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土耳其裔塞浦路斯患者接受血液透析的疾病认知:一项定性研究。

Illness perceptions of Turkish Cypriot patients receiving haemodialysis: A qualitative study.

机构信息

School of Life and Medical Sciences, University of Hertfordshire, Hatfield, UK.

Department of Psychology, Bahçeşehir Cyprus University, Nicosia, North Cyprus.

出版信息

J Ren Care. 2021 Jun;47(2):113-122. doi: 10.1111/jorc.12351. Epub 2020 Oct 10.

Abstract

BACKGROUND

Illness perceptions refer to cognitive appraisals that help patients understand and make sense of their condition. Although their importance in health behaviour and outcomes has been evidenced, less is known about cultural influences on mental representations of kidney failure amongst patients receiving haemodialysis in different settings.

OBJECTIVE

To explore the illness perceptions of Turkish patients receiving haemodialysis in North Cyprus (Turkish Cypriots).

DESIGN

A qualitative study involving individual semistructured interviews.

PARTICIPANTS

Fourteen patients receiving haemodialysis, recruited from three state hospitals in North Cyprus.

APPROACH

All interviews were conducted in Turkish, audio-recorded, and transcribed verbatim. They were analysed inductively in the original language using reflexive thematic analysis. Once the analysis was completed, it was translated into English. Quality assurance was integral to the research process to retain semantic equivalence.

FINDINGS

Three themes were developed. "Illness appraisal" highlighted a lack of factual knowledge about kidney failure and how this is related to attempts at sense-making, whilst retaining hope for the future. "Life-changing effects" centred around the negative consequences of haemodialysis across multiple domains (e.g., emotional and physical). "Active coping strategies" focused on mechanisms that patients adopt to manage the burden of haemodialysis, particularly approaches that are culturally rooted.

CONCLUSION

There is a need for better communication to address the lack of individual patient knowledge about kidney failure. Haemodialysis is described as a burdensome treatment though existing coping mechanisms suggest that psycho-spiritual interventions may be advantageous to aid adjustment for Turkish Cypriots receiving haemodialysis.

摘要

背景

疾病认知是指帮助患者理解和理解自身状况的认知评估。尽管已经证实了它们在健康行为和结果中的重要性,但对于在不同环境中接受血液透析的患者的心理表现对肾脏衰竭的文化影响知之甚少。

目的

探讨北塞浦路斯(土族塞人)接受血液透析的土耳其患者的疾病认知。

设计

一项涉及个体半结构式访谈的定性研究。

参与者

从北塞浦路斯的三家公立医院招募了 14 名接受血液透析的患者。

方法

所有访谈均以土耳其语进行,录音并逐字转录。使用反思性主题分析,以原始语言进行归纳分析。分析完成后,将其翻译成英语。质量保证是研究过程的一个组成部分,以保持语义等效。

结果

提出了三个主题。“疾病评估”强调了对肾衰竭缺乏事实性知识,以及这如何与试图理解相关,同时保留对未来的希望。“改变生活的影响”集中在血液透析对多个领域(例如情感和身体)的负面影响。“积极应对策略”侧重于患者采用的管理血液透析负担的机制,特别是具有文化根源的方法。

结论

需要进行更好的沟通,以解决个别患者对肾衰竭缺乏了解的问题。血液透析被描述为一种负担沉重的治疗方法,但现有的应对机制表明,心理-精神干预可能有助于帮助接受血液透析的土族塞人进行调整。

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