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Anticipatory Waivers of Consent for Pediatric Biobanking.
Hartsock, Jane A; Schwartz, Peter H; Waltz, Amy C; Ott, Mary A.
Afiliação
  • Hartsock JA; Faculty investigator with the Indiana University Center for Bioethics at the Indiana University School of Medicine and the director of clinical ethics for the Academic Health Center at Indiana University Health.
  • Schwartz PH; Director of the Indiana University Center for Bioethics at the Indiana University School of Medicine and an associate professor of medicine at Indiana University School of Medicine.
  • Waltz AC; Associate director of the Indiana University Human Subjects Office and an adjunct professor at the Indiana University Robert H. McKinney School of Law.
  • Ott MA; Pediatric ethicist at the Indiana University Center for Bioethics at the Indiana University School of Medicine and an associate professor of pediatrics in the Indiana University School of Medicine.
Ethics Hum Res ; 41(2): 14-21, 2019 Mar.
Article em En | MEDLINE | ID: mdl-30895753
As pediatric biobank research grows, additional guidance will be needed about whether researchers should always obtain consent from participants when they reach the legal age of majority. Biobanks struggle with a range of practical and ethical issues related to this question. We propose a framework for the use of anticipatory waivers of consent that is empirically rooted in research that shows that children and adolescents are often developmentally capable of meaningful deliberation about the risks and benefits of participation in research. Accordingly, bright-line legal concepts of majority or competency do not accurately capture the emerging capacity for autonomous decision-making of many pediatric research participants and unnecessarily complicate the issues about contacting participants at the age of majority to obtain consent for the continued or first use of their biospecimens that were obtained during childhood. We believe the proposed framework provides an ethically sound balance between the concern for potential exploitation of vulnerable populations, the impetus for the federal regulations governing research with children, and the need to conduct valuable research in the age of genomic medicine.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pediatria / Competência Mental / Bancos de Espécimes Biológicos / Consentimento Informado por Menores / Consentimento Livre e Esclarecido Tipo de estudo: Guideline / Prognostic_studies Aspecto: Ethics Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Ethics Hum Res Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pediatria / Competência Mental / Bancos de Espécimes Biológicos / Consentimento Informado por Menores / Consentimento Livre e Esclarecido Tipo de estudo: Guideline / Prognostic_studies Aspecto: Ethics Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Ethics Hum Res Ano de publicação: 2019 Tipo de documento: Article