submission deadlines for the FY 2022 APU are in Table 17.
CAHPS[supreg] Hospice Survey vendors must submit data by the deadlines
listed in Table 17 for all APU periods listed in the table and moving
forward. There are no late submissions permitted after the deadlines,
except for extraordinary circumstances beyond the control of the
provider as discussed above.
d. Measure Calculations
As noted above, we are proposing to adopt six composite
CAHPS[supreg] Hospice Survey-based measures and two global survey-based
measures. As with other measures adopted for HQRP, a hospice's
performance for a given payment determination year will be based upon
the successful submission of data required in accordance with the
administrative, form, manner and timing requirements established for
the program. Therefore, hospices' scores on the CAHPS[supreg] Hospice
Survey-based measures will not affect whether they are subject to the
2.0 percentage point payment reduction for hospices that fail to report
data required to be submitted.
We propose that CAHPS Hospice Survey scores for a given hospice be
displayed as ``top-box'' scores, with the national average top-box
score for participating hospices provided for comparison. Top-box
scores reflect the proportion of caregiver respondents that endorse the
most positive response(s) to a given measure, such as the proportion
that rate the hospice a 9 or 10 out of 10 on a 0 to 10 scale, or the
proportion that report that they ``always'' received timely care. The
top-box numerator for each question within a measure is the number of
respondents that endorse the most positive response(s) to the question.
The denominator includes all respondents eligible to respond to the
question, with one exception. The exception is the Getting Hospice Care
Training measure; for this measure, the measure score is calculated
only among those respondents who indicated that their family member
received hospice care at home or in an assisted living facility.
For additional information on the specifications of these measures,
including details regarding top-box scoring methodology and mode and
case-mix adjustment, please refer to the CAHPS[supreg] Hospice Survey
Web page at https://www.hospicecahpssurvey.org/en/.
i. Composite Survey-Based Measures
Unadjusted hospice scores on each composite CAHPS[supreg] Hospice
Survey-based measure would be calculated by determining the proportion
of ``top-box'' responses for each question within the composite and
averaging these proportions over all the questions in the composite
measure. For example, to assess hospice performance on the composite
measure CAHPS[supreg] Hospice Survey--Hospice Team Communication, we
would calculate the proportion of top-box responses for each of the
measure's six questions, add those proportions together, and divide by
the number of questions in the composite measure (in this case, six).
As a specific example, we take a theoretical hospice facility that
had 50 surveys completed and received the proportions of ``top-box''
responses through sample calculations:
25 ``top-box'' responses out of 50 total responses on Question
One
40 ``top-box'' responses out of 50 total responses on Question
Two
50 ``top-box'' responses out of 50 total responses on Question
Three
35 ``top-box'' responses out of 50 total responses on Question
Four
45 ``top-box'' responses out of 50 total responses on Question
Five
40 ``top-box'' responses out of 50 total responses on Question
Six
Based on the above responses, we would calculate that hospice's
unadjusted measure score for public reporting as follows:
[GRAPHIC] [TIFF OMITTED] TP03MY17.005
This calculation would give this example hospice an unadjusted
score of 0.78 or 78 percent for the Hospice Team Communication measure
for purposes of public reporting. We note that an adjusted hospice
score would be calculated by adjusting the score for each question for
differences in the characteristics of decedents and caregivers across
hospices and for mode as described in section 11.e, and then averaging
across questions within the measure as described here. Further detailed
information regarding scoring and risk adjustment can be found at the
CAHPS[supreg] Hospice Survey Web site (https://www.hospicecahpssurvey.org/en/technical-specifications/).
ii. Global Survey-Based Measures
We are proposing to adopt two global CAHPS[supreg] Hospice Survey
measures. CAHPS[supreg] Hospice Survey--Rating of Hospice asks the
primary caregiver of the decedent to rate the care provided by the
hospice on a scale of 0 to 10, and CAHPS[supreg] Hospice Survey--
Willingness to Recommend asks about the caregiver's willingness to
recommend the hospice to family and friends on a scale of ``Definitely
No'' to ``Definitely Yes''. Unadjusted hospice performance on each of
the two global CAHPS[supreg] Hospice Survey-based measures would be
calculated by the proportion of respondents providing high-value
responses (that is, a 9 to 10 rating or ``Definitely Yes'') to the
survey questions over the total number of respondents. For example, if
a hospice received 45 9- and 10-point ratings out of 50 responses, this
hospital would receive a 0.9 or 90 percent unadjusted score, which
would then be adjusted for differences in the characteristics of
decedents and caregivers across hospices and modes, as described in
section 12.E.
iii. Cohort
The CAHPS[supreg] Hospice Survey is administered to all eligible
patients/caregivers--or a random sample thereof--who meet the
eligibility criteria. Eligible patients, regardless of insurance or
payment, can participate.
For purposes of each survey-based measure captured in the
CAHPS[supreg] Hospice Survey, an ``eligible patient'' is a decedent 18
years or older:
With death at least 48 hours following last admission to
hospice care
for whom there is a caregiver of record
whose caregiver is someone other than a non-familial legal
guardian
for whom the caregiver has a U.S. or U.S. Territory home
address
Patients who are still alive or whose admission to the hospice
resulted in a
[[Page 20785]]
live discharge, are not eligible to participate in the survey. In
addition, decedents/caregivers who initiate or voluntarily request that
the hospice not reveal the patient's identity; and/or not survey the
patient/caregiver (``no publicity patients/caregivers'') are excluded
from the sample.
e. Risk Adjustment
The CAHPS[supreg] Hospice Survey measures assess activities that
are fully under the control of hospice care professionals and/or
hospice organizations. In order to ensure fair comparisons in public
reporting, we believe it is necessary and appropriate to adjust for
factors that are not directly related to hospice performance, such as
patient mix, for these CAHPS[supreg] Hospice Survey measures. The
survey based measures are adjusted for decedent and caregiver
characteristics (including the lag time between patient death and
survey response; decedent's age, payer for hospice care, decedent's
primary diagnosis, decedent's length of final episode of hospice care,
caregiver's education, decedent's relationship to caregiver,
caregiver's preferred language and language in which the survey was
completed, and caregiver's age) known to be associated with systematic
difference in survey responses.
