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Respecting autonomy in the end-of-life care of people with intellectual disabilities: a qualitative multiple-case study

机译:尊重具有智力残疾人终生关怀中的自治:一个定性的多案例研究

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摘要

Background: The aim of this article was to describe how caregivers and relatives shape respect for autonomy in the end-of-life care for people with intellectual disabilities (ID) and to discuss to what extent this corresponds with a relational concept of autonomy, such as described in care ethics. Method: This study consisted of a qualitative design in which the cases of 12 recently deceased people with ID were reconstructed by interviewing the caregivers and relatives who were closest to the person at the end of their life. A cyclic process of data collection and analysis was used. Interviews were transcribed verbatim and data were analysed inductively. Results: Respect for autonomy in the end-of-life care of people with ID was mainly reflected in helping the person with ID familiarise with three transitions: new information on the diagnosis and prognosis, changing care needs and wishes, and important decisions that were at stake. In respecting autonomy, relatives and caregivers encountered several challenges. These concerned ascertaining information needs, communicating about illness and death, inexperience in end-of-life care, eliciting current and hidden last wishes, the dependence of people with ID and conflicting wishes. Several qualities were important for respecting autonomy: attention to information needs, connecting, recognising end-of-life care needs, giving space to show wishes and preferences, and discussing dilemmas. Conclusions: If caregivers and relatives embrace autonomy as a relational construct, attained through an open, active and reflective attitude, and have more access to knowledge about communication and how to identify end-of-life care needs, this could lead to improved respect for the ID persons' autonomy at the end of life. We discuss the view that a relational concept of autonomy is useful for describing respect for autonomy in end-of-life care for people with ID, but that more reflection and openness is needed to sufficiently employ relationships and regard autonomy as a product of joint work. © 2013 John Wiley & Sons Ltd, MENCAP & IASSIDD.
机译:背景:这篇文章的目的是描述如何照顾者和亲属在结束生命的关怀自主权形状尊重智障人士(ID),并讨论在何种程度上与此对应的自治关系的概念,这样的在护理伦理学描述。方法:这项研究包括了质的设计,其中的12最近去世的人ID的情况下,被采访最接近的人谁是在其寿命结束照顾者和亲属重建的。用于数据收集和分析的一个循环过程。访谈转录逐字记录和数据分析电感。结果:尊重以结束生命的照顾人的ID自主权主要体现在帮助ID为他们熟悉的人有三个转变:新的信息,对诊断和预后,不断变化的保健需求和愿望,而且是重要的决定危在旦夕。在尊重自主权,亲属和医护人员遇到了一些挑战。这些关注查明信息的需求,有关生老病死,经验不足最终的生活护理沟通,引起电流和隐藏的遗愿,人与ID的依赖性和相互矛盾的愿望。有几个特质是尊重自主权重要:注意信息的需求,连接,确认最终的生活护理的需求,展现意愿和喜好给予空间,并讨论困境。结论:如果照顾者和亲属拥抱自治关系结构,通过一个开放的,积极的和反思的态度实现,并有知识有关的沟通和如何识别结束生活护理需要更多的访问,这可能导致改善尊重该ID的人在生命的尽头自主权。我们讨论认为,自治关系的概念是在结束生活护理描述尊重自治人ID是有用的,但更多的思考和开放性,需要充分雇佣关系,对于自主性的联合工作产品。 ©2013 John Wiley和Sons有限公司,MENCAP&IASSIDD。

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