Medicare Program; Request for Information To Aid in the Design and Development of a Survey Regarding Patient and Family Member Experiences With Care Received in Long-Term Care Hospitals, 72722-72725 [2015-29622]
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tkelley on DSK3SPTVN1PROD with NOTICES
72722
Federal Register / Vol. 80, No. 224 / Friday, November 20, 2015 / Notices
Appendix I of the Auction 1000
Application Procedures Public Notice,
80 FR 66429, October 29, 2015. The
revision corrected information for a
small number of stations, and adjusts
population data for stations that are
affected by these corrections. The Task
Force also updated the constraint files
(https://data.fcc.gov/download/
incentive-auctions/Constraint_Files/)
that will be used in the repacking
process to reflect these corrections and
adjustments. The revised data will be
used to determine feasible channel
assignments for each station. These
revisions serve the Commission’s
statutory mandate to ‘‘make all
reasonable efforts’’ to preserve each
station’s coverage area and population
served. The revised Appendix I listing
is an attachment to the Auction 1001
Baseline Data PN and may be found on
the Auction 1001 Web page: https://
wireless.fcc.gov/auctions/incentiveauctions/auction-1001.html.
2. The Task Force also announced
revised reverse auction opening bid
prices in the Attachment to the Auction
1001 Baseline Data PN; these opening
bid prices may be found on the Auction
1001 Web page: https://wireless.fcc.gov/
auctions/incentive-auctions/auction1001.html. The opening bid prices were
recalculated to reflect the corrected
baseline and constraint files. The
opening bid prices were recalculated
using the formula adopted by the
Commission in the Auction 1000
Bidding Procedures PN, 80 FR 61918,
October 14, 2015.
3. In order to provide broadcasters
with at least 60 days after the release of
the recalculated prices to evaluate
whether to apply to voluntarily
participate in the reverse auction in
light of such prices, the Task Force
revised the filing window for FCC Form
177, the reverse auction application
form. Specifically, the FCC Form 177
filing window will open at 12:00 noon
Eastern Time on December 8, 2015, and
close at 6:00 p.m. Eastern Time on
January 12, 2016. Applications must be
filed prior to the closing of the filing
window.
4. Given the revised reverse auction
filing window, the Task Force revised
the filing window for FCC Form 175, the
forward auction application form.
Specifically, the FCC Form 175 filing
window will open at 12:00 noon Eastern
Time on January 26, 2016, and close at
6:00 p.m. Eastern Time on February 9,
2016. Applications must be filed prior
to the closing of the filing window.
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Federal Communications Commission.
William Huber,
Associate Chief, Auctions and Spectrum
Access Division, WTB.
[FR Doc. 2015–29792 Filed 11–19–15; 8:45 am]
BILLING CODE 6712–01–P
FEDERAL RESERVE SYSTEM
Change in Bank Control Notices;
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies;
Correction
This notice corrects a notice (80 FR
71801, FR Doc. 2015–29298) of the issue
for Tuesday, November 17, 2015.
Under the Federal Reserve Bank of
Atlanta heading, the entry for Donald
Joseph Leeper, Adairsville, Georgia, is
revised to read as follows:
1. Donald Joseph Leeper, Cartersville,
Georgia; to acquire voting shares of
NorthSide Bancshares, Inc., and thereby
indirectly acquire voting shares of
NorthSide Bank, both in Adairsville,
Georgia.
Comments on this application must
be received by December 2, 2015.
Board of Governors of the Federal Reserve
System, November 17, 2015.
Michael J. Lewandowski,
Associate Secretary of the Board.
[FR Doc. 2015–29678 Filed 11–19–15; 8:45 am]
BILLING CODE 6210–01–P
FEDERAL RESERVE SYSTEM
Change in Bank Control Notices;
Acquisitions of Shares of a Bank or
Bank Holding Company
The notificants listed below have
applied under the Change in Bank
Control Act (12 U.S.C. 1817(j)) and
§ 225.41 of the Board’s Regulation Y (12
CFR 225.41) to acquire shares of a bank
or bank holding company. The factors
that are considered in acting on the
notices are set forth in paragraph 7 of
the Act (12 U.S.C. 1817(j)(7)).
