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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:对学习的范围审查,以告知政策和未来研究

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Abstract 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:摘要性别是与痴呆症的人有关的公共话语中的忽视维度。生活在这种情况下的人通常在性别中立术语中被描绘为“有痴呆症”和“家庭照顾者”的政策和策略,好像性别无关紧要,当清楚它确实如此。该裁视审查的目的是对痴呆症关心的性别差异进行关于性别差异的知识,以告知政策和未来的研究。这项工作基于女权主义者对公民身份进行了基础,因为这提供了一种镜片,用于在痴呆研究中暴露和检查性别假设。在2014年5月和7月之间的系统技术中搜索了四个数据库,包括Cinahl,Medicine和Cochrane,并在2015年2月进行了重复搜索。我们发现了一项大量的有价值的研究,涉及关系性别差异从1990年到2014年出版的痴呆症护理;其中大多数缺乏女权主义公民身份的角度。此外,不成比例的研究数量仅关注护理人员而不是痴呆症的公民。因此,关于性别平等的问题没有提出,男性和痴呆症的声音是沉默的。因此,我们争论政策制定中的性别敏感性提高,建议社会科学家注入女权主义公民身份的观点。

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