Agency Information Collection Activities: Submission for OMB Review; Comment Request, 51569-51571 [2014-20589]
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Federal Register / Vol. 79, No. 168 / Friday, August 29, 2014 / Notices
• Do facilitators and barriers that
impact use vary by health care settings
and systems?
• Do facilitators and barriers that
impact use vary by IT system
characteristics?
KQ 8: What factors influence
sustainability of HIE?
PICOTS (Populations, Interventions,
Comparators, Outcomes, Timing,
Setting)
Populations
Any individual or group of health
care providers, patients, managers,
health care institutions, or regional
organizations.
Intervention
Heath Information Exchange (HIE).
HIE is defined as the electronic sharing
of clinical information among users
such as health care providers, patients,
administrators or policy makers across
the boundaries of health care
institutions, health data repositories,
States and others, typically not within a
single organization or among affiliated
providers, while protecting the integrity,
privacy, and security of the information.
Comparators
• Time period prior to HIE
implementation
• Locations (geographic or
organizational without HIE)
• Situations in which HIE is not
available, akin to ‘‘usual care’’ in a
clinical study
• Comparisons across types of HIE
• Comparisons of the characteristics
of the different settings, health care
system, and IT systems in which HIE is
used
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Outcomes (specified for each Key
Question)
KQ 1: Effectiveness is defined in
terms of clinical outcomes (e.g.,
mortality and morbidity), economic
outcomes (e.g., costs and resource use,
the value proposition for HIE) and
population outcomes (e.g., syndromic
surveillance for the identification of
trends or clusters).
KQ 2: Harms include unintended
negative consequence or adverse events
experienced by individuals, institutions,
or organizations. Harms from HIE may
include negative outcomes or the risk of
negative outcomes resulting from
information that is wrong, not provided
in a timely manner, or in formats that
inhibit its identification,
comprehension, and use. Harms also
may result from too much information
as well as lack of information. Harms
can also include negative impacts on
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attitudes (e.g., patients not trusting the
privacy will be protected, clinicians’
concerns about legal liability).
KQ 3: Intermediate outcomes include
outcomes such as provider and patient
experience and perceptions; changes in
provider behavior and health care
processes; and changes in the
availability, completeness, or accuracy
of information.
KQ 4: Level of use is the rate of HIE
use by individuals, health care
institutions, or regional organizations.
KQ 5: Usability focuses on the
function of the HIE in terms of the
interaction between users and HIE and
their ability to navigate and accomplish
tasks.
KQ 6: Implementation of HIE is
defined as the realization of an HIE
project such that the exchange of data is
operational.
KQ 7: Use is the incorporation of the
HIE into the workflow and decisions of
patients, providers or organizations.
KQ 8: Sustainability is long-term
maintenance, and improvement or
expansion of HIE, after the
implementation period.
Timing
No minimum duration of time lapsed
from implementation of HIE to the
measurement of outcomes.
Settings
Any aspect of the setting in which
health information is exchanged for the
purpose of improving health or health
care decisions that is hypothesized to
impact effectiveness, use, usability or
sustainability. This may include the
type(s) of clinical environments (e.g.,
ambulatory care, hospital, nursing
home, etc.), payment/reimbursement
model(s) (e.g., fee-for-service, managed
care setting, risk/value-based model
such as an accountable care
organization, etc.), and legislative
requirements (e.g., participation in HIE
required to participate in Medicaid).
Dated: August 20, 2014.
Richard Kronick,
AHRQ Director.
[FR Doc. 2014–20425 Filed 8–28–14; 8:45 am]
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51569
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10147, CMS–
2540–10, CMS–265–11, CMS–10106 and
CMS–10537]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
ACTION:
Notice.
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including any of the
following subjects: (1) The necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions; (2) the accuracy
of the estimated burden; (3) ways to
enhance the quality, utility, and clarity
of the information to be collected; and
(4) the use of automated collection
techniques or other forms of information
technology to minimize the information
collection burden.
DATES: Comments on the collection(s) of
information must be received by the
OMB desk officer by September 29,
2014.
SUMMARY:
When commenting on the
proposed information collections,
please reference the document identifier
or OMB control number. To be assured
consideration, comments and
recommendations must be received by
the OMB desk officer via one of the
following transmissions: OMB, Office of
Information and Regulatory Affairs,
Attention: CMS Desk Officer, Fax
Number: (202) 395–5806 or Email:
OIRA_submission@omb.eop.gov.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
https://www.cms.hhs.gov/
PaperworkReductionActof1995.
