Agency Information Collection Activities: Proposed Collection; Comment Request, 33349-33352 [2024-09071]
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Federal Register / Vol. 89, No. 83 / Monday, April 29, 2024 / Notices
eleven attachments associated with the
application and notification
requirements in Subparts A and C of
Regulation K. The Board requires the
information collected by the FR K–1 for
regulatory and supervisory purposes
and to allow the Board to fulfill its
statutory obligations under the Federal
Reserve Act (FRA) and the Bank
Holding Company Act of 1956 (BHC
Act).
Frequency: Event-generated.
Respondents: Member banks, Edge
and agreement corporations, BHCs, and
with regard to certain investments,
foreign organizations.
Total estimated number of
respondents: 119.
Total estimated annual burden hours:
1,009.2
Board of Governors of the Federal Reserve
System, April 23, 2024.
Michele Taylor Fennell,
Deputy Associate Secretary of the Board.
[FR Doc. 2024–09115 Filed 4–26–24; 8:45 am]
GENERAL SERVICES
ADMINISTRATION
[Notice–IEB–2024–03; Docket No. 2024–
0002; Sequence No. 21]
Privacy Act of 1974; Rescindment of a
System of Records Notice
General Services
Administration (GSA).
ACTION: Rescindment of a System of
Records Notice.
AGENCY:
Pursuant to the provisions of
the Privacy Act of 1974, notice is given
that the General Services
Administration (GSA) proposes to
rescind a System of Records Notice,
GSA/GOVT–10, Login.gov. This system
of records contains information related
to the development and operation of a
citizen-centric platform for delivering
government services through a
centralized single sign-on platform.
DATES: This system of records stopped
being maintained in 2017.
ADDRESSES: Comments may be
submitted to the Federal eRulemaking
Portal, https://www.regulations.gov.
Submit comments by searching for
GSA/GOVT–10.
FOR FURTHER INFORMATION CONTACT: Call
or email Richard Speidel, Chief Privacy
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
2 More detailed information regarding this
collection, including more detailed burden
estimates, can be found in the OMB Supporting
Statement posted at https://www.federalreserve.gov/
apps/reportingforms/home/review. On the page
displayed at the link, you can find the OMB
Supporting Statement by referencing the collection
identifier, FR K–1.
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Officer at (202) 969–5830 and
gsa.privacyact@gsa.gov.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
GSA
proposes to rescind a System of Records
Notification, GSA/GOVT–10, Login.gov.
This Notice is being rescinded because
no records were ever collected under
the government-wide SORN GSA/
GOVT–10. GSA/GOVT–10 was
published in the Federal Register in
August 2016 and is directed to a version
of Login.gov that did not enter
production. No records were ever
collected or used under this proposed
system of records.
Agency-specific SORN GSA/TTS–1
was published less than five months
later and includes an administratively
incorrect attempt to rescind GSA/
GOVT–10. The following rescindment
attempt appears in the Supplementary
Information section of GSA/TTS–1
(January 19, 2017):
Agency for Healthcare Research and
Quality
SUPPLEMENTARY INFORMATION:
‘‘The previously published notice, at 81 FR
57912, on August 24, 2016, is being
replaced.’’
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GSA did not timely file a SORN
rescindment notice for GSA/GOVT–10
at the time of publication of GSA/TTS–
1. The present notice addresses this
issue.
Moreover, this rescindment addresses
an instance where the same number was
inadvertently used for two separate
Notices. GSA published GSA/GOVT–10
(Login.gov) in 2016 and inadvertently
reused the same SORN number for GSA/
GOVT–10 (Federal Acquisition
Regulation (FAR) Data Collection
System), which was published in 2017.
This rescindment action resolves the
discrepancy with only the 2017 GSA/
GOVT–10 (Federal Acquisition
Regulation (FAR) Data Collection
System) remaining in effect.
SYSTEM NAME:
Login.gov.
SYSTEM NUMBER:
GSA/GOVT–10.
HISTORY:
This system was previously published
in the Federal Register at 81 FR 57912,
August 24, 2016.
Richard Speidel,
Chief Privacy Officer, Office of Enterprise
Data & Privacy Management, General Services
Administration.
