Proposed Data Collection Submitted for Public Comment and Recommendations, 34592-34593 [2018-15528]

Download as PDF 34592 Federal Register / Vol. 83, No. 140 / Friday, July 20, 2018 / Notices Centers for Disease Control and Prevention [60Day–18–18AJJ; Docket No. CDC–2018– 0056] 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 and/or continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled Knowledge, Attitudes, and Practices of US Large Animal Veterinarians Concerning Common Veterinary Infection Control Measures When Working with Animal Obstetric Cases. The goals of this survey are to better describe veterinarians’ current knowledge of zoonotic infectious diseases that cause abortion in large animals, determine common veterinary infection control practices when working up obstetric cases, and identify common barriers to personal protective equipment use. DATES: CDC must receive written comments on or before September 18, 2018. SUMMARY: You may submit comments, identified by Docket No. CDC–2018– 0056 by any of the following methods: • Federal eRulemaking Portal: Regulations.gov. Follow the instructions for submitting comments. • Mail: Jeffrey Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS–D74, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to Regulations.gov. daltland on DSKBBV9HB2PROD with NOTICES ADDRESSES: Please note: Submit all comments through the Federal eRulemaking portal (regulations.gov) or by U.S. mail to the address listed above. VerDate Sep<11>2014 18:06 Jul 19, 2018 Jkt 244001 To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Jeffrey Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS– D74, Atlanta, Georgia 30329; phone: 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 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; and 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. 5. Assess information collection costs. FOR FURTHER INFORMATION CONTACT: DEPARTMENT OF HEALTH AND HUMAN SERVICES Proposed Project Knowledge, Attitudes, and Practices of U.S. Large Animal Veterinarians Concerning Common Veterinary Infection Control Measures When Working with Animal Obstetric Cases— New ICR—National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention (CDC). PO 00000 Frm 00057 Fmt 4703 Sfmt 4703 Background and Brief Description Veterinarians are particularly at risk of contracting zoonotic infectious diseases due to their close proximity to animals, especially during times of injury or illness. Some veterinarians may be unaware of recommended personal protection measures or opt not to participate in measures that would decrease their risk of contracting a zoonotic disease (Wright et al. 2008). In 1977, a survey conducted of 1182 veterinarians showed that approximately 43% of the respondents had contracted an infectious zoonotic disease (Schnurrenberger & Martin 1977). Today, this elevated zoonotic disease risk persists; the seroprevalence of Q fever in U.S. veterinarians is 22% (Whitney, Massung, et al. 2009) and the seroprevalance of leptospirosis is 2.5% (Whitney, Ailes, et al. 2009). Within the veterinary profession, large animal practitioners might have an increased risk of occupational exposure to infectious zoonotic diseases for many reasons, including decreased biosecurity measures available in the field and the limited space available on a mobile practice for PPE. The goals of this study are to establish veterinarians’ knowledge of zoonotic infectious disease, identify veterinarians’ attitudes towards zoonotic infectious disease and personal risk, and determine practices to decrease personal risk of infection. By identifying knowledge gaps in personal protective equipment (PPE) use, transmission risk factors, and disease identification/diagnosis, we aim to determine the best methods for education of veterinarians on relevant abortion-associated zoonotic infectious diseases. The purpose of this study is to better describe veterinarians’ current knowledge of zoonotic diseases that cause abortion in large animals, determine common veterinary infection control practices when working up obstetric cases, and identify common barriers to PPE use. In order to develop effective messaging strategies, a deeper understanding of the attitudes and barriers to PPE use is needed. The information collected will be used to improve and enhance zoonotic disease education and PPE guidance targeted to veterinarians. The estimated annual burden hours are 125. There is no cost to respondents other than their time. E:\FR\FM\20JYN1.SGM 20JYN1 34593 Federal Register / Vol. 83, No. 140 / Friday, July 20, 2018 / Notices ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Number of responses per respondent Average burden per response (in hours) Total burden (in hours) Type of respondents Form name Veterinarian ....................................... ........................................................... 500 1 15/60 125 Total ........................................... ........................................................... ........................ ........................ ........................ 