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A comparison of spouse and non-spouse carers of people with dementia: a descriptive analysis of Swedish national survey data
Dalarna University, School of Health and Welfare, Care Sciences.ORCID iD: 0000-0002-8480-190x
Dalarna University, School of Health and Welfare, Social Work.ORCID iD: 0000-0002-8795-7555
Dalarna University, School of Health and Welfare, Social Work. Karolinska Institutet; Stockholm University.ORCID iD: 0000-0002-7685-3216
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2021 (English)In: BMC Geriatrics, E-ISSN 1471-2318, Vol. 21, article id 338Article in journal (Refereed) Published
Abstract [en]

Being an informal carer of a person with dementia (PwD) can have a negative effect on the carer’s health and quality of life, and spouse carers have been found to be especially vulnerable. Yet relatively little is known about the care provided and support received by spouse carers. This study compares spouse carers to other informal carers of PwDs regarding their care provision, the support received and the psychosocial impact of care.

Place, publisher, year, edition, pages
2021. Vol. 21, article id 338
National Category
Nursing
Research subject
Research Profiles 2009-2020, Health and Welfare
Identifiers
URN: urn:nbn:se:du-37261DOI: 10.1186/s12877-021-02264-0ISI: 000660608300001PubMedID: 34078292Scopus ID: 2-s2.0-85107220762OAI: oai:DiVA.org:du-37261DiVA, id: diva2:1559967
Available from: 2021-06-03 Created: 2021-06-03 Last updated: 2024-07-04Bibliographically approved
In thesis
1. For better and for worse, till death do us part: Support needs of persons caring for a co-habitant spouse or partner with dementia
Open this publication in new window or tab >>For better and for worse, till death do us part: Support needs of persons caring for a co-habitant spouse or partner with dementia
2024 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Background: Caring for a partner with dementia is typically stressful and challenging. Such carers can become overwhelmed by their responsibilities, neglecting their personal needs as well as their need for support as a carer. Receipt of support is low among spouse carers, while the support received may not be appropriate for their needs. More research is required to develop effective support for this important group of carers. 

Overall aim: To explore the life- and caring situation of spouses caring for a partner with dementia and to increase the understanding of their needs and experiences of support.  

Methods: This thesis consists of four papers (I-IV): I, Analysis of data on informal carers of persons with dementia (n=330) from a cross-sectional survey of a stratified random probability sample of adults in Sweden (N=30 009); II and III, a cross-sectional survey of a convenience sample of people aged 65 years or older caring for a partner with dementia (N=175). Hierarchal regression models explored positive and negative aspects of caring (II), and principal component analysis examined carers’ perceptions of support (III); IV, a thematic analysis of semi-structured telephone interviews with 24 spouse carers, exploring their caring experiences. 

Results: Compared to other carers, spouses of persons with dementia received less support from family or local authorities, while experiencing more negative impact from caring (I). Negative impact from, and positive value of, caring among spouses, were associated with different aspects of their situation (II). Support was perceived as important, yet spouses may not perceive support to themselves as more important than support to their partner (III). Spouse carers experienced a loss of self and felt confined in their situation, finding it hard to distinguish between their needs and those of their partner (IV). 

Conclusion: Compared to other carers, spouses are more exposed to the negative aspects of caring, while being less supported. Support to spouse carers should focus on strengthening the positive aspects of caring to mitigate the negative aspects. As a spouse’s needs are conditioned by their partner’s, support should focus on spouses’ personal needs and their partners’ care needs.

Place, publisher, year, edition, pages
Falun: Dalarna University, 2024
Series
Dalarna Doctoral Dissertations ; 30
Keywords
Informal care, spouse, dementia, support, needs, experiences
National Category
Nursing
Identifiers
urn:nbn:se:du-47671 (URN)978-91-88679-58-1 (ISBN)
Public defence
2024-04-19, lecture hall 105 (Fö 5), campus Falun, 09:00 (Swedish)
Opponent
Supervisors
Available from: 2024-03-15 Created: 2024-01-04 Last updated: 2024-03-15Bibliographically approved

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Falk Johansson, MarcusMcKee, KevinDahlberg, LenaMarmstål Hammar, Lena

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Falk Johansson, MarcusMcKee, KevinDahlberg, LenaMarmstål Hammar, Lena
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