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. 2017 Jul 18;18(1):69. doi: 10.1186/s10194-017-0776-4

Table 1.

Characteristics of Studies Included in the Meta-Analysis

First authors, year Diagnostic tool Topiramate Placebo
N Age (years),mean ± SD Gender
(male:female,%)
Dose& Duration Side effects/Adverse events N Age (years),mean ± SD Gender (male: female,%)
Titration Maintenance
Paul Winner,2005 International Headache Society (IHS) diagnostic criteria for pediatric migraine 108 11.3 ± 2.5 50.9:49.1 8-week:
Week 1 = 15 mg/d
Week 2 = 30 mg/d
Week 3 = 50 mg/d
(dose increased to 2–3 mg/kg/d)
12-week: 2–3 mg/kg/d upper respiratory tract infection, anorexia, weight decrease, gastroenteritis, paresthesia, somnolence 49 10.7 ± 2.6 53.1:46.9
C. V. S. Lakshmi,2007 International Classification of Headache Disorders, 2nd Edition (ICHD-II) 21 10.95 ± 1.53 85.7:14.3 1-month: 25-mg incremented to 100 mg/d 3-month: 100 mg/d weight loss, lack of concentration in school, parasthesia, sedation, loss of appetite, pain in abdomen 21 10.14 ± 1.35 52.4:47.6
Donald Lewis,2009 International Classification of Headache Disorders, 2nd Edition (ICHD-II) 70 14.2 ± 1.54 40:60 4-week: 25-mg incremented to 50 or 100 mg/d 12-week: 50 or 100 mg/d upper respiratory tract infection, paresthesia, abdominal pain, anorexia, injury, rhinitis, coughing, viral infection, pharyngitis, fatigue, nausea, dizziness, taste perversion, insomnia, back pain, conjunctivitis, sinusitis, asthma, pneumonia, fever, allergy, vomiting, nervousness, somnolence, abnormal vision, eye pain 33 14.4 ± 1.7 36:64
Scott W.Powers,2017a International Classification of Headache Disorders, 2nd Edition (ICHD-II) 145 14.2 ± 2.5 30:70 8-week: 2 mg/Kg.d, dose escalation occurred every 2 weeks 16-week: average 1.93 ± 0.40 mg mg/Kg.d aphasia, cognitive disorder, dizziness, memory impairment, paresthesia, general: fatigue, dry mouth, intussusception, streptococcal pharyngitis, upper respiratory tract infection, altered mood, suicide attempt, investigations: decreased weight, contusion, traumatic liver injury, respiratory: bronchospasm 33 14.2 ± 2.2 32:68

SD standard deviations, N Total number in group

aThe analysis population included patients who ended trial early

†35 subjects treated with topiramate at 50 mg/day, 35 subjects treated with topiramate at 100 mg/day