G. Coppola et al., VIGABATRIN AS ADD-ON THERAPY IN CHILDREN AND ADOLESCENTS WITH REFRACTORY EPILEPSY - AN OPEN TRIAL, Brain & development, 19(7), 1997, pp. 459-463
Seventy-seven children and adolescents with drug-resistant epilepsies
received vigabatrin as add-on therapy for a median of 18 months (range
4-36 months) at a dose of 50 mg/kg/day divided in two doses. patients
with spasms were given a maximum dose of 100 mg/kg/day. In 23 patient
s (29.9%), seizure frequency decreased by 50-130% and in 12 patients (
15.6%) by 25-50%. The number of seizures remained unchanged in 34 pati
ents (44.1%) and increased in seven (9.1%). Vigabatrin was most effect
ive in cryptogenic and symptomatic partial seizures (39% and 43%, resp
ectively), and in infantile spasms (25%). Adverse events occurred in 2
0 patients (26%), though they were generally mild and transient, sugge
sting that vigabatrin is well tolerated. (C) 1997 Elsevier Science B.V
.