Agency Information Collection Activities: Proposed Collection; Comment Request, 78048-78050 [2023-25059]

Download as PDF 78048 Federal Register / Vol. 88, No. 218 / Tuesday, November 14, 2023 / Notices some data elements (e.g., date of birth, date of diagnosis, county of residence) could potentially be combined with other information to identify individuals. Private information is not disclosed unless otherwise compelled by law, and all data are treated in a secure manner consistent with the technical, administrative, and operational controls required by the Federal Information Security Management Act of 2002 (FISMA) and the 2010 National Institute of Standards and Technology (NIST) Recommended Security Controls for Federal Information Systems and Organizations. Weekly tables of nationally notifiable diseases are available through CDC WONDER and www.data.cdc.gov. Annual summaries of finalized nationally notifiable disease data are burden estimates for the one-time burden for reporting jurisdictions are for the addition of case notification data for Cronobacter and Ehrlichiosis, new notifiable conditions; the addition of case notification data for Congenital cytomegalovirus infection and Toxoplasmosis, new conditions under standardized surveillance; and the addition of new disease-specific data elements for Cronobacter, Hansen’s Disease (Leprosy) and Leptospirosis. Because there were fewer diseasespecific data elements added in this Revision, the total burden hours decreased from 18,594 to 18,414. CDC requests OMB approval for an estimated 18,414 annual burden hours from the 257 respondents. published on CDC WONDER and www.data.cdc.gov and disease-specific data are published by individual CDC programs. The burden estimates include the number of hours that the public health department uses to process and send case notification data from their jurisdiction to CDC. Specifically, the burden estimates include separate burden hours incurred for automated and non-automated transmissions, separate weekly burden hours incurred for modernizing surveillance systems as part of CDC’s Data Modernization Initiative (DMI) implementation, separate burden hours incurred for annual data reconciliation and submission, and separate one-time burden hours incurred for the addition of new diseases and data elements. The ESTIMATED ANNUALIZED BURDEN HOURS Type of respondent States States States States States ............................. ............................. ............................. ............................. ............................. Territories Territories Territories Territories Territories ....................... ....................... ....................... ....................... ....................... Freely Freely Freely Freely Associated Associated Associated Associated States States States States Cities Cities Cities Cities Cities .............................. .............................. .............................. .............................. .............................. Total ........................ 50 10 50 50 50 52 52 52 1 1 20/60 2 4 75 3 867 1,040 10,400 3,750 150 5 5 5 5 5 52 56 52 1 1 20/60 20/60 4 5 3 87 93 1,040 25 15 3 3 3 3 52 56 1 1 20/60 20/60 5 3 52 56 15 9 2 2 2 2 2 52 52 52 1 1 20/60 2 4 75 3 35 208 416 150 6 .............................................................................. ........................ ........................ ........................ 18,414 [FR Doc. 2023–25088 Filed 11–13–23; 8:45 am] BILLING CODE 4163–18–P khammond on DSKJM1Z7X2PROD with NOTICES Total burden (in hours) Weekly (Automated) ............................................ Weekly (Non-automated) ..................................... Weekly (DMI Implementation) ............................. Annual .................................................................. One-time Addition of Diseases and Data Elements. Weekly (Automated) ............................................ Weekly, Quarterly (Non-automated) .................... Weekly (DMI Implementation) ............................. Annual .................................................................. One-time Addition of Diseases and Data Elements. Weekly (Automated) ............................................ Weekly, Quarterly (Non-automated) .................... Annual .................................................................. One-time Addition of Diseases and Data Elements. Weekly (Automated) ............................................ Weekly (Non-automated) ..................................... Weekly (DMI Implementation) ............................. Annual .................................................................. One-time Addition of Diseases and Data Elements. Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Public Health Ethics and Regulations, Office of Science, Centers for Disease Control and Prevention. DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier: CMS–10552] Agency Information Collection Activities: Proposed Collection; Comment Request Centers for Medicare & Medicaid Services, Health and Human Services (HHS). ACTION: Notice. AGENCY: VerDate Sep<11>2014 Average burden per response (in hours) Number of responses per respondent Number of respondents Form name 16:48 Nov 13, 2023 Jkt 262001 PO 00000 Frm 00101 Fmt 4703 Sfmt 4703 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 SUMMARY: E:\FR\FM\14NON1.SGM 14NON1 Federal Register / Vol. 88, No. 218 / Tuesday, November 14, 2023 / Notices 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 January 16, 2024. ADDRESSES: When commenting, please reference the document identifier or OMB control number. To be assured consideration, comments and 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:__, 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, please access the CMS PRA website by copying and pasting the following web address into your web browser: https://www.cms.gov/ Regulations-and-Guidance/Legislation/ PaperworkReductionActof1995/PRAListing. FOR FURTHER INFORMATION CONTACT: William N. Parham at (410) 786–4669. SUPPLEMENTARY INFORMATION: khammond on DSKJM1Z7X2PROD with NOTICES 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–10552 Implementation of Medicare Programs;—Medicare Promoting Interoperability Program Under the PRA (44 U.S.C. 3501– 3520), Federal agencies must obtain approval from the Office of Management VerDate Sep<11>2014 16:48 Nov 13, 2023 Jkt 262001 and Budget (OMB) for each collection of information they conduct or sponsor. The term ‘‘collection of information’’ is 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: Revision of a currently approved collection; Title of Information Collection: Implementation of Medicare Programs;—Medicare Promoting Interoperability Program; Use: The Centers for Medicare & Medicaid Services (CMS) is requesting approval to collect information from eligible hospitals and critical access hospitals (CAHs). We have finalized changes to this program as discussed in the FY 2024 Inpatient Prospective Payment System (IPPS)/Long-term Care Hospital Prospective Payment System (LTCH PPS) final rule. This is a revision of the information collection request. The American Recovery and Reinvestment Act of 2009 (Recovery Act) (Pub. L. 111–5) was enacted on February 17, 2009. Title IV of Division B of the Recovery Act amended Titles XVIII and XIX of the Social Security Act (the Act) by establishing incentive payments to eligible professionals (EPs), eligible hospitals and CAHs, and Medicare Advantage (MA) organizations participating in the Medicare and Medicaid programs that adopt and successfully demonstrate meaningful use of certified EHR technology (CEHRT). These Recovery Act provisions, together with Title XIII of Division A of the Recovery Act, may be cited as the ‘‘Health Information Technology for Economic and Clinical Health Act’’ or the ‘‘HITECH Act.’’ The HITECH Act created incentive programs for EPs, eligible hospitals including CAHs, and MA organizations in the Medicare Fee-for-Service (FFS), and Medicaid programs that successfully demonstrated meaningful use of CEHRT. In their first payment year, Medicaid EPs, eligible hospitals including MA organizations and CAHs could adopt, implement, or upgrade to certified EHR technology. It also PO 00000 Frm 00102 Fmt 4703 Sfmt 4703 78049 allowed for negative payment adjustments in the Medicare FFS and MA programs starting in 2015 for EPs, eligible hospitals including MA organizations and CAHs participating in Medicare that are not meaningful users of CEHRT. The Medicaid Promoting Interoperability Program did not authorize negative payment adjustments, but its participants were eligible for incentive payments until December 31, 2021, when the program ended. In CY 2017, we began collecting data from eligible hospitals and CAHs to determine the application of the Medicare payment adjustments. This information collection was also used to make incentive payments to eligible hospitals in Puerto Rico from 2016 through 2021. At this time, Medicare eligible professionals no longer reported to the EHR Incentive Program, as they began reporting under the Merit-based Incentive Payment System’s (MIPS) Promoting Interoperability Performance Category. In 2019, the EHR Incentives Program for eligible hospitals and CAHs was subsequently renamed the Medicare Promoting Interoperability Program. In subsequent years, we have focused on balancing reporting burden for eligible hospitals and CAHs while also implementing changes designed to incentivize the advanced use of CEHRT to support health information exchange, interoperability, advanced quality measurement, and maximizing clinical effectiveness and efficiencies. In the FY 2024 IPPS/LTCH PPS final rule, we finalized the following policy changes for eligible hospitals and CAHs that attest to CMS under the Medicare Promoting Interoperability Program. None of the policies we finalized will affect the information collection burden: (i) to adopt three electronic clinical quality measures (eCQMs) beginning with the CY 2025 reporting period: (1) Hospital Harm—Pressure Injury eCQM; (2) Hospital Harm—Acute Kidney Injury eCQM; and (3) Excessive Radiation Dose or Inadequate Image Quality for Diagnostic Computed Tomography (CMT) in Adults eCQM; (ii) to modify the Safety Assurance Factors for EHR Resilience (SAFER) Guides measure to require eligible hospitals and CAHs to submit a ‘‘yes’’ attestation to fulfill the measure beginning with the EHR reporting period in CY 2024; and (iii) to establish an EHR reporting period of a minimum of any continuous 180-day period in CY 2025. Form Number: CMS–10552 (OMB control number: 0938–1278); Frequency: Annually; Affected Public: State, Local or Private Government; Business and for-profit and Not-for-profit; Number of E:\FR\FM\14NON1.SGM 14NON1 78050 Federal Register / Vol. 88, No. 218 / Tuesday, November 14, 2023 / Notices Respondents: 4,500; Total Annual Responses: 4,500; Total Annual Hours: 29,625. (For policy questions regarding this collection, contact Jessica Warren at 410–786–7519.) DEPARTMENT OF HEALTH AND HUMAN SERVICES Dated: November 8, 2023. William N. Parham, III, Director, Paperwork Reduction Staff, Office of Strategic Operations and Regulatory Affairs. National Rural Health Information Clearinghouse Program Health Resources and Services Administration FOR FURTHER INFORMATION CONTACT: Health Resources and Services Administration (HRSA), Department of Health and Human Services. ACTION: Announcing Funding Supplement for National Rural Health Information Clearinghouse Program recipient. AGENCY: [FR Doc. 2023–25059 Filed 11–13–23; 8:45 am] BILLING CODE 4120–01–P Program recipient to develop toolkits and other resources that address strategies to promote rural community health. HRSA provided supplemental award funds to the National Rural Health Information Clearinghouse SUMMARY: Sarah Scott, Federal Office of Rural Health Policy, HRSA, at sscott2@ hrsa.gov and (301) 287–2619. SUPPLEMENTARY INFORMATION: Intended Recipient of the Award: The University of North Dakota. Amount of Non-Competitive Award: One award for $485,000. Project Period: June 1, 2023, to May 31, 2024. CFDA Number: 93.223. Award Instrument: Supplement. Authority: Social Security Act 711(b) (42 U.S.C. 912(b)). TABLE 1—RECIPIENTS AND AWARD AMOUNTS Grant No. Award recipient name City, State U56RH05539 ........................................... University of North Dakota ...................... Grand Forks, ND ..................................... Justification: