Intravitreal Bevacizumab (Avastin) for Diabetic Retinopathy: The 2010 GLADAOF Lecture

Author:

Arevalo J. Fernando1,Sanchez Juan G.2,Lasave Andres F.1,Wu Lihteh3,Maia Mauricio4,Bonafonte Sergio5,Brito Miguel6,Alezzandrini Arturo A.7,Restrepo Natalia2,Berrocal Maria H.8,Saravia Mario9,Farah Michel Eid4,Fromow-Guerra Jans10,Morales-Canton Virgilio10

Affiliation:

1. Retina and Vitreous Service, Caracas Clinical Opthalmology Center, Caracas 1010, Venezuela

2. Retina and Vitreous Service, Instituto Nacional de Investigación en Oftalmologica (INIO), Medellín, Colombia

3. Retina and Vitreous Service, Instituto de Cirugia Ocular, San José, Costa Rica

4. Departamento de Oftalmologica, Instituto da Visão, Universidad Federal de São Paulo, 04021-001 São Paulo, SP, Brazil

5. Retina and Vitreous Service, Centro de Oftalmología Bonafonte, Barcelona, Spain

6. Retina and Vitreous Service, Instituto Docente de Especialidades Oftalmológicas (IDEO), Maracaibo, Venezuela

7. OFTALMOS, Facultad de Medicina, Universidad de Buenos Aires, Buenos Aires, Argentina

8. Department of Ophthalmology, University of Puerto Rico, San Juan, Puerto Rico

9. Department of Ophthalmology, Hospital Universitario Austral, Buenos Aires, Argentina

10. Hospital Dr. Luis Sanchez Bulnes, Asociación Para Evitar la Ceguera en Mexico 04030, Mexico City, Mexico

Abstract

This paper demonstrates multiple benefits of intravitreal bevacizumab (IVB) on diabetic retinopathy (DR) including diabetic macular edema (DME) and proliferative diabetic retinopathy (PDR) at 24 months of followup. This is a retrospective multicenter interventional comparative case series of intravitreal injections of 1.25 or 2.5 mg of bevacizumab for DME, PDR without tractional retinal detachment (TRD), and patients who experienced the development or progression of TRD after an intravitreal injection of 1.25 or 2.5 mg of bevacizumab before vitrectomy for the management of PDR. The results indicate that IVB injections may have a beneficial effect on macular thickness and visual acuity (VA) in diffuse DME. Therefore, in the future this new therapy could complement focal/grid laser photocoagulation in DME. In PDR, this new option could be an adjuvant agent to panretina photocoagulation so that more selective therapy may be applied. Finally, TRD in PDR may occur or progress after IVB used as an adjuvant to vitrectomy. Surgery should be performed 4 days after IVB. Most patients had poorly controlled diabetes mellitus associated with elevated HbA1c, insulin administration, PDR refractory to panretinal photocoagulation, and longer time between IVB and vitrectomy.

Funder

Arevalo-Coutinho Foundation for Research in Ophthalmology

Publisher

Hindawi Limited

Subject

Ophthalmology

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