April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Comparison of 2 Doses of Intravitreal Bevacizumab (Avastin) for Proliferative Diabetic Retinopathy: Results From the Pan-American Collaborative Retina Study Group (PACORES) at 24-Month Follow-Up
Author Affiliations & Notes
  • N. Restrepo
    Retina, Instituto Nacional de Investigacion en Oftalmologia, Medellin, Colombia
  • L. Wu
    Vitreoretinal, Instituto De Cirugia Ocular, San Jose, Costa Rica
  • J. G. Sanchez
    Retina, Instituto Nacional de Investigacion en Oftalmologia, Medellin, Colombia
  • M. Maia
    Retina, the Universidade Federal de São Paulo Instituto da Visão, Sao Paulo, Brazil
  • M. J. Saravia
    Ophthalmology /Retina, Hospital Austral, Buenos Aires, Argentina
  • J. Arevalo
    Retina and Vitreous, Clinica Oftal Centro Caracas, Caracas, Venezuela
  • for the Pan-American Collaborative Retina Study Group
    Retina, Instituto Nacional de Investigacion en Oftalmologia, Medellin, Colombia
  • Footnotes
    Commercial Relationships  N. Restrepo, None; L. Wu, None; J.G. Sanchez, None; M. Maia, None; M.J. Saravia, None; J. Arevalo, None.
  • Footnotes
    Support  in part by the Arevalo-Coutinho Foundation for Research in Ophthalmology, Caracas, Venezuela
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 4233. doi:
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      N. Restrepo, L. Wu, J. G. Sanchez, M. Maia, M. J. Saravia, J. Arevalo, for the Pan-American Collaborative Retina Study Group; Comparison of 2 Doses of Intravitreal Bevacizumab (Avastin) for Proliferative Diabetic Retinopathy: Results From the Pan-American Collaborative Retina Study Group (PACORES) at 24-Month Follow-Up. Invest. Ophthalmol. Vis. Sci. 2010;51(13):4233.

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

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Abstract

Purpose: : To compare the effects of two doses (1.25 vs 2.5 mg) of intravitreal bevacizumab (Avastin) on retinal neovascularization (RN) in patients with proliferative diabetic retinopathy (PDR)

Methods: : In this interventional, retrospective, multicenter study, we reviewed the clinical records of 39 consecutive patients (43 eyes) with RN due to PDR with a mean age of 54 ± 12.5 years and a follow-up of 24 months. Patients were treated with at least 1 intravitreal injection of 1.25 mg or 2.5 mg of bevacizumab (IVB). Patients underwent ETDRS BCVA testing, ophthalmoscopic examination, optical coherence tomography (OCT), and fluorescein angiography (FA) at baseline and follow-up visits

Results: : The mean number of IVB injections per eye was 3.6 ± 1.6 (range: 1 to 7 injections). Twenty-four (55.8%) eyes received IVB at a dose of 1.25 mg, and 19 (44.2%) eyes received a dose of 2.5 mg. Thirty-one eyes (72.1%) had previous panretinal photocoagulation (PRP). In the 1.25 mg group, 8 eyes (33.3%) showed total regression of NVE and 6 eyes (25%) showed total regression of NVD, 5 (20.8%) showed partial regression of NVE and 5 eyes (20.8%) showed partial regression of NVD, and 9 eyes (37.5%) showed no regression of NVE and 13 eyes (54.2%) showed no regression of NVD. In the 2.5 mg group, 7 eyes (36.8%) showed total regression of NVE and 7 eyes (36.8%) showed total regression of NVD, 5 (26.3%) showed partial regression of NVE and 9 eyes (47.4%) showed partial regression of NVD, and 3 eyes (15.8%) showed no regression of NVE and 3 eyes (15.8%) showed no regression of NVD. Comparing the two groups, the difference was not statistically significant considering the number of eyes, which showed NVE regression (P = 0.09) and was statistically significant considering NVD regression (P = 0.005) in favor of the 2.5 mg group

Conclusions: : IVB at doses of 1.25 mg or 2.5 provides total or partial regression of RN associated to PDR in 67.2% of eyes with improvement in BCVA and OCT. There was a statistically significant difference in eyes with more regression of NVD with the 2.5mg dose. No tachyphylaxis was identified at 24 months

Keywords: diabetic retinopathy • retinal neovascularization • vascular endothelial growth factor 
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