ADDRESSES:
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2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. The term ‘‘collection of
information’’ is defined in 44 U.S.C.
3502(3) and 5 CFR 1320.3(c) and
includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension or
reinstatement of an existing collection
of information, before submitting the
collection to OMB for approval. To
comply with this requirement, CMS is
publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Medicare
Prescription Drug Coverage and Your
Rights; Use: Through the delivery of this
standardized notice, Part D plan
sponsors’ network pharmacies are in the
best position to inform enrollees (at the
point of sale) about how to contact their
Part D plan if their prescription cannot
be filled and how to request an
exception to the Part D plan’s formulary.
The notice restates certain rights and
protections related to the enrollees
Medicare prescription drug benefits,
including the right to receive a written
explanation from the drug plan about
why a prescription drug is not covered.
Form Number: CMS–10147 (OMB
control number: 0938–0975); Frequency:
Occasionally; Affected Public: Private
sector—Business or other for-profits;
Number of Respondents: 56,000; Total
Annual Responses: 37,620,000; Total
Annual Hours: 626,749. (For policy
questions regarding this collection
contact Kathryn M. Smith at 410–786–
7623).
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Skilled Nursing
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Facility and Skilled Nursing Facility
Health Care Complex Cost Report; Use:
Providers of services participating in the
Medicare program are required under
sections 1815(a), 1833(e) and
1861(v)(1)(A) of the Social Security Act
(42 USC 1395g) to submit annual
information to achieve settlement of
costs for health care services rendered to
Medicare beneficiaries. In addition,
regulations at 42 CFR 413.20 and 413.24
require adequate cost data and cost
reports from providers on an annual
basis. Form CMS–2540–10 is used by
Skilled Nursing Facilities (SNFs) and
Skilled Nursing Facility Complexes
participating in the Medicare program to
report health care costs to determine the
amount of reimbursable costs for
services rendered to Medicare
beneficiaries.
Form Number: CMS–2540–10 (OMB
control number: 0938–0463); Frequency:
Yearly; Affected Public: Private Sector—
Business or other for-profits and Notfor-profit institutions; Number of
Respondents: 14,185; Total Annual
Responses: 14,185; Total Annual Hours:
2,865,370. (For policy questions
regarding this collection contact Amelia
Citerone at 410–786–3901.)
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Independent
Renal Dialysis Facility Cost Report and
Supporting Regulations; Use: Providers
of services participating in the Medicare
program are required under sections
1815(a) and 1861(v)(1)(A) of the Social
Security Act (42 U.S.C. 1395g) to submit
annual information to achieve
settlement of costs for health care
services rendered to Medicare
beneficiaries. In addition, regulations at
42 CFR 413.20 and 413.24 require
adequate cost data and cost reports from
providers on an annual basis. The Form
CMS–265–11 cost report is needed to
determine a provider’s reasonable costs
incurred in furnishing medical services
to Medicare beneficiaries.
Form Number: CMS–265–11 (OMB
control number: 0938–0263); Frequency:
Yearly; Affected Public: Private Sector—
Business or other for-profits and Notfor-profit institutions; Number of
Respondents: 5,677; Total Annual
Responses: 5,677; Total Annual Hours:
369,005. (For policy questions regarding
this collection contact Gail Duncan at
410–786–7278.)
4. Type of Information Collection
Request: Reinstatement without change
of a previously approved collection;
Title of Information Collection:
Medicare Authorization to Disclose
Personal Health Information; Use:
Unless permitted or required by law, the
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Health Insurance Portability and
Accountability Act (HIPAA) Privacy
Rule (§ 164.508) prohibits Medicare (a
HIPAA covered entity) from disclosing
an individual’s protected health
information without a valid
authorization. In order to be valid, an
authorization must include specified
core elements and statements. Medicare
will make available to Medicare
beneficiaries a standard, valid
authorization to enable beneficiaries to
request the disclosure of their protected
health information. This standard
authorization will simplify the process
of requesting information disclosure for
beneficiaries and minimize the response
time for Medicare. Form CMS–10106,
the Medicare Authorization to Disclose
Personal Health Information, will be
used by Medicare beneficiaries to
authorize Medicare to disclose their
protected health information to a third
party. Form Number: CMS–10106 (OMB
control number: 0938–0930); Frequency:
Occasionally; Affected Public:
Individuals or Households; Number of
Respondents: 1,298,329; Total Annual
Responses: 1,298,329; Total Annual
Hours: 324,582. (For policy questions
regarding this collection contact Sam
Jenkins at 410–786–3261.)
