Feeding back of individual genetic results in Botswana: mapping opportunities and challenges
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Published:2023-06-03
Issue:1
Volume:24
Page:
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ISSN:1472-6939
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Container-title:BMC Medical Ethics
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language:en
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Short-container-title:BMC Med Ethics
Author:
Kasule Mary,Matshaba Mogomotsi,Wonkam Ambroise,de Vries Jantina
Abstract
Abstract
Purpose
We explored the views of Botswana stakeholders involved in developing, implementing and applying ethical standards for return of individual study results from genomic research. This allowed for mapping opportunities and challenges regarding actionability requirements that determine whether individual genomic research results should be fed back.
Methods
Using in-depth interviews, this study explored the views of sixteen (16) stakeholders about the extent, nature and timing of feedback of individual genomic research findings, including incidental findings that arise in the context of African genomics research. Coded data was analyzed through an iterative process of analytic induction to document and interpret themes.
Results
Overall, respondents were of the view that feedback of actionable individual genomic results was an important outcome that could benefit participants. However, a number of themes surfaced that pointed to opportunities and challenges that exist in Botswana that could help in planning for feeding back of individual genomic results that were mapped. Some of the opportunities cited by the respondents included the existence of good governance; democracy and humanitarianism; universal healthcare system; national commitment to science; research and innovation to transform Botswana into a knowledge-based economy; and applicable standard of care which could promote actionability. On the other hand, contextual issues like the requirement for validation of genomic research results in accredited laboratories, high cost of validation of genomic results, and linkage to care, as well as lack of experts like genomic scientists and counselors were considered as challenges for return of individual results.
Conclusion
We propose that decisions whether and which genomic results to return take into consideration contextual opportunities and challenges for actionability for return of results in a research setting. This is likely to avoid or minimize ethical issues of justice, equity and harm regarding actionability decisions.
Funder
National Institutes of Health (NIH) Common Fund H3Africa Initiative
Publisher
Springer Science and Business Media LLC
Subject
Health Policy,Health (social science),Issues, ethics and legal aspects
Reference44 articles.
1. Wonkam A, de Vries J. Returning incidental findings in African genomics research. Nat Genet. 2020.
2. Fabsitz RR, McGuire A, Sharp RR, Puggal M, Beskow LM, Biesecker LG, et al. Ethical and practical guidelines for reporting genetic research results to study participants. Circulation: Cardiovasc Genet. 2010;3:574–80.
3. Consortium A, Consortium A, Whilst F. H3Africa Guideline for the Return of Individual Genetic Res Find. 2016;:1–14.
4. Williams JR. The 2016 CIOMS guidelines and public-health research ethics. South Afr J Bioeth Law. 2017.
5. Kong H, West S. WMA DECLARATION OF HELSINKI – ETHICAL PRINCIPLES FOR Scienti c Requirements and Research Protocols. 2013; October 1975.