April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Long Term Follow-Up of Intravitreous Bevacizumab (Avastin) for Neovascular Glaucoma Secondary to Proliferate Diabetic Retinopathy
Author Affiliations & Notes
  • T. D. Albright
    Ophthalmology, Cook County Hospital, Chicago, Illinois
  • K. C. LaMattina
    Ophthalmology, New York Medical College, Valhalla, New York
  • J. M. Roberts
    Ophthalmology, Cook County Hospital, Chicago, Illinois
  • P. MacIntosh
    Ophthalmology, Cook County Hospital, Chicago, Illinois
  • A. Desai
    Ophthalmology, Chicago Medical School/RFUMS, North Chicago, Illinois
  • R. M. Ahuja
    Ophthalmology, Cook County Hospital, Chicago, Illinois
    Ophthalmology, Chicago Medical School/RFUMS, North Chicago, Illinois
  • Footnotes
    Commercial Relationships  T.D. Albright, None; K.C. LaMattina, None; J.M. Roberts, None; P. MacIntosh, None; A. Desai, None; R.M. Ahuja, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 4236. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      T. D. Albright, K. C. LaMattina, J. M. Roberts, P. MacIntosh, A. Desai, R. M. Ahuja; Long Term Follow-Up of Intravitreous Bevacizumab (Avastin) for Neovascular Glaucoma Secondary to Proliferate Diabetic Retinopathy. Invest. Ophthalmol. Vis. Sci. 2010;51(13):4236.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose: : To examine the visual acuity and intraocular pressure (IOP) outcomes of patients treated with intravitreous bevacizumab (Avastin) for neovascular glaucoma (NVG) secondary to proliferative diabetic retinopathy (PDR)

Methods: : We conducted a retrospective study of patients receiving intravitreous injections of 1.25 mg per 0.05cc bevacizumab for NVG secondary to PDR at the Stroger Cook County Hospital Division of Ophthalmology. All eyes displayed neovascularization of the iris (NVI) and/or neovascularization of the angle (NVA) at presentation. Patients with NVG secondary to other causes were excluded. All patients enrolled gave informed consent including off-label use of bevacizumab. A complete ophthalmic examination was performed on initial examination, and follow-up was as medically indicated.

Results: : A total of 16 eyes of 16 patients were included in the study. Twelve patients were male, and 4 were female. The average age was 49.1 years (range 28-63). Ten were Hispanic, 3 White, and 3 African American. The mean and median number of intravitreous injections per eye was 2 (range 1-4). Average follow-up was 413 days (range 53-1000). Visual acuity at last examination improved in 1 eye (6%), remained the same in 9 (56%), and declined in 6 (38%). Final visual acuity ranged from 20/40 to no light perception. Intraocular pressure decreased in 14 eyes (86%) and increased in 2 (12%). All patients also had standard treatment for NVG. Twelve patients (75%) required glaucoma surgery. Six underwent alloplastic tube shunt surgery, 5 had cyclodestructive procedures, and 1 had both. No patients had adverse events secondary to the intravitreous bevacizumab.

Conclusions: : Neovascular glaucoma is a rare complication of PDR, and traditional treatment regimens are often ineffective in halting or reversing vision loss. Adjunctive intravitreous bevacizumab helped to maintain or improve visual acuity in almost two thirds of our patients. This is rare in NVG. However, a majority of patients did require glaucoma surgery to manage IOP. No patients suffered adverse events from injection of intravitreous bevacizumab. Our average follow-up was greater than one year, which demonstrates long-term safety and efficacy of intravitreous bevacizumab with few injections. Further studies to examine visual acuity outcomes in patients with NVG secondary to PDR are warranted.

Keywords: clinical (human) or epidemiologic studies: outcomes/complications • injection • retinal neovascularization 
×
×

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.

×