Research Online

Logo

Goldsmiths - University of London

To Tell or Not to Tell: The Ethics and Law of Disclosing Health-Related Genetic Information to Family Members

Chapman, Robert; Devereux, Johanna; Nanau, Victoria; Smereczynska, Vanessa; Matsepuro, Daria and Selita, Fatos. 2018. To Tell or Not to Tell: The Ethics and Law of Disclosing Health-Related Genetic Information to Family Members. Psychology in Russia: State of the Art, 11(4), pp. 68-78. ISSN 2074-6857 [Article]

[img]
Preview
Text
psych_4_2018_5_chapman.pdf - Published Version
Available under License Creative Commons Attribution Non-commercial.

Download (373kB) | Preview

Abstract or Description

Background. Genetic conditions and susceptibilities differ from other diseases and health-related risks. Genetic characteristics are shared between blood relatives, and therefore a genetic finding can have implications for the wider family.

Objective. The present study investigates people’s views on issues related to disclosing genetic information to relatives. Specifically, the study assesses opinions in relation to two issues: 1) whether people have a moral obligation to share their genetic data with family members; and 2) whether healthcare providers should have a legal obligation to share such data when consent is withheld.

Design. A public engagement event was held based on the real-life court case of ABC vs the UK National Health Service (NHS). Participants were provided with information in three phases: first, about the case; then, with progressively more details of the case; and finally, with other relevant information. After being given each portion of information, the participants were asked to disclose their views on the rights and responsibilities related to the sharing of this information.

Results. The results clearly demonstrate that people hold strong and polarized views regarding confidentiality, and the moral and legal duties to disclose genetic information to family members. Even when withholding information could have an adverse impact on the health and life choices of relatives, participants disagreed about the legal obligations for healthcare providers to disclose a person’s genetic information to those relatives.

Conclusion. The results suggest that the issues of privacy and disclosure of genetic information are complex and divisive.

Item Type:

Article

Identification Number (DOI):

https://doi.org/10.11621/pir.2018.0405

Keywords:

genetics, ethics, public engagement, patient con dentiality, duty of care, data access rights

Departments, Centres and Research Units:

Psychology

Dates:

DateEvent
30 September 2018Accepted
30 December 2018Published

Item ID:

25913

Date Deposited:

28 Feb 2019 14:39

Last Modified:

06 Mar 2019 06:29

Peer Reviewed:

Yes, this version has been peer-reviewed.

URI:

http://research.gold.ac.uk/id/eprint/25913

View statistics for this item...

Edit Record Edit Record (login required)