Abstract

BackgroundIncidental findings (IFs) and secondary findings (SFs), being results that are unrelated to the diagnostic question, are the subject of an important debate in the practice of clinical genomic medicine. Arguments for reporting these results or not doing so typically relate to the principles of autonomy, non-maleficence and beneficence. However, these principles frequently conflict and are insufficient by themselves to come to a conclusion. This study investigates empirically how ethical principles are considered when actually reporting IFs or SFs and how value conflicts are weighed.MethodsA qualitative focus group study has been undertaken, including a multidisciplinary group of professionals from Belgian centres for medical genetics. The data were analysed thematically.ResultsAll eight Belgian centres participated in this study. Ethical values were frequently referred to for disclosure policies on IFs and SFs. Participants invoked respect for patient autonomy to support the disclosure of IFs and opt-out options for IFs and SFs, non-maleficence for the professional delineation of reportable IFs and opt-out options for IFs and SFs and (the particular scope of) beneficence for the mandatory reporting of actionable IFs, the delineation of reportable IFs and a current decline of actively pursued SFs. Professional assumptions about patients’ genetic literacy were an important factor in the weighing of values.ConclusionsIn line with the traditional bioethical discourse, the mandatory reporting of actionable IFs might be interpreted as a “technological, soft paternalism”. Restricting patients’ choices might be acceptable, but then its motives should be valid and its beneficent outcomes highly plausible. Hence, the presuppositions of technological, soft paternalism - patients’ inability to make informed decisions, normative rationality, the efficacy of beneficent outcomes and the delineated spectrum of beneficence - should be approached critically. Moreover, distributive justice should be considered an important value in the delineation of the current scope of the ethical debate on IFs and SFs.This study of guiding values may stimulate the debate on the ethical grounds for a solid policy on IFs and SFs internationally.

Highlights

  • Incidental findings (IFs) and secondary findings (SFs), being results that are unrelated to the diagnostic question, are the subject of an important debate in the practice of clinical genomic medicine

  • Even though participants were not explicitly asked for principles that supported their reporting practices regarding IFs and SFs, professionals frequently referred to ethical values including autonomy, non-maleficence and beneficence, and these concepts emerged from the data as a specific theme

  • Professionals at Belgian centres for medical genetics (CMGs) frequently refer to ethical values for disclosure policies on IFs and SFs

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Summary

Introduction

Incidental findings (IFs) and secondary findings (SFs), being results that are unrelated to the diagnostic question, are the subject of an important debate in the practice of clinical genomic medicine Arguments for reporting these results or not doing so typically relate to the principles of autonomy, nonmaleficence and beneficence. The European Society of Human Genetics (ESHG), EuroGentest and the Canadian College of Medical Geneticists (CCMG) are more cautious with diagnostically unrelated results; they recommend a minimisation of IFs and they explicitly discourage or seem not to support the active pursuit of SFs [2, 4, 6] Arguments for this cautiousness are the possibility of physical and/or emotional harm (by overwhelming patients with unnecessary or harmful tests, diagnoses or interventions) and the professional duty of non-maleficence [3, 8]. When IFs are unintentionally identified, these results should only be disclosed if they are highly significant, highly penetrant and medically actionable [17,18,19]

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