首页> 外文期刊>Retina >COMPARISON OF TWO DOSES OF INTRAVITREAL BEVACIZUMAB (AVASTIN) FOR TREATMENT OF MACULAR EDEMA SECONDARY TO BRANCH RETINAL VEIN OCCLUSION: Results From the Pan-American Collaborative Retina Study Group at 6 Months of Follow-Up.
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COMPARISON OF TWO DOSES OF INTRAVITREAL BEVACIZUMAB (AVASTIN) FOR TREATMENT OF MACULAR EDEMA SECONDARY TO BRANCH RETINAL VEIN OCCLUSION: Results From the Pan-American Collaborative Retina Study Group at 6 Months of Follow-Up.

机译:比较两种剂量的贝伐单抗(阿瓦斯汀)治疗继发于分支静脉视网膜的黄斑水肿:在术后6个月进行的泛美视网膜研究小组的研究结果。

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PURPOSE:: To report the 6-month anatomical and visual outcomes after injecting two different doses of intravitreal bevacizumab in patients with macular edema secondary to branch retinal vein occlusion (BRVO). METHODS:: An interventional, retrospective multicenter study of 45 eyes that were treated with at least one intravitreal injection (24 eyes, 1.25 mg; 21 eyes, 2.5 mg) of bevacizumab is reported. The main outcome measures were the central 1-mm macular thickness (CMT) and the change in ETDRS lines of best-corrected visual acuity (BCVA) at 6 months. RESULTS:: Forty-five eyes were injected on average 26.1 months (range, 3-86 months) after the diagnosis. The average follow-up was 35.2 weeks (range, 24-52 weeks). All patients completed at least 6 months of follow-up. In the 1.25-mg dose group, at 1 month, there was an average gain of 4.5 lines of BCVA; at 3 months, 5.1 lines of BCVA; and at 6 months, 5.1 lines of BCVA (P < 0.005). In the 2.5-mg dose group, at 1 month, there was an average gain of 2.3 lines of BCVA; at 3 months, 3.8 lines of BCVA; and at 6 months, 4.8 lines of BCVA (P = 0.05). In the 1.25-mg dose group, the mean CMT +/- SD decreased from 461 +/- 211 mum at baseline to 321 +/- 152 mum at 1 month, 273 +/- 99 mum at 3 months, and 277 +/- 114 mum at 6 months (P = 0.0002). In the 2.5-mg group, the mean CMT +/- SD decreased from 385 +/- 168 mum at baseline to 279 +/- 111 mum at 1 month, 249 +/- 97 mum at 3 months, and 240 +/- 93 mum at 6 months (P = 0.011). CONCLUSION:: There were no statistically significant differences between the two dose groups with regard to the number of injections and anatomical and functional outcomes. Intravitreal injection of bevacizumab at doses up to 2.5 mg appears to be effective in improving BCVA and reducing CMT in BRVO in the short term. Multiple injections are needed in a large number of eyes for continued control of macular edema and preservation of visual acuity in the short term. Longer studies are needed to determine what role if any intravitreal injection of bevacizumab may play in the long-term treatment of this condition.
机译:目的:报告在视网膜分支支静脉闭塞(BRVO)继发的黄斑水肿患者中注射两种不同剂量的玻璃体内贝伐单抗后的六个月的解剖和视觉结果。方法:一项介入性,回顾性多中心研究报道了45眼接受至少一次玻璃体内注射贝伐珠单抗(24眼,1.25 mg; 21眼,2.5 mg)治疗的贝伐单抗。主要结局指标为中心性1mm黄斑厚度(CMT)和6个月时最佳矫正视力(BCVA)的ETDRS谱线变化。结果:在诊断后平均26.1个月(范围3-86个月)注射了45只眼。平均随访时间为35.2周(范围24-52周)。所有患者至少完成了6个月的随访。在1.25 mg剂量组中,在1个月时,平均增加了4.5行BCVA;而在1-4个月时,BCVA平均增加了4.5行。 3个月时,BCVA为5.1行;在6个月时,有5.1行BCVA(P <0.005)。在2.5 mg剂量组中,在1个月时,平均增加了2.3株BCVA;而在1个月时,平均增加了BCVA。在3个月时,有3.8行BCVA;在6个月时,有4.8行BCVA(P = 0.05)。在1.25 mg剂量组中,平均CMT +/- SD从基线的461 +/- 211妈妈降低到1个月的321 +/- 152妈妈,3个月的273 +/- 99妈妈和277 + / -6个月时114胎(P = 0.0002)。在2.5毫克组中,平均CMT +/- SD从基线的385 +/- 168毫米降低到1个月的279 +/- 111毫米,3个月的249 +/- 97毫米和240 +/-降低6个月时93个月的妈妈(P = 0.011)。结论:两个剂量组之间在注射次数以及解剖和功能结局方面无统计学差异。在短期内玻璃体内注射贝伐单抗最高剂量为2.5 mg,似乎可以有效改善BRVO中的BCVA和降低CMT。大量眼睛需要多次注射,以在短期内持续控制黄斑水肿并保持视力。需要更长的研究以确定玻璃体内注射贝伐单抗在长期治疗该病中可能起什么作用。

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