Agency Forms Undergoing Paperwork Reduction Act Review, 14268-14269 [2022-05298]
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14268
Federal Register / Vol. 87, No. 49 / Monday, March 14, 2022 / Notices
majority of livestock (96%) and wildlife
(58%) cases resulted in death.
Factors that influence the occurrence
of HABs include water temperature and
nutrient levels. Warm waters with
abundant phosphorus and nitrogen
content (e.g., from urban or agricultural
run-off) are more likely to form HABs.
These conditions promote the growth of
phytoplankton or algae that can produce
toxins or otherwise cause illness in
animals, people, and negatively impact
the local ecology (e.g., reduced oxygen
and light available for aquatic
organisms) or economy (e.g., beach
closures, shellfish bed closures). There
is evidence that the frequency and
severity of HABs may be affected by
climate change, but that the impacts
might vary due to the causal species,
bloom location, or other factors.
In response to HAB-related public
health events in 2018, Congress
appropriated funds to CDC to enhance
HAB exposure activities, including
surveillance, mitigation, and event
response efforts. In years since,
Congress has directed CDC to continue
efforts to respond to HAB events,
including OHHABS as a tool for
national surveillance. OHHABS is a
centralized data source for public health
surveillance of HAB events and HAB-
associated illnesses. It uses a One
Health approach that takes into
consideration information from the
environment, animal cases, and human
cases. Outbreaks of HAB-associated
human illnesses may already be
reported to CDC by state and territorial
public health agencies within the
electronic National Outbreak Reporting
System (NORS) (OMB Control No.
0920–0004). OHHABS is the national
database used for public health
surveillance of HAB events and single
cases of HAB-associated human or
animal illness. A standardized datacollection system for HAB events and
HAB-associated illnesses continues to
be necessary to quantify and
characterize HAB-associated illnesses,
refine HAB event and case definitions,
and inform One Health prevention
efforts.
OHHABS was approved for data
collection in 2016. The system was
launched in June 2016 along with a CDC
HAB-associated illnesses website to
provide more information for the
general public about potential illnesses
and to share resources for HAB
awareness and OHHABS with public
health partners. Since 2016, CDC has
provided technical assistance and
training to states and territories
interested in OHHABs and worked with
contractors to implement new features
for OHHABS. In 2020, CDC and partners
published the first summary of
OHHABS data (years 2016—2018) in the
Morbidity and Mortality Weekly Report
(MMWR). In 2021, CDC released a 2019
OHHABS data summary online (https://
www.cdc.gov/habs/data/)
and upgraded the electronic platform to
improve the user interface and system
functionality. During this time CDC has
also continued to coordinate a series of
conference calls where state and federal
partners may discuss their surveillance
activities, needs, and priorities. CDC has
also had the opportunity to
communicate with additional HAB
surveillance stakeholders, such as
members of the veterinary community,
state and federal environmental health
staff, and others to provide information
about OHHABS reporting through
webinars, posters, and other
presentations.
This activity is authorized by Section
301 of the Public Health Service Act (42
U.S.C. 241). CDC requests OMB
approval for an estimated 76 annual
burden hours. There is no cost to
respondents other than their time to
participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
State/Territory .................................................
One Health Harmful Algal Bloom System
(OHHABS) (electronic, year-round).
