Agency Forms Undergoing Paperwork Reduction Act Review, 22055-22056 [2021-08573]
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22055
Federal Register / Vol. 86, No. 78 / Monday, April 26, 2021 / Notices
(2) Identify potentially new courses
that may be of some use to HIV CBO
leadership;
(3) Provide a timely and accurate
aggregated accounting of patterns of
usage and enrollment trends to CDC and
other state, and local agencies, and other
stakeholders seeking information about
the services delivered in the Learning
Community.
No other federal agency collects these
types of national HIV prevention
capacity building data. The total
annualized burden is 89 hours. There
are no other costs to respondents other
than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hr.)
Total burden
(in hr.)
Type of respondent
Form name
CBO Managers .................................
CBO Managers .................................
CBO Managers .................................
Registration Form .............................
Post Participation Survey .................
Semi-Structured Zoom Interview .....
270
270
135
1
1
1
3/60
9/60
15/60
14
41
34
Total ...........................................
...........................................................
........................
........................
........................
89
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–08578 Filed 4–23–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–21–1108]
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Paul Coverdell
National Acute Stroke Program
(PCNASP) to the Office of Management
and Budget (OMB) for review and
approval. CDC previously published a
‘‘Proposed Data Collection Submitted
for Public Comment and
Recommendations’’ notice on December
3, 2020 to obtain comments from the
public and affected agencies. CDC did
not receive comments related to the
previous notice. This notice serves to
allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
VerDate Sep<11>2014
18:01 Apr 23, 2021
Jkt 253001
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
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
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Paul Coverdell National Acute Stroke
Program (PCNASP) (OMB Control No.
0920–1108, Exp. 09/30/2022)—
Revision—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
PO 00000
Frm 00046
Fmt 4703
Sfmt 4703
Background and Brief Description
Stroke is the fifth leading cause of
death in the United States, and results
in approximately 145,000 deaths per
year. However, many strokes are
preventable, or patient outcomes poststroke can be improved through
coordinated care that begins at stroke
onset, and is delivered in a timely
manner.
Through the Paul Coverdell National
Acute Stroke Program (PCNASP), CDC
has continuously worked to measure
and improve acute stroke care using
well-known quality improvement
strategies coupled with frequent
evaluation of results. There remains a
national need to understand best
practices of stroke systems of care,
which includes prevention and
awareness, use of EMS, in-hospital care,
and rehabilitation and recovery.
PCNASP awardees work statewide with
participating hospitals, Emergency
Medical Services (EMS) agencies, and
other healthcare partners (e.g.,
community clinical partners) to improve
quality of care for stroke patients. These
efforts include implementing strategies
to close the gap on stroke disparities,
identifying effective stroke treatment
centers, building capacity and
infrastructure to ensure that stroke
patients are routed to effective treatment
centers in a timely manner, and
improving transitions of care from the
hospital to the next care setting.
The PCNASP’s current five-year
cooperative agreement started on July 1,
2015 and includes nine state health
department awardees and their selected
partners (hospitals, EMS agencies, other
healthcare facilities). This current
funding period reflects additional
emphasis on pre-hospital quality of care
as well as the post-hospital transition of
care setting from hospital to home or
other healthcare facility. With technical
E:\FR\FM\26APN1.SGM
26APN1
22056
Federal Register / Vol. 86, No. 78 / Monday, April 26, 2021 / Notices
assistance provided by CDC, awardees
have worked on identifying and using
data systems to systematically collect
and report data on all three phases of
the stroke care continuum and on
hospital capacity.
PCNASP currently has OMB approval
for the collection of pre-hospital (EMS),
in-hospital, and post-hospital patient
care data, as well as hospital inventory
data (OMB Control No. 0920–1108, Exp.
09/30/2022). CDC plans to request a
revision of this currently approved
collection, with an extension of three
years, reflecting a new Notice of
Funding Opportunity (NOFO). The new
PCNASP cooperative agreement will be
expanded to include 13 awardees,
which will be awarded on or about July
1, 2021.
In-hospital patient care data will
continue to align with standards set by
The Joint Commission (TJC) and the
American Heart Association’s Get With
The Guidelines (GWTG) Program.
Estimated burden for the collection of
in-hospital data will increase by a net
increase of eight hours due to added
program awardees under the new
cooperative agreement. The average
burden per response remains 30
minutes for awardees, for a total of 26
hours annually.
Data collection methods for prehospital care will continue to be
collected similarly to the two current
methods, depending on awardees’
access to data sources. These two
methods are existing data systems
currently available to awardees,
including the AHA’s GWTG and the
National Emergency Medical Services
Information System (NEMSIS). CDC has
worked to reduce the overall number of
required data elements and identified
areas of alignment with AHA’s GWTG.
