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苯妥英钠和左乙拉西坦治疗急性脑炎综合征儿童急性症状性发作的疗效和安全性:一项开放标签、随机对照试验。

Efficacy and safety of phenytoin and levetiracetam for acute symptomatic seizures in children with acute encephalitis syndrome: an open label, randomised controlled trial.

机构信息

Pediatric Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, Rishikesh, Uttarakhand 249203, India.

Pediatric Intensive Care Division, Department of Pediatrics, All India Institute of Medical Sciences, Rishikesh, Uttarakhand 249203, India.

出版信息

Seizure. 2024 May;118:110-116. doi: 10.1016/j.seizure.2024.04.015. Epub 2024 Apr 18.

Abstract

INTRODUCTION

Seizures represent a significant comorbidity in children with acute encephalitis syndrome (AES). Despite this, there is a notable absence of randomized controlled trials (RCTs) directly comparing antiseizure medications (ASMs) in children with AES.

MATERIALS AND METHODS

This RCT aimed to assess the efficacy and safety of phenytoin and levetiracetam in controlling seizures among children with AES. Both ASMs were administered with a loading followed by maintenance dose. After a 12-week period, children exhibiting a normal electroencephalogram and no seizure recurrence underwent tapering and discontinuation of ASM. Clinical follow-up occurred daily for the first week, and subsequently at 4, 12, and 24 weeks, evaluating seizure recurrence, incidence of status epilepticus, cognition, behavior, functional status, ASM acquisition cost, and adverse effects.

RESULTS

A total of 100 children (50 in each group) were enrolled. Within the first week, 5 and 3 children in the phenytoin and levetiracetam groups expired. Up to 1 week or death (whichever occurred earliest), 46 (92 %) and 44 (88 %) children remained seizure-free. Intention-to-treat analysis for both best and worst-case scenarios showed insignificant differences (p=0.52 and 1.0). No children experienced seizure recurrence after 1 week in either group. The number of patients with breakthrough status epilepticus, need for mechanical ventilation, duration of hospital stay, presence of epileptiform abnormalities in repeat electroencephalogram at 12 weeks, functional outcomes at 1, 12, and 24 weeks, as well as cognition and behavioral profiles at 24 weeks, were comparable in both groups (p>0.05 for all). However, the incidence of treatment-emergent adverse events (TEAEs) causally related to study medications was significantly higher in the phenytoin group (p=0.04).

CONCLUSION

Levetiracetam and phenytoin are comparable in efficacy in terms of achieving clinical seizure control in children with acute encephalitis syndrome, although levetiracetam group demonstrated fewer adverse effects.

摘要

介绍

癫痫发作是急性脑炎综合征(AES)患儿的一种重要合并症。尽管如此,目前仍缺乏直接比较 AES 患儿抗癫痫药物(ASM)的随机对照试验(RCT)。

材料和方法

本 RCT 旨在评估苯妥英钠和左乙拉西坦控制 AES 患儿癫痫发作的疗效和安全性。两种 ASM 均采用负荷剂量加维持剂量给药。12 周后,脑电图正常且无癫痫发作复发的患儿逐渐减少并停用 ASM。临床随访在第 1 周每天进行,随后在第 4、12 和 24 周时进行,评估癫痫发作复发、癫痫持续状态的发生率、认知、行为、功能状态、ASM 获得成本和不良反应。

结果

共纳入 100 例患儿(每组 50 例)。苯妥英钠组和左乙拉西坦组分别有 5 例和 3 例患儿在第 1 周内死亡。在第 1 周或死亡(以先发生者为准)前,46 例(92%)和 44 例(88%)患儿无癫痫发作。最佳和最差情况的意向治疗分析显示差异无统计学意义(p=0.52 和 1.0)。两组患儿均在第 1 周后无癫痫发作复发。两组患儿的突破性癫痫持续状态、机械通气需要、住院时间、第 12 周重复脑电图出现癫痫样异常、第 1、12 和 24 周的功能结局以及第 24 周的认知和行为特征的数量均无差异(p>0.05)。然而,苯妥英钠组与研究药物相关的治疗中出现的不良事件(TEAE)发生率明显高于左乙拉西坦组(p=0.04)。

结论

左乙拉西坦和苯妥英钠在 AES 患儿的临床癫痫控制方面疗效相当,尽管左乙拉西坦组的不良反应较少。

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