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Anesthetic experience of a patient with Ohtahara syndrome -A case report-

By Eun Mi Choi, Kyeong Tae Min, Jin Sun Cho and Seung Ho Choi

Abstract

Ohtahara syndrome (OS) is a rare epileptic encephalopathy that is characterized by an abnormal electroencephalogram (EEG) and intractable seizures in the neonatal and early infantile period. The patient of this reported case was delivered normally at 39 weeks of gestation without any complication. One week after birth, seizures that were refractory to anticonvulsants started with repetitive clustered tonic spasms. The child had no abnormal findings on the initial laboratory investigations. But he was diagnosed with OS according to the frequent tonic spasms, an abnormal EEG pattern of suppression-burst and magnetic resonance imaging of cortical dysplasia. He was planned to undergo an operation for brain lesion. This report describes our experience with the general anesthetic management when we performed craniotomy and right hemispherotomy for a patient with OS

Topics: Case Report
Publisher: The Korean Society of Anesthesiologists
OAI identifier: oai:pubmedcentral.nih.gov:3049880
Provided by: PubMed Central

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