United States 118th Congress Status: In Committee 1 D cosponsors

S 3757 — Congenital Heart Futures Reauthorization Act of 2024

Last action — Placed on Senate Legislative Calendar under General Orders. Calendar No. 429.

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  1. ✓
    Introduced
  2. 2
    In Committee
  3. 3
    Passed Senate
  4. 4
    Passed House
  5. 5
    To Executive
  6. 6
    Enacted

This bill died with 118th Congress. It reached “In Committee” and never advanced before the session ended, so it can no longer move — a new version would have to be reintroduced in the current session.

This bill is no longer active — its legislative session has ended, so there is no live prognosis. It would have to be reintroduced in the current session to move again.

Bill Text

What changed in the latest version

83 added · 24 removed

Plain-language change summary

The amendment adds a requirement for the Secretary to convene a workshop focused on the needs of adult patients living with congenital heart disease. This workshop will gather subject matter experts to discuss areas such as long-term health outcomes, quality of life, and the utilization of healthcare services. The change emphasizes collaboration among various stakeholders, which may enhance understanding and support for adult congenital heart disease patients.

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3757 Introduced in Senate (IS)] <DOC> 118th CONGRESS 2d Session S.
3757 Reported in Senate (RS)] <DOC> Calendar No.
429 118th CONGRESS 2d Session S.
Durbin (for himself and Mr.
Durbin (for himself, Mr.
Young) introduced the following bill;
Young, Mr.
which was read twice and referred to the Committee on Health, Education, Labor, and Pensions _______________________________________________________________________ A BILL To reauthorize the congenital heart disease research, surveillance, and awareness program of the Centers for Disease Control and Prevention, and for other purposes.
Casey, Ms.
Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled, SECTION 1.
Smith, and Mrs.
Gillibrand) introduced the following bill;
which was read twice and referred to the Committee on Health, Education, Labor, and Pensions June 18, 2024 Reported by Mr.
Sanders, with an amendment [Strike out all after the enacting clause and insert the part printed in italic] _______________________________________________________________________ A BILL To reauthorize the congenital heart disease research, surveillance, and awareness program of the Centers for Disease Control and Prevention, and for other purposes.
Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled, <DELETED>SECTION 1.
SHORT TITLE.</DELETED> <DELETED> This Act may be cited as the ``Congenital Heart Futures Reauthorization Act of 2024''.</DELETED> <DELETED>SEC.
2.
NATIONAL CONGENITAL HEART DISEASE RESEARCH, SURVEILLANCE, AND AWARENESS.</DELETED> <DELETED> Section 399V-2 of the Public Health Service Act (42 U.S.C.
280g-13) is amended--</DELETED> <DELETED> (1) by redesignating subsections (f) and (g) as subsections (h) and (i), respectively;</DELETED> <DELETED> (2) by inserting after subsection (e) the following:</DELETED> <DELETED> ``(f) Stakeholder Workshop.--</DELETED> <DELETED> ``(1) In general.--Not later than 1 year after the date of enactment of the Congenital Heart Futures Reauthorization Act of 2024, the Secretary shall convene a workshop composed of subject matter experts, on adult patients living with congenital heart disease, to--</DELETED> <DELETED> ``(A) identify research gaps and opportunities related to the lifelong needs of congenital heart disease patients, including long-term health outcomes, quality of life, mental health, and health care utilization;</DELETED> <DELETED> ``(B) assess the workforce capacity in the United States of health care providers who treat adult patients living with congenital heart disease, and options to address any such shortages in such workforce, which may include strategies to expand fellowship training programs and support regional care centers;
and</DELETED> <DELETED> ``(C) foster collaboration and dissemination of information across Federal agencies, health care providers, researchers, and patient organizations.</DELETED> <DELETED> ``(2) Composition.--The workshop described in paragraph (1) shall be led by the Secretary, and shall involve participants that include, as appropriate, stakeholders representing patient organizations, health care professionals, research entities, health insurance providers, accrediting organizations, and relevant Federal agencies, including the Centers for Disease Control and Prevention, the National Institutes of Health, and the Health Resources and Services Administration.</DELETED> <DELETED> ``(g) Report.--Not later than 3 years after the date of enactment of the Congenital Heart Futures Reauthorization Act of 2024, the Secretary shall issue a report to the Committee on Health, Education, Labor, and Pensions of the Senate and the Committee on Energy and Commerce of the House of Representatives on findings and recommendations of the Secretary with respect to strategies to advance research related to the lifelong needs of congenital heart disease patients and address workforce shortages of providers for adult patients living with congenital heart disease, and, as appropriate, progress made by the Secretary to implement such strategies and a plan for implementing such recommendations.'';
and</DELETED> <DELETED> (3) in subsection (i), as so redesignated, by striking ``2020 through 2024'' and inserting ``2025 through 2029''.</DELETED> SECTION 1.
``(f) Stakeholder Workshop.-- ``(1) In general.--Not later than 1 year after the date of enactment of the Congenital Heart Futures Reauthorization Act of 2024, the Secretary shall convene a workshop composed of subject matter experts, on adult patients living with congenital heart disease, to-- ``(A) identify research gaps and opportunities related to the lifelong needs of congenital heart disease patients, including long-term health outcomes, quality of life, mental health, and health care utilization;
``(f) Stakeholder Workshop.-- ``(1) In general.--Not later than 1 year after the date of enactment of the Congenital Heart Futures Reauthorization Act of 2024, the Secretary shall convene a workshop on congenital heart disease, to-- ``(A) identify research gaps and opportunities related to the needs of adults with congenital heart disease, including with respect to long-term health outcomes, quality of life, mental health, and health care utilization;
``(B) assess the workforce capacity in the United States of health care providers who treat adult patients living with congenital heart disease, and options to address any such shortages in such workforce, which may include strategies to expand fellowship training programs and support regional care centers;
``(B) assess the workforce capacity in the United States to treat adults with congenital heart disease, and options to address any shortages in such workforce, which may include strategies related to fellowship training programs;
and ``(C) foster collaboration and dissemination of information across Federal agencies, health care providers, researchers, and patient organizations.
and ``(C) foster collaboration and dissemination of information related to congenital heart disease among Federal agencies, health care providers, researchers, patient advocates, and other relevant stakeholders.
``(2) Composition.--The workshop described in paragraph (1) shall be led by the Secretary, and shall involve participants that include, as appropriate, stakeholders representing patient organizations, health care professionals, research entities, health insurance providers, accrediting organizations, and relevant Federal agencies, including the Centers for Disease Control and Prevention, the National Institutes of Health, and the Health Resources and Services Administration.
``(2) Composition.--The workshop described in paragraph (1) shall include relevant stakeholders, such as patient advocates, health care providers, researchers, and health insurance issuers, and representatives of relevant Federal agencies, including the Centers for Disease Control and Prevention, the National Institutes of Health, and the Health Resources and Services Administration.
``(g) Report.--Not later than 3 years after the date of enactment of the Congenital Heart Futures Reauthorization Act of 2024, the Secretary shall issue a report to the Committee on Health, Education, Labor, and Pensions of the Senate and the Committee on Energy and Commerce of the House of Representatives on findings and recommendations of the Secretary with respect to strategies to advance research related to the lifelong needs of congenital heart disease patients and address workforce shortages of providers for adult patients living with congenital heart disease, and, as appropriate, progress made by the Secretary to implement such strategies and a plan for implementing such recommendations.'';
``(g) Report.--Not later than 3 years after the date of enactment of the Congenital Heart Futures Reauthorization Act of 2024, the Secretary shall issue a report to the Committee on Health, Education, Labor, and Pensions of the Senate and the Committee on Energy and Commerce of the House of Representatives on findings and recommendations of the Secretary with respect to strategies to advance research related to the needs of individuals of all ages with congenital heart disease and address workforce shortages of providers for adults with congenital heart disease, and, as appropriate, a plan for implementing such strategies, including any progress to date.'';
<all>
Calendar No.
429 118th CONGRESS 2d Session S.
3757 _______________________________________________________________________ A BILL To reauthorize the congenital heart disease research, surveillance, and awareness program of the Centers for Disease Control and Prevention, and for other purposes.
_______________________________________________________________________ June 18, 2024 Reported with an amendment
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Action History

