van der Meché F G
Department of Neurology, University Hospital Dijkzigt, Rotterdam, The Netherlands.
Wien Klin Wochenschr Suppl. 1991;190:17-8.
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.
据报道,荷兰一项多中心试验的初步结果,该试验比较了血浆置换(PE)与大剂量静脉注射免疫球蛋白(IgIV)(连续5天,剂量为0.4g/kg,总剂量为2.0g/kg)。该试验对150名患者进行。4周后,34.2%的血浆置换患者和52.7%的IgIV患者病情有所改善。虽然有11名患者因医学原因不得不停止血浆置换,但大剂量免疫球蛋白治疗组未出现严重副作用。在30%的患者中发现了抗GM1神经节苷脂抗体。此类抗体的存在与更严重的临床病程和恢复延迟相关。由于GM1阴性患者中IgIV组病情改善的频率几乎是GM1阳性患者的两倍,因此GM1阳性患者的治疗效果似乎有限,显然需要额外治疗。目前一项多中心试验正在使用IgIV联合大剂量甲基强的松龙。