Bevacizumab versus ziv-aflibercept in branch retinal vein occlusion

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Wolters Kluwer Medknow Publications

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Purpose: To compare the effectiveness of treatment with intravitreal bevacizumab (IVB) and ziv-aflibercept (IVZ) in patients with macular edema (ME) post-branch retinal vein occlusion (BRVO). Methods: Patients with treatment naïve ME post-BRVO were included retrospectively if they received either IVB (0.05 ml/1.25 mg) or IVZ (0.05 ml/1.25 mg) monotherapy with a follow up of 12 months. Results: Thirty-two and 17 eyes received IVB and IVZ, respectively. The mean improvement in best corrected visual acuity (BCVA) was 0.36 ± 0.3 logarithm of minimum angle of resolution (logMAR) in the IVB group and 0.27 ± 0.3 in the IVZ group (P = 0.35). The mean change in central macular thickness was 178.9 ± 180.9 and 173.5 ± 344.4 μm in IVB and IVZ groups, respectively (P = 0.94). The mean number of injections was higher in the IVB group (4.0 ± 1.8) compared with 1.82 ± 0.8 in the IVZ group (P < 0.0001). The IVZ group had significantly fewer number of visits (P < 0.0001) and longer maximum treatment-free intervals (P = 0.0081). Conclusion: IVZ appears to be cost-effective with the similar visual outcome and less number of visits in comparison to IVB. © 2019 Indian Journal of Ophthalmology Published by Wolters Kluwer - Medknow.

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Bevacizumab, Branch retinal venous occlusion, Macular edema, Optical coherence tomography, Ziv-aflibercept, Aged, Angiogenesis inhibitors, Dose-response relationship, drug, Female, Fluorescein angiography, Follow-up studies, Fundus oculi, Humans, Intravitreal injections, Male, Middle aged, Ophthalmoscopy, Receptors, vascular endothelial growth factor, Recombinant fusion proteins, Retina, Retinal vein occlusion, Slit lamp microscopy, Tomography, optical coherence, Treatment outcome, Visual acuity, Aflibercept, Angiogenesis inhibitor, Fusion protein, Vasculotropin receptor, Antagonists and inhibitors, Clinical trial, Comparative study, Diagnostic imaging, Dose response, Eye fundus, Fluorescence angiography, Follow up, Human, Intravitreal drug administration, Multicenter study, Retina vein occlusion

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