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Gender, citizenship and dementia care: a scoping review of studies to inform policy and future research

机译:性别,公民身份和痴呆症护理:对研究进行范围审查,为政策和未来研究提供信息

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摘要

Gender is a neglected dimension in public discourse related to people with dementia. Those living with this condition are typically portrayed in policies and strategies in gender neutral terms as ‘people with dementia’ and ‘family carers’ as if gender does not matter, when clearly it does. The purpose of this scoping review was to take stock of knowledge about gender differences in relation to dementia care to inform policy and future research. The work is grounded in a feminist perspective to citizenship, as this provide a lens with which to expose and examine gendered assumptions within dementia studies. A search of four databases, including CINAHL, Web of Science, Medline and Cochrane was conducted using systematic techniques between May and July 2014. A repeat search was conducted in February 2015. We found a significant amount of valuable research concerned with gender differences in relation to dementia care published from 1990 to 2014; the majority of which lacks a feminist citizenship perspective. Moreover, a disproportionate number of studies focused solely on caregivers rather than citizens with dementia. As such, questions about gender equality are not being raised and the voices of men and women with dementia are silent. Thus we argue for increased gender-sensitivity in policy making and recommend that social scientists inject a feminist citizenship perspective into their work.
机译:性别是与痴呆症患者有关的公共话语中被忽略的一个方面。患有这种疾病的人在政策和策略中通常会以性别中立的态度刻画为“痴呆症患者”和“家庭照料者”,似乎性别无关紧要,但显然性别无关紧要。范围界定审查的目的是评估与痴呆症护理有关的性别差异知识,以为政策和未来研究提供信息。这项工作以女性主义的公民身份为基础,因为这为在痴呆研究中揭示和检验性别假设提供了一个视角。在2014年5月至2014年7月之间使用系统技术对四个数据库进行了搜索,包括CINAHL,Web of Science,Medline和Cochrane。2015年2月进行了重复搜索。我们发现了大量有关性别差异的有价值的研究1990年至2014年发表的痴呆症护理;其中大多数缺乏女权主义公民观。此外,不成比例的研究仅集中于看护者,而不是痴呆症患者。因此,没有提出有关性别平等的问题,患有痴呆症的男人和女人的声音都保持沉默。因此,我们主张在决策中提高性别敏感性,并建议社会科学家在其工作中注入女性主义的公民观。

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