[FR Doc. 2024–09106 Filed 4–26–24; 8:45 am]
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Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
AGENCY:
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve a revision of the
currently approved information
collection project: ‘‘The AHRQ Safety
Program for Telemedicine: Improving
the Diagnostic Process and Improving
Antibiotic Use.’’ In accordance with the
Paperwork Reduction Act of 1995,
AHRQ invites the public to comment on
this proposed information collection.
DATES: Comments on this notice must be
received by June 28, 2024.
ADDRESSES: Written comments should
be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by
email at REPORTSCLEARANCE
OFFICER@ahrq.hhs.gov.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
email at REPORTSCLEARANCE
OFFICER@ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
Proposed Project
AHRQ Safety Program for Telemedicine:
Improving Antibiotic Use
This Information Collection Request
(ICR) is for a revision to the AHRQ
Safety Program for Telemedicine:
Improving the Diagnostic Process and
Improving Antibiotic Use. These
changes include the removal of the
Diagnostic Process Cohort, updates to
the Improving Antibiotic Use Data
Collection Tools and changing the name
of the project to the ‘‘AHRQ Safety
Program for Telemedicine: Improving
Antibiotic Use.’’ The OMB control
number for the AHRQ Safety Program
for Telemedicine is 0935–0265 and will
expire on April 30, 2026. Supporting
documents can be downloaded from
OMB’s website at: https://
www.reginfo.gov/public/do/
PRAViewICR?ref_nbr=202303-0935-001.
AHRQ is requesting a new expiration
date, three years from approval.
Since the project received OMB
approval, there have been two
developments that require changes to
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the project’s goals and design. First, the
Improving the Diagnostic Process
Cohort was canceled because there was
insufficient recruitment. Second, the
materials approved by OMB for the
Improving Antibiotic Use Cohort
included a single version of the
Structural Assessment and Participant
Experience Survey, to be completed by
all participants in the improving
antibiotic use cohort. However,
following pre-recruitment discussions
with AHRQ’s Technical Expert Panel
(TEP) and potential participants, it was
learned that the target audience for the
improving antibiotic use cohort is
comprised of healthcare providers from
two distinctly different settings (brickand-mortar and telemedicine-only)
settings. Providers that practice in brickand-mortar settings provide care both
in-person and via telemedicine whereas
providers that practice in telemedicineonly settings provide care exclusively
using telemedicine. Based on this
information AHRQ decided to create
separate data collection tools, one for
providers in a brick-and-mortar setting,
and one for providers in telemedicine
only. Practices and providers receive
information about the program from
newsletters, listservs, and direct
outreach through public and private
organizations. They attend an
information webinar and may join the
program if interested and eligible.
As in the currently approved design,
the program will incorporate CUSP
strategies to improve antibiotic
prescribing in telemedicine. The new
program goals are to:
• Identify best practices in
implementing interventions to improve
antibiotic use in telemedicine.
• Determine how best to adapt CUSP
to enhance antibiotic use in
telemedicine.
• Use a CUSP approach to design and
implement the interventions for
improving antibiotic use across
telemedicine practices.
• Reduce inappropriate antibiotic
prescribing among telemedicine
practices.
To achieve these goals the following
data collections will be implemented:
1. Structural Assessment Antibiotic
Use Cohort—There will be two versions
of the Structural Assessment, one for
providers in a brick-and-mortar setting,
and one for providers in telemedicine
only. Both versions ask the same
questions but vary slightly in how they
refer to the practice. The assessment
asks about the practice’s characteristics,
experience related to antibiotic
stewardship activities, and any existing
supports the practice may have in place
that are intended to improve antibiotic
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prescribing. The assessment will be
administered to the Safety Program
leader/champion at each participating
brick-and-mortar practice or
telemedicine-only organization at
baseline (pre-intervention) and at the
end of the intervention. The results will
be used to assess changes in the
practice’s infrastructure and capacity to
implement the Safety Program over
time. The data will provide information
about any existing quality improvement
initiatives currently in place, their
existing infrastructure and capacity to
carry out the program, as well as
changes in the infrastructure and quality
improvement activities as a result of
participation in the Safety Program.
