Abstract | OBJECTIVE: METHODS: Eighty-five children with BECTS receiving topiramate treatment were randomly divided into A group (44 patients) and B group (41 patients). In A group, topiramate was orally administrated once a night, with a final dose of 2 mg/kg/day. In B group, topiramate was orally administrated twice a day, with a final dose of 4 mg/kg/day. At the end of the 12-month follow-up period, clinical efficacy, changes in electroencephalographic (EEG) activity, and adverse reactions were analyzed. RESULTS: There was no significant difference in overall efficacy rate, percentages of patients achieving seizure free, or changes in EEG activity between the two groups (P > 0.05). The rate of adverse reactions for A group was 9.1 %, which was significantly lower than the 29.3 % for B group (χ (2) = 4.262, P < 0.05). CONCLUSION: Nightly oral administration of topiramate is a feasible strategy for the treatment of BECTS, with the advantages of comparable efficacy, convenience, and fewer adverse reactions.
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Authors | Chunrong Liu, Mei Song, Jiwen Wang |
Journal | Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
(Childs Nerv Syst)
Vol. 32
Issue 5
Pg. 839-43
(May 2016)
ISSN: 1433-0350 [Electronic] Germany |
PMID | 26984807
(Publication Type: Journal Article, Randomized Controlled Trial)
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Chemical References |
- Anticonvulsants
- Topiramate
- Fructose
|
Topics |
- Administration, Oral
- Adolescent
- Anticonvulsants
(administration & dosage, therapeutic use)
- Brain
(physiopathology)
- Child
- Child, Preschool
- Drug Administration Schedule
- Electroencephalography
- Epilepsy, Rolandic
(drug therapy, physiopathology)
- Female
- Fructose
(administration & dosage, analogs & derivatives, therapeutic use)
- Humans
- Male
- Topiramate
- Treatment Outcome
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