首页> 美国卫生研究院文献>The Journal of Neurology and Psychopathology >A double-blind controlled trial of high dose methylprednisolone in patients with multiple sclerosis: 1. Clinical effects.
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A double-blind controlled trial of high dose methylprednisolone in patients with multiple sclerosis: 1. Clinical effects.

机译:高剂量甲基强的松龙对多发性硬化症患者的双盲对照试验:1.临床效果。

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摘要

A randomised double-blind, placebo-controlled trial of high-dose, pulsed intravenous methylprednisolone was carried out in 50 individuals with multiple sclerosis; 22 patients were in acute relapse and 28 had chronic progressive disease. After a baseline assessment using the Kurtzke functional and expanded disability status scales each patient was randomly allocated to intravenous treatment with methylprednisolone (500 mg) or a saline placebo administered as a single daily dose for 5 days. Clinical assessments were repeated at 1 and 4 weeks after starting treatment. The results from all 50 patients showed a highly significant effect in favour of methylprednisolone treatment (p less than 0.001). In patients with relapse, there was a significant decrease in clinical disability scores at 1 and 4 weeks in the methylprednisolone treated group compared with controls (p less than 0.05 for each comparison). In the chronic progressive group, disability scores at 4 weeks only were significantly lower after treatment with methylprednisolone (p less than 0.01), mainly attributable to improvement in pyramidal function.
机译:在50名多发性硬化症患者中进行了大剂量脉冲静脉注射甲基强的松龙的随机双盲,安慰剂对照试验。急性复发22例,慢性进行性疾病28例。在使用Kurtzke功能和扩展的残疾状态量表进行基线评估后,将每位患者随机分配为接受甲基泼尼松龙(500 mg)或生理盐水安慰剂的静脉内治疗,每日剂量为5天。开始治疗后第1和4周重复进行临床评估。所有50例患者的结果均显示出了对甲基强的松龙治疗的高度显着效果(p小于0.001)。在复发患者中,甲基泼尼松龙治疗组在第1周和第4周时的临床残疾评分与对照组相比有显着降低(每次比较p均小于0.05)。在慢性进行性组中,甲基强的松龙治疗后仅4周时的残疾评分显着降低(p小于0.01),主要归因于锥体功能的改善。

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