Proposed Data Collection Submitted for Public Comment and Recommendations, 75595-75596 [2023-24345]
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Federal Register / Vol. 88, No. 212 / Friday, November 3, 2023 / Notices
God). Studies have found contradictory
findings, suggesting that Mexican
American women have increased
awareness of the association between
folate and birth defects compared to
English-speaking women. More research
is needed to determine cultural factors
in the decision-making process around
folic acid intake for Hispanic WRA,
though several studies have examined
beliefs and best practices for promoting
folic acid consumption.
The purpose of this project is to
conduct formative research with
Hispanic/Latina women of reproductive
age to examine folic acid and fortified
food awareness, food and supplement
use practices, as well as messaging and
channels to reach Hispanic/Latina
women. The resulting data are expected
to be used for developing new
messaging and communication products
to improve knowledge, awareness, and
practices regarding folic acid
fortification and supplementation
among Hispanic/Latina women of
reproductive age. Additionally, the
findings from the project will inform
future intervention activities to prevent
neural tube defects among Hispanic
women of reproductive age.
This information collection will
involve focus groups with Hispanic/
Latina WRA. CDC requests OMB
approval for an estimated 122 annual
burden hours. There are no costs to
respondents other than their time to
participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Hispanic/Latina Women of Reproductive Age (WRA).
Knowledge, Attitudes, and Practices (KAPs) of Hispanic/Latina Women of Reproductive Age: Focus
Group Moderator Guide (English/Spanish).
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. 2023–24343 Filed 11–2–23; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–24AL; Docket No. CDC–2023–
0089]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Occupational
exposures to surgical smoke in
veterinary personnel which will
characterize occupational exposure to
surgical smoke and related respiratory
health effects in clinical veterinary
settings and provide guidance on
SUMMARY:
lotter on DSK11XQN23PROD with NOTICES1
Number of
respondents
Type of respondents
VerDate Sep<11>2014
17:02 Nov 02, 2023
Jkt 262001
engineering controls to improve air
quality in veterinary medicine/animal
care personnel’s work environment by
reducing exposure to surgical smoke.
DATES: CDC must receive written
comments on or before January 2, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2023–
0089 by either of the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road, NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.regulations.gov) or by U.S. mail to
the address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road, NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 404–639–7570; Email: omb@
cdc.gov.
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
PO 00000
Frm 00059
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
81
1
Average
burden per
response
(in hours)
90/60
information they conduct or sponsor. In
addition, the PRA also requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each new proposed
collection, each proposed extension of
existing collection of information, and
each reinstatement of previously
approved information collection before
submitting the collection to the OMB for
approval. To comply with this
requirement, we are publishing this
notice of a proposed data collection as
described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. 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 submissions
of responses; and
5. Assess information collection costs.
E:\FR\FM\03NON1.SGM
03NON1
75596
Federal Register / Vol. 88, No. 212 / Friday, November 3, 2023 / Notices
Proposed Project
Occupational Exposures to Surgical
Smoke in Veterinary Personnel—New—
National Institute for Occupational
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
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.
Participating VM/AC personnel at
collaborating field study sites 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.
CDC requests OMB approval for an
estimated 59 annual burden hours.
There are no costs to respondents other
than their time to participate.
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
ESTIMATED ANNUALIZED BURDEN HOURS
Total burden
(in hours)
Form name
VM/AC personnel ..............................
VM/AC personnel ..............................
Baseline Questionnaire ....................
Post-shift Questionnaire ...................
33
33
1
10
28/60
8/60
15
44
Total ...........................................
...........................................................
........................
........................
........................
59
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. 2023–24345 Filed 11–2–23; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
Privacy Act of 1974; Matching Program
Center for Consumer
Information and Insurance Oversight
(CCIIO), Centers for Medicare &
Medicaid Services (CMS), Department
of Health and Human Services (HHS).
AGENCY:
Notice of a new matching
program.
ACTION:
lotter on DSK11XQN23PROD with NOTICES1
Average
burden per
response
(in hours)
Number of
responses per
respondent
Number of
respondents
Type of respondents
In accordance with the
Privacy Act of 1974, as amended, the
Department of Health and Human
Services (HHS), Centers for Medicare &
Medicaid Services (CMS) is providing
notice of the re-establishment of a
computer matching program between
SUMMARY:
VerDate Sep<11>2014
17:02 Nov 02, 2023
Jkt 262001
CMS and the Office of Personnel
Management (OPM), ‘‘Verification of
Eligibility of Minimum Essential
Coverage Under the Patient Protection
and Affordable Care Act through an
Office of Personnel Management Health
Benefit Plan.’’
