May 2003
Volume 44, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2003
Intravitreal Triamcinolone Acetonide for the Treatment of Diabetic Macular Edema Refractory to Laser Photocoagulation
Author Affiliations & Notes
  • V. Cruz-Villegas
    Ophthalmology-Retina, Bascom Palmer Eye Inst-U Miami, Miami, FL, United States
  • I.U. Scott
    Ophthalmology-Retina, Bascom Palmer Eye Inst-U Miami, Miami, FL, United States
  • H.W. Flynn Jr
    Ophthalmology-Retina, Bascom Palmer Eye Inst-U Miami, Miami, FL, United States
  • Footnotes
    Commercial Relationships  V. Cruz-Villegas, None; I.U. Scott, None; H.W. Flynn Jr, None.
Investigative Ophthalmology & Visual Science May 2003, Vol.44, 3967. doi:
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      V. Cruz-Villegas, I.U. Scott, H.W. Flynn Jr; Intravitreal Triamcinolone Acetonide for the Treatment of Diabetic Macular Edema Refractory to Laser Photocoagulation . Invest. Ophthalmol. Vis. Sci. 2003;44(13):3967.

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

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Abstract

Abstract: : Purpose: To investigate the safety and efficacy of intravitreal triamcinolone for the treatment of diabetic macular edema refractory to laser photocoagulation. Methods: The medical records were reviewed of all patients treated for diabetic macular edema refractory to laser photocoagulation with 4mg/0.1cc intravitreal triamcinolone acetonide by two vitreoretinal surgeons at a single institution between January 1, 2001 and August 31, 2002. Results: The study included 14 eyes of 14 patients with a median age of 66 years (range, 32-80 years) and followed for a median of 4.5 months (range, 1-6 months). The median duration of macular edema was 18 months (range, 6-54 months). Median visual acuity was 20/300 (range, 20/60-CF) pre-treatment, 20/200 (range, 20/40-20/400) at 1 month following treatment, 20/150 (range, 20/25 to 20/400) at 3 months, and 20/100 (range, 20/25-20/400) at 6 months. The mean change in logMAR visual acuity was 0.3 (halving of the visual angle) at both 3 and 6 months (range, -0.3 to 0.6). Vision improved at 1, 3, and 6 months post-injection (p=0.23, p=0.019, and p=0.093, respectively, paired t-test). Visual acuity was improved by at least one Snellen line in 8/13 eyes (62%) at 1 month, 7/10 (70%) at 3 months, and 5/7 (71%) at 6 months. Visual acuity was stable in 3/13 eyes (23%) at 1 month, 2/10 (20%) at 3 months, and 1/7 (14%) at 6 months. Compared to baseline, acuity was decreased in 2/13 patients (15%) at 1 month, 1/10 (10%) at 3 months and 1/7 (14%) at 6 months. Median foveal thickness as measured by optical coherence tomography (OCT) was 453 µm (range, 259-755 µm) at baseline, compared to 255 µm (range 154-350 µm) at 1 month, 251 µm (range, 116-434 µm) at 3 months, and 214 µm (range, 192-268 µm) at 6 months. Mean foveal thickness decreased at 1, 3, and 6 months post-injection (p=0.017, 0.039, and 0.056, respectively, paired t-test). Intraocular pressure (IOP) was increased >10 mmHg compared to baseline in 3/13 patients (23%) at 1 month, 1/10 (10%) at 3 months, and 1/7 (14%) at 6 months following injection. Two patients (14%) developed recurrence of macular edema and underwent a second injection of intravitreal triamcinolone acetonide. Two patients (14%) experienced progressive lens opacification. No other adverse events occurred. Conclusions: In the current series, intravitreal triamcinolone acetonide was associated with a reduction in macular edema and visual acuity improvement in most patients with diabetic macular edema refractory to laser photocoagulation.

Keywords: diabetes • clinical (human) or epidemiologic studies: out • diabetic retinopathy 
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