125 Jeffrey M. Zirger, Acting Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2018–15528 Filed 7–19–18; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier CMS–10675] Agency Information Collection Activities: Proposed Collection; Comment Request Centers for Medicare & Medicaid Services, HHS. ACTION: Notice. AGENCY: The Centers for Medicare & Medicaid Services (CMS) is announcing an opportunity for the public to comment on CMS’ intention to collect information from the public. Under the Paperwork Reduction Act of 1995 (the PRA), federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information (including each proposed extension or reinstatement of an existing collection of information) and to allow 60 days for public comment on the proposed action. Interested persons are invited to send comments regarding our burden estimates or any other aspect of this collection of information, including the necessity and utility of the proposed information collection for the proper performance of the agency’s functions, the accuracy of the estimated burden, ways to enhance the quality, utility, and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden. DATES: Comments must be received by September 18, 2018. ADDRESSES: When commenting, please reference the document identifier or OMB control number. To be assured consideration, comments and daltland on DSKBBV9HB2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 18:06 Jul 19, 2018 Jkt 244001 recommendations must be submitted in any one of the following ways: 1. Electronically. You may send your comments electronically to https:// www.regulations.gov. Follow the instructions for ‘‘Comment or Submission’’ or ‘‘More Search Options’’ to find the information collection document(s) that are accepting comments. 2. By regular mail. You may mail written comments to the following address: CMS, Office of Strategic Operations and Regulatory Affairs, Division of Regulations Development, Attention: Document Identifier/OMB Control Number ll, Room C4–26–05, 7500 Security Boulevard, Baltimore, Maryland 21244–1850. To obtain copies of a supporting statement and any related forms for the proposed collection(s) summarized in this notice, you may make your request using one of following: 1. Access CMS’ website address at https://www.cms.gov/Regulations-andGuidance/Legislation/Paperwork ReductionActof1995/PRA-Listing.html. 2. Email your request, including your address, phone number, OMB number, and CMS document identifier, to Paperwork@cms.hhs.gov. 3. Call the Reports Clearance Office at (410) 786–1326. FOR FURTHER INFORMATION CONTACT: William Parham at (410) 786–4669. SUPPLEMENTARY INFORMATION: Contents This notice sets out a summary of the use and burden associated with the following information collections. More detailed information can be found in each collection’s supporting statement and associated materials (see ADDRESSES). CMS–10675 Evaluation of the CMS Quality Improvement Organizations: Medication Safety and Adverse Drug Event Prevention Under the 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. The term ‘‘collection of information’’ is PO 00000 Frm 00058 Fmt 4703 Sfmt 4703 defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and includes agency requests or requirements that members of the public submit reports, keep records, or provide information to a third party. Section 3506(c)(2)(A) of the PRA requires federal agencies to publish a 60-day notice in the Federal Register concerning each proposed collection of information, including each proposed extension or reinstatement of an existing collection of information, before submitting the collection to OMB for approval. To comply with this requirement, CMS is publishing this notice. Information Collection 1. Type of Information Collection Request: New Collection of Information Request; Title of Information Collection: Evaluation of the CMS Quality Improvement Organizations: Medication Safety and Adverse Drug Event Prevention; Use: The purpose of this Information Collection Request (ICR) is to collect data to inform the program evaluation of the Centers for Medicare & Medicaid Services (CMS) Quality Improvement Organizations (QIO) current contract known as the 11th Scope of Work (SOW). The current ICR focuses on evaluating one component of the quality improvement activities of the Quality Innovation Network Quality Improvement Organizations (QIN–QIOs) and is part of a larger evaluation of the overall impact of the QIO program. This ICR aims to assess the QIN–QIO Task which focuses on Medication Safety and Adverse Drug Event Prevention. For this evaluation, we are using a mixedmethods design to compare quality improvement activities of pharmacists, physicians, and nursing home administrators or directors of nursing at nursing homes participating in the QIN– QIO program (participating) with those not participating in the QIN–QIO program (non-participating). As mandated by Sections 1152–1154 of the Social Security Act, CMS directs the QIO program, which is one of the largest federal programs dedicated to improving health quality for Medicare beneficiaries. QIOs are groups of health quality experts, clinicians, and E:\FR\FM\20JYN1.SGM 20JYN1