5. Type of Information Collection
Request: New collection (Request for a
new control number); Title of
Information Collection: National
Implementation of the Hospice
Experience of Care Survey (CAHPs
Hospice Survey); Use: We are requesting
a three-year clearance from the Office of
Management and Budget (OMB) under
the Paperwork Reduction Act of 1995 to
implement the Hospice Experience of
Care Survey (HECS), also called the
Consumer Assessment of Healthcare
Providers and Systems (CAHPS®)
Hospice Survey, and to conduct an
assessment of the effects of survey
administration mode. Under Contract
Number HHSM–500–2014–00350G, the
project team will implement and
analyze a hospice experience of care
survey for primary caregivers (i.e.,
bereaved family members or close
friends) of patients who died while
receiving hospice care (‘‘decedents’’).
Specifically, we will: (1) Implement a
survey to collect data on experiences of
hospice care, and (2) conduct an
experiment to examine effects of survey
mode (i.e., mail-only, telephone-only,
and mail with telephone follow-up).
This survey supports the National
Quality Strategy developed by the U.S.
Department of Health and Human
Services (HHS) that was called for under
the Affordable Care Act to create
national aims and priorities to guide
local, state, and national efforts to
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improve the quality of health care. This
strategy has established six priorities
that support a three-part aim focusing
on better care, better health, and lower
costs through improvement. The six
priorities include: Making care safer by
reducing harm caused by the delivery of
care; ensuring that each person and
family are engaged as partners in their
care; promoting effective
communication and coordination of
care; promoting the most effective
prevention and treatment practices for
the leading causes of mortality, starting
with cardiovascular disease; working
with communities to promote wide use
of best practices to enable healthy
living; and making quality care more
affordable for individuals, families,
employers, and governments by
developing and spreading new health
care delivery models. Because the
hospice survey focuses on experiences
of care, implementation of the survey
supports the following national
priorities for improving care: Engaging
patients and families in care and
promoting effective communication and
coordination. In addition, national
implementation and public reporting of
hospice survey results will provide data
on experiences with hospice care that
enable consumers to make meaningful
comparisons between hospices across
the nation.
Form Number: CMS–10537 (OMB
control number: 0938–New); Frequency:
Occasionally; Affected Public:
Individuals or Households; Number of
Respondents: 561,026; Total Annual
Responses: 561,026; Total Annual
Hours: 98,179.55. (For policy questions
regarding this collection contact Lori
Teichman at 410–786–6684.)
Dated: August 26, 2014.
Martique Jones,
Deputy Director, Regulations Development
Group, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2014–20589 Filed 8–28–14; 8:45 am]
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HUMAN SERVICES
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Centers for Medicare & Medicaid
Services
[Document Identifier CMS–10536]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
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The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
any of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
SUMMARY:
Comments must be received by
October 28, 2014.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number (OCN). To be
assured consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Numberlllll, Room C4–
26–05, 7500 Security Boulevard,
Baltimore, Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
https://www.cms.hhs.gov/
PaperworkReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
DATES:
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51571
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10536 Medicaid Eligibility and
Enrollment (EE) Implementation
Advanced Planning Document (IAPD)
Template
Under the PRA (44 U.S.C. 3501–
3520), federal agencies must obtain
approval from the Office of Management
and Budget (OMB) for each collection of
information they conduct or sponsor.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection
Request: New collection (request for a
new OMB Control Number); Title of
Information Collection: Medicaid
Eligibility and Enrollment (EE)
Implementation Advanced Planning
Document (IAPD) Template; Use: To
assess the appropriateness of states’
requests for enhanced federal financial
participation for expenditures related to
Medicaid eligibility determination
systems, we will review the submitted
information and documentation to make
an approval determination for the
advanced planning document.
Form Number: CMS–10536 (OMB
control number: 0938-New); Frequency:
Yearly, once, and occasionally; Affected
Public: State, Local, or Tribal
Governments; Number of Respondents:
56; Total Annual Responses: 168; Total
Annual Hours: 1,344. (For policy
questions regarding this collection
contact Christine Gerhardt at 410–786–
0693).
