Dementia care‐giving from a family network perspective in Germany: A typology.

Sustaining informal care‐giving for people living with dementia (PWD) is a common objective of societies worldwide. Families can contribute substantially to the support of care‐giving relatives. However, a deeper understanding of the impact of informal care‐giving for PWD on family life is needed. I...

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Publicado en:Health & Social Care in the Community Vol. 30; no. 2; pp. 579 - 592
Autores principales: Neubert, Lydia, Gottschalk, Sophie, König, Hans‐Helmut, Brettschneider, Christian
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell Feb2022
Acceso en línea:Ver este registro en EBSCOhost
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      pub: Wiley-Blackwell
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        10.1111/hsc.13161
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        atl: Dementia care‐giving from a family network perspective in Germany: A typology.
      aug:
        au:
          Neubert, Lydia
          Gottschalk, Sophie
          König, Hans‐Helmut
          Brettschneider, Christian
        affil: Department of Health Economics and Health Services Research, Hamburg Center for Health Economics, University Medical Center Hamburg‐Eppendorf, Hamburg, Germany
      sug:
        subj:
          Dementia Germany
          Caregivers Psychosocial Factors
          Family Attitudes Germany
          Caregiver Attitudes
          Human
          Germany
          Dementia Patients
          Primary Health Care
          Pilot Studies
          Qualitative Studies
          Life Experiences
          Purposive Sample
          Funding Source
      ab: Sustaining informal care‐giving for people living with dementia (PWD) is a common objective of societies worldwide. Families can contribute substantially to the support of care‐giving relatives. However, a deeper understanding of the impact of informal care‐giving for PWD on family life is needed. Interviewing of multiple family network members—in addition to the primary carer—provides more insight into familial contexts of care‐giving. This pilot study aims to explore how informal carers reconcile dementia care‐giving and family life from a family network perspective. Therefore, we conducted 14 narrative interviews with family carers from seven care‐giving networks in Germany, which we interpreted using the documentary method. The yielded relational typology describes five types of family carers of PWD. These types reflect the way the families deal with dementia care‐giving based on the interrelation between relationship quality and the distribution of care‐giving tasks within the family. Depending on the constellation of this interrelationship, family carers either experience care as a joint project, as co‐operation with external support or within the family, as disappointment or as a predicament without alternatives. Finally, if the care‐giving tasks are not shared, or if the distribution is perceived as unequal, relationship break downs can occur, especially in family ties that are already strained. However, joint care‐giving and strong ties can also bring the family closer together and enhance care experiences. Care professionals and social workers should be aware of the family network of dementia carers and support the development of a sense of family unity. This can contribute to positive care experiences among family carers and thus increase the maintenance of informal dementia care.
      pubtype: Academic Journal
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      ougenre: Article
    language: English
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