The notices are available for
immediate inspection at the Federal
Reserve Bank indicated. The notices
also will be available for inspection at
the offices of the Board of Governors.
Interested persons may express their
views in writing to the Reserve Bank
indicated for that notice or to the offices
of the Board of Governors. Comments
must be received not later than
December 7, 2015.
A. Federal Reserve Bank of Atlanta
(Chapelle Davis, Assistant Vice
President) 1000 Peachtree Street NE.,
Atlanta, Georgia 30309:
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Frm 00043
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1. Harbour FM, L.P., New York, New
York and its general partner, the Linda
S. Lucas 2015 Revocable Trust, New
York, New York (Co-trustees Linda S.
Lucas, Fort Myers, Florida; David H.
Lucas, Fort Myers, Florida; and Edward
G. Beimfohr, Bonita Springs, Florida); to
join the Lucas family control group,
which was previously approved on
January 13, 2015; David H. Lucas, and
The Amended and Restated Edward G.
Beimfohr Revocable Trust (Trustee
Edward G. Beimfohr); The Thomas A.
Lucas Trust, dated January 27, 2015
(Trustee Thomas Lucas, Laguna Niguel,
California); Michael Lucas, Las Vegas,
Nevada; The Connelly Living Trust,
dated March 12, 1998 (Trustee Gene
Connelly, Irvine, California); and
Rebecca Sanders, Fort Myers, Florida; to
acquire voting shares of FineMark
Holdings, Inc., and thereby indirectly
acquire voting shares of FineMark
National Bank & Trust, both in Fort
Myers, Florida.
B. Federal Reserve Bank of Kansas
City (Dennis Denney, Assistant Vice
President) 1 Memorial Drive, Kansas
City, Missouri 64198–0001:
1. Jennifer Whitham-Jensik, and
Jessica P. Frampton, both of Fredonia,
Kansas, as trustees of the Tyler F.
Whitham Irrevocable Trust and the
Jessica P. Frampton Irrevocable Trust,
both of Garden City, Kansas,
individually, to acquire additional
voting shares of Whitcorp Financial
Company, Leoti, Kansas, and thereby
indirectly acquire additional voting
shares of Western State Bank, Garden
City, Kansas, and Frontier Bank, Lamar,
Colorado.
Board of Governors of the Federal Reserve
System, November 17, 2015.
Michael J. Lewandowski,
Associate Secretary of the Board.
[FR Doc. 2015–29679 Filed 11–19–15; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3327–NC]
Medicare Program; Request for
Information To Aid in the Design and
Development of a Survey Regarding
Patient and Family Member
Experiences With Care Received in
Long-Term Care Hospitals
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Request for information.
AGENCY:
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Federal Register / Vol. 80, No. 224 / Friday, November 20, 2015 / Notices
This request for information
will aid in the design and development
of a survey regarding patient and family
member experiences with the care
received in long-term care hospitals
(LTCHs).
Comment Date: To be assured
consideration, comments must be
received at one of the addresses
provided below, no later than 5 p.m. on
January 19, 2016.
ADDRESSES: In commenting, refer to file
code CMS–3327–NC. 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–3327–NC, P.O. Box 8016,
Baltimore, MD 21244–8016.
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–3327–NC,
Mail Stop C4–26–05, 7500 Security
Boulevard, Baltimore, MD 21244–8016.
4. By hand or courier. Alternatively,
you may deliver (by hand or courier)
your written comments only to the
following addresses:
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 21244–8016.
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SUMMARY:
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If you intend to deliver your
comments to the Baltimore address, call
telephone number (410) 786–7195 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 FURTHER INFORMATION CONTACT:
Judith Harvilchuck, 410–786–3527.
SUPPLEMENTARY INFORMATION:
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.
