Literature DB >> 19191998

Informal carers of older family members: how they manage and what support they receive from respite care.

Sirpa Salin1, Marja Kaunonen, Päivi Astedt-Kurki.   

Abstract

AIMS: To describe informal carers' coping strategies and their experiences of the support provided by respite care.
BACKGROUND: The target set in the Finnish national old age policy strategy is that 90% of the population over 75 should be able to live at home. A major source of support for older people and their families is respite care in an institution.
DESIGN: Survey.
METHODS: The data were collected among informal carers who regularly use respite care services (n = 143). Two structured questionnaires were used: the Carers' Assessment of Managing Index (Nolan et al. 1995) and an index developed by the researchers.
RESULTS: Informal carers who provided care for younger individuals or people who needed less help had a better quality of life. Spouse carers and older informal carers were less satisfied with their quality of life than younger carers. Periods of respite care had a major influence on informal carers' quality of life: 93% said they felt invigorated. Care periods remained rather isolated episodes in the lives of the older patients in that there was hardly any discussion at the institution about the family's situation, the objectives of respite care, or about how the informal carer was coping. Altogether, 47% of the nurses remained fairly distant. The most useful coping strategies involved creating alternative perspectives in the caring relationship.
CONCLUSIONS: The results strengthen the knowledge base of informal caregiving by showing how caregivers cope and what kind of support they need in their demanding caring role. RELEVANCE TO CLINICAL PRACTICE: Respite care nurses should invest greater effort in supporting informal carers. The service should be developed as an integral part of home care for older people. Nurses and informal carers should see each other as partners who share a common goal, i.e. the well-being of the entire family.

Entities:  

Mesh:

Year:  2009        PMID: 19191998     DOI: 10.1111/j.1365-2702.2008.02550.x

Source DB:  PubMed          Journal:  J Clin Nurs        ISSN: 0962-1067            Impact factor:   3.036


  12 in total

1.  Spouses, adult children, and children-in-law as caregivers of older adults: a meta-analytic comparison.

Authors:  Martin Pinquart; Silvia Sörensen
Journal:  Psychol Aging       Date:  2011-03

2.  [Users and utilization of support groups among caregivers of dementia patients : Results of a naturalistic observational study].

Authors:  O Riedel; H-U Wittchen
Journal:  Z Gerontol Geriatr       Date:  2015-12-14       Impact factor: 1.281

3.  The Impact of Multiple Roles on Psychological Distress among Japanese Workers.

Authors:  Ayumi Honda; Yasuyo Abe; Yutaka Date; Sumihisa Honda
Journal:  Saf Health Work       Date:  2015-01-12

4.  Comparative analysis of the expected demands for nursing care services among older people from urban, rural, and institutional environments.

Authors:  Ewa Borowiak; Joanna Kostka; Tomasz Kostka
Journal:  Clin Interv Aging       Date:  2015-02-02       Impact factor: 4.458

5.  Providing care to relatives with mental illness: reactions and distress among primary informal caregivers.

Authors:  Sherilyn Chang; Yunjue Zhang; Anitha Jeyagurunathan; Ying Wen Lau; Vathsala Sagayadevan; Siow Ann Chong; Mythily Subramaniam
Journal:  BMC Psychiatry       Date:  2016-03-25       Impact factor: 3.630

6.  Family carers' experience of caring for an older parent with severe and persistent mental illness.

Authors:  Terence V McCann; John Bamberg; Flora McCann
Journal:  Int J Ment Health Nurs       Date:  2015-05-11       Impact factor: 3.503

7.  "Never at ease" - family carers within integrated palliative care: a multinational, mixed method study.

Authors:  Gülay Ateş; Anne Frederieke Ebenau; Csilla Busa; Ágnes Csikos; Jeroen Hasselaar; Birgit Jaspers; Johan Menten; Sheila Payne; Karen Van Beek; Sandra Varey; Marieke Groot; Lukas Radbruch
Journal:  BMC Palliat Care       Date:  2018-03-01       Impact factor: 3.234

8.  Work-related Stress, Caregiver Role, and Depressive Symptoms among Japanese Workers.

Authors:  Ayumi Honda; Yutaka Date; Yasuyo Abe; Kiyoshi Aoyagi; Sumihisa Honda
Journal:  Saf Health Work       Date:  2013-12-12

9.  Communication, support and psychosocial work environment affecting psychological distress among working women aged 20 to 39 years in Japan.

Authors:  Ayumi Honda; Yutaka Date; Yasuyo Abe; Kiyoshi Aoyagi; Sumihisa Honda
Journal:  Ind Health       Date:  2015-08-28       Impact factor: 2.179

10.  Experiences of family caregivers of persons living with mental illness: A meta-synthesis.

Authors:  Esther I Ntsayagae; Marie Poggenpoel; Chris Myburgh
Journal:  Curationis       Date:  2019-09-19
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