Overview

Title

To establish a national plan to coordinate research on epilepsy, and for other purposes.

ELI5 AI

The bill is like a big plan to help people who have epilepsy, a condition that makes them have seizures. It wants to find better ways to understand, treat, and maybe even cure epilepsy by having smart people work together and talk about it often to make sure progress is made.

Summary AI

H.R. 10210, titled the "National Plan for Epilepsy Act," proposes the creation of a comprehensive national plan to advance the prevention, diagnosis, treatment, and cure of epilepsy in the United States. The bill outlines the establishment of an integrated national strategy, with the Secretary of Health and Human Services coordinating research, services, and the development of effective treatments. Furthermore, it includes setting up an Advisory Council on Epilepsy Research, Care, and Services to help guide epilepsy-related issues and submit annual progress reports to Congress. The proposed plan aims to address the health, social, and financial impacts of epilepsy and will remain in effect until December 31, 2035.

Published

2024-11-21
Congress: 118
Session: 2
Chamber: HOUSE
Status: Introduced in House
Date: 2024-11-21
Package ID: BILLS-118hr10210ih

Bill Statistics

Size

Sections:
4
Words:
1,870
Pages:
10
Sentences:
40

Language

Nouns: 498
Verbs: 160
Adjectives: 103
Adverbs: 24
Numbers: 57
Entities: 89

Complexity

Average Token Length:
4.20
Average Sentence Length:
46.75
Token Entropy:
5.09
Readability (ARI):
24.91

AnalysisAI

General Summary of the Bill

The proposed legislation, titled the "National Plan for Epilepsy Act," aims to create a comprehensive national strategy for addressing epilepsy in the United States. Introduced in the House of Representatives, this bill seeks to coordinate efforts across various federal entities to prevent, diagnose, treat, and ultimately cure epilepsy. The plan would involve establishing an Advisory Council to help guide these efforts through research, community engagement, and periodic evaluations. The bill provides a structured framework extending through December 31, 2035.

Summary of Significant Issues

The bill's broad scope raises several concerns regarding federal spending, as it outlines extensive activities without specifying budgetary constraints, potentially leading to inefficient expenditure. Additionally, the requirement for cooperation with international bodies lacks clear directives, which might result in unnecessary costs.

The establishment of an Advisory Council introduces potential bureaucracy and ambiguity. For instance, the diversity criteria for selecting non-Federal members are undefined, risking favoritism. Moreover, the mandate for frequent meetings could result in administrative challenges and increased costs.

Concerns also arise around data sharing among federal agencies, as the bill does not provide comprehensive guidance on ensuring data security and privacy. Finally, while the bill is ambitious with a long implementation period, the absence of metrics for evaluating effectiveness could lead to subjective assessments and missed opportunities for course corrections.

Broad Impact on the Public

If implemented effectively, the National Plan for Epilepsy could significantly improve the lives of individuals living with epilepsy. The coordinated national effort may lead to advancements in treatment and management of the condition, potentially reducing healthcare costs and enhancing quality of life for millions of Americans. Moreover, by promoting awareness and reducing stigma, the bill could foster a more inclusive society for those affected by epilepsy.

However, potential inefficiencies and oversight problems might limit these benefits. Without clear spending controls or evaluation criteria, resources might not be allocated optimally, delaying progress in research and treatment development. These issues could impair the plan's capacity to deliver its intended positive impacts.

Impact on Specific Stakeholders

Individuals with Epilepsy: Individuals and families affected by epilepsy stand to gain improved access to medical care, increased support services, and better-tailored research. For those with uncontrolled seizures, advances in treatment options could significantly transform their daily lives.

Healthcare Providers: Healthcare practitioners, especially neurologists and epileptologists, may benefit from improved resources and research findings, enabling them to offer more effective patient care. However, the increased involvement in federal initiatives might require additional training or adaptation to new guidelines.

Federal and Non-Federal Entities: Government agencies tasked with implementing the National Plan might face increased administrative responsibilities, needing to coordinate more effectively while managing budget constraints. Non-governmental organizations could see new opportunities for partnership and influence but may also encounter challenges navigating the bureaucratic processes outlined in the bill.

In conclusion, while the National Plan for Epilepsy Act presents a forward-thinking approach to addressing epilepsy, careful consideration of its implementation and oversight mechanisms is crucial. Balancing ambition with practical details will determine whether this well-intentioned effort can truly achieve the significant benefits it envisions.

Financial Assessment

The proposed bill, the "National Plan for Epilepsy Act," aims to create a national plan to address epilepsy in terms of prevention, diagnosis, treatment, and a potential cure. The bill emphasizes the importance of coordinating research and improving services. It involves setting up an Advisory Council and requires annual reporting to Congress about progress and needs related to epilepsy strategies.

Financial References

The bill provides two notable financial references:

  1. Epilepsy and its Economic Impact: It highlights that 53% of individuals with uncontrolled seizures are in households earning less than $25,000 per year. This points to the significant socio-economic challenges faced by those affected and suggests a potential need for financial intervention or support programs to relieve some of the burdens on these households.