i. Patient Mix Adjustment
Previous research, on both CAHPS[supreg] surveys and other types of
surveys, has identified respondent characteristics that are not under
the control of the entities being assessed but tend to be related to
survey responses. Hence, variations in the proportion of respondents
with such characteristics will be associated with variations in survey
responses that are unrelated to the actual quality of hospice care. To
ensure that comparisons between hospices reflect differences in
performance rather than differences in patient and/or caregiver
characteristics, publicly reported hospice scores will be adjusted for
variations of such characteristics across hospices. This adjustment is
performed using a linear regression model applied to all data within a
quarter, with indicator variables for each hospice and each
characteristic as an independent variable in the model.
ii. Mode Adjustment
We conducted an experiment to determine whether survey mode
adjustments were needed to fairly compare CAHPS[supreg] Hospice Survey
scores. The experiment found that mode adjustments are needed. Publicly
reported CAHPS[supreg] Hospice Survey scores will be adjusted for the
mode of survey administration, which affects scores but is not related
to quality of hospice care. (Authorized survey modes are: Mail-only,
telephone-only, and mail with telephone follow up, also called mixed
mode.) Mode adjustment is performed prior to patient-mix adjustment; a
mode adjustment value is added/subtracted (depending on the mode) to
each response to the survey by mail-only mode or mixed mode. Responses
obtained using telephone-only mode are not adjusted since this is the
reference mode.
As a result of the risk adjustment methodologies proposed here, the
final percentages may vary from the unadjusted percentage as calculated
in the examples provided above.
f. For Further Information About the CAHPS[supreg] Hospice Survey
We encourage hospices and other entities to learn more about the
survey on www.hospicecahpssurvey.org. For direct questions, please
contact the CAHPS[supreg] Hospice Survey Team at
hospicecahpssurvey@HCQIS.org or telephone 1-844-472-4621.
12. HQRP Reconsideration and Appeals Procedures for the FY 2018 Payment
Determination and Subsequent Years
In the FY 2015 Hospice Wage Index final rule (79 FR 50496), we
notified hospice providers on how to seek reconsideration if they
received a noncompliance decision for the FY 2016 payment determination
and subsequent years. A hospice may request reconsideration of a
decision by CMS that the hospice has not met the requirements of the
HQRP for a particular period.
We clarified that any hospice that wishes to submit a
reconsideration request must do so by submitting an email to CMS
containing all of the requirements listed on the HQRP Web site at
https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Hospice-Quality-Reporting/Reconsideration-Requests.html.
Electronic email sent to HospiceQRPReconsiderations@cms.hhs.gov is the
only form of submission that will be accepted. Any reconsideration
requests received through any other channel including the United States
Postal Service (USPS) or phone will not be considered as a valid
reconsideration request. In the FY 2017 final rule we further clarified
that providers should submit reconsideration requests of decision by
CMS that the hospice has not met the CAHPS[supreg] Hospice Survey
requirements using the same process (81 FR 52181) (Details about the
reports and emails received after data submission are in the
CAHPS[supreg] Hospice Quality Assurance Guidelines, which is available
on the official CAHPS[supreg] Hospice Survey Web site,
www.hospicecahpssurvey.org). We codified this process at Sec.
418.312(h). In addition, we codified at Sec. 418.306(b)(2) that
beginning with FY 2014 and each subsequent FY, the Secretary shall
reduce the market basket update by 2 percentage points for any hospice
that does not comply with the quality data submission requirements for
that FY and solicited comments on all of the proposals and the
associated regulations text at Sec. 418.312 and in Sec. 418.306 in
section VI. Official instructions regarding the payment reduction
reconsideration process can be located under the Regulations and
Guidance, Transmittals, 2015 Transmittals Web site at https://www.cms.gov/Regulations-and-Guidance/Guidance/Transmittals/2017-Transmittals.html.
In the past, only hospices found to be non-compliant with the
reporting requirements set forth for a given payment determination
received a notification from CMS of this finding along with
instructions for requesting reconsideration in the form of a USPS
letter. In the FY 2016 Hospice Wage Index final rule (80 FR 47198), we
stated that we would use the QIES CASPER reporting system as an
additional mechanism to communicate to hospices regarding their
compliance with the reporting requirements for the given reporting
cycle. We have implemented this additional communication mechanism via
the CASPER Hospice Timeliness Compliance Threshold Report previously
discussed in the FY 2017 Hospice Wage Index rule at 81 FR 25527 and
25528. We will continue to send notification of noncompliance via
delivery of a letter via the USPS. We previously finalized our proposal
(80 FR 47198) to publish a list of hospices who successfully meet the
reporting requirements for the applicable payment determination on the
CMS HQRP Web site. The list of providers found to be compliant with the
FY 2017 APU requirements can be found on the CMS HQRP Web site here:
https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Hospice-Quality-Reporting/HQRP-Requirements-and-Best-Practices.html.
13. Confidential Feedback Reports
As part of our effort to promote use of standardized quality data
to improve quality of care, in December 2016, we made available two new
provider feedback reports: The Hospice-Level
[[Page 20786]]
Quality Measure Report and the Patient Stay-Level Quality Measure
Report. These confidential feedback reports are available to each
hospice using the CASPER system, and are part of the class of CASPER
reports known as Quality Measure (QM) Reports. These reports are
separate from public reporting and are for provider viewing only, for
the purposes of internal provider quality improvement. These reports
are on-demand and thus enable hospice providers to view and compare
their performance to the national average for a reporting period of
their choice.
Providers are able to view their data and information at both the
hospice and patient stay levels for it's HIS based quality measures.
The CASPER hospice-level QM Reports contain information such as the
numerator, denominator, hospice-level QM score, and national average.
The CASPER patient stay-level QM Reports show whether each patient stay
is counted toward each quality measure. The HIS based QMs reported in
both reports include:
NQF #1641 Treatment Preferences
NQF #1647 Beliefs/Values
NQF #1634 Pain Screening
NQF #1637 Pain Assessment
NQF #1639 Dyspnea Screening
NQF #1638 Dyspnea Treatment
NQF #1617 Bowel Regimen
For more information on the CASPER QM Reports, we refer readers to
the CASPER QM Factsheet on the HQRP Web site at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Hospice-Quality-Reporting/HQRP-Requirements-and-Best-Practices.html. This fact
sheet contains detailed information about each CASPER QM report
currently available, the data included in the reports, and how
providers can use the reports as part of their Quality Assessment and
Performance Improvement (QAPI) efforts. For technical information on
the reports and how to access the CASPER QM Reports, we refer readers
to: https://www.qtso.com/hospicetrain.html.
