Literature DB >> 27862072

Views of American OB/GYNs on the ethics of prenatal whole-genome sequencing.

Michelle J Bayefsky1, Amina White2, Paul Wakim3, Sara Chandros Hull1,4, David Wasserman1, Stephanie Chen1, Benjamin E Berkman1,4.   

Abstract

OBJECTIVE: Given public demand for genetic information, the potential to perform prenatal whole-genome sequencing (PWGS) non-invasively in the future, and decreasing costs of whole-genome sequencing, it is likely that OB/GYN practice will include PWGS. The goal of this project was to explore OB/GYNs' views on the ethical issues surrounding PWGS and their preparedness for counseling patients on its use.
METHODS: A national survey was administered to 2500 members of American Congress of Obstetricians and Gynecologists.
RESULTS: A total of 1114 respondents completed the survey (response rate = 45%). OB/GYNs are most concerned with ordering non-medical fetal genetic information, are worried about increasing parental anxiety, and feel it is appropriate to be directive when counseling parents about PWGS. Furthermore, most OB/GYNs have limited knowledge of genetics, rely heavily on genetic counselors and would like more guidance regarding the clinical adoption of PWGS.
CONCLUSION: OB/GYNs do not completely accept or reject PWGS, but a substantial number have significant ethical and practical concerns. They are most concerned with issues that will directly affect their practices and interactions with patients, such as increasing parental anxiety and costs of care. Professional guidance would be instrumental in directing the adoption of PWGS and alleviating the ethical burden posed by PWGS on individual OB/GYNs. Published 2016. This article is a U.S. Government work and is in the public domain in the USA. Published 2016. This article is a U.S. Government work and is in the public domain in the USA.

Entities:  

Mesh:

Year:  2016        PMID: 27862072     DOI: 10.1002/pd.4968

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  7 in total

1.  Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care.

Authors:  Zornitza Stark; Amy Nisselle; Belinda McClaren; Fiona Lynch; Stephanie Best; Janet C Long; Melissa Martyn; Chirag Patel; Luregn J Schlapbach; Christopher Barnett; Christiane Theda; Jason Pinner; Marcel E Dinger; Sebastian Lunke; Clara L Gaff
Journal:  Eur J Hum Genet       Date:  2019-05-31       Impact factor: 4.246

Review 2.  Prenatal diagnosis by chromosomal microarray analysis.

Authors:  Brynn Levy; Ronald Wapner
Journal:  Fertil Steril       Date:  2018-02       Impact factor: 7.329

3.  Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service [version 2; peer review: 2 approved].

Authors:  Melissa Hill; Sian Ellard; Jane Fisher; Naomi Fulop; Marian Knight; Mark Kroese; Jean Ledger; Kerry Leeson-Beevers; Alec McEwan; Dominic McMullan; Rhiannon Mellis; Stephen Morris; Michael Parker; Dagmar Tapon; Emma Baple; Laura Blackburn; Asya Choudry; Caroline Lafarge; Hannah McInnes-Dean; Michelle Peter; Rema Ramakrishnan; Lauren Roberts; Beverly Searle; Emma Smith; Holly Walton; Sarah L Wynn; Wing Han Wu; Lyn S Chitty
Journal:  NIHR Open Res       Date:  2022-07-18

Review 4.  Promises, pitfalls and practicalities of prenatal whole exome sequencing.

Authors:  Sunayna Best; Karen Wou; Neeta Vora; Ignatia B Van der Veyver; Ronald Wapner; Lyn S Chitty
Journal:  Prenat Diagn       Date:  2017-07-25       Impact factor: 3.050

5.  Noninvasive Prenatal Whole Genome Sequencing: Pregnant Women's Views and Preferences.

Authors:  Haley K Sullivan; Michelle Bayefsky; Paul G Wakim; Kathi Huddleston; Barbara B Biesecker; Sara Chandros Hull; Benjamin E Berkman
Journal:  Obstet Gynecol       Date:  2019-03       Impact factor: 7.623

6.  Time Costs for Genetic Counseling in Preconception Carrier Screening with Genome Sequencing.

Authors:  Frances L Lynch; Patricia Himes; Marian J Gilmore; Elissa M Morris; Jennifer L Schneider; Tia L Kauffman; Elizabeth Shuster; Jacob A Reiss; John F Dickerson; Michael C Leo; James V Davis; Carmit K McMullen; Benjamin S Wilfond; Katrina A B Goddard
Journal:  J Genet Couns       Date:  2018-02-08       Impact factor: 2.537

Review 7.  A framework for reporting secondary and incidental findings in prenatal sequencing: When and for whom?

Authors:  Danya Vears; David J Amor
Journal:  Prenat Diagn       Date:  2022-01-19       Impact factor: 3.242

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.