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Neurology 2002;59:S41-S45
© 2002 American Academy of Neurology

Neurology supplements are not peer-reviewed. Information contained in Neurology supplements represent the opinions of the authors and are not endorsed by nor do they reflect the views of the American Academy of Neurology, Editor-in-Chief, or Associate Editors of Neurology.

Regulatory and reimbursement issues in treating patients with immune-mediated neuropathies

Peter D. Donofrio, MD and Neil A. Busis, MD

From the Department of Neurology, Wake Forest University School of Medicine, Winston-Salem, NC (Dr. Donofrio) and the Pittsburgh Neurology Group, Pittsburgh, PA (Dr. Busis).

Address correspondence and reprint requests to Dr. Peter D. Donofrio, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157-1078.

Neurologists are prescribing intravenous immunoglobulin (IVIg) with increasing frequency to treat many neurologic conditions that have a proven or presumed autoimmune or inflammatory pathogenesis. Although IVIg is not FDA approved for any neurologic condition, physicians can safely prescribe it for several disorders with reasonable certainty that the cost for the agent will be reimbursed by third-party carriers. This article discusses present FDA indications for using IVIg, off-label uses of IVIg, policies of third-party payers toward reimbursement, the Local Medical Review Policy of Medicare, coding, billing, and reimbursement for IVIg infusion, and approaches to use when reimbursement is delayed or denied.




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