DATES: The deadline for comments on
this notice is December 4, 2023. The reestablished matching program will
commence not sooner than 30 days after
publication of this notice, provided no
comments are received that warrant a
change to this notice. The matching
program will be conducted for an initial
term of 18 months (from approximately
December 8, 2023 to June 7, 2025) and
within three months of expiration may
be renewed for up to one additional year
if the parties make no change to the
matching program and certify that the
program has been conducted in
compliance with the matching
agreement.
ADDRESSES: Interested parties may
submit comments on this notice to the
CMS Privacy Act Officer by mail at:
Division of Security, Privacy Policy &
Governance, Information Security &
Privacy Group, Office of Information
Technology, Centers for Medicare &
PO 00000
Frm 00060
Fmt 4703
Sfmt 4703
Medicaid Services, Location: N1–14–56,
7500 Security Blvd., Baltimore, MD
21244–1850 or by email at
Barbara.Demopulos@cms.hhs.gov.
FOR FURTHER INFORMATION CONTACT: If
you have questions about the matching
program, you may contact Anne Pesto,
Senior Advisor, Marketplace Eligibility
and Enrollment Group, Center for
Consumer Information and Insurance
Oversight, Centers for Medicare &
Medicaid Services, at 443–955–9966, by
email at anne.pesto@cms.hhs.gov, or by
mail at 7500 Security Blvd., Baltimore,
MD 21244.
SUPPLEMENTARY INFORMATION: The
Privacy Act of 1974, as amended (5
U.S.C. 552a) provides certain
protections for individuals applying for
and receiving federal benefits. The law
governs the use of computer matching
by federal agencies when records in a
system of records (meaning, federal
agency records about individuals
retrieved by name or other personal
identifier) are matched with records of
other federal or non-federal agencies.
The Privacy Act requires agencies
involved in a matching program to:
1. Enter into a written agreement,
which must be prepared in accordance
E:\FR\FM\03NON1.SGM
03NON1
]]>Agencies
[Federal Register Volume 88, Number 212 (Friday, November 3, 2023)]
[Notices]
[Pages 75595-75596]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-24345]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-24-24AL; Docket No. CDC-2023-0089]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a proposed information
collection, as required by the Paperwork Reduction Act of 1995. This
notice invites comment on a proposed information collection project
titled Occupational exposures to surgical smoke in veterinary personnel
which will characterize occupational exposure to surgical smoke and
related respiratory health effects in clinical veterinary settings and
provide guidance on engineering controls to improve air quality in
veterinary medicine/animal care personnel's work environment by
reducing exposure to surgical smoke.
DATES: CDC must receive written comments on or before January 2, 2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2023-
0089 by either of the following methods:
Federal eRulemaking Portal: www.regulations.gov. Follow
the instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road,
NE, MS H21-8, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to www.regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (www.regulations.gov) or by U.S. mail to the address listed
above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road, NE, MS H21-8, Atlanta, Georgia 30329; Telephone: 404-639-7570;
Email: [email protected].
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. In addition, the PRA also requires Federal agencies
to provide a 60-day notice in the Federal Register concerning each
proposed collection of information, including each new proposed
collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. 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;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected;
4. 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
submissions of responses; and
5. Assess information collection costs.
[[Page 75596]]
Proposed Project
Occupational Exposures to Surgical Smoke in Veterinary Personnel--
New--National Institute for Occupational 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. Participating VM/AC personnel at collaborating field study
sites 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.
CDC requests OMB approval for an estimated 59 annual burden hours.
There are no costs to respondents other than their time to participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondents Form name respondents responses per response (in (in hours)
respondent hours)
----------------------------------------------------------------------------------------------------------------
VM/AC personnel............... Baseline 33 1 28/60 15
Questionnaire.
VM/AC personnel............... Post-shift 33 10 8/60 44
Questionnaire.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 59
----------------------------------------------------------------------------------------------------------------
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. 2023-24345 Filed 11-2-23; 8:45 am]
BILLING CODE 4163-18-P
