The Safety, Effectiveness and Prognostic Factors of Intravitreal Avastin (Bevacizumab) Injection for the Treatment of Macular Edema at the University of Gondar Tertiary Eye Care and Training Center, NW Ethiopia

Yoseph Gizachew, Asamere Tsegaw, Tarekegn Wuletaw
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Abstract

Introduction: The current management of macular edema (ME) is intravitreal injection of anti-vascular endothelial growth factor (anti-VEGF) drugs and this represents an important advance in the treatment of ME. Studies done in the western eye care settings have confirmed that intravitreal injection of Avastin is effective for the treatment of ME. However, data on this drugs efficacy and safety in African eye care settings are very scarce. Objective: To assess the Safety and Effectiveness of intravitreal Bevacizumab (Avastin) injection for the treatment of Macular Edema (ME) due to retina vascular diseases at university of Gondar tertiary eye care and training center, NW Ethiopia. Method: A retrospective study was done on patients who were given intravitreal avastin (IVA) for the treatment of diabetic macular edema (DME), retinal vein occlusion (RVO) and Neovascular Age related macular degeneration (AMD). The main outcome measure was visual acuity (VA) and central macular thickness (CMT) measured by spectral domain OCT. Results: Medical records of 50 patients (66 eyes) were reviewed of which 46 (69.7%) were males and mean age of 54.2 years (range 20-80). The means of baseline VA and CMT were 1.0logMAR and 379.4 micron respectively. At the end of follow up and after mean injection of 2.5 times per eye, the mean VA improved to 0.7 logMAR (p=0.001) and the mean CMT reduced to 295 micron (p=0.0001). Baseline mean VA was significant prognostic factor for VA improvement (p=0.0001). Baseline mean CMT (P=0.007), number of injection (P=0.009) and diffuse macular edema (P=0.03) were significant factors for CMT reduction. Conclusions: IVA injection for ME edema due to retinal vascular diseases resulted in a significant improvement in mean VA (p=0.001) and CMT (p=0.0001) at the end of follow up. There was no any ocular or systemic complication of IVA injection.
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在埃塞俄比亚西北部贡达尔大学眼科三级护理和培训中心注射玻璃体内阿瓦斯汀(贝伐单抗)治疗黄斑水肿的安全性、有效性和预后因素
导言:目前治疗黄斑水肿(ME)的方法是在玻璃体内注射抗血管内皮生长因子(anti-VEGF)药物,这是治疗黄斑水肿的重要进展。在西方眼科医疗机构进行的研究证实,玻璃体内注射阿瓦斯汀可有效治疗黄斑水肿。然而,有关这种药物在非洲眼科治疗环境中的疗效和安全性的数据却非常稀少。目的评估在埃塞俄比亚西北部贡达尔大学三级眼科护理和培训中心静脉注射贝伐单抗(安维汀)治疗视网膜血管疾病引起的黄斑水肿(ME)的安全性和有效性:这项回顾性研究的对象是接受静脉注射阿瓦斯汀(IVA)治疗糖尿病黄斑水肿(DME)、视网膜静脉阻塞(RVO)和新生血管性老年黄斑变性(AMD)的患者。主要结果指标是视力(VA)和光谱域 OCT 测量的黄斑中心厚度(CMT):回顾了 50 名患者(66 只眼睛)的医疗记录,其中 46 名(69.7%)为男性,平均年龄为 54.2 岁(20-80 岁不等)。基线视力和CMT的平均值分别为1.0logMAR和379.4微米。随访结束时,平均每只眼睛注射 2.5 次后,平均视力提高到 0.7 logMAR(p=0.001),平均 CMT 降低到 295 微米(p=0.0001)。基线平均视力是视力改善的重要预后因素(P=0.0001)。基线平均 CMT(P=0.007)、注射次数(P=0.009)和弥漫性黄斑水肿(P=0.03)是 CMT 减少的重要因素。结论IVA 注射治疗视网膜血管疾病引起的 ME 水肿,在随访结束时可显著改善平均视力(P=0.001)和 CMT(P=0.0001)。IVA 注射未引起任何眼部或全身并发症。
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