Total average burden will decrease due
to the reduction in data elements under
the new NOFO. Depending on the
awardees’ access to data sources (GWTG
or NEMSIS), the average burden per
response will vary from 30 minutes to
one hour. Thus, the burden for prehospital data is estimated to decrease
from 60 to 46 burden hours annually.
Under the scope of the new NOFO,
patient level post-hospital quality of
care data will not be collected. Poststroke transitions of care, rehabilitation,
and follow-up will be assessed in
alignment with existing CDC
cooperative agreements, such as
supporting the development of
approaches to link patients with
community resources and clinical
services through CDC–RFA–DP18–1817.
As a result, burden for this collection
and transmission will not be included
in the overall estimation of average
burden.
Primary data collection of hospital
inventory data will continue to be
collected to understand the capacity and
infrastructure of the hospitals that admit
and treat stroke patients. Each hospital
will report inventory information to its
PCNASP awardee annually. The average
burden per response remains 30
minutes for hospitals. In addition, each
PCNASP awardee prepares an annual
aggregate hospital inventory file for
transmission to CDC. The average
burden of reporting hospital inventory
information for each PCNASP awardee
remains eight hours per response. Based
on current data and expected number of
awardees under the new NOFO, we are
estimating the number of hospital
partners per awardee to be 50 hospitals.
Due to this increase in awardees, the
estimated number of hospital
respondents is anticipated to increase
from 378 to 650. Thus, there is a net
increase of 136 hours for hospitals to
collect and transmit this data. The total
burden for hospital inventory data is
increasing from 189 to 325 hours
annually.
These requested changes will result in
a net increase in total average burden
from 361 to 501 hours. All patient,
hospital, and EMS provider data that is
submitted to CDC by PCNASP awardees
will be de-identified and occur through
secure data systems. Proposed data
elements and quality indicators may be
updated over time to include new or
revised items based on evolving
recommendations and standards in the
field to improve the quality of stroke
care.
OMB approval is requested for three
years. CDC requests approval for an
estimated 501 annualized burden hours.
Participation is voluntary, and there are
no costs to respondents other than their
time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
PCNASP Awardee ..........................................
Hospital inventory ...........................................
In-hospital care data ......................................
Pre-hospital care data ....................................
PCNASP Hospital Partners ............................
Hospital Inventory ..........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–08573 Filed 4–23–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Submission for OMB Review;
Community Services Block Grant
(CSBG) Annual Report (OMB #0970–
0492)
Office of Community Services,
Administration for Children and
Families, Department of Health and
Human Services.
18:01 Apr 23, 2021
Jkt 253001
ACTION:
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
1
4
4
4
1
Average
burden per
response
(in hours)
8
30/60
30/60
1
30/60
Request for public comment.
The Office of Community
Services (OCS), Administration for
Children and Families (ACF), U.S.
Department of Health and Human
Services (HHS), is requesting expedited
review of an information collection
request from the Office of Management
and Budget (OMB) and is inviting
public comments on the collection of
data for the new Community Services
Block Grant (CSBG) CARES Act
Supplemental and CSBG Disaster
Supplemental funding. This information
SUMMARY:
Administration for Children and
Families
AGENCY:
VerDate Sep<11>2014
13
13
3
10
650
Number of
responses per
respondent
E:\FR\FM\26APN1.SGM
26APN1
Agencies
[Federal Register Volume 86, Number 78 (Monday, April 26, 2021)]
[Notices]
[Pages 22055-22056]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-08573]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-21-1108]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled Paul Coverdell National Acute Stroke Program
(PCNASP) to the Office of Management and Budget (OMB) for review and
approval. CDC previously published a ``Proposed Data Collection
Submitted for Public Comment and Recommendations'' notice on December
3, 2020 to obtain comments from the public and affected agencies. CDC
did not receive comments related to the previous notice. This notice
serves to allow an additional 30 days for public and affected agency
comments.
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(a) Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
(b) Evaluate the accuracy of the agencies estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and clarity of the information to
be collected;
(d) Minimize the burden of the collection of information on those
who are to respond, including, through the use of appropriate
automated, electronic, mechanical, or other technological collection
techniques or other forms of information technology, e.g., permitting
electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570. 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 for Public Comments'' or by using the search function. Direct
written comments and/or suggestions regarding the items contained in
this notice to the Attention: CDC Desk Officer, Office of Management
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202)
395-5806. Provide written comments within 30 days of notice
publication.
Proposed Project
Paul Coverdell National Acute Stroke Program (PCNASP) (OMB Control
No. 0920-1108, Exp. 09/30/2022)--Revision--National Center for Chronic
Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Stroke is the fifth leading cause of death in the United States,
and results in approximately 145,000 deaths per year. However, many
strokes are preventable, or patient outcomes post-stroke can be
improved through coordinated care that begins at stroke onset, and is
delivered in a timely manner.