As new HIS measures are implemented in the HQRP, we will continue
to expand the functionality of the QM reports to allow providers to
view data on additional HIS measures. We will announce refinements and
additions to the QM reports through sub-regulatory communication
channels and in future rulemaking cycles.
We also propose to provide hospices with preview reports of their
data prior to the quarterly publication of CAHPS[supreg] Hospice Survey
data on the Compare site. The reports will be provided through the
CASPER reporting system. Each hospice will receive only its own,
individual reports.
14. Public Display of Quality Measures and Other Hospice Data for the
HQRP
Under section 1814(i)(5)(E) of the Act, the Secretary is required
to establish procedures for making any quality data submitted by
hospices available to the public. These procedures shall ensure that a
hospice has the opportunity to review the data that is to be made
public for the hospice prior to such data being made public. The
Secretary shall report quality measures that relate to hospice care
provided by hospice programs on a publicly available CMS Web site.
In the FY 2017 rule, we discussed our analysis of HIS data to
inform which measures were eligible for public reporting and
reportability analysis to determine data selection period and minimum
denominator size for measures to be publicly reported. Based on
analysis results, we determined that all 7 HIS quality measures adopted
for the FY 2016 and beyond (NQF #1634, NQF #1637, NQF #1639, NQF #1638,
NQF #1641, NQF #1647, NQF #1617), calculated based on a rolling 12
month data selection period, to be eligible for public reporting with a
minimum denominator size of 20 patient stays. For additional details on
these analyses, we refer readers to the FY 2017 final rule (81 FR 52183
through 52184).
In the FY 2017 final rule we also clarified policies for
reportability analyses for new measures. As stated in the FY 2017 final
rule, new measures will undergo reportability analysis to determine (1)
appropriateness for public reporting and (2) appropriate data selection
period. In accordance with discussion in the prior year's rule, we will
use the same analytic approach used in previous reportability analyses
to determine data selection period and minimum denominator size for the
Hospice and Palliative Care Composite Process Measure--Comprehensive
Assessment at Admission. We will begin reportability analyses for the
Hospice Visits When Death is Imminent Measure Pair once data for the
measure are available. Results of reportability analyses conducted for
these new measures will be communicated through future rulemaking.
To meet the Affordable Care Act's requirement for making quality
measure data public, we are developing a CMS Hospice Compare Web site,
which will allow consumers, providers and stakeholders to search for
all Medicare-certified hospice providers and view their information and
quality measure scores. We anticipate that public reporting of HQRP
data on the CMS Compare Web site will begin sometime in the summer of
CY 2017. To help providers prepare for public reporting, we will offer
opportunities for stakeholder engagement and education prior to the
rollout of a CMS Hospice Compare site. We will offer outreach
opportunities for providers through CMS HQRP Public reporting Web page:
https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Hospice-Quality-Reporting/Hospice-Quality-Public-Reporting.html, listserv messages via the Post-Acute Care QRP listserv,
MLN Connects[supreg] National Provider Calls & Events, MLN
Connects[supreg] Provider eNews and announcements on Open Door Forums
and Special Open Door Forums. Finally, we will offer educational
support and outreach to all hospice providers on the systems and
processes for reviewing their data prior to public reporting;
availability of educational support and outreach opportunities will be
communicated through the listed channels above.
We will provide hospices an opportunity to preview their quality
measure data prior to publicly reporting information. These quality
measure data reports or ``preview reports'' will be made available in
the CASPER system prior to public reporting and will offer providers
the opportunity to preview their quality measure data prior to public
reporting on the CMS Hospice Compare Web site. We will provide hospices
30 days to review the preview report beginning from the date on which
they can access the report. Hospices will have an opportunity to
request review of their data by CMS during the 30-day preview period if
they believe that errors in data submitted to CMS may have resulted in
incorrect measure scores and can submit proof along with a plan
describing how the errors will be corrected. We will review these
requests and if we confirm that the errors have affected the measures
and agree to correct the measure, we will suppress the measure on the
Hospice Compare Web site for one time only and display the corrected
measure during the subsequent quarterly refresh of the Compare Web
site. When the preview reports are ready for providers to access,
anticipated summer of CY 2017 prior to the release of Hospice Compare,
we will post the policies and procedures for providers to submit
requests for reviewing of their data by CMS on the CMS HQRP Web site:
https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-
[[Page 20787]]
Instruments/Hospice-Quality-Reporting/Hospice-Quality-Public-
Reporting.html.
CMS encourages hospices to use CASPER QM Reports (see section
III.D.14 of this proposed rule) to review their HIS quality measures
after they submit the HIS data to CMS. If hospices determine that
erroneous data have been submitted, they should submit either of these
two types of HIS records: Modify existing record or inactivate existing
record to correct their data. HIS data corrected before the data are
frozen for the creation of the preview reports will be reflected in the
preview reports.
We propose to begin public reporting of CAHPS[supreg] Hospice
Survey measures in 2018. Specifically, we are proposing to publicly
report data in winter CY 2018 on all eight CAHPS[supreg] Hospice Survey
measures. Scores would be displayed based on eight rolling quarters of
data and would initially use CAHPS[supreg] Hospice Survey data
collected from caregivers of patients who died while receiving hospice
care between April 1, 2015 and March 31, 2017. We are proposing that
the display of these scores be updated quarterly, and that scores be
displayed only for those hospices for which there are 30 or more
completed questionnaires during the reporting period. Scores will not
be displayed for hospices with fewer than 30 completed questionnaires
during the reporting period.
Like other CMS Compare Web sites, the Hospice Compare Web site
will, in time, feature a quality rating system that gives each hospice
a rating of between 1 and 5 stars. Hospices will have prepublication
access to their own agency's quality data, which enables each agency to
know how it is performing before public posting of data on the Hospice
Compare Web site. Public comments regarding how the rating system would
determine a hospice's star rating and the methods used for
calculations, as well as a proposed timeline for implementation will be
announced via the CMS HQRP Web page, listserv messages via the Post-
Acute Care QRP listserv, MLN Connects[supreg] National Provider Calls &
Events, MLN Connects[supreg] Provider eNews and announcements on Open
Door Forums and Special Open Door Forums. We will announce the timeline
for development and implementation of the star rating system in future
rulemaking.
