Randomized, controlled trial of intravenous immunoglobulin in myasthenia gravis
✍ Scribed by Gil I. Wolfe; Richard J. Barohn; Barbara M. Foster; Carlayne E. Jackson; John T. Kissel; John W. Day; Charles A. Thornton; Sharon P. Nations; Wilson W. Bryan; Anthony A. Amato; Miriam L. Freimer; Gareth J. Parry
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 80 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0148-639X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
We initiated a randomized, double‐blinded, placebo‐controlled trial of intravenous immunoglobulin (IVIG) treatment in myasthenia gravis (MG). Patients received IVIG 2 gm/kg at induction and 1 gm/kg after 3 weeks vs. 5% albumin placebo. The primary efficacy measurement was the change in the quantitative MG Score (QMG) at day 42. Fifteen patients were enrolled (6 to IVIG; 9 to placebo) before the study was terminated because of insufficient IVIG inventories. At day 42, there was no significant difference in primary or secondary outcome measurements between the two groups. In a subsequent 6‐week open‐label study of IVIG, positive trends were observed. © 2002 Wiley Periodicals, Inc. Muscle Nerve 26: 549–552, 2002
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## Abstract Twenty‐three myasthenia gravis (MG) subjects, mean (SD) age 41.6 years (14), showing poor disease control or steroid‐related side effects, received treatment for 12 months with intravenous cyclophosphamide (CP; __n__ = 12) or placebo (PL; __n__ = 11) in a randomized, double‐blind trial.