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下肢截肢者的生活体验。

The lived experience of persons with lower extremity amputation.

机构信息

Department of Nursing, Chang Gung Institute of Technology and PhD Student, Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Tao-Yuan, Taiwan.

出版信息

J Clin Nurs. 2010 Aug;19(15-16):2152-61. doi: 10.1111/j.1365-2702.2010.03256.x.

Abstract

AIM

The aim of this study was to describe and understand the lived experience of people with lower extremity amputation.

BACKGROUND

The loss of a body part can cause physical, psychological and social disturbances. The majority of previous studies in this area focus on the impact of amputation or the effectiveness of rehabilitation programmes. This is the first study in Taiwan exploring the holistic experiences of persons with amputation.

DESIGN

A phenomenological research design was used.

METHODS

Semi-structured interviews were performed with 22 people with lower extremity amputation. Interviews were tape-recorded and transcribed verbatim. Data were analysed using Colaizzi's phenomenological analysis method.

RESULTS

The lived experience of persons with lower extremity amputation could be categorised into the following four themes: 'lost in the dark woods', 'emotional collapse', 'difficulty in passing through the shadow' and 'igniting a gleam of hope'.

CONCLUSIONS

Participants described suffering in physical, psychological and sociocultural realms and the ways they strived to cope with these challenges. The findings of this study provide an enhanced understanding of the experiences of people with lower extremity amputation and underscore the importance of truly listening and responding to their concerns. The need to appreciate cultural context and to develop the peer-based support programme was highlighted.

RELEVANCE TO CLINICAL PRACTICE

Health professionals need to acknowledge the real needs of people with lower extremity amputation and provide them a clear explanation regarding the short-term and long-term health issues associated with amputation during the pre- and post-amputation phase. Health professionals also need to expand the scope of services beyond a physical and prosthetic focus. Supportive psychological and social interventions such as formal support groups and peer support programmes may provide a powerful and inexpensive addition to routine care. Currently, such programmes are unavailable in Taiwan.

摘要

目的

本研究旨在描述和理解下肢截肢患者的生活体验。

背景

失去身体的一部分会导致身体、心理和社会的紊乱。以往在这一领域的大多数研究都集中在截肢的影响或康复计划的有效性上。这是台湾首例探索截肢患者整体体验的研究。

设计

采用现象学研究设计。

方法

对 22 名下肢截肢患者进行半结构式访谈。访谈进行录音并逐字转录。使用 Colaizzi 的现象学分析方法对数据进行分析。

结果

下肢截肢患者的生活体验可分为以下四个主题:“迷失在黑暗的树林中”、“情绪崩溃”、“难以穿过阴影”和“点燃一线希望”。

结论

参与者描述了身体、心理和社会文化领域的痛苦,以及他们努力应对这些挑战的方式。本研究的结果提供了对下肢截肢患者体验的更深入理解,并强调了真正倾听和回应他们关切的重要性。需要重视文化背景,并开发基于同伴的支持计划。

临床相关性

健康专业人员需要了解下肢截肢患者的真实需求,并在截肢前和截肢后阶段向他们清楚地解释与截肢相关的短期和长期健康问题。健康专业人员还需要将服务范围从身体和假肢方面扩展到其他方面。支持性的心理和社会干预措施,如正式的支持小组和同伴支持计划,可能是常规护理的有力和廉价的补充。目前,这些计划在台湾还没有。

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