I. Background
In accordance with section 3011 of
the Affordable Care Act, the Department
of Health and Human Services (HHS)
developed the National Quality Strategy
(NQS), which is led by the Agency for
Healthcare Research and Quality
(AHRQ), to create national aims and
priorities to guide local, state, and
national efforts to improve the quality of
health care (https://www.ahrq.gov/
workingforquality/). The NQS
established three aims supported by six
priorities.
The three aims are as follows:
• Better Care: Improve the overall
quality, by making health care more
patient-centered, reliable, accessible,
and safe.
• Healthy People/Healthy
Communities: Improve the health of the
U.S. population by supporting proven
interventions to address behavioral,
social, and environmental determinants
of health in addition to delivering
higher-quality care.
• Affordable Care: Reduce the cost of
quality health care for individuals,
families, employers, and government.
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The six priorities are: ‘‘(1) Making
care safer by reducing harm caused by
the delivery of care; (2) ensuring that
each person and family are engaged as
partners in their care; (3) promoting
effective communication and
coordination of care; (4) promoting the
most effective prevention and treatment
practices for the leading causes of
mortality, starting with cardiovascular
disease; (5) working with communities
to promote wide use of best practices to
enable healthy living; and (6) making
quality care more affordable for
individuals, families, employers, and
governments by developing and
spreading new health care delivery
models.’’
To support the collection of data that
can be used to pursue these aims and
progress on these priorities in the longterm care hospital (LTCH) setting, we
are developing a survey hereinafter
referred to as the ‘‘LTCH Patient and
Family Member Experience of Care
(PEC) Survey,’’ which supports the NQS
goal of Better Care and the priorities of:
• Ensuring that each person and
family are engaged as partners in their
care (priority #2); and
• Promoting effective communication
and coordination of care (priority #3).
We plan to collect this information in
support of the NQS and, under sections
1886(m)(5) and 1890A(e) of the Social
Security Act (the Act) and develop the
LTCH PEC Survey into a quality
measure that we may consider
proposing for adoption in the LTCH
Quality Reporting Program (QRP) (for
details on CMS’ measure development
process, please see the Blueprint at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/MMS/Measures
ManagementSystemBlueprint.html). We
will develop the CMS LTCH PEC in
accordance with Consumer Assessment
of Healthcare Providers and Systems
(CAHPS®) Survey Design Principles and
are developing this survey and plans to
submit the resulting instrument to
AHRQ for recognition as a CAHPS®
survey. CAHPS® Survey Design
Principles and implementation
instructions can be found at (https://
www.cahps.ahrq.gov/about-cahps/
principles/).
We have previously implemented a
number of nationwide patient
experience CAHPS® surveys in both inpatient and out-patient settings and for
different services. Specifically, we
implemented CAHPS® surveys for
Medicare health and drug plans,
inpatient hospitals, home health
agencies, in-center dialysis facilities,
hospices, and Accountable Care
Organizations, and recently developed a
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CAHPS® survey for outpatient and
ambulatory surgery centers; and we
have also begun development of an
Inpatient Rehabilitation Facility Patient
Experience of Care Survey. The planned
CMS LTCH PEC Survey differs from the
other CMS PEC surveys, because the
target population for the LTCH PEC
Survey consists of patients who have
complex and severe conditions and are
in need of critical care-related services
for an extended period of time.
Certified as acute-care hospitals,
LTCHs furnish care to beneficiaries who
need hospital-level care for relatively
extended periods. To qualify as an
LTCH for Medicare payment, a facility
must meet Medicare’s conditions of
participation for acute care hospitals,
and its Medicare patients generally must
have an average length of stay greater
than 25 days.1 LTCHs provide extended
medical and rehabilitative hospital-level
care to patients that are clinically
complex, or may suffer from multiple
acute or chronic conditions.2 3 Services
provided typically include: medical and
nursing care, critical care,
comprehensive rehabilitation, wound
care, respiratory therapy (for example,
ventilator support), head trauma
treatment, pain management, case
management, and social services.
We believe that the following aspects
of LTCH care would have to be taken
into account in the development of the
LTCH PEC survey, but we invite
comment on these considerations as
well as any potential omissions from
this list:
• Complexity and severity of illness
is marked for this population, resulting
in an average inpatient length of stay
greater than 25 days.
• Patient-centered goals/preferences
with a possible need to include family
as proxies for patients, since LTCH
patients are very ill and may not be the
best source of information for the
trajectory of their episode of LTCH care.
• Services are often critical care
based, due to the critical nature of the
illness or injury that requires such
hospitalization.
• Comprehensive array of services
and levels of care.
• Interdisciplinary team approach to
the delivery of care.
• A higher mortality rate exists
among this population compared with
other settings.
1 https://www.medpac.gov/documents/reports/
chapter-11-long-term-care-hospital-services-(march2013-report).pdf?sfvrsn=2.
2 https://www.cms.gov/Medicare/Medicare-Fee-forService-Payment/SNFPPS/post_acute_care_reform_
plan.html.
3 https://www.medicare.gov/Pubs/pdf/11347.pdf.
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• Consideration of post-LTCH care
and transitions to other possible care
settings.
Given the unique environment and
patient population of LTCH facilities,
we are exploring the level of adequacy
of existing patient experience of care
instruments for capturing LTCH care
experiences. Therefore, we are in the
process of reviewing potential topic
areas (as discussed in section II of this
RFI), as well as publicly available
instruments and measures, for the
purpose of developing a LTCH Survey
that will enable objective comparisons
of LTCH experiences across the country.
A rigorous, well-designed LTCH Survey
will allow us to understand patient
experiences throughout their LTCH
care, as reported by the patients
themselves, if possible, or by family
members. Should we ultimately adopt
the LTCH PEC Survey as a quality
measure in the LTCH QRP, public
reporting of data from the measure
could help consumers make more
informed decisions about LTCH
settings, as well as drive improvements
in the quality of LTCH care.
II. Solicitation of Information
We are soliciting the submission of
suggested topic areas such as
communication with providers,
mechanical ventilation, therapy
services, wound care, pain
management/control or non-pain
symptom management (including
offering of alternative non-opioid pain
management, discussion of safe storage
and proper disposal of opioids,
screening for overdose risk, and review
the history of substance use),
rehabilitation services, medical and
nursing care, interdisciplinary team goal
setting and care planning, family
training, and discharge planning. We are
also soliciting information on publicly
available instruments and measures that
can be used to capture patients’ or
family members’ experiences with
LTCH care in a variety of formats (for
example, standardized, computer
readable format) that can be collected by
providers or CAHPS® survey vendors.
We are interested in suggested topic
areas and the identification of publicly
available instruments that can measure
the quality of care from the patients’ or
family member’s perspective in LTCH
settings; instruments that can be used to
track changes over time; and items that
are developed for or can be modified to
address low case volume. Existing
instruments are preferred if they have
been tested, have been found to have a
high degree of reliability and validity, or
are in wide use already in the industry/
hospital settings, including those in
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rural and frontier communities.
Instruments capable of risk adjustment,
and/or instruments that minimize
duplication of efforts and/or that utilize
common quality measures, where
available, are preferred. Whenever
possible, preference will be given to
quality measures identified by the
Secretary under section 1139A or 1139B
of the Act, or endorsed under section
1890 of the Act.
The following information would be
especially helpful in any comments
responding to this request for
information:
• A brief cover letter summarizing the
information requested for submitted
instruments and topic areas,
respectively, and how the submitted
materials could be used to fulfill the
intent of the survey.
• (Optional) Information about the
person submitting the materials for the
purpose of allowing for follow-up
questions about the submission,
including the following:
++ Name.
++ Title.
++ Organization.
++ Mailing address.
++ Telephone number.
++ Email address.
• When submitting topic areas, we
encourage including, to the extent
available, the following information:
++ Detailed descriptions of the
suggested topic area(s) and specific
purpose(s).
++ Relevant peer-reviewed journal
articles or full citations.
