A new anti-epileptic drug, tiagabine, is a potent inhibitor of GABA up
take into neurons and glia. Tiagabine has shown promising efficacy and
safety profiles as add-on treatment for partial seizures. We evaluate
d the long-term effects of tiagabine on cognition and EEG in 37 patien
ts with partial epilepsy. The study protocol consisted of a randomized
, double-blind, placebo-controlled, parallel-group add-on study and an
open-label extension study. During the 3 month double-blind phase at
low doses (30 mg/day) tiagabine treatment did not cause any cognitive
or EEG changes as compared with placebo. Tiagabine treatment did not c
ause deterioration in cognitive performance or produce any rhythmic sl
ow-wave activity or other constant, new abnormalities on EEG during lo
nger follow-up with successful treatment on higher doses after 6-12 mo
nths (mean 65.7 mg/day, range 30-80 mg/day) and after 18-24 months (me
an dose 67.6 mg/day, range 24-80 mg/day). The daily dosages in the lon
g-term follow-up of the present study are higher than in the previous
reports.