General practitioners' perceptions on the feasibility and acceptability of implementing a risk prediction checklist to support their end-of-life discussions in routine care: a qualitative study.


Journal

Family practice
ISSN: 1460-2229
Titre abrégé: Fam Pract
Pays: England
ID NLM: 8500875

Informations de publication

Date de publication:
19 10 2020
Historique:
pubmed: 17 4 2020
medline: 26 10 2021
entrez: 17 4 2020
Statut: ppublish

Résumé

General practitioners' (GPs) play a central role in facilitating end-of-life discussions with older patients nearing the end-of-life. However, prognostic uncertainty of time to death is one important barrier to initiation of these discussions. To explore GPs' perceptions of the feasibility and acceptability of a risk prediction checklist to identify older patients in their last 12 months of life and describe perceived barriers and facilitators for implementing end-of-life planning. Qualitative, semi-structured interviews were conducted with 15 GPs practising in metropolitan locations in New South Wales and Queensland between May and June 2019. Data were analysed thematically. Eight themes emerged: accessibility and implementation of the checklist, uncertainty around checklist's accuracy and usefulness, time of the checklist, checklist as a potential prompt for end-of-life conversations, end-of-life conversations not an easy topic, end-of-life conversation requires time and effort, uncertainty in identifying end-of-life patients and limited community literacy on end-of-life. Most participants welcomed a risk prediction checklist in routine practice if assured of its accuracy in identifying which patients were nearing end-of-life. Most participating GPs saw the value in risk assessment and end-of-life planning. Many emphasized the need for appropriate support, tools and funding for prognostic screening and end-of-life planning for this to become routine in general practice. Well validated risk prediction tools are needed to increase clinician confidence in identifying risk of death to support end-of-life care planning.

Sections du résumé

BACKGROUND
General practitioners' (GPs) play a central role in facilitating end-of-life discussions with older patients nearing the end-of-life. However, prognostic uncertainty of time to death is one important barrier to initiation of these discussions.
OBJECTIVE
To explore GPs' perceptions of the feasibility and acceptability of a risk prediction checklist to identify older patients in their last 12 months of life and describe perceived barriers and facilitators for implementing end-of-life planning.
METHODS
Qualitative, semi-structured interviews were conducted with 15 GPs practising in metropolitan locations in New South Wales and Queensland between May and June 2019. Data were analysed thematically.
RESULTS
Eight themes emerged: accessibility and implementation of the checklist, uncertainty around checklist's accuracy and usefulness, time of the checklist, checklist as a potential prompt for end-of-life conversations, end-of-life conversations not an easy topic, end-of-life conversation requires time and effort, uncertainty in identifying end-of-life patients and limited community literacy on end-of-life. Most participants welcomed a risk prediction checklist in routine practice if assured of its accuracy in identifying which patients were nearing end-of-life.
CONCLUSIONS
Most participating GPs saw the value in risk assessment and end-of-life planning. Many emphasized the need for appropriate support, tools and funding for prognostic screening and end-of-life planning for this to become routine in general practice. Well validated risk prediction tools are needed to increase clinician confidence in identifying risk of death to support end-of-life care planning.

Identifiants

pubmed: 32297645
pii: 5820803
doi: 10.1093/fampra/cmaa036
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

703-710

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Ebony T Lewis (ET)

School of Public Health and Community Medicine, University of New South Wales, Sydney, Australia.
School of Psychology, University of New South Wales, Sydney, Australia.

Abela Mahimbo (A)

Centre for Primary Health Care & Equity, University of New South Wales, Sydney, Australia.

Christine Linhart (C)

School of Public Health and Community Medicine, University of New South Wales, Sydney, Australia.

Margaret Williamson (M)

School of Public Health and Community Medicine, University of New South Wales, Sydney, Australia.
Centre for Primary Health Care & Equity, University of New South Wales, Sydney, Australia.

Mark Morgan (M)

Faculty of Health Sciences and Medicine, Bond University, Gold Coast, Australia.

Kathrine Hammill (K)

School of Science & Health, Western Sydney University, Sydney, Australia.

John Hall (J)

School of Public Health and Community Medicine, University of New South Wales, Sydney, Australia.

Magnolia Cardona (M)

Gold Coast University Hospital, Gold Coast, Australia.
Institute for Evidence-Based Healthcare, Bond University, Gold Coast, Australia.

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Classifications MeSH