首页> 外文期刊>National Journal of Medical Research >Role of intravitreal Bevacizumab Injection for Management of Neovascular Age Related Macular Degeneration
【24h】

Role of intravitreal Bevacizumab Injection for Management of Neovascular Age Related Macular Degeneration

机译:玻璃体内贝伐单抗注射液在管理新生血管性年龄相关性黄斑变性中的作用

获取原文
       

摘要

Background: Age related macular degeneration ( ARMD ) is the major cause of severe visual loss in older adults. Different treatment modalities are available such as: Laser photocoagulation, photodynamic therapy,transpupillary thermotherapy,submacular surgery & anti-veg. Aims & Objectives: The aim of our study was to evaluate the efficacy and safety of intravitreally administered Bevacizumab a humanized monoclonal anti ?VEGF in Neovascular Age related Macular Degeneration. Methodology: This non randomized, prospective study was carried out on 75 eyes of 75 patients attending the OPD at M & J Institute Of Ophthalmology and diagnosed as having Neovascular ARMD confirmed on FFA and SD-OCT . After taking written informed consent all patients were injected with intravitreal Bevacizumab 1.25 mg/0.05 ml. Follow up visits were scheduled one week, one month post procedure and every monthly thereafter. Results: 75 eyes of 75 patients were included in this non randomized prospective study. & 29.33% patients required 2 injections. Visual acuity is improved more than 3 lines from baseline in 21.33% patient, 64% patient have 2-3 lines gain & 6.66% patients showed 0-1 line gain in snellen?s visual acuity. 5.33% patients have a loss of 1 line from baseline & 2.66% patients showed loss of 2-3 lines. Central foveal thickness decreased more than 200 microns from baseline in 52% patients, 28% patients have decreased of 100-200 microns & 20% patients have decreased of less than 100 microns. Discussion: Approximately 10 % of ARMD patients manifest the neovascular form of the disease. 12 weeks). Our study showed that 80% patients had decrease in central foveal thickness more than 100 microns from baseline at the end of one year. 85% patients had gain of 2 or more lines on Snellen?s visual acuity chart from baseline.No patient had any serious local or systemic adverse reactions.Limitations of our study is small number of patients,ICG not done,not compared with other anti-vegf drugs. Conclusion: Intravitreal Bevacizumab is a safe and effective drug in treatment of neovascular age related macular degeneration without any serious systemic or local adverse effects
机译:背景:与年龄相关的黄斑变性(ARMD)是老年人严重视力丧失的主要原因。提供不同的治疗方式,例如:激光光凝,光动力疗法,经瞳孔热疗,黄斑下手术和抗植物。目的与目的:本研究的目的是评估玻璃体腔注射贝伐单抗(人源化单克隆抗βVEGF)在新生血管性年龄相关性黄斑变性中的疗效和安全性。方法:这项非随机,前瞻性研究在M&J眼科研究所接受OPD治疗的75例患者的75只眼中进行,并经FFA和SD-OCT确诊为新血管性ARMD。征得书面知情同意后,所有患者均注射1.25 mg / 0.05 ml玻璃体内贝伐单抗。随访时间安排为一周,手术后一个月,此后每月一次。结果:这项非随机前瞻性研究纳入了75例患者的75眼。 &29.33%的患者需要注射2次。视力较基线提高了3行以上,占21.33%,64%的患者获得2-3行,6.66%的患者的Snellen视力提高了0-1行。 5.33%的患者较基线减少了1行,而2.66