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首页> 外文期刊>JMIR Research Protocols >Valproic Acid as an Adjuvant Treatment for Generalized Convulsive Status Epilepticus in Adults Admitted to Intensive Care Units: Protocol for a Double-Blind, Multicenter Randomized Controlled Trial
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Valproic Acid as an Adjuvant Treatment for Generalized Convulsive Status Epilepticus in Adults Admitted to Intensive Care Units: Protocol for a Double-Blind, Multicenter Randomized Controlled Trial

机译:丙戊酸作为一般性痉挛状态癫痫的辅助治疗成人入备到密集护理单位:双盲,多中心随机对照试验的议定书

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Background Generalized convulsive status epilepticus (GCSE) is a frequent medical emergency. GCSE treatment focuses on the administration of benzodiazepines followed by a second-line antiepileptic drug (AED). Despite this stepwise strategy, GCSE is not controlled in one-quarter of patients and is associated with protracted hospitalization, high mortality, and long-term disability. Valproic acid (VPA) is an AED with good tolerability and neuroprotective properties. Objective This study aims to demonstrate that administration of VPA as an adjuvant for first- and second-line treatment in GCSE can improve outcomes. Methods A multicenter, double-blind, randomized controlled trial was conducted, comparing VPA with a placebo in adults admitted to intensive care units (ICUs) for GCSE in France. GCSE was diagnosed by specifically trained ICU physicians according to standard criteria. All patients received standard of care, including a benzodiazepine and a second-line AED (not VPA), at the discretion of the treating medical team. In the intervention arm, VPA was administered intravenously at a loading dose of 30 mg/kg over 15 minutes, followed by a continuous infusion of 1 mg/kg/hour over the next 12 hours. In the placebo group, an identical intravenous administration of 0.9% saline was used. The primary outcome was the proportion of patients discharged alive from the hospital by day 15. Secondary outcomes were frequency of refractory and super refractory GCSE, ICU-related morbidity, adverse events related to VPA, and cognitive dysfunction at 3 months. Statistical analyses will be performed according to the intent-to-treat principle. Results The first patient was randomized on February 18, 2013, and the last patient was randomized on July 7, 2018. Of 248 planned patients, 98.7% (245/248) were enrolled across 20 ICUs. At present, data management is still ongoing, and all parties involved in the trial remain blinded. Conclusions The Valproic Acid as an Adjuvant Treatment for Generalized Convulsive Status Epilepticus (VALSE) trial will evaluate whether the use of VPA as an adjuvant for first- and second-line treatment in GCSE improves outcomes.
机译:背景技术广义痉挛状态癫痫症(GCSE)是经常医疗紧急情况。 GCSE治疗侧重于苯并二氮卓的施用,然后是二线抗癫痫药物(AED)。尽管这一练习策略,GCSE在四分之一的患者中没有控制,并且与长期住院,高死亡率和长期残疾有关。丙戊酸(VPA)是具有良好耐受性和神经保护性的AEd。目的本研究旨在证明VPA作为佐剂在GCSE中施用第一和二线治疗可以改善结果。方法进行多中心,双盲,随机对照试验,将VPA与入住的成人安慰剂的VPA进行比较,以便在法国的GCSE中录取为重症监护单位(ICU)。根据标准标准,通过专门培训的ICU医生诊断GCSE。所有患者都接受了护理标准,包括苯二氮卓和第二行AED(不是VPA),由治疗医疗团队决定。在干预臂中,在15分钟内以30mg / kg的装载剂量静脉内施用VPA,然后在接下来的12小时内连续输注1mg / kg /小时。在安慰剂组中,使用相同的静脉施用0.9%盐水。主要结果是在第15天从医院排出的患者的比例。二次结果是难治性和超级难治性GCSE的频率,ICU相关的发病率,与VPA相关的不良事件,以及3个月内的认知功能障碍。统计分析将根据意图的原则进行。结果第一款患者于2013年2月18日随机随机化,最后一名患者于2018年7月7日随机分组。在248名计划的患者中,98.7%(245/248)注册了20个ICU。目前,数据管理仍然正在进行中,涉及审判中涉及的各方都仍然蒙蔽。结论丙戊酸作为广义痉挛状态癫痫病毒治疗的佐剂治疗,将评估VPA作为GCSE中首先和二线治疗的佐剂是否改善了结果。

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