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Balancing needs as a family caregiver in Huntington's disease: a qualitative interview study

机译:亨廷顿氏病作为家庭照顾者的需求平衡:一项定性访谈研究

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Family members in families with severe chronic disease play important roles in care-giving. In families affected by Huntington's disease (HD), caregivers encounter practical and emotional challenges and distress. Enduring caregiver burdens may lead to problems and caregivers are in need of social support and health services to deal with challenges. We wanted to explore coping strategies and behaviour patterns used by family caregivers to care for themselves, while caring for a family member with HD. Participants were recruited from hospitals and community-based healthcare. The sample represents experiences from care-giving in all stages of the disease. We conducted semi-structured interviews with 15 family caregivers in Norway. The transcribed material was analysed by use of systematic text condensation, a method for cross-case thematic analysis of qualitative data. We found that family members used various coping strategies, adjusted to the stage and progression of HD. They tried to regulate information about the disease, balancing considerations for protection and disclosure, within and outside the family. The participants made efforts to maintain a balance between their own needs in everyday life and the need for care for affected family member(s). As the disease progressed, the balance was skewed, and the family caregivers' participation in social activities gradually decreased, resulting in experiences of isolation and frustration. In later stages of the disease, the need for care gradually overshadowed the caregivers' own activities, and they put their own life on hold. Health professionals and social workers should acknowledge that family caregivers balance their needs and considerations in coping with HD. They should, therefore, tailor healthcare services and social support to family caregivers' needs during the different stages of HD to improve caregivers' abilities to maintain some of their own activities, in balance with care-giving.
机译:患有严重慢性疾病的家庭中的家庭成员在照料中起着重要作用。在受亨廷顿舞蹈病(HD)影响的家庭中,护理人员会遇到实际和情感上的挑战和困扰。持久的照顾者负担可能会导致问题,并且照顾者需要社会支持和卫生服务以应对挑战。我们想探究家庭照顾者用来照顾自己的同时应对HD家人的应对策略和行为模式。参与者是从医院和基于社区的医疗保健中招募的。该样本代表疾病各个阶段的护理经历。我们对挪威的15位家庭护理人员进行了半结构化访谈。通过使用系统的文本压缩分析转录的材料,这是一种跨案例的定性数据专题分析方法。我们发现家庭成员使用了多种应对策略,适应了HD的阶段和进展。他们试图规范有关该疾病的信息,在家庭内外兼顾保护和披露方面的考虑。参与者努力在自己的日常生活需求和对受影响家庭成员的照料需求之间保持平衡。随着疾病的发展,平衡出现了偏差,家庭照顾者对社会活动的参与逐渐减少,导致了孤立和沮丧的经历。在疾病的后期阶段,对护理的需求逐渐掩盖了护理人员的活动,他们搁置了自己的生命。卫生专业人员和社会工作者应认识到,家庭护理人员在应对HD时要平衡他们的需求和考虑因素。因此,他们应在房屋署的不同阶段针对家庭护理人员的需求量身定制医疗保健服务和社会支持,以提高护理人员维持自己的某些活动的能力,同时兼顾护理工作。

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