A follow-up study on newer anti-epileptic drugs as add-on and monotherapy for partial epilepsy in China.
- Author:
Hui-cong KANG
1
;
Qi HU
;
Xiao-yan LIU
;
Zhi-guang LIU
;
Zheng ZENG
;
Jian-lin LIU
;
Min WANG
;
Yan-ling LIANG
;
Sui-qiang ZHU
Author Information
- Publication Type:Journal Article
- MeSH: Anticonvulsants; therapeutic use; Carbamazepine; analogs & derivatives; therapeutic use; China; Epilepsies, Partial; drug therapy; Follow-Up Studies; Fructose; analogs & derivatives; therapeutic use; Humans; Treatment Outcome; Triazines; therapeutic use
- From: Chinese Medical Journal 2012;125(4):646-651
- CountryChina
- Language:English
-
Abstract:
BACKGROUNDRecently, new anti-epileptic drugs (AEDs) have been more frequently selected to treat epilepsy. In the present study, we evaluated the dynamic changes of efficacy and safety of three newer AEDs for treating partial epilepsy in China.
METHODSPatients were collected sequentially and were divided into three groups which accepted oxcarbazepine (OXC), lamotrigine (LTG) or topiramate (TPM) therapy. Each group included monotherapy and add-on therapy subgroups. We followed all patients for one year and recorded the indexes of efficacy and safety in detail.
RESULTSA total of 909 patients finished the follow-up observation. No significant difference was found in proportion of patients with > or = 50% reduction, > or = 75% reduction and 100% seizure reduction in the LTG and OXC groups between the first and the second six months. In the TPM group there was a statistical difference between the first and the second six months in proportion of patients with > or = 50% reduction (P = 0.002), > or = 75% reduction (P < 0.0001) and 100% seizure reduction (P = 0.009) in the monotherapy subgroup, and about > or = 75% reduction and 100% seizure reduction in the add-on therapy subgroup (P < 0.0001). The efficacy between the add-on and monotherapy subgroups showed a statistical difference. The safety of the three newer AEDs was good.
CONCLUSIONSThe three newer AEDs all showed good efficacy and tolerability for partial epilepsy. And the efficacy can be maintained for at least one year.