Lastly, as part of our ongoing efforts to make healthcare more
transparent, affordable, and accountable for all hospice stakeholders,
we have posted a hospice directory and quality data on a public data
set located at https://data.medicare.gov. This data will serve as a
helpful resource regarding information on Medicare-certified hospice
agencies throughout the nation. In an effort to move toward public
reporting of hospice data, we have initially posted demographic data of
hospice agencies that have been registered with Medicare. This list
includes high-level demographic data for each agency, including
provider name, address, phone numbers, ownership type, CCN, profit
status, and date of original CMS certification. The posting of this
hospice data directory occurred on June 14, 2016 and will be refreshed
quarterly. Information can be located at https://data.medicare.gov/data/hospice-directory. Additionally, we have posted two hospice data
files containing national level aggregate quality data regarding seven
HIS quality measures and CAHPS[supreg] Hospice Survey measures in
December 2016. These data file are a one-time release with a goal to
make quality data available prior to the release of the Hospice Compare
in summer of CY 2017. Additional details regarding hospice datasets
will be announced via the CMS HQRP Web page, listserv messages via the
Post-Acute Care QRP listserv, MLN Connects[supreg] National Provider
Calls & Events, MLN Connects[supreg] Provider eNews and announcements
on Open Door Forums and Special Open Door Forums. In addition, we have
provided the list of CASPER/ASPEN contacts, Regional Office and State
coordinators in the event that a Medicare-certified agency is either
not listed in the database or the characteristics/administrative data
(name, address, phone number, services, or type of ownership) are
incorrect or have changed. To continue to meet Medicare enrollment
requirements, all Medicare providers are required to report changes to
their information in their enrollment application as outlined in the
Provider-Supplier Enrollment Fact Sheet Series located at https://www.cms.gov/Outreach-and-Education/Medicare-Learning-Network-MLN/MLNProducts/downloads/MedEnroll_InstProv_FactSheet_ICN903783.pdf. Once
the Hospice Compare Web site is released in the summer of CY 2017,
https://data.medicare.gov will post the official datasets used on the
Medicare.gov Compare Web sites provided by CM.
IV. Collection of Information Requirements
Under the Paperwork Reduction Act of 1995, we are required to
provide 60-day notice in the Federal Register and solicit public
comment before a collection of information requirement is submitted to
the Office of Management and Budget (OMB) for review and approval. In
order to fairly evaluate whether an information collection should be
approved by OMB, section 3506(c)(2)(A) of the Paperwork Reduction Act
of 1995 requires that we solicit comment on the following issues:
The need for the information collection and its usefulness
in carrying out the proper functions of our agency.
The accuracy of our estimate of the information collection
burden.
The quality, utility, and clarity of the information to be
collected.
Recommendations to minimize the information collection
burden on the affected public, including automated collection
techniques.
Unless noted otherwise, all salary information is from the Bureau
of Labor Statistics (BLS) Web site at https://www.bls.gov/oes and
includes a fringe benefits package worth 100 percent of the base
salary. The mean hourly wage rates are based on May, 2015 BLS data for
each discipline.
Section 1814(i)(5)(C) of the Act requires that each hospice submit
data to the Secretary on quality measures specified by the Secretary.
This data must be submitted in a form and manner, and at a time
specified by the Secretary.
We are soliciting public comment on each of these issues for the
following sections of this document that contain information collection
requirements (ICRs):
A. Hospice Item Set
In the FY 2014 Hospice Wage Index final rule (78 FR 48257), and in
compliance with section 1814(i)(5)(C) of the Act, we finalized the
specific collection of data items that support the following 7 NQF
endorsed measures for hospice:
NQF #1617 Patients Treated with an Opioid who are Given a
Bowel Regimen,
NQF #1634 Pain Screening,
NQF #1637 Pain Assessment,
NQF #1638 Dyspnea Treatment,
NQF #1639 Dyspnea Screening,
NQF #1641 Treatment Preferences,
NQF #1647 Beliefs/Values Addressed (if desired by the
patient).
We finalized the following two additional measures in the FY 2017
Hospice Wage Index final rule affecting FY 2019 payment determinations
(81 FR 52163 through 52173):
Hospice Visits when Death is Imminent
Hospice and Palliative Care Composite Process Measure--
Comprehensive Assessment at Admission
Data for the aforementioned 9 measures is collected via the HIS as
[[Page 20788]]
discussed in the FY 2017 Hospice Wage Index final rule (81 FR 52189)
and covered under OMB control number 0938-1153. The HIS V2.00.0 was
approved by the Office of Management and Budget on April 17, 2017 under
control number 0938-1153. We are not proposing any new updates or
additional collections of information in this proposed rule in regards
to the Hospice Item Set or its constituent quality measures.
B. Summary of CAHPS[supreg] Hospice Survey Information Collection
Requirements (OMB Control Number 0938-1257)
National Implementation of the Hospice Experience of Care Survey
(CAHPs Hospice Survey) data measures are covered under OMB control
number 0938-1257 and is summarized here for convenience. We have
implemented patient experience surveys in a number of settings
including Medicare, Medicare Advantage, and Part D Prescription Drug
Plans, hospitals, and home health agencies. Other CAHPS[supreg] surveys
exist for hemodialysis facilities, nursing homes, and physician
practices. The hospice survey differs from most other CMS patient
experience surveys because its target population is bereaved family
members or close friends of patients who died in hospice care. Family
members and friends are the best source of information regarding the
entire trajectory of hospice care. In addition, many hospice patients
are very ill and unable to answer survey questions.
Surveys are administered by CMS-approved survey vendors hired by
hospice providers to conduct the survey on their behalf. The survey
vendor may collect data in one of three modes: Mail-only, telephone-
only, or mixed mode (mail with telephone follow-up). The sample
consists of bereaved family members or close friends of patients who
died while receiving hospice care (1) at home, (2) in a nursing home,
or (3) an inpatient setting (that is, freestanding inpatient unit or
acute care hospital). The questionnaire is composed of 47 items.
