PMID- 29784458 OWN - NLM STAT- MEDLINE DCOM- 20190326 LR - 20190326 IS - 1872-6844 (Electronic) IS - 0920-1211 (Linking) VI - 143 DP - 2018 Jul TI - Efficacy of antiepileptic drugs in the adjunctive treatment of refractory partial-onset seizures: Meta-analysis of pivotal trials. PG - 120-129 LID - S0920-1211(17)30176-6 [pii] LID - 10.1016/j.eplepsyres.2017.10.004 [doi] AB - OBJECTIVE: In the absence of randomized clinical trials (RCTs) assessing the relative efficacy of antiepileptic drugs (AEDs), meta-analyses are useful resources for informing treatment choices. This meta-analysis assesses the relative efficacy and tolerability of AEDs for adjunctive treatment of refractory partial onset seizures (POS). METHODS: A systematic literature review was conducted to identify pivotal AED trials serving as the basis for US Food and Drug Administration (FDA) approval. INCLUSION CRITERIA: 1) double-blind, placebo-controlled, parallel-group design, with 8- to 14-week maintenance period; 2) enrolled patients >/=16years with refractory POS, including complex partial seizures; 3) study was conducted between 1993 and 2013; and; 4) patients received FDA-approved dosage. Outcomes analyzed: 1) 50% responder rate (>/=50% reduction from baseline in seizure frequency); 2) seizure freedom (proportion of seizure-free patients); and 3) discontinuation due to adverse events (AEs). DerSimonian and Laird random-effects model was used to derive odds ratios (OR) and 95% confidence intervals (CI). RESULTS: A total of 29 publications for 11 AEDs (eslicarbazepine, ezogabine, gabapentin, lacosamide, levetiracetam, perampanel, pregabalin, tiagabine, topiramate, vigabatrin, and zonisamide) were included in the meta-analysis. Tiagabine 56mg/day (OR 8.82, 95% CI: 2.77-28.11), pregabalin 600mg/day (OR 8.08, 95% CI: 5.45-11.98), and vigabatrin 3000mg/day (OR 6.23, 95% CI: 1.46-26.20) had the highest OR versus placebo of 50% response. The odds of seizure freedom were >/=7 times greater than placebo for levetiracetam 3000mg/day (OR 11.00, 95% CI: 2.08-58.06), vigabatrin 3000mg/day (OR 7.41, 95% CI: 1.31-41.84), and ezogabine 1200mg/day (OR 7.09, 95% CI: 0.36-58.06). Patients were more likely to discontinue any AED (except low-dose pregabalin) than placebo. CONCLUSION: In this meta-analysis of >9000 patients, those treated with AEDs were more likely than placebo to achieve seizure response or freedom. Patients receiving pregabalin, tiagabine, and vigabatrin had the highest odds of >/=50% reduction in seizures, and patients receiving ezogabine, levetiracetam, and vigabatrin had the highest odds of seizure freedom. CI - Copyright (c) 2017 The Authors. Published by Elsevier B.V. All rights reserved. FAU - Slater, Jeremy AU - Slater J AD - University of Texas Health Science Center at Houston, Houston, TX, USA. Electronic address: Jeremy.D.Slater@uth.tmc.edu. FAU - Chung, Steve AU - Chung S AD - Banner University Medical Center, Phoenix, AZ, USA. FAU - Huynh, Lynn AU - Huynh L AD - Analysis Group, Inc, Boston, MA, USA. FAU - Duh, Mei Sheng AU - Duh MS AD - Analysis Group, Inc, Boston, MA, USA. FAU - Gorin, Brian AU - Gorin B AD - Analysis Group, Inc, Boston, MA, USA. FAU - McMicken, Carolyn AU - McMicken C AD - Lundbeck LLC, Deerfield, IL, USA. FAU - Ziemann, Adam AU - Ziemann A AD - Lundbeck LLC, Deerfield, IL, USA. FAU - Isojarvi, Jouko AU - Isojarvi J AD - Lundbeck LLC, Deerfield, IL, USA. LA - eng PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't PT - Systematic Review PL - Netherlands TA - Epilepsy Res JT - Epilepsy research JID - 8703089 RN - 0 (Anticonvulsants) SB - IM MH - Anticonvulsants/*therapeutic use MH - Chemotherapy, Adjuvant MH - Drug Resistance MH - Drug Resistant Epilepsy/drug therapy MH - Epilepsies, Partial/drug therapy MH - Humans MH - Seizures/*drug therapy OTO - NOTNLM OT - AEDs OT - Antiepileptic drugs OT - Meta-analysis OT - Refractory partial-onset seizures OT - rPOS EDAT- 2018/05/23 06:00 MHDA- 2019/03/27 06:00 CRDT- 2018/05/23 06:00 PHST- 2017/03/24 00:00 [received] PHST- 2017/07/14 00:00 [revised] PHST- 2017/10/03 00:00 [accepted] PHST- 2018/05/23 06:00 [entrez] PHST- 2018/05/23 06:00 [pubmed] PHST- 2019/03/27 06:00 [medline] AID - S0920-1211(17)30176-6 [pii] AID - 10.1016/j.eplepsyres.2017.10.004 [doi] PST - ppublish SO - Epilepsy Res. 2018 Jul;143:120-129. doi: 10.1016/j.eplepsyres.2017.10.004.