Overview

Title

To amend the Public Health Service Act to reauthorize a national congenital heart disease research, surveillance, and awareness program, and for other purposes.

ELI5 AI

This bill wants to keep helping doctors and scientists study and learn more about a heart problem some babies are born with, by continuing a program that helps them share what they know and find new ways to teach people about it. They want to make sure this program keeps going until 2029.

Summary AI

H.R. 7189 aims to amend the Public Health Service Act to continue supporting a national program focused on congenital heart disease research, awareness, and surveillance. It mandates the Secretary of Health and Human Services to issue a report within two years on current efforts to increase public awareness and improve healthcare provider education on the disease. Additionally, within a year after submitting this report, a strategy must be developed to address awareness gaps, workforce shortages, and promote collaboration involving various stakeholders. This reauthorization extends the program from 2025 to 2029.

Published

2024-05-22
Congress: 118
Session: 2
Chamber: HOUSE
Status: Reported in House
Date: 2024-05-22
Package ID: BILLS-118hr7189rh

Keywords AI

congenital heart disease public health service act reauthorization healthcare provider education public awareness workforce shortages health services research funding surveillance program healthcare collaboration

Sources

Bill Statistics

Size

Sections:
2
Words:
906
Pages:
8
Sentences:
9

Language

Nouns: 316
Verbs: 65
Adjectives: 38
Adverbs: 5
Numbers: 36
Entities: 52

Complexity

Average Token Length:
4.43
Average Sentence Length:
100.67
Token Entropy:
4.88
Readability (ARI):
53.16

AnalysisAI

General Summary

The proposed bill, titled the "Congenital Heart Futures Reauthorization Act of 2024," seeks to amend the Public Health Service Act to reauthorize a national program focused on research, surveillance, and raising awareness about congenital heart disease (CHD). The bill mandates the preparation of comprehensive reports and strategies to enhance public knowledge and healthcare provider education regarding congenital heart disease. It also evaluates the current healthcare workforce dedicated to treating adult CHD patients and extends funding for the program from 2025 through 2029.

Summary of Significant Issues

This bill does not explicitly outline significant controversial issues or debates surrounding its contents. It straightforwardly aims to continue and expand efforts in addressing congenital heart disease—a condition present at birth that affects the structure and function of the heart. The bill emphasizes reporting and strategizing around better public awareness, enhanced training for healthcare providers, and assessing and potentially improving the specialized healthcare workforce for congenital heart disease.

Impact on the Public

Broadly, the bill has the potential to improve long-term health outcomes and quality of life for individuals living with congenital heart disease. By raising public awareness and providing better education for healthcare providers, early diagnosis and more effective treatment plans for CHD patients might be facilitated. Additionally, gaining a clearer understanding of workforce capacity could lead to improvements in the availability and quality of care for adult patients living with CHD. Extending the program's funding ensures continued national focus and resources dedicated to these initiatives.

Impact on Specific Stakeholders

  1. Healthcare Providers: The bill is likely to have positive implications for healthcare professionals by offering them more education and training opportunities related to CHD, potentially improving patient outcomes.

  2. CHD Patients and Families: Patients with congenital heart disease and their families could experience significant benefits from increased public awareness and improved healthcare practices, which may lead to better management of the disease and overall quality of life.

  3. Healthcare Systems and Workforce: The evaluation of workforce capacity to treat adult CHD patients could highlight gaps and lead to strategic development of specialized training programs, fostering a more capable and prepared healthcare system.

  4. Government and Federal Agencies: For agencies such as the CDC and NIH, the bill reinforces collaborative efforts and information dissemination about CHD, strengthening public health initiatives and research.

Overall, while the bill does not present contentious issues, its focus is clear in advocating for enhanced resources and strategic planning in addressing congenital heart disease on a national level. The anticipated positive impacts on patient care and public awareness exemplify the bill's potential to drive meaningful advancements in healthcare related to congenital heart disease.

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 specifies that it can be referred to as the “Congenital Heart Futures Reauthorization Act of 2024.”

2. Reauthorization of national congenital heart disease research, surveillance, and awareness program Read Opens in new tab

Summary AI

The section amends a part of the Public Health Service Act to require a report and strategy focused on congenital heart disease. It calls for increased public awareness and education for healthcare providers, assesses workforce capacity, and extends funding for the program through 2029.