The place of high dose immunoglobulins in the treatment of Guillain-Barré patients based upon the dutch trial.

F G van der Meché
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Abstract

The preliminary results of a multicenter trial in the Netherlands comparing plasma exchange (PE) with high-dose intravenous immunoglobulin (IgIV) (dose 0.4 g/kg during 5 consecutive days, total dose of 2.0 g/kg) are reported. The trial was performed on 150 patients. After 4 weeks, 34.2% of the PE patients and 52.7% of the IgIV patients showed improvement. While in 11 patients plasma exchange had to be discontinued for medical reasons, no serious side effects were seen in the high-dose immunoglobulin treatment group. In 30% of the patients antibodies to GM1 ganglioside were found. The presence of such antibodies was correlated with a more severe clinical course and delayed recovery. Since improvement in the IgIV group occurred almost twice as often in GM1 negative patients, the effect appears to be limited in GM1-positive patients, who obviously need additional treatment. A current multicenter trial uses IgIV combined with high-dose methylprednisolone.

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基于荷兰试验的高剂量免疫球蛋白在格林-巴氏综合征治疗中的地位。
报道了荷兰一项比较血浆置换(PE)与高剂量静脉注射免疫球蛋白(IgIV)(连续5天剂量为0.4 g/kg,总剂量为2.0 g/kg)的多中心试验的初步结果。这项试验在150名患者身上进行。4周后,34.2%的PE患者和52.7%的IgIV患者出现改善。虽然有11例患者因医疗原因不得不停止血浆置换,但在高剂量免疫球蛋白治疗组中未见严重副作用。30%的患者发现GM1神经节苷脂抗体。这种抗体的存在与更严重的临床病程和延迟恢复相关。由于IgIV组在GM1阴性患者中出现改善的频率几乎是其两倍,因此对GM1阳性患者的效果似乎有限,他们显然需要额外的治疗。目前的一项多中心试验使用IgIV联合大剂量甲基强的松龙。
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