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Vivências de cuidadores familiares de pessoas portadoras da doen?a de Alzheimer

机译:阿尔茨海默氏病患者家庭照顾者的经历

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Alzheimer disease may be considered as a familiar disease by interfering in the quotidian of families. The search seeks to know experiences of family with Alzheimer disease. It is qualitative, descriptive, comprising six familiar caregivers who got in tauch with the sick person continuously, residents in four cities in the northwest region of Rio Grande do Sul. The data collection occurred in November 2006, through open interview, with the following guiding question: "How is/was for you to take care of your familiar Alzheimer disease?". The data analysis followed the steps recommended for thematic analysis and the ethical aspects involving studies with people were observed. The analysis of the testimonies appeared the theme: Experiences of family caregivers of people with Alzheimer's Disease: the impact of the disease in everyday family. They expressed difficulties in the management of the patient, ignorance of the disease, sadness and insecurity. We can identify the need to home care by health professionals to the family caregivers of people with Alzheimer, including guidelines and support concerning the illness and care. The results of this research also show that the relatives are not element of intervention of health teams and the actions are fragmented and specific.
机译:阿尔茨海默氏病可以通过干扰家庭的日常生活而被视为一种熟悉的疾病。该搜索旨在了解患有阿尔茨海默氏病的家庭的经历。它是定性的,描述性的,由六名熟悉的照料者组成,这些照料者不断与病人打交道,是南里奥格兰德州西北四个城市的居民。数据收集是在2006年11月通过公开采访进行的,有以下指导性问题:“您如何/如何照顾自己熟悉的阿尔茨海默氏病?”。数据分析遵循建议进行主题分析的步骤,并观察到涉及与人研究的道德方面。对证词的分析出现了一个主题:阿尔茨海默氏病患者的家庭看护人的经历:该疾病对日常家庭的影响。他们表示在患者管理,疾病的无知,悲伤和不安全感方面存在困难。我们可以确定医疗专业人员对老年痴呆症患者的家庭护理人员进行家庭护理的必要性,包括有关疾病和护理的指南和支持。这项研究的结果还表明,亲属不是卫生小组干预的内容,行动是零散而具体的。

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