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Patient Engagement, Chronic Illness, and the Subject of Health Care Reform

Datos Bibliográficos

ID4564508
AutoresMark D Fleming (0000-0002-3037-704X, Schlumberger (Ireland), autor de correspondencia), Janet K Shim (0000-0002-4597-7961, Twitter (United States)), Irene H Yen (0000-0002-2954-6109), Irene Yen, Ariana Thompson-Lastad (0000-0002-4880-1371), Nancy J Burke (0000-0002-2269-3341)
Año2021
Volumen40
Número3
Páginas214-227
Fecha de publicación2021-04-03
Peer ReviewedSí
Open AccessNo
TipoARTICLE
RevistaMedical Anthropology (JOURNAL)
Identificadores de la revistaISSN: 0145-9740 • E-ISSN: 1545-5882
EditorialInforma UK Limited (PUBLISHER • GB)
DOI10.1080/01459740.2020.1820500
PMID32946278
OpenAlexW3087614282
IdiomaEN
Citas recibidas3
Referencias citadas26

In the United States, in the wake of health care reform, health care systems have been subject to intensifying demands to increase patient engagement , a term that refers broadly to participation in care. We draw from ethnographic research in urban health care safety-net settings in California to examine efforts to increase patient engagement among chronically ill, marginalized patients who have long been disconnected from outpatient care. We suggest that the work of engagement in this context involved getting people to accept the norms of biomedicine while also reworking these norms to account for the complex circumstances of their lives

Biomedicine · Context (archaeology · Ethnography · Health care · Political science · Public relations · Sociology · Subject (documents · Work (physics · Medicine · Mental Health and Patient Involvement · Nursing · Patient-Provider Communication in Healthcare · Primary Care and Health Outcomes · Psychology

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Obras citantes distintas3
Citas por año0,6
Intervalo de citas2021 - 2024 (4)
Velocidad de citaciónrecent
Altamente citadoNo
Tipos de citaNeutras: 3
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