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dc.rights.licenseCreative Commons Attribution 4.0 International License
dc.contributor.authorMarulappa, Nidhi
dc.contributor.authorAnderson, Natalie N.
dc.contributor.authorBethell, Jennifer
dc.contributor.authorBourbonnais, Anne
dc.contributor.authorKelly, Fiona
dc.contributor.authorMcMurray, Josephine
dc.contributor.authorRogers, Heather L.
dc.contributor.authorVedel, Isabelle
dc.contributor.authorGagliardi, Anna R.
dc.identifierpublisher-id: s12913-022-07875-w
dc.identifiermanuscript: 7875
dc.identifierdoi: 10.1186/s12913-022-07875-w
dc.identifier.citationMarulappa, N., Anderson, N.N., Bethell, J., Bourbonnais, A., Kelly, F., McMurray, J., Rogers, H.L., Vedel, I. and Gagliardi, A.R. (2022) 'How to implement person-centred care and support for dementia in outpatient and home/community settings: Scoping review', BMC Health Services Research, 22, article no. 541.
dc.descriptionFrom Springer Nature via Jisc Publications Router
dc.description.abstractBackground: Little prior research focused on person-centred care and support (PCCS) for dementia in home, community or outpatient care. We aimed to describe what constitutes PCCS, how to implement it, and considerations for women who comprise the majority of affected persons (with dementia, carers). Methods: We conducted a scoping review by searching multiple databases from 2000 inclusive to June 7, 2020. We extracted data on study characteristics and PCCS approaches, evaluation, determinants or the impact of strategies to implement PCCS. We used summary statistics to report data and interpreted findings with an existing person-centred care framework. Results: We included 22 studies with qualitative (55%) or quantitative/multiple methods design (45%) involving affected persons (50%), or healthcare workers (50%). Studies varied in how PCCS was conceptualized; 59% cited a PCC definition or framework. Affected persons and healthcare workers largely agreed on what constitutes PCCS (e.g. foster partnership, promote autonomy, support carers). In 4 studies that evaluated care, barriers of PCCS were reported at the affected person (e.g. family conflict), healthcare worker (e.g. lack of knowledge) and organizational (e.g. resource constraints) levels. Studies that evaluated strategies to implement PCCS approaches were largely targeted to healthcare workers, and showed that in-person inter-professional educational meetings yielded both perceived (e.g. improved engagement of affected persons) and observed (e.g. use of PCCS approaches) beneficial outcomes. Few studies reported results by gender or other intersectional factors, and none revealed if or how to tailor PCCS for women. This synthesis confirmed and elaborated the PCC framework, resulting in a Framework of PCCS for Dementia. Conclusion: Despite the paucity of research on PCCS for dementia, synthesis of knowledge from diverse studies into a Framework provides interim guidance for those planning or evaluating dementia services in outpatient, home or community settings. Further research is needed to elaborate the Framework, evaluate PCCS for dementia, explore determinants, and develop strategies to implement and scale-up PCCS approaches. Such studies should explore how to tailor PCCS needs and preferences based on input from persons with dementia, and by sex/gender and other intersectional factors such as ethnicity or culture.
dc.relation.ispartofBMC Health Services Research
dc.subjectNeurocognitive Disorder
dc.subjectPerson-centred Care
dc.subjectOutpatient Care
dc.subjectHome Care
dc.subjectScoping Review
dc.titleHow to implement person-centred care and support for dementia in outpatient and home/community settings: Scoping review
qmu.authorKelly, Fiona
qmu.centreCentre for Person-centred Practise Research

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Except where otherwise noted, this item's license is described as Creative Commons Attribution 4.0 International License