Agency Forms Undergoing Paperwork Reduction Act Review, 79926-79927 [2024-22471]
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79926
Federal Register / Vol. 89, No. 190 / Tuesday, October 1, 2024 / Notices
To meet CDC’s goal for a rigorous,
comprehensive evaluation, this
collection is proposing a mixed-method
quasi-experimental design with the
following three aims to evaluate the
2022 CDC Clinical Practice Guideline:
• Aim 1: Dissemination—Assess
CDC’s efforts in disseminating the 2022
CDC Clinical Practice Guideline.
• Aim 2: Impact—Evaluate the impact
of the 2022 CDC Clinical Practice
Guideline through population-wide
changes in prescribing practices for
opioids and medications for opioid use
disorder.
• Aim 3: Implementation—Evaluate
the implementation of the 2022 CDC
Number of
respondents
interviews with dentists, virtual
interviews with leaders from
professional organizations, payers,
medical boards, and health systems, and
virtual focus groups with patients and
caregivers.
The CDC will use this information
collection to evaluate the dissemination,
impact, and implementation of the 2022
CDC Clinical Practice Guideline to
ensure that Americans have access to
safer, effective ways of managing their
pain. CDC requests OMB approval for an
estimated 325 annual burden hours.
There is no cost to respondents other
than their time.
Estimated Annualized Burden Hours
Average
burden per
response
(in hours)
Number of
responses per
respondent
Total burden
(in hours)
Type of respondents
Form name
Clinicians ...........................................
200
1,000
1,000
10
2
3
3
3
1
1
1
1
1
2
2
2
10/60
5/60
5/60
1
1
1
1
1
33
83
83
10
2
6
6
6
Medical Board Leaders .....................
Patients .............................................
Caregivers .........................................
Clinician Survey ...............................
Invitation ...........................................
Follow up Emails ..............................
Clinician Interview ............................
Dentist Interview ...............................
Health System Leaders Interview ....
Payer Interview ................................
Professional Association Leaders
Interview.
Medical Board Leaders Interview ....
Patient Focus Groups ......................
Caregiver Focus Groups ..................
3
15
15
2
3
2
1
1
1
6
45
30
Total ...........................................
...........................................................
........................
........................
........................
325
Dentists .............................................
Health System Leaders ....................
Payers ...............................................
Professional Association Leaders .....
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
[FR Doc. 2024–22474 Filed 9–30–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–24–24AL]
Agency Forms Undergoing Paperwork
Reduction Act Review
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Clinical Practice Guideline from
perspectives of patients, caregivers,
clinicians; and leaders from health
systems, payers, professional
associations, and medical boards.
This evaluation will include
systematic collection and analysis of a
range of primary and secondary data
sources. To answer the research
questions, we will employ qualitative
synthesis and analytic approaches,
quantitative analyses, and various
mixed-methods approaches. Primary
data collection efforts include a webbased survey conducted among a
national sample of clinicians, virtual
interviews with clinicians, virtual
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Occupational
Exposures to Surgical Smoke in
Veterinary Personnel’’ 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 November
VerDate Sep<11>2014
17:42 Sep 30, 2024
Jkt 265001
3, 2023 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
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
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
Occupational Exposures to Surgical
Smoke in Veterinary Personnel—New—
National Institute for Occupational
E:\FR\FM\01OCN1.SGM
01OCN1
79927
Federal Register / Vol. 89, No. 190 / Tuesday, October 1, 2024 / Notices
Safety and Health (NIOSH), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Surgical smoke produced during
tissue cutting and cauterizing tissues
and blood vessels generates hazardous
gaseous compounds and aerosols that
are associated with cancer and
respiratory irritation; however, no
research has characterized surgical
smoke generated from animal tissue in
clinical veterinary settings. Surgical
smoke exposure is an emerging concern
in human operating rooms, and several
states have either passed or are
considering bills requiring surgical
smoke evacuation systems in human
operating rooms to mitigate this
occupational hazard. Surgical suites in
veterinary clinics are often multiple bay
suites or have less effective ventilation
systems than human operating rooms,
potentially leading to higher exposure
levels, yet no research has examined
barriers and aids to the use of surgical
smoke evacuation systems among
veterinary medicine/animal care (VM/
AC) personnel.
The proposed project will
characterize occupational exposure to
surgical smoke and related respiratory
health effects in clinical veterinary
settings. Data will be used to examine:
(1) work-related factors that contribute
to exposure to surgical smoke in clinical
veterinary settings; (2) relationships
between surgical smoke exposure in
clinical veterinary settings and
respiratory health; and (3) barriers and
aids to implementing surgical smoke
extraction systems that reduce
occupational exposures to surgical
smoke. Findings from this study will
help to provide guidance on engineering
controls to improve air quality in VM/
AC personnel’s work environment by
reducing exposure to surgical smoke.
