Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.690289
Title: Incidental findings from genomic tests : exploring the ethical issues and implications for practice
Author: Crawford, Gillian
ISNI:       0000 0004 5922 6709
Awarding Body: University of Southampton
Current Institution: University of Southampton
Date of Award: 2016
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Abstract:
Rapidly declining costs and increasing availability of whole-genome analysis means that clinical genetic testing has shifted from a targeted approach to broad analysis that can provide many more clinical predictions than previously possible. This thesis explores ethical issues in the discovery of clinically relevant findings not suspected from signs, symptoms or family history. In particular the consent and disclosure practices pertaining to such incidental findings (IFs) were explored from both health professional (HCP) and patient perspectives. Phase 1 reviewed current practices and explored lay and professional experiences of and views about ethical issues surrounding IFs. 27 clinic observations and 48 in-depth interviews (32 HCP and 16 patient) were analysed thematically. Observations demonstrated that the concept of IFs was often not explained at the point of testing, or if it was, this was rarely recalled by patients. In-depth interviews demonstrated that the concept of IFs was variably understood. Some findings, classed as ‘incidental’ were in fact only potential IFs at the time of reporting. Only a sub-group of these became clear IFs, and then only when other complex investigations, including ones in relatives, had been analysed. Both patients and HCPs thought that seeking explicit consent for IFs was important, often using rights-based language, but both groups also described difficulties in gaining explicit consent for a broad and open ended concept. Some thought that actionable results should be provided regardless of consent but acknowledged that this might result in perceptions of paternalism. Furthermore, there were very different perceptions of what a good definition of actionable would be. Despite these concerns patients who had received an IF without giving specific consent, were pleased to receive them and did not feel their rights had been infringed. The aim of Phase 2 was to design a questionnaire to examine whether key findings from phase 1 resonate with a larger and representative sample of UK HCPs who manage genetic testing. The questionnaire was developed through a process of cognitive interviewing and pre-testing and is now ready for piloting and administration as post-doctoral work. Despite the focus on specific or ‘informed’ consent, this research found support for broad consent for the notion of IFs rather than specific consent to any particular IF or type of IF. This research provides an insight into the gap between the technological advances in genomics and their translation into clinical practice. Infrastructures to support consent and communication of IFs, need to be developed as genetic tests become routine for most medical specialities.
Supervisor: Lucassen, Anneke ; Foster, Claire ; Fenwick, Angela Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.690289  DOI: Not available
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