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The Right to Know or Not to Know: Risk Notification and Genetic Counselling

Genetics, Health and Society

ISBN: 978-1-78350-581-4, eISBN: 978-1-78350-568-5

Publication date: 16 July 2015

Abstract

Purpose

Risk notification is part of a focus on preventive medicine that is dominant in contemporary Western biomedicine. Genomics has forecasted great advances in alleviating disease and prolonging human life, moving from a reactive to a preventative practice. However, in doing so, genomics redraws boundaries, potentially classifying all people as possible carriers of malfunctioning genes. This chapter presents a critical review of the practice of ‘risk notification’ as undertaken by familial cancer genetic testing services, focusing on the right to be informed or not to be informed and implications of knowing.

Methodology/approach

With backgrounds in anthropology, psychology and public health, the authors draw upon literature around risk notification from a range of disciplines.

Findings

In the context of familial cancer, clients may be asked to provide contact information for biological family members to inform them of their potential genetic risk. Through these processes a number of tensions and issues may emerge that relate to fundamental bioethical principles. The ability and decision whether to know, or conversely, to not know, is ethically fraught. We consider the roles and rights of family members and clients, as well as the broader goal of population health.

Originality/value

While much attention has been devoted to clients’ right to know in the context of medical research and treatment, relatively little work has examined the right not to know and adverse consequences of knowing. This review addresses concerns which have rarely been critically examined and debated in the context of risk notification of biological family members.

Keywords

Citation

Gilson, A., Hemer, S.R., Chur-Hansen, A. and Crabb, S. (2015), "The Right to Know or Not to Know: Risk Notification and Genetic Counselling", Genetics, Health and Society (Advances in Medical Sociology, Vol. 16), Emerald Group Publishing Limited, Leeds, pp. 249-267. https://doi.org/10.1108/S1057-629020150000016009

Publisher

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Emerald Group Publishing Limited

Copyright © 2015 Emerald Group Publishing Limited