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患者及家属对家庭腹膜透析的看法:一项人种志研究的结果

Patient and family perspectives on peritoneal dialysis at home: findings from an ethnographic study.

作者信息

Baillie Jessica, Lankshear Annette

机构信息

School of Healthcare Sciences, Cardiff University, Cardiff, UK.

出版信息

J Clin Nurs. 2015 Jan;24(1-2):222-34. doi: 10.1111/jocn.12663. Epub 2014 Sep 25.

Abstract

AIMS AND OBJECTIVES

To discuss findings from an ethnographic study, considering the experiences of patients and families, using peritoneal dialysis at home in the United Kingdom.

BACKGROUND

Peritoneal dialysis is a daily, life-preserving treatment for end-stage renal disease, undertaken in the patient's home. With ever-growing numbers of patients requiring treatment for this condition, the increased use of peritoneal dialysis is being promoted. While it is known that quality of life is reduced when using dialysis, few studies have sought to explore experiences of peritoneal dialysis specifically. No previous studies were identified that adopted an ethnographic approach.

DESIGN

A qualitative design was employed, utilising ethnographic methodology.

METHODS

Ethical and governance approvals were gained in November 2010 and data were generated in 2011. Patients (n = 16) and their relatives (n = 9) were interviewed and observed using peritoneal dialysis in their homes. Thematic analysis was undertaken using Wolcott's (1994) three stage process: Description, Analysis and Interpretation.

RESULTS

This article describes four themes: initiating peritoneal dialysis; the constraints of peritoneal dialysis due to medicalisation of the home environment and the imposition of rigid timetables; the uncertainty of managing crises and inevitable deterioration; and seeking freedom through creativity and hope of a kidney transplant.

CONCLUSIONS

This study highlights the culture of patients and their families living with peritoneal dialysis. Despite the challenges posed by the treatment, participants were grateful they were able to self-manage at home. Furthermore, ethnographic methods offer an appropriate and meaningful way of considering how patients live with home technologies.

RELEVANCE TO CLINICAL PRACTICE

Participants reported confusion about kidney transplantation and also how to identify peritonitis, and ongoing education from nurses and other healthcare professionals is thus vital. Opportunities for sharing experiences of peritoneal dialysis were valued by participants and further peer-support services should thus be considered.

摘要

目的与目标

探讨一项人种志研究的结果,该研究考量了英国在家中进行腹膜透析的患者及其家庭的经历。

背景

腹膜透析是终末期肾病的一种日常维持生命的治疗方法,在患者家中进行。随着需要这种治疗的患者数量不断增加,腹膜透析的使用正在得到推广。虽然已知透析会降低生活质量,但很少有研究专门探讨腹膜透析的经历。此前未发现采用人种志方法的研究。

设计

采用定性设计,运用人种志方法。

方法

2010年11月获得伦理和管理批准,并于2011年收集数据。对16名患者及其9名亲属进行了访谈,并观察他们在家中进行腹膜透析的情况。采用沃尔科特(1994年)的三阶段过程进行主题分析:描述、分析和解释。

结果

本文描述了四个主题:开始腹膜透析;由于家庭环境医学化和严格时间表的强制实施导致的腹膜透析限制;处理危机和不可避免的病情恶化的不确定性;以及通过创造力和肾移植希望寻求自由。

结论

本研究突出了腹膜透析患者及其家庭的文化。尽管治疗带来了挑战,但参与者很感激他们能够在家中自我管理。此外,人种志方法为考量患者如何与家用技术共处提供了一种合适且有意义的方式。

与临床实践的相关性

参与者报告了对肾移植以及如何识别腹膜炎的困惑,因此护士和其他医护人员持续的教育至关重要。参与者重视分享腹膜透析经历的机会,因此应考虑进一步的同伴支持服务。

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