Literature DB >> 33389383

'We Should View Him as an Individual': The Role of the Child's Future Autonomy in Shared Decision-Making About Unsolicited Findings in Pediatric Exome Sequencing.

W Dondorp1, I Bolt2, A Tibben3, G De Wert4, M Van Summeren5.   

Abstract

In debates about genetic testing of children, as well as about disclosing unsolicited findings (UFs) of pediatric exome sequencing, respect for future autonomy should be regarded as a prima facie consideration for not taking steps that would entail denying the future adult the opportunity to decide for herself about what to know about her own genome. While the argument can be overridden when other, morally more weighty considerations are at stake, whether this is the case can only be determined in concrete cases. Importantly, when children grow into adolescents, respect for future autonomy will have to give way to respecting their emerging autonomy. When pediatric exome sequencing is done for complex conditions not involving developmental delay, respect for the child's future or emerging autonomy should be a primary consideration for those charged with deciding on behalf of the child. Building on what Emanuel and Emanuel have termed the 'deliberative model' of shared decision making, we argue that if parents fail to give these considerations their due, professionals should actively invite them to do so. Taking a directive stance may be needed in order to make sure that the future or emerging autonomy of the child are duly considered in the decision-making process, but also to help the parents and themselves to shape their respective roles as responsible care-givers.
© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature.

Entities:  

Keywords:  Clinical sequencing; Ethics; Future autonomy; Pediatrics; Shared decision making; Unsollicited findings

Year:  2021        PMID: 33389383     DOI: 10.1007/s10728-020-00425-7

Source DB:  PubMed          Journal:  Health Care Anal        ISSN: 1065-3058


  32 in total

1.  Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations.

Authors:  Pascal Borry; Gerry Evers-Kiebooms; Martina C Cornel; Angus Clarke; Kris Dierickx
Journal:  Eur J Hum Genet       Date:  2009-03-11       Impact factor: 4.246

2.  Next-generation sequencing: does the next generation still have a right to an open future?

Authors:  Annelien L Bredenoord; Martine C de Vries; Johannes J M van Delden
Journal:  Nat Rev Genet       Date:  2013-05       Impact factor: 53.242

Review 3.  Managing the ethical challenges of next-generation sequencing in genomic medicine.

Authors:  Angus J Clarke
Journal:  Br Med Bull       Date:  2014-08-13       Impact factor: 4.291

Review 4.  Ethical issues in pediatric genetic testing and screening.

Authors:  Jeffrey R Botkin
Journal:  Curr Opin Pediatr       Date:  2016-12       Impact factor: 2.856

Review 5.  Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers.

Authors:  P Borry; L Stultiens; H Nys; J-J Cassiman; K Dierickx
Journal:  Clin Genet       Date:  2006-11       Impact factor: 4.438

Review 6.  Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.

Authors:  Jeffrey R Botkin; John W Belmont; Jonathan S Berg; Benjamin E Berkman; Yvonne Bombard; Ingrid A Holm; Howard P Levy; Kelly E Ormond; Howard M Saal; Nancy B Spinner; Benjamin S Wilfond; Joseph D McInerney
Journal:  Am J Hum Genet       Date:  2015-07-02       Impact factor: 11.025

Review 7.  Unsolved challenges in pediatric whole-exome sequencing: A literature analysis.

Authors:  Gabrielle Bertier; Karine Sénécal; Pascal Borry; Danya F Vears
Journal:  Crit Rev Clin Lab Sci       Date:  2017-01-28       Impact factor: 6.250

8.  The genetic testing of children. Working Party of the Clinical Genetics Society (UK)

Authors:  A Clarke
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

9.  "Is it going to hurt?": the impact of the diagnostic odyssey on children and their families.

Authors:  Nikkola Carmichael; Judith Tsipis; Gail Windmueller; Leslie Mandel; Elicia Estrella
Journal:  J Genet Couns       Date:  2014-10-04       Impact factor: 2.537

10.  Opinion: predictive testing for Huntington disease in childhood: challenges and implications.

Authors:  M Bloch; M R Hayden
Journal:  Am J Hum Genet       Date:  1990-01       Impact factor: 11.025

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