Dados Bibliográficos

AUTOR(ES) C. Kendall , S.H. Lee , Susannah Johnston , S Collin , Maya Gibb , Sathya Karunananthan , Margaret Cody , Peter Tanuseputro , Daniel Bedard , Krystal Kehoe MacLeod
AFILIAÇÃO(ÕES) Faculty of Medicine, University of Ottawa, Canada, École des Hautes Études Publiques, Université de Moncton, Canada, Clinical Epidemiology Program, Ottawa Hospital Research Institute, Canada, Department of Palliative Care, Bruyère Research Institute, Canada, Institute du Savoir Monfort, Canada
ANO 2023
TIPO Artigo
PERIÓDICO International Journal of Qualitative Methods
ISSN 1609-4069
E-ISSN 1609-4069
EDITORA SAGE Publications Inc.
DOI 10.1177/16094069231205202
ADICIONADO EM 2025-08-18

Resumo

Health disparities exist across different linguistic groups. Language barriers in primary care can negatively affect access to healthcare services and the quality and safety of care at the end-of-life. This study will take a novel, in-depth look at the experience of language- and/or cultural-discordant care for adults from linguistic minority groups through the eyes of primary care physicians providing palliative and/or end-of-life care. Language and cultural discordance means that the physician and patient do not speak the same language or are not from the same cultural background. Qualitative data from primary care physicians ( n = 12–24) providing language-discordant end-of-life care to Francophone and/or Allophone older adults across different care models and diverse geographies in Ontario will be collected through semi-structured interviews. Reflexive thematic analysis will be used to report themes within the data and consider the influence of the social locations of the researcher and research participants, geographic considerations impacting service provision, and barriers imposed by differing primary care funding structures on the provision of palliative and end-of-life care for linguistic and cultural minority groups in Ontario. Findings from this study will identify the interconnections among language and cultural discordance, care model, geographic region, and physician perceptions of their combined effects on access to, and quality of, palliative and end-of-life care. This evidence will be key to informing clinical practice guidelines and mobilizing change to improve primary care access and quality for adults at the end-of-life from linguistic and cultural minority populations across Ontario.

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