The EEG pattern marked A — generalized, bilaterally synchronous 3 Hz spike-and-wave discharges provoked by hyperventilation — is the pathognomonic hallmark of childhood absence epilepsy (CAE). The clinical presentation (brief unresponsiveness, vacant stare, multiple daily episodes, school-age onset) combined with this EEG finding confirms CAE. Ethosuximide is the first-line drug for CAE, particularly when seizures are limited to absences. The landmark NEJM 2010 CAE Trial demonstrated that ethosuximide achieved absence-freedom in 62% of patients, superior to lamotrigine (58%) and more effective than valproate (29%) for absence control alone, while causing fewer attentional adverse effects than valproate. Ethosuximide works by blocking T-type calcium channels in the thalamocortical circuit, directly addressing the pathophysiology underlying the 3 Hz spike-and-wave pattern (Nelson 21e Ch 611; NEJM 2010;362:790).
Nelson 21e Ch 611; NEJM 2010;362:790 (CAE Trial)
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