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在家庭痴呆症护理中关于非自愿治疗的护理人员决策。

Caregiver decision-making concerning involuntary treatment in dementia care at home.

机构信息

Maastricht University, The Netherlands; White Yellow Cross Limburg, Belgium; Living Lab in Ageing and Long-Term Care, the Netherlands.

Maastricht University, The Netherlands; Living Lab in Ageing and Long-Term Care, The Netherlands.

出版信息

Nurs Ethics. 2022 Mar;29(2):330-343. doi: 10.1177/09697330211041742. Epub 2021 Dec 6.

Abstract

BACKGROUND

Dementia care at home often involves decisions in which the caregiver must weigh safety concerns with respect for autonomy. These dilemmas can lead to situations where caregivers provide care against the will of persons living with dementia, referred to as involuntary treatment. To prevent this, insight is needed into how family caregivers of persons living with dementia deal with care situations that can lead to involuntary treatment.

OBJECTIVE

To identify and describe family caregivers' experiences regarding care decisions for situations that can lead to involuntary treatment use in persons living with dementia at home.

RESEARCH DESIGN

A qualitative descriptive interview design. Data were analysed using the Qualitative Analysis Guide of Leuven.

PARTICIPANTS AND RESEARCH CONTEXT

A total of 10 family caregivers providing care for 13 persons living with dementia participated in in-depth semi-structured interviews. Participants were recruited by registered nurses via purposive sampling.

ETHICAL CONSIDERATION

The study protocol was approved by the Ethics Committee of the University Hospitals Leuven and the Medical Ethical Test Committee Zuyderland.

FINDINGS

Family caregivers experience the decision-making process concerning care dilemmas that can lead to involuntary treatment as complicated, stressful and exhausting. Although they consider safety and autonomy as important values, they struggle with finding the right balance between them. Due to the progressive and unpredictable nature of dementia, they are constantly seeking solutions while they adapt to new situations. Family caregivers feel responsible and experience social pressure for the safety of persons living with dementia. They may be blamed if something adverse happens to the persons living with dementia, which increases an already stressful situation. Their experience is influenced by characteristics of the care triad (persons living with dementia, professional and family caregivers) such as practical and emotional support, knowledge, and previous experiences.

DISCUSSION AND CONCLUSION

To prevent involuntary treatment, professionals need to proactively inform family caregivers, and they need to support each other in dealing with complex care situations.

摘要

背景

家庭中的痴呆症护理常常涉及到照顾者必须权衡安全问题与尊重自主权之间的决策。这些困境可能导致照顾者违背痴呆症患者的意愿提供护理,这种情况被称为非自愿治疗。为了防止这种情况发生,需要深入了解家庭照顾者在处理可能导致非自愿治疗的护理情况时的想法。

目的

确定并描述家庭照顾者在家庭中照顾患有痴呆症的人时,对于可能导致非自愿治疗的情况的护理决策的体验。

研究设计

定性描述性访谈设计。使用莱顿定性分析指南对数据进行分析。

参与者和研究背景

共有 10 名家庭照顾者为 13 名患有痴呆症的人提供了深入的半结构化访谈。参与者是由注册护士通过目的抽样招募的。

伦理考虑

该研究方案得到了鲁汶大学医院伦理委员会和祖伊德兰德医学伦理测试委员会的批准。

结果

家庭照顾者在考虑可能导致非自愿治疗的护理困境的决策过程中,会感到复杂、有压力和疲惫。尽管他们认为安全和自主权是重要的价值观,但他们在两者之间找到平衡却很困难。由于痴呆症的进行性和不可预测性,他们在适应新情况的同时,不断寻求解决方案。家庭照顾者感到对痴呆症患者的安全负责,并感受到社会压力。如果患者发生任何不良事件,他们可能会受到指责,这会增加本来就有压力的情况。他们的体验受到护理三角(痴呆症患者、专业人员和家庭照顾者)的特征的影响,例如实际和情感支持、知识和以前的经验。

讨论和结论

为了防止非自愿治疗,专业人员需要主动告知家庭照顾者,并在处理复杂的护理情况时相互支持。

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