Table 2.
Epilepsy and neurodevelopmental outcomes in children with West syndrome
Outcomes | N = 114 |
---|---|
Clinical response to standard therapy; N (%) | |
Complete cessation of spasms | 61 (53.5) |
No response | 53 (46.5) |
Evolution to Lennox–Gastaut syndrome; N (%) | 17 (15%) |
Seizure status at 2 y; N (%) | |
Seizure freedom | 42 (36) |
Ongoing seizures | 72 (64) |
Social quotient as per VSMS; N (%) | |
≥ 70 | 16 (14) |
55–69 | 11 (9.6) |
40–54 | 9 (7.9) |
26–39 | 19 (16.7) |
≤ 25 | 59 (51.8) |