May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Efficacy of Intravitreal Bevacizumab (BV) Injection for the Treatment of Retinal Vein Occlusion
Author Affiliations & Notes
  • T.M. O'Hearn
    Ophthalmology, Doheny Eye Institute, Los Angeles, CA
  • E. Thomas
    Retina–Vitreous Associates, Los Angeles, CA
  • R. Gallemore
    Retina–Vitreous Associates, Los Angeles, CA
  • D. Boyer
    Retina–Vitreous Associates, Los Angeles, CA
  • R. Novack
    Retina–Vitreous Associates, Los Angeles, CA
  • T. Chu
    Retina–Vitreous Associates, Los Angeles, CA
  • F. Rahhal
    Retina–Vitreous Associates, Los Angeles, CA
  • Footnotes
    Commercial Relationships  T.M. O'Hearn, None; E. Thomas, None; R. Gallemore, None; D. Boyer, None; R. Novack, None; T. Chu, None; F. Rahhal, None.
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 4290. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      T.M. O'Hearn, E. Thomas, R. Gallemore, D. Boyer, R. Novack, T. Chu, F. Rahhal; Efficacy of Intravitreal Bevacizumab (BV) Injection for the Treatment of Retinal Vein Occlusion . Invest. Ophthalmol. Vis. Sci. 2006;47(13):4290.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose: : To asses the effects of the anti–VEGF antibody Bevacizumab (BV) on retinal edema in retinal vein occlusions.

Methods: : Retrospective uncontrolled study of the effects of BV on visual acuity, intraocular pressure (IOP), and central retinal thickness measured by OCT in branch retinal (BRVO) and central retinal vein occlusions (CRVO).

Results: : A total of 50 eyes in 49 patients received an intravitreal injection of 1.25mg of BV for BRVO and CRVO. Early follow up (n=6) demonstrated statistically significant reduction (P<0.05) in central retinal thickness at both 1 week (527µm vs 263µm) and 4–6 weeks (527µm vs 247µm). Mean IOP fell at both 1week (20.7 vs.19.2mmHg) and 4–6 weeks (20.7 vs.16.6mmHg) of follow up. Visual acuity improved from 1.29 to 1.14 LogMAR at 1 week follow up (P<0.05), but at 4–6 weeks follow up was no longer statistically improved (1.29 vs.1.18, P>0.05).

Conclusions: : Bevacizumab injection produced significantly reduced central retinal thickness in BRVO/CRVO patients at 1 week and 4–6 week follow up as well as limited improvement in visual acuity at 1 week follow up. There was also a trend towards lower IOP. Effects were transient consistent with the limited half–life of bevacizumab. Re–injection may be beneficial in these patients. Extended follow–up will be presented.

Keywords: retinal neovascularization • injection • vascular occlusion/vascular occlusive disease 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×