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纳入CLASS(一项氯美噻唑与安慰剂治疗急性卒中患者的对照试验)的95例出血性卒中患者的结果。

Results in 95 hemorrhagic stroke patients included in CLASS, a controlled trial of clomethiazole versus placebo in acute stroke patients.

作者信息

Wahlgren N G, Díez-Tejedor E, Teitelbaum J, Arboix A, Leys D, Ashwood T, Grossman E

机构信息

Stroke Research Unit, Department of Neurology, Karolinska Hospital, Stockholm, Sweden.

出版信息

Stroke. 2000 Jan;31(1):82-5. doi: 10.1161/01.str.31.1.82.

Abstract

BACKGROUND AND PURPOSE

Clomethiazole is a neuroprotective drug that enhances gamma-aminobutyrate type A (GABA(A)) receptor activity. Its efficacy and safety were tested in the CLomethiazole Acute Stroke Study (CLASS). The protocol allowed a CT scan to be done after randomization but within 7 days of stroke onset to minimize delays before start of treatment. Ninety-five of the 1360 patients randomized were diagnosed as having intracranial hemorrhage rather than ischemic stroke. Safety results for clomethiazole compared with placebo in this group are reported.

METHODS

The study included patients with a clinical diagnosis of acute hemispheric cerebral infarction. Treatment was a 24-hour intravenous infusion of 75 mg/kg clomethiazole or placebo. Patients with intracranial hemorrhage discovered on a postrandomization CT were withdrawn from study treatment if treatment was ongoing, and all patients were followed up to 90 days.

RESULTS

Ninety-four patients received treatment, 47 in each group. The hemorrhage was classified as intracerebral in 89 patients (94%). Mortality at 90 days was 19.1% in the clomethiazole group and 23.4% in the placebo group. Sedation was the most common adverse event, occurring at a higher incidence in clomethiazole-treated patients (clomethiazole 53%, placebo 17%), followed by rhinitis and coughing. The incidence and pattern of serious adverse events was similar between the treatment groups. The percentage of patients reaching relative functional independence on the Barthel Index (score >/=60) at 90 days was 59.6% in the clomethiazole group and 53.2% in the placebo group.

CONCLUSIONS

Clomethiazole appears safe to administer to hemorrhagic stroke patients compared with placebo. These results would obviate the need for a CT scan before therapy is initiated in acute stroke. The safety of clomethiazole in hemorrhagic stroke patients will be further evaluated in a prospective study that is under way in North America.

摘要

背景与目的

氯美噻唑是一种增强γ-氨基丁酸A型(GABAA)受体活性的神经保护药物。其疗效和安全性在氯美噻唑急性卒中研究(CLASS)中进行了测试。该方案允许在随机分组后但在卒中发作7天内进行CT扫描,以尽量减少治疗开始前的延迟。1360例随机分组的患者中有95例被诊断为颅内出血而非缺血性卒中。本文报告了该组中氯美噻唑与安慰剂相比的安全性结果。

方法

该研究纳入临床诊断为急性半球性脑梗死的患者。治疗方法为静脉输注24小时、剂量为75mg/kg的氯美噻唑或安慰剂。随机分组后CT检查发现颅内出血的患者,若正在接受治疗则退出研究治疗,所有患者均随访至90天。

结果

94例患者接受了治疗,每组47例。89例患者(94%)的出血被分类为脑内出血。氯美噻唑组90天死亡率为19.1%,安慰剂组为23.4%。镇静是最常见的不良事件,在接受氯美噻唑治疗的患者中发生率更高(氯美噻唑组为53%,安慰剂组为17%),其次是鼻炎和咳嗽。治疗组之间严重不良事件的发生率和模式相似。氯美噻唑组90天时Barthel指数(评分≥60)达到相对功能独立的患者百分比为59.6%,安慰剂组为53.2%。

结论

与安慰剂相比,氯美噻唑用于出血性卒中患者似乎是安全的。这些结果将消除在急性卒中治疗开始前进行CT扫描的必要性。氯美噻唑在出血性卒中患者中的安全性将在北美正在进行的一项前瞻性研究中进一步评估。

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