Stiripentol in atypical absence seizures in children: an open trial

JR Farwell, GD Anderson, BM Kerr, JA Tor… - Epilepsia, 1993 - Wiley Online Library
JR Farwell, GD Anderson, BM Kerr, JA Tor, RH Levy
Epilepsia, 1993Wiley Online Library
Stiripentol (STP) was added to the antiepileptic drug (AED) regimen of 10 patients with
uncontrolled atypical absence seizures (more than one seizure a day). Seven boys and
three girls aged 6–16 years participated in the study. Concomitant AEDs included various
combinations of phenobarbital (PB), phenytoin (PHT), carbamazepine (CBZ), and valproate
(VPA). Parents counted daily seizures over a 4‐week baseline period before institution of
STP, and in a 20‐week period during STP therapy. To compensate for drug interactions …
Summary
Stiripentol (STP) was added to the antiepileptic drug (AED) regimen of 10 patients with uncontrolled atypical absence seizures (more than one seizure a day). Seven boys and three girls aged 6–16 years participated in the study. Concomitant AEDs included various combinations of phenobarbital (PB), phenytoin (PHT), carbamazepine (CBZ), and valproate (VPA). Parents counted daily seizures over a 4‐week baseline period before institution of STP, and in a 20‐week period during STP therapy. To compensate for drug interactions, doses of other AEDs were adjusted during STP administration to keep serum levels close to levels of the baseline period. Maintenance doses of STP were 1,000–3,000 mg/day, giving serum levels of 4–22 μg/mL. All patients experienced a decrease in atypical absence seizures. Average decrease was 70% (range 5–95%). Side effects experienced by some patients were dose related and included anorexia, nausea, vomiting, and lethargy. In only 1 patient did an adverse effect (vomiting) require discontinuation of STP. We conclude that STP shows promise in treatment of atypical absence seizures in children, and further trials are warranted.
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