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Volume 116, Issue 8, Pages 1481-1487.e1 (August 2009)


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Intravitreal Bevacizumab for Refractory Pseudophakic Cystoid Macular Edema: The Pan-American Collaborative Retina Study Group Results

Presented in part at: American Academy of Ophthalmology Annual Meeting, November 2008, Atlanta, Georgia.

Pan-American Collaborative Retina Study Group (PACORES)J. Fernando Arevalo, MD, FACS1Corresponding Author Informationemail address, Mauricio Maia, MD2, Rafael A. Garcia-Amaris, MD1, Jose A. Roca, MD3, Juan G. Sanchez, MD1, Maria H. Berrocal, MD4, Lihteh Wu, MD5

Received 25 September 2008; received in revised form 21 February 2009; accepted 1 April 2009. published online 22 June 2009.

Objective

To determine the feasibility, safety, and clinical effect of intravitreal (IVT) bevacizumab (Avastin; Genentech, Inc., San Francisco, CA) in patients with refractory cystoid macular edema (CME) after cataract surgery.

Design

Interventional, retrospective, multicenter study.

Participants

Thirty-six eyes of 31 patients with refractory CME after cataract surgery and with a mean age of 68.2 years (range, 67–87 years).

Methods

Patients were treated with at least 1 IVT injection of 1.25 or 2.5 mg bevacizumab. Patients were followed up for 12 months.

Main Outcome Measures

Best-corrected visual acuity (BCVA) and central macular thickness (CMT) by optical coherence tomography (OCT).

Results

Twenty-six eyes (72.2%) demonstrated improvement of BCVA (≥2 Early Treatment Diabetic Retinopathy Study [ETDRS] lines), and no eye experienced worsening of visual acuity (≥2 ETDRS lines). Mean baseline BCVA was 20/200 (0.96 logarithm of the minimum angle of resolution [logMAR] units), and the mean 12-month BCVA was 20/80 (0.62 logMAR units; P<0.0001). Optical coherence tomography demonstrated that mean CMT at baseline was 499.9 μm (range, 298–784 μm) and decreased to a mean of 286.1 μm (range, 168–499 μm) at 12 months (P<0.0001). Four (11%) eyes received 2 injections, 10 (27.8%) eyes received 3 injections, 10 (27.8%) eyes received 4 injections, 1 (2.8%) eye received 5 injections, and 1 (2.8%) eye received 6 injections. The mean number of injections was 2.7 (range, 1–6), and the mean interval between injections was 15.1 weeks (range, 4–45 weeks). No ocular or systemic adverse events were observed.

Conclusions

Short-term results suggest that IVT bevacizumab is well tolerated in patients with refractory pseudophakic CME. Treated eyes had a significant improvement in BCVA and decrease in macular thickness by OCT at 12 months.

Financial Disclosure(s)

The author(s) have no proprietary or commercial interest in any materials discussed in this article.

Available online: June 21, 2009.

1 Retina and Vitreous Service, Clinica Oftalmológica Centro Caracas, Caracas, Venezuela

2 Departamento de Oftalmologia, Instituto da Visão, Universidade Federal de São Paulo, São Paulo, Brazil

3 Clínica Ricardo Palma, Lima, Peru

4 Department of Ophthalmology, University of Puerto Rico, San Juan, Puerto Rico

5 Retina and Vitreous Service, Instituto de Cirugia Ocular, San Jose, Costa Rica

Corresponding Author InformationCorrespondence: J. Fernando Arevalo, MD, FACS, Clinica Oftalmológica Centro Caracas, Edif. Centro Caracas PH-1, Av. Panteon, San Bernardino, Caracas 1010, Venezuela

 Manuscript no. 2008-1157.

 For a complete listing of participating members of PACORES, see Appendix 1 (available at http://aaojournal.org).

 Financial Disclosure(s): The author(s) have no proprietary or commercial interest in any materials discussed in this article.

 Supported in part by the Arevalo-Coutinho Foundation for Research in Ophthalmology, Caracas, Venezuela.

 Group members listed online in Appendix 1 (available at http://aaojournal.org).

PII: S0161-6420(09)00358-3

doi:10.1016/j.ophtha.2009.04.006


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