2. Medical Office Survey on Patient
Safety Culture (MOSOPS): As currently
approved, the Safety Program for
Telemedicine included completion of
the MOSOPS by all participating staff
across all participating practices. In this
revision, AHRQ will administer the
MOSOPS to HCPs practicing in brickand-mortar settings only. The MOSOPS
was designed to assess key
characteristics of HCPs working inperson in a single medical office and
results are unlikely to be reliable or
valid if administered among HCPs
practicing in telemedicine-only settings.
The MOSOPS will be administered to
all participating staff at brick-andmortar practices at baseline (preintervention) and at the end of the
intervention. The survey collects
information on patient safety issues,
patient safety culture, medical errors,
and event reporting. The data will be
used to assess changes in safety culture
following implementation of the Safety
Program.
3. Participant Experience Survey
Antibiotic Use Cohort—Based on
feedback from the TEP and
conversations with telemedicine-only
organizations, this revision includes
changes to the Participant Experience
Survey as well as unique versions for
brick-and-mortar and telemedicine-only
participants. The survey will be
administered to the clinical leader/
champion at each practice at the end of
the program (post-intervention). The
survey will assess how participants
approached implementation of the
Safety Program.
4. Semi-Structured Interviews
Antibiotic Use Cohort—A proportion of
practices from both brick-and-mortar
practices and telemedicine-only
organizations will be selected to
participate in telephone/virtual
discussions to understand the
facilitators and barriers to implementing
the Safety Program. This interview
guide includes four core domains that
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are intended to capture characteristics
of health care providers (physicians,
nurse practitioners, and physician
assistants) and their perception of the
AHRQ Safety Program for Telemedicine:
Improving Antibiotic Use (‘‘the Safety
Program’’) on pre- and postimplementation changes. All interviews
will occur at the end of the intervention
period
5. Antibiotic Prescription Data
Template Antibiotic Use Cohort—Each
month starting at baseline (preintervention) until the end of the
intervention, each participating practice
will extract antibiotic prescribing data
from their electronic health record
(EHR) system. The data will be
submitted quarterly using a secure
online data submission portal. The
prescribing data will evaluate changes
in antibiotic usage, clinical outcomes,
and other effectiveness measures
resulting from participation in the
Safety Program. Based on feedback from
participants in the prior AHRQ Safety
Program, this updated version includes
revisions to the EHR template to
simplify the data requested in the
template from aggregate to visit-level.
Participating practices will submit two
key types of data related to antibiotic
prescribing: (1) Total antibiotic
prescriptions per 100 respiratory tract
infection telemedicine visits and (2)
Antibiotic prescriptions per 100
antibiotic-inappropriate respiratory tract
infection telemedicine visits. This data
will be an important way for the
practice to monitor its prescribing
practices throughout the course of the
program and will be used by the
assessment team to monitor and
describe prescribing trends across
practices enrolled in the program.
This study is being conducted by
AHRQ through its contractor, NORC at
the University of Chicago and Johns
Hopkins Medicine, pursuant to AHRQ’s
statutory authority to conduct and
support research on healthcare and on
systems for the delivery of such care,
including activities with respect to the
quality, effectiveness, efficiency,
appropriateness, and value of healthcare
services and with respect to quality
measurement and improvement. 42
U.S.C. 299a(a)(1) and (2).
Method of Collection
To minimize respondent burden and
to permit the electronic submission of
survey responses and data collection
forms, the structural assessment, AHRQ
MOSOPS, participant experience
survey, and antibiotic prescription data
template will be web-based and
deployed using a well-designed, low
burden, and respondent-friendly survey
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administration process. In addition, the
EHR data extracted by practice staff that
are requested for this program may
already be collected by practices as part
of their ongoing quality improvement
initiatives. Practices will receive access
to the online data collection platform
and detailed instructions on completing
the online forms and EHR data
submissions.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated
annualized burden hours for the
respondents’ time to participate in this
project.
1. Structural Assessment Antibiotic
Use Cohort—The assessment will be
administered twice to the Safety
Program leader/champion at each
participating brick-and-mortar practice
or telemedicine-only organization, once
at baseline (pre-intervention) and again
at the end of the intervention. AHRQ
expects 188 respondents at each
administration. The Assessment
requires 12 minutes to complete.