  1. Committee on Health, Education, Labor, and Pensions. Reported by Senator Sanders with an amendment in the nature of a substitute. Without written report.

  2. Committee on Health, Education, Labor, and Pensions. Reported by Senator Sanders with an amendment in the nature of a substitute. Without written report.

  3. Placed on Senate Legislative Calendar under General Orders. Calendar No. 429.

  4. Committee on Health, Education, Labor, and Pensions. Ordered to be reported with an amendment in the nature of a substitute favorably.

  5. Introduced in Senate

  6. Read twice and referred to the Committee on Health, Education, Labor, and Pensions.

Sponsors

Sponsorship breakdown

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1 sponsors · 0 co-sponsors · 546 not signed on

Sponsors (1)

Co-sponsors (0)

None.

Not signed on (546)

546 members have not signed on to this bill.

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"Not signed on" means a member has not sponsored or co-sponsored this bill — it does not imply opposition. Members flagged Voted No have a recorded No vote on this bill.

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Subjects

healthcare health-insurance
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Frequently asked questions

Who sponsors S 3757?
S 3757 is sponsored by Durbin, Richard J. (Democratic).
What is the current status of S 3757?
This bill died with 118th Congress. It reached “In Committee” and never advanced before the session ended, so it can no longer move — a new version would have to be reintroduced in the current session.
Where can I track S 3757?
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