Public Comment Period Extended for Strategies To Improve Patient Safety: Draft Report to Congress for Public Comment and Review by the National Academy of Medicine, 14752-14753 [2021-05605]
Download as PDF
14752
Federal Register / Vol. 86, No. 51 / Thursday, March 18, 2021 / Notices
by a system of records, FCC/WTB–1,
‘‘Wireless Services Licensing Records’’,
and these and all other records may be
disclosed pursuant to the Routine Uses
as stated in the SORN.
Needs and Uses: The information
collected is necessary to require owners
of marine VHF radios with Digital
Selective Calling (DSC) capability to
register information such as the name,
address, type of vessel with a private
entity issuing marine mobile service
identities (MMSI). The information
would be used by search and rescue
personnel to identify vessels in distress
and to select the proper rescue units and
search methods.
The requirement to collect this
information is contained in
international agreements with the U.S.
Coast Guard and private sector entities
that issue MMSI’s.
The information is used by private
entities to maintain a database used to
provide information about the vessel
owner in distress using marine VHF
radios with DSC capability. If the data
were not collected, the U.S. Coast Guard
would not have access to this
information which would increase the
time and effort needed to complete a
search and rescue operation.
Federal Communications Commission.
Cecilia Sigmund,
Federal Register Liaison Officer.
[FR Doc. 2021–05563 Filed 3–17–21; 8:45 am]
BILLING CODE 6712–01–P
FEDERAL ELECTION COMMISSION
Sunshine Act Meeting
Tuesday, March 23, 2021
at 10:00 a.m. and its continuation at the
conclusion of the open meeting on
March 25, 2021.
TIME AND DATE:
1050 First Street NE,
Washington, DC. (This meeting will be
a virtual meeting).
PLACE:
This meeting will be closed to
the public.
STATUS:
jbell on DSKJLSW7X2PROD with NOTICES
MATTERS TO BE CONSIDERED:
Compliance matters pursuant to 52
U.S.C. 30109.
Information the premature disclosure
of which would be likely to have a
considerable adverse effect on the
implementation of a proposed
Commission action.
Matters concerning participation in
civil actions or proceedings or
arbitration.
*
*
*
*
*
VerDate Sep<11>2014
16:49 Mar 17, 2021
Jkt 253001
CONTACT PERSON FOR MORE INFORMATION:
Judith Ingram, Press Officer, Telephone:
(202) 694–1220.
Vicktoria J. Allen,
Acting Deputy Secretary of the Commission.
[FR Doc. 2021–05816 Filed 3–16–21; 4:15 pm]
BILLING CODE 6715–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Public Comment Period Extended for
Strategies To Improve Patient Safety:
Draft Report to Congress for Public
Comment and Review by the National
Academy of Medicine
Agency for Healthcare Research
and Quality (AHRQ), Department of
Health and Human Services (HHS).
AGENCY:
ACTION:
Notice of extension in comment
period.
As required by the Patient
Safety and Quality Improvement Act of
2005 (Patient Safety Act), the Secretary
of HHS (the Secretary) is making this
draft report on effective strategies for
reducing medical errors and increasing
patient safety available to the public for
review and comment. Through this
notice the comment period is extended.
The subject matter content remains
unchanged from the original notice
which was published on December 16,
2020 (https://www.federalregister.gov/
documents/2020/12/16/2020-27589/
notice-of-opportunity-to-comment-onstrategies-to-improve-patient-safetydraft-report-to-congress).
SUMMARY:
Submit comments on or before
April 5, 2021.