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Agencies
[Federal Register Volume 79, Number 168 (Friday, August 29, 2014)]
[Notices]
[Pages 51569-51571]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-20589]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10147, CMS-2540-10, CMS-265-11, CMS-10106 and
CMS-10537]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. Under the Paperwork Reduction
Act of 1995 (PRA), federal agencies are required to publish notice in
the Federal Register concerning each proposed collection of
information, including each proposed extension or reinstatement of an
existing collection of information, and to allow a second opportunity
for public comment on the notice. Interested persons are invited to
send comments regarding the burden estimate or any other aspect of this
collection of information, including any of the following subjects: (1)
The necessity and utility of the proposed information collection for
the proper performance of the agency's functions; (2) the accuracy of
the estimated burden; (3) ways to enhance the quality, utility, and
clarity of the information to be collected; and (4) the use of
automated collection techniques or other forms of information
technology to minimize the information collection burden.
DATES: Comments on the collection(s) of information must be received by
the OMB desk officer by September 29, 2014.
ADDRESSES: When commenting on the proposed information collections,
please reference the document identifier or OMB control number. To be
assured consideration, comments and recommendations must be received by
the OMB desk officer via one of the following transmissions: OMB,
Office of Information and Regulatory Affairs, Attention: CMS Desk
Officer, Fax Number: (202) 395-5806 or Email:
OIRAsubmission@omb.eop.gov.
To obtain copies of a supporting statement and any related forms
for the proposed collection(s) summarized in this notice, you may make
your request using one of following:
1. Access CMS' Web site address at https://www.cms.hhs.gov/PaperworkReductionActof1995.
[[Page 51570]]
2. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at (410) 786-1326.
FOR FURTHER INFORMATION CONTACT: Reports Clearance Office at (410) 786-
1326.
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. The term ``collection of
information'' is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and
includes agency requests or requirements that members of the public
submit reports, keep records, or provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires
federal agencies to publish a 30-day notice in the Federal Register
concerning each proposed collection of information, including each
proposed extension or reinstatement of an existing collection of
information, before submitting the collection to OMB for approval. To
comply with this requirement, CMS is publishing this notice that
summarizes the following proposed collection(s) of information for
public comment:
1. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Medicare
Prescription Drug Coverage and Your Rights; Use: Through the delivery
of this standardized notice, Part D plan sponsors' network pharmacies
are in the best position to inform enrollees (at the point of sale)
about how to contact their Part D plan if their prescription cannot be
filled and how to request an exception to the Part D plan's formulary.
The notice restates certain rights and protections related to the
enrollees Medicare prescription drug benefits, including the right to
receive a written explanation from the drug plan about why a
prescription drug is not covered.
Form Number: CMS-10147 (OMB control number: 0938-0975); Frequency:
Occasionally; Affected Public: Private sector--Business or other for-
profits; Number of Respondents: 56,000; Total Annual Responses:
37,620,000; Total Annual Hours: 626,749. (For policy questions
regarding this collection contact Kathryn M. Smith at 410-786-7623).
2. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Skilled Nursing
Facility and Skilled Nursing Facility Health Care Complex Cost Report;
Use: Providers of services participating in the Medicare program are
required under sections 1815(a), 1833(e) and 1861(v)(1)(A) of the
Social Security Act (42 USC 1395g) to submit annual information to
achieve settlement of costs for health care services rendered to
Medicare beneficiaries. In addition, regulations at 42 CFR 413.20 and
413.24 require adequate cost data and cost reports from providers on an
annual basis. Form CMS-2540-10 is used by Skilled Nursing Facilities
(SNFs) and Skilled Nursing Facility Complexes participating in the
Medicare program to report health care costs to determine the amount of
reimbursable costs for services rendered to Medicare beneficiaries.
Form Number: CMS-2540-10 (OMB control number: 0938-0463);
Frequency: Yearly; Affected Public: Private Sector--Business or other
for-profits and Not-for-profit institutions; Number of Respondents:
14,185; Total Annual Responses: 14,185; Total Annual Hours: 2,865,370.
(For policy questions regarding this collection contact Amelia Citerone
at 410-786-3901.)
3. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Independent Renal
Dialysis Facility Cost Report and Supporting Regulations; Use:
Providers of services participating in the Medicare program are
required under sections 1815(a) and 1861(v)(1)(A) of the Social
Security Act (42 U.S.C. 1395g) to submit annual information to achieve
settlement of costs for health care services rendered to Medicare
beneficiaries. In addition, regulations at 42 CFR 413.20 and 413.24
require adequate cost data and cost reports from providers on an annual
basis. The Form CMS-265-11 cost report is needed to determine a
provider's reasonable costs incurred in furnishing medical services to
Medicare beneficiaries.