This funding will provide a one-time supplement to the University of North Dakota via the National Rural Health Information Clearinghouse Program. This supplement will allow the University of North Dakota to build on past and ongoing projects supported by HRSA to improve health care in rural areas by serving as a primary resource for information, opportunities, and tools related to rural health. The supplement will allow the University of North Dakota to create new toolkits and resources on important topics related to rural community health. This builds upon the planned work within the scope of its existing award. Carole Johnson, Administrator. [FR Doc. 2023–25068 Filed 11–13–23; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES khammond on DSKJM1Z7X2PROD with NOTICES Health Resources and Services Administration National Vaccine Injury Compensation Program; List of Petitions Received Health Resources and Services Administration (HRSA), Department of Health and Human Services (HHS). ACTION: Notice. AGENCY: HRSA is publishing this notice of petitions received under the SUMMARY: VerDate Sep<11>2014 16:48 Nov 13, 2023 Jkt 262001 National Vaccine Injury Compensation Program (the Program), as required by the Public Health Service (PHS) Act, as amended. While the Secretary of HHS is named as the respondent in all proceedings brought by the filing of petitions for compensation under the Program, the United States Court of Federal Claims is charged by statute with responsibility for considering and acting upon the petitions. FOR FURTHER INFORMATION CONTACT: For information about requirements for filing petitions, and the Program in general, contact Lisa L. Reyes, Clerk of Court, United States Court of Federal Claims, 717 Madison Place NW, Washington, DC 20005, (202) 357–6400. For information on HRSA’s role in the Program, contact the Director, National Vaccine Injury Compensation Program, 5600 Fishers Lane, Room 08N146B, Rockville, Maryland 20857; (301) 443– 6593, or visit our website at: https:// www.hrsa.gov/vaccinecompensation/ index.html. SUPPLEMENTARY INFORMATION: The Program provides a system of no-fault compensation for certain individuals who have been injured by specified childhood vaccines. Subtitle 2 of title XXI of the PHS Act, 42 U.S.C. 300aa– 10 et seq., provides that those seeking compensation are to file a petition with the United States Court of Federal Claims and to serve a copy of the petition to the Secretary of HHS, who is named as the respondent in each proceeding. The Secretary has delegated this responsibility under the Program to PO 00000 Frm 00103 Fmt 4703 Sfmt 4703 Supplemental award amount $485,000 HRSA. The Court is directed by statute to appoint special masters who take evidence, conduct hearings as appropriate, and make initial decisions as to eligibility for, and amount of, compensation. A petition may be filed with respect to injuries, disabilities, illnesses, conditions, and deaths resulting from vaccines described in the Vaccine Injury Table (the Table) set forth at 42 CFR 100.3. This Table lists for each covered childhood vaccine the conditions that may lead to compensation and, for each condition, the time period for occurrence of the first symptom or manifestation of onset or of significant aggravation after vaccine administration. Compensation may also be awarded for conditions not listed in the Table and for conditions that are manifested outside the time periods specified in the Table, but only if the petitioner shows that the condition was caused by one of the listed vaccines. Section 2112(b)(2) of the PHS Act, 42 U.S.C. 300aa–12(b)(2), requires that ‘‘[w]ithin 30 days after the Secretary receives service of any petition filed under section 2111 the Secretary shall publish notice of such petition in the Federal Register.’’ Set forth below is a list of petitions received by HRSA on September 1, 2023, through September 30, 2023. This list provides the name of the petitioner, city, and state of vaccination (if unknown then the city and state of the person or attorney filing the claim), and case number. In cases where the Court has redacted the name E:\FR\FM\14NON1.SGM 14NON1

