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肠皮肤瘘的生活体验。

Experience of living with an enterocutaneous fistula.

作者信息

Härle Karolina, Lindgren Margareta, Hallböök Olof

机构信息

Department of Surgery, Linköping University, Linköping, Sweden.

Department of Medical and Health Science, Division of Nursing Science, Linköping University, Linköping, Sweden.

出版信息

J Clin Nurs. 2015 Aug;24(15-16):2175-83. doi: 10.1111/jocn.12857. Epub 2015 May 11.

Abstract

AIMS AND OBJECTIVES

The purpose of this study was to describe patients' experiences of living with an enterocutaneous fistula.

BACKGROUND

An enterocutaneous fistula is a complex and serious illness that usually occurs as a complication from surgery or spontaneously as a result of an underlying disease. The illness is demanding both physically and mentally and causes substantial medical and nursing problems for the afflicted individual.

DESIGN

A descriptive design with a qualitative approach.

METHODS

In-depth interviews were performed with nine participants who had experiences of living with an enterocutaneous fistula. The analysis was conducted using descriptive phenomenology according to Giorgi.

RESULTS

The essence of this study was that living with an enterocutaneous fistula is about handling an illness that causes several limitations in daily life and the following five themes emerged from the data: restrictions in daily life, approaches to illness, emotions, dependence and need of support. A constant fear of leakage from the fistula appliance, being dependent on intravenous fluids and being dependent on health care professionals caused isolation and social restriction.

CONCLUSIONS

The participants had many strategies for handling their illness. By being well trained, engaged and having a positive and understanding approach, health care professionals can encourage hope, motivation and self-care. This can lead to decreased dependence and help the patient to better handle their illness.

RELEVANCE TO CLINICAL PRACTICE

The competence of health care professionals is essential in the care of patients with an enterocutaneous fistula.

摘要

目的与目标

本研究的目的是描述肠造口瘘患者的生活体验。

背景

肠造口瘘是一种复杂且严重的疾病,通常作为手术并发症出现,或因潜在疾病自发产生。这种疾病对患者的身心都有很高要求,给患者带来了大量医疗和护理问题。

设计

采用定性方法的描述性设计。

方法

对九名有肠造口瘘生活经历的参与者进行了深入访谈。根据 Giorgi 的方法,使用描述性现象学进行分析。

结果

本研究的核心是,患有肠造口瘘意味着应对一种在日常生活中造成多种限制的疾病,数据中出现了以下五个主题:日常生活中的限制、应对疾病的方式、情绪、依赖和支持需求。对瘘管装置渗漏的持续恐惧、对静脉输液的依赖以及对医护人员的依赖导致了孤立和社交限制。

结论

参与者有许多应对疾病的策略。通过良好的培训、参与以及积极理解的态度,医护人员可以激发希望、动力和自我护理能力。这可以减少依赖,帮助患者更好地应对疾病。

与临床实践的相关性

医护人员的能力在肠造口瘘患者的护理中至关重要。

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