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Minimally Invasive Endoscopic Surgery for Infantile Craniosynostosis: A Longitudinal Cohort Study.
Riordan, Coleman P; Zurakowski, David; Meier, Petra M; Alexopoulos, Georgios; Meara, John G; Proctor, Mark R; Goobie, Susan M.
Afiliación
  • Riordan CP; Department of Neurosurgery, Boston Children's Hospital, Harvard Medical School, Boston, MA.
  • Zurakowski D; Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA; Department of General Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA.
  • Meier PM; Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA.
  • Alexopoulos G; Department of Neurosurgery, Boston Children's Hospital, Harvard Medical School, Boston, MA.
  • Meara JG; Department of Plastic and Oral Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA.
  • Proctor MR; Department of Neurosurgery, Boston Children's Hospital, Harvard Medical School, Boston, MA.
  • Goobie SM; Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA. Electronic address: Susan.Goobie@childrens.harvard.edu.
J Pediatr ; 216: 142-149.e2, 2020 01.
Article en En | MEDLINE | ID: mdl-31685225
OBJECTIVE: To evaluate patient outcomes of minimally invasive endoscopic strip craniectomy (ESC) for craniosynostosis. STUDY DESIGN: This is a retrospective cohort analysis (2004-2018) of 500 consecutive infants with craniosynostosis treated by ESC with orthotic therapy at a single center. Operative outcomes included transfusions, complications, and reoperations as well as head circumference change based on World Health Organization percentiles. Multivariable logistic regression was used to identify risk factors associated with blood transfusion. Paired t tests were used for within-patient comparisons and Fisher exact test to compare syndromic and nonsyndromic subgroups. RESULTS: ESC was associated with low rates of blood transfusion (6.6%), complications (1.4%), and reoperations (3.0%). Risk factors for transfusion included syndromic craniosynostosis (P = .01) and multiple fused sutures (P = .02). Median surgical time was 47 minutes, and hospital length of stay 1 day. Transfusion and reoperation rates were higher among syndromic patients (both P < .001). Head circumference normalized by 12 months of age relative to World Health Organization criteria in infants with sagittal, coronal, and multisuture craniosynostosis (all P < .001). CONCLUSIONS: ESC is a safe, effective, and durable correction of infantile craniosynostosis. ESC can achieve head growth normalization with low risks of blood transfusion, complications, or reoperation. Early identification of craniosynostosis in the newborn period and prompt referral by pediatricians allows families the option of ESC vs larger and riskier open reconstruction procedures.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Craneosinostosis / Craneotomía / Endoscopía Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Infant / Male Idioma: En Revista: J Pediatr Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Craneosinostosis / Craneotomía / Endoscopía Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Infant / Male Idioma: En Revista: J Pediatr Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos