Agency Forms Undergoing Paperwork Reduction Act Review, 14268-14269 [2022-05298]

Download as PDF 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 Jkt 256001 (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 Sfmt 4703 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: VerDate Sep<11>2014 17:51 Mar 11, 2022 Jkt 256001 PO 00000 Frm 00033 Fmt 4703 Sfmt 4703 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
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