May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
Intravitreal Triamcinolone Acetonide Improves Macular Thickness in Three Days
Author Affiliations & Notes
  • S. Smetana
    Ophthalmology, St. Louis University, Saint Louis, MO
  • L. Akduman
    Ophthalmology, St. Louis University, Saint Louis, MO
  • Footnotes
    Commercial Relationships  S. Smetana, None; L. Akduman, None.
  • Footnotes
    Support  Research to Prevent Blindness
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 1928. doi:
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      S. Smetana, L. Akduman; Intravitreal Triamcinolone Acetonide Improves Macular Thickness in Three Days . Invest. Ophthalmol. Vis. Sci. 2004;45(13):1928.

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

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Abstract

Abstract: : Purpose: To investigate the efficacy and onset of action ofintravitreal triamcinolone acetonide in macular edema secondaryto various disorders.Methods: Twenty–two eyes of 18 patients with macular edemasecondary to pseudophakia (12), uveitis (5), diabetic retinopathy(4), and BRVO (1) were given 4 mg of intravitreal triamcinoloneacetonide. Preoperative and postoperative visual acuity, fovealthickness measured by OCT and fluorescein angiograms were usedto assess the response. Complications and side effects of theprocedure were noted.Results: Sixteen eyes (73%) had two lines or more improvementin visual acuity. Follow up–time was 1 to 6 months (median3 months). The best response was seen in pseudophakic CME (11/12improved) and uveitic CME (4/5 improved). OCT showed significantimprovement in macular thickness as early as 3 days after injectionwith average macular thickness improving from 435+/–22microns to 269+/–22 microns (Fig 1a and Fig 1b). Improvementin the leakage in the fluorescein angiogram was correlated withdecreasing foveal thickness in the OCT. The only complicationseen was a transient moderate increase in the intraocular pressurecontrolled by topical anti–glaucoma medications.Conclusions: Intravitreal triamcinolone acetonide improves therefractory macular edema effectively in cases with pseudophakicCME and uveitic CME. Improvement is seen and can be assessedby OCT as early as 3 days after injection. Long term efficacyand safety need to be determined with larger series. 

 

Keywords: macula/fovea • imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • clinical (human) or epidemiologic studies: treatment/prevention assessment/controlled clinical trials 
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