Evidence map›Paper›PMID 40552368›Full record

ArticleAge and ageing2025

End-of-life dementia care: a qualitative study of the experiences and perceptions of minority ethnic and economically disadvantaged groups.

Louise Tomkow, Marie Poole, Efioanwan Damisa, Barbara Hanratty, Faith Tissa, Malcolm Ngouala, Josie Dixon, Maria Karagiannidou, Margaret Ogden, Felicity Dewhurst

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Article in Age and ageing, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Louise TomkowHumanitarian and Conflict Response Institute, School of Arts, Languages and Cultures, The University of Manchester, Manchester, UK.ORCID 0000-0002-6453-9019
Marie PoolePopulation health sciences institute, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0001-8379-7462
Efioanwan DamisaPopulation health and primary care, The University of Manchester, Manchester, UK.
Barbara HanrattyPopulation Health Sciences Institute, Biomedical Research Building Newcastle University, Newcastle upon Tyne NE4 5PL, UK.ORCID 0000-0002-3122-7190
Faith TissaPopulation Health Sciences Institute, Newcastle Biomedical Research Building Campus for Ageing , Newcastle upon Tyne NE4 5PL, UK.
Malcolm NgoualaPopulation health sciences institute, Newcastle University, Newcastle upon Tyne, UK.
Josie DixonDepartment of Health Policy, London School of Economics and Political Science, PSSRU Houghton Street, London WC2A 2AE, UK.ORCID 0000-0003-4772-6450
Maria KaragiannidouSchool of Public Policy, The London School of Economics and Political Science, London, UK.
Margaret OgdenAlzheimer's Society, London, UK.
Felicity DewhurstPopulation health sciences institute, Newcastle University, Newcastle upon Tyne, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDementia is a leading cause of morbidity and mortality amongst ageing populations. However, palliative care is often poor or non-existent. People from minority ethnic and economically disadvantaged communities are especially likely to miss out. Research exploring how inclusive end-of-life (EOL) care should be provided for people living with dementia (PLWD) is limited and commonly fails to include sufficient representation of people from minority ethnic groups and those living in poverty.

aimsOur aim was to understand the experiences and perceptions of EOL dementia care amongst underserved groups and investigate how ethnicity and socioeconomic status influence experiences and perceptions of EOL dementia care.

methodsTen workshops were held with a total of 29 Experts-by-Experience (EbE). All had professional and/or personal experience of care for people from disadvantaged groups living with dementia in England. The groups explored (i) current evidence gaps, (ii) barriers and facilitators to EOL care for PLWD across different ethnic and socioeconomic groups and (iii) recommendations for care and future research. The discussions were recorded, transcribed and the qualitative data analysed thematically.

resultsData point to cultural, socioeconomic and systemic barriers to accessing quality EOL care for PLWD. EbE described how there is fear and stigma of talking about dementia and EOL care, and a mistrust of health and care services. Financial concerns were pervasive throughout the data and were described by EbE as significant drivers of inequalities in access to quality care.

conclusionEbE from minority ethnic and socioeconomically disadvantaged groups report poor experiences of EOL dementia care. Our data suggests there is a need to improve multiple aspects of care, including access and coordination. Future research should work with underserved communities to co-produce culturally sensitive interventions to address inequalities in dementia EOL care.

Indexed as

DementiaEthnicityHealthcare DisparitiesHealth Knowledge, Attitudes, PracticeMinority GroupsPovertyTerminal CareVulnerable PopulationsAttitude of Health PersonnelEnglandFemaleHealth Services AccessibilityHumansMaleQualitative ResearchSocioeconomic Factorscarersdementiaend-of-lifeexperiencesminority ethnicolder peoplequalitative research

Identifiers

PMID40552368
PMCPMC12206086

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.