PMID- 35301936 OWN - NLM STAT- MEDLINE DCOM- 20230810 LR - 20230810 IS - 1563-5279 (Electronic) IS - 0020-7454 (Linking) VI - 133 IP - 9 DP - 2023 Dec TI - Efficacy and safety of perampanel for the treatment of epilepsy in adolescents: a meta-analysis. PG - 1008-1016 LID - 10.1080/00207454.2022.2032045 [doi] AB - BACKGROUND: In the present meta-analysis, the efficacy and safety of perampanel (PER) for the treatment of adolescents with epilepsy were assessed. METHODS: Keyword searches were performed in Embase, PubMed, Cochrane Library, Web of Science, EBSCO and CNKI from 1 January 2020 to 10 October 2020. The randomized controlled trials (RCTs) and case-control studies in which PER was compared with other Anti-seizure drugs (ASDs) and/or placebo in children with epilepsy, were considered eligible studies. Odds ratio (OR) with 95% confidence interval (95% CI) for the dichotomous outcome statistic was calculated using a fixed-effects or random-effects model. RESULTS: Three RCTs with a total of 372 adolescents' patients were included in this meta-analysis. Placebo was used as a control in these studies. Compared with placebo, PER showed better efficacy in median seizure frequency reduction from baseline per 28 days (OR = 2.49, 95% CI: 1.25-4.96, p = 0.009) and in responder rate (OR = 1.87, 95% CI: 1.15-3.05, p = 0.01); both were considered statistically increased in PER group. Regarding adverse effects (AEs), significant differences between PER and placebo (OR = 1.47, 95% CI: 0.92-2.41, p = 0.11) were not found, and the most common AEs of PER were dizziness (24.0%), somnolence (15.9%), headache (11.2%), nasopharyngitis (9.7%), upper respiratory tract infection (7.0%) and aggression (7.0%). CONCLUSION: Based on the results in this study, PER showed better efficacy than placebo therapy in children with epilepsy and the AEs were similar in PER group and placebo group. PER showed good efficacy and a low risk of AEs, and might be a promising medication for the treatment of pediatric epilepsy. In the future, well-designed and large-scale RCTs are necessary to validate the present findings. FAU - Wang, Ting AU - Wang T AD - Department of Pediatrics, The First Affiliated Hospital of Xi'an Jiaotong University, Shaanxi, China. FAU - Li, Limin AU - Li L AD - Department of Pediatrics, The First Affiliated Hospital of Xi'an Jiaotong University, Shaanxi, China. FAU - Sun, Fei AU - Sun F AD - Department of Pediatrics, The First Affiliated Hospital of Xi'an Jiaotong University, Shaanxi, China. FAU - Yang, Yonghua AU - Yang Y AD - Department of Pediatrics, The First Affiliated Hospital of Xi'an Jiaotong University, Shaanxi, China. FAU - Liu, Xiaohong AU - Liu X AD - Department of Pediatrics, The First Affiliated Hospital of Xi'an Jiaotong University, Shaanxi, China. LA - eng PT - Journal Article PT - Meta-Analysis DEP - 20220318 PL - England TA - Int J Neurosci JT - The International journal of neuroscience JID - 0270707 RN - H821664NPK (perampanel) RN - 0 (Anticonvulsants) SB - IM MH - Humans MH - Child MH - Adolescent MH - Anticonvulsants/adverse effects MH - Treatment Outcome MH - *Epilepsies, Partial/drug therapy MH - *Epilepsy/drug therapy/chemically induced OTO - NOTNLM OT - Epilepsy OT - adolescents OT - efficacy OT - meta-analysis OT - perampanel OT - safety EDAT- 2022/03/19 06:00 MHDA- 2023/08/10 06:43 CRDT- 2022/03/18 08:39 PHST- 2023/08/10 06:43 [medline] PHST- 2022/03/19 06:00 [pubmed] PHST- 2022/03/18 08:39 [entrez] AID - 10.1080/00207454.2022.2032045 [doi] PST - ppublish SO - Int J Neurosci. 2023 Dec;133(9):1008-1016. doi: 10.1080/00207454.2022.2032045. Epub 2022 Mar 18.