• When submitting publicly available
instruments or survey questions, we
encourage including to the extent
available the following information:
++ Name of the instrument.
++ Indication that the instrument is
publicly available.
++ Copies of the full instrument in all
available languages.
++ Topic areas included in the
instrument.
++ Measures that can be derived from
data collected using the instrument.
++ Information regarding instrument
reliability (internal consistency, testretest, etc.) and validity (content,
construct, criterion related).
++ Results of cognitive testing (oneon-one testing with a small number of
respondents to ensure that they
understand the questionnaire.)
++ Results of field testing.
++ Current use of the instrument
(who is using it, for what it is being
used, with what population it is being
used, how instrument findings are
reported, and by whom the findings are
used).
++ Relevant peer-reviewed journal
articles or full citations.
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++ CAHPS® trademark status.
++ NQF endorsement status.
++ Survey administration
instructions.
++ Data analysis instructions.
++ Guidelines for reporting survey
data.
If you wish to provide comment on
this information collection, please
submit your comments as specified in
the ADDRESSES section of this request for
information.
Comments must be received on/by
January 19, 2016.
III. Collection of Information
Requirements
This RFI does not impose any
information collection requirements. We
believe it is a solicitation of comments
from the general public. As stated in the
implementing regulations of the
Paperwork Reduction Act of 1995 (PRA)
at 5 CFR 1320.3(h)(4), it is exempt from
the requirements of the PRA (44 U.S.C.
3501 et seq.) .
The data collected via this RFI will be
used to develop the LTCH PEC Survey.
While surveys are generally subject to
the requirements of the PRA, we believe
the LTCH PEC Survey is exempt.
Section I of this RFI explains that we
plan to collect this information in
support of the NQS and, under sections
1886(m)(5) and 1890A(e) of the the Act
and develop the LTCH PEC Survey into
a quality measure that we may consider
proposing for adoption in the LTCH
Quality Reporting Program (QRP). In
accordance with section 102 of the
Medicare Access and CHIP
Reauthorization Act of 2015 (MACRA)
(Pub. L. 114–110), the PRA shall not
apply to the collection of information
for the development of quality
measures.
Also, as stated earlier in section I. of
this RFI, we will develop the CMS
LTCH PEC Survey in accordance with
CAHPS® Survey Design Principles and
are developing this survey and plans to
submit the resulting instrument to
AHRQ for recognition as a CAHPS®
survey. Upon receiving recognition as a
CAHPS® survey and prior to
implementation, CMS will submit the
CAHPS recognized LTCH PEC Survey
through the OMB approval process. At
that time, the public will have the
opportunity to review, comment, or
review and comment on the proposed
information collection request prior to
its submission to OMB for review and
approval.
IV. Response to Comments
Because of the large number of public
comments we normally receive on
Federal Register documents, we are not
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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.
Dated: November 6, 2015.
Andrew M. Slavitt,
Acting Administrator, Centers for Medicare
& Medicaid Services.
[FR Doc. 2015–29622 Filed 11–19–15; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3328–NC]
Medicare Program; Request for
Information To Aid in the Design and
Development of a Survey Regarding
Patient and Family Member
Experiences With Care Received in
Inpatient Rehabilitation Facilities
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Request for information.
AGENCY:
This request for information
will aid in the design and development
of a survey regarding patient and family
member experiences with the care
received in inpatient rehabilitation
facilities (IRFs).
Comment Date: To be assured
consideration, comments must be
received at one of the addresses
provided below, no later than 5 p.m. on
January 19, 2016.
ADDRESSES: In commenting, refer to file
code CMS–3328–NC. 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–3328–NC, P.O. Box 8016,
Baltimore, MD 21244–8016.
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
SUMMARY:
PO 00000
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72725
following address only: Centers for
Medicare & Medicaid Services,
Department of Health and Human
Services, Attention: CMS–3328–NC,
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:
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) 786–7195 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 FURTHER INFORMATION CONTACT:
Judith Harvilchuck, Ph.D., 410–786–
3527.
