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“It doesn’t exist…”: negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective
BACKGROUND: The end of life represents a therapeutic context that acutely raises cultural and linguistic specificities, yet there is very little evidence illustrating the importance of such dynamics in shaping choices, trajectories and care practices. Culture and language interplay to offer consider...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027583/ https://www.ncbi.nlm.nih.gov/pubmed/29966521 http://dx.doi.org/10.1186/s12904-018-0343-z |
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author | Kirby, Emma Lwin, Zarnie Kenny, Katherine Broom, Alex Birman, Holi Good, Phillip |
author_facet | Kirby, Emma Lwin, Zarnie Kenny, Katherine Broom, Alex Birman, Holi Good, Phillip |
author_sort | Kirby, Emma |
collection | PubMed |
description | BACKGROUND: The end of life represents a therapeutic context that acutely raises cultural and linguistic specificities, yet there is very little evidence illustrating the importance of such dynamics in shaping choices, trajectories and care practices. Culture and language interplay to offer considerable potential challenges to both patient and provider, with further work needed to explore patient and caregiver perspectives across cultures and linguistic groups, and provider perspectives. The objective of this study was to develop a critical, evidence-based understanding of the experiences of people from Culturally and Linguistically Diverse (CALD) backgrounds, and their caregivers, in a palliative care setting. METHODS: A qualitative study, using semi-structured interviews to explore key experiences and perspectives of CALD patients and caregivers currently undergoing treatment under oncology or palliative care specialists in two Australian hospitals. Interviews were digitally audio recorded and transcribed in full. A thematic analysis was conducted utilising the framework approach. RESULTS: Sixteen patients and fourteen caregivers from a range of CALD backgrounds participated in semi-structured interviews. The research identified four prevalent themes among participants: (1) Terminology in the transition to palliative care; (2) Communication, culture and pain management; (3) (Not) Talking about death and dying; and, (4) Religious faith as a coping strategy: challenging the terminal diagnosis. CONCLUSIONS: CALD patients and caregivers’ experiences are multifaceted, particularly in negotiating linguistic difficulties, beliefs about treatment, and issues related to death and dying. Greater attention is needed to develop effective communication skills, recognise CALD patients’ particular cultural, linguistic and spiritual values and needs, and acknowledge the unique nature of each doctor-patient interaction. |
format | Online Article Text |
id | pubmed-6027583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60275832018-07-09 “It doesn’t exist…”: negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective Kirby, Emma Lwin, Zarnie Kenny, Katherine Broom, Alex Birman, Holi Good, Phillip BMC Palliat Care Research Article BACKGROUND: The end of life represents a therapeutic context that acutely raises cultural and linguistic specificities, yet there is very little evidence illustrating the importance of such dynamics in shaping choices, trajectories and care practices. Culture and language interplay to offer considerable potential challenges to both patient and provider, with further work needed to explore patient and caregiver perspectives across cultures and linguistic groups, and provider perspectives. The objective of this study was to develop a critical, evidence-based understanding of the experiences of people from Culturally and Linguistically Diverse (CALD) backgrounds, and their caregivers, in a palliative care setting. METHODS: A qualitative study, using semi-structured interviews to explore key experiences and perspectives of CALD patients and caregivers currently undergoing treatment under oncology or palliative care specialists in two Australian hospitals. Interviews were digitally audio recorded and transcribed in full. A thematic analysis was conducted utilising the framework approach. RESULTS: Sixteen patients and fourteen caregivers from a range of CALD backgrounds participated in semi-structured interviews. The research identified four prevalent themes among participants: (1) Terminology in the transition to palliative care; (2) Communication, culture and pain management; (3) (Not) Talking about death and dying; and, (4) Religious faith as a coping strategy: challenging the terminal diagnosis. CONCLUSIONS: CALD patients and caregivers’ experiences are multifaceted, particularly in negotiating linguistic difficulties, beliefs about treatment, and issues related to death and dying. Greater attention is needed to develop effective communication skills, recognise CALD patients’ particular cultural, linguistic and spiritual values and needs, and acknowledge the unique nature of each doctor-patient interaction. BioMed Central 2018-07-02 /pmc/articles/PMC6027583/ /pubmed/29966521 http://dx.doi.org/10.1186/s12904-018-0343-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kirby, Emma Lwin, Zarnie Kenny, Katherine Broom, Alex Birman, Holi Good, Phillip “It doesn’t exist…”: negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective |
title | “It doesn’t exist…”: negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective |
title_full | “It doesn’t exist…”: negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective |
title_fullStr | “It doesn’t exist…”: negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective |
title_full_unstemmed | “It doesn’t exist…”: negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective |
title_short | “It doesn’t exist…”: negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective |
title_sort | “it doesn’t exist…”: negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027583/ https://www.ncbi.nlm.nih.gov/pubmed/29966521 http://dx.doi.org/10.1186/s12904-018-0343-z |
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