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A meta‐synthesis of how parents of children with autism describe their experience of advocating for their children during the process of diagnosis

机译:荟萃综合患有自闭症儿童的父母如何描述他们在诊断过程中倡导他们的孩子的经验

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Abstract The diagnostic process for children with autism can be complex for parents to navigate as they advocate for their child in order to obtain answers to their concerns, and receive the subsequent support they need. Gaining an understanding of parents’ experiences during this process, will assist service providers in supporting families adequately. This systematic review was undertaken to consolidate in‐depth qualitative data from parents of their experience of advocating for their child with autism, during the process of diagnosis. A qualitative meta‐synthesis was conducted, whereby fifteen databases were systematically searched. Twenty‐two studies were identified and appraised using an adapted version of the Critical Appraisal Skills Programme tool. Data were synthesised into themes through the steps of review, meta‐aggregation, integration, and interpretation. The date range of the included studies spans 1999–2016. The voices of 1,178 parents are presented in this review describing their experiences in two overarching themes: “Pathway to diagnosis—Confusion and not feeling heard”; and “Pursuing diagnosis—Resilience and commitment.” Each one of these main themes had sub‐themes. Our findings highlight the intense emotional journey for parents during identification of their initial concerns and the formal process of diagnosis, and their perceptions of not being supported by others on this journey. This review illustrates the significant impact that positive experiences with first‐line professionals have during the process of diagnosis, and how these experiences lay the foundation for all future relationships with other service providers. As a result, awareness of parents’ experiences will assist service providers to reconsider their communication style, information sharing, provision of support and to incorporate parents’ contributions in facilitating a more streamlined and more supportive process of diagnosis.
机译:摘要自闭症儿童的诊断过程对于父母来说可以复杂,因为他们倡导他们的孩子,以获得他们的关切的答案,并获得他们所需的随后支持。在此过程中获得对父母的经验,将帮助服务提供商充分支持家庭。在诊断过程中,在诊断过程中,进行了系统审查,以巩固他们对自闭症倡导的经验的深入定性数据。进行了定性的荟萃合成,从而系统地搜索了十五个数据库。使用适应的关键评估技能计划工具的适应版本确定并评估了二十两项研究。通过审查,元聚集,集成和解释的步骤综合数据以主题综合。 1999-2016的附录研究日期范围。本次审查中提出了1,178名父母的声音,描述了他们在两个总体主题中的经验:“诊断 - 混乱的途径,感觉不清楚”;并“追求诊断 - 弹性和承诺”。这些主要主题中的每一个都有子主题。我们的调查结果突出了父母在确定其初步担忧和正式诊断过程中的激烈情感旅程,以及他们对这一旅程不支持的看法。本综述说明了在诊断过程中与一线专业人士的积极经验以及这些经验如何为与其他服务提供商的所有关系奠定基础的重大影响。因此,对父母经验的认识将协助服务提供商重新考虑他们的沟通方式,信息共享,提供支持,并将父母的贡献纳入促进更精简和更具支持性诊断过程。

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