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儿童肾脏科的人种志研究:长期肾病患儿及青少年的经历

An ethnography of a children's renal unit: experiences of children and young people with long-term renal illness.

作者信息

Lindsay Waters Anne

机构信息

Royal College of Surgeons, Ireland, Medical University of Bahrain, Faculty of Nursing and Midwifery, Building 2441, Road, 2835, Block Busaiteen 228, Muharraq, Kingdom of Bahrain.

出版信息

J Clin Nurs. 2008 Dec;17(23):3103-14. doi: 10.1111/j.1365-2702.2008.02645.x.

Abstract

AIM

This study explored the experience of long-term renal illness, including issues concerning compliance with treatment, from the perspectives of children and young people.

BACKGROUND

Children and young people have difficulty complying with renal treatment; research in this area usually focuses on their compliance with a narrow range of behaviours: compliance with dialysis, tablet taking and dietary and fluid restrictions. Renal compliance studies are usually premised on the assumption that children will automatically comply with treatment and/or that blame for non-compliance rests with the child and family.

DESIGN

The study, underpinned by a view of children as competent social agents, used ethnography to explore and describe the everyday experience of long-term renal illness.

METHOD

Ethnographic fieldwork--involving participant observation, informal interviews and the use of children's drawings--took place over 16 months in a hospital renal unit comprising an inpatient ward, a haemodialysis unit and an outpatient clinic. The primary participants were 13 children; 14 carers and 36 staff members also participated. Data were interrogated through descriptive and thematic forms of analysis.

RESULTS

This study reveals participants' perspectives on the physical and social impact of renal treatment. It also provides a conceptualisation of life with long-term renal illness that highlights children's management of 'illness labour', their inhabitation 'renal geographical space', 'a renal body' and a 'renal social world'.

CONCLUSIONS

These findings show how compliance with renal treatment involves particular embodied experiences that are hard for children to manage. Traditional views of compliance/non-compliance render children's embodied experience and their labour in managing dialysis, thirst and their difficulties with tablet taking irrelevant, whilst this study shows these as highly relevant to children.

RELEVANCE TO CLINICAL PRACTICE

The conceptualisation of children's experience arising in this study provides a new way of considering the embodied experience of children with long-term renal illness.

摘要

目的

本研究从儿童和青少年的角度探讨了长期肾病的经历,包括与治疗依从性相关的问题。

背景

儿童和青少年在遵守肾病治疗方面存在困难;该领域的研究通常集中在他们对一系列有限行为的依从性上:透析依从性、服药依从性以及饮食和液体限制。肾病依从性研究通常基于这样的假设,即儿童会自动遵守治疗,和/或不依从的责任在于儿童及其家庭。

设计

该研究以儿童是有能力的社会行为者这一观点为基础,采用民族志方法来探索和描述长期肾病的日常经历。

方法

民族志田野调查——包括参与观察、非正式访谈以及使用儿童绘画——在一个医院肾病科进行,为期16个月,该科室包括一个住院病房、一个血液透析室和一个门诊诊所。主要参与者是13名儿童;14名护理人员和36名工作人员也参与其中。通过描述性和主题性分析形式对数据进行了审视。

结果

本研究揭示了参与者对肾病治疗的身体和社会影响的看法。它还提供了一种对长期肾病生活的概念化理解,突出了儿童对“疾病劳作”的管理、他们对“肾病地理空间”、“肾病身体”和“肾病社会世界”的体验。

结论

这些发现表明,遵守肾病治疗涉及儿童难以应对的特定身体体验。传统的依从/不依从观点认为儿童的身体体验以及他们在管理透析、口渴和服药困难方面的劳作无关紧要,而本研究表明这些对儿童非常重要。

与临床实践的相关性

本研究中出现的儿童经历的概念化为考虑长期肾病儿童的身体体验提供了一种新方式。

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