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. Author manuscript; available in PMC: 2010 Apr 1.
Published in final edited form as: J Child Neurol. 2009 Feb 18;24(4):400–405. doi: 10.1177/0883073808324538

Table 1. Patient demographics.

Thirty-one patients met inclusion criteria. A clinical diagnosis of spasms and an EEG report with hypsarrhythmia were both required for inclusion. The only difference we found between treatment groups was an older age at diagnosis in the topiramate treatment group. The rest of the demographics were similar between the ACTH and topiramate groups.

Initial Treatment
Topiramate ACTH
Male 8 7
Female 11 5
Average Age (months) 8.05 4.68*
Cryptogenic 2 3
Genetic 2 2
Clinical Etiology
HIE 3 1
Stroke 1 1
TS 0 0
Neurologic Exam Abnormality 17 8
MRI Abnormality 13 6
Other Physical Abnormality 6 2
Clinical Infantile Spasms
Average Duration Prior to
Treatment
2 (<1->12months) 1.5 (<1-3 months)
Flexor 15 8
Extensor 4 3
EEG Hypsarrhythmia 19 12

Average Age at diagnosis in months; cryptogenic= a normal MRI and clinical exams at the time of diagnosis. HIE - hypoxic ischemic encephalopathy, TS-tuberous sclerosis. Other physical abnormalities= non-neurologic disorders or congenital anomalies.

*

P=0.03 T-test with Welch correction.