DATES:
The draft report, Strategies
to Improve Patient Safety: Draft Report
to Congress for Public Comment and
Review by the National Academy of
Medicine, can be accessed electronically
at the following HHS website: https://
pso.ahrq.gov/legislation/act. Comments
on the draft report must be submitted by
email to PSQIA.RC@ahrq.hhs.gov.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Paula DiStabile, Patient Safety
Organization Division, Center for
Quality Improvement and Patient
Safety, AHRQ; telephone (toll free):
(866) 403–3697; telephone (local): (301)
427–1111; TTY (toll free): (866) 438–
7231; TTY (local): (301) 427–1130;
email: PSQIA.RC@ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00033
Fmt 4703
Sfmt 4703
Background
The Secretary, in consultation with
the Director of AHRQ, has prepared a
draft report on effective strategies for
reducing medical errors and increasing
patient safety as required by the Patient
Safety Act. The report includes
measures determined appropriate by the
Secretary to encourage the appropriate
use of such strategies, including use in
any federally funded programs. The
draft report is now available for public
comment and has been submitted to the
National Academy of Medicine for
review. The final report is required to be
submitted to Congress no later than
December 21, 2021. The specific
provision describing these requirements
can be found at 42 U.S.C. 299b–22(j).
The Patient Safety Act created a
framework for the development of a
voluntary patient safety event reporting
system to advance patient safety and
quality of care across the Nation.
Without limiting patients’ rights to their
medical information, the law created
Federal legal privilege and
confidentiality protections for patient
safety work product; that is, information
exchanged between healthcare
providers and organizations listed by
the Secretary that specialize in patient
safety and quality improvement, called
patient safety organizations (PSOs). The
law charged PSOs with analyzing and
using this information to provide
feedback and assistance to help
providers minimize patient risk and
improve the safety and quality of their
care. More information about the Patient
Safety Act, its implementing regulation,
and PSOs can be found at https://
pso.ahrq.gov/.
In addition to creating a protected
legal environment where healthcare
providers can share information and
learning for improvement purposes
beyond organizational and State
boundaries, Congress also envisioned
and created the potential for aggregating
and analyzing patient safety data on a
national scale. This part of the Patient
Safety Act, the network of patient safety
databases (NPSD), is a mechanism that
can leverage data contributed by
individual healthcare providers and
PSOs across the United States into a
valuable national resource for
improving patient safety. Congress
required the draft report that is the
subject of this Notice to be made
available for public comment and
submitted to the Institute of Medicine
(now the National Academy of
Medicine) no later than 18 months after
the NPSD became operational. The
NPSD became operational on June 21,
2019. More information about the NPSD
E:\FR\FM\18MRN1.SGM
18MRN1
Federal Register / Vol. 86, No. 51 / Thursday, March 18, 2021 / Notices
jbell on DSKJLSW7X2PROD with NOTICES
can be found at https://www.ahrq.gov/
npsd/.
Overview of the Draft Report
The draft report contains three
chapters. It begins with an overview of
the impetus for and objectives of the
Patient Safety Act, its key provisions,
and some milestones in its
implementation. Chapter 2 reviews
some of the principles and concepts
underlying effective patient safety
improvement, provides an overview of
research and measurement in patient
safety, and presents the strategies and
practices for reducing medical errors
and increasing patient safety reviewed
in AHRQ’s Making Healthcare Safer
reports, published in 2001, 2013, and
2020. Together, these reports reviewed
the existing evidence for the
effectiveness of more than 100 patient
safety strategies and practices used in
hospitals, primary care practices, longterm care facilities, and other healthcare
settings. They include cross-cutting
strategies and topics such as patient and
family engagement and teamwork
training; safety topics specific to
particular clinical interventions, such as
medications and surgery; a variety of
tools and processes, such as rapid
response teams and antimicrobial
stewardship; and practices that target
prevention of specific harms, such as
healthcare-associated infections and
pressure injuries. Hyperlinks in the
draft report lead to the full text of the
evidence review and to later updates
regarding the assessment of evidence for
the effectiveness for each strategy and
practice. The final chapter in the draft
report begins with an overview of
learning health systems and concepts
underlying effective implementation of
patient safety strategies. It provides
examples of resources Federal agencies
make available to encourage healthcare
providers to use effective patient safety
strategies and describes ‘‘Safer Together:
A National Action Plan to Advance
Patient Safety,’’ recently released by the
National Steering Committee for Patient
Safety that was convened by the
Institute for Healthcare Improvement.
