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House Bill 6829
118th Congress(2023-2024)
HEARTS Act of 2024
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Passed House on Sep 23, 2024
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H. R. 6829 (Introduced-in-House)


118th CONGRESS
1st Session
H. R. 6829


To amend the Public Health Service Act to authorize and support the creation and dissemination of cardiomyopathy education, awareness, and risk assessment materials and resources to identify more at-risk families, to authorize research and surveillance activities relating to cardiomyopathy, and for other purposes.


IN THE HOUSE OF REPRESENTATIVES

December 14, 2023

Mr. Pallone (for himself and Mr. Kim of New Jersey) introduced the following bill; which was referred to the Committee on Energy and Commerce


A BILL

To amend the Public Health Service Act to authorize and support the creation and dissemination of cardiomyopathy education, awareness, and risk assessment materials and resources to identify more at-risk families, to authorize research and surveillance activities relating to cardiomyopathy, and for other purposes.

Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled,

SECTION 1. Short title.

This Act may be cited as the “Cardiomyopathy Health Education, Awareness, Research, and Training in the Schools Act of 2023” or the “HEARTS Act of 2023”.

SEC. 2. Materials and resources to increase education and awareness of cardiomyopathy among school administrators, educators, and families.

Part P of title III of the Public Health Service Act (42 U.S.C. 280g et seq.) is amended by adding at the end the following new section:

“SEC. 399V–8. Materials and resources to increase education and awareness of cardiomyopathy among school administrators, educators, and families.

“(a) Materials and resources.—Not later than 18 months after the date of the enactment of this section, the Secretary, in consultation with the Director of the Centers for Disease Control and Prevention (in this section referred to as the ‘Director’) shall develop public education materials and resources to be disseminated to school administrators, educators, school health professionals, coaches, families, guardians, caregivers, and other appropriate individuals. The materials and resources shall include—

“(1) background information to increase education and awareness of cardiomyopathy;

“(2) guidelines regarding the placement of automated external defibrillators in schools, early childhood education programs, and child care centers;

“(3) training information on automated external defibrillators and cardiopulmonary resuscitation; and

“(4) recommendations for how schools, early childhood education programs, and child care centers can develop and implement a cardiac emergency response plan.

“(b) Dissemination of materials and resources.—Not later than 30 months after the date of the enactment of this section, the Secretary shall disseminate the materials and resources developed under subsection (a) in accordance with the following:

“(1) DISTRIBUTION BY STATE EDUCATIONAL AGENCIES.—The Secretary shall make available such materials and resources to State educational agencies to distribute—

“(A) to school administrators, educators, school health professionals, coaches, families, guardians, caregivers, and other appropriate individuals, the background materials developed under subsection (a)(1);

“(B) to parents, guardians, or other caregivers, the risk assessment for individuals with or at risk for cardiomyopathy developed pursuant to section 399V–9(b)(1); and

“(C) to school administrators, educators, school health professionals, and coaches—

“(i) the guidelines described in subsection (a)(2);

“(ii) the training information described in subsection (a)(3); and

“(iii) the recommendations described in subsection (a)(4).

“(2) DISSEMINATION TO HEALTH DEPARTMENTS AND PROFESSIONALS.—The Secretary shall make available the materials and resources developed under subsection (a) to State and local health departments, pediatricians, hospitals, and other health professionals, such as nurses and first responders.

“(3) POSTING ON WEBSITE.—

“(A) CDC.—

“(i) IN GENERAL.—The Secretary, through the Director, shall post the materials and resources developed under subsection (a) on the public Internet website of the Centers for Disease Control and Prevention.

“(ii) ADDITIONAL INFORMATION.—The Director is encouraged to maintain on such public Internet website such additional information regarding cardiomyopathy as deemed appropriate by the Director.

“(B) STATE EDUCATIONAL AGENCIES.—State educational agencies are encouraged to create public Internet webpages dedicated to cardiomyopathy and post the materials and resources developed under subsection (a) on such webpages.

“(c) Definitions.—In this section:

“(1) The term ‘school administrator’ means a principal, director, manager, or other supervisor or leader within an elementary school, secondary school, State-based early childhood education program, or child care center.

“(2) The term ‘school health professional’ means a health professional serving at an elementary school, secondary school, State-based early childhood education program, or child care center.

“(3) The terms ‘early childhood education program’, ‘elementary school’, and ‘secondary school’ have the meanings given to those terms in section 8101 of the Elementary and Secondary Education Act of 1965.

“(4) The term ‘cardiomyopathy’ has the meaning given such term in section 399V–9(c).

“(d) Authorization of appropriations.—For carrying out this section and section 399V–9, there is authorized to be appropriated $5,000,000 for each of fiscal years 2025 through 2028.”.

SEC. 3. Research and surveillance activities relating to cardiomyopathy.

(a) CDC research and surveillance.—Part P of title III of the Public Health Service Act (42 U.S.C. 280g et seq.), as amended by section 2, is further amended by adding at the end the following new section:

“SEC. 399V–9. Research and surveillance activities relating to cardiomyopathy.