The estimated annualized burden hours and costs to respondents for
the national implementation of the CAHPS[supreg] Hospice Survey are
shown in Tables 18 and 19. Based on participation in national
implementation in the CAHPS[supreg] Hospice Survey from Quarter 2 2015
through Quarter 1 2016, we assume that 3,414 hospices will administer
the survey to an average of 278.7 cases. Thus, we estimate that the
CAHPS[supreg] Hospice Survey will be administered to a maximum of
951,482 individuals each year for the duration of the collection period
covered by this application for the purposes of national
implementation. As not all sampled cases will complete the survey, this
estimate reflects the maximum burden possible. The estimated number of
responses is based on actual hospice participation in national
implementation of the CAHPS[supreg] Hospice Survey.
Table 18 shows the estimated annualized burden for the respondents'
time to participate in the national implementation data collection. The
survey contains 47 items and is estimated to require an average
administration time of 10.4 minutes in English (at a pace of 4.5 items
per minute) and 12.5 minutes in Spanish (assuming 20 percent more words
in the Spanish translation), for an average response time of 10.47
minutes or 0.174 hours (assuming that 1 percent of survey respondents
complete the survey in Spanish). These burden and pace estimates are
based on CMS' experience with the CAHPS[supreg] Hospice Survey and
surveys of similar length that were fielded with Medicare
beneficiaries. As indicated below, the annual total burden hours for
survey participants are estimated to be 165,959.57 for the continued
national implementation of the survey.
Table 18--Estimated Annualized Burden Hours for Respondents: National Implementation of the CAHPS[supreg]
Hospice Survey
----------------------------------------------------------------------------------------------------------------
Number of
Survey version Number of responses per Hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
CAHPS[supreg] Hospice Survey.................... 951,482 1 0.174 165,959.57
---------------------------------------------------------------
Total....................................... 951,482 1 0.174 165,959.57
----------------------------------------------------------------------------------------------------------------
Table 19 shows the cost burden to respondents associated with their
time to complete a survey as part of national implementation. The
annual total cost burden is estimated to be $7,710,481.60. This
estimate is higher than the $3,034,789.70 estimated in the prior OMB
filing, due to the increased number of hospices participating (and
correspondingly, the increased number of respondents), as well as an
increase in the average hourly rate.
Table 19--Estimated Annualized Cost Burden for Respondents: National Implementation
----------------------------------------------------------------------------------------------------------------
Average
Form name Number of Total burden hourly wage Total cost
respondents hours rate* burden
----------------------------------------------------------------------------------------------------------------
CAHPS[supreg] Hospice Survey.................... 951,482 165,959.57 * $46.46 $7,710,481.60
----------------------------------------------------------------------------------------------------------------
Total....................................... 951,482 165,959.57 * $46.46 $7,710,481.60
----------------------------------------------------------------------------------------------------------------
* Source: Data from the U.S. Bureau of Labor Statistics' May 2015 National Occupational Employment and Wage
Estimates for all salary estimates (https://www.bls.gov/oes). This figure includes a 100% fringe benefit on an
average wage of $23.23. Retrieved April 10, 2017.
If you comment on these information collection, that is, reporting,
recordkeeping or third-party disclosure requirements, please submit
your comments electronically as specified in the ADDRESSES section of
this proposed rule.
Comments must be received by 5 p.m. June 26, 2017.
[[Page 20789]]
V. Response to Comments
Because of the large number of public comments we normally receive
on Federal Register documents, we are not able to acknowledge or
respond to them individually. We will consider all comments we receive
by the date and time specified in the DATES section of this preamble,
and, when we proceed with a subsequent document, we will respond to the
comments in the preamble to that document.
VI. Request for Information on CMS Flexibilities and Efficiencies
CMS is committed to transforming the health care delivery system--
and the Medicare program--by putting an additional focus on patient-
centered care and working with providers, physicians, and patients to
improve outcomes. We seek to reduce burdens for hospitals, physicians,
and patients, improve the quality of care, decrease costs, and ensure
that patients and their providers and physicians are making the best
health care choices possible. These are the reasons we are including
this Request for Information in this proposed rule.
As we work to maintain flexibility and efficiency throughout the
Medicare program, we would like to start a national conversation about
improvements that can be made to the health care delivery system that
reduce unnecessary burdens for clinicians, other providers, and
patients and their families. We aim to increase quality of care, lower
costs improve program integrity, and make the health care system more
effective, simple and accessible.
We would like to take this opportunity to invite the public to
submit their ideas for regulatory, subregulatory, policy, practice, and
procedural changes to better accomplish these goals. Ideas could
include payment system redesign, elimination or streamlining of
reporting, monitoring and documentation requirements, aligning Medicare
requirements and processes with those from Medicaid and other payers,
operational flexibility, feedback mechanisms and data sharing that
would enhance patient care, support of the physician-patient
relationship in care delivery, and facilitation of individual
preferences. Responses to this Request for Information could also
include recommendations regarding when and how CMS issues regulations
and policies and how CMS can simplify rules and policies for
beneficiaries, clinicians, physicians, providers, and suppliers. Where
practicable, data and specific examples would be helpful. If the
proposals involve novel legal questions, analysis regarding CMS'
authority is welcome for CMS' consideration. We are particularly
interested in ideas for incentivizing organizations and the full range
of relevant professionals and paraprofessionals to provide screening,
assessment and evidence-based treatment for individuals with opioid use
disorder and other substance use disorders, including reimbursement
methodologies, care coordination, systems and services integration, use
of paraprofessionals including community paramedics and other
strategies. We are requesting commenters to provide clear and concise
proposals that include data and specific examples that could be
implemented within the law.
We note that this is a Request for Information only. Respondents
are encouraged to provide complete but concise responses. This Request
for Information is issued solely for information and planning purposes;
it does not constitute a Request for Proposal (RFP), applications,
proposal abstracts, or quotations. This Request for Information does
not commit the U.S. Government to contract for any supplies or services
or make a grant award. Further, CMS is not seeking proposals through
this Request for Information and will not accept unsolicited proposals.
