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Published in

Policy Press, Evidence and Policy, 1(3), p. 47-65, 2007

DOI: 10.1332/174426407779702201

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Evaluating the impact of patient and public involvement initiatives on UK health services: a systematic review

Journal article published in 2007 by Norma Daykin ORCID, David Evans, Christina Petsoulas, Adrian Sayers
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

English This article reports on a systematic review of the patient and public involvement (PPI) literature in the UK that was undertaken in 2005 to support an evaluation of the Patient Advice and Liaison Services (PALS) in England. The general PPI literature has been extensively reviewed; here we focus on the relatively small empirically based evaluation literature. The research adopts the framework of realistic evaluation, which identifies contexts, mechanisms and outcomes that lead to favourable and unfavourable outcomes. The question guiding the review is therefore: ‘What context and mechanism factors can be identified from empirical research that will lead to successful PPI outcomes?’.