Superior seizure control with first-line levetiracetam in very low birth weight neonates: a 10-year comparative retrospective study.

Q2 Pharmacology, Toxicology and Pharmaceutics
Drug metabolism and personalized therapy Pub Date : 2026-05-28 eCollection Date: 2026-06-01 DOI:10.1515/dmpt-2026-0011
Coşkun Armağan, Begüm Nişancı Öğünçlü, Mustafa Halk, Uluç Yiş, Ayşe Semra Hız Kurul, Funda Erdoğan, Nuray Duman, Hasan Özkan
{"title":"Superior seizure control with first-line levetiracetam in very low birth weight neonates: a 10-year comparative retrospective study.","authors":"Coşkun Armağan, Begüm Nişancı Öğünçlü, Mustafa Halk, Uluç Yiş, Ayşe Semra Hız Kurul, Funda Erdoğan, Nuray Duman, Hasan Özkan","doi":"10.1515/dmpt-2026-0011","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Very low birth weight (VLBW) infants are at disproportionately high risk for neonatal seizures, yet optimal first-line antiseizure medication (ASM) strategies in this vulnerable population remain a matter of debate. Over the past decade, levetiracetam (LEV) has emerged as a promising alternative to phenobarbital (PB), driven by growing concerns over PB's limited efficacy and potential neurotoxic effects.</p><p><strong>Methods: </strong>This retrospective cohort study analyzed medical records of VLBW infants treated for seizures at our Neonatal Intensive Care Unit from 2013 to 2023. We compared the efficacy and safety of LEV and PB as initial antiepileptic treatments. Data on gestational age, birth weight, type of seizures, electroencephalogram findings, and treatment outcomes were meticulously collected and analyzed.</p><p><strong>Results: </strong>The study included 103 VLBW infants (mean gestational age 26.17±2.31 weeks); 27 received LEV and 76 received PB. Baseline demographic and clinical characteristics were comparable between the two groups. Although the LEV group had a higher proportion of infants with severe intraventricular hemorrhage and necrotizing enterocolitis indicating a potentially more critical baseline, these differences were not statistically significant. The primary outcome revealed that significantly fewer infants in the LEV group were unresponsive to initial treatment compared to the PB group (14.8 vs. 56.6 %; p<0.001). Furthermore, lower gestational age was identified as a significant risk factor for PB unresponsiveness.</p><p><strong>Conclusions: </strong>This study supports that LEV is more successful in clinical seizure control compared to PB as the first choice in ASM selection in VLBW. If our study results are supported by randomized controlled prospective studies, LEV, with its potentially fewer side effects, could be included in clinical algorithms as the first-choice ASM especially for VLBW.</p>","PeriodicalId":11332,"journal":{"name":"Drug metabolism and personalized therapy","volume":" ","pages":"109-117"},"PeriodicalIF":0.0000,"publicationDate":"2026-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug metabolism and personalized therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/dmpt-2026-0011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/6/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: Very low birth weight (VLBW) infants are at disproportionately high risk for neonatal seizures, yet optimal first-line antiseizure medication (ASM) strategies in this vulnerable population remain a matter of debate. Over the past decade, levetiracetam (LEV) has emerged as a promising alternative to phenobarbital (PB), driven by growing concerns over PB's limited efficacy and potential neurotoxic effects.

Methods: This retrospective cohort study analyzed medical records of VLBW infants treated for seizures at our Neonatal Intensive Care Unit from 2013 to 2023. We compared the efficacy and safety of LEV and PB as initial antiepileptic treatments. Data on gestational age, birth weight, type of seizures, electroencephalogram findings, and treatment outcomes were meticulously collected and analyzed.

Results: The study included 103 VLBW infants (mean gestational age 26.17±2.31 weeks); 27 received LEV and 76 received PB. Baseline demographic and clinical characteristics were comparable between the two groups. Although the LEV group had a higher proportion of infants with severe intraventricular hemorrhage and necrotizing enterocolitis indicating a potentially more critical baseline, these differences were not statistically significant. The primary outcome revealed that significantly fewer infants in the LEV group were unresponsive to initial treatment compared to the PB group (14.8 vs. 56.6 %; p<0.001). Furthermore, lower gestational age was identified as a significant risk factor for PB unresponsiveness.

Conclusions: This study supports that LEV is more successful in clinical seizure control compared to PB as the first choice in ASM selection in VLBW. If our study results are supported by randomized controlled prospective studies, LEV, with its potentially fewer side effects, could be included in clinical algorithms as the first-choice ASM especially for VLBW.

极低出生体重新生儿一线左乙拉西坦优越的癫痫控制:一项10年比较回顾性研究
目的:极低出生体重(VLBW)婴儿的新生儿癫痫发作风险高得不成比例,但这一弱势群体的最佳一线抗癫痫药物(ASM)策略仍存在争议。在过去的十年中,由于人们越来越关注苯巴比妥有限的疗效和潜在的神经毒性作用,左乙拉西坦(LEV)已成为苯巴比妥(PB)的一种有希望的替代品。方法:本回顾性队列研究分析了2013年至2023年在我院新生儿重症监护室治疗癫痫发作的VLBW婴儿的医疗记录。我们比较了LEV和PB作为初始抗癫痫治疗的疗效和安全性。仔细收集和分析孕龄、出生体重、癫痫发作类型、脑电图结果和治疗结果等数据。结果:研究纳入103例VLBW婴儿(平均胎龄26.17±2.31周);LEV 27例,PB 76例。两组患者的基线人口学和临床特征具有可比性。虽然LEV组婴儿出现严重脑室内出血和坏死性小肠结肠炎的比例更高,表明基线可能更为关键,但这些差异没有统计学意义。主要结果显示,与PB组相比,LEV组对初始治疗无反应的婴儿显著减少(14.8% vs. 56.6% %)。结论:本研究支持LEV在临床癫痫控制方面比PB更成功,是VLBW患者ASM选择的首选。如果我们的研究结果得到随机对照前瞻性研究的支持,LEV可能副作用更小,可以作为首选ASM纳入临床算法,特别是VLBW。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Drug metabolism and personalized therapy
Drug metabolism and personalized therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
2.30
自引率
0.00%
发文量
35
期刊介绍: Drug Metabolism and Personalized Therapy (DMPT) is a peer-reviewed journal, and is abstracted/indexed in relevant major Abstracting Services. It provides up-to-date research articles, reviews and opinion papers in the wide field of drug metabolism research, covering established, new and potential drugs, environmentally toxic chemicals, the mechanisms by which drugs may interact with each other and with biological systems, and the pharmacological and toxicological consequences of these interactions and drug metabolism and excretion. Topics: drug metabolizing enzymes, pharmacogenetics and pharmacogenomics, biochemical pharmacology, molecular pathology, clinical pharmacology, pharmacokinetics and drug-drug interactions, immunopharmacology, neuropsychopharmacology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书