Responders are advised that the U.S. Government will not pay for any
information or administrative costs incurred in response to this
Request for Information; all costs associated with responding to this
Request for Information will be solely at the interested party's
expense. We note that not responding to this Request for Information
does not preclude participation in any future procurement, if
conducted. It is the responsibility of the potential responders to
monitor this Request for Information announcement for additional
information pertaining to this request. In addition, we note that CMS
will not respond to questions about the policy issues raised in this
Request for Information. CMS will not respond to comment submissions in
response to this Request for Information in the FY 2018 Hospice Wage
Index and Payment Rate Update and Hospice Quality Reporting
Requirements final rule. Rather, CMS will actively consider all input
as we develop future regulatory proposals or future subregulatory
policy guidance. CMS may or may not choose to contact individual
responders. Such communications would be for the sole purpose of
clarifying statements in the responders' written responses. Contractor
support personnel may be used to review responses to this Request for
Information. Responses to this notice are not offers and cannot be
accepted by the Government to form a binding contract or issue a grant.
Information obtained as a result of this Request for Information may be
used by the Government for program planning on a nonattribution basis.
Respondents should not include any information that might be considered
proprietary or confidential. This Request for Information should not be
construed as a commitment or authorization to incur cost for which
reimbursement would be required or sought. All submissions become U.S.
Government property and will not be returned. CMS may publicly post the
public comments received, or a summary of those public comments.
VII. Regulatory Impact Analyses
A. Statement of Need
This proposed rule meets the requirements of our regulations at
Sec. 418.306(c), which requires annual issuance, in the Federal
Register, of the hospice wage index based on the most current available
CMS hospital wage data, including any changes to the definitions of
Core-Based Statistical Areas (CBSAs), or previously used Metropolitan
Statistical Areas (MSAs). This proposed rule would also update payment
rates for each of the categories of hospice care, described in Sec.
418.302(b), for FY 2018 as required under section
1814(i)(1)(C)(ii)(VII) of the Act. Section 411(d) of the Medicare
Access and CHIP Reauthorization Act of 2015 (MACRA) amended section
1814(i)(1)(C) of the Act such that for hospice payments for FY 2018,
the market basket percentage increase shall be 1 percent. Finally,
section 3004 of the Affordable Care Act amended the Act to authorize a
quality reporting program for hospices and this rule discusses changes
in the requirements for the hospice quality reporting program in
accordance with section 1814(i)(5) of the Act.
B. Overall Impacts
We estimate that the aggregate impact of the payment provisions in
this proposed rule would result in an increase of $180 million in
payments to hospices, resulting from the hospice payment update
percentage of 1.0 percent. The impact analysis of this proposed rule
represents the projected effects of the changes in hospice payments
from FY 2017 to FY 2018. Using the most recent data available at the
time of rulemaking, in this case FY
[[Page 20790]]
2016 hospice claims data, we apply the current FY 2017 wage index and
labor-related share values to the level of care per diem payments and
SIA payments for each day of hospice care to simulate FY 2017 payments.
Then, using the same FY 2016 data, we apply the proposed FY 2018 wage
index and labor-related share values to simulate FY 2018 payments.
Certain events may limit the scope or accuracy of our impact analysis,
because such an analysis is susceptible to forecasting errors due to
other changes in the forecasted impact time period. The nature of the
Medicare program is such that the changes may interact, and the
complexity of the interaction of these changes could make it difficult
to predict accurately the full scope of the impact upon hospices.
We have examined the impacts of this rule as required by Executive
Order 12866 on Regulatory Planning and Review (September 30, 1993),
Executive Order 13563 on Improving Regulation and Regulatory Review
(January 18, 2011), the Regulatory Flexibility Act (RFA) (September 19,
1980, Pub. L. 96-354), section 1102(b) of the Social Security Act,
section 202 of the Unfunded Mandates Reform Act of 1995 (March 22,
1995; Pub. L. 104-4), Executive Order 13132 on Federalism (August 4,
1999), the Congressional Review Act (5 U.S.C. 804(2) and Executive
Order 13771 on Reducing Regulation and Controlling Regulatory Costs
(January 30, 2017).
Executive Orders 12866 and 13563 direct agencies to assess all
costs and benefits of available regulatory alternatives and, if
regulation is necessary, to select regulatory approaches that maximize
net benefits (including potential economic, environmental, public
health and safety effects, distributive impacts, and equity). Section
3(f) of Executive Order 12866 defines a ``significant regulatory
action'' as an action that is likely to result in a rule: (1) Having an
annual effect on the economy of $100 million or more in any 1 year, or
adversely and materially affecting a sector of the economy,
productivity, competition, jobs, the environment, public health or
safety, or state, local or tribal governments or communities (also
referred to as ``economically significant''); (2) creating a serious
inconsistency or otherwise interfering with an action taken or planned
by another agency; (3) materially altering the budgetary impacts of
entitlement grants, user fees, or loan programs or the rights and
obligations of recipients thereof; or (4) raising novel legal or policy
issues arising out of legal mandates, the President's priorities, or
the principles set forth in the Executive Order.
A regulatory impact analysis (RIA) must be prepared for major rules
with economically significant effects ($100 million or more in any 1
year). We estimate that this rulemaking is ``economically significant''
as measured by the $100 million threshold, and hence also a major rule
under the Congressional Review Act. Accordingly, we have prepared a RIA
that, to the best of our ability presents the costs and benefits of the
rulemaking.
C. Anticipated Effects
The RFA requires agencies to analyze options for regulatory relief
of small businesses if a rule has a significant impact on a substantial
number of small entities. The great majority of hospitals and most
other health care providers and suppliers are small entities by meeting
the Small Business Administration (SBA) definition of a small business
(in the service sector, having revenues of less than $7.5 million to
$38.5 million in any 1 year), or being nonprofit organizations. For
purposes of the RFA, we consider all hospices as small entities as that
term is used in the RFA. HHS's practice in interpreting the RFA is to
consider effects economically ``significant'' only if they reach a
threshold of 3 to 5 percent or more of total revenue or total costs.
The effect of the proposed FY 2018 hospice payment update percentage
results in an overall increase in estimated hospice payments of 1.0
percent, or $180 million. Therefore, the Secretary has determined that
this proposed rule will not create a significant economic impact on a
substantial number of small entities.
In addition, section 1102(b) of the Act requires us to prepare a
regulatory impact analysis if a rule may have a significant impact on
the operations of a substantial number of small rural hospitals. This
analysis must conform to the provisions of section 604 of the RFA. For
purposes of section 1102(b) of the Act, we define a small rural
hospital as a hospital that is located outside of a metropolitan
statistical area and has fewer than 100 beds. This proposed rule only
affects hospices. Therefore, the Secretary has determined that this
proposed rule would not have a significant impact on the operations of
a substantial number of small rural hospitals.
