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Suffering and loss in Lewy body dementia: applying a palliative care lens to a longitudinal narrative study

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Suffering and loss in Lewy body dementia: applying a palliative care lens to a longitudinal narrative study. / Bentley, Allison; Salifu, Yakubu; Walshe, Catherine.
In: Palliative and Supportive Care, Vol. 23, e117, 31.12.2025.

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Bentley A, Salifu Y, Walshe C. Suffering and loss in Lewy body dementia: applying a palliative care lens to a longitudinal narrative study. Palliative and Supportive Care. 2025 Dec 31;23:e117. Epub 2025 Jun 20. doi: 10.1017/S1478951524001962

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@article{f4999041173942b68cdc634221b18e73,
title = "Suffering and loss in Lewy body dementia: applying a palliative care lens to a longitudinal narrative study",
abstract = "ObjectivesThis study aims to explore the everyday experiences of people living with Lewy body dementia and their families, to deepen understanding of their care needs. Lewy body dementia is a neurodegenerative condition associated with shorter life-expectancy and poorer quality of life than other forms of dementia. Cognitive fluctuations, visual hallucinations, falls, and motor features of Parkinsonism gives rise to complex and debilitating symptoms. Other prominent features include behavioral and emotional problems, rapid eye movement sleep disorder, and autonomic dysfunction. Improving palliative care for people with dementia continues to be an international priority; however, little is known as to how a palliative care approach could support people living with Lewy body dementia and their families.MethodsDrawing on narrative theory of self and personhood, a qualitative, longitudinal narrative approach provided unique insights into 5 couples{\textquoteright} experiences of living with Lewy body dementia. Analysis was conducted using Murray{\textquoteright}s levels of narrative analysis in health psychology to explore stories at the personal, interpersonal, positional, and societal level.ResultsParticipants with Lewy body dementia described losses associated with communication, continence, and energy leading to a progressive loss of independence. For their family caregivers a loss of companionship was particularly salient. These losses, compounded by a perceived lack of clinical support, resulted in suffering both for the person with Lewy body dementia, and for those close to them.Significance of resultsThere has been a societal and political shift to move beyond loss in dementia, to a focus on abilities and living well. However, acknowledging loss, while supporting symptom management is an important aspect of Lewy body dementia care. Providing person-centered, palliative supportive care throughout the disease trajectory could reduce suffering and enhance well-being.",
author = "Allison Bentley and Yakubu Salifu and Catherine Walshe",
year = "2025",
month = jun,
day = "20",
doi = "10.1017/S1478951524001962",
language = "English",
volume = "23",
journal = "Palliative and Supportive Care",
issn = "1478-9515",
publisher = "Cambridge University Press",

}

RIS

TY - JOUR

T1 - Suffering and loss in Lewy body dementia

T2 - applying a palliative care lens to a longitudinal narrative study

AU - Bentley, Allison

AU - Salifu, Yakubu

AU - Walshe, Catherine

PY - 2025/6/20

Y1 - 2025/6/20

N2 - ObjectivesThis study aims to explore the everyday experiences of people living with Lewy body dementia and their families, to deepen understanding of their care needs. Lewy body dementia is a neurodegenerative condition associated with shorter life-expectancy and poorer quality of life than other forms of dementia. Cognitive fluctuations, visual hallucinations, falls, and motor features of Parkinsonism gives rise to complex and debilitating symptoms. Other prominent features include behavioral and emotional problems, rapid eye movement sleep disorder, and autonomic dysfunction. Improving palliative care for people with dementia continues to be an international priority; however, little is known as to how a palliative care approach could support people living with Lewy body dementia and their families.MethodsDrawing on narrative theory of self and personhood, a qualitative, longitudinal narrative approach provided unique insights into 5 couples’ experiences of living with Lewy body dementia. Analysis was conducted using Murray’s levels of narrative analysis in health psychology to explore stories at the personal, interpersonal, positional, and societal level.ResultsParticipants with Lewy body dementia described losses associated with communication, continence, and energy leading to a progressive loss of independence. For their family caregivers a loss of companionship was particularly salient. These losses, compounded by a perceived lack of clinical support, resulted in suffering both for the person with Lewy body dementia, and for those close to them.Significance of resultsThere has been a societal and political shift to move beyond loss in dementia, to a focus on abilities and living well. However, acknowledging loss, while supporting symptom management is an important aspect of Lewy body dementia care. Providing person-centered, palliative supportive care throughout the disease trajectory could reduce suffering and enhance well-being.

AB - ObjectivesThis study aims to explore the everyday experiences of people living with Lewy body dementia and their families, to deepen understanding of their care needs. Lewy body dementia is a neurodegenerative condition associated with shorter life-expectancy and poorer quality of life than other forms of dementia. Cognitive fluctuations, visual hallucinations, falls, and motor features of Parkinsonism gives rise to complex and debilitating symptoms. Other prominent features include behavioral and emotional problems, rapid eye movement sleep disorder, and autonomic dysfunction. Improving palliative care for people with dementia continues to be an international priority; however, little is known as to how a palliative care approach could support people living with Lewy body dementia and their families.MethodsDrawing on narrative theory of self and personhood, a qualitative, longitudinal narrative approach provided unique insights into 5 couples’ experiences of living with Lewy body dementia. Analysis was conducted using Murray’s levels of narrative analysis in health psychology to explore stories at the personal, interpersonal, positional, and societal level.ResultsParticipants with Lewy body dementia described losses associated with communication, continence, and energy leading to a progressive loss of independence. For their family caregivers a loss of companionship was particularly salient. These losses, compounded by a perceived lack of clinical support, resulted in suffering both for the person with Lewy body dementia, and for those close to them.Significance of resultsThere has been a societal and political shift to move beyond loss in dementia, to a focus on abilities and living well. However, acknowledging loss, while supporting symptom management is an important aspect of Lewy body dementia care. Providing person-centered, palliative supportive care throughout the disease trajectory could reduce suffering and enhance well-being.

U2 - 10.1017/S1478951524001962

DO - 10.1017/S1478951524001962

M3 - Journal article

VL - 23

JO - Palliative and Supportive Care

JF - Palliative and Supportive Care

SN - 1478-9515

M1 - e117

ER -