2. Medical Office Survey on Patient
Safety (MOSOPS)—The MOSOPS will
be completed by all participating staff at
brick-and-mortar practices to assess
patient safety issues, medical errors, and
event reporting practices. The survey
will be completed twice, once at
baseline (pre-intervention) and at the
end of the intervention to measure the
changes in patient safety culture
resulting from participation in the
Safety Program. The survey will be
completed by 438 staff members at each
administration and requires 30 minutes
to complete.
3. Participant Experience Survey
Antibiotic Use Cohort—The Participant
Experience Survey will be administered
once to the Safety Program leader/
champion at the end of the intervention
to assess participant engagement and
progress; understand providers’
experience using materials and
participating in the Safety Program; and
identify processes used and changes
made to implement and sustain the
Safety Program. The survey is estimated
to require 20 minutes to complete.
4. Semi-Structured Interviews
Antibiotic Use Cohort—Semi-structured
interviews will be conducted at the end
of the intervention among clinical and
professional support staff from a sample
of practices to collect qualitative
information on the implementation of
the program. Interviews will be
conducted with 18 participating
practices/organizations and requires one
hour to complete.
5. Antibiotic Prescription Data
Template Antibiotic Use Cohort—The
Antibiotic Prescription Data Template
will be completed each month and
submitted quarterly starting in the
baseline (pre-intervention) period until
the end of the intervention to measure
changes in antibiotic usage resulting
from the intervention. The data will be
extracted from the practice/
organization’s electronic health records,
by a staff member, and entered into the
data template. AHRQ expects 225
practices/organizations to extract data
monthly for 18 months. Each monthly
data extraction should require one hour
of a staff members time.
The total burden for the respondents’
time to participate in this research is
estimated to be 4,644 hours.
EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents *
Form name
1.
2.
3.
4.
5.
Number of
responses per
respondent
Hours per
response
Total burden
hours
Structural Assessment .................................................................................
MOSOPS (brick-and-mortar only) ...............................................................
Participant Experience Survey ....................................................................
Semi-structured interviews ..........................................................................
Antibiotic Prescription Data Template .........................................................
188
438
188
18
225
2
2
1
1
18
12/60
30/60
20/60
1
1
75
438
63
18
4,050
Total ..........................................................................................................
1,057
na
na
4,644
* Annualized number of respondents is based on maximum practices recruited, assuming 50% of the practices are telemedicine-only and 50%
are brick-and-mortar, and 75% response rate for forms 1 and 3, 50% response rate for form 2, and 90% response rate for forms 4 and 5.
Exhibit 2 shows the estimated
annualized cost burden based on the
respondents’ time to complete the data
collection forms. The total cost burden
is estimated to be $348,868.
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Total burden
hours
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Form name
Average
hourly wage
rate **
Total burden
cost
1. Structural Assessment .............................................................................................................
2. MOSOPS (brick-and-mortar only).
a. Physicians ........................................................................................................................
b. Other Health Practitioners ................................................................................................
3. Participant Experience Survey ................................................................................................
4. Semi-structured qualitative interviews .....................................................................................
5. Antibiotic Prescription Data Template .....................................................................................
75
a $114.76
$8,607
219
219
63
18
4,050
a 114.76
c 73.77
25,132
7,179
7,115
2,066
298,769
Total ...............................................................................................................................
4,644
........................
348,868
b 32.78
a 114.76
a 114.76
** Annualized number of respondents is based on maximum practices recruited, assuming 50% of the practices are telemedicine-only and 50%
are brick-and-mortar, and 75% response rate for forms 1 and 3, 50% response rate for form 2, and 90% response rate for forms 4 and 5.
** National Compensation Survey: Occupational wages in the United States May 2022 ‘‘U.S. Department of Labor, Bureau of Labor Statistics:’’
https://www.bls.gov/oes/current/oes_stru.htm.
a Based on the mean wages for 29–1069 Physicians and Surgeons, All Other.
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b Based on the mean wages for 29–9099 Miscellaneous Health Practitioners and Technical Workers: Healthcare Practitioners and Technical
Workers, All Other.
c Based on an average of the mean wages for 29–1069 Physicians and Surgeons, All Other and 29–9099 Miscellaneous Health Practitioners
and Technical Workers: Healthcare Practitioners and Technical Workers, All Other.
