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创伤性蛛网膜下腔出血及其尼莫地平治疗。德国创伤性蛛网膜下腔出血研究组

Traumatic subarachnoid hemorrhage and its treatment with nimodipine. German tSAH Study Group.

作者信息

Harders A, Kakarieka A, Braakman R

机构信息

Department of Neurosurgery, Ruhr University Bochum, Germany.

出版信息

J Neurosurg. 1996 Jul;85(1):82-9. doi: 10.3171/jns.1996.85.1.0082.

Abstract

A prospective, randomized, double-blind, placebo-controlled study of nimodipine used to treat traumatic subarachnoid hemorrhage (tSAH) was conducted in 21 German neurosurgical centers between January 1994 and April 1995. One hundred twenty-three patients with tSAH appearing on initial computerized tomography (CT) scanning were entered into the study. Requirements for inclusion included age between 16 and 70 and admission into the study within 12 hours after head injury, regardless of the patient's level of consciousness. Eligible patients received either a sequential course of intravenous and oral nimodipine or placebo treatment for 3 weeks. Patients were closely monitored using clinical neurology, computerized tomography, laboratory, and transcranial Doppler ultrasound parameters. Patients treated with nimodipine had a significantly less unfavorable outcome (death, vegetative survival, or severe disability) at 6 months than placebo-treated patients (25% vs. 46%, p = 0.02). The relative reduction in unfavorable outcome in the nimodipine-treated group was even higher (55%, p = 0.002) when only patients who complied with the protocol were considered.

摘要

1994年1月至1995年4月期间,在21个德国神经外科中心进行了一项前瞻性、随机、双盲、安慰剂对照研究,以评估尼莫地平治疗创伤性蛛网膜下腔出血(tSAH)的效果。123例初次计算机断层扫描(CT)显示有tSAH的患者纳入研究。纳入标准包括年龄在16至70岁之间,且在头部受伤后12小时内入组,无论患者意识水平如何。符合条件的患者接受静脉和口服尼莫地平序贯治疗或安慰剂治疗3周。通过临床神经学、计算机断层扫描、实验室检查和经颅多普勒超声参数对患者进行密切监测。与接受安慰剂治疗的患者相比,接受尼莫地平治疗的患者在6个月时出现不良结局(死亡、植物生存或严重残疾)的比例显著更低(25%对46%,p = 0.02)。仅考虑符合方案的患者时,尼莫地平治疗组不良结局的相对降低幅度更高(55%,p = 0.002)。

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