[1982年至1991年间老年痴呆症护理人员的比较研究]。

K Nakajima, K Nagata, K Kitagawa, Y Kudo, R Yamada
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引用次数: 0

摘要

本研究的目的是透过两项横断面研究的比较,来厘清照顾者地位的变化。研究对象为“老年痴呆家庭护理协会”组成员658名(1982年)和705名(1991年)。结果总结如下:1)1991年痴呆症患者的平均寿命比1992年更长。2) 1991年,各年龄组中约30%的患者住院,约70%的患者在家接受治疗。这些事实表明,医疗设施在9年期间扩大了接收老年痴呆症患者的能力。希望独立生活的家庭成员支持由家庭中越来越少的人来照顾的观点。从这个意义上说,家庭的照顾能力被削弱了。(4)主要照顾者的非正式社会支持网络范围显著扩大。(5)服务规模越大,被照顾者对服务的利用程度越高。然而,所提供服务的质量和数量仍不足以满足照顾者的需求。6)总的来说,照顾者过去所面临的困难在1991年似乎有所减少。
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[A comparative study of caregivers of the elderly with dementia between 1982 and 1991].

The purpose of this study is to clarify the changes of the caregivers'status with comparison of two cross-sectional studies. The subjects were 658 (primary, in 1982) and 705 (secondary, in 1991) group members of "The Association of Families Caring for Elderly Persons with Dementia". The summary of results are as follows: 1) The mean life span of a person suffering dementia was found to be longer in 1991 than 1992. 2) In 1991, about 30 percent of the patients in all age groups were hospitalized and about 70 percent of the patients were treated at home. These facts indicated that the medical facilities had expanded their capacities during the 9 year period for receiving the elderly with dementia. 3) Family members who wished to live independently supported the idea that care should be given by a decreased number of individuals within the family. In that sense, the family's power of caregiving was decreased. 4) The range of main caregivers' informal social-support-network was remarkably expanded. 5) The more the service were expanded, the more the service were utilized by the caregivers. However, the quality and the quantity of the services provided are still not sufficient to meet the caregivers' need. 6) In balance, the difficulties caregivers used to face, seemed to be decreased in 1991.

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