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      Patient and public involvement in priority‐setting decisions in England's Transforming NHS: An interview study with Clinical Commissioning Groups in South London sustainability transformation partnerships

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          Abstract

          Background

          Patient and public involvement (PPI) in health‐care commissioning decisions has always been a contentious issue. However, the current moves towards Sustainability and Transformation Partnerships (STPs) in England's NHS are viewed as posing the risk of reducing the impact of current structures for PPI.

          Objective

          To understand how different members in clinical commissioning groups (CCGs) understand PPI as currently functioning in their decision‐making practices, and the implications of the STPs for it.

          Design

          Thematic analysis of 18 semi‐structured interviews with CCG governing body voting members (e.g. clinicians and lay members), non‐voting governing body members (e.g. Healthwatch representatives) and CCG staff with roles focussed on PPI, recruited from CCGs in South London STPs.

          Results

          There are contestations amongst CCG members regarding not only what PPI is, but also the role that it currently plays and could play in commissioning decision making in the context of STPs. Three main themes were identified: PPI is ‘going out’ into the community; PPI as a disruptive power; and PPI as co‐production, a ‘utopian dream’?

          Conclusions

          Long‐standing issues distinctive to PPI in NHS prioritization decisions are resurfacing with the moves towards STPs, particularly in relation to contradictions between the rhetoric of ‘partnership’ and reorganizations that foster more top‐down control. The interviews reveal pervasive distrusts across a number of levels that are counterproductive to the collaborations upon which STPs rely. And it is argued that such distrust and contestations will continue until a formalized space for PPI in STP priority‐setting is created.

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          Most cited references33

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          Revolution or evolution: the challenges of conceptualizing patient and public involvement in a consumerist world.

          Changing the relationship between citizens and the state is at the heart of current policy reforms. Across England and the developed world, from Oslo to Ontario, Newcastle to Newquay, giving the public a more direct say in shaping the organization and delivery of healthcare services is central to the current health reform agenda. Realigning public services around those they serve, based on evidence from service user's experiences, and designed with and by the people rather than simply on their behalf, is challenging the dominance of managerialism, marketization and bureaucratic expertise. Despite this attention there is limited conceptual and theoretical work to underpin policy and practice. This article proposes a conceptual framework for patient and public involvement (PPI) and goes on to explore the different justifications for involvement and the implications of a rights-based rather than a regulatory approach. These issues are highlighted through exploring the particular evolution of English health policy in relation to PPI on the one hand and patient choice on the other before turning to similar patterns apparent in the United States and more broadly. A framework for conceptualizing PPI is presented that differentiates between the different types and aims of involvement and their potential impact. Approaches to involvement are different in those countries that adopt a rights-based rather than a regulatory approach. I conclude with a discussion of the tension and interaction apparent in the globalization of both involvement and patient choice in both policy and practice.
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            What is the evidence base for public involvement in health-care policy?: results of a systematic scoping review.

            Public involvement in health-care policy has been advocated as a means to enhance health system responsiveness, yet evidence for its impact has been difficult to ascertain.
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              A Hierarchy of Power: The Place of Patient and Public Involvement in Healthcare Service Development

              Amidst statutory and non-statutory calls for effective patient and public involvement (PPI), questions continue to be raised about the impact of PPI in healthcare services. Stakeholders, policy makers, researchers, and members of the public ask in what ways and at what level PPI makes a difference. Patient experience is widely seen as an important and valuable resource to the development of healthcare services, yet there remain legitimacy issues concerning different forms of knowledge that members of the public and professionals bring to the table, and related power struggles. This paper draws on data from a qualitative study of PPI in a clinical commissioning group (CCG) in the UK. The study looked at some of the activities in which there was PPI; this involved researchers conducting observations of meetings, and interviews with staff and lay members who engaged in CCG PPI activities. This paper explores power imbalances when it comes to influencing the work of the CCG mainly between professionals and members of public, but also between different CCG staff members and between different groups of members of public. The authors conclude that a hierarchy of power exists, with some professionals and public and lay members afforded more scope for influencing healthcare service development than others—an approach which is reflected in the ways and extent to which different forms and holders of knowledge are viewed, managed, and utilized.
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                Author and article information

                Contributors
                Role: Research Associateclare.coultas@kcl.ac.uk
                Role: Postdoctoral Researcher in Comparative Public Policy
                Role: Professor of Public Health
                Journal
                Health Expect
                Health Expect
                10.1111/(ISSN)1369-7625
                HEX
                Health Expectations : An International Journal of Public Participation in Health Care and Health Policy
                John Wiley and Sons Inc. (Hoboken )
                1369-6513
                1369-7625
                14 August 2019
                December 2019
                : 22
                : 6 ( doiID: 10.1111/hex.v22.6 )
                : 1223-1230
                Affiliations
                [ 1 ] School of Population Health & Environmental Sciences, Faculty of Life Sciences & Medicine King's College London London UK
                [ 2 ] Department of Political Science Universitat Wien Vienna Austria
                [ 3 ]Present address: King's College London, Universitat Wien Vienna Austria
                Author notes
                [*] [* ] Correspondence

                Clare Coultas, School of Population Health & Environmental Sciences, Faculty of Life Sciences & Medicine, King's College London, 5th Floor, Addison House, Guy's Campus, London SE1 1UL, UK.

                Email: clare.coultas@ 123456kcl.ac.uk

                Author information
                https://orcid.org/0000-0002-8506-8287
                https://orcid.org/0000-0002-0126-6949
                https://orcid.org/0000-0003-2503-9692
                Article
                HEX12948
                10.1111/hex.12948
                6882255
                31410967
                3567777d-8fb9-42ce-b505-76359dd9ce3e
                © 2019 The Authors Health Expectations published by John Wiley & Sons Ltd

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 September 2018
                : 12 July 2019
                : 16 July 2019
                Page count
                Figures: 0, Tables: 1, Pages: 8, Words: 6897
                Funding
                Funded by: National Institute for Health Research (NIHR)
                Funded by: Applied Health Research and Care (CLAHRC) South London at King’s College Hospital NHS Foundation Trust
                Categories
                Original Research Paper
                Original Research Papers
                Custom metadata
                2.0
                hex12948
                December 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.7.2 mode:remove_FC converted:28.11.2019

                Health & Social care
                activism,clinical commissioning groups,co‐production,england's national health service,integrated care systems,patient and public involvement,priority‐setting,sustainability and transformation partnerships,trust

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