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Unlabelled: Surgical correction of craniosynostosis addresses potentially elevated intracranial pressure and the cranial deformity. In nonsyndromic sagittal synostosis, approximately 15% of patients have elevated intracranial pressure. The decision to operate therefore likely reflects a combination of aesthetic goals, prevention of brain growth restriction over time, surgeon training and experience, and parental expectations. This study examines clinical factors that influence surgical decision-making in nonsyndromic sagittal synostosis.
Methods: An online survey sent to craniofacial and neurosurgeons presented 5 theoretical patients with varying severities of sagittal synostosis. For each cephalic index, 4 separate clinical scenarios were presented to assess influences of parental concern and developmental delay on the decision to operate.
Results: Fifty-six surveys were completed (response rate = 28%). Participants were predominantly from North America (57%), had over 10 years of experience (75%), and performed over 20 craniosynostosis procedures annually (50%). Thirty percent of respondents indicated they would operate regardless of head shape and without clinical and/or parental concern. Head shape was the greatest predictor of decision to operate ( < 0.001). Parental concern and developmental delay were independently associated with decision to operate ( < 0.001). Surgeons with more experience were also more likely to operate across all phenotypes (OR: 2.69, < 0.004).
Conclusions: Surgeons responding to this survey were more strongly compelled to operate on children with nonsyndromic sagittal craniosynostosis when head shape was more severe. Additional factors, including parental concern and developmental delay, also influence the decision to operate, especially for moderate phenotypes. Geographic and subspecialty variations were not significant.
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http://dx.doi.org/10.1097/GOX.0000000000003493 | DOI Listing |
Cleft Palate Craniofac J
August 2025
Phoenix Children's Center for Cleft and Craniofacial Care, Division of Plastic, Reconstructive, and Maxillofacial Surgery, Phoenix Children's, Phoenix, AZ, USA.
Our objective is to examine which sociodemographic factors may influence the time of presentation of patients with craniosynostosis, which can impact perioperative outcomes. Retrospective cohort study. Tertiary pediatric hospital.
View Article and Find Full Text PDFOrphanet J Rare Dis
August 2025
Integrative Neuromedicine, Community Hospital Herdecke, Witten/Herdecke University, Gerhard-Kienle-Weg 4, 58313, Herdecke, Germany.
Background: Sagittal suture craniosynostosis is the most usual subtype of craniosynostosis which results from premature fusion of the sagittal suture. It leads to an elongated skull shape known as scaphocephaly. This condition necessitates timely surgical intervention to correct cranial deformities and prevent the associated complications.
View Article and Find Full Text PDFChilds Nerv Syst
July 2025
Division of Plastic & Reconstructive Surgery, Department of Surgery, Yale School of Medicine, 330 Cedar Street, Boardman Building, New Haven, CT, 06510, USA.
Purpose: While previous studies have investigated behavioral development after non-syndromic sagittal craniosynostosis (NSSC) repair, there is limited information available about the influence of surgical technique. This study examined behavioral differences among patients with NSSC following cranial vault remodeling (CVR) versus strip craniectomy (SC).
Methods: Parents of patients ages 6-18 years old with NSSC repaired before 6 months via either CVR or SC completed four behavioral surveys: Conners Short 3rd Edition (ADHD), Social Responsiveness Scale 2nd edition (ASD), Behavior Rating Inventory of Executive Function 2nd Edition (executive functioning), and Child Behavior Checklist (emotional/behavioral regulation).
Cleft Palate Craniofac J
June 2025
Division of Pediatric Plastic Surgery, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
ObjectiveTo develop and validate machine learning (ML) models for objective and comprehensive quantification of sagittal craniosynostosis (SCS) severity, enhancing clinical assessment, management, and research.DesignA cross-sectional study that combined the analysis of computed tomography (CT) scans and expert ratings.SettingThe study was conducted at a children's hospital and a major computer imaging institution.
View Article and Find Full Text PDFJ Craniofac Surg
May 2025
Department of Pediatric Neurosurgery, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Yangpu, Shanghai, China.
Craniosynostosis is the premature fusion of the cranial sutures, a heterogeneous disorder with a prevalence of ~1 in 2200. The etiology of craniosynostosis is largely unknown. However, several recent genomic discoveries have elucidated the genetic basis for nonsyndromic craniosynostosis, particularly unicoronal or bicoronal craniosynostosis.
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