Caregiver perspectives of scoliosis surgery for children with cerebral palsy: a qualitative study.

Stewart, Kirsty; Price, Georgia; Kelderman, Jayne; Carman, Sarah; Imms, Christine; Wallen, Margaret

Purpose: To explore the perspectives of primary caregivers of children with cerebral palsy (CP) who had spinal surgery for scoliosis. Materials and Methods: A qualitative study was conducted using semi-structured interviews and guided by qualitative description methodology. Participants were caregivers of children with CP aged 5–18, who had undergone spinal surgery for scoliosis in Australia. The research team included a parent with lived experience. Results: Fourteen participants (8 biological mothers), aged 40–49 years, completed online semi-structured interviews. Four themes were identified emerged. Life with a child with CP underpinned all experiences which were founded on familiarity with their child, medical procedures, and hospitalisation. Three subthemes were parents are the experts in knowing their child, children are vulnerable, and impact on caregivers. Theme 2 involved the significance of decision making to proceed with surgery. Theme 3 underscored a need to be prepared for the surgical journey and, in Theme 4, participants spoke of needing to expect the unexpected. Conclusion: The findings highlight the importance of understanding caregiver experiences and can help inform health professionals and other families in the decision-making process, preparing for and navigating spinal surgery. IMPLICATIONS FOR REHABILITATION: Spinal surgery for scoliosis in children with cerebral palsy is a major surgery and poses substantial challenges for the family. Understanding the magnitude of the decision for families to proceed with surgery will equip health professionals to adequately support and partner with families. Detailed information and extensive preparation are necessary for families to proceed with and navigate surgery, the hospital stay and to return home and to the community.

AUSTRALIA; CHILDREN with disabilities; QUALITATIVE research; SCOLIOSIS; INTERVIEWING; HOSPITAL care; STATISTICAL sampling; DESCRIPTIVE statistics; DECISION making; CHILDREN with cerebral palsy; THEMATIC analysis; EXPERIENCE; RESEARCH methodology; CHILD care; CAREGIVER attitudes; PATIENT participation; CHILDREN

Disability & Rehabilitation, 2025, Vol 47, Issue 2, p459

0963-8288

Academic Journal

10.1080/09638288.2024.2342501