Efficacy, tolerability and safety of add-on third-generation antiseizure medications in treating focal seizures worldwide: a network meta-analysis of randomised, placebo-controlled trials.

Journal: EClinicalMedicine

Volume: 70

Issue: 

Year of Publication: 

Affiliated Institutions:  Department of Neurology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, , China. Department of Respiratory, The Ninth People's Hospital of Chongqing, Chongqing, , China. Department of Medical Records, Heze Municipal Hospital, Heze, , China. Department of Neurology, Heze Third People's Hospital, Heze, , China. Department of Neurology, Shandong Provincial Hospital Heze Branch, Heze, , China. Department of Neurology, Heze Mudan District People's Hospital, Heze, , China. Department of Neurology, Juancheng County People's Hospital, Juancheng, , China. Department of Neurology, Heze Municipal Hospital Brain Hospital, Heze, , China. Mental Health Center, University-Town Hospital of Chongqing Medical University, Chongqing, , China.

Abstract summary 

Adjunctive newer antiseizure medications (ASMs) are being used in patients with treatment-resistant focal-onset seizures (FOS). An updated network meta-analysis (NMA) was necessary to compile evidence in this critical area.We systematically searched PubMed, Embase, Cochrane Library, Web of Science, and Scopus from their inception until 17 January 2024, evaluating the efficacy, tolerability, and safety of rufinamide (RUF), brivaracetam (BRV), cenobamate (CNB), eslicarbazepine (ESL), lacosamide (LCM), retigabine (RTG), and perampanel (PER) as adjunctive treatments for FOS. Efficacy outcomes included seizure response and seizure freedom. Tolerability was assessed by discontinuation due to adverse events (AEs). Safety outcomes were evaluated based on the number of patients experiencing at least one AE and serious adverse events (SAEs). This review is registered with PROSPERO (CRD42023485130).A total of 29 studies involving 11,750 participants were included. For seizure response, all ASMs were significantly superior to placebo, with RTG ranking highest, followed by CNB. Considering dosage, CNB 400 mg/d was top-ranked, followed by RTG 1200 mg/d. For seizure freedom, BRV was highest-ranked, followed by CNB, with BRV 100 mg/d leading, followed by CNB 400 mg/d. Regarding tolerability, LCM 600 mg/d had the lowest ranking, followed by CNB 400 mg/d. For the safety outcome of AEs, ESL 1200 mg/d was ranked lowest, followed by CNB 400 mg/d. Regarding SAEs, LCM 400 mg/d was ranked lowest, followed by RTG 1200 mg/d.ASMs at different dosages have varying efficacy and tolerability profiles. We have provided hierarchical rankings of ASMs for efficacy and safety outcomes. Our findings offer the most comprehensive evidence available to inform patients, families, physicians, guideline developers, and policymakers about the choice of ASMs in patients with treatment-resistant FOS.None.

Authors & Co-authors:  Chen Li Lu Gao Song Zhang Zhao Cai Guo Zhou Chen

Study Outcome 

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Statistics
Citations :  Chang B.S., Lowenstein D.H. Epilepsy. N Engl J Med. 2003;349(13):1257–1266. doi: 10.1056/NEJMra022308.
Authors :  11
Identifiers
Doi : 102513
SSN : 2589-5370
Study Population
Male,Female
Mesh Terms
Other Terms
Antiseizure medications;Epilepsy;Focal seizures;Network meta-analysis;Seizure
Study Design
Study Approach
Country of Study
Publication Country
England