Literature DB >> 30600266

Rapid Challenges: Ethics and Genomic Neonatal Intensive Care.

Christopher Gyngell1,2, Ainsley J Newson3, Dominic Wilkinson4,5, Zornitza Stark6,2,7, Julian Savulescu2,5.   

Abstract

NICUs are a priority implementation area for genomic medicine. Rapid genomic testing in the NICU is expected to be genomic medicine's "critical application," providing such clear benefits that it drives the adoption of genomics more broadly. Studies from multiple centers worldwide have now demonstrated the clinical utility and cost-effectiveness of rapid genomic sequencing in this setting, paving the way for widespread implementation. However, the introduction of this potentially powerful tool for predicting future impairment in the NICU also raises profound ethical challenges. Developing models of good practice that incorporate the identification, exploration, and analysis of ethical issues will be critical for successful implementation. In this article, we analyze 3 such issues: (1) the value and meaning of gaining consent to a complex test in a stressful, emotionally charged environment; (2) the effect of rapid diagnosis on parent-child bonding and its implications for medical and family decisions, particularly in relation to treatment limitation; and (3) distributive justice (ie, whether the substantial cost and diversion of resources to deliver rapid genomic testing in the NICU can be justified).
Copyright © 2019 by the American Academy of Pediatrics.

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Year:  2019        PMID: 30600266      PMCID: PMC6379057          DOI: 10.1542/peds.2018-1099D

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  47 in total

1.  Resources, Down's syndrome, and cardiac surgery.

Authors:  J Savulescu
Journal:  BMJ       Date:  2001-04-14

2.  Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process.

Authors:  Carmen Ayuso; José M Millán; Marta Mancheño; Rafael Dal-Ré
Journal:  Eur J Hum Genet       Date:  2013-01-16       Impact factor: 4.246

Review 3.  Genomic Testing in The Paediatric Population: Ethical Considerations in Light of Recent Policy Statements.

Authors:  Ainsley J Newson; Lisa Schonstein
Journal:  Mol Diagn Ther       Date:  2016-10       Impact factor: 4.074

4.  Anticipating uncertainty and irrevocable decisions: provider perspectives on implementing whole-genome sequencing in critically ill children with heart disease.

Authors:  Danton S Char; Sandra Soo-Jin Lee; David Magnus; Mildred Cho
Journal:  Genet Med       Date:  2018-03-01       Impact factor: 8.822

5.  Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time.

Authors:  Jonathan S Berg; Muin J Khoury; James P Evans
Journal:  Genet Med       Date:  2011-06       Impact factor: 8.822

6.  Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis.

Authors:  Sophie Nambot; Julien Thevenon; Paul Kuentz; Yannis Duffourd; Emilie Tisserant; Ange-Line Bruel; Anne-Laure Mosca-Boidron; Alice Masurel-Paulet; Daphné Lehalle; Nolwenn Jean-Marçais; Mathilde Lefebvre; Pierre Vabres; Salima El Chehadeh-Djebbar; Christophe Philippe; Frederic Tran Mau-Them; Judith St-Onge; Thibaud Jouan; Martin Chevarin; Charlotte Poé; Virginie Carmignac; Antonio Vitobello; Patrick Callier; Jean-Baptiste Rivière; Laurence Faivre; Christel Thauvin-Robinet
Journal:  Genet Med       Date:  2017-11-02       Impact factor: 8.822

7.  Psychological effects of false-positive results in expanded newborn screening in China.

Authors:  Wen-Jun Tu; Jian He; Hui Chen; Xiao-Dong Shi; Ying Li
Journal:  PLoS One       Date:  2012-04-27       Impact factor: 3.240

8.  Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders.

Authors:  Caroline F Wright; Jeremy F McRae; Stephen Clayton; Giuseppe Gallone; Stuart Aitken; Tomas W FitzGerald; Philip Jones; Elena Prigmore; Diana Rajan; Jenny Lord; Alejandro Sifrim; Rosemary Kelsell; Michael J Parker; Jeffrey C Barrett; Matthew E Hurles; David R FitzPatrick; Helen V Firth
Journal:  Genet Med       Date:  2018-01-11       Impact factor: 8.822

9.  Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.

