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From a Single Voice to Diversity

Reframing 'Representation' in Patient Engagement

Dados Bibliográficos

ID4611690
AutoresBrett Scholz (0000-0003-2819-994X, School of Medicine and Psychology, The Australian National University, Canberra, ACT, Australia, autor correspondente), Lucy Kirk (0000-0003-3462-3890, School of Medicine and Psychology, The Australian National University, Canberra, ACT, Australia), Terri Warner (0000-0001-9345-8907, School of Medicine and Psychology, The Australian National University, Canberra, ACT, Australia), Lauren O’brien (0000-0002-7336-2171, ACT Disability, Aged and Carer Advocacy Service, Canberra, ACT, Australia), Zsuzsoka Kecskes (0000-0002-9722-1509, University of Wollongong), Imogen Mitchell (0000-0001-6013-4922, School of Medicine and Psychology, The Australian National University, Canberra, ACT, Australia)
Ano2024
Volume34
Fascículo11
Páginas1007-1018
Data de publicação2024-09-01
Peer ReviewedSim
Open AccessSim
TipoARTICLE
PeriódicoQualitative Health Research (JOURNAL)
Identificadores do periódicoISSN: 1049-7323 • E-ISSN: 1552-7557
EditoraSAGE Publications Inc (PUBLISHER)
DOI10.1177/10497323231221674
PMID38229426
OpenAlexW4390952499
IdiomaEN
Citações recebidas7
Referências citadas41

There has been a growing emphasis on consumer representation in the development of health policy, services, research, and education. Existing literature has critiqued how discourses of representativeness can disempower consumers working in health systems. The context of the current study is consumer engagement in the development of COVID-19 triage policy and practice in a local health service. Consumer engagement has often been an afterthought in the COVID response, with few examples of consumers in agenda-setting or decision-making roles. In the Australian Capital Territory, 26 consumer, carer, and community groups worked together with academics and clinicians to develop these principles. Interviews were conducted with stakeholders (including consumers, clinicians, and other health professionals) to evaluate the development of triage principles. A discursive psychological approach to analysis was used to explore participants' understandings about and constructions of consumers being representative (or not) and how this may reproduce power imbalances against consumers. The results explore two distinct ways in which participants talked about consumer representativeness: the first drawing on rhetoric about consumers as lay members of the public (as distinct from being professionally engaged in the health sector), and the second in terms of consumer representatives being diverse and having intersectional identities and experiences. Expectations about consumers to be representative of the general population may reproduce traditional power imbalances and silence lived experience expertise. These power imbalances may be challenged by a shift in the way representativeness is conceptualised to requiring health services to seek out diverse and intersectionally marginalised consumers

Cognitive reframing · Health care · Political science · Public relations · Representativeness heuristic · Sociology · Empathy and Medical Education · Mental Health and Patient Involvement · Patient-Provider Communication in Healthcare · Psychology · Social Psychology

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Obras citantes distintas7
Citações por ano3,5
Intervalo de citações2024 - 2026 (3)
Velocidade de citaçãocurrent
Altamente citadoNão
Tipos de citaçãoNeutras: 7
Ethnos_APP • Projeto Open Source • Licença MIT • Frontend v2.0.0 • Privacidade e Cookies • Documentação da API: api.ethnos.app/docs • Código da API: GitHub • DOI: 10.5281/zenodo.17049435 • Código do Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae