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Department of Neurology (Drs. Amato and Pappert), Wilford Hall Medical Center, Lackland Air Force Base, TX; the Department of Neurology (Dr. Barohn), University of Texas Southwestern Medical Center, Dallas, TX; the Division of Neurology, Department of Medicine (Dr. Jackson), The University of Texas Health Science Center at San Antonio, San Antonio, TX; and the Department of Neurology (Drs. Sahenk and Kissel), The Ohio State University School of Medicine, Columbus, OH.
We report the results of nine patients with inclusion body myositis treated with intravenous immunoglobulin in an open-label uncontrolled study. None of our patients improved on objective manual muscle testing or functional disability scores. One patient developed mild neutropenia, complicating the intravenous immunoglobulin treatment. Our results do not exclude the possibility that intravenous immunoglobulin could be beneficial in some patients by slowing the rate of deterioration or perhaps stabilizing the disease. However, given the lack of objective improvement and high cost of treatment, we would not recommend intravenous immunoglobulin in the treatment of inclusion body myositis unless a blinded, controlled trial demonstrates clear benefit.
Address correspondence and reprint requests to Dr. Anthony A. Amato, WHMC/PSMN, 2200 Bergquist Dr, Ste 1, Lackland AFB, TX 78236-5300.
Received November 8, 1993. Accepted in final form February 7, 1994.
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