SUPPLEMENTARY INFORMATION:
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
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Agencies
[Federal Register Volume 80, Number 224 (Friday, November 20, 2015)]
[Notices]
[Pages 72722-72725]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-29622]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-3327-NC]
Medicare Program; Request for Information To Aid in the Design
and Development of a Survey Regarding Patient and Family Member
Experiences With Care Received in Long-Term Care Hospitals
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Request for information.
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SUMMARY: This request for information will aid in the design and
development of a survey regarding patient and family member experiences
with the care received in long-term care hospitals (LTCHs).
Comment Date: To be assured consideration, comments must be
received at one of the addresses provided below, no later than 5 p.m.
on January 19, 2016.
ADDRESSES: In commenting, refer to file code CMS-3327-NC. 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-3327-NC, P.O. Box 8016,
Baltimore, MD 21244-8016.
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-3327-NC, Mail
Stop C4-26-05, 7500 Security Boulevard, Baltimore, MD 21244-8016.
4. By hand or courier. Alternatively, you may deliver (by hand or
courier) your written comments only to the following addresses:
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 21244-8016.
If you intend to deliver your comments to the Baltimore address,
call telephone number (410) 786-7195 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 FURTHER INFORMATION CONTACT: Judith Harvilchuck, 410-786-3527.
SUPPLEMENTARY INFORMATION:
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.
I. Background
In accordance with section 3011 of the Affordable Care Act, the
Department of Health and Human Services (HHS) developed the National
Quality Strategy (NQS), which is led by the Agency for Healthcare
Research and Quality (AHRQ), to create national aims and priorities to
guide local, state, and national efforts to improve the quality of
health care (https://www.ahrq.gov/workingforquality/). The NQS
established three aims supported by six priorities.
The three aims are as follows:
Better Care: Improve the overall quality, by making health
care more patient-centered, reliable, accessible, and safe.
Healthy People/Healthy Communities: Improve the health of
the U.S. population by supporting proven interventions to address
behavioral, social, and environmental determinants of health in
addition to delivering higher-quality care.
Affordable Care: Reduce the cost of quality health care
for individuals, families, employers, and government.
The six priorities are: ``(1) Making care safer by reducing harm
caused by the delivery of care; (2) ensuring that each person and
family are engaged as partners in their care; (3) promoting effective
communication and coordination of care; (4) promoting the most
effective prevention and treatment practices for the leading causes of
mortality, starting with cardiovascular disease; (5) working with
communities to promote wide use of best practices to enable healthy
living; and (6) making quality care more affordable for individuals,
families, employers, and governments by developing and spreading new
health care delivery models.''
To support the collection of data that can be used to pursue these
aims and progress on these priorities in the long-term care hospital
(LTCH) setting, we are developing a survey hereinafter referred to as
the ``LTCH Patient and Family Member Experience of Care (PEC) Survey,''
which supports the NQS goal of Better Care and the priorities of:
Ensuring that each person and family are engaged as
partners in their care (priority #2); and
Promoting effective communication and coordination of care
(priority #3).
We plan to collect this information in support of the NQS and,
under sections 1886(m)(5) and 1890A(e) of the Social Security Act (the
Act) and develop the LTCH PEC Survey into a quality measure that we may
consider proposing for adoption in the LTCH Quality Reporting Program
(QRP) (for details on CMS' measure development process, please see the
Blueprint at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/MMS/MeasuresManagementSystemBlueprint.html). We
will develop the CMS LTCH PEC in accordance with Consumer Assessment of
Healthcare Providers and Systems (CAHPS[supreg]) Survey Design
Principles and are developing this survey and plans to submit the
resulting instrument to AHRQ for recognition as a CAHPS[supreg] survey.
CAHPS[supreg] Survey Design Principles and implementation instructions
can be found at (https://www.cahps.ahrq.gov/about-cahps/principles/).
