Who cares for the carer? The suffering, struggles and unmet needs of older women caring for husbands living with cognitive decline

M. Munkejord, O. Stefansdottir, E. Sveinbjarnardóttir
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引用次数: 9

Abstract

Background: The Nordic welfare states have been called the ‘caring states’. However, increasingly, less money is spent on long-term care for older persons than on care for younger persons. Additionally, a strong de-institutionalisation of care coupled with an ageing at home ideology means older persons are expected to remain in their own home, even when they are frail and in need of comprehensive care. As a result, family members, particularly older women, are increasingly expected to take on caring roles, sometimes at the expense of their own health and wellbeing. Aim: The aim of this article is to examine the experiences of older women caring for a spouse living with cognitive decline in a Nordic context. Methods: A qualitative study was designed, in which 11 women in Iceland and Norway were interviewed in their own homes about their past and current experiences as care partners. Findings: Our participants reported that despite receiving home-based care services from the municipality, living with a husband with cognitive decline consisted of constantly being on the alert and assisting with various practicalities. It entailed being woken up night after night, always having to repeat the same bits of conversation, dealing with accusations of infidelity, episodes of aggression, and sometimes hallucinations, violence and fear. The women needed more information, more assistance and time away from care, and emotional and psychological support. Conclusions and implications for practice: The care partners were not treated as persons with their own care needs, and their voices were not heard. A relational person-centred approach in homebased elderly care is needed, placing the couple, not the individual, at the core of service provision. A tool for systematic collaboration between home care services and families should be developed so that both partners’ needs may be met in a more coherent and holistic way.
谁在乎看护人?老年妇女照顾认知能力下降的丈夫的痛苦、挣扎和未满足的需求
背景:北欧福利国家被称为“关爱国家”。然而,用于老年人长期护理的资金越来越少于用于年轻人护理的资金。此外,护理的强烈去制度化,加上居家养老的意识形态,意味着老年人即使身体虚弱,需要全面护理,也应该留在自己的家里。因此,家庭成员,尤其是老年妇女,越来越被期望承担起照顾他人的角色,有时会以牺牲自己的健康和福祉为代价。目的:本文的目的是考察北欧背景下老年女性照顾认知能力下降配偶的经历。方法:设计了一项定性研究,在该研究中,冰岛和挪威的11名女性在自己的家中接受了采访,了解她们作为护理伙伴的过去和现在的经历。调查结果:我们的参与者报告说,尽管接受了市政当局的家庭护理服务,但与认知能力下降的丈夫一起生活包括不断保持警惕并协助处理各种实际问题。这需要一晚又一晚地被吵醒,总是要重复同样的对话,处理不忠的指控、侵犯行为,有时还有幻觉、暴力和恐惧。这些妇女需要更多的信息、更多的帮助和远离护理的时间,以及情感和心理支持。结论和对实践的影响:护理伙伴没有被视为有自己护理需求的人,他们的声音也没有被听到。居家养老需要一种以关系人为中心的方法,将夫妻而非个人置于服务提供的核心。应开发一种在家庭护理服务和家庭之间进行系统合作的工具,以便以更一致和全面的方式满足双方的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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