Family‐centred care in early intervention: A systematic review of the processes and outcomes of family‐centred care and impacting factors.

Family‐centred care (FCC) has been established as a best practice model for child disability services internationally. However, further empirical support is required to explore the operationalization and efficacy of FCC, in the absence of a universal practice model. This review aimed to identify the...

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Publicado en:Child: Care, Health & Development Vol. 48; no. 1; pp. 1 - 33
Autores principales: McCarthy, Elaine, Guerin, Suzanne
Formato: research systematic review tables/charts Journal Article
Publicado: Wiley-Blackwell Jan2022
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jan2022
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      pub: Wiley-Blackwell
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        atl: Family‐centred care in early intervention: A systematic review of the processes and outcomes of family‐centred care and impacting factors.
      aug:
        au:
          McCarthy, Elaine
          Guerin, Suzanne
        affil: UCD School of Psychology, University College Dublin, Dublin, Ireland
      sug:
        subj:
          Family Centered Care
          Early Intervention
          Outcomes (Health Care)
          Children with Disabilities
          Parents of Children with Disabilities
          Human
          Systematic Review
          Infant, Newborn
          Infant
          Child, Preschool
          Child
          Family
          Descriptive Statistics
          Family Characteristics
          Parental Attitudes
          Infant, Newborn: birth-1 month
          Infant: 1-23 months
          Child, Preschool: 2-5 years
          Child: 6-12 years
      ab: Family‐centred care (FCC) has been established as a best practice model for child disability services internationally. However, further empirical support is required to explore the operationalization and efficacy of FCC, in the absence of a universal practice model. This review aimed to identify the key processes and outcomes of FCC in early intervention (EI) settings and the factors that impact FCC. A systemic review was conducted exploring the processes and outcomes of FCC delivered to children predominantly aged 0–6 years with disabilities/suspected disabilities and families as part of EI or early services. The search procedure was informed by the Preferred Reporting Items for Systematic Reviews and Meta‐Analyses (PRISMA) guidelines (Moher et al., 2009). Narrative analysis of data was guided by Braun and Clarke (2006, 2014). Data were presented as per the standards for reporting qualitative research (SRQR; O'Brien et al., 2014). Forty‐two studies were included. The majority (90.5%) outlined the processes of FCC, with 59.5% of studies detailing outcomes. Processes were largely reported as qualitative data and/or subscales of the Measure of Processes of Care (MPOC; King et al., 1995), which were subsequently collated. Findings indicated eight key operational processes and corresponding outcomes. Variables that hinder or facilitate FCC included family/professional characteristics, family/service resources, and parent attitudes, engagement and agency. FCC was largely conceptualized as the application of services to children and their families. Critical perspectives on FCC are discussed. It is hoped this research will contribute to the development of a framework of FCC in EI to inform services provided to young children with complex needs and their families and future research.
      pubtype: Academic Journal
      doctype:
        research
        systematic review
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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