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Emerging communities of child-healthcare practice in the management of long-term conditions such as chronic kidney disease: qualitative study of parents’ accounts

机译:新兴的儿童保健实践社区在诸如慢性肾脏疾病等长期疾病的管理中:对父母陈述的定性研究

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Background Parents of children and young people with long-term conditions who need to deliver clinical care to their child at home with remote support from hospital-based professionals, often search the internet for care-giving information. However, there is little evidence that the information available online was developed and evaluated with parents or that it acknowledges the communities of practice that exist as parents and healthcare professionals share responsibility for condition management. Methods The data reported here are part of a wider study that developed and tested a condition-specific, online parent information and support application with children and young people with chronic-kidney disease, parents and professionals. Semi-structured interviews were conducted with 19 fathers and 24 mothers who had recently tested the novel application. Data were analysed using Framework Analysis and the Communities of Practice concept. Results Evolving communities of child-healthcare practice were identified comprising three components and several sub components: (1) Experiencing (parents making sense of clinical tasks) through Normalising care, Normalising illness, Acceptance & action, Gaining strength from the affected child and Building relationships to formalise a routine; (2) Doing (Parents executing tasks according to their individual skills) illustrated by Developing coping strategies, Importance of parents’ efficacy of care and Fear of the child’s health failing; and (3) Belonging/Becoming (Parents defining task and group members’ worth and creating a personal identity within the community) consisting of Information sharing, Negotiation with health professionals and Achieving expertise in care. Parents also recalled factors affecting the development of their respective communities of healthcare practice; these included Service transition, Poor parent social life, Psycho-social affects, Family chronic illness, Difficulty in learning new procedures, Shielding and avoidance, and Language and cultural barriers. Health care professionals will benefit from using the communities of child-healthcare practice model when they support parents of children with chronic kidney disease. Conclusions Understanding some of the factors that may influence the development of communities of child-healthcare practice will help professionals to tailor information and support for parents learning to manage their child’s healthcare. Our results are potentially transferrable to professionals managing the care of children and young people with other long-term conditions.
机译:背景技术需要长期护理的儿童和年轻人的父母,需要在医院专业人员的远程支持下在家中为他们的孩子提供临床护理,他们经常在互联网上搜索提供护理的信息。但是,几乎没有证据表明在线可用信息是由父母开发和评估的,或者它承认当父母和医疗保健专业人员共同负责病情管理时存在的实践社区。方法此处报告的数据是更广泛研究的一部分,该研究开发并测试了针对特定条件的在线父母信息,并向患有慢性肾脏病的儿童和青少年,父母和专业人员提供了支持应用程序。对最近测试过该新颖应用程序的19位父亲和24位母亲进行了半结构化访谈。使用框架分析和实践社区概念对数据进行了分析。结果确定了不断发展的儿童保健实践社区,包括三个组成部分和几个子组成部分:(1)通过规范照料,规范疾病,接纳和行动,从患病儿童那里获得力量和建立人际关系来体验(父母理解临床任务)制定例行程序; (2)做(制定父母应对策略,父母重视照料功效的重要性和对孩子健康状况的恐惧的例证)(父母根据自己的技能来执行任务); (3)归属/成为(父母确定任务和小组成员的价值并在社区内建立个人身份),包括信息共享,与卫生专业人员的谈判以及在护理方面的专业知识。家长们还回顾了影响其各自医疗保健社区发展的因素;这些包括服务过渡,父母社交生活差,心理社会影响,家庭慢性疾病,学习新程序的困难,屏蔽和回避以及语言和文化障碍。当医疗保健专业人员为患有慢性肾脏病的儿童的父母提供支持时,他们将从使用儿童保健实践模式社区中受益。结论了解可能影响儿童保健实践社区发展的某些因素,将有助于专业人士定制信息并为父母学习如何管理其孩子的保健提供支持。我们的结果可能会转移给管理其他长期病情的儿童和年轻人的专业人员。

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