Request for Comments
In accordance with the Paperwork
Reduction Act, 44 U.S.C. 3501–3520,
comments on AHRQ’s information
collection are requested with regard to
any of the following: (a) whether the
proposed collection of information is
necessary for the proper performance of
AHRQ’s health care research and health
care information dissemination
functions, including whether the
information will have practical utility;
(b) the accuracy of AHRQ’s estimate of
burden (including hours and costs) of
the proposed collection(s) of
information; (c) ways to enhance the
quality, utility and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
Dated: April 23, 2024.
Marquita Cullom,
Associate Director.
[FR Doc. 2024–09071 Filed 4–26–24; 8:45 am]
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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 ‘‘Colorectal
Cancer Control Program (CRCCP)
Monitoring Activities’’ 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
22, 2023 to obtain comments from the
public and affected agencies. CDC
received one comment related to the
previous notice. This notice serves to
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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
Colorectal Cancer Control Program
(CRCCP) Monitoring Activities (OMB
Control No. 0920–1074)—
Reinstatement—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
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Background and Brief Description
CDC is requesting a Reinstatement of
OMB No. 0920–1074. Colorectal cancer
(CRC) is the second leading cause of
death from cancer in the United States
among cancers that affect both men and
women. There is substantial evidence
that CRC screening reduces the
incidence of and death from the disease.
Screening for CRC can detect disease
early when treatment is more effective,
and prevent cancer by finding and
removing precancerous polyps. Of
individuals diagnosed with early stage
CRC, more than 90% live five or more
years. To reduce CRC morbidity,
mortality, and associated costs, use of
CRC screening tests must be increased
among age-eligible adults with the
lowest CRC screening rates.
The purpose of the Colorectal Cancer
Control Program (CRCCP) is to partner
with health systems and their
individual primary care clinics to
implement evidence-based
interventions (EBIs) to increase CRC
screening among defined populations of
adults ages 50–75 that have CRC
screening rates lower than the national,
regional, or local rate. In 2020, CDC
issued the funding opportunity, Public
Health and Health System Partnerships
to Increase Colorectal Cancer Screening
in Clinical Settings (DP20–2002), a fiveyear cooperative agreement to increase
CRC screening among defined
populations of adults ages 50–75 that
have CRC screening rates lower than the
national, regional, or local rate. DP20–
2002 funds recipients to partner with
health systems and their primary care
clinics to implement multiple EBIs,
partner with organizations to support
implementation of EBIs in those clinics,
and collect high-quality clinic-level data
to monitor EBI implementation and
assess screening rate changes.
CDC proposes information collection
using three data collection tools: the
Annual Awardee Survey, Clinic-Level
Data Collection Instrument, and
Quarterly Program Update.
The Annual Awardee Survey is
administered once per year and
assesses: program management, clinic
readiness assessment activities, data
management, technical assistance (TA)
needs, partnerships, and the effect of
COVID–19 on CRC implementation. The
Clinic-Level Information Collection
Instrument is administered three
months following each program year
end and assesses: health system and
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Agencies
[Federal Register Volume 89, Number 83 (Monday, April 29, 2024)]
[Notices]
[Pages 33349-33352]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-09071]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Agency for Healthcare Research and Quality, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the intention of the Agency for
Healthcare Research and Quality (AHRQ) to request that the Office of
Management and Budget (OMB) approve a revision of the currently
approved information collection project: ``The AHRQ Safety Program for
Telemedicine: Improving the Diagnostic Process and Improving Antibiotic
Use.'' In accordance with the Paperwork Reduction Act of 1995, AHRQ
invites the public to comment on this proposed information collection.
DATES: Comments on this notice must be received by June 28, 2024.
ADDRESSES: Written comments should be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by email at
[email protected].
FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427-1477, or by email at
[email protected].
