van der Meché F G
Department of Neurology, University Hospital Dijkzig, Rotterdam, The Netherlands.
Clin Exp Immunol. 1994 Jul;97 Suppl 1(Suppl 1):43-7.
Guillain-Barré syndrome is an acute immune-mediated polyneuropathy with a severe clinical course. Plasma exchange (PE) was the first proven effective treatment ameliorating morbidity and outcome. However, it is not readily available and contraindications and complications frequently occur. High-dose intravenous immune globulin (IVIG) was demonstrated recently to be at least as effective and possibly more effective. The evidence is summarized in this article. Although specific treatment is now available, a proportion of patients do deteriorate with either IVIG (25%) or PE (34%) over the first 2 weeks after onset of treatment. A new dilemma has therefore arisen: is it worthwhile to switch therapy in patients who show further deterioration during therapy? As will be discussed, only a pragmatic approach is possible for the moment. In general it will be most effective to give just one full dose of IVIG or, alternatively, a full course of PE. More effective treatments are still being developed. The results of a pilot study of IVIG combined with high-dose methyl-prednisolone are promising and warrant a large scale clinical trial for further confirmation.
格林-巴利综合征是一种急性免疫介导的多神经病,临床过程严重。血浆置换(PE)是首个被证实能改善发病率和预后的有效治疗方法。然而,它并非随时可用,且经常出现禁忌症和并发症。大剂量静脉注射免疫球蛋白(IVIG)最近被证明至少同样有效,甚至可能更有效。本文总结了相关证据。尽管现在有了特异性治疗方法,但仍有一部分患者在治疗开始后的头2周内,接受IVIG(25%)或PE(34%)治疗时病情会恶化。因此出现了一个新的困境:对于治疗期间病情进一步恶化的患者,更换治疗方法是否值得?正如将要讨论的,目前只能采取务实的方法。一般来说,仅给予一剂完整剂量的IVIG或一个完整疗程的PE最为有效。更有效的治疗方法仍在研发中。IVIG联合大剂量甲基强的松龙的一项初步研究结果很有前景,值得进行大规模临床试验以进一步证实。