Literature DB >> 30275112

The biobank consent debate: Why 'meta-consent' is not the solution?

Neil C Manson.   

Abstract

Over the past couple of decades, there has been an ongoing, often fierce, debate about the ethics of biobank participation. One central element of that debate has concerned the nature of informed consent, must specific reconsent be gained for each new use, or user, or is broad consent ethically adequate? Recently, Thomas Ploug and Søren Holm have developed an alternative to both specific and broad consent: what they call a meta-consent framework. On a meta-consent framework, participants can choose the type of consent framework they require, for different kinds of use, different types of user and so on. Meta-consent involves a distinctive kind of design of the consent process. Here it is argued, first, that although a meta-consent framework does not wrong participants, Ploug and Holm understate the likely costs and burdens of such a framework, so there are good practical reasons not to offer it. Second, although Ploug and Holm allude to some ethical considerations that might seem to ground an ethical argument for providing meta-consent, they do not offer any sound argument, and it does not wrong participants in any way to fail to offer them the opportunity to design their own consent process. © Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  informed consent; research ethics

Mesh:

Year:  2018        PMID: 30275112     DOI: 10.1136/medethics-2018-105007

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  7 in total

1.  Evaluating models of consent in changing health research environments.

Authors:  Svenja Wiertz; Joachim Boldt
Journal:  Med Health Care Philos       Date:  2022-03-14

2.  Ethical Issues in Consent for the Reuse of Data in Health Data Platforms.

Authors:  Alex McKeown; Miranda Mourby; Paul Harrison; Sophie Walker; Mark Sheehan; Ilina Singh
Journal:  Sci Eng Ethics       Date:  2021-02-04       Impact factor: 3.525

3.  Better governance starts with better words: why responsible human tissue research demands a change of language.

Authors:  Michael A Lensink; Karin R Jongsma; Sarah N Boers; Annelien L Bredenoord
Journal:  BMC Med Ethics       Date:  2022-09-01       Impact factor: 2.834

4.  A concentric circles view of health data relations facilitates understanding of sociotechnical challenges for learning health systems and the role of federated data networks.

Authors:  Richard Milne; Mark Sheehan; Brendan Barnes; Janek Kapper; Nathan Lea; James N'Dow; Gurparkash Singh; Amelia Martín-Uranga; Nigel Hughes
Journal:  Front Big Data       Date:  2022-09-16

5.  Stakeholder perspectives on the ethico-legal dimensions of biobanking in South Africa.

Authors:  Shenuka Singh; Keymanthri Moodley
Journal:  BMC Med Ethics       Date:  2021-07-01       Impact factor: 2.652

6.  In Defence of informed consent for health record research - why arguments from 'easy rescue', 'no harm' and 'consent bias' fail.

Authors:  Thomas Ploug
Journal:  BMC Med Ethics       Date:  2020-08-20       Impact factor: 2.652

7.  Authority and the Future of Consent in Population-Level Biomedical Research.

Authors:  Mark Sheehan; Rachel Thompson; Jon Fistein; Jim Davies; Michael Dunn; Michael Parker; Julian Savulescu; Kerrie Woods
Journal:  Public Health Ethics       Date:  2019-10-30       Impact factor: 1.940

  7 in total

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