Suppr超能文献

神经发育障碍青少年从儿童医疗保健服务向成人医疗保健服务过渡的经验。

Experiences of transition from children's to adult's healthcare services for young people with a neurodevelopmental condition.

机构信息

Your Healthcare CIC, Surbiton, Surrey, UK.

出版信息

Health Soc Care Community. 2021 Sep;29(5):1429-1438. doi: 10.1111/hsc.13198. Epub 2020 Oct 16.

Abstract

Previous research has highlighted a lack of continuity of care when young people with a neurodevelopmental condition make the transition from children's to adult specialist healthcare services. A lack of planning, consistency, and availability of adult services has been found to lead to; increased anxiety, poor health outcomes, reduced support and some young people not receiving healthcare. The majority of transition research has focused on what health professionals consider important in the transition process, rather than focusing on the experiences of the young people and those closest to them. Our objective was to gather evidence from young people (and their families) who had experienced transition from children's to adult specialist healthcare services through semi-structured interviews. Volunteers were recruited from two London boroughs. All young people were aged between 18 and 25 years with a neurodevelopmental condition (Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder and/or an Intellectual Disability). Overall, we interviewed six young people with support from a family member. Five further family members were interviewed on behalf of the young person. In total, ten semi-structured interviews were transcribed verbatim and analysed using Interpretative Phenomenological Analysis. Four themes emerged from the analysis: (a) Parents as advocates, (b) Availability of adult's specialist health and social care services, (c) Lack of information sharing and (d) Transition as a binary, abrupt change. Our findings suggest the transition experience could be improved by changing service specifications to incorporate assessment and handover across the age range of 16-20 years. Additionally, statutory services should understand and provide the coordination role now offered by parents in transition. We suggest future research could evaluate the feasibility of a patient-owned online information sharing tool with information about relevant services for young people and their families.

摘要

先前的研究强调了,当患有神经发育疾病的年轻人从儿童专科医疗服务过渡到成人专科医疗服务时,医疗服务的连续性存在不足。研究发现,缺乏规划、服务的一致性和成人服务的可及性会导致:焦虑增加、健康状况恶化、支持减少,以及一些年轻人无法获得医疗保健。大多数过渡研究侧重于卫生专业人员认为在过渡过程中重要的内容,而不是关注年轻人及其最亲近的人的经历。我们的目的是通过半结构化访谈,从经历过从儿童专科医疗服务过渡到成人专科医疗服务的年轻人(及其家人)那里收集证据。志愿者从伦敦的两个行政区招募。所有年轻人的年龄都在 18 至 25 岁之间,患有神经发育疾病(注意力缺陷多动障碍、自闭症谱系障碍和/或智力残疾)。总体而言,我们采访了六名年轻人,有一名家庭成员提供支持。另外五名家庭成员代表年轻人接受了采访。共有十份半结构化访谈被逐字转录,并使用解释现象学分析进行分析。分析中出现了四个主题:(a)父母作为倡导者,(b)成人专科医疗和社会保健服务的可用性,(c)信息共享的缺乏,以及(d)过渡是一种二元的、突然的变化。我们的研究结果表明,可以通过改变服务规范来改善过渡体验,将评估和交接纳入 16-20 岁年龄段。此外,法定服务部门应该理解并发挥家长在过渡中提供的协调作用。我们建议未来的研究可以评估一个由患者拥有的在线信息共享工具的可行性,该工具包含有关年轻人及其家庭的相关服务的信息。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验