“The final arbiter of everything”: a genealogy of concern with patient experience in Britain
Author:
Publisher
Springer Science and Business Media LLC
Subject
Sociology and Political Science,Health (social science)
Link
http://link.springer.com/article/10.1057/s41285-017-0045-2/fulltext.html
Reference87 articles.
1. Ashley, L., H. Jones, J. Thomas, et al. 2013. Integrating patient reported outcomes with clinical cancer registry data. Journal of Medical Internet Research 15: e230.
2. Asprey, A., J.L. Campbell, J. Newbould, et al. 2013. Challenges to the credibility of patient feedback in primary healthcare settings: A qualitative study. British Journal of General Practice 63: 200–208.
3. Aujoulat, I., W. d’Hoore, and A. Deccache. 2007. Patient empowerment in theory and practice: Polysemy or cacophony? Patient Education and Counseling 66 (1): 13–20.
4. Baggott, R. 2005. A funny thing happened on the way to the forum? Reforming patient and public involvement in the NHS in England. Public Administration 83 (3): 533–551.
5. Barnes, M., and P. Cotterell (eds.). 2012. Critical Perspectives on User Involvement. Bristol: Policy Press.
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