Through the Paul Coverdell National Acute Stroke Program (PCNASP),
CDC has continuously worked to measure and improve acute stroke care
using well-known quality improvement strategies coupled with frequent
evaluation of results. There remains a national need to understand best
practices of stroke systems of care, which includes prevention and
awareness, use of EMS, in-hospital care, and rehabilitation and
recovery. PCNASP awardees work statewide with participating hospitals,
Emergency Medical Services (EMS) agencies, and other healthcare
partners (e.g., community clinical partners) to improve quality of care
for stroke patients. These efforts include implementing strategies to
close the gap on stroke disparities, identifying effective stroke
treatment centers, building capacity and infrastructure to ensure that
stroke patients are routed to effective treatment centers in a timely
manner, and improving transitions of care from the hospital to the next
care setting.
The PCNASP's current five-year cooperative agreement started on
July 1, 2015 and includes nine state health department awardees and
their selected partners (hospitals, EMS agencies, other healthcare
facilities). This current funding period reflects additional emphasis
on pre-hospital quality of care as well as the post-hospital transition
of care setting from hospital to home or other healthcare facility.
With technical
[[Page 22056]]
assistance provided by CDC, awardees have worked on identifying and
using data systems to systematically collect and report data on all
three phases of the stroke care continuum and on hospital capacity.
PCNASP currently has OMB approval for the collection of pre-
hospital (EMS), in-hospital, and post-hospital patient care data, as
well as hospital inventory data (OMB Control No. 0920-1108, Exp. 09/30/
2022). CDC plans to request a revision of this currently approved
collection, with an extension of three years, reflecting a new Notice
of Funding Opportunity (NOFO). The new PCNASP cooperative agreement
will be expanded to include 13 awardees, which will be awarded on or
about July 1, 2021.
In-hospital patient care data will continue to align with standards
set by The Joint Commission (TJC) and the American Heart Association's
Get With The Guidelines (GWTG) Program. Estimated burden for the
collection of in-hospital data will increase by a net increase of eight
hours due to added program awardees under the new cooperative
agreement. The average burden per response remains 30 minutes for
awardees, for a total of 26 hours annually.
Data collection methods for pre-hospital care will continue to be
collected similarly to the two current methods, depending on awardees'
access to data sources. These two methods are existing data systems
currently available to awardees, including the AHA's GWTG and the
National Emergency Medical Services Information System (NEMSIS). CDC
has worked to reduce the overall number of required data elements and
identified areas of alignment with AHA's GWTG. Total average burden
will decrease due to the reduction in data elements under the new NOFO.
Depending on the awardees' access to data sources (GWTG or NEMSIS), the
average burden per response will vary from 30 minutes to one hour.
Thus, the burden for pre-hospital data is estimated to decrease from 60
to 46 burden hours annually.
Under the scope of the new NOFO, patient level post-hospital
quality of care data will not be collected. Post-stroke transitions of
care, rehabilitation, and follow-up will be assessed in alignment with
existing CDC cooperative agreements, such as supporting the development
of approaches to link patients with community resources and clinical
services through CDC-RFA-DP18-1817. As a result, burden for this
collection and transmission will not be included in the overall
estimation of average burden.
Primary data collection of hospital inventory data will continue to
be collected to understand the capacity and infrastructure of the
hospitals that admit and treat stroke patients. Each hospital will
report inventory information to its PCNASP awardee annually. The
average burden per response remains 30 minutes for hospitals. In
addition, each PCNASP awardee prepares an annual aggregate hospital
inventory file for transmission to CDC. The average burden of reporting
hospital inventory information for each PCNASP awardee remains eight
hours per response. Based on current data and expected number of
awardees under the new NOFO, we are estimating the number of hospital
partners per awardee to be 50 hospitals. Due to this increase in
awardees, the estimated number of hospital respondents is anticipated
to increase from 378 to 650. Thus, there is a net increase of 136 hours
for hospitals to collect and transmit this data. The total burden for
hospital inventory data is increasing from 189 to 325 hours annually.
These requested changes will result in a net increase in total
average burden from 361 to 501 hours. All patient, hospital, and EMS
provider data that is submitted to CDC by PCNASP awardees will be de-
identified and occur through secure data systems. Proposed data
elements and quality indicators may be updated over time to include new
or revised items based on evolving recommendations and standards in the
field to improve the quality of stroke care.
OMB approval is requested for three years. CDC requests approval
for an estimated 501 annualized burden hours. Participation is
voluntary, and there are no costs to respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
PCNASP Awardee........................ Hospital inventory...... 13 1 8
In-hospital care data... 13 4 30/60
Pre-hospital care data.. 3 4 30/60
10 4 1
PCNASP Hospital Partners.............. Hospital Inventory...... 650 1 30/60
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2021-08573 Filed 4-23-21; 8:45 am]
BILLING CODE 4163-18-P