Relevance of surgical strategies for the management of pediatric Chiari type I malformation

Male Adolescent Infant Decompression, Surgical Neurosurgical Procedures Syringomyelia Arnold-Chiari Malformation 03 medical and health sciences Postoperative Complications Treatment Outcome 0302 clinical medicine Cerebellum Child, Preschool Humans Female Dura Mater Child Craniotomy Retrospective Studies
DOI: 10.1007/s00381-007-0297-6 Publication Date: 2007-01-25T02:43:06Z
ABSTRACT
In face of continuing controversy to the optimal treatment of Chiari type I malformation, the authors analyzed three different surgical strategies.Sixty patients (30 boys and 30 girls, mean age 8.2 years) presented with clinical Chiari malformation. Additional syringomyelia was present in 24 children, whereas cine flow studies showed no flow in the craniocervical junction in 48 children. All patients underwent a limited occipital craniectomy; a duraplasty was performed in 21 cases; and additional tonsillar reduction was performed in 19 cases. Clinical improvement was seen in 24 patients who underwent posterior decompression with or without duraplasty. In the tonsillar group, clinical improvement was evident in 18 patients.Duraplasty and tonsillar reduction were equally effective but significantly better than bone decompression alone. Among patients with syringomyelia, tonsillar reduction was associated with a significantly better outcome. Postoperative flow studies improved in 39 patients but did not correlate to the clinical outcome.
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