PMID- 21159526 OWN - NLM STAT- MEDLINE DCOM- 20110701 LR - 20221207 IS - 1532-2688 (Electronic) IS - 1059-1311 (Linking) VI - 20 IP - 3 DP - 2011 Apr TI - Comparison of the retention rates between carbamazepine and valproate as an initial monotherapy in Chinese patients with partial seizures: A ten-year follow-up, observational study. PG - 208-13 LID - 10.1016/j.seizure.2010.11.020 [doi] AB - PURPOSE: To compare the long-term retention rates of the two most commonly prescribed antiepileptic drugs (AEDs), carbamazepine (CBZ) and valproate (VPA) as an initial monotherapy in Chinese patients with partial seizures. METHODS: This is a retrospective, observational study in a tertiary epilepsy centre. Overall, 584 patients were followed during a ten-year period. Kaplan-Meier survival analysis was used to estimate the cumulative probability of retention. Cox proportional hazard model was used to analyze the risk factors for retention rate. RESULTS: The calculated retention rates estimated by Kaplan-Meier survival analysis showed no difference between CBZ and VPA (p=0.074). During the time period from the first six months to two years, the lack of efficacy (LE) that led to drug discontinuation was 10.7% for CBZ compared to 4.5% for VPA (p=0.004). The adverse effects (AEs) that led to discontinuation was 2.4% for CBZ compared to 6.3% for VPA (p=0.025). Clinical control that led to discontinuation was 15.9% for CBZ compared to 7.5% for VPA (p=0.001). The five-year remission rate was higher in the CBZ group (33.3%) than in the VPA group (23.2%, p=0.006). Yet in the complex partial seizure subgroup, there was no significant difference between the two drugs (p=0.61). CONCLUSION: Compared with VPA, patients treated with CBZ were more likely to discontinue treatment for LE, and were less likely to discontinue for AEs; however, the two differences above only occurred in the time period between the first six months to two years of treatment. Long-term treatment with CBZ appeared to be more effective in terms of five-year remission and clinical control than VPA. CI - Copyright (c) 2010 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved. FAU - Hu, Yida AU - Hu Y AD - Department of Neurology, The First Affiliated Hospital, Chongqing Medical University, Chongqing 400016, People's Republic of China. FAU - Huang, Yuanyuan AU - Huang Y FAU - Quan, Fengying AU - Quan F FAU - Hu, Yuming AU - Hu Y FAU - Lu, Yang AU - Lu Y FAU - Wang, Xue-Feng AU - Wang XF LA - eng PT - Comparative Study PT - Journal Article DEP - 20101215 PL - England TA - Seizure JT - Seizure JID - 9306979 RN - 0 (Anticonvulsants) RN - 33CM23913M (Carbamazepine) RN - 614OI1Z5WI (Valproic Acid) SB - IM MH - Adult MH - Anticonvulsants/*therapeutic use MH - Asian People MH - Carbamazepine/*therapeutic use MH - Epilepsies, Partial/*drug therapy MH - Female MH - Humans MH - Kaplan-Meier Estimate MH - Longitudinal Studies MH - Male MH - Observation MH - Proportional Hazards Models MH - *Treatment Outcome MH - Valproic Acid/*therapeutic use MH - Young Adult EDAT- 2010/12/17 06:00 MHDA- 2011/07/02 06:00 CRDT- 2010/12/17 06:00 PHST- 2010/09/09 00:00 [received] PHST- 2010/11/18 00:00 [revised] PHST- 2010/11/22 00:00 [accepted] PHST- 2010/12/17 06:00 [entrez] PHST- 2010/12/17 06:00 [pubmed] PHST- 2011/07/02 06:00 [medline] AID - S1059-1311(10)00303-1 [pii] AID - 10.1016/j.seizure.2010.11.020 [doi] PST - ppublish SO - Seizure. 2011 Apr;20(3):208-13. doi: 10.1016/j.seizure.2010.11.020. Epub 2010 Dec 15.