The draft report concludes by describing
an approach that has a track record of
success in encouraging providers to use
effective practices to improve patient
safety and outlines measures that could
accelerate progress in improving patient
safety and encouraging the use of
effective patient safety improvement
strategies.
Where To View the Draft Report and
How To Submit Comments
The draft report is posted on the
AHRQ PSO Program website at https://
VerDate Sep<11>2014
16:49 Mar 17, 2021
Jkt 253001
pso.ahrq.gov/legislation/act. The
website contains a link to the email
address for submitting comments on the
draft report, which is PSQIA.RC@
ahrq.hhs.gov.
Dated: March 15, 2021.
Marquita Cullom,
Associate Director.
[FR Doc. 2021–05605 Filed 3–17–21; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10198]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
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 the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
the estimated burden, ways to enhance
the quality, utility, and clarity of the
information to be collected, and the use
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
SUMMARY:
Comments on the collection(s) of
information must be received by the
OMB desk officer by April 19, 2021.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
DATES:
PO 00000
Frm 00034
Fmt 4703
Sfmt 4703
14753
for Public Comments’’ or by using the
search function.
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’ website address at:
https://www.cms.gov/Regulations-andGuidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
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: Creditable
Coverage Disclosure to CMS On-Line
Form and Instructions; Use: Section
1860D–13 of the Social Security Act, as
established by the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA) and
implementing regulations at 42 CFR
423.56(e), require that entities that offer
prescription drug benefits under any of
the types of coverage described in 42
CFR 423.56(b) provide a disclosure of
creditable coverage to CMS.
There are other disclosure and
notification requirements to Part D
eligible individuals in § 423.56(c), (d),
and (f); this PRA covers the requirement
in subsection (e). Entities required to
make this disclosure state whether their
prescription drug coverage meets the
actuarial requirements defined in
§ 423.56(a). Most entities that currently
provide prescription drug benefits to
any Medicare Part D eligible individual
must disclose whether their prescription
E:\FR\FM\18MRN1.SGM
18MRN1
Agencies
[Federal Register Volume 86, Number 51 (Thursday, March 18, 2021)]
[Notices]
[Pages 14752-14753]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-05605]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Public Comment Period Extended for Strategies To Improve Patient
Safety: Draft Report to Congress for Public Comment and Review by the
National Academy of Medicine
AGENCY: Agency for Healthcare Research and Quality (AHRQ), Department
of Health and Human Services (HHS).
ACTION: Notice of extension in comment period.
-----------------------------------------------------------------------
SUMMARY: As required by the Patient Safety and Quality Improvement Act
of 2005 (Patient Safety Act), the Secretary of HHS (the Secretary) is
making this draft report on effective strategies for reducing medical
errors and increasing patient safety available to the public for review
and comment. Through this notice the comment period is extended. The
subject matter content remains unchanged from the original notice which
was published on December 16, 2020 (https://www.federalregister.gov/documents/2020/12/16/2020-27589/notice-of-opportunity-to-comment-on-strategies-to-improve-patient-safety-draft-report-to-congress).
DATES: Submit comments on or before April 5, 2021.
ADDRESSES: The draft report, Strategies to Improve Patient Safety:
Draft Report to Congress for Public Comment and Review by the National
Academy of Medicine, can be accessed electronically at the following
HHS website: https://pso.ahrq.gov/legislation/act. Comments on the
draft report must be submitted by email to [email protected].
FOR FURTHER INFORMATION CONTACT: Paula DiStabile, Patient Safety
Organization Division, Center for Quality Improvement and Patient
Safety, AHRQ; telephone (toll free): (866) 403-3697; telephone (local):
(301) 427-1111; TTY (toll free): (866) 438-7231; TTY (local): (301)
427-1130; email: [email protected].
