Use of Pediatric Outcomes Data Collection Instrument to Evaluate Functional Outcomes in Multiple Hereditary Exostoses

Nathalia Sundin Palmeira de Oliveira1, Marcela Rocha Dias da Silva2, Camila Bedeschi Rego de Mattos3

  • 1Oncology Orthopedist, Orthopaedic department, Hospital Universitário Pedro Ernesto (HUPE-UERJ), Rio de Janeiro, RJ.

Insights

The Pediatric Outcomes Data Collection Instrument (PODCI) effectively measures quality of life in children with multiple hereditary exostosis (MHE), showing lower functional levels compared to healthy peers.

Area of Science:

  • Orthopedics
  • Pediatric Health
  • Quality of Life Research

Background:

  • The Pediatric Outcomes Data Collection Instrument (PODCI) is a validated tool for assessing quality of life in pediatric musculoskeletal conditions.
  • Multiple hereditary exostosis (MHE) is a genetic disorder affecting bone development, with limited research on its impact on children's general health status and daily functioning.
  • Existing studies on MHE primarily focus on surgical interventions and deformity correction, neglecting the broader health and functional implications for pediatric patients.

Purpose of the Study:

  • To evaluate the functional levels and quality of life in pediatric patients diagnosed with multiple hereditary exostosis (MHE) using the PODCI questionnaire.
  • To establish a baseline understanding of how MHE affects pain, function, and daily activities in children.
  • To explore the utility of the PODCI in assessing outcomes for MHE patients.

Main Methods:

  • A cross-sectional study involving 34 pediatric patients with MHE and their families.
  • Prospective administration of the PODCI questionnaire to assess functional status.
  • Statistical analysis including Student and Welch t tests for group comparisons, Wilcoxon signed rank test for parent-child report differences, and Spearman test for correlation with physical examination findings.

Main Results:

  • Pediatric patients with MHE demonstrated significantly lower PODCI scores across all domains compared to unaffected children (P < 0.05).
  • Statistically significant differences were observed between parent and child reports in the pain and comfort domain (P < 0.5).
  • A significant negative correlation was found between physical examination findings and PODCI scores, indicating poorer function with more severe physical signs.

Conclusions:

  • The PODCI questionnaire is a capable tool for evaluating functional outcomes in pediatric patients with multiple hereditary exostosis (MHE).
  • The findings highlight the significant impact of MHE on the quality of life and functional status of affected children.
  • Further research utilizing the PODCI can aid in developing targeted interventions and improving care for children with MHE.
Abstract