Patient empowerment, what does it mean for adults in the advanced stages of a life-limiting illness: A systematic review using critical interpretive synthesis

Author:

Wakefield Dominique1ORCID,Bayly Jo1,Selman Lucy Ellen2ORCID,Firth Alice M1,Higginson Irene J1ORCID,Murtagh Fliss EM3

Affiliation:

1. Department of Palliative Care, Policy & Rehabilitation, Cicely Saunders Institute, King’s College London, London, UK

2. Bristol Randomised Trials Collaboration (BRTC), School of Social and Community Medicine, Faculty of Health Sciences, University of Bristol, Bristol, UK

3. Wolfson Palliative Care Research Centre, Hull York Medical School, University of Hull, Hull, UK

Abstract

Background: Patient empowerment, defined as ‘a process through which people gain greater control over decisions and actions affecting their health’ (World Health Organization) is a key theme within global health and social care strategies. The benefits of incorporating empowerment strategies in care are well documented, but little is known about their application or impact for patients with advanced, life-limiting illness(s). Aim: To identify and synthesise the international evidence on patient empowerment for adults with advanced, life-limiting illness(s). Design: Systematic review (PROSPERO no. 46113) with critical interpretive synthesis methodology. Data sources: Five databases (MEDLINE, Embase, CINHAL, PsycINFO and Cochrane) were searched from inception to March 2018. Grey literature and reference list/citation searches of included papers were undertaken. Inclusion criteria: empirical research involving patients with advanced life-limiting illness including descriptions of, or references to, patient empowerment within the study results. Results: In all, 13 papers met inclusion criteria. Two qualitative studies explored patient empowerment as a study objective. Six papers evaluated interventions, referencing patient empowerment as an incidental outcome. The following themes were identified from the interpretive synthesis: self-identity, personalised knowledge in theory and practice, negotiating personal and healthcare relationships, acknowledgement of terminal illness, and navigating continued losses. Conclusion: There are features of empowerment, for patients with advanced life-limiting illness distinct to those of other patient groups. Greater efforts should be made to progress the empowerment of patients nearing the end of their lives. We propose that the identified themes may provide a useful starting point to guide the assessment of existing or planned services and inform future research.

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,General Medicine

Reference43 articles.

1. World Health Organization (WHO). Global Health Observatory data – life expectancy, www.who.int/gho/mortality_burden_disease/life_tables/situation_trends_text/ (2017, accessed 20 June 2017).

2. The Growing Burden of Chronic Disease in America

3. World Health Organization (WHO). Global health and aging, www.who.int/ageing/publications (2011, accessed 20 June 2017).

4. Conceptualising patient empowerment: a mixed methods study

5. Assessment of Patient Empowerment - A Systematic Review of Measures

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