Section 202 of the Unfunded Mandates Reform Act of 1995 (UMRA) also
requires that agencies assess anticipated costs and benefits before
issuing any rule whose mandates require spending in any 1 year of $100
million in 1995 dollars, updated annually for inflation. In 2017, that
threshold is approximately $148 million. This proposed rule is not
anticipated to have an effect on state, local, or tribal governments,
in the aggregate, or on the private sector of $148 million or more.
Executive Order 13132 establishes certain requirements that an
agency must meet when it promulgates a proposed rule (and subsequent
final rule) that imposes substantial direct requirement costs on state
and local governments, preempts State law, or otherwise has Federalism
implications. We have reviewed this proposed rule under these criteria
of Executive Order 13132, and have determined that it will not impose
substantial direct costs on state or local governments.
If regulations impose administrative costs on private entities,
such as the time needed to read and interpret this proposed rule, we
should estimate the cost associated with regulatory review. Due to the
uncertainty involved with accurately quantifying the number of entities
that will review the rule, we assume that the total number of unique
commenters on last year's proposed rule will be the number of reviewers
of this proposed rule. We acknowledge that this assumption may
understate or overstate the costs of reviewing this rule. It is
possible that not all commenters reviewed last year's rule in detail,
and it is also possible that some reviewers chose not to comment on the
proposed rule. For these reasons we thought that the number of past
commenters would be a fair estimate of the number of reviewers of this
rule. We welcome any comments on the approach in estimating the number
of entities which will review this proposed rule.
We also recognize that different types of entities are in many
cases affected by mutually exclusive sections of this proposed rule,
and therefore for the purposes of our estimate we assume that each
reviewer reads approximately 50 percent of the rule. We seek comments
on this assumption.
Using the wage information from the BLS for medical and health
service managers (Code 11-9111), we estimate that the cost of reviewing
this rule is $90.16 per hour, including overhead and fringe benefits
(https://www.bls.gov/oes/2015/may/naics4_621100.htm). Assuming an
average reading speed, we estimate that it would take approximately 1.3
hours for the staff to review half of this proposed rule. For each
hospice that reviews the rule, the estimated cost is $117.21 (1.3 hours
x
[[Page 20791]]
$90.16). Therefore, we estimate that the total cost of reviewing this
regulation is $7, 032.60 ($117.21 x 60 reviewers).
D. Detailed Economic Analysis
The proposed FY 2018 hospice payment impacts appear in Table 20. We
tabulate the resulting payments according to the classifications in
Table 20 (for example, facility type, geographic region, facility
ownership), and compare the difference between current and proposed
payments to determine the overall impact.
The first column shows the breakdown of all hospices by urban or
rural status, census region, hospital-based or freestanding status,
size, and type of ownership, and hospice base. The second column shows
the number of hospices in each of the categories in the first column.
The third column shows the effect of the annual update to the wage
index. This represents the effect of using the proposed FY 2018 hospice
wage index. The aggregate impact of this change is zero percent, due to
the proposed hospice wage index standardization factor. However, there
are distributional effects of the proposed FY 2018 hospice wage index.
The fourth column shows the effect of the proposed hospice payment
update percentage for FY 2018. The proposed FY 2018 hospice payment
update percentage of 1 percent is mandated by section 1814(i)(1)(C) of
the Act, as amended by section 411(d) of the MACRA.
The fifth column shows the effect of all the proposed changes on FY
2018 hospice payments. It is projected that aggregate payments will
increase by 1.0 percent, assuming hospices do not change their service
and billing practices in response.
As illustrated in Table 20, the combined effects of all the
proposals vary by specific types of providers and by location. For
example, due to the changes proposed in this rule, the estimated
impacts on FY 2018 payments range from a 0.9 percent decrease for
hospices providing care in the rural outlying region to a 1.7 percent
increase for hospices providing care in the urban Pacific region.
Table 20--Projected Impact to Hospices for FY 2018
----------------------------------------------------------------------------------------------------------------
Proposed FY
Number of Updated wage 2018 hospice FY 2018 total
providers data (%) payment change (%)
update (%)
(1) (2) (3) (4) (5)
----------------------------------------------------------------------------------------------------------------
All Hospices.................................... 4,295 0.0 1.0 1.0
Urban Hospices.................................. 3,323 0.0 1.0 1.0
Rural Hospices.................................. 972 0.1 1.0 1.1
Urban Hospices--New England..................... 134 -0.7 1.0 0.3
Urban Hospices--Middle Atlantic................. 249 0.1 1.0 1.1
Urban Hospices--South Atlantic.................. 429 -0.3 1.0 0.7
Urban Hospices--East North Central.............. 405 -0.1 1.0 0.9
Urban Hospices--East South Central.............. 159 0.0 1.0 1.0
Urban Hospices--West North Central.............. 229 -0.2 1.0 0.8
Urban Hospices--West South Central.............. 648 0.0 1.0 1.0
Urban Hospices--Mountain........................ 315 -0.1 1.0 0.9
Urban Hospices--Pacific......................... 716 0.7 1.0 1.7
Urban Hospices--Outlying........................ 39 -0.6 1.0 0.4
Rural Hospices--New England..................... 23 0.0 1.0 1.0
Rural Hospices--Middle Atlantic................. 40 0.6 1.0 1.6
Rural Hospices--South Atlantic.................. 134 0.1 1.0 1.1
Rural Hospices--East North Central.............. 140 0.2 1.0 1.2
Rural Hospices--East South Central.............. 124 -0.1 1.0 0.9
Rural Hospices--West North Central.............. 181 0.2 1.0 1.2
Rural Hospices--West South Central.............. 180 0.1 1.0 1.1
Rural Hospices--Mountain........................ 101 0.2 1.0 1.2
Rural Hospices--Pacific......................... 46 0.3 1.0 1.3
Rural Hospices--Outlying........................ 3 -1.9 1.0 -0.9
0--3,499 RHC Days (Small)....................... 960 0.2 1.0 1.2
3,500-19,999 RHC Days (Medium).................. 2,001 0.1 1.0 1.1
20,000+ RHC Days (Large)........................ 1,334 0.0 1.0 1.0
Non-Profit Ownership............................ 1,058 0.0 1.0 1.0
For Profit Ownership............................ 2,682 0.1 1.0 1.1
Government Ownership............................ 155 -0.3 1.0 0.7
Other Ownership................................. 400 -0.2 1.0 0.8
Freestanding Facility Type...................... 3,323 0.0 1.0 1.0
HHA/Facility-Based Facility Type................ 972 0.0 1.0 1.0
----------------------------------------------------------------------------------------------------------------
Source: FY 2016 hospice claims from the Chronic Condition Data Warehouse (CCW) Research Identifiable File (RIF)
in January 2017.
