Chapter

<i>Participating in Health Decisions: Patient and Community Empowerment</i>

Alan Cribb

in Health and the Good Society

Published in print October 2005 | ISBN: 9780199242733
Published online May 2006 | e-ISBN: 9780191603549 | DOI: http://dx.doi.org/10.1093/0199242739.003.0003

Series: Issues in Biomedical Ethics

 							Participating in Health Decisions: Patient and Community Empowerment

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This chapter focuses on one of the most important dimensions of the diffusion of the health agenda: the opening up of levels of ‘involvement’ in healthcare and policy. It reviews the nature and ethical significance of participation in both healthcare and health policy. It considers the relationship between participation at the levels of care and policy, including the relationship between people participating as patients and as citizens. The discussion is designed not only to highlight the central ethical importance of participation, but also to specify the reasons it falls far short of an ‘ethical panacea’. Participation has to be understood as only one element in a complex nexus of competing healthcare goods.

Keywords: healthcare; health policy; health agenda; participation; patients; citizen

Chapter.  9434 words. 

Subjects: Moral Philosophy

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