Misra Shubham, Wang Selena, Quinn Terence J, Dawson Jesse, Zelano Johan, Tanaka Tomotaka, Grotta James C, Khan Erum, Beriwal Nitya, Funaro Melissa C, Perla Sravan, Dev Priya, Larsson David, Hussain Taimoor, Liebeskind David S, Yasuda Clarissa Lin, Altalib Hamada Hamid, Zaveri Hitten P, Elshahat Amr, Hitawala Gazala, Wang Ethan Y, Kitagawa Rachel, Pathak Abhishek, Scalzo Fabien, Ihara Masafumi, Sunnerhagen Katharina S, Walters Matthew R, Zhao Yize, Jette Nathalie, Kasner Scott E, Kwan Patrick, Mishra Nishant K
Department of Neurology, Yale University School of Medicine, New Haven, CT.
Department of Biostatistics, Yale University School of Public Health, New Haven, CT.
Neurology. 2025 Feb 11;104(3):e210231. doi: 10.1212/WNL.0000000000210231. Epub 2025 Jan 14.
The most effective antiseizure medications (ASMs) for poststroke seizures (PSSs) remain unclear. We aimed to determine outcomes associated with ASMs in people with PSS.
We systematically searched electronic databases for studies on patients with PSS on ASMs. Our outcomes were seizure recurrence, adverse events, drug discontinuation rate, and mortality. We assessed the risk of bias using Cochrane Risk of Bias tool for randomized controlled trials and Risk Of Bias In Non-randomized Studies of Interventions tools. Using levetiracetam as the reference treatment, we conducted a frequentist network meta-analysis and determined the certainty of evidence using the Grading of Recommendations Assessment, Development, and Evaluation methodology.
Our search yielded 15 studies (3 randomized, 12 nonrandomized, N = 18,676 patients (121 early and 18,547 late seizures), 60% male, mean age 69 years) comparing 13 ASMs. Three studies had moderate and 12 had high risk of bias. Seizure recurrence was 24.8%. Compared with levetiracetam, very low-certainty evidence suggested that phenytoin was associated with higher seizure recurrences (odds ratio [OR] 7.3, 95% CI 3.7-14.5) and more adverse events (OR 5.2, 95% CI 1.2-22.9). Low-certainty evidence suggested that carbamazepine (OR 1.8, 95% CI 1.5-2.2) and phenytoin (OR 1.9, 95% CI 1.4-2.8) were associated with high drug discontinuation rates. Moderate to high-certainty evidence suggested that valproic acid (OR 4.7, 95% CI 3.6-6.3) and phenytoin (OR 8.3, 95% CI 5.7-11.9) were associated with higher mortality rates. Considering all treatments and using the GRADE approach for treatment ranking, very low-certainty evidence suggested that eslicarbazepine, lacosamide, and levetiracetam had the fewest seizure recurrences. Low to very low-certainty evidence suggested that lamotrigine had the fewest adverse events and drug discontinuations, whereas lamotrigine and levetiracetam exhibited low mortality rates with moderate-certainty evidence.
We found that levetiracetam and lamotrigine may be safe and tolerable ASMs for PSS. Despite ASM use, the seizure recurrence rate remains high in the PSS population. Owing to bias and confounding risks, these findings should be interpreted cautiously.
PROSPERO: CRD42022363844.
治疗卒中后癫痫(PSS)最有效的抗癫痫药物(ASM)仍不明确。我们旨在确定ASM治疗PSS患者的疗效。
我们系统检索电子数据库,查找有关使用ASM治疗PSS患者的研究。我们的观察指标为癫痫复发、不良事件、停药率和死亡率。我们使用Cochrane偏倚风险工具评估随机对照试验的偏倚风险,并使用干预性非随机研究中的偏倚风险工具。以左乙拉西坦作为对照治疗,我们进行了频率学派网状Meta分析,并使用推荐分级的评估、制定与评价方法确定证据的确定性。
我们的检索共纳入15项研究(3项随机对照试验,12项非随机对照试验,N = 18,676例患者(121例早期癫痫和18,547例晚期癫痫),男性占60%,平均年龄69岁),比较了13种ASM。3项研究存在中度偏倚风险,12项研究存在高度偏倚风险。癫痫复发率为24.8%。与左乙拉西坦相比,极低确定性证据表明苯妥英钠与更高的癫痫复发率相关(比值比[OR] 7.3,95%置信区间[CI] 3.7 - 14.5)以及更多的不良事件(OR 5.2,95% CI 1.2 - 22.9)。低确定性证据表明卡马西平(OR 1.8,95% CI 1.5 - 2.2)和苯妥英钠(OR 1.9,95% CI 1.4 - 2.8)与高停药率相关。中度至高度确定性证据表明丙戊酸(OR 4.7,95% CI 3.6 - 6.3)和苯妥英钠(OR 8.3,95% CI 5.7 - 11.9)与更高的死亡率相关。考虑所有治疗方法并使用GRADE方法进行治疗排序,极低确定性证据表明艾司利卡西平、拉科酰胺和左乙拉西坦的癫痫复发最少。低至极低确定性证据表明拉莫三嗪的不良事件和停药最少,而拉莫三嗪和左乙拉西坦在中度确定性证据下显示出低死亡率。
我们发现左乙拉西坦和拉莫三嗪可能是治疗PSS安全且耐受性良好的ASM。尽管使用了ASM,但PSS患者的癫痫复发率仍然很高。由于存在偏倚和混杂风险,这些结果应谨慎解释。
PROSPERO:CRD42022363844。