Article
How do officially organized services meet the needs of elderly caregivers and their spouses with Alzheimer's disease?
Memory Research and Treatment Centers Finland, Medical Center Hemo Oy, Lahti, Social Insurance Institution of Finland.
American Journal of Alzheimer s Disease and Other Dementias (impact factor:
1.45).
22(5):360-8.
DOI:10.1177/1533317507305178
pp.360-8
Source: PubMed
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Citations (0)
- Cited In (2)
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Article: Carers’ experiences with overnight respite care : a qualitative study
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ABSTRACT: Aim: The aim of this study was to explore experiences with overnight respite care (ORC) of Norwegian carers who provided care to frail elderly awaiting nursing home placement. Background: In many Western countries respite care has become part of health care service provision, and various types of respite care are available. The intent with respite care can be twofold; caring for the care receiver and supporting the carer. Methods: This is a descriptive qualitative study. Interviews were conducted with 15 carers, transcribed and analysed by qualitative content analysis. Findings: The carers described various experiences with ORC. If ORC supported the whole family, it was welcomed by carers and experienced as supportive. If ORC did not support the whole family, many carers rejected ORC, and it was experienced as non-supportive. Two categories were constructed: ‘experiencing ORC as supportive for the family as a whole’ and ‘not experiencing ORC as supportive for the family as a whole’. Conclusion: To support more carers, nurses have to listen to carers’ experiences about ORC. Nurses need to take responsibility for the family as a whole and provide more flexible ORC services based on both carers’ and elderly’s needs. -
Article: Alzheimer's patients' spouses critiques of the support services.
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ABSTRACT: Introduction. Caregiving families of patients with dementia are often reluctant to use support services. The aim of this study was to describe their subjective critiques of these services. Material and Methods. A cross-sectional questionnaire was sent to a random sample (N = 1943) of Alzheimer's patients' spouses in Finland with an open-ended question: "What kind of problems have you faced with the services?" Their responses were analyzed with thematic content analysis. Results. Of the responders identifying themselves as caregivers (N = 1386), 728 (mean age 77.8, 65.1% females) responded. Opinions could be divided into two categories: (1) problems with the service application process (N = 296); (2) critiques of the services offered (N = 270) including either problems with community care support services or institutional care. 74 indicated that they had no need for services, and 15 praised the services they had received. Conclusions. From the caregiver's perspective, the service system is complicated, bureaucratic and works organization centredly.ISRN nursing. 01/2011; 2011:943059.
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Keywords
Alzheimer's disease
behavioral symptoms
caregivers
caregivers' satisfaction
caregiving situation
dementia
Disabilities
financial support
home respite
house-cleaning
Mean age
nursing homes
official services
physiotherapy
random sample
respite care
services
spouses
technical devices