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

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Autores
Arevalo, J. Fernando
Maia, Mauricio
Garcia-Amaris, Rafael A.
Roca, Jose A.
Sanchez, Juan G.
Berrocal, Maria H.
Wu, Lihteh

Fecha
2009-06-22

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Elsevier

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Abstract
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.
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Keywords
Aged , Aged , 80 and over , Angiogenesis Inhibitors , Antibodies , Monoclonal , Antibodies , Monoclonal , Humanized , Bevacizumab , Cataract Extraction , Feasibility Studies , Female , Fluorescein Angiography , Follow-Up Studies , Humans , Injections , Macular Edema , Male , Postoperative Complications , Pseudophakia , Retrospective Studies , Tomography , Optical Coherence , Treatment Outcome , Vascular Endothelial Growth Factor A , Visual Acuity , Vitreous Body
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