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[Federal Register Volume 83, Number 140 (Friday, July 20, 2018)]
[Notices]
[Pages 34592-34593]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-15528]



[[Page 34592]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-18-18AJJ; Docket No. CDC-2018-0056]


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 and/or 
continuing information collection, as required by the Paperwork 
Reduction Act of 1995. This notice invites comment on a proposed 
information collection project titled Knowledge, Attitudes, and 
Practices of US Large Animal Veterinarians Concerning Common Veterinary 
Infection Control Measures When Working with Animal Obstetric Cases. 
The goals of this survey are to better describe veterinarians' current 
knowledge of zoonotic infectious diseases that cause abortion in large 
animals, determine common veterinary infection control practices when 
working up obstetric cases, and identify common barriers to personal 
protective equipment use.

DATES: CDC must receive written comments on or before September 18, 
2018.

ADDRESSES: You may submit comments, identified by Docket No. CDC-2018-
0056 by any of the following methods:
     Federal eRulemaking Portal: Regulations.gov. Follow the 
instructions for submitting comments.
     Mail: Jeffrey Zirger, Information Collection Review 
Office, Centers for Disease Control and Prevention, 1600 Clifton Road 
NE, MS-D74, Atlanta, Georgia 30329.
    Instructions: All submissions received must include the agency name 
and Docket Number. CDC will post, without change, all relevant comments 
to Regulations.gov.

    Please note:
     Submit all comments through the Federal eRulemaking portal 
(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 Zirger, Information Collection Review 
Office, Centers for Disease Control and Prevention, 1600 Clifton Road 
NE, MS-D74, Atlanta, Georgia 30329; phone: 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; and
    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.
    5. Assess information collection costs.

Proposed Project

    Knowledge, Attitudes, and Practices of U.S. Large Animal 
Veterinarians Concerning Common Veterinary Infection Control Measures 
When Working with Animal Obstetric Cases--New ICR--National Center for 
Emerging and Zoonotic Infectious Diseases, Centers for Disease Control 
and Prevention (CDC).

Background and Brief Description

    Veterinarians are particularly at risk of contracting zoonotic 
infectious diseases due to their close proximity to animals, especially 
during times of injury or illness. Some veterinarians may be unaware of 
recommended personal protection measures or opt not to participate in 
measures that would decrease their risk of contracting a zoonotic 
disease (Wright et al. 2008). In 1977, a survey conducted of 1182 
veterinarians showed that approximately 43% of the respondents had 
contracted an infectious zoonotic disease (Schnurrenberger & Martin 
1977). Today, this elevated zoonotic disease risk persists; the 
seroprevalence of Q fever in U.S. veterinarians is 22% (Whitney, 
Massung, et al. 2009) and the seroprevalance of leptospirosis is 2.5% 
(Whitney, Ailes, et al. 2009). Within the veterinary profession, large 
animal practitioners might have an increased risk of occupational 
exposure to infectious zoonotic diseases for many reasons, including 
decreased biosecurity measures available in the field and the limited 
space available on a mobile practice for PPE.
    The goals of this study are to establish veterinarians' knowledge 
of zoonotic infectious disease, identify veterinarians' attitudes 
towards zoonotic infectious disease and personal risk, and determine 
practices to decrease personal risk of infection. By identifying 
knowledge gaps in personal protective equipment (PPE) use, transmission 
risk factors, and disease identification/diagnosis, we aim to determine 
the best methods for education of veterinarians on relevant abortion-
associated zoonotic infectious diseases.
    The purpose of this study is to better describe veterinarians' 
current knowledge of zoonotic diseases that cause abortion in large 
animals, determine common veterinary infection control practices when 
working up obstetric cases, and identify common barriers to PPE use. In 
order to develop effective messaging strategies, a deeper understanding 
of the attitudes and barriers to PPE use is needed. The information 
collected will be used to improve and enhance zoonotic disease 
education and PPE guidance targeted to veterinarians. The estimated 
annual burden hours are 125. There is no cost to respondents other than 
their time.

[[Page 34593]]



                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
      Type of respondents           Form name        Number of     responses per   per response    Total burden
                                                    respondents     respondent      (in hours)      (in hours)
----------------------------------------------------------------------------------------------------------------
Veterinarian..................  ................             500               1           15/60             125
                                                 ---------------------------------------------------------------
    Total.....................  ................  ..............  ..............  ..............             125
----------------------------------------------------------------------------------------------------------------


Jeffrey M. Zirger,
Acting Chief, Information Collection Review Office, Office of 
Scientific Integrity, Office of the Associate Director for Science, 
Office of the Director, Centers for Disease Control and Prevention.
[FR Doc. 2018-15528 Filed 7-19-18; 8:45 am]
 BILLING CODE 4163-18-P


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