"It doesn't exist…": negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective
- PMID: 29966521
- PMCID: PMC6027583
- DOI: 10.1186/s12904-018-0343-z
"It doesn't exist…": negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective
Abstract
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.
Keywords: Australia; Cultural and linguistic diversity; Palliative care; Qualitative.
Conflict of interest statement
Ethics approval and consent to participate
Ethics approval was granted by Mater Human Research Ethics Committee (HREC) (NHMRC certified; approval number: HREC/14/MHS/22). Written informed consent was obtained by all participants prior to each interview.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Similar articles
-
'Death is difficult in any language': A qualitative study of palliative care professionals' experiences when providing end-of-life care to patients from culturally and linguistically diverse backgrounds.Palliat Med. 2018 Sep;32(8):1419-1427. doi: 10.1177/0269216318776850. Epub 2018 May 16. Palliat Med. 2018. PMID: 29767578
-
Health professionals' views on health literacy issues for culturally and linguistically diverse women in maternity care: barriers, enablers and the need for an integrated approach.Aust Health Rev. 2018 Feb;42(1):10-20. doi: 10.1071/AH17067. Aust Health Rev. 2018. PMID: 29081348
-
Negotiating palliative care in the context of culturally and linguistically diverse patients.Intern Med J. 2013 Sep;43(9):1043-6. doi: 10.1111/imj.12244. Intern Med J. 2013. PMID: 24004395 Review.
-
Socio-cultural contexts of end- of- life conversations and decisions: bereaved family cancer caregivers' retrospective co-constructions.BMC Palliat Care. 2017 Aug 14;16(1):40. doi: 10.1186/s12904-017-0222-z. BMC Palliat Care. 2017. PMID: 28806952 Free PMC article.
-
Thinking ahead about medical treatments in advanced illness: a qualitative study of barriers and enablers in end-of-life care planning with patients and families from ethnically diverse backgrounds.Health Soc Care Deliv Res. 2023 Jun;11(7):1-135. doi: 10.3310/JVFW4781. Health Soc Care Deliv Res. 2023. PMID: 37464868
Cited by
-
Experiences of Medical Interpreters During Palliative Care Encounters With Limited English Proficiency Patients: A Qualitative Study.J Palliat Med. 2023 Jun;26(6):784-789. doi: 10.1089/jpm.2022.0320. Epub 2022 Dec 13. J Palliat Med. 2023. PMID: 36516127 Free PMC article.
-
The (un)caring experienced by racialized and/or ethnoculturally diverse residents in supportive living: a qualitative study.BMC Geriatr. 2024 Jan 20;24(1):78. doi: 10.1186/s12877-023-04636-0. BMC Geriatr. 2024. PMID: 38245697 Free PMC article.
-
Healthcare practitioners' perspectives of providing palliative care to patients from culturally diverse backgrounds: a qualitative systematic review.BMC Palliat Care. 2023 Nov 17;22(1):182. doi: 10.1186/s12904-023-01285-3. BMC Palliat Care. 2023. PMID: 37978500 Free PMC article.
-
Living and dying between cultural traditions in African & Caribbean Heritage families: a constructivist grounded theory.BMC Palliat Care. 2024 Jul 18;23(1):176. doi: 10.1186/s12904-024-01503-6. BMC Palliat Care. 2024. PMID: 39026241 Free PMC article.
-
The Experience of Informal Newcomer Cancer Caregivers with Limited Language Proficiency: A Scoping Review.J Immigr Minor Health. 2023 Apr;25(2):436-448. doi: 10.1007/s10903-022-01442-5. Epub 2022 Dec 20. J Immigr Minor Health. 2023. PMID: 36538206
References
-
- Broom A. Dying: a social perspective on the end of life. Surrey, England: Ashgate; 2015.
-
- Kirby E, Broom A, Good P, et al. Families and the transition to specialist palliative care. Mortality. 2014;19(4):323–341. doi: 10.1080/13576275.2014.916258. - DOI
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical