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针对痴呆症患者的玩偶疗法的伦理考量。

Ethical considerations of doll therapy for people with dementia.

作者信息

Mitchell Gary, Templeton Michelle

机构信息

Queen's University Belfast, UK

Queen's University Belfast, UK.

出版信息

Nurs Ethics. 2014 Sep;21(6):720-30. doi: 10.1177/0969733013518447. Epub 2014 Feb 3.

Abstract

The use of doll therapy for people with dementia has been emerging in recent years. Providing a doll to someone with dementia has been associated with a number of benefits which include a reduction in episodes of distress, an increase in general well-being, improved dietary intake and higher levels of engagement with others. It could be argued that doll therapy fulfils the concepts of beneficence (facilitates the promotion of well-being) and respect for autonomy (the person with dementia can exercise their right to engage with dolls if they wish). However, some may believe that doll therapy is inappropriate when applied to the concepts of dignity (people with dementia are encouraged to interact with dolls) and non-maleficence (potential distress this therapy could cause for family members). The absence of rigorous empirical evidence and legislative guidelines render this a therapy that must be approached cautiously owing to the varied subjective interpretations of Kitwood's 'malignant social psychology' and bioethics. This article suggests that by applying a 'rights-based approach', healthcare professionals might be better empowered to resolve any ethical tensions they may have when using doll therapy for people with dementia. In this perspective, the internationally agreed upon principles of the United Nations Convention on the Rights of Persons with Disabilities provide a legal framework that considers the person with dementia as a 'rights holder' and places them at the centre of any ethical dilemma. In addition, those with responsibility towards caring for people with dementia have their capacity built to respect, protect and fulfil dementia patient's rights and needs.

摘要

近年来,针对痴呆症患者的玩偶疗法开始兴起。为痴呆症患者提供一个玩偶与诸多益处相关联,这些益处包括减少痛苦发作、提高总体幸福感、改善饮食摄入以及增强与他人的互动程度。可以说,玩偶疗法符合 beneficence(促进幸福感)和尊重自主性(痴呆症患者若愿意可行使与玩偶互动的权利)的概念。然而,有些人可能认为,当涉及尊严概念(鼓励痴呆症患者与玩偶互动)和不伤害原则(这种疗法可能给家庭成员带来潜在痛苦)时,玩偶疗法并不合适。由于缺乏严格的实证证据和立法指南,鉴于对基特伍德“恶性社会心理”和生物伦理学存在各种主观解读,这种疗法必须谨慎对待。本文认为,通过采用“基于权利的方法”,医疗保健专业人员在为痴呆症患者使用玩偶疗法时,可能更有能力解决他们可能面临的任何伦理困境。从这个角度来看,联合国《残疾人权利公约》国际商定的原则提供了一个法律框架,将痴呆症患者视为“权利持有者”,并将他们置于任何伦理困境的核心。此外,那些负责照顾痴呆症患者的人有能力尊重、保护和满足痴呆症患者的权利和需求。

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