在决策中保持一定的自主权:配偶护理人员如何支持这一点?

IF 2.4 3区 社会学 Q2 GERONTOLOGY
D. Fetherstonhaugh, Jo-Anne Rayner, Laura Tarzia
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引用次数: 10

摘要

在澳大利亚,大多数痴呆症患者生活在由家庭(通常是配偶)提供非正式护理的社区中。痴呆症的诊断对一个人的人格构成威胁,通常伴随着对未来依赖性的感知,这将涉及无法履行传统角色和完成包括决策在内的日常任务。然而,能够做出决定是作为一个“人”的一部分,正是通过关系来定义和构建人格。在对七对夫妇(一对护理人员和痴呆症患者)和两对配偶护理人员的面对面采访中,这项研究探讨了配偶护理人员为什么以及如何支持痴呆症患者继续参与决策。研究结果强调了爱和尊重关系在制定支持痴呆症患者持续决策的策略中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hanging on to Some Autonomy in Decisionmaking: How do Spouse Carers Support this?
In Australia, the majority of people with dementia live in the community with informal care provided by family, commonly a spouse. A diagnosis of dementia is a threat to one’s personhood and is often accompanied by perceptions of future dependency, which will involve the inability to carry out conventional roles and complete everyday tasks including making decisions. Being able to make decisions, however, is part of being a ‘person’ and it is through relationships that personhood is defined and constructed. In face-to-face interviews with seven couples (a carer and person with dementia dyad) and two spouse carers, this study explored why, and how, spouse carers support continued involvement in decision-making for people with dementia. The findings highlight the importance of loving and respectful relationships in the development of strategies to support continued decision-making for people with dementia.
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来源期刊
CiteScore
5.60
自引率
12.50%
发文量
114
期刊介绍: Dementia acts as a major forum for social research of direct relevance to improving the quality of life and quality of care for people with dementia and their families. For the first time an international research journal is available for academics and practitioners that has as its primary paradigm the lived experience of dementia.
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