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肌萎缩侧索硬化症患者整个照护过程中非正式照护者的需求:一项定性分析

Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis.

作者信息

Galvin Miriam, Carney Sile, Corr Bernie, Mays Iain, Pender Niall, Hardiman Orla

机构信息

Academic Unit of Neurology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.

Department of Psychology, Beaumont Hospital, Dublin, Ireland.

出版信息

BMJ Open. 2018 Jan 27;8(1):e018721. doi: 10.1136/bmjopen-2017-018721.

Abstract

OBJECTIVES

Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND), is a debilitating terminal condition. Informal caregivers are key figures in ALS care provision. The physical, psychological and emotional impact of providing care in the home requires appropriate assistance and support. The objective of this analysis is to explore the needs of informal ALS caregivers across the caregiving course.

DESIGN

In an open-ended question as part of a semistructured interview, caregivers were asked what would help them in their role. Interviews took place on three occasions at 4-month to 6-month intervals. Demographic, burden and quality of life data were collected, in addition to the open-ended responses. We carried out descriptive statistical analysis and thematic analysis of qualitative data.

SETTING AND PARTICIPANTS

Home interviews at baseline (n=81) and on two further occasions (n=56, n=41) with informal caregivers of people with ALS attending the National ALS/MND Clinic at Beaumont Hospital, Dublin, Ireland.

RESULTS

The majority of caregivers were family members. Hours of care provided and caregiver burden increased across the interview series. Thematic analysis identified what would help them in their role, and needs related to external support and services, psychological-emotional factors, patient-related behaviours, a cure and 'nothing'. Themes were interconnected and their prevalence varied across the interview time points.

CONCLUSION

This study has shown the consistency and adaptation in what caregivers identified as helpful in their role, across 12-18 months of a caregiving journey. Support needs are clearly defined, and change with time and the course of caregiving. Caregivers need support from family, friends and healthcare professionals in managing their tasks and the emotional demands of caregiving. Identifying the specific needs of informal caregivers should enable health professionals to provide tailored supportive interventions.

摘要

目的

肌萎缩侧索硬化症(ALS),也称为运动神经元病(MND),是一种使人衰弱的终末期疾病。非正式照护者是ALS护理工作中的关键人物。在家中提供照护所带来的身体、心理和情感影响需要适当的协助和支持。本分析的目的是探讨非正式ALS照护者在整个照护过程中的需求。

设计

在半结构化访谈的一个开放式问题环节中,询问照护者哪些因素对他们履行职责有帮助。访谈分三次进行,间隔时间为4至6个月。除了开放式回答外,还收集了人口统计学、负担和生活质量数据。我们对定性数据进行了描述性统计分析和主题分析。

地点和参与者

对爱尔兰都柏林博蒙特医院国家ALS/MND诊所的ALS患者的非正式照护者进行家访,基线时81人,之后两次分别为56人和41人。

结果

大多数照护者是家庭成员。在整个访谈系列中,提供照护的时长和照护者负担都有所增加。主题分析确定了哪些因素对他们履行职责有帮助,以及与外部支持和服务、心理情感因素、患者相关行为、治愈方法和“无帮助因素”相关的需求。各主题相互关联,其普遍性在不同访谈时间点有所不同。

结论

本研究表明,在12至18个月的照护过程中,照护者所认定的对其履行职责有帮助的因素具有一致性和适应性变化。支持需求明确,且会随时间和照护过程而变化。照护者在管理照护任务和应对情感需求方面需要家人、朋友和医疗保健专业人员的支持。确定非正式照护者的具体需求应能使卫生专业人员提供量身定制的支持性干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a4/5829772/5e8473031fdb/bmjopen-2017-018721f01.jpg

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