Agencies

[Federal Register Volume 88, Number 218 (Tuesday, November 14, 2023)]
[Notices]
[Pages 78048-78050]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-25059]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

[Document Identifier: CMS-10552]


Agency Information Collection Activities: Proposed Collection; 
Comment Request

AGENCY: Centers for Medicare & Medicaid Services, Health and Human 
Services (HHS).

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: 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

[[Page 78049]]

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 January 16, 2024.

ADDRESSES: When commenting, please reference the document identifier or 
OMB control number. To be assured consideration, comments and 
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:__, 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, please access 
the CMS PRA website by copying and pasting the following web address 
into your web browser: https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.

FOR FURTHER INFORMATION CONTACT: William N. 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-10552 Implementation of Medicare Programs;--Medicare Promoting 
Interoperability Program

    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 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: Revision of a currently 
approved collection; Title of Information Collection: Implementation of 
Medicare Programs;--Medicare Promoting Interoperability Program; Use: 
The Centers for Medicare & Medicaid Services (CMS) is requesting 
approval to collect information from eligible hospitals and critical 
access hospitals (CAHs). We have finalized changes to this program as 
discussed in the FY 2024 Inpatient Prospective Payment System (IPPS)/
Long-term Care Hospital Prospective Payment System (LTCH PPS) final 
rule. This is a revision of the information collection request.
    The American Recovery and Reinvestment Act of 2009 (Recovery Act) 
(Pub. L. 111-5) was enacted on February 17, 2009. Title IV of Division 
B of the Recovery Act amended Titles XVIII and XIX of the Social 
Security Act (the Act) by establishing incentive payments to eligible 
professionals (EPs), eligible hospitals and CAHs, and Medicare 
Advantage (MA) organizations participating in the Medicare and Medicaid 
programs that adopt and successfully demonstrate meaningful use of 
certified EHR technology (CEHRT). These Recovery Act provisions, 
together with Title XIII of Division A of the Recovery Act, may be 
cited as the ``Health Information Technology for Economic and Clinical 
Health Act'' or the ``HITECH Act.''
    The HITECH Act created incentive programs for EPs, eligible 
hospitals including CAHs, and MA organizations in the Medicare Fee-for-
Service (FFS), and Medicaid programs that successfully demonstrated 
meaningful use of CEHRT. In their first payment year, Medicaid EPs, 
eligible hospitals including MA organizations and CAHs could adopt, 
implement, or upgrade to certified EHR technology. It also allowed for 
negative payment adjustments in the Medicare FFS and MA programs 
starting in 2015 for EPs, eligible hospitals including MA organizations 
and CAHs participating in Medicare that are not meaningful users of 
CEHRT. The Medicaid Promoting Interoperability Program did not 
authorize negative payment adjustments, but its participants were 
eligible for incentive payments until December 31, 2021, when the 
program ended.
    In CY 2017, we began collecting data from eligible hospitals and 
CAHs to determine the application of the Medicare payment adjustments. 
This information collection was also used to make incentive payments to 
eligible hospitals in Puerto Rico from 2016 through 2021. At this time, 
Medicare eligible professionals no longer reported to the EHR Incentive 
Program, as they began reporting under the Merit-based Incentive 
Payment System's (MIPS) Promoting Interoperability Performance 
Category. In 2019, the EHR Incentives Program for eligible hospitals 
and CAHs was subsequently renamed the Medicare Promoting 
Interoperability Program. In subsequent years, we have focused on 
balancing reporting burden for eligible hospitals and CAHs while also 
implementing changes designed to incentivize the advanced use of CEHRT 
to support health information exchange, interoperability, advanced 
quality measurement, and maximizing clinical effectiveness and 
efficiencies.
    In the FY 2024 IPPS/LTCH PPS final rule, we finalized the following 
policy changes for eligible hospitals and CAHs that attest to CMS under 
the Medicare Promoting Interoperability Program. None of the policies 
we finalized will affect the information collection burden: (i) to 
adopt three electronic clinical quality measures (eCQMs) beginning with 
the CY 2025 reporting period: (1) Hospital Harm--Pressure Injury eCQM; 
(2) Hospital Harm--Acute Kidney Injury eCQM; and (3) Excessive 
Radiation Dose or Inadequate Image Quality for Diagnostic Computed 
Tomography (CMT) in Adults eCQM; (ii) to modify the Safety Assurance 
Factors for EHR Resilience (SAFER) Guides measure to require eligible 
hospitals and CAHs to submit a ``yes'' attestation to fulfill the 
measure beginning with the EHR reporting period in CY 2024; and (iii) 
to establish an EHR reporting period of a minimum of any continuous 
180-day period in CY 2025. Form Number: CMS-10552 (OMB control number: 
0938-1278); Frequency: Annually; Affected Public: State, Local or 
Private Government; Business and for-profit and Not-for-profit; Number 
of

[[Page 78050]]

Respondents: 4,500; Total Annual Responses: 4,500; Total Annual Hours: 
29,625. (For policy questions regarding this collection, contact 
Jessica Warren at 410-786-7519.)

    Dated: November 8, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and 
Regulatory Affairs.
[FR Doc. 2023-25059 Filed 11-13-23; 8:45 am]
BILLING CODE 4120-01-P
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