SUPPLEMENTARY INFORMATION:
Background
The Secretary, in consultation with the Director of AHRQ, has
prepared a draft report on effective strategies for reducing medical
errors and increasing patient safety as required by the Patient Safety
Act. The report includes measures determined appropriate by the
Secretary to encourage the appropriate use of such strategies,
including use in any federally funded programs. The draft report is now
available for public comment and has been submitted to the National
Academy of Medicine for review. The final report is required to be
submitted to Congress no later than December 21, 2021. The specific
provision describing these requirements can be found at 42 U.S.C. 299b-
22(j).
The Patient Safety Act created a framework for the development of a
voluntary patient safety event reporting system to advance patient
safety and quality of care across the Nation. Without limiting
patients' rights to their medical information, the law created Federal
legal privilege and confidentiality protections for patient safety work
product; that is, information exchanged between healthcare providers
and organizations listed by the Secretary that specialize in patient
safety and quality improvement, called patient safety organizations
(PSOs). The law charged PSOs with analyzing and using this information
to provide feedback and assistance to help providers minimize patient
risk and improve the safety and quality of their care. More information
about the Patient Safety Act, its implementing regulation, and PSOs can
be found at https://pso.ahrq.gov/.
In addition to creating a protected legal environment where
healthcare providers can share information and learning for improvement
purposes beyond organizational and State boundaries, Congress also
envisioned and created the potential for aggregating and analyzing
patient safety data on a national scale. This part of the Patient
Safety Act, the network of patient safety databases (NPSD), is a
mechanism that can leverage data contributed by individual healthcare
providers and PSOs across the United States into a valuable national
resource for improving patient safety. Congress required the draft
report that is the subject of this Notice to be made available for
public comment and submitted to the Institute of Medicine (now the
National Academy of Medicine) no later than 18 months after the NPSD
became operational. The NPSD became operational on June 21, 2019. More
information about the NPSD
[[Page 14753]]
can be found at https://www.ahrq.gov/npsd/.
Overview of the Draft Report
The draft report contains three chapters. It begins with an
overview of the impetus for and objectives of the Patient Safety Act,
its key provisions, and some milestones in its implementation. Chapter
2 reviews some of the principles and concepts underlying effective
patient safety improvement, provides an overview of research and
measurement in patient safety, and presents the strategies and
practices for reducing medical errors and increasing patient safety
reviewed in AHRQ's Making Healthcare Safer reports, published in 2001,
2013, and 2020. Together, these reports reviewed the existing evidence
for the effectiveness of more than 100 patient safety strategies and
practices used in hospitals, primary care practices, long-term care
facilities, and other healthcare settings. They include cross-cutting
strategies and topics such as patient and family engagement and
teamwork training; safety topics specific to particular clinical
interventions, such as medications and surgery; a variety of tools and
processes, such as rapid response teams and antimicrobial stewardship;
and practices that target prevention of specific harms, such as
healthcare-associated infections and pressure injuries. Hyperlinks in
the draft report lead to the full text of the evidence review and to
later updates regarding the assessment of evidence for the
effectiveness for each strategy and practice. The final chapter in the
draft report begins with an overview of learning health systems and
concepts underlying effective implementation of patient safety
strategies. It provides examples of resources Federal agencies make
available to encourage healthcare providers to use effective patient
safety strategies and describes ``Safer Together: A National Action
Plan to Advance Patient Safety,'' recently released by the National
Steering Committee for Patient Safety that was convened by the
Institute for Healthcare Improvement. The draft report concludes by
describing an approach that has a track record of success in
encouraging providers to use effective practices to improve patient
safety and outlines measures that could accelerate progress in
improving patient safety and encouraging the use of effective patient
safety improvement strategies.
Where To View the Draft Report and How To Submit Comments
The draft report is posted on the AHRQ PSO Program website at
https://pso.ahrq.gov/legislation/act. The website contains a link to
the email address for submitting comments on the draft report, which is
[email protected].
Dated: March 15, 2021.
Marquita Cullom,
Associate Director.
[FR Doc. 2021-05605 Filed 3-17-21; 8:45 am]
BILLING CODE 4160-90-P