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Post-diagnostic support for persons with young-onset dementia - a retrospective analysis based on data from the Swedish dementia registry SveDem
Jönköping University, Hälsohögskolan, HHJ, Institutet för gerontologi. Jönköping University, Hälsohögskolan, HHJ. Studies on Integrated Health and Welfare (SIHW).ORCID-id: 0009-0003-2261-0635
Jönköping University, Hälsohögskolan, HHJ, Institutet för gerontologi. Jönköping University, Hälsohögskolan, HHJ. Studies on Integrated Health and Welfare (SIHW). Center for Economic and Social Research, University of Southern California, Los Angeles, USA.ORCID-id: 0000-0003-2346-2470
Jönköping University, Hälsohögskolan, HHJ, Institutet för gerontologi. Department of Human Development and Family Studies, Penn State University, University Park, USA.ORCID-id: 0000-0002-0351-2090
Institute of Health and Care Science, The Sahlgrenska Academy at Gothenburg University, Gothenburg, Sweden; Department of Architecture and Civil Engineering, Chalmers University of Technology, Gothenburg, Sweden.
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2024 (Engelska)Ingår i: BMC Health Services Research, E-ISSN 1472-6963, Vol. 24, nr 1, artikel-id 649Artikel i tidskrift (Refereegranskat) Published
Hållbar utveckling
00. Hållbar utveckling, 3. God hälsa och välbefinnande
Abstract [en]

BACKGROUND: Approximately 3.9 million persons worldwide have young-onset dementia. Symptoms related to young-onset dementia present distinct challenges related to finances, employment, and family. To provide tailored support, it is important to gain knowledge about the formal support available for persons with young-onset dementia. Therefore, this paper aims to describe formal support for persons with young-onset dementia in Sweden and the factors influencing this support.

METHODS: This retrospective study used data on persons under 65 years of age (n = 284) from The Swedish Registry for Cognitive/Dementia Disorders (SveDem) between 2021 and 2022. SveDem was established to monitor the quality of dementia care in Sweden. Characteristics of participants were obtained, including age, sex, dementia diagnosis, MMSE, medications, accommodation, and care setting. Descriptive statistics and logistic regression were used to test for associations between participant characteristics and post-diagnostic support.

RESULTS: Information and educational support were usually offered to the person with young-onset dementia (90.1%) and their family (78.9%). Approximately half of the sample were offered contact with a dementia nurse (49.3%), counsellor (51.4%), or needs assessor (47.9%). A minority (28.5%) were offered cognitive aids. Six regression models were conducted based on participant characteristics to predict the likelihood that persons were offered support. Support was not predicted by age, sex, children at home, accommodation, or medications. Lower MMSE scores (p < .05) and home help (p < .05) were significantly associated with offer of a needs assessor. Living together was a significant predictor (p < .01) for information and educational support offered to the family. Care setting significantly predicted (p < .01) an offer of information and educational support for the person and family members, as well as contact with a counsellor.

CONCLUSION: This study indicates potential formal support shortages for persons with young-onset dementia in some areas of dementia care. Despite equal support across most characteristics, disparities based on care setting highlight the importance of specialised dementia care. Pre-diagnostic support is minimal, indicating challenges for persons with young-onset dementia to access these services before diagnosis. While our study has identified areas in need of improvement, we recommend further research to understand the changing support needs of those with young-onset dementia.

Ort, förlag, år, upplaga, sidor
BioMed Central (BMC), 2024. Vol. 24, nr 1, artikel-id 649
Nyckelord [en]
Dementia care, Early-onset dementia, Formal support services, Memory clinics, Quality registry, YOD, Young-onset dementia
Nationell ämneskategori
Geriatrik Hälso- och sjukvårdsorganisation, hälsopolitik och hälsoekonomi
Identifikatorer
URN: urn:nbn:se:hj:diva-64404DOI: 10.1186/s12913-024-11108-7ISI: 001228894700002PubMedID: 38773535Scopus ID: 2-s2.0-85193987921Lokalt ID: GOA;;954111OAI: oai:DiVA.org:hj-64404DiVA, id: diva2:1862878
Forskningsfinansiär
Forte, Forskningsrådet för hälsa, arbetsliv och välfärd, 2021−01799Tillgänglig från: 2024-05-30 Skapad: 2024-05-30 Senast uppdaterad: 2024-05-30Bibliografiskt granskad

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Kårelind, FannyFinkel, DeborahZarit, Steven H.Bielsten, ThereseJohansson, Linda

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Kårelind, FannyFinkel, DeborahZarit, Steven H.Bielsten, ThereseJohansson, Linda
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BMC Health Services Research
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