Your browser doesn't support javascript.
loading
Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project.
Pereira, Stacey; Robinson, Jill Oliver; Gutierrez, Amanda M; Petersen, Devan K; Hsu, Rebecca L; Lee, Caroline H; Schwartz, Talia S; Holm, Ingrid A; Beggs, Alan H; Green, Robert C; McGuire, Amy L.
Afiliação
  • Pereira S; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas.
  • Robinson JO; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas.
  • Gutierrez AM; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas.
  • Petersen DK; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas.
  • Hsu RL; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas.
  • Lee CH; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas.
  • Schwartz TS; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital.
  • Holm IA; Department of Medicine, Harvard Medical School, Harvard University, Boston, Massachusetts.
  • Beggs AH; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital.
  • Green RC; Department of Medicine, Harvard Medical School, Harvard University, Boston, Massachusetts.
  • McGuire AL; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital.
Pediatrics ; 143(Suppl 1): S6-S13, 2019 01.
Article em En | MEDLINE | ID: mdl-30600265
ABSTRACT
BACKGROUND AND

OBJECTIVES:

There is interest in applying genomic sequencing (GS) to newborns' clinical care. Here we explore parents' and clinicians' attitudes toward and perceptions of the risks, benefits, and utility of newborn GS compared with newborn screening (NBS) prior to receiving study results.

METHODS:

The BabySeq Project is a randomized controlled trial used to explore the impact of integrating GS into the clinical care of newborns. Parents (n = 493) of enrolled infants (n = 309) and clinicians (n = 144) completed a baseline survey at enrollment. We examined between-group differences in perceived utility and attitudes toward NBS and GS. Open-ended responses about risks and benefits of each technology were categorized by theme.

RESULTS:

The majority of parents (71%) and clinicians (51%) agreed that there are health benefits of GS, although parents and clinicians agreed more that there are risks associated with GS (35%, 70%) than with NBS (19%, 39%; all P < .05). Parents perceived more benefit and less risk of GS than did clinicians. Clinicians endorsed concerns about privacy and discrimination related to genomic information more strongly than did parents, and parents anticipated benefits of GS that clinicians did not.

CONCLUSIONS:

Parents and clinicians are less confident in GS than NBS, but parents perceive a more favorable risk/benefit ratio of GS than do clinicians. Clinicians should be aware that parents' optimism may stem from their perceived benefits beyond clinical utility.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pais / Atitude do Pessoal de Saúde / Atitude Frente a Saúde / Triagem Neonatal / Sequenciamento Completo do Genoma Tipo de estudo: Clinical_trials / Etiology_studies / Qualitative_research / Risk_factors_studies Limite: Adult / Female / Humans / Male / Newborn Idioma: En Revista: Pediatrics Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pais / Atitude do Pessoal de Saúde / Atitude Frente a Saúde / Triagem Neonatal / Sequenciamento Completo do Genoma Tipo de estudo: Clinical_trials / Etiology_studies / Qualitative_research / Risk_factors_studies Limite: Adult / Female / Humans / Male / Newborn Idioma: En Revista: Pediatrics Ano de publicação: 2019 Tipo de documento: Article