Purpose: The efficacy and tolerability of vigabatrin (VGB) as an add-o
n therapy in the treatment of infantile spasm (IS) prompted physicians
to explore its use as the first drug in this seizure type. Methods: O
ur retrospective study included 250 infants diagnosed with IS; the dat
a obtained were subjected to peer-group review. Of this infant populat
ion, 192 infants were considered to have classic IS and had received V
GB as their first treatment for the spasms. There was a slight prepond
erance of boys (57%) in this population. Mean age of IS onset was 5.8
months; 60% had typical hypsarrhythmia. Results: Initial suppression o
f spasms was obtained in 68% of infants with a median time to response
of 4 days at an average VGB dose of 99 mg/kg/day. The best response w
as seen in those infants with tuberous sclerosis (96% response) and in
those younger than 3 months at onset of spasms (90% response). Of the
se infants, 43 (22%) of 192 subsequently had other types of seizures,
and a recurrence of infantile spasms occurred in 28 (21%) of 131 respo
nders. At the end of this study, 96 of 192 infants who could be evalua
ted were seizure free with VGB monotherapy. Treatment appeared to be w
ell tolerated, with only 33 (13%) infants with adverse events, of whic
h the most common were somnolence (15 patients) and hyperkinesia (eigh
t patients). In only two cases did adverse events require VGB withdraw
al. Conclusion: This study supports the opinion that VGB may be consid
ered an initial treatment for IS regardless of cause.