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甲基强的松龙用于心肌梗死后的干预。甲强龙无菌粉剂急性心肌梗死研究组。

Methylprednisolone as an intervention following myocardial infarction. The Solu-Medrol Sterile Powder AMI Studies Group.

出版信息

J Int Med Res. 1986;14 Suppl 1:1-10.

PMID:2875003
Abstract

Results of early studies support the concept that steroid treatment may reduce mortality from acute myocardial infarction. This double-blind, randomized, 1118-patient study was performed to determine if methylprednisolone sodium succinate (MPSS, Solu-Medrol Sterile Powder, The Upjohn Company) reduced 28-day mortality following myocardial infarction complicated by cardiac failure. Treatment with 30 mg/kg intravenous MPSS (maximum dose, 3 g) resulted in 28-day mortality rates of 11.7% with MPSS and 9.9% with placebo when treatment was initiated within six hours of the onset of chest pain (Group 1). Mortality rates at 28 days were 10.4% with MPSS and 14.7% with placebo when the treatment was initiated 6-12 hours after onset of chest pain (Group 2). In the late-treatment group, six-month mortality rates were 13.7% with MPSS and 20.3% with placebo (p = 0.08). Analysis of data by life table methods showed similar survival rates between MPSS- and placebo-treated patients in Group 1. In Group 2, survival rates were increased in MPSS-treated patients in the intervals from 48 hours through seven days (p = 0.04) and from three months through six months (p = 0.03). A Cox regression analysis showed that the relative risk of death for Group 1 patients was similar, regardless of treatment; Group 2 patients on MPSS had a significantly decreased relative risk of death (p less than 0.01). MPSS treatment was not associated with increased incidence of myocardial rupture, cardiac aneurysm, early malignant ventricular arrhythmias, or other adverse cardiac events.

摘要

早期研究结果支持类固醇治疗可能降低急性心肌梗死死亡率这一概念。本项双盲、随机、纳入1118例患者的研究旨在确定琥珀酸甲泼尼龙(MPSS,甲强龙无菌粉末,优普强公司)是否能降低心肌梗死合并心力衰竭后的28天死亡率。胸痛发作6小时内开始治疗时,静脉注射30mg/kg MPSS(最大剂量3g),MPSS组28天死亡率为11.7%,安慰剂组为9.9%(第1组)。胸痛发作6 - 12小时后开始治疗时,MPSS组28天死亡率为10.4%,安慰剂组为14.7%(第2组)。在延迟治疗组中,MPSS组6个月死亡率为13.7%,安慰剂组为20.3%(p = 0.08)。采用生命表方法分析数据显示,第1组中MPSS治疗组和安慰剂治疗组患者的生存率相似。在第2组中,MPSS治疗组患者在48小时至7天期间(p = 0.04)以及3个月至6个月期间(p = 0.03)的生存率有所提高。Cox回归分析表明,第1组患者无论接受何种治疗,死亡相对风险相似;第2组接受MPSS治疗的患者死亡相对风险显著降低(p < 0.01)。MPSS治疗与心肌破裂、心脏动脉瘤、早期恶性室性心律失常或其他不良心脏事件的发生率增加无关。

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