Literature DB >> 19205854

Professional ambivalence: accounts of ethical practice in childhood genetic testing.

Michael Arribas-Ayllon1, Srikant Sarangi, Angus Clarke.   

Abstract

Childhood genetic testing raises complex ethical and moral dilemmas for both families and professionals. In the family sphere, the role of communication is a key aspect in the transmission of 'genetic responsibility' between adults and children. In the professional sphere, genetic responsibility is an interactional accomplishment emerging from the sometimes competing views over what constitutes the 'best interests' of the child in relation to parental preferences on the one hand, and professional judgements on the other. In the present paper we extend our previous research into parental accounts of childhood genetic testing and explore the ethical accounts of professionals in research interviews. Interviews (n = 20) were conducted with professional practitioners involved in the genetic diagnosis and management of children and their families. We first identify four inter-related themes-juxtaposition of parental rights vis-à-vis child's autonomy, elicitation of the child's autonomy, avoidance of parental responsibility and recognition of professional uncertainty. Then, using Rhetorical Discourse Analysis, we examine the range of discourse devices through which ethical accounts are situationally illustrated: contrast, reported speech, constructed dialogue, character and event work. An overarching device in these ethical accounts is the use of extreme case scenarios, which reconstruct dilemmas as justifications of professional conduct. While acknowledging ambivalence, our analysis suggests that professional judgement is not a simple matter of implementing ethical principles but rather of managing the practical conditions and consequences of interactions with parents and children. We conclude that more attention is needed to understand the way professional practitioners formulate judgements about ethical practice.

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Year:  2009        PMID: 19205854     DOI: 10.1007/s10897-008-9201-0

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  23 in total

1.  Predictive and carrier testing of children: professional dilemmas for clinical geneticists.

Authors:  Alison Chapple; Carl May; Peter Campion
Journal:  Eur J Genet Soc       Date:  1996

2.  Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information.

Authors:  N Hallowell; C Foster; R Eeles; A Ardern-Jones; V Murday; M Watson
Journal:  J Med Ethics       Date:  2003-04       Impact factor: 2.903

Review 3.  Genetic dilemmas and the child's right to an open future.

Authors:  D S Davis
Journal:  Hastings Cent Rep       Date:  1997 Mar-Apr       Impact factor: 2.683

4.  Ethics and practice: two worlds? The example of genetic counselling.

Authors:  Kerstin Wustner
Journal:  New Genet Soc       Date:  2003-04

5.  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

6.  Attitudes toward the genetic testing of children among adults in a Utah-based kindred tested for a BRCA1 mutation.

Authors:  H A Hamann; R T Croyle; V L Venne; B J Baty; K R Smith; J R Botkin
Journal:  Am J Med Genet       Date:  2000-05-01

7.  Ethical and professional challenges posed by patients with genetic concerns: a report of focus group discussions with genetic counselors, physicians, and nurses.

Authors:  P M Veach; D M Bartels; B S LeRoy
Journal:  J Genet Couns       Date:  2001-04       Impact factor: 2.537

Review 8.  The autonomy paradox: predictive genetic testing and autonomy: three essential problems.

Authors:  A K Huibers; A van 't Spijker
Journal:  Patient Educ Couns       Date:  1998-09

9.  Professional and personal attitudes about access and confidentiality in the genetic testing of children: a pilot study.

Authors:  Elizabeth Campbell; Lainie Friedman Ross
Journal:  Genet Test       Date:  2003

10.  Adolescent carrier testing in practice: the impact of legal rulings and problems with "gillick competence".

Authors:  Paula Boddington; Maggie Gregory
Journal:  J Genet Couns       Date:  2008-08-29       Impact factor: 2.537

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  7 in total

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Authors:  Lilian Liou Cohen; Marina Stolerman; Christine Walsh; David Wasserman; Siobhan M Dolan
Journal:  J Med Ethics       Date:  2011-09-27       Impact factor: 2.903

2.  A qualitative study to explore how professionals in the United Kingdom make decisions to test children for a sickle cell carrier status.

Authors:  Melissa Noke; Sarah Peters; Alison Wearden; Fiona Ulph
Journal:  Eur J Hum Genet       Date:  2015-05-27       Impact factor: 4.246

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Journal:  J Genet Couns       Date:  2014-07-11       Impact factor: 2.537

4.  Support Seeking or Familial Obligation: An Investigation of Motives for Disclosing Genetic Test Results.

Authors:  Marisa Greenberg; Rachel A Smith
Journal:  Health Commun       Date:  2015-10-27

5.  DSD and Professionalism from a Multilateral View: Supplementing the Consensus Statement on the Basis of a Qualitative Survey.

Authors:  Jürg C Streuli; Birgit Köhler; Knut Werner-Rosen; Christine Mitchell
Journal:  Adv Urol       Date:  2012-07-09

6.  Failed surrogate conceptions: social and ethical aspects of preconception disruptions during commercial surrogacy in India.

Authors:  Sayani Mitra; Silke Schicktanz
Journal:  Philos Ethics Humanit Med       Date:  2016-09-19       Impact factor: 2.464

7.  Professionals' accounts of genetic testing in adoption: a qualitative study.

Authors:  Michael Arribas-Ayllon; Angus Clarke; Katherine Shelton
Journal:  Arch Dis Child       Date:  2019-07-11       Impact factor: 3.791

  7 in total

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