Region Key: New England=Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont; Middle
Atlantic=Pennsylvania, New Jersey, New York; South Atlantic=Delaware, District of Columbia, Florida, Georgia,
Maryland, North Carolina, South Carolina, Virginia, West Virginia; East North Central=Illinois, Indiana,
Michigan, Ohio, Wisconsin; East South Central=Alabama, Kentucky, Mississippi, Tennessee; West North
Central=Iowa, Kansas, Minnesota, Missouri, Nebraska, North Dakota, South Dakota; West South Central=Arkansas,
Louisiana, Oklahoma, Texas; Mountain=Arizona, Colorado, Idaho, Montana, Nevada, New Mexico, Utah, Wyoming;
Pacific=Alaska, California, Hawaii, Oregon, Washington; Outlying=Guam, Puerto Rico, Virgin Islands
[[Page 20792]]
E. Alternatives Considered
Since the hospice payment update percentage is determined based on
statutory requirements, we did not consider not updating hospice
payment rates by the payment update percentage. Payment rates since FY
2002 have been updated according to section 1814(i)(1)(C)(ii)(VII) of
the Act, which states that the update to the payment rates for
subsequent years must be the market basket percentage for that FY.
Section 3401(g) of the Affordable Care Act also mandates that, starting
with FY 2013 (and in subsequent years), the hospice payment update
percentage will be annually reduced by changes in economy-wide
productivity as specified in section 1886(b)(3)(B)(xi)(II) of the Act.
In addition, section 3401(g) of the Affordable Care Act mandates that
in FY 2013 through FY 2019, the hospice payment update percentage will
be reduced by an additional 0.3 percentage point (although for FY 2014
to FY 2019, the potential 0.3 percentage point reduction is subject to
suspension under conditions specified in section 1814(i)(1)(C)(v) of
the Act). For FY 2018, since the hospice payment update percentage is
determined based on statutory requirements at section 1814(i)(1)(C) of
the Act, as amended by section 411(d) of the MACRA, we cannot consider
not updating the hospice payment rates by the hospice payment update
percentage, nor can we consider updating the hospice payment rates by
the hospice payment update percentage absent the change to section
1814(i)(1)(C) as amended by MACRA.
F. Accounting Statement
As required by OMB Circular A-4 (available at https://www.whitehouse.gov/omb/circulars/a004/a-4.pdf), in Table 21, we have
prepared an accounting statement showing the classification of the
expenditures associated with the provisions of this proposed rule.
Table 21 provides our best estimate of the possible changes in Medicare
payments under the hospice benefit as a result of the policies in this
proposed rule. This estimate is based on the data for 4,295 hospices in
our impact analysis file, which was constructed using FY 2016 claims
available in January 2017. All expenditures are classified as transfers
to hospices.
Table 21--Accounting Statement: Classification of Estimated Transfers
and Costs, From FY 2017 to FY 2018
------------------------------------------------------------------------
Category Transfers
------------------------------------------------------------------------
Annualized Monetized Transfers......... $ 180 million.\*\
From Whom to Whom?..................... Federal Government to Medicare
Hospices.
------------------------------------------------------------------------
* The net increase of $180 million in transfer payments is a result of
the 1.0 percent hospice payment update compared to payments in FY
2017.
G. Reducing Regulation and Controlling Regulatory Costs
Executive Order 13771, titled ``Reducing Regulation and Controlling
Regulatory Costs,'' was issued on January 30, 2017 (82 FR 9339,
February 3, 2017). Section 2(a) of Executive Order 13771 requires an
agency, unless prohibited by law, to identify at least two existing
regulations to be repealed when the agency publicly proposes for notice
and comment, or otherwise promulgates, a new regulation. In furtherance
of this requirement, section 2(c) of Executive Order 13771 requires
that the new incremental costs associated with new regulations shall,
to the extent permitted by law, be offset by the elimination of
existing costs associated with at least two prior regulations. OMB's
implementation guidance, issued on April 5, 2017, explains that
``Federal spending regulatory actions that cause only income transfers
between taxpayers and program beneficiaries (for example, regulations
associated with . . . Medicare spending) are considered `transfer
rules' and are not covered by EO 13771. . . . However . . . such
regulatory actions may impose requirements apart from transfers . . .
In those cases, the actions would need to be offset to the extent they
impose more than de minimis costs. Examples of ancillary requirements
that may require offsets include new reporting or recordkeeping
requirements.'' It has been determined that this proposed rule is a
transfer rule that does not impose more than de minimis costs as
described above and thus is not a regulatory action for the purposes of
EO 13771.
H. Conclusion
We estimate that aggregate payments to hospices in FY 2018 would
increase by $180 million, or 1.0 percent, compared to payments in FY
2017. We estimate that in FY 2018, hospices in urban and rural areas
would experience, on average, 1.0 percent and 1.1 percent increases,
respectively, in estimated payments compared to FY 2017. Hospices
providing services in the urban Pacific and rural Middle Atlantic
regions would experience the largest estimated increases in payments of
1.7 percent and 1.6 percent, respectively. Hospices serving patients in
urban areas in the New England region would experience, on average, the
lowest estimated increase of 0.3 percent in FY 2018 payments.
In accordance with the provisions of Executive Order 12866, this
regulation was reviewed by the Office of Management and Budget.
Dated: April 12, 2017.
Seema Verma,
Administrator, Centers for Medicare & Medicaid Services.
Dated: April 17, 2017.
Thomas E. Price,
Secretary, Department of Health and Human Services.
[FR Doc. 2017-08563 Filed 4-27-17; 4:15 pm]
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