Why we should not seek individual informed consent for participation in health services research.

Abstract:

:Ethics committees now require that individuals give informed consent to much health services research, in the same way as for clinical research. This is misguided. Existing ethical guidelines do not help us decide how to seek consent in these cases, and have allowed managerial experimentation to remain largely unchecked. Inappropriate requirements for individual consent can institutionalise health inequalities and reduce access to services for vulnerable groups. This undermines the fundamental purpose of the National Health Service (NHS), and ignores our rights and duties as its members, explored here. Alternative forms of community consent should be actively pursued.

journal_name

J Med Ethics

authors

Cassell J,Young A

doi

10.1136/jme.28.5.313

keywords:

subject

Has Abstract

pub_date

2002-10-01 00:00:00

pages

313-7

issue

5

eissn

0306-6800

issn

1473-4257

journal_volume

28

pub_type

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