Motivating donors to genetic research? Anthropological reasons to rethink the role of informed consent

Matti Hayry, Klaus Hoeyer, Niels Lynöe

    Research output: Contribution to journalArticlepeer-review

    Abstract

    In this article we explore the contribution from social anthropology to the medical ethical debates about the use of informed consent in research, based on blood samples and other forms of tissue. The article springs from a project exploring donors' motivation for providing blood and healthcare data for genetic research to be executed by a Swedish start-up genomics company. This article is not confined to empirical findings, however, as we suggest that anthropology provides reason to reassess the theoretical understanding of autonomy as generally defined by Beauchamp and Childress. Careful consideration of the trust expressed by donors through the act of donation, furthermore, suggests that there is reason to redirect the ethical scrutiny from informed consent to issues concerning institutional arrangements and social responsibility. In particular, we suggest that an anthropological approach could facilitate a reconsideration of the political implications of using informed consent as a regulatory practice in tissue-based research. © Springer 2006.
    Original languageEnglish
    Pages (from-to)13-23
    Number of pages10
    JournalMedicine, Health Care and Philosophy
    Volume9
    Issue number1
    DOIs
    Publication statusPublished - Mar 2006

    Keywords

    • Anthropology
    • Biobanks
    • Informed consent
    • Pragmatic ethics
    • Principle ethics

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