April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Long-Term Outcomes of Ranibizumab for Uveitic Macular Edema and the Effect on Contralateral Eyes
Author Affiliations & Notes
  • Y. Qian
    F. I. Proctor Foundation, San Francisco, California
  • W. Sittavarakul
    F. I. Proctor Foundation, San Francisco, California
  • K. Hong
    F. I. Proctor Foundation, San Francisco, California
  • S. M. Lee
    F. I. Proctor Foundation, San Francisco, California
  • N. R. Acharya
    Ophthal-Proctor Foundation, Univ of California - SF, San Francisco, California
  • Footnotes
    Commercial Relationships  Y. Qian, None; W. Sittavarakul, None; K. Hong, None; S.M. Lee, None; N.R. Acharya, None.
  • Footnotes
    Support  Genentech, Inc: investigator-initiated trial program. NEI: EY02162. NEI: K23EY017897. Research to Prevent Blindness Career Development Award
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 5115. doi:
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    • Get Citation

      Y. Qian, W. Sittavarakul, K. Hong, S. M. Lee, N. R. Acharya; Long-Term Outcomes of Ranibizumab for Uveitic Macular Edema and the Effect on Contralateral Eyes. Invest. Ophthalmol. Vis. Sci. 2010;51(13):5115.

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

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Abstract

Purpose: : Our previous study on ranibizumab for uveitic macular edema demonstrated a statistically significant improvement in macular edema and visual acuity at 6 months (AJO 2009; 148: 303-309). Here, we report on the 12-month results as well an observed effect on the non-injected contralateral eyes with refractory bilateral cystoid macular edema due to uveitis.

Methods: : Seven patients with controlled uveitis and longstanding cystoid macular edema were enrolled in a prospective, interventional open-label trial for three monthly injections of 0.5 mg intravitreal ranibizumab for the eye with worse vision, followed by repeat injections based on macular thickness. Baseline best spectacle-corrected visual acuity (BSCVA) and optical coherence tomography were performed for central retinal thickness (CRT) of both eyes monthly.

Results: : Of the seven patients enrolled in this study, five patients completed the study at 12 months. From baseline to 6 months, there was improvement of mean BSCVA from 50 letters (20/100) to 63 letters (P=0.03) and improvement of mean CRT from 555µm to 213µm (P=0.03). Between 6 to 12 months, there was little change in BSCVA with a median loss of 2 letters (range -6 to +2 letters, P=0.08). Between 6 to 12 months, the median CRT worsened by 83µm (range 6µm improvement to 502µm worsening, P=0.08). There were three patients with bilateral cystoid macular edema who received unilateral intravitreal injections of ranibizumab. No other treatment changes were made during the study. The contralateral eyes of each of these patients experienced improvement in CRT at 3 months, which was sustained to 12 months in one eye and to 6 months in another eye, but not sustained beyond 3 months in the third eye. At 6 months, the contralateral eyes gained 2, 6, and 1 lines of BSCVA, respectfully. At 12 months, the BSCVA was 1 line gain (2 eyes) to 1 line loss (1 eye). One patient with bilateral neovascularization of the optic nerve had regression of neovascularization in both study and fellow eye at 3 months, which was sustained at 12 months.

Conclusions: : Intravitreal ranibizumab in uveitic eyes with refractory macular edema led to an increase in BSCVA which was sustained from months 6 to 12. There was an increase in CRT from months 6 to 12, after most patients stopped receiving injections. Contralateral effect of intravitreal ranibizumab has not been reported. The benefit of reduced cystoid macular edema and improvement in visual acuity observed in contralateral eyes raises questions on the pharmacokinetics of ranibizumab in eyes with uveitis.

Clinical Trial: : www.clinicaltrials.gov NCT00498355

Keywords: clinical (human) or epidemiologic studies: treatment/prevention assessment/controlled clinical trials • inflammation • macula/fovea 
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