Abstract
Introduction: A palliative care approach can improve quality-of-life for people with dementia. It is the preference of many people with dementia to remain living at home until death, with the appropriate care. To develop a successful model for dementia palliative care in the community, it is essential to assimilate the perspectives and experiences of those affected. The guiding research question for this study was: What are people with dementia and family carers’ views on a model for dementia palliative care?
Methods: Focus groups (n=3) were conducted with bereaved or current family carers (n=11), and people with dementia (n=2). Discussions centred around a proposed model of dementia palliative care. These were transcribed and analysed using thematic analysis.
Results: Three main themes were identified: living and dying well with dementia; reducing carer burden to fulfil the wish for home care; and lack of faith in the healthcare system. One statement which summarised the analysis was: “Dementia palliative care is a dream, but not a reality.” This reflected participants’ repeated “wish” for this “ideal” model of care, but simultaneous scepticism regarding its implementation, based on their prior experiences of healthcare services.
Conclusion: All participants were welcoming of the proposed model for dementia palliative care and were generally positive about palliative care as a concept relating to dementia. There was consensus that the model would allow people to live and die well with dementia, and reducing the carer burden would fulfil the wish to remain at home. However systemic changes in the healthcare system will be needed to facilitate a truly person-centred, holistic, individualised and flexible model of care.
Methods: Focus groups (n=3) were conducted with bereaved or current family carers (n=11), and people with dementia (n=2). Discussions centred around a proposed model of dementia palliative care. These were transcribed and analysed using thematic analysis.
Results: Three main themes were identified: living and dying well with dementia; reducing carer burden to fulfil the wish for home care; and lack of faith in the healthcare system. One statement which summarised the analysis was: “Dementia palliative care is a dream, but not a reality.” This reflected participants’ repeated “wish” for this “ideal” model of care, but simultaneous scepticism regarding its implementation, based on their prior experiences of healthcare services.
Conclusion: All participants were welcoming of the proposed model for dementia palliative care and were generally positive about palliative care as a concept relating to dementia. There was consensus that the model would allow people to live and die well with dementia, and reducing the carer burden would fulfil the wish to remain at home. However systemic changes in the healthcare system will be needed to facilitate a truly person-centred, holistic, individualised and flexible model of care.
| Original language | English |
|---|---|
| Article number | DEM-23-0337r1 |
| Pages (from-to) | 91-110 |
| Number of pages | 20 |
| Journal | Dementia: The International Journal of Social Research and Practice |
| Volume | 24 |
| Issue number | 1 |
| Early online date | 9 Aug 2024 |
| DOIs | |
| Publication status | Published (in print/issue) - 31 Jan 2025 |
Bibliographical note
Publisher Copyright:© The Author(s) 2024.
Data Availability Statement
Raw data (i.e., interview transcripts) are not publicly available due to their potentially identifiable nature.*Funding
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This research was supported by a grant from the Health Research Board (ILPHSR-2017-020).
| Funder number |
|---|
| ILPHSR-2017-020 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- Dementia
- palliative care
- advance care planning
- end- of-life
- home care
- community care
- Model
- end-of-life
- dementia
- model
- Palliative Care/psychology
- Humans
- Middle Aged
- Focus Groups
- Male
- Caregivers/psychology
- Quality of Life/psychology
- Aged, 80 and over
- Female
- Aged
- Qualitative Research
- Dementia/psychology
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