Department of Emergency Medicine, University of Cincinnati, Cincinnati, OH, USA.
Acad Emerg Med. 2010 Jun;17(6):575-82. doi: 10.1111/j.1553-2712.2010.00751.x.
Rapid treatment of status epilepticus (SE) is associated with better outcomes. Diazepam and midazolam are commonly used, but the optimal agent and administration route is unclear.
The objective was to determine by systematic review if nonintravenous (non-IV) midazolam is as effective as diazepam, by any route, in terminating SE seizures in children and adults. Time to seizure cessation and respiratory complications was examined.
We performed a search of PubMed, Web of Knowledge, Embase, Cochrane Database of Systematic Reviews, Database of Abstracts of Reviews of Effects, American College of Physicians Journal Club, Cochrane Central Register of Controlled Trials, the Cumulative Index to Nursing and Allied Health Literature, and International Pharmaceutical Abstracts for studies published January 1, 1950, through July 4, 2009. English language quasi-experimental or randomized controlled trials comparing midazolam and diazepam as first-line treatment for SE, and meeting the Consolidated Standards of Reporting Trials (CONSORT)-based quality measures, were eligible. Two reviewers independently screened studies for inclusion and extracted outcomes data. Administration routes were stratified as non-IV (buccal, intranasal, intramuscular, rectal) or IV. Fixed-effects models generated pooled statistics.
Six studies with 774 subjects were included. For seizure cessation, midazolam, by any route, was superior to diazepam, by any route (relative risk [RR] = 1.52; 95% confidence interval [CI] = 1.27 to 1.82). Non-IV midazolam is as effective as IV diazepam (RR = 0.79; 95% CI = 0.19 to 3.36), and buccal midazolam is superior to rectal diazepam in achieving seizure control (RR = 1.54; 95% CI = 1.29 to 1.85). Midazolam was administered faster than diazepam (mean difference = 2.46 minutes; 95% CI = 1.52 to 3.39 minutes) and had similar times between drug administration and seizure cessation. Respiratory complications requiring intervention were similar, regardless of administration route (RR = 1.49; 95% CI = 0.25 to 8.72).
Non-IV midazolam, compared to non-IV or IV diazepam, is safe and effective in treating SE. Comparison to lorazepam, evaluation in adults, and prospective confirmation of safety and efficacy is needed.
快速治疗癫痫持续状态(SE)与更好的结果相关。地西泮和咪达唑仑通常被使用,但最佳的药物和给药途径尚不清楚。
通过系统评价确定非静脉(非-IV)咪达唑仑是否通过任何途径与地西泮一样有效,用于终止儿童和成人 SE 发作。检查了发作停止时间和呼吸并发症。
我们对 PubMed、Web of Knowledge、Embase、Cochrane 系统评价数据库、效果评价文摘数据库、美国医师学院杂志俱乐部、Cochrane 对照试验中心注册、护理和相关健康文献累积索引以及国际药学文摘进行了检索,检索时间为 1950 年 1 月 1 日至 2009 年 7 月 4 日。符合 CONSORT(报告试验的统一标准)质量标准的比较咪达唑仑和地西泮作为 SE 一线治疗的半实验或随机对照试验被纳入。两名评审员独立筛选纳入的研究并提取结局数据。给药途径分层为非-IV(颊、鼻内、肌内、直肠)或 IV。固定效应模型生成汇总统计。
纳入了 6 项共 774 例患者的研究。对于发作停止,咪达唑仑通过任何途径都优于地西泮通过任何途径(相对风险[RR] = 1.52;95%置信区间[CI] = 1.27 至 1.82)。非-IV 咪达唑仑与 IV 地西泮一样有效(RR = 0.79;95% CI = 0.19 至 3.36),而颊部咪达唑仑优于直肠地西泮(RR = 1.54;95% CI = 1.29 至 1.85)控制发作。咪达唑仑的给药速度快于地西泮(平均差值= 2.46 分钟;95% CI = 1.52 至 3.39 分钟),且从药物给药到发作停止的时间相似。无论给药途径如何,需要干预的呼吸并发症相似(RR = 1.49;95% CI = 0.25 至 8.72)。
与非-IV 或 IV 地西泮相比,非-IV 咪达唑仑在治疗 SE 方面是安全有效的。需要与劳拉西泮进行比较,评估在成人中的安全性和有效性,并进行前瞻性确认。