Authors:  Dimitri J Stavropoulos; Daniele Merico; Rebekah Jobling; Sarah Bowdin; Nasim Monfared; Bhooma Thiruvahindrapuram; Thomas Nalpathamkalam; Giovanna Pellecchia; Ryan K C Yuen; Michael J Szego; Robin Z Hayeems; Randi Zlotnik Shaul; Michael Brudno; Marta Girdea; Brendan Frey; Babak Alipanahi; Sohnee Ahmed; Riyana Babul-Hirji; Ramses Badilla Porras; Melissa T Carter; Lauren Chad; Ayeshah Chaudhry; David Chitayat; Soghra Jougheh Doust; Cheryl Cytrynbaum; Lucie Dupuis; Resham Ejaz; Leona Fishman; Andrea Guerin; Bita Hashemi; Mayada Helal; Stacy Hewson; Michal Inbar-Feigenberg; Peter Kannu; Natalya Karp; Raymond Kim; Jonathan Kronick; Eriskay Liston; Heather MacDonald; Saadet Mercimek-Mahmutoglu; Roberto Mendoza-Londono; Enas Nasr; Graeme Nimmo; Nicole Parkinson; Nada Quercia; Julian Raiman; Maian Roifman; Andreas Schulze; Andrea Shugar; Cheryl Shuman; Pierre Sinajon; Komudi Siriwardena; Rosanna Weksberg; Grace Yoon; Chris Carew; Raith Erickson; Richard A Leach; Robert Klein; Peter N Ray; M Stephen Meyn; Stephen W Scherer; Ronald D Cohn; Christian R Marshall
Journal:  NPJ Genom Med       Date:  2016-01-13       Impact factor: 8.617

10.  Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization.

Authors:  Lauge Farnaes; Amber Hildreth; Nathaly M Sweeney; Michelle M Clark; Shimul Chowdhury; Shareef Nahas; Julie A Cakici; Wendy Benson; Robert H Kaplan; Richard Kronick; Matthew N Bainbridge; Jennifer Friedman; Jeffrey J Gold; Yan Ding; Narayanan Veeraraghavan; David Dimmock; Stephen F Kingsmore
Journal:  NPJ Genom Med       Date:  2018-04-04       Impact factor: 8.617

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  11 in total

1.  Australian Genomics: A Federated Model for Integrating Genomics into Healthcare.

Authors:  Zornitza Stark; Tiffany Boughtwood; Peta Phillips; John Christodoulou; David P Hansen; Jeffrey Braithwaite; Ainsley J Newson; Clara L Gaff; Andrew H Sinclair; Kathryn N North
Journal:  Am J Hum Genet       Date:  2019-07-03       Impact factor: 11.025

2.  Influence of Genetic Information on Neonatologists' Decisions: A Psychological Experiment.

Authors:  Katharine Press Callahan; John Flibotte; Cara Skraban; Katherine Taylor Wild; Steven Joffe; David Munson; Chris Feudtner
Journal:  Pediatrics       Date:  2022-03-01       Impact factor: 7.124

Review 3.  Rapid genomic testing for critically ill children: time to become standard of care?

Authors:  Zornitza Stark; Sian Ellard
Journal:  Eur J Hum Genet       Date:  2021-11-08       Impact factor: 4.246

4.  The fetus in the age of the genome.

Authors:  Dagmar Schmitz; Wolfram Henn
Journal:  Hum Genet       Date:  2021-08-23       Impact factor: 5.881

5.  Preferences and values for rapid genomic testing in critically ill infants and children: a discrete choice experiment.

Authors:  Ilias Goranitis; Stephanie Best; John Christodoulou; Tiffany Boughtwood; Zornitza Stark
Journal:  Eur J Hum Genet       Date:  2021-04-02       Impact factor: 4.246

6.  Parents' experiences of decision making for rapid genomic sequencing in intensive care.

Authors:  Fiona Lynch; Amy Nisselle; Zornitza Stark; Clara L Gaff; Belinda McClaren
Journal:  Eur J Hum Genet       Date:  2021-08-23       Impact factor: 4.246

7.  Personalized medicine, digital technology and trust: a Kantian account.

Authors:  Bjørn K Myskja; Kristin S Steinsbekk
Journal:  Med Health Care Philos       Date:  2020-09-04

8.  Measures of Utility Among Studies of Genomic Medicine for Critically Ill Infants: A Systematic Review.

Authors:  Katharine Press Callahan; Rebecca Mueller; John Flibotte; Emily A Largent; Chris Feudtner
Journal:  JAMA Netw Open       Date:  2022-08-01

9.  Moving from 'fully' to 'appropriately' informed consent in genomics: The PROMICE framework.

Authors:  Julian J Koplin; Christopher Gyngell; Julian Savulescu; Danya F Vears
Journal:  Bioethics       Date:  2022-04-07       Impact factor: 2.512

10.  'Diagnostic shock': the impact of results from ultrarapid genomic sequencing of critically unwell children on aspects of family functioning.

Authors:  Hilary Bowman-Smart; Danya F Vears; Gemma R Brett; Melissa Martyn; Zornitza Stark; Christopher Gyngell
Journal:  Eur J Hum Genet       Date:  2022-07-13       Impact factor: 5.351

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