Efficacy of Ranibizumab in the Treatment of Macular Edema Secondary to Retinal Vein Occlusion

Zehra Tunçbilek, Bedriye Nur Ayrancıoğlu, Ayşe Feyza Önder
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Abstract

Objective: Branch retinal vein occlusion (BRVO), a major cause of vision loss, is a significant ocular health concern. The frequency of macular edema due to BRVO is a critical area of study because of its profound impact on patient quality of life. This study investigated the effectiveness of ranibizumab, a monoclonal antibody fragment and VEGF inhibitor, in the treatment of macular edema in patients with BRVO. Material and Methods: Twelve patients (12 eyes) diagnosed with macular edema secondary to BRVO were included in this study. Patients were selected on the basis of specific visual acuity and macular thickness criteria, excluding those with other ocular conditions or systemic diseases. 0.05 milligrams of ranibizumab was administered intravitreally to each patient. Ophthalmological assessments were conducted both before and after the injection and at 1, 2, 3, and 6-month intervals following medication administration. Results: The average follow-up duration was 5.5±1.16 months (ranging from 2 to 6 months). The average central macular thickness before the injection was 542.66±191.44 µm, which decreased to 320.50±101.44 µm at 1-month post-injection, 283.66±125.01 µm at 2 months, 299.40±91.52 µm at 3 months, and 260.90±144.97 µm at 6 months. The reduction in central macular thickness at all time points was statistically significant (p<0.01). The mean Early Treatment Diabetic Retinopathy Study (ETDRS) letter score was 55.83±23.91 before the injection and improved to 71.25±17.07 at 1 month, 74.33±15.97 at 2 months, 66.7±21.60 at 3 months, and 71.2±17.38 at 6 months post-injection. The increase in visual acuity at 1, 2, 3, and 6 months after the injection was statistically significant compared to the pre-injection ETDRS letter scores (p<0.05). An improvement of two or more lines in visual acuity was observed in 58.3% of cases at 1 month, 58.3% at 2 months, 50% at 3 months, and 80% at 6 months (one line equivalent to five letters). Conclusion: Intravitreal Ranibizumab injections have been found to be effective and reliable in the early stages of treating macular edema due to branch retinal vein occlusion.
雷珠单抗治疗视网膜静脉闭塞继发性黄斑水肿的疗效
目的:视网膜分支静脉阻塞(BRVO)是视力丧失的主要原因,也是眼部健康的一个重要问题。视网膜静脉阻塞导致的黄斑水肿对患者的生活质量影响深远,因此黄斑水肿的发病率是一个重要的研究领域。本研究探讨了单克隆抗体片段和血管内皮生长因子抑制剂雷尼珠单抗治疗 BRVO 患者黄斑水肿的有效性:本研究纳入了 12 名确诊为 BRVO 继发性黄斑水肿的患者(12 只眼)。根据特定的视力和黄斑厚度标准选择患者,排除患有其他眼部疾病或全身性疾病的患者。每位患者均在玻璃体内注射了0.05毫克的雷尼珠单抗。在注射前后以及用药后的 1、2、3 和 6 个月期间进行了眼科评估:平均随访时间为 5.5±1.16 个月(2 至 6 个月)。注射前黄斑中心厚度平均为 542.66±191.44 µm,注射后 1 个月时降至 320.50±101.44 µm,2 个月时降至 283.66±125.01 µm,3 个月时降至 299.40±91.52 µm,6 个月时降至 260.90±144.97 µm。所有时间点黄斑中心厚度的减少均有统计学意义(P<0.01)。注射前,早期治疗糖尿病视网膜病变研究(ETDRS)的平均字母评分为 55.83±23.91,注射后 1 个月时提高到 71.25±17.07,2 个月时提高到 74.33±15.97,3 个月时提高到 66.7±21.60,6 个月时提高到 71.2±17.38。与注射前的 ETDRS 字母评分相比,注射后 1、2、3 和 6 个月视力的提高具有统计学意义(P<0.05)。58.3%的病例在注射 1 个月后视力提高了两行或两行以上,58.3%的病例在注射 2 个月后视力提高了两行或两行以上,50%的病例在注射 3 个月后视力提高了两行或两行以上,80%的病例在注射 6 个月后视力提高了两行或两行以上(一行相当于 5 个字母):结论:在治疗视网膜分支静脉闭塞引起的黄斑水肿的早期阶段,玻璃体内注射雷珠单抗是有效和可靠的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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