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


Journal

Health & social care in the community
ISSN: 1365-2524
Titre abrégé: Health Soc Care Community
Pays: England
ID NLM: 9306359

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 06 06 2018
revised: 23 10 2018
accepted: 30 10 2018
pubmed: 15 12 2018
medline: 2 6 2020
entrez: 15 12 2018
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 30548710
doi: 10.1111/hsc.12691
doi:

Types de publication

Journal Article Meta-Analysis Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e143-e157

Informations de copyright

© 2018 John Wiley & Sons Ltd.

Auteurs

Kobie Boshoff (K)

School of Health Sciences, International Centre for Allied Health Evidence, University of South Australia, Adelaide, South Australia, Australia.

Deanna Gibbs (D)

Nursing, Midwifery & Allied Health Professions, Barts Health NHS Trust, London, UK.

Rebecca L Phillips (RL)

ANU Medical School, Centre for Health Stewardship, The Australian National University, Canberra, Australia.

Louise Wiles (L)

School of Health Sciences, International Centre for Allied Health Evidence, University of South Australia, Adelaide, South Australia, Australia.

Lisa Porter (L)

University of South Australia, Adelaide, South Australia, Australia.

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Classifications MeSH