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. 2017 Apr 23;2017(4):CD010008. doi: 10.1002/14651858.CD010008.pub3
Methods Randomized open‐label observational study
Participants 33 participants with juvenile myoclonic epilepsy
Interventions Participants were assigned as 1:1 ratio to topiramate (16 participants) or valproate (17 participants) for 32 weeks. The assigned antiepileptic drug was titrated up to 1200 mg/day for valproate or 100 mg/day for topiramate. The dose of valproate was titrated up 300 mg/day for 2 weeks, whereas topiramate was increased 25 mg/day for 2 weeks. In participants with a poor response to medication during the 24‐week maintenance phase, the dose of valproate was increased 300 mg/day for 1 month to a maximum dose of 2400 mg/day, and the dose of topiramate was increased 50 mg/day for 1 month to a maximum 300 mg/day
Outcomes Number of days without myoclonic seizures during the 24‐week maintenance period, adverse events
Notes Baseline period was not clear. An 8‐week titration phase was followed by a 24‐week maintenance phase
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Low risk Participants underwent computerized randomization in a 1 : 1 ratio to primary treatment with topiramate or valproate
Allocation concealment (selection bias) Unclear risk Not reported
Blinding of participants and personnel (performance bias) All outcomes Unclear risk Not reported
Blinding of outcome assessment (detection bias) All outcomes Unclear risk Not reported
Incomplete outcome data (attrition bias) All outcomes High risk 1 (6%) participant who was randomized to topiramate was removed from the study due to severe anorexia. 4 (25%) participants from the topiramate group and 1 (6%) participant from the valproate group were lost to follow‐up
Selective reporting (reporting bias) Unclear risk No pre published protocol
Other bias Low risk No other bias was found

PGTCS: primarily generalized tonic‐clonic seizures.