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大剂量皮质类固醇治疗视神经炎。

Treatment of optic neuritis with megadose corticosteroids.

作者信息

Spoor T C

出版信息

J Clin Neuroophthalmol. 1986 Sep;6(3):137-43.

PMID:2946719
Abstract

Difficulty in distinguishing between monosymptomatic optic neuritis due to autoimmune disease or to intrinsic demyelination in young adults prompted a trial administration of megadose corticosteroids in a series of patients. Treatment with 1 g daily of intravenous methylprednisolone (Solu-Medrol) for 2 to 5 days led to the rapid resolution and restoration of visual function in five patients. Two untreated patients suffered irreversible loss of vision. One patient with known autoimmune disease required a higher dose. The author suggests a trial of megadose, intravenous corticosteroids in patients between the ages of 21 and 45 years with optic neuropathies of uncertain or suspected autoimmune etiology after appropriate neuro-ophthalmologic evaluation.

摘要

区分年轻成人中由自身免疫性疾病或内在脱髓鞘引起的单症状性视神经炎存在困难,这促使对一系列患者进行大剂量皮质类固醇的试验性给药。每天静脉注射1克甲泼尼龙(甲强龙),持续2至5天的治疗使5例患者的视觉功能迅速恢复。2例未接受治疗的患者视力出现不可逆丧失。1例已知自身免疫性疾病的患者需要更高剂量。作者建议,在经过适当的神经眼科评估后,对年龄在21至45岁之间、病因不确定或疑似自身免疫性的视神经病变患者进行大剂量静脉注射皮质类固醇的试验。

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