We have previously implemented a number of nationwide patient
experience CAHPS[supreg] surveys in both in-patient and out-patient
settings and for different services. Specifically, we implemented
CAHPS[supreg] surveys for Medicare health and drug plans, inpatient
hospitals, home health agencies, in-center dialysis facilities,
hospices, and Accountable Care Organizations, and recently developed a
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CAHPS[supreg] survey for outpatient and ambulatory surgery centers; and
we have also begun development of an Inpatient Rehabilitation Facility
Patient Experience of Care Survey. The planned CMS LTCH PEC Survey
differs from the other CMS PEC surveys, because the target population
for the LTCH PEC Survey consists of patients who have complex and
severe conditions and are in need of critical care-related services for
an extended period of time.
Certified as acute-care hospitals, LTCHs furnish care to
beneficiaries who need hospital-level care for relatively extended
periods. To qualify as an LTCH for Medicare payment, a facility must
meet Medicare's conditions of participation for acute care hospitals,
and its Medicare patients generally must have an average length of stay
greater than 25 days.\1\ LTCHs provide extended medical and
rehabilitative hospital-level care to patients that are clinically
complex, or may suffer from multiple acute or chronic
conditions.2 3 Services provided typically include: medical
and nursing care, critical care, comprehensive rehabilitation, wound
care, respiratory therapy (for example, ventilator support), head
trauma treatment, pain management, case management, and social
services.
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\1\ https://www.medpac.gov/documents/reports/chapter-11-long-term-care-hospital-services-(march-2013-report).pdf?sfvrsn=2.
\2\ https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/SNFPPS/post_acute_care_reform_plan.html.
\3\ https://www.medicare.gov/Pubs/pdf/11347.pdf.
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We believe that the following aspects of LTCH care would have to be
taken into account in the development of the LTCH PEC survey, but we
invite comment on these considerations as well as any potential
omissions from this list:
Complexity and severity of illness is marked for this
population, resulting in an average inpatient length of stay greater
than 25 days.
Patient-centered goals/preferences with a possible need to
include family as proxies for patients, since LTCH patients are very
ill and may not be the best source of information for the trajectory of
their episode of LTCH care.
Services are often critical care based, due to the
critical nature of the illness or injury that requires such
hospitalization.
Comprehensive array of services and levels of care.
Interdisciplinary team approach to the delivery of care.
A higher mortality rate exists among this population
compared with other settings.
Consideration of post-LTCH care and transitions to other
possible care settings.
Given the unique environment and patient population of LTCH
facilities, we are exploring the level of adequacy of existing patient
experience of care instruments for capturing LTCH care experiences.
Therefore, we are in the process of reviewing potential topic areas (as
discussed in section II of this RFI), as well as publicly available
instruments and measures, for the purpose of developing a LTCH Survey
that will enable objective comparisons of LTCH experiences across the
country. A rigorous, well-designed LTCH Survey will allow us to
understand patient experiences throughout their LTCH care, as reported
by the patients themselves, if possible, or by family members. Should
we ultimately adopt the LTCH PEC Survey as a quality measure in the
LTCH QRP, public reporting of data from the measure could help
consumers make more informed decisions about LTCH settings, as well as
drive improvements in the quality of LTCH care.
II. Solicitation of Information
We are soliciting the submission of suggested topic areas such as
communication with providers, mechanical ventilation, therapy services,
wound care, pain management/control or non-pain symptom management
(including offering of alternative non-opioid pain management,
discussion of safe storage and proper disposal of opioids, screening
for overdose risk, and review the history of substance use),
rehabilitation services, medical and nursing care, interdisciplinary
team goal setting and care planning, family training, and discharge
planning. We are also soliciting information on publicly available
instruments and measures that can be used to capture patients' or
family members' experiences with LTCH care in a variety of formats (for
example, standardized, computer readable format) that can be collected
by providers or CAHPS[supreg] survey vendors. We are interested in
suggested topic areas and the identification of publicly available
instruments that can measure the quality of care from the patients' or
family member's perspective in LTCH settings; instruments that can be
used to track changes over time; and items that are developed for or
can be modified to address low case volume. Existing instruments are
preferred if they have been tested, have been found to have a high
degree of reliability and validity, or are in wide use already in the
industry/hospital settings, including those in rural and frontier
communities. Instruments capable of risk adjustment, and/or instruments
that minimize duplication of efforts and/or that utilize common quality
measures, where available, are preferred. Whenever possible, preference
will be given to quality measures identified by the Secretary under
section 1139A or 1139B of the Act, or endorsed under section 1890 of
the Act.
