Methods: We compared treatment patterns and craniometric changes of children presenting with syndromic craniosynostosis before (2003-2008) and after (2009-2014) implementation of PVDO.
Results: 64 children with syndromic craniosynostosis presented during the study period. 40 met inclusion criteria with complete medical records and care continuity since birth: 22 prior to and 18 after implementation of PVDO. Patients with computed tomographic studies before and after PVDO demonstrate significant reduction in frontal bossing (FNS angle decreased 125.4 to 118.8, p = 0.005.) Cranial volume increased after PVDO by a mean 21.5%, and by 28.4% in the subset of patients under 1 year of age, compared to 8.6% in patients undergoing FOA with or without posterior cranial vault remodeling (p = 0.041). Only 10 (56%) of patients who underwent initial PVDO required frontal advancement, at a mean follow-up of 4.0 years of age (range 1.5-7.5 years,) compared to 22 (100%) prior to implementation of PVDO, at a mean initial age of 1.3 years. Kaplan-Meier survival analysis indicates significant delay in need for subsequent FOA in patients who underwent early PVDO compared to early FOA or monobloc (p=0.011).
Conclusions:
Early PVDO confers improved frontal morphologic changes in children with syndromic craniosynostosis, and increased cranial volume expansion compared with those treated initially with FOA and/or posterior cranial vault remodeling. Consequently, these children are less likely to undergo FOA early in life. We have developed an evidence-based algorithm for syndromic synostosis based on these results that employs early PVDO.