A meta‐synthesis of how parents of children with autism describe their experience of accessing and using routine healthcare services for their children.

In order to present a greater understanding to parental experiences of supporting their child with autism to access healthcare services, a systematic review of qualitative research was undertaken, addressing the review question: 'How do parents of children with autism describe their experiences of u...

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Published in:Health & Social Care in the Community Vol. 29; no. 6; pp. 1668 - 1683
Main Authors: Boshoff, Kobie, Bowen‐Salter, Holly, Gibbs, Deanna, Phillips, Rebecca L., Porter, Lisa, Wiles, Louise
Format: research systematic review tables/charts meta synthesis Journal Article
Published: Wiley-Blackwell Nov2021
Online Access:View this record in EBSCOhost
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      dt: Nov2021
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1111/hsc.13369
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        atl: A meta‐synthesis of how parents of children with autism describe their experience of accessing and using routine healthcare services for their children.
      aug:
        au:
          Boshoff, Kobie
          Bowen‐Salter, Holly
          Gibbs, Deanna
          Phillips, Rebecca L.
          Porter, Lisa
          Wiles, Louise
        affil: International Centre for Allied Health Evidence, Allied Health and Human Performance, University of South Australia, Adelaide SA,, Australia
      sug:
        subj:
          Autism Spectrum Disorder
          Parents of Children with Disabilities
          Parental Attitudes Evaluation
          Attitude to Health Evaluation
          Health Services Accessibility
          Child Health Services
          Human
          Systematic Review
          Meta Synthesis
          Medline
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          Psycinfo
          ERIC Database
          Cochrane Library
          Thematic Analysis
          Professional-Patient Relations
          Professional-Family Relations
      ab: In order to present a greater understanding to parental experiences of supporting their child with autism to access healthcare services, a systematic review of qualitative research was undertaken, addressing the review question: 'How do parents of children with autism describe their experiences of utilising routine healthcare services?'. After a systematic search and selection process, 12 studies were identified and appraised independently by paired reviewers using an adapted version of the Critical Appraisal Skills Programme (CASP) tool. Data were synthesised by two reviewers in line with the Joanna Briggs Approach for meta‐aggregation. The 12 studies included in this review (spanning 2012–2020), represented the voices of 240 parents. The synthesis resulted in the following synthesised finding (based on four categories that emerged from the original studies' themes): parents report challenges in accessing and use of mainstream health services, for their child with autism, due to not having a voice, inadequate communication and lack of understanding from health service providers. This review raises our awareness of parents' experiences of healthcare services and will assist healthcare practitioners to reconsider their own communication style, understanding and approach with children with autism and their families. From these findings, we recommend that healthcare practitioners more readily incorporate parents' contributory expertise into healthcare visits. These recommendations will help facilitate effective, supportive and positive healthcare experiences for all involved.
      pubtype: Academic Journal
      doctype:
        research
        systematic review
        tables/charts
        meta synthesis
        Journal Article
      ougenre: Article
    language: English
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