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. 2021 Oct 8;89(8):765–770. doi: 10.1007/s12098-021-03918-y

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)