The following information would be especially helpful in any
comments responding to this request for information:
A brief cover letter summarizing the information requested
for submitted instruments and topic areas, respectively, and how the
submitted materials could be used to fulfill the intent of the survey.
(Optional) Information about the person submitting the
materials for the purpose of allowing for follow-up questions about the
submission, including the following:
++ Name.
++ Title.
++ Organization.
++ Mailing address.
++ Telephone number.
++ Email address.
When submitting topic areas, we encourage including, to
the extent available, the following information:
++ Detailed descriptions of the suggested topic area(s) and
specific purpose(s).
++ Relevant peer-reviewed journal articles or full citations.
When submitting publicly available instruments or survey
questions, we encourage including to the extent available the following
information:
++ Name of the instrument.
++ Indication that the instrument is publicly available.
++ Copies of the full instrument in all available languages.
++ Topic areas included in the instrument.
++ Measures that can be derived from data collected using the
instrument.
++ Information regarding instrument reliability (internal
consistency, test-retest, etc.) and validity (content, construct,
criterion related).
++ Results of cognitive testing (one-on-one testing with a small
number of respondents to ensure that they understand the
questionnaire.)
++ Results of field testing.
++ Current use of the instrument (who is using it, for what it is
being used, with what population it is being used, how instrument
findings are reported, and by whom the findings are used).
++ Relevant peer-reviewed journal articles or full citations.
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++ CAHPS[supreg] trademark status.
++ NQF endorsement status.
++ Survey administration instructions.
++ Data analysis instructions.
++ Guidelines for reporting survey data.
If you wish to provide comment on this information collection,
please submit your comments as specified in the ADDRESSES section of
this request for information.
Comments must be received on/by January 19, 2016.
III. Collection of Information Requirements
This RFI does not impose any information collection requirements.
We believe it is a solicitation of comments from the general public. As
stated in the implementing regulations of the Paperwork Reduction Act
of 1995 (PRA) at 5 CFR 1320.3(h)(4), it is exempt from the requirements
of the PRA (44 U.S.C. 3501 et seq.) .
The data collected via this RFI will be used to develop the LTCH
PEC Survey. While surveys are generally subject to the requirements of
the PRA, we believe the LTCH PEC Survey is exempt. Section I of this
RFI explains that we plan to collect this information in support of the
NQS and, under sections 1886(m)(5) and 1890A(e) of the the Act and
develop the LTCH PEC Survey into a quality measure that we may consider
proposing for adoption in the LTCH Quality Reporting Program (QRP). In
accordance with section 102 of the Medicare Access and CHIP
Reauthorization Act of 2015 (MACRA) (Pub. L. 114-110), the PRA shall
not apply to the collection of information for the development of
quality measures.
Also, as stated earlier in section I. of this RFI, we will develop
the CMS LTCH PEC Survey in accordance with CAHPS[supreg] Survey Design
Principles and are developing this survey and plans to submit the
resulting instrument to AHRQ for recognition as a CAHPS[supreg] survey.
Upon receiving recognition as a CAHPS[supreg] survey and prior to
implementation, CMS will submit the CAHPS recognized LTCH PEC Survey
through the OMB approval process. At that time, the public will have
the opportunity to review, comment, or review and comment on the
proposed information collection request prior to its submission to OMB
for review and approval.
IV. 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.
Dated: November 6, 2015.
Andrew M. Slavitt,
Acting Administrator, Centers for Medicare & Medicaid Services.
[FR Doc. 2015-29622 Filed 11-19-15; 8:45 am]
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