April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Clinical Outcomes of Ocular Inflammatory Disease Patients Treated With Cyclosporine-A as a Single Immunomodulatory Agent
Author Affiliations & Notes
  • R. Kacmaz
    Mount Sinai School of Medicine, New York, New York
  • J. H. Kempen
    Ocular Inflammation Service, Scheie Eye Institute, Philadelphia, Pennsylvania
  • C. Newcomb
    Department of Biostatistics and Epidemiology, University of Pennsylvania, Philadelphia, Pennsylvania
  • R. B. Nussenblatt
    Laboratory of Immunology, National Eye Institute, Bethesda, Maryland
  • J. T. Rosenbaum
    Department of Ophthalmology, Departments of Ophthalmology and Medicine,
    Oregon Health & Science University, Portland, Oregon
  • E. B. Suhler
    Department of Ophthalmology,
    Oregon Health & Science University, Portland, Oregon
  • J. E. Thorne
    Departments of Ophthalmology and Epidemiology, The Johns Hopkins University, Baltimore, Maryland
  • D. A. Jabs
    Department of Ophthalmology, Departments of Ophthalmology and Medicine,
    Mount Sinai School of Medicine, New York, New York
  • G. A. Levy-Clarke
    St. Luke’s Cataract and Laser Institute, Tarpon Springs, Florida
  • C. Foster
    Massachusetts Eye Research and Surgery Institute, Cambridge, Massachusetts
  • Footnotes
    Commercial Relationships  R. Kacmaz, None; J.H. Kempen, None; C. Newcomb, None; R.B. Nussenblatt, None; J.T. Rosenbaum, received $10,000 for consulting fees or paid advisory boards for both Novartis and Abbott Laboratories, and having a research grant pending from Abbott Laboratories, C; E.B. Suhler, received a research grant from Abbott Laboratories, F; J.E. Thorne, None; D.A. Jabs, received $10,000 for consulting fees or paid advisory boards for Novartis., C; G.A. Levy-Clarke, None; C. Foster, None.
  • Footnotes
    Support  National Eye Institute Grant EY014943, Paul and Evanina Mackall Foundation and Research to Prevent Blindness
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 2699. doi:
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      R. Kacmaz, J. H. Kempen, C. Newcomb, R. B. Nussenblatt, J. T. Rosenbaum, E. B. Suhler, J. E. Thorne, D. A. Jabs, G. A. Levy-Clarke, C. Foster; Clinical Outcomes of Ocular Inflammatory Disease Patients Treated With Cyclosporine-A as a Single Immunomodulatory Agent. Invest. Ophthalmol. Vis. Sci. 2009;50(13):2699.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To evaluate the clinical outcomes of cyclosporine-A used as a single immunomodulatory agent for non-infectious ocular inflammation

Methods: : 444 consecutive patients with non-infectious ocular inflammation started on cyclosporine as a single immunomodulatory agent at five ocular inflammation subspecialty centers between 1979-2007 were included. Demographic and clinical characteristics, including dosage of cyclosporine-A and main outcome measures (control of inflammation, corticosteroid-sparing effects, incidence of and reason for discontinuation of therapy) were obtained for every eye of every patient at every visit by medical record review.

Results: : Of the 444 patients (819 eyes with ocular inflammation) observed to start cyclosporine-A monotherapy, 16.7%, 30.5%, 47.3%, 2.8%, and 2.6% respectively had anterior uveitis, intermediate uveitis,posterior/panuveitis, scleritis, and other forms of ocular inflammation. Within these groups, complete suppression of inflammation sustained for ≥28 days was achieved in ≤6 months in 29.2%, 29.2%, 23.7%, 62.3%, and 20% respectively. Corticosteroid-sparing success (controlled inflammation with prednisone ≤10 mg/day for ≥28 days) was achieved within 6 months among 27.5%, 18.7%, 14.1%, 52.8%, and 20% of the respective groups. However, results were substantially better using less stringent sucsess criteria. Cyclosporine-A was discontinued within ≤1 year by 210 (47%) patients. Side effects were the cause of discontinuation in 50 patients (11%), and typically were reversible with dose reduction/discontinuation.

Keywords: clinical (human) or epidemiologic studies: outcomes/complications • cyclosporine • uveitis-clinical/animal model 
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