Hooper Robert G, Ramaswamy Viraraghavan Vadakkencherry, Wahid Rachael M, Satodia Prakash, Bhulani Adarsh
University of Warwick, Coventry, UK.
University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
Dev Med Child Neurol. 2021 Nov;63(11):1283-1293. doi: 10.1111/dmcn.14943. Epub 2021 Jun 13.
To assess the effectiveness and safety of levetiracetam when used as first-line treatment of neonatal seizures.
Four electronic databases, Medline, Embase, Web of Science, and ClinicalTrials.gov were systematically searched from inception until 20th November 2020. Randomized controlled trials (RCTs) and observational studies that included neonates born preterm and term were eligible for inclusion. The primary outcome measure was levetiracetam effectiveness, defined as seizure cessation within 24 hours of starting treatment. Secondary outcomes included short-term adverse events, mortality before discharge, and long-term neurodevelopmental outcomes.
Fourteen studies assessing 1188 neonates were included: four RCTs, three observational trials with phenobarbital as the control arm, and seven observational studies of levetiracetam with no control arm. Pooled efficacy of levetiracetam from observational studies was 45% (95% confidence interval [CI] 34-57%) (GRADE - very low). Meta-analysis of RCTs evaluating levetiracetam versus phenobarbital showed that both were equally effective (risk ratio [95% CI] 0.6 [0.30-1.20]) (GRADE - very low). Levetiracetam resulted in a lower risk of short-term adverse events compared to phenobarbital (risk ratio [95% CI] 0.24 [0.06-0.92]) (GRADE - moderate).
Very low certainty of evidence suggests levetiracetam might not be more effective than phenobarbital. Moderate certainty of evidence indicates levetiracetam is associated with a lower risk of adverse events. Future trials on neonatal antiseizure medication therapy should include continuous electroencephalogram (EEG) monitoring as standard of care and enrol a homogenous population with similar seizure aetiology. What this paper adds Levetiracetam is effective in 45% of neonatal seizures. Levetiracetam might not be more effective than phenobarbital. Levetiracetam is likely to be safer than phenobarbital. Evidence available is limited and of very low certainty.
评估左乙拉西坦作为新生儿惊厥一线治疗药物的有效性和安全性。
系统检索了4个电子数据库,即Medline、Embase、Web of Science和ClinicalTrials.gov,检索时间从建库至2020年11月20日。纳入包括早产和足月出生新生儿的随机对照试验(RCT)和观察性研究。主要结局指标是左乙拉西坦的有效性,定义为开始治疗后24小时内惊厥停止。次要结局包括短期不良事件、出院前死亡率和长期神经发育结局。
纳入了评估1188例新生儿的14项研究:4项RCT、3项以苯巴比妥为对照臂的观察性试验以及7项无对照臂的左乙拉西坦观察性研究。观察性研究中左乙拉西坦的合并疗效为45%(95%置信区间[CI]34 - 57%)(GRADE - 极低)。评估左乙拉西坦与苯巴比妥对比的RCT的荟萃分析表明,两者同样有效(风险比[95%CI]0.6[0.30 - 1.20])(GRADE - 极低)。与苯巴比妥相比,左乙拉西坦导致短期不良事件的风险更低(风险比[95%CI]0.24[0.06 - 0.92])(GRADE - 中等)。
证据的确定性极低表明左乙拉西坦可能并不比苯巴比妥更有效。证据的确定性中等表明左乙拉西坦与较低的不良事件风险相关。未来关于新生儿抗惊厥药物治疗的试验应将连续脑电图(EEG)监测作为标准治疗措施,并纳入具有相似惊厥病因的同质人群。本文补充内容:左乙拉西坦对45%的新生儿惊厥有效。左乙拉西坦可能并不比苯巴比妥更有效。左乙拉西坦可能比苯巴比妥更安全。现有证据有限且确定性极低。