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INTRAVITREAL BEVACIZUMAB (AVASTIN) FOR MACULAR EDEMA SECONDARY TO RETINAL VEIN OCCLUSION.
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Aim: The purpose of this study is to evaluate the efcacy and safety prole of intravitreal injection of bevacizumab for
macular edema secondary to retinal vein occlusion. A prospective analysis w Methods: as conducted on patients with
macular edema because of retinal vein occlusion, who had been administered three doses of intravitreal injections of bevacizumab at four weeks
interval and further retreatment was based on optical coherence tomography (OCT) ndings. The changes in the retinal thickness and visual
acuity were evaluated to judge the efcacy, and adverse events were noted for the safety prole over a period of 6 months. A total of 37 Results:
eyes of thirty seven patients were included in the study. The mean age of the patients was 59 ± 14 years. The mean pre-injection best corrected
visual acuity (BCVA) was 1.14± 0.48 log minimum angle of resolution (logMAR) and central foveal thickness (CFT)of 449.8 ± 115.22μm, and
the post-injection BCVA at 6 months was 0.51 ± 0.36 logMAR with a CFT of259.9 ± 87.08μm, this change was statistically signicant (P <
0.05). During the follow-up period after injection, no patient had inammation, endophthalmitis, an increase in intra-ocular pressure, or systemic
side effects. Intravitreal bevacizumab appears to be a safe and effective Conclusion: treatment in patients with macular edema secondary to
retinal vein occlusion.
World Wide Journals
Title: INTRAVITREAL BEVACIZUMAB (AVASTIN) FOR MACULAR EDEMA SECONDARY TO RETINAL VEIN OCCLUSION.
Description:
Aim: The purpose of this study is to evaluate the efcacy and safety prole of intravitreal injection of bevacizumab for
macular edema secondary to retinal vein occlusion.
A prospective analysis w Methods: as conducted on patients with
macular edema because of retinal vein occlusion, who had been administered three doses of intravitreal injections of bevacizumab at four weeks
interval and further retreatment was based on optical coherence tomography (OCT) ndings.
The changes in the retinal thickness and visual
acuity were evaluated to judge the efcacy, and adverse events were noted for the safety prole over a period of 6 months.
A total of 37 Results:
eyes of thirty seven patients were included in the study.
The mean age of the patients was 59 ± 14 years.
The mean pre-injection best corrected
visual acuity (BCVA) was 1.
14± 0.
48 log minimum angle of resolution (logMAR) and central foveal thickness (CFT)of 449.
8 ± 115.
22μm, and
the post-injection BCVA at 6 months was 0.
51 ± 0.
36 logMAR with a CFT of259.
9 ± 87.
08μm, this change was statistically signicant (P <
0.
05).
During the follow-up period after injection, no patient had inammation, endophthalmitis, an increase in intra-ocular pressure, or systemic
side effects.
Intravitreal bevacizumab appears to be a safe and effective Conclusion: treatment in patients with macular edema secondary to
retinal vein occlusion.
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