A bad time to die? Exploring bereaved families/wha-nau experiences of end-of-life care under COVID-19 restrictions: a qualitative interview study.

COVID-19 bereavement cultural safety family caregiving grief holistic health care palliative

Journal

Palliative care and social practice
ISSN: 2632-3524
Titre abrégé: Palliat Care Soc Pract
Pays: United States
ID NLM: 101754997

Informations de publication

Date de publication:
2023
Historique:
received: 17 04 2023
accepted: 05 07 2023
pubmed: 16 8 2023
medline: 16 8 2023
entrez: 16 8 2023
Statut: epublish

Résumé

There have been international concerns raised that, during the COVID-19 pandemic, there was an absence of good palliative care resulting in poor end-of-life care experiences. To date, there have been few studies considering the pandemic's impact on people dying from non-COVID-19 causes and their families and friends. In particular, there has been very less empirical research in relation to end-of-life care for Indigenous, migrant and minoritised ethnic communities. To explore bereaved next-of-kin's views and experiences of end-of-life care under COVID-19 pandemic regulations. This qualitative study involved in-depth one-off interviews with 30 ethnically diverse next-of-kin who had a family member die in the first year of the pandemic in Aotearoa, New Zealand. Interviews were conducted by ethnically matched interviewers/interviewees. A reflexive thematic analysis was used to explore and conceptualise their accounts. A key finding was that dying alone and contracting COVID-19 were seen as equally significant risks by bereaved families. Through this analysis, we identified five key themes: (1) compromised connection; (2) uncertain communication; (3) cultural safety; (4) supported grieving and (5) silver linings. This article emphasises the importance of enabling safe and supported access for family/whanau to be with their family/wha-nau member at end-of-life. We identify a need for wider provision of bereavement support. We recommend that policy makers increase resourcing of palliative care services to ensure that patients and their families receive high-quality end-of-life care, both during and post this pandemic. Policy makers could also promote a culturally-diverse end-of-life care work force and the embedding of culturally-safety practices across a range of institutions where people die.

Sections du résumé

Background UNASSIGNED
There have been international concerns raised that, during the COVID-19 pandemic, there was an absence of good palliative care resulting in poor end-of-life care experiences. To date, there have been few studies considering the pandemic's impact on people dying from non-COVID-19 causes and their families and friends. In particular, there has been very less empirical research in relation to end-of-life care for Indigenous, migrant and minoritised ethnic communities.
Objectives UNASSIGNED
To explore bereaved next-of-kin's views and experiences of end-of-life care under COVID-19 pandemic regulations.
Design UNASSIGNED
This qualitative study involved in-depth one-off interviews with 30 ethnically diverse next-of-kin who had a family member die in the first year of the pandemic in Aotearoa, New Zealand.
Methods UNASSIGNED
Interviews were conducted by ethnically matched interviewers/interviewees. A reflexive thematic analysis was used to explore and conceptualise their accounts.
Results UNASSIGNED
A key finding was that dying alone and contracting COVID-19 were seen as equally significant risks by bereaved families. Through this analysis, we identified five key themes: (1) compromised connection; (2) uncertain communication; (3) cultural safety; (4) supported grieving and (5) silver linings.
Conclusion UNASSIGNED
This article emphasises the importance of enabling safe and supported access for family/whanau to be with their family/wha-nau member at end-of-life. We identify a need for wider provision of bereavement support. We recommend that policy makers increase resourcing of palliative care services to ensure that patients and their families receive high-quality end-of-life care, both during and post this pandemic. Policy makers could also promote a culturally-diverse end-of-life care work force and the embedding of culturally-safety practices across a range of institutions where people die.

Identifiants

pubmed: 37584059
doi: 10.1177/26323524231189525
pii: 10.1177_26323524231189525
pmc: PMC10424543
doi:

Types de publication

Journal Article

Langues

eng

Pagination

26323524231189525

Informations de copyright

© The Author(s), 2023.

Déclaration de conflit d'intérêts

The authors declared no potential conflicts of interest with respect to the research, authorship and/or publication of this article.

Auteurs

Tessa Morgan (T)

Applied Social Science Group, Department of Public Health and Primary Care, The University of Cambridge, Forvie Site, Cambridge CB2 0SR, UK.

Merryn Gott (M)

School of Nursing, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

Lisa Williams (L)

School of Nursing, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

Joe Naden (J)

School of Nursing, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

Yingmin Wang (Y)

School of Foreign Studies and School of International Culture, South China Normal University, Guangzhou, China.

Brianna Smith (B)

School of Nursing, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

Elizabeth Fanueli (E)

School of Population Health, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

Martyarini Budi Setyawati (M)

School of Nursing, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

Kathryn Morgan (K)

School of Nursing, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

Jackie Robinson (J)

School of Nursing, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

Natalie Anderson (N)

School of Nursing, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

Melissa Carey (M)

School of Nursing, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

Tess Moeke-Maxwell (T)

School of Nursing, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

Classifications MeSH