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静脉注射甲基强的松龙治疗格林-巴利综合征的双盲试验。格林-巴利综合征类固醇试验组。

Double-blind trial of intravenous methylprednisolone in Guillain-Barré syndrome. Guillain-Barré Syndrome Steroid Trial Group.

出版信息

Lancet. 1993 Mar 6;341(8845):586-90.

PMID:8094828
Abstract

Steroids have been beneficial in the treatment of demyelinating diseases with features similar to those of Guillain-Barré syndrome (GBS). However, steroid treatment of GBS has been disappointing; in an earlier trial oral prednisolone was ineffective, although the dose was low and the sample small. We assessed the benefit of a high-dose steroid regimen in a large sample of patients with GBS in a multicentre, randomised, double-blind trial. 242 adult patients were randomised to receive intravenous methylprednisolone (IVMP) 500 mg (124 patients) or a placebo (118) daily for 5 days. Patients were diagnosed by standard clinical criteria and entered the trial within 15 days of onset of neurological symptoms. All patients were too weak to run. Some patients received plasma exchange depending on the practice of their centre. Disability was graded on a scale from 0 (healthy) to 6 (dead) at intervals for 48 weeks. There was no significant difference in any outcome variable between patients treated with IVMP and those given placebo. The most important outcome was the difference between the groups in disability grade 4 weeks after randomisation, which was only a 0.06 grade (95% Cl -0.23 to 0.36) greater improvement in the IVMP than the placebo group. The 39 patients in the IVMP group who required ventilation did so for a median of 18 days, 9 days fewer than the 44 patients who had a placebo and required ventilation (95% Cl -9.6 to 27.6). Median time to walk unaided was 38 days in the IVMP patients and 50 days in the placebo patients (difference 12 days, (95% Cl -21.3 to 45.3). A short course of high-dose IVMP given early in GBS is ineffective.

摘要

类固醇对治疗具有与吉兰-巴雷综合征(GBS)相似特征的脱髓鞘疾病有益。然而,类固醇治疗GBS的效果却令人失望;在一项早期试验中,口服泼尼松龙无效,尽管剂量低且样本量小。我们在一项多中心、随机、双盲试验中,对大量GBS患者评估了高剂量类固醇方案的益处。242名成年患者被随机分为两组,一组每天接受500毫克静脉注射甲泼尼龙(IVMP)(124例患者),另一组接受安慰剂(118例),持续5天。患者根据标准临床标准进行诊断,并在神经症状出现后15天内进入试验。所有患者都过于虚弱而无法跑步。一些患者根据其所在中心的惯例接受了血浆置换。在48周内定期对残疾程度进行评分,范围从0(健康)到6(死亡)。接受IVMP治疗的患者与接受安慰剂治疗的患者在任何结局变量上均无显著差异。最重要的结局是随机分组后4周时两组在残疾程度上的差异,IVMP组比安慰剂组仅多改善了0.06级(95%可信区间为-0.23至0.36)。IVMP组中需要通气的39例患者,通气的中位时间为18天,比接受安慰剂且需要通气的44例患者少9天(95%可信区间为-9.6至27.6)。IVMP组患者独立行走的中位时间为38天,安慰剂组为50天(差异为12天,95%可信区间为-21.3至45.3)。GBS早期给予短疗程高剂量IVMP无效。

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