Perceptions of participation: child patients with a disability in the doctor-parent-child partnership

Belinda Garth1, Gregory C Murphy, Dinah S Reddihough

  • 1School of Public Health, Faculty of Health Science, La Trobe University, Bundoora 3086, Victoria, Australia. B.Garth@latrobe.edu.au

Insights

Children contribute to the doctor-parent-child partnership, but their involvement varies. Understanding these complexities requires moving beyond dyadic models to embrace a social model of care for triadic partnerships.

Area of Science:

  • Pediatric healthcare
  • Family-centered care
  • Qualitative research

Background:

  • The traditional doctor-parent partnership often excludes the child.
  • Understanding the child's role in healthcare decisions is crucial.

Purpose of the Study:

  • To investigate the child's experience and contribution within the doctor-parent-child partnership.
  • To explore how children with cerebral palsy participate in healthcare discussions.

Main Methods:

  • Qualitative study utilizing semi-structured interviews.
  • 33 participants: 9 pediatricians, 14 parents, 10 children (aged 8-12) with cerebral palsy.
  • Data collected from a pediatric teaching hospital in Victoria, Australia.

Main Results:

  • Children were reported to participate in the doctor-parent-child partnership.
  • Child involvement was variable, not perceived as 'equal' or 'regular'.
  • Key themes: creating space for involvement, acknowledging preferences, and negotiating age/developmental factors.

Conclusions:

  • The doctor-parent-child partnership is often triadic, not exclusively dyadic.
  • Children contribute to the partnership, though limitations exist.
  • A social model of care is essential for developing effective triadic partnerships.
Abstract

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