SUPPLEMENTARY INFORMATION:
Proposed Project
AHRQ Safety Program for Telemedicine: Improving Antibiotic Use
This Information Collection Request (ICR) is for a revision to the
AHRQ Safety Program for Telemedicine: Improving the Diagnostic Process
and Improving Antibiotic Use. These changes include the removal of the
Diagnostic Process Cohort, updates to the Improving Antibiotic Use Data
Collection Tools and changing the name of the project to the ``AHRQ
Safety Program for Telemedicine: Improving Antibiotic Use.'' The OMB
control number for the AHRQ Safety Program for Telemedicine is 0935-
0265 and will expire on April 30, 2026. Supporting documents can be
downloaded from OMB's website at: https://www.reginfo.gov/public/do/PRAViewICR?ref_nbr=202303-0935-001. AHRQ is requesting a new expiration
date, three years from approval.
Since the project received OMB approval, there have been two
developments that require changes to
[[Page 33350]]
the project's goals and design. First, the Improving the Diagnostic
Process Cohort was canceled because there was insufficient recruitment.
Second, the materials approved by OMB for the Improving Antibiotic Use
Cohort included a single version of the Structural Assessment and
Participant Experience Survey, to be completed by all participants in
the improving antibiotic use cohort. However, following pre-recruitment
discussions with AHRQ's Technical Expert Panel (TEP) and potential
participants, it was learned that the target audience for the improving
antibiotic use cohort is comprised of healthcare providers from two
distinctly different settings (brick-and-mortar and telemedicine-only)
settings. Providers that practice in brick-and-mortar settings provide
care both in-person and via telemedicine whereas providers that
practice in telemedicine-only settings provide care exclusively using
telemedicine. Based on this information AHRQ decided to create separate
data collection tools, one for providers in a brick-and-mortar setting,
and one for providers in telemedicine only. Practices and providers
receive information about the program from newsletters, listservs, and
direct outreach through public and private organizations. They attend
an information webinar and may join the program if interested and
eligible.
As in the currently approved design, the program will incorporate
CUSP strategies to improve antibiotic prescribing in telemedicine. The
new program goals are to:
Identify best practices in implementing interventions to
improve antibiotic use in telemedicine.
Determine how best to adapt CUSP to enhance antibiotic use
in telemedicine.
Use a CUSP approach to design and implement the
interventions for improving antibiotic use across telemedicine
practices.
Reduce inappropriate antibiotic prescribing among
telemedicine practices.
To achieve these goals the following data collections will be
implemented:
1. Structural Assessment Antibiotic Use Cohort--There will be two
versions of the Structural Assessment, one for providers in a brick-
and-mortar setting, and one for providers in telemedicine only. Both
versions ask the same questions but vary slightly in how they refer to
the practice. The assessment asks about the practice's characteristics,
experience related to antibiotic stewardship activities, and any
existing supports the practice may have in place that are intended to
improve antibiotic prescribing. The assessment will be administered to
the Safety Program leader/champion at each participating brick-and-
mortar practice or telemedicine-only organization at baseline (pre-
intervention) and at the end of the intervention. The results will be
used to assess changes in the practice's infrastructure and capacity to
implement the Safety Program over time. The data will provide
information about any existing quality improvement initiatives
currently in place, their existing infrastructure and capacity to carry
out the program, as well as changes in the infrastructure and quality
improvement activities as a result of participation in the Safety
Program.
2. Medical Office Survey on Patient Safety Culture (MOSOPS): As
currently approved, the Safety Program for Telemedicine included
completion of the MOSOPS by all participating staff across all
participating practices. In this revision, AHRQ will administer the
MOSOPS to HCPs practicing in brick-and-mortar settings only. The MOSOPS
was designed to assess key characteristics of HCPs working in-person in
a single medical office and results are unlikely to be reliable or
valid if administered among HCPs practicing in telemedicine-only
settings. The MOSOPS will be administered to all participating staff at
brick-and-mortar practices at baseline (pre-intervention) and at the
end of the intervention. The survey collects information on patient
safety issues, patient safety culture, medical errors, and event
reporting. The data will be used to assess changes in safety culture
following implementation of the Safety Program.
3. Participant Experience Survey Antibiotic Use Cohort--Based on
feedback from the TEP and conversations with telemedicine-only
organizations, this revision includes changes to the Participant
Experience Survey as well as unique versions for brick-and-mortar and
telemedicine-only participants. The survey will be administered to the
clinical leader/champion at each practice at the end of the program
(post-intervention). The survey will assess how participants approached
implementation of the Safety Program.
