We reviewed the outcome (developmental, neurologic, and seizure) and p
rognostic factors of 57 cases of infantile spasms (17 cryptogenic, 40
symptomatic). The mean developmental score of the cryptogenic group (7
1.2 +/- 24.2) was significantly higher than that of the symptomatic gr
oup (48.4 +/- 24.5), as assessed by the Griffith Mental Developmental
Scale. A resultant neurologic deficit was present in 23.5% of the cryp
togenic group and 75.0% of the symptomatic group. Coexistence of other
forms of seizures was observed in 35.3% of the cryptogenic group and
57.5% of the symptomatic group. Outcome was affected by the coexistenc
e of other seizures, presence of neurologic deficit, time lag in initi
ation of treatment (cognitive outcome only), poor response to ACTH tre
atment, and persistent EEG abnormality. Character of spasms and time l
ag in initiation of treatment (seizure outcome only) did not have any
significant effect on outcome.