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  Vol. 127 No. 6, June 2009 TABLE OF CONTENTS
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Uncovering the Risks of Immunosuppressive Therapy in Patients With Uveitis

Debra A. Goldstein, MD

Arch Ophthalmol. 2009;127(6):799-800.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

The systemic treatment of potentially blinding ocular inflammatory disease is fraught with challenges, ranging from lack of efficacy to serious safety concerns. Systemic corticosteroids, which have been used since the 1950s, have a host of potential adverse effects. Steroid-sparing agents such as methotrexate, azathioprine, and mycophenolate may reduce the need for corticosteroids, but carry with them their own set of adverse effects, and may be of limited efficacy in some cases. The biologic agents, including the tumor necrosis factor (TNF) inhibitors, have been more recently introduced and are being used with increasing frequency. The TNF inhibitor infliximab has been reported in case series and retrospective studies as effective in managing treatment-resistant ocular inflammation.1-3 Adverse effects have been reported as minimal in most series in the uveitis literature,3-5 but more significant in the rheumatologic literature.6-8 The adverse effect profile of infliximab, as with most agents, seems better . . . [Full Text of this Article]


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RELATED ARTICLE

Infliximab Therapy for Refractory Uveitis: 2-Year Results of a Prospective Trial
Eric B. Suhler, Justine R. Smith, Tracy R. Giles, Andreas K. Lauer, Michael S. Wertheim, Daryl E. Kurz, Paul A. Kurz, Lyndell Lim, Friederike Mackensen, Terri D. Pickard, and James T. Rosenbaum
Arch Ophthalmol. 2009;127(6):819-822.
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