Three veterinary teaching hospitals
and a national network of community
veterinary clinics have been recruited to
participate in this research. VM/AC
personnel at collaborating field study
sites will have the opportunity to
voluntarily express interest in
participating by completing a brief
expression of interest form. Study
participants will complete: (1) a
baseline questionnaire that collects data
on demographics, work history, job
tasks, exposures to respiratory hazards
(including surgical smoke), use of
personal protective equipment,
workplace safety climate, and
respiratory health and symptoms; and
(2) a post-shift questionnaire assessing
acute respiratory symptoms and job
tasks during the work shift.
This is a new data collection, with
approval requested for three years. CDC
requests OMB approval for an estimated
107 annual burden hours. There are no
costs to respondents other than their
time to participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
VM/AC
VM/AC
VM/AC
VM/AC
personnel
personnel
personnel
personnel
............................................
............................................
............................................
............................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
[FR Doc. 2024–22471 Filed 9–30–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–24–0950]
khammond on DSKJM1Z7X2PROD with NOTICES
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 ‘‘National
Health and Nutrition Examination
Survey (NHANES)’’ 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 May 13,
VerDate Sep<11>2014
17:42 Sep 30, 2024
Jkt 265001
Number of
respondents
Form name
Expression of Interest Form ...........................
Informed Consent ...........................................
Baseline Questionnaire ..................................
Post-shift Questionnaire .................................
2024 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
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
50
50
50
50
Number of
responses
per
respondent
1
1
1
10
Average
burden per
response
(in hours)
3/60
15/60
28/60
8/60
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
National Health and Nutrition
Examination Survey (NHANES) (OMB
Control No. 0920–0950, Exp. 04/30/
E:\FR\FM\01OCN1.SGM
01OCN1
Agencies
[Federal Register Volume 89, Number 190 (Tuesday, October 1, 2024)]
[Notices]
[Pages 79926-79927]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-22471]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-24-24AL]
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 ``Occupational Exposures to Surgical Smoke in
Veterinary Personnel'' 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
November 3, 2023 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
Occupational Exposures to Surgical Smoke in Veterinary Personnel--
New--National Institute for Occupational
[[Page 79927]]
Safety and Health (NIOSH), Centers for Disease Control and Prevention
(CDC).
Background and Brief Description
Surgical smoke produced during tissue cutting and cauterizing
tissues and blood vessels generates hazardous gaseous compounds and
aerosols that are associated with cancer and respiratory irritation;
however, no research has characterized surgical smoke generated from
animal tissue in clinical veterinary settings. Surgical smoke exposure
is an emerging concern in human operating rooms, and several states
have either passed or are considering bills requiring surgical smoke
evacuation systems in human operating rooms to mitigate this
occupational hazard. Surgical suites in veterinary clinics are often
multiple bay suites or have less effective ventilation systems than
human operating rooms, potentially leading to higher exposure levels,
yet no research has examined barriers and aids to the use of surgical
smoke evacuation systems among veterinary medicine/animal care (VM/AC)
personnel.
The proposed project will characterize occupational exposure to
surgical smoke and related respiratory health effects in clinical
veterinary settings. Data will be used to examine: (1) work-related
factors that contribute to exposure to surgical smoke in clinical
veterinary settings; (2) relationships between surgical smoke exposure
in clinical veterinary settings and respiratory health; and (3)
barriers and aids to implementing surgical smoke extraction systems
that reduce occupational exposures to surgical smoke. Findings from
this study will help to provide guidance on engineering controls to
improve air quality in VM/AC personnel's work environment by reducing
exposure to surgical smoke.
Three veterinary teaching hospitals and a national network of
community veterinary clinics have been recruited to participate in this
research. VM/AC personnel at collaborating field study sites will have
the opportunity to voluntarily express interest in participating by
completing a brief expression of interest form. Study participants will
complete: (1) a baseline questionnaire that collects data on
demographics, work history, job tasks, exposures to respiratory hazards
(including surgical smoke), use of personal protective equipment,
workplace safety climate, and respiratory health and symptoms; and (2)
a post-shift questionnaire assessing acute respiratory symptoms and job
tasks during the work shift.
This is a new data collection, with approval requested for three
years. CDC requests OMB approval for an estimated 107 annual burden
hours. There are no costs to respondents other than their time to
participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
VM/AC personnel....................... Expression of Interest 50 1 3/60
Form.
VM/AC personnel....................... Informed Consent........ 50 1 15/60
VM/AC personnel....................... Baseline Questionnaire.. 50 1 28/60
VM/AC personnel....................... Post-shift Questionnaire 50 10 8/60
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Public Health
Ethics and Regulations, Office of Science, Centers for Disease Control
and Prevention.
[FR Doc. 2024-22471 Filed 9-30-24; 8:45 am]
BILLING CODE 4163-18-P