Retrospective review was performed of children aged <3 years with epileptic
spasms at our center from 2004-2010. Short-term (<6 months) and long-term (≥6 months) outcomes were assessed. We included 173 children (104 boys; median age of onset, 6.8 months) with epileptic
spasms of known (62%) and unknown (38%) etiology. Treatments included
adrenocorticotropic hormone (n = 103),
vigabatrin (n = 82),
phenobarbital (n = 34), and other agents (n = 121). Short-term treatment with
adrenocorticotropic hormone and
vigabatrin provided better epileptic
spasm control in groups with known and unknown etiology than other agents. At follow-up (6-27 months), 54% of children manifested
seizures, and 83% manifested developmental delay. Known etiology was a predictor of poor developmental outcome (P = 0.006), whereas bilateral/diffuse brain lesions predicted both poor development and
seizures (P = 0.001 and 0.005, respectively). Initial presentations of epileptic
spasms with
hypotonia or developmental delay most strongly predicted both
seizures and neurodevelopmental outcomes (P < 0.001). In a child presenting with epileptic
spasms with developmental delay or
hypotonia, no specific treatment may offer superior benefit.