Precarious hope: Ethical considerations for offering experimental fetal therapies outside of research after initial studies in humans.


Journal

Prenatal diagnosis
ISSN: 1097-0223
Titre abrégé: Prenat Diagn
Pays: England
ID NLM: 8106540

Informations de publication

Date de publication:
09 Dec 2023
Historique:
revised: 24 10 2023
received: 20 09 2023
accepted: 20 11 2023
medline: 10 12 2023
pubmed: 10 12 2023
entrez: 9 12 2023
Statut: aheadofprint

Résumé

Risks and benefits of experimental fetal therapies can remain uncertain after initial clinical studies, especially long-term effects. Nevertheless, pregnant individuals may request them, hoping to benefit their future child. Guidance about offering experimental fetal therapies outside research (as "innovative therapy") is limited, despite their ethical complexity. We propose points for clinicians and reviewers to consider when deciding whether and how to offer experimental fetal therapies as innovative therapies after initial clinical studies. We used conceptual analysis and a current case to develop points for consideration, grounded in broader debates on innovative therapy and the unique challenges associated with experimental fetal therapies. Clinicians should evaluate whether offering experimental fetal therapies as innovative therapy is appropriate for a pregnant individual and their fetus. The anticipated risk-benefit ratio for the fetus should be favorable. For the pregnant individual, risks may outweigh benefits, within reasonable limits. Medical resources should be sufficient to ensure appropriate care. Clinicians should support pregnant individuals in making informed choices. Clinicians offering innovative therapies with more than minimal risk should collect and report data on outcomes. Independent review should take place. Considering these points may advance the interests of fetuses, future children, and their families.

Identifiants

pubmed: 38069681
doi: 10.1002/pd.6474
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
Pays : United States

Informations de copyright

© 2023 John Wiley & Sons Ltd. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

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Auteurs

Saskia Hendriks (S)

Department of Bioethics, NIH Clinical Center, Bethesda, Maryland, USA.

Janyne Althaus (J)

Department of Obstetrics, Gynecology and Reproductive Sciences, University of Maryland, Baltimore, Maryland, USA.

Meredith A Atkinson (MA)

Department of Pediatrics, Division of Nephrology, Johns Hopkins University, Baltimore, Maryland, USA.

Ahmet A Baschat (AA)

Department of Gynecology and Obstetrics, Center for Fetal Therapy, Johns Hopkins University, Baltimore, Maryland, USA.

Benjamin E Berkman (BE)

Department of Bioethics, NIH Clinical Center, Bethesda, Maryland, USA.
National Human Genome Research Institute, Bethesda, Maryland, USA.

Christine Grady (C)

Department of Bioethics, NIH Clinical Center, Bethesda, Maryland, USA.

David Wasserman (D)

Department of Bioethics, NIH Clinical Center, Bethesda, Maryland, USA.

David Wendler (D)

Department of Bioethics, NIH Clinical Center, Bethesda, Maryland, USA.

Jena L Miller (JL)

Department of Gynecology and Obstetrics, Center for Fetal Therapy, Johns Hopkins University, Baltimore, Maryland, USA.

Classifications MeSH