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A qualitative investigation into third-party functioning and third-party disability in aphasia: Positive and negative experiences of family members of people with aphasia

机译:对失语症的第三方功能和第三方残疾的定性调查:失语症患者家庭成员的正面和负面经历

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Background: In the International Classification of Functioning, Disability and Health (ICF), the World Health Organization introduces the term "third-party disability" and identifies the need for further investigation into family members' Functioning and Disability in relation to a significant other's health condition. Aims: This qualitative investigation represents the first phase of a mixed methods study to develop a tool for measuring third-party functioning and third-party disability in aphasia. The aims of this phase of the study were to explore: (1) the positive aphasia-related changes associated with third-party functioning, and; (2) the negative aphasia-related changes associated with third-party disability, as experienced by family members of adults with aphasia post-stroke. Methods & Procedures: This study used an inductive design with a qualitative descriptive research strategy to explore the lived experience of having a relative with aphasia. Twenty family members (e.g., spouses, parents, children, siblings, etc.) of individuals with aphasia participated in individual in-depth semi-structured interviews. The interviews were analysed using qualitative content analysis. Outcomes & Results: Analysis revealed five categories of positive aphasia-related changes associated with third-party functioning: (1) emotions; (2) communication; (3) relationships; (4) recreational activities and social life; and (5) paid/volunteer work or education. In addition, seven categories of negative aphasia-related changes associated with third-party disability were revealed: (1) physical, mental, and emotional health; (2) communication; (3) relationships; (4) recreational activities and social life; (5) paid/volunteer work or education; (6) domestic and caregiving responsibilities; and (7) finances. Conclusions: Interpreted within the framework of the ICF, this study showed how the pervasive effects of aphasia are associated with changes in Functioning and Disability in family members, providing a holistic description of family members' experience using the standardised language of the ICF. Clinically, these results emphasise the importance of recognising the positive and negative outcomes for close family members in the development of a rehabilitation plan for the family to address their experience of third-party disability.
机译:背景:在《国际功能,残疾与健康分类》(ICF)中,世界卫生组织引入了“第三方残疾”一词,并指出有必要进一步调查家庭成员与其他重要健康状况相关的功能和残疾健康)状况。目的:这项定性研究代表了混合方法研究的第一阶段,该研究旨在开发一种用于测量失语症的第三方功能和第三方残疾的工具。该研究阶段的目的是探索:(1)与第三方功能相关的与失语症有关的积极变化;以及(2)中风后失语症成人家庭成员所经历的与第三方残疾相关的与失语相关的负面变化。方法和步骤:本研究采用归纳性设计和定性描述性研究策略,探讨了患有失语症亲戚的生活经历。失语症患者的二十名家庭成员(例如配偶,父母,子女,兄弟姐妹等)参加了深入的半结构化访谈。使用定性内容分析法对访谈进行了分析。结果与结果:分析显示与第三方功能相关的与失语症有关的五种积极变化:(1)情绪; (2)沟通; (3)关系; (四)娱乐活动和社会生活; (5)有偿/志愿工作或教育。此外,揭示了与第三方残疾相关的与失语相关的负面消极变化的七种类型:(1)身体,心理和情感健康; (2)沟通; (3)关系; (四)娱乐活动和社会生活; (五)有偿/志愿工作或教育; (6)家政和看护责任; (7)财务。结论:在ICF框架内解释,这项研究表明失语症的普遍影响如何与家庭成员的功能和残疾变化相关联,使用ICF的标准语言全面描述了家庭成员的经历。临床上,这些结果强调了在制定家庭康复计划以解决他们的第三方残疾经历时,必须认识到亲密家庭成员的正面和负面结果的重要性。

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