Boshoff K, Gibbs D, Phillips R L, Wiles L, Porter L
International Centre for Allied Health Evidence, School of Health Sciences, University of South Australia, Adelaide, South Australia.
Barts Health NHS Trust, Royal London Hospital, London, UK.
Child Care Health Dev. 2018 Jan;44(1):147-160. doi: 10.1111/cch.12504. Epub 2017 Aug 23.
Advocacy has been described by parents of children with autism as an important coping strategy, enabling them to move forward by redirecting emotions into actions. A key factor in the development of collaborative and constructive partnerships between service providers and parents is having an understanding of how parents engage in advocacy and the support needed to do so. This meta-synthesis was undertaken to consolidate in-depth qualitative data from parents' perspectives of the process that they use to advocate for their children with autism.
A qualitative meta-synthesis was conducted, whereby 15 databases were systematically searched. Thirty-one studies were identified and appraised using an adapted version of the Critical Appraisal Skills Programme tool. Data were synthesized into themes through the steps of review, meta-aggregation, integration, and interpretation.
The voices of 1,662 parents are presented describing the process of advocacy in the stages of seeking a diagnosis, seeking self-education, and taking action. Taking action includes 2 subthemes: seeking, access, and use of support services and community engagement and educating others.
Results highlight the significant impact that positive experiences with first-line professionals have during the diagnosis process and how these experiences lay the foundation for all future relationships with other service providers. Important implications arise from this meta-synthesis for service providers in supporting parents' advocacy and hence building constructive relationships with families with a child with autism.
自闭症患儿的家长将自我维权描述为一种重要的应对策略,能让他们将情绪转化为行动,从而不断前行。服务提供者与家长之间建立合作性和建设性伙伴关系的一个关键因素,是要了解家长如何进行自我维权以及这样做所需的支持。本次元综合研究旨在整合来自家长视角的关于他们为自闭症患儿维权过程的深度定性数据。
进行了一项定性元综合研究,系统检索了15个数据库。使用经改编的批判性评估技能计划工具对31项研究进行了识别和评估。通过回顾、元聚合、整合和解释等步骤将数据综合为主题。
呈现了1662名家长的声音,描述了在寻求诊断、自我教育和采取行动等阶段的维权过程。采取行动包括两个子主题:寻求、获取和使用支持服务以及社区参与和教育他人。
结果突出了一线专业人员在诊断过程中的积极体验所产生的重大影响,以及这些体验如何为未来与其他服务提供者的所有关系奠定基础。本次元综合研究对服务提供者在支持家长维权从而与自闭症患儿家庭建立建设性关系方面具有重要启示。