4.2 Article

Intravenous Immunoglobulin for Inflammatory Myositis Experience in a Tertiary Medical Center

Journal

JCR-JOURNAL OF CLINICAL RHEUMATOLOGY
Volume 27, Issue 8, Pages E616-E621

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/RHU.0000000000001418

Keywords

dermatomyositis; inflammatory myopathy; intravenous immunoglobulin; IVIG; polymyositis

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IVIG treatment for patients with inflammatory myopathies resulted in significant improvement in muscle strength, reduction in creatinine phosphokinase levels, and steroid dosage. Majority of patients experienced clinical and laboratory improvement, suggesting IVIG as a potential alternative treatment option for those with limited responsiveness to conventional methods.
Introduction Inflammatory myopathies are treated with glucocorticoids and other immunosuppressive medications. Intravenous immunoglobulin (IVIG) is increasingly used for refractory or severe cases; however, the evidence for their effectiveness is limited. We assessed effectiveness and safety of IVIG when used with other immunomodulatory agents in the treatment of inflammatory myopathies. Methods This study reviewed records of patients diagnosed with dermatomyositis or polymyositis and treated with IVIG, from 2009 through 2016 in 1 tertiary medical center. Mixed-effects general linear regression models were applied to determine effectiveness of treatment on muscle strength, creatinine phosphokinase levels, and steroid dosage. Results Twenty-three patients with dermatomyositis/polymyositis treated with IVIG were followed up for a mean of 31 (SD, +/- 25) months. During this period, a significant improvement in muscle strength was demonstrated, with a mean increase of 0.92 Medical Research Council scale points (beta = 0.14; confidence interval [CI], 0.136-0.149; p < 0.0001), a significant reduction of creatinine phosphokinase levels and steroid dosage with a mean decrease of 1140 IU/L (beta = -0.274; CI, -0.354 to -0.195; p < 0.0001), and 36 mg/d (beta = -0.008; CI, -0.011 to -0.006; p < 0.0001), respectively. Overall, remission was observed in 10 patients (43.5%), and partial remission in 6 patients (26%), whereas 1 patient (17%) remained refractory to treatment, and 6 patients (27%) were lost to follow-up. Conclusions The majority of patients with inflammatory myopathies experienced a clinical and laboratory improvement during IVIG treatment. In addition, a steroid-sparing effect was noticed in most patients. These results encourage the use of IVIG as an alternative treatment option for patients with limited responsiveness to conventional methods.

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