Fasanaro A M, Pizza V, Rossi V
Neurology Department, A. Cardarelli Hospital, Naples.
Minerva Med. 1996 Jan-Feb;87(1-2):17-20.
We report the results obtained with intravenous immunoglobulin (IVGG) in 15 patients suffering from Guillain Barré syndrome (GBS) with substantial motor damage. All of them met the NINCDS criteria for a diagnosis of certain GBS and were graded using a specific scale on entry, after 2 weeks, one month, two months, six months and one year. The clinical data were correlated to neurophysiological results. The patients were treated within the seventh day of the disease with IVGG (0.4 g/kg/day) for 5 days. Complete recovery was obtained in all but 2 patients died. We measured the mean time taken to improve one grade of the evaluation scale and the mean time taken to achieve walking unassisted. We obtained 11 days and 14 days respectively, that is, times significantly shorter than those reported in studies employing plasma exchange. No adverse effect was found except in one case. No relapse was observed. Even the patients with more clinical and neurophysiological damage had a rapid recovery. We advocate IVGG therapy for GBS, as it is effective, safe and easy to use.
我们报告了静脉注射免疫球蛋白(IVGG)治疗15例患有严重运动损伤的格林-巴利综合征(GBS)患者的结果。所有患者均符合美国国立神经病学、语言障碍和卒中研究所(NINCDS)关于确诊GBS的标准,并在入院时、2周后、1个月、2个月、6个月和1年时使用特定量表进行分级。临床数据与神经生理学结果相关联。患者在疾病第7天内接受IVGG(0.4 g/kg/天)治疗5天。除2例死亡患者外,所有患者均完全康复。我们测量了评估量表提高一个等级所需的平均时间以及实现独立行走所需的平均时间。我们分别获得了11天和14天,即,这些时间明显短于采用血浆置换的研究报告的时间。除1例患者外未发现不良反应。未观察到复发情况。即使是临床和神经生理学损伤更严重的患者也恢复迅速。我们提倡将IVGG疗法用于GBS,因为它有效、安全且易于使用。