N200 and P300 of event-related potentials (ERPs) were recorded from 22
epileptic children receiving high-dose antiepileptic drugs. The patie
nts were undergoing monotherapy with supratherapeutic serum level and
were not mentally retarded. P300 latency was prolonged in 5 of 8 patie
nts (62.5%) of the carbamazepine (CBZ) group and in 4 of 7 patients (5
7.1%) of the phenytoin (PHT) group. Only one child of the PHT group sh
owed abnormality in brain-stem auditory evoked potentials (BAEPs). Abn
ormality of P300 was more frequent than that of BAEP. In patients of t
he PHT group who underwent examinations consecutively before and after
changing the dose, P300 latency was prolonged rapidly when the PHT le
vel exceeded 30 mu g/ml. This suggested that the prolongation was dose
dependent. In all patients of the valproic acid (VPA) group, P300 lat
ency was normal. Only 2 patients of the PHT group had P300 prolongatio
n simultaneously with clinical signs of intoxication. Others demonstra
ted changes in P300 without symptoms of side effects.