首页> 美国卫生研究院文献>Journal of Clinical Medicine >Efficacy of Modified Treat-and-Extend Regimen of Aflibercept for Macular Edema from Branch Retinal Vein Occlusion: 2-Year Prospective Study Outcomes
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Efficacy of Modified Treat-and-Extend Regimen of Aflibercept for Macular Edema from Branch Retinal Vein Occlusion: 2-Year Prospective Study Outcomes

机译:从分支视网膜静脉闭塞治疗AfliBercept的修饰治疗和延伸方案的疗效:2年前瞻性研究结果

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摘要

This study aimed to evaluate the long-term (24-month) efficacy and safety of a modified treat-and-extend (mTAE) regimen of aflibercept for macular edema (ME) due to branch retinal vein occlusion (BRVO). This was a prospective multicenter intervention study. We evaluated 50 eyes in 50 patients with ME due to BRVO enrolled between October 2016 and September 2017. The patients received intravitreal aflibercept (IVA) injections according to a mTAE regimen for 24 months. This study reports the secondary endpoints of best-corrected visual acuity (BCVA) and central subfield thickness (CST) at 24 months and compares them with previously reported primary endpoints. Compared with baseline BCVA and CST of 0.33 (0.27) and 488 (165) µm (mean (standard deviation)), respectively, BCVA and CST were significantly improved at 12 and 24 months (12 months: 0.059 (0.19) LogMAR and 299 (112) µm; 24 months: 0.034 (0.18) LogMAR and 272 (81) µm, respectively; both p < 0.0001). Over the 24-month period, the mean number of IVA injections and clinic visits was 7.4 (3.3) and 11.1 (2.0), respectively. The mTAE regimen of IVA injections for ME due to BRVO was effective for improving BCVA and reducing CST over 24 months. This regimen shows promise for reducing the number of injections and clinic visits.
机译:本研究旨在评估由于分支视网膜静脉闭塞(BRVO),为黄斑水肿(ME)的改良治疗和延伸(MTAE)方案的长期(24个月)的疗效和安全性。这是一个未来的多中心干预研究。由于2016年10月至2017年9月在2016年10月至9月期间,我们评估了50名患者50名患者。根据MTAE方案24个月,患者接受术治疗术治疗术术治疗术治疗术语AFLIBERCEPT(IVA)注射。本研究报告了24个月的最佳校正的视力(BCVA)和中央子场厚度(CST)的次要终点,并将其与先前报告的主要终点进行比较。与基线BCVA和0.33(0.27)和488(165)μm(平均值(标准偏差))相比,BCVA和CST在12和24个月(12个月:0.059(0.19)logmar和299( 112)μm; 24个月:0.034(0.18)Logmar和272(81)μm;两个p <0.0001)。在24个月期间,IVA注射和临床访问的平均数分别为7.4(3.3)和11.1(2.0)。由于BRVO,IVA注射的MTAE方案对于改善BCVA并在24个月内减少CST。这个方案显示了减少注射次数和诊所访问的承诺。

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