Factors influencing adult carer support planning for unpaid caregiving at the end of life in Scotland: Qualitative insights from triangulated interviews and focus groups.


Journal

Health & social care in the community
ISSN: 1365-2524
Titre abrégé: Health Soc Care Community
Pays: England
ID NLM: 9306359

Informations de publication

Date de publication:
07 2022
Historique:
revised: 24 02 2021
received: 12 07 2020
accepted: 18 05 2021
pubmed: 25 8 2021
medline: 9 6 2022
entrez: 24 8 2021
Statut: ppublish

Résumé

Caring for a relative or friend at the end of life can be rewarding but all-encompassing. These caregivers are often not identified, meaning their diverse needs remain unmet, and the lack of assessment, support and planning increases the likelihood of crisis and burnout. The Carers (Scotland) Act 2016 places responsibility on local authorities to implement such a plan, which will be fast-tracked for carers supporting someone at the end of life. Our research described the factors which might influence this planning, triangulating primary focus groups with 15 carers and secondary qualitative data from transcripts with 30 carers, all of whom who had looked after someone with a terminal illness. Analysis was iterative, and constant comparative analysis of the secondary data informed the primary focus groups. Three main themes were identified; 1. The importance of early identification as a carer to enable timely assessment and support. 2. Carers experience isolation and loneliness which limits opportunities for support. 3. Responding in a timely fashion to carer assessment and support is vital to avoid crises. This research confirms that identifying carers early in the illness trajectory, ideally at diagnosis, is vital to avoid carer burnout. Health and social care providers have a key role in identification and should ensure, where possible, that carer needs are dynamically assessed, supported and documented. Finally, caring does not end after death, it extends into bereavement. Thus, we need to consider system and cultural change to ensure the experiences and needs of carers are addressed and valued.

Identifiants

pubmed: 34427355
doi: 10.1111/hsc.13472
pmc: PMC9290463
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1422-1432

Subventions

Organisme : Chief Scientist Office
ID : CZH/4/1033
Pays : United Kingdom

Informations de copyright

© 2021 The Authors. Health and Social Care in the Community published by John Wiley & Sons Ltd.

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Auteurs

Susan Swan (S)

Marie Curie Hospice, Glasgow, UK.

Richard Meade (R)

Marie Curie, Edinburgh, UK.

Debbie Cavers (D)

Usher Institute, University of Edinburgh, Old Medical School, Edinburgh, UK.

Barbara Kimbell (B)

Usher Institute, University of Edinburgh, Old Medical School, Edinburgh, UK.

Anna Lloyd (A)

Usher Institute, University of Edinburgh, Old Medical School, Edinburgh, UK.
St Columba's Hospice, Edinburgh, UK.

Emma Carduff (E)

Marie Curie Hospice, Glasgow, UK.

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