Published 10 July 2008, doi:10.1136/bmj.a337
Cite this as: BMJ 2008;337:a337

Editorials

Evidence of support for biobanking practices

Lack of dissent in opt-in mechanisms does not necessarily support a move to opt-out

The first 150 words of the full text of this article appear below.

In the linked study, Johnsson and colleagues report levels of dissent in Swedish patients who are asked about storage and future research use of samples collected during health care.1 Only 0.14% of patients dissented to either storage or use of their samples, and 0.063% confirmed their decision by completing a dissent form.

The authors conclude that their survey provides evidence of high levels of trust in the Swedish system, and although this might not translate to other countries or contexts, it may support a move to opt-out systems of regulatory governance. Although the study concerns samples rather than data derived from them, the research value of samples lies in the generalisable data that they can generate, so questions about control of information and access to it are crucial. The suggestion that lack of dissent in an explicit consent system (opt-in) may support a move to presumed consent (opt-out) requires close . . . [Full text of this article]

Graeme Laurie, professor of medical jurisprudence

1 School of Law, University of Edinburgh, Edinburgh EH8 9YL

Graeme.Laurie@ed.ac.uk


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This article has been cited by other articles:

  • Johnsson, L., Hansson, M. G, Eriksson, S., Helgesson, G. (2008). Opt-out from biobanks better respects patients' autonomy. BMJ 337: a1580-a1580 [Full text]  

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Opt-out from biobanks better respects patients' autonomy and trust
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