“(a) Reports on CDC national cardiomyopathy surveillance research activities.—

“(1) INITIAL REPORT.—Not later than June 1, 2024, the Secretary, acting through the Director of the Centers for Disease Control and Prevention, shall submit to Congress an initial report on findings and data generated from surveillance and research activities conducted by the Centers for Disease Control and Prevention to improve the understanding of the prevalence and epidemiology of cardiomyopathy across the lifespan, from birth to adulthood, with particular interest in the following:

“(A) The health care costs, utilization, and natural history of individuals with cardiomyopathy, in both the pediatric and adult population.

“(B) Estimates of cardiomyopathy-related emergency department visits and hospitalizations, in both the pediatric and adult population.

“(2) FINAL REPORT.—Not later than January 1, 2029, the Secretary, acting through the Director of the Centers for Disease Control and Prevention, shall submit to Congress a final report on the content described in paragraph (1).

“(3) PUBLIC ACCESS.—Subject to paragraph (4), the reports submitted under this subsection shall be made available to the public.

“(4) PRIVACY PROTECTIONS.—The Secretary shall ensure that this subsection is carried out in a manner that complies with all applicable privacy laws under Federal and State law.

“(b) Improving risk assessments for individuals with cardiomyopathy.—

“(1) IN GENERAL.—The Secretary shall develop and make publicly available a risk assessment for individuals with or at risk for cardiomyopathy. Such risk assessment shall, at a minimum, include the following:

“(A) Background information of the prevalence, incidence, and health impact of cardiomyopathy, including all forms of cardiomyopathy and their effects on pediatric, adolescent, and adult individuals.

“(B) A worksheet with variables and conditions for an individual or health care provider to use in assessing whether the individual is at risk for cardiomyopathy.

“(C) A worksheet with variables and stages of progression for an individual or health care provider to use in assessing whether and to what extent cardiomyopathy has progressed in the individual.

“(D) Guidelines on cardiomyopathy screenings for individuals who are at risk for, or have a family history of, cardiomyopathy.

“(2) STAKEHOLDER INPUT.—In carrying out paragraph (1), the Director of the Centers for Disease Control and Prevention shall seek input from external stakeholders including—

“(A) representatives from national patient advocacy organizations expert in all forms of cardiomyopathy;

“(B) representatives from medical professional societies that specialize in the care of adults and pediatrics with cardiomyopathy; and

“(C) representatives from other relevant Federal agencies.

“(c) Cardiomyopathy defined.—For purposes of this section, the term ‘cardiomyopathy’ means a heart disease that affects the heart’s muscle (myocardium)—

“(1) the symptoms of which may vary from case to case, including—

“(A) cases in which no symptoms are present (asymptomatic); and

“(B) cases in which there are symptoms of a progressive condition that may result from an impaired ability of the heart to pump blood, such as fatigue, irregular heartbeats (arrhythmia), heart failure, and, potentially, sudden cardiac death; and

“(2) the recognized types of which include dilated, hypertrophic, restrictive, arrhythmogenic right ventricular dysplasia, and left ventricular non-compaction.”.

(b) NIH research.—Part A of title IV of the Public Health Service Act (42 U.S.C. 281 et seq.) is amended by inserting after section 404E the following new section:

“SEC. 404F. Cardiomyopathy research.

“(a) In general.—The Director of NIH may expand, intensify, and coordinate research and related activities of the National Institutes of Health with respect to cardiomyopathy, which may include research with respect to—

“(1) causation of cardiomyopathy, including genetic causes and molecular biomarkers;

“(2) long-term health outcomes in individuals with cardiomyopathy, including infants, children, teenagers, adults, and elderly individuals; and

“(3) studies using longitudinal data and retrospective analysis to identify effective treatments and outcomes for individuals with cardiomyopathy.

“(b) Cardiomyopathy defined.—For purposes of this section, the term ‘cardiomyopathy’ means a heart disease that affects the heart’s muscle (myocardium)—

“(1) the symptoms of which may vary from case to case, including—

“(A) cases in which no symptoms are present (asymptomatic); and

“(B) cases in which there are symptoms of a progressive condition that may result from an impaired ability of the heart to pump blood, such as fatigue, irregular heartbeats (arrhythmia), heart failure, and, potentially, sudden cardiac death; and

“(2) the recognized types of which include dilated, hypertrophic, restrictive, arrhythmogenic right ventricular dysplasia, and left ventricular non-compaction.”.

(c) NIH report.—Not later than 18 months after the date of the enactment of this Act, the Director of the National Institutes of Health shall submit to Congress a report—

(1) outlining the ongoing research efforts of the National Institutes of Health regarding cardiomyopathy; and

(2) identifying—

(A) a research agenda regarding adult forms of cardiomyopathy;

(B) plans for researching cardiomyopathy affecting the pediatric population; and

(C) the areas of greatest need for such research.