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–05299 Filed 3–11–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–22–1092]
Agency Forms Undergoing Paperwork
Reduction Act Review
jspears on DSK121TN23PROD with NOTICES1
Number of
respondents
Type of respondents
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Sudden Death
in the Young (SDY) Case Registry’’ to
the Office of Management and Budget
VerDate Sep<11>2014
17:51 Mar 11, 2022
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(OMB) for review and approval. CDC
previously published a ‘‘Proposed Data
Collection Submitted for Public
Comment and Recommendations’’
notice on September 7, 2021 to obtain
comments from the public and affected
agencies. CDC received two 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
PO 00000
Frm 00032
Fmt 4703
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Number of
responses per
respondent
57
4
Average
burden per
response
(in hours)
20/60
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
E:\FR\FM\14MRN1.SGM
14MRN1
14269
Federal Register / Vol. 87, No. 49 / Monday, March 14, 2022 / Notices
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
Sudden Death in the Young (SDY)
Case Registry (OMB Control No. 0920–
1092, Exp. 04/30/2022)—Revision—
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Sudden Death in the Young (SDY) is
defined as a sudden and unexpected
death among an infant, child, or young
adults (up to age 20), which is not
explained by homicide, suicide,
overdose, or the result of an external
cause that was the only and obvious
reason for the fatal injury, or terminal
illnesses. Injury deaths where there may
have been an initiating natural cause
(e.g., drowning or death of the driver in
a motor vehicle accident, which may
have been triggered by an underlying
cardiac or neurological condition) are
also included in the definition.
SDY deaths are not systematically
monitored and estimates of the annual
incidence of SDY vary due to
differences in definitions,
inconsistencies in classifying cause,
variable age and study populations, and
differing case ascertainment
methodologies. Because standardized
information has not been collected on
the incidence, causes, and risk factors,
developing evidence-based prevention
measures has been challenging.
To address these gaps, CDC, in
collaboration with the National Heart,
Lung, and Blood Institute and the
National Institute of Neurological
Disorders and Stroke at the National
Institutes of Health, implemented the
SDY Case Registry. Standardized data
collected through the SDY Case Registry
has been used by the NIH and CDC
awardees to generate estimates of the
incidence of SDY; to elucidate risk
factors; and to develop evidence-based
prevention strategies for SDY. The SDY
Registry also creates infrastructure for
future research about previously
unknown or unrecognized risk factors
for, and causes of, these deaths.
This information collection request is
to extend OMB approval for the SDY
Registry. By continuing the prior work
of the SDY Registry, the information
collected under this request will allow
CDC to provide technical assistance to
awardees so they can improve their state
or local jurisdiction’s information on
SDY. This includes two additions to
their existing Child Death Review (CDR)
program: (1) Entering SDY information
from existing data sources (e.g., medical
records, autopsy reports) used during
CDR review into the established webbased NCFRP Case Reporting System;
and (2) convening clinicians with three
different types of expertise (pediatric
cardiology; pediatric neurology or
epileptology; and forensic pathology) to
conduct advanced clinical reviews of a
subset of SDY cases to allow for a more
thorough review of information
compiled, and to generate additional
data about the classification of the
death. The intended result will be data
that can establish incidence and guide
program and policy decisions at the
state/local jurisdiction levels.
CDC estimates that the participating
state/local jurisdictions will collect data
on approximately 720 SDY cases per
year. For participating state/local
jurisdictions, burden is estimated for
reporting required case information.
Based on historical program
information, it is estimated that
approximately half (360) of the 720
estimated SDY cases each year will
undergo an advanced clinical review
and classification of cause by a team of
three medical experts.
OMB approval is requested for three
years. The total estimated annual
burden is 511 hours which is a decrease
of 10 hours from the previously
approved information collection request
due to a decrease in the number of
participating states/local jurisdictions
from 14 to 13. There are no costs to
respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
State or Local Health Department Personnel
Medical Experts ..............................................
State or Local Health Department Personnel
SDY Module I .................................................
Advanced Review ..........................................
SDY Module N ...............................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–05298 Filed 3–11–22; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–22–0457; Docket No. CDC–2022–
0033]
BILLING CODE 4163–18–P
jspears on DSK121TN23PROD with NOTICES1
Number of
respondents
Type of respondents
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
SUMMARY:
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Number of
responses per
respondent
13
39
13
55
28
55
Average
burden per
response
(in hours)
10/60
15/60
10/60
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 and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on an
information collection titled, Aggregate
Reports for Tuberculosis Program
Evaluation. The goal of the study is to
allow CDC to collect and monitor
indicators for key program activities,
such as finding tuberculosis infections
in recent contacts of cases and in other
high-risk persons likely to be infected,
and providing therapy for latent
E:\FR\FM\14MRN1.SGM
14MRN1
Agencies
[Federal Register Volume 87, Number 49 (Monday, March 14, 2022)]
[Notices]
[Pages 14268-14269]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-05298]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-22-1092]
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 ``Sudden Death in the Young (SDY) Case
Registry'' 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 September
7, 2021 to obtain comments from the public and affected agencies. CDC
received two 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
[[Page 14269]]
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
Sudden Death in the Young (SDY) Case Registry (OMB Control No.
0920-1092, Exp. 04/30/2022)--Revision--National Center for Chronic
Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Sudden Death in the Young (SDY) is defined as a sudden and
unexpected death among an infant, child, or young adults (up to age
20), which is not explained by homicide, suicide, overdose, or the
result of an external cause that was the only and obvious reason for
the fatal injury, or terminal illnesses. Injury deaths where there may
have been an initiating natural cause (e.g., drowning or death of the
driver in a motor vehicle accident, which may have been triggered by an
underlying cardiac or neurological condition) are also included in the
definition.
SDY deaths are not systematically monitored and estimates of the
annual incidence of SDY vary due to differences in definitions,
inconsistencies in classifying cause, variable age and study
populations, and differing case ascertainment methodologies. Because
standardized information has not been collected on the incidence,
causes, and risk factors, developing evidence-based prevention measures
has been challenging.
To address these gaps, CDC, in collaboration with the National
Heart, Lung, and Blood Institute and the National Institute of
Neurological Disorders and Stroke at the National Institutes of Health,
implemented the SDY Case Registry. Standardized data collected through
the SDY Case Registry has been used by the NIH and CDC awardees to
generate estimates of the incidence of SDY; to elucidate risk factors;
and to develop evidence-based prevention strategies for SDY. The SDY
Registry also creates infrastructure for future research about
previously unknown or unrecognized risk factors for, and causes of,
these deaths.
This information collection request is to extend OMB approval for
the SDY Registry. By continuing the prior work of the SDY Registry, the
information collected under this request will allow CDC to provide
technical assistance to awardees so they can improve their state or
local jurisdiction's information on SDY. This includes two additions to
their existing Child Death Review (CDR) program: (1) Entering SDY
information from existing data sources (e.g., medical records, autopsy
reports) used during CDR review into the established web-based NCFRP
Case Reporting System; and (2) convening clinicians with three
different types of expertise (pediatric cardiology; pediatric neurology
or epileptology; and forensic pathology) to conduct advanced clinical
reviews of a subset of SDY cases to allow for a more thorough review of
information compiled, and to generate additional data about the
classification of the death. The intended result will be data that can
establish incidence and guide program and policy decisions at the
state/local jurisdiction levels.
CDC estimates that the participating state/local jurisdictions will
collect data on approximately 720 SDY cases per year. For participating
state/local jurisdictions, burden is estimated for reporting required
case information. Based on historical program information, it is
estimated that approximately half (360) of the 720 estimated SDY cases
each year will undergo an advanced clinical review and classification
of cause by a team of three medical experts.
OMB approval is requested for three years. The total estimated
annual burden is 511 hours which is a decrease of 10 hours from the
previously approved information collection request due to a decrease in
the number of participating states/local jurisdictions from 14 to 13.
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)
----------------------------------------------------------------------------------------------------------------
State or Local Health Department SDY Module I............ 13 55 10/60
Personnel.
Medical Experts....................... Advanced Review......... 39 28 15/60
State or Local Health Department SDY Module N............ 13 55 10/60
Personnel.
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2022-05298 Filed 3-11-22; 8:45 am]
BILLING CODE 4163-18-P