从活得好到死得好与痴呆症:扩大对损失的理解对临终关怀的意义。

IF 2.2 Q2 HEALTH CARE SCIENCES & SERVICES
Palliative Care and Social Practice Pub Date : 2025-09-01 eCollection Date: 2025-01-01 DOI:10.1177/26323524251347653
Joseph M Sawyer, Paul Higgs
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引用次数: 0

摘要

随着痴呆症发病率的上升,对护理的需求是显而易见的。了解这是什么样子的,以及人们如何根据普遍相关的成功版本来定位护理的叙述和实践,这是不太明确的,但如果我们要朝着一种理想的护理发展,即通过姑息治疗实现“良好”或“有尊严”的死亡,这似乎至关重要。以这为中心焦点,本文探讨了指导当前痴呆症护理方法的定向原则。我们描绘了学术理论的演变,从以缺陷为基础的护理模式(将缺陷识别为一种手段)到建立资源以对抗它们,再到以能力为导向的方法(侧重于适应痴呆症带来的新体验)。我们描述了这些框架是如何主要针对早期痴呆症的,它们是如何支持人们以积极和富有社会生产力的方式生活的,以及当它们被转移到生命末期时,衰退和依赖是主要的经历,是如何产生紧张的。我们的分析表明,目前痴呆症护理的理论方法需要被认为是与生活经历的衰退、依赖和损失相关的辩证方法。我们认为,娱乐这样的辩证法可以提供见解,如何在老年痴呆症临终关怀的方法可能会适应损失,紧张和悖论的存在,这样的方式不排除成功,同时提供更广泛的社会价值。我们得出的结论是,在没有对价值所在有一些愿景的情况下,进一步干预需求规模只会增加进一步的紧张。传统上,人们认为痴呆症是一种生物或社会挑战,应该有一种匹配的解决方案,而从内到外看待它,从痴呆症及其相关脆弱性可能给人类带来的教训中吸取教训,可能更有用。我们认为,这可能为该领域的知识进步提供一条途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

From living well to dying well with dementia: The significance of an expanded understanding of loss for end-of-life care.

From living well to dying well with dementia: The significance of an expanded understanding of loss for end-of-life care.

As rates of dementia increase, the need for care is clear. Understanding what this looks like and how people might orientate the narratives and practices of care against a universally relatable version of success is less clear cut yet seems crucial if we are to progress towards an ideal of care that allows for a 'good' or 'dignified' death with palliative care. With this as a central focus, the paper examines the orientating principles that govern the current approach to dementia care. We map the evolution in academic theory from deficit-based models of care that identify impairments as a means to building resources to counter them, towards capacity-oriented approaches that focus on accommodating the new experiences that dementia brings. We describe how these frameworks are predominantly orientated towards early dementia, where they work to support people to live in an active and socially productive way, and how tensions arise when they are transposed to the end-of-life where decline and dependency are the dominant experience. Our analysis suggests that the current theoretical approaches to dementia care need to be thought of as dialectical in relation to the lived experiences of decline, dependency and loss. We argue that entertaining such a dialectic can offer insights into how the approach to end-of-life care in dementia might accommodate the presence of loss, tension and paradox in such a way that does not preclude success whilst offering wider social value. We conclude that further interventions that respond to the scale of need will only add further tension without first having some vision of where value might lie. Where conventionally dementia has been viewed through the reductionist lens of being either a biological or social challenge to which there should be a matching solution, it is perhaps more useful to look at it from the inside out, to learn the lessons that dementia and its associated vulnerabilities may hold for humanity. This, we suggest, may offer a route to knowledge progression in the field.

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来源期刊
Palliative Care and Social Practice
Palliative Care and Social Practice Nursing-Advanced and Specialized Nursing
CiteScore
2.90
自引率
0.00%
发文量
37
审稿时长
9 weeks
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