FR 2025-00589

Overview

Title

Agency Information Collection Activities: Submission for OMB Review; Comment Request

Agencies

ELI5 AI

CMS wants to know what people think about their plan to ask for information on Medicare health, but they need help in making sure it's useful and not too hard for people to give.

Summary AI

The Centers for Medicare & Medicaid Services (CMS) is inviting public comments on their plan to collect information, as required by the Paperwork Reduction Act of 1995. This includes gathering data on the Medicare Health Outcomes Survey, which measures the quality of life and daily functioning of Medicare beneficiaries. Public input is wanted to assess the necessity of this information collection and its potential burden on participants. Comments must be submitted by February 13, 2025, to ensure they are considered before final approval by the Office of Management and Budget.

Abstract

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 (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 a second opportunity for public comment on the notice. Interested persons are invited to send comments regarding the burden estimate 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.

Type: Notice
Citation: 90 FR 3222
Document #: 2025-00589
Date:
Volume: 90
Pages: 3222-3223

AnalysisAI

The document entitled "Agency Information Collection Activities: Submission for OMB Review; Comment Request" outlines a notice from the Centers for Medicare & Medicaid Services (CMS), a branch of the U.S. Department of Health and Human Services. It invites public comment on CMS's proposed collection of information from Medicare beneficiaries through the Medicare Health Outcomes Survey (HOS). This request is part of a legal requirement under the Paperwork Reduction Act of 1995, which mandates that federal agencies seek public feedback and gain approval from the Office of Management and Budget (OMB) before collecting data from the public.

Summary of the Document

The core purpose of this notice is to gather feedback on the usefulness, necessity, and potential burden of collecting health outcome information from Medicare recipients. CMS employs the Health Outcomes Survey to assess the overall quality of life and daily functioning among its beneficiaries. The agency seeks comments on whether the data collection is necessary for its functions, the accuracy of the expected burden, and whether automation could reduce paperwork.

Significant Issues or Concerns

Several issues arise from the document:

  • Lack of Clarity on Costs: The document does not provide specific details on the costs associated with collecting this information. Without such data, it becomes challenging for stakeholders to evaluate if this initiative is a judicious use of taxpayer funds.

  • Utility of Information Volume: The notice indicates a significant volume of total annual responses (663,150). However, it does not elaborate on why such a large sample is required or how effectively all of this data will be utilized, potentially implying inefficiencies.

  • Methodological Details: The proposed methodology for using the gathered data to enhance health outcomes is insufficiently detailed. It is unclear how CMS plans to transform the information from the survey into actionable insights that will genuinely benefit patients.

  • Complex Terminology: The use of terms such as "longitudinal patient-reported outcome measure (PROM)" and the "Meaningful Measures Framework" without definitions might obscure understanding for readers who are not familiar with medical or regulatory jargon.

  • Dense Bureaucratic Language: The document employs language that may not be easily accessible to all members of the public, despite their potential interest and stake in the Medicare system.

  • Limited Contact Information: While contact details are provided, the document does not clarify if other communication channels are available for inquiries or assistance.

Potential Impact on the Public

For the general public, particularly Medicare beneficiaries and their families, the survey represents both an opportunity and a burden. On the positive side, gathering this data could potentially lead to improved healthcare outcomes if CMS translates insights into policy and practice. However, respondents may find participation time-consuming or intrusive, particularly if the benefits of participation are not immediately apparent.

Impact on Specific Stakeholders

Medicare Beneficiaries: These individuals are likely the direct subjects of the survey, and their feedback will be crucial in fine-tuning Medicare services. However, the unaddressed issues such as unclarified costs and the survey’s utility may influence their willingness to participate.

Healthcare Providers: Providers could benefit from the broader insights into patient outcomes the survey aims to collect. Nevertheless, they might also face increased administrative pressure if the data collection results in additional reporting or compliance requirements.

Policy Makers and Taxpayers: For policy makers, thorough participant feedback could guide more effective and efficient healthcare policies. Meanwhile, taxpayers could potentially benefit from more effective use of Medicare funds, but only if the findings lead to actionable policy improvements, which the document does not sufficiently guarantee.

Overall, while the initiative outlined in the document has the potential to better health outcomes and streamline Medicare services, its current presentation leaves significant questions unanswered about its cost-effectiveness and practical impact. More transparency and clarity would likely enhance stakeholder engagement and trust.

Issues

  • • The document does not clearly specify the cost associated with the collection of information, which makes it difficult to assess the potential for wasteful spending.

  • • The notice lists a large number of total annual responses (663,150) but does not separately clarify the expected utility or necessity of such a large volume of information collected, which could imply inefficiency.

  • • The document mentions the use of the Health Outcomes Survey to improve health outcomes for beneficiaries but does not provide detailed methods on how this data will be specifically used to achieve these improvements.

  • • Terms like 'longitudinal patient-reported outcome measure (PROM)' and 'Meaningful Measures Framework' are used without definition, which could cause confusion for lay readers.

  • • The document is dense and uses bureaucratic language that may be difficult for the general public to fully comprehend, especially regarding the impact of the survey data.

  • • Contact information for further inquiries is provided, but it is unclear if this is sufficient or if additional channels for assistance are available.

Statistics

Size

Pages: 2
Words: 853
Sentences: 26
Entities: 66

Language

Nouns: 302
Verbs: 82
Adjectives: 24
Adverbs: 5
Numbers: 36

Complexity

Average Token Length:
5.66
Average Sentence Length:
32.81
Token Entropy:
5.20
Readability (ARI):
25.16

Reading Time

about 3 minutes