4. Semi-Structured Interviews Antibiotic Use Cohort--A proportion
of practices from both brick-and-mortar practices and telemedicine-only
organizations will be selected to participate in telephone/virtual
discussions to understand the facilitators and barriers to implementing
the Safety Program. This interview guide includes four core domains
that are intended to capture characteristics of health care providers
(physicians, nurse practitioners, and physician assistants) and their
perception of the AHRQ Safety Program for Telemedicine: Improving
Antibiotic Use (``the Safety Program'') on pre- and post-implementation
changes. All interviews will occur at the end of the intervention
period
5. Antibiotic Prescription Data Template Antibiotic Use Cohort--
Each month starting at baseline (pre-intervention) until the end of the
intervention, each participating practice will extract antibiotic
prescribing data from their electronic health record (EHR) system. The
data will be submitted quarterly using a secure online data submission
portal. The prescribing data will evaluate changes in antibiotic usage,
clinical outcomes, and other effectiveness measures resulting from
participation in the Safety Program. Based on feedback from
participants in the prior AHRQ Safety Program, this updated version
includes revisions to the EHR template to simplify the data requested
in the template from aggregate to visit-level. Participating practices
will submit two key types of data related to antibiotic prescribing:
(1) Total antibiotic prescriptions per 100 respiratory tract infection
telemedicine visits and (2) Antibiotic prescriptions per 100
antibiotic-inappropriate respiratory tract infection telemedicine
visits. This data will be an important way for the practice to monitor
its prescribing practices throughout the course of the program and will
be used by the assessment team to monitor and describe prescribing
trends across practices enrolled in the program.
This study is being conducted by AHRQ through its contractor, NORC
at the University of Chicago and Johns Hopkins Medicine, pursuant to
AHRQ's statutory authority to conduct and support research on
healthcare and on systems for the delivery of such care, including
activities with respect to the quality, effectiveness, efficiency,
appropriateness, and value of healthcare services and with respect to
quality measurement and improvement. 42 U.S.C. 299a(a)(1) and (2).
Method of Collection
To minimize respondent burden and to permit the electronic
submission of survey responses and data collection forms, the
structural assessment, AHRQ MOSOPS, participant experience survey, and
antibiotic prescription data template will be web-based and deployed
using a well-designed, low burden, and respondent-friendly survey
[[Page 33351]]
administration process. In addition, the EHR data extracted by practice
staff that are requested for this program may already be collected by
practices as part of their ongoing quality improvement initiatives.
Practices will receive access to the online data collection platform
and detailed instructions on completing the online forms and EHR data
submissions.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annualized burden hours for the
respondents' time to participate in this project.
1. Structural Assessment Antibiotic Use Cohort--The assessment will
be administered twice to the Safety Program leader/champion at each
participating brick-and-mortar practice or telemedicine-only
organization, once at baseline (pre-intervention) and again at the end
of the intervention. AHRQ expects 188 respondents at each
administration. The Assessment requires 12 minutes to complete.
2. Medical Office Survey on Patient Safety (MOSOPS)--The MOSOPS
will be completed by all participating staff at brick-and-mortar
practices to assess patient safety issues, medical errors, and event
reporting practices. The survey will be completed twice, once at
baseline (pre-intervention) and at the end of the intervention to
measure the changes in patient safety culture resulting from
participation in the Safety Program. The survey will be completed by
438 staff members at each administration and requires 30 minutes to
complete.
3. Participant Experience Survey Antibiotic Use Cohort--The
Participant Experience Survey will be administered once to the Safety
Program leader/champion at the end of the intervention to assess
participant engagement and progress; understand providers' experience
using materials and participating in the Safety Program; and identify
processes used and changes made to implement and sustain the Safety
Program. The survey is estimated to require 20 minutes to complete.
4. Semi-Structured Interviews Antibiotic Use Cohort--Semi-
structured interviews will be conducted at the end of the intervention
among clinical and professional support staff from a sample of
practices to collect qualitative information on the implementation of
the program. Interviews will be conducted with 18 participating
practices/organizations and requires one hour to complete.