  2. Health Care Costs: The bill outlines that the healthcare costs associated with epilepsy and seizures exceed $54 billion per year in the United States. This staggering figure underscores the high economic impact epilepsy has on the healthcare system and society at large.

Analysis of Financial Implications

Given these references, several issues can be related directly to the financial components of the proposed legislation:

  • Lack of Specific Budgetary Allocations: Although the bill addresses the urgent need to tackle epilepsy, it lacks detailed financial allocations or controls. Without explicit budget plans, there is a risk of excessive federal spending without clear oversight or specific resource allocation, leading to potential inefficiencies and the urgent issue of wasteful expenditures (Issue 1).

  • Potential Administrative Costs: The bill could result in significant administrative costs due to the frequent required meetings of the Advisory Council and the necessity for multiple reports and assessments. These requirements could lead to redundant efforts that may demand substantial federal resources, further intensifying concerns about effective spending management (Issue 5, 6, 7).

  • Data Sharing Concerns: Subsection 320C (e) encourages data sharing among agencies, but it does not address specific financial implications or investment in data security and privacy, potentially leading to increased costs if these aspects are overlooked (Issue 2).

Overall, while the bill aims to address an important health issue, the financial elements risk being overlooked without well-defined budgetary frameworks, which could undermine the efficiency and effectiveness of the legislative intent.

Issues

  • The broad scope of the 'National Plan for Epilepsy' and its listed activities (Section 320C (a)) may result in significant Federal spending, but lacks specific budgetary allocations or spending controls, potentially leading to wasteful expenditures.

  • Subsection 320C (e) addresses data sharing among agencies but lacks specific guidance on data security and privacy protection, posing risks to sensitive information related to epilepsy.

  • The language around 'coordinating with international bodies' (Section 320C (a)(2)(H)) is vague, potentially leading to unnecessary international travel or partnerships without clear outcomes, resulting in inefficient spending.

  • The establishment of an Advisory Council (Section 320C (c)) could introduce additional bureaucratic layers and delays due to the large number of required representatives and experts.

  • Subsection 320C (c)(2)(B) does not define 'diversity of epilepsy', leading to ambiguity and potential favoritism in appointing non-Federal members.

  • The requirement for the Advisory Council to meet at least once each quarter (Section 320C (c)(3)(A)) could result in increased administrative costs, with the meeting frequency potentially excessive and costly.

  • The requirement for multiple reports and assessments by both the Advisory Council and the Secretary (Section 320C (b), (c)(4), and (d)) could be seen as redundant and bureaucratic, needing considerable administrative effort with ambiguous benefits.

  • Subsection 320C (f) indicates a sunset date in 2035, allowing a long implementation period that might not be regularly evaluated for effectiveness or necessity.

  • Subsection 320C (c)(4)(C)(x) requires evaluating the National Plan's implementation but provides no criteria or metrics, leading to subjective assessments.

  • The complexity of language in detailing responsibilities and scope in this bill (e.g., Section 320C (a)(2), (c)(4), and (d)) could be simplified for better understanding, potentially obscuring key responsibilities.

Sections

Sections are presented as they are annotated in the original legislative text. Any missing headers, numbers, or non-consecutive order is due to the original text.

1. Short title Read Opens in new tab

Summary AI

The first section of the bill states that this legislation is officially named the "National Plan for Epilepsy Act."

2. Findings Read Opens in new tab

Summary AI

Congress makes the following findings: Epilepsy is a brain condition causing seizures, affecting millions of adults and children in the U.S., with various causes and often resulting in uncontrolled seizures for some. The condition increases the risk of early death and impacts the ability to work, with significant healthcare costs; many affected people live in low-income households.

Money References

  • (8) Fifty-three percent of individuals with uncontrolled seizures live in households earning less than $25,000 per year.
  • (9) Health care costs associated with epilepsy and seizures exceed $54,000,000,000 per year in the United States.

3. Establishing a National Plan for Epilepsy Read Opens in new tab

Summary AI

The National Plan for Epilepsy aims to prevent, diagnose, treat, and cure epilepsy through a variety of coordinated efforts by the Secretary, including forming an Advisory Council, conducting annual progress assessments, collaborating with federal and international bodies, and ensuring public involvement. It also involves regular meetings and reports to Congress to evaluate and improve epilepsy-related research and services, with a focus on direct impact on individuals living with epilepsy and their caregivers, until its expiration on December 31, 2035.

320C. Programs relating to epilepsy Read Opens in new tab

Summary AI

The section outlines the creation of a "National Plan for Epilepsy," which involves the Secretary carrying out various activities to address epilepsy through prevention, diagnosis, treatment, research coordination, and public engagement. It also establishes an Advisory Council to provide recommendations and evaluate progress, requires annual assessments and reports to Congress, and includes provisions for sharing epilepsy-related data among federal agencies, with the section set to expire on December 31, 2035.