Form Number: CMS-265-11 (OMB control number: 0938-0263); Frequency:
Yearly; Affected Public: Private Sector--Business or other for-profits
and Not-for-profit institutions; Number of Respondents: 5,677; Total
Annual Responses: 5,677; Total Annual Hours: 369,005. (For policy
questions regarding this collection contact Gail Duncan at 410-786-
7278.)
4. Type of Information Collection Request: Reinstatement without
change of a previously approved collection; Title of Information
Collection: Medicare Authorization to Disclose Personal Health
Information; Use: Unless permitted or required by law, the Health
Insurance Portability and Accountability Act (HIPAA) Privacy Rule
(Sec. 164.508) prohibits Medicare (a HIPAA covered entity) from
disclosing an individual's protected health information without a valid
authorization. In order to be valid, an authorization must include
specified core elements and statements. Medicare will make available to
Medicare beneficiaries a standard, valid authorization to enable
beneficiaries to request the disclosure of their protected health
information. This standard authorization will simplify the process of
requesting information disclosure for beneficiaries and minimize the
response time for Medicare. Form CMS-10106, the Medicare Authorization
to Disclose Personal Health Information, will be used by Medicare
beneficiaries to authorize Medicare to disclose their protected health
information to a third party. Form Number: CMS-10106 (OMB control
number: 0938-0930); Frequency: Occasionally; Affected Public:
Individuals or Households; Number of Respondents: 1,298,329; Total
Annual Responses: 1,298,329; Total Annual Hours: 324,582. (For policy
questions regarding this collection contact Sam Jenkins at 410-786-
3261.)
5. Type of Information Collection Request: New collection (Request
for a new control number); Title of Information Collection: National
Implementation of the Hospice Experience of Care Survey (CAHPs Hospice
Survey); Use: We are requesting a three-year clearance from the Office
of Management and Budget (OMB) under the Paperwork Reduction Act of
1995 to implement the Hospice Experience of Care Survey (HECS), also
called the Consumer Assessment of Healthcare Providers and Systems
(CAHPS[supreg]) Hospice Survey, and to conduct an assessment of the
effects of survey administration mode. Under Contract Number HHSM-500-
2014-00350G, the project team will implement and analyze a hospice
experience of care survey for primary caregivers (i.e., bereaved family
members or close friends) of patients who died while receiving hospice
care (``decedents''). Specifically, we will: (1) Implement a survey to
collect data on experiences of hospice care, and (2) conduct an
experiment to examine effects of survey mode (i.e., mail-only,
telephone-only, and mail with telephone follow-up).
This survey supports the National Quality Strategy developed by the
U.S. Department of Health and Human Services (HHS) that was called for
under the Affordable Care Act to create national aims and priorities to
guide local, state, and national efforts to
[[Page 51571]]
improve the quality of health care. This strategy has established six
priorities that support a three-part aim focusing on better care,
better health, and lower costs through improvement. The six priorities
include: Making care safer by reducing harm caused by the delivery of
care; ensuring that each person and family are engaged as partners in
their care; promoting effective communication and coordination of care;
promoting the most effective prevention and treatment practices for the
leading causes of mortality, starting with cardiovascular disease;
working with communities to promote wide use of best practices to
enable healthy living; and making quality care more affordable for
individuals, families, employers, and governments by developing and
spreading new health care delivery models. Because the hospice survey
focuses on experiences of care, implementation of the survey supports
the following national priorities for improving care: Engaging patients
and families in care and promoting effective communication and
coordination. In addition, national implementation and public reporting
of hospice survey results will provide data on experiences with hospice
care that enable consumers to make meaningful comparisons between
hospices across the nation.
Form Number: CMS-10537 (OMB control number: 0938-New); Frequency:
Occasionally; Affected Public: Individuals or Households; Number of
Respondents: 561,026; Total Annual Responses: 561,026; Total Annual
Hours: 98,179.55. (For policy questions regarding this collection
contact Lori Teichman at 410-786-6684.)
Dated: August 26, 2014.
Martique Jones,
Deputy Director, Regulations Development Group, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2014-20589 Filed 8-28-14; 8:45 am]
BILLING CODE 4120-01-P