5. Antibiotic Prescription Data Template Antibiotic Use Cohort--The
Antibiotic Prescription Data Template will be completed each month and
submitted quarterly starting in the baseline (pre-intervention) period
until the end of the intervention to measure changes in antibiotic
usage resulting from the intervention. The data will be extracted from
the practice/organization's electronic health records, by a staff
member, and entered into the data template. AHRQ expects 225 practices/
organizations to extract data monthly for 18 months. Each monthly data
extraction should require one hour of a staff members time.
The total burden for the respondents' time to participate in this
research is estimated to be 4,644 hours.
Exhibit 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of
Form name Number of responses per Hours per Total burden
respondents * respondent response hours
----------------------------------------------------------------------------------------------------------------
1. Structural Assessment........................ 188 2 12/60 75
2. MOSOPS (brick-and-mortar only)............... 438 2 30/60 438
3. Participant Experience Survey................ 188 1 20/60 63
4. Semi-structured interviews................... 18 1 1 18
5. Antibiotic Prescription Data Template........ 225 18 1 4,050
---------------------------------------------------------------
Total....................................... 1,057 na na 4,644
----------------------------------------------------------------------------------------------------------------
* Annualized number of respondents is based on maximum practices recruited, assuming 50% of the practices are
telemedicine-only and 50% are brick-and-mortar, and 75% response rate for forms 1 and 3, 50% response rate for
form 2, and 90% response rate for forms 4 and 5.
Exhibit 2 shows the estimated annualized cost burden based on the
respondents' time to complete the data collection forms. The total cost
burden is estimated to be $348,868.
Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Total burden Average hourly Total burden
Form name hours wage rate ** cost
----------------------------------------------------------------------------------------------------------------
1. Structural Assessment........................................ 75 \a\ $114.76 $8,607
2. MOSOPS (brick-and-mortar only)...............................
a. Physicians............................................... 219 \a\ 114.76 25,132
b. Other Health Practitioners............................... 219 \b\ 32.78 7,179
3. Participant Experience Survey................................ 63 \a\ 114.76 7,115
4. Semi-structured qualitative interviews....................... 18 \a\ 114.76 2,066
5. Antibiotic Prescription Data Template........................ 4,050 \c\ 73.77 298,769
-----------------------------------------------
Total................................................... 4,644 .............. 348,868
----------------------------------------------------------------------------------------------------------------
** Annualized number of respondents is based on maximum practices recruited, assuming 50% of the practices are
telemedicine-only and 50% are brick-and-mortar, and 75% response rate for forms 1 and 3, 50% response rate for
form 2, and 90% response rate for forms 4 and 5.
** National Compensation Survey: Occupational wages in the United States May 2022 ``U.S. Department of Labor,
Bureau of Labor Statistics:'' https://www.bls.gov/oes/current/oes_stru.htm.
\a\ Based on the mean wages for 29-1069 Physicians and Surgeons, All Other.
[[Page 33352]]
\b\ Based on the mean wages for 29-9099 Miscellaneous Health Practitioners and Technical Workers: Healthcare
Practitioners and Technical Workers, All Other.
\c\ Based on an average of the mean wages for 29-1069 Physicians and Surgeons, All Other and 29-9099
Miscellaneous Health Practitioners and Technical Workers: Healthcare Practitioners and Technical Workers, All
Other.
Request for Comments
In accordance with the Paperwork Reduction Act, 44 U.S.C. 3501-
3520, comments on AHRQ's information collection are requested with
regard to any of the following: (a) whether the proposed collection of
information is necessary for the proper performance of AHRQ's health
care research and health care information dissemination functions,
including whether the information will have practical utility; (b) the
accuracy of AHRQ's estimate of burden (including hours and costs) of
the proposed collection(s) of information; (c) ways to enhance the
quality, utility and clarity of the information to be collected; and
(d) ways to minimize the burden of the collection of information upon
the respondents, including the use of automated collection techniques
or other forms of information technology.
Comments submitted in response to this notice will be summarized
and included in the Agency's subsequent request for OMB approval of the
proposed information collection. All comments will become a matter of
public record.
Dated: April 23, 2024.
Marquita Cullom,
Associate Director.
[FR Doc. 2024-09071 Filed 4-26-24; 8:45 am]
BILLING CODE 4160-90-P