School-Aged Anthropometric Outcomes After Endoscopic or Open Repair of Metopic Synostosis

Austin Y Ha1, Gary B Skolnick1, David Chi1

  • 1Division of Plastic and Reconstructive Surgery, Department of Surgery and.

Pediatrics
|August 14, 2020
PubMed

Insights

Endoscopic repair for metopic craniosynostosis offers equivalent or superior 5-year outcomes compared to open surgery, with reduced morbidity and faster recovery. This approach is recommended for infants under six months.

Area of Science:

  • Craniofacial Surgery
  • Pediatric Neurosurgery
  • Plastic Surgery

Background:

  • Metopic craniosynostosis is a premature fusion of the metopic suture.
  • Treatment options include fronto-orbital advancement (open repair) and endoscopic strip craniectomy.
  • Endoscopic repair is typically indicated for infants under 6 months.

Purpose of the Study:

  • To compare 5-year anthropometric outcomes of endoscopic versus open repair for metopic craniosynostosis.
  • To evaluate peri-operative variables and long-term morbidity associated with each surgical technique.

Main Methods:

  • Retrospective chart review of 31 nonsyndromic patients with isolated metopic craniosynostosis.
  • Comparison of frontal width, interfrontal divergence angle, Whitaker classification, and lateral frontal retrusion at 5 years.
  • Analysis of peri-operative data including blood loss, transfusion rates, length of stay, and operative time.

Main Results:

  • Endoscopic repair showed a significantly lower rate of lateral frontal retrusion at 5 years.
  • No significant differences were observed in other anthropometric outcomes between the groups.
  • The endoscopic group experienced shorter operating times, hospital stays, and less blood loss.

Conclusions:

  • Endoscopic repair provides superior or equivalent anthropometric outcomes and reduced morbidity in school-aged children with metopic craniosynostosis.
  • Endoscopic repair is associated with a faster recovery and decreased complications.
  • Consider endoscopic repair for metopic craniosynostosis in infants diagnosed before 6 months of age.
Abstract