City, University of London Department of Health Services Research and Management, United Kingdom.
UCL Great Ormond Street Institute of Child Health, United Kingdom.
Child Care Health Dev. 2024 Jul;50(4):e13303. doi: 10.1111/cch.13303.
Children and young people (CYP) with complex neurodisability experience multiple physical, communication, educational and social challenges, which require complex packages of multidisciplinary care. Part of the holistic care required includes supporting the families and parents/caregivers. The aim of the wider study was to introduce a new programme ('Ubuntu') to parents/caregivers and healthcare professionals (HCPs) in order to test the feasibility and acceptability of the concept and content, with the goal of potential adaptation for the UK in mind. Data collection and analysis uncovered rich data on caregiving journeys, navigation of health services, and perceived service gaps. This paper focuses solely on these topics. Further papers will report on the feasibility and adaptation data.
Two rounds of semi-structured interviews were conducted with 12 caregivers of CYP with complex neurodisability and six HCPs from a variety of disciplines, recruited from a community child health service in London Borough of Newham, UK in 2020. The interviews included open-ended questions to explore caregiving journeys, experiences of navigating health services and perceived service gaps. Transcripts were analysed using a data-driven inductive thematic analysis.
Three themes were identified that related to the aim of understanding caregivers' experiences and unmet needs relating to current service provision. These were (1) Caregiver Mental Health, (2) The Information Gap and (3) The Need for Holistic Support. Mental health difficulties were reported, particularly around the period of diagnosis. Priority needs included the provision of clear information about the diagnosis and services offered, opportunities to forge peer support networks and for services across the community to collaborate.
The delivery of health services for CYP with neurodisability should encompass the broad needs of the family as well as meeting the clinical needs of the CYP.
患有复杂神经残疾的儿童和青少年 (CYP) 面临多种身体、沟通、教育和社会挑战,需要复杂的多学科护理包。所需整体护理的一部分包括支持家庭和父母/照顾者。更广泛研究的目的是向父母/照顾者和医疗保健专业人员 (HCP) 介绍一个新方案(“Ubuntu”),以测试该概念和内容的可行性和可接受性,同时考虑到在英国的潜在适应性。数据收集和分析揭示了有关照顾者旅程、健康服务导航和感知服务差距的丰富数据。本文仅关注这些主题。其他论文将报告可行性和适应性数据。
2020 年,在英国伦敦纽汉姆区的社区儿童健康服务机构中,对 12 名患有复杂神经残疾的 CYP 的照顾者和 6 名来自各种学科的 HCP 进行了两轮半结构化访谈。访谈包括开放式问题,以探索照顾者的旅程、健康服务的导航体验和感知到的服务差距。使用数据驱动的归纳主题分析对转录本进行分析。
确定了与了解照顾者与当前服务提供相关的经验和未满足需求的目标相关的三个主题。这些主题是:(1)照顾者心理健康,(2)信息差距和(3)对整体支持的需求。报告了心理健康困难,尤其是在诊断期间。优先需求包括提供有关诊断和提供的服务的明确信息、有机会建立同行支持网络以及整个社区的服务进行协作的机会。
为神经残疾的 CYP 提供的卫生服务应包括家庭的广泛需求,以及满足 CYP 的临床需求。