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首页> 外文期刊>Health & social care in the community >'The child's got a complete circle around him'. The care of younger children (5-11 years) with CFS/ME. A qualitative study comparing families', teachers' and clinicians' perspectives'
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'The child's got a complete circle around him'. The care of younger children (5-11 years) with CFS/ME. A qualitative study comparing families', teachers' and clinicians' perspectives'

机译:“孩子周围有一个完整的圈子”。 CFS / ME的小孩(5-11岁)的照顾。 比较家庭,教师和临床医生的观点的定性研究

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摘要

Society needs to improve the care of children with complex needs. Guidelines recommend integrating care across health and educational settings, however, there is little research on whether this is achieved or how this can be done in practice. Our aim was to address this gap by examining how the care of children (aged 5-11 years) with Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis (CFS/ME) is shared across home, education and health settings, in order to generate recommendations for integrating care. We undertook semi-structured interviews with families (22 participants), teachers (11 participants) and healthcare providers (9 participants), analysing the data thematically and comparatively. Our analysis of the data was informed by a socio-ecological perspective as we sought to understand the complexity of the relationships and systems around the child. The first theme focuses on the child ("individual level"); child-centred care is seen as essential whilst acknowledging that the child has limited capacity to manage their own care. The second theme presents the distinct roles of parents, teachers and clinicians ("interpersonal and organisational levels"). The third describes how these three levels interact in the management of the child's care, in the context of the health and education systems and policies ("policy levels"). The fourth explores optimal ways to integrate care across home, school and clinical settings. In conclusion, there is opportunity to support a child with complex health needs by targeting the systems around the child; parents, teachers and clinicians, as well as education and health policy that can enable shared-care. Involving schools in assessment, communicating diagnosis across settings and using a stepped-care approach to integrated care may be beneficial. Further work is needed to explore these recommendations, with attention to the policy factors that may act as barriers and enablers.
机译:社会需要改善对有复杂需求儿童的照顾。指导方针建议将医疗服务整合到医疗和教育环境中,然而,关于这是否实现或如何在实践中实现的研究很少。我们的目标是通过研究如何在家庭、教育和健康环境中共享对患有慢性疲劳综合征/肌痛性脑脊髓炎(CFS/ME)的儿童(5-11岁)的护理,以解决这一差距,从而提出整合护理的建议。我们对家庭(22名参与者)、教师(11名参与者)和医疗保健提供者(9名参与者)进行了半结构式访谈,对数据进行了主题分析和比较。我们对数据的分析是从社会生态的角度进行的,因为我们试图了解儿童周围关系和系统的复杂性。第一个主题关注儿童(“个人层面”);以儿童为中心的护理被视为至关重要的,同时承认儿童管理自己护理的能力有限。第二个主题介绍了父母、教师和临床医生的不同角色(“人际和组织层面”)。第三部分描述了在卫生和教育系统和政策的背景下,这三个层面如何在儿童护理管理中相互作用(“政策层面”)。第四部分探索了整合家庭、学校和临床环境的最佳方式。总之,有机会通过针对儿童周围的系统来支持有复杂健康需求的儿童;家长、教师和临床医生,以及能够实现共享护理的教育和卫生政策。让学校参与评估,在不同的环境中交流诊断,以及在综合护理中使用阶梯式护理方法可能是有益的。需要进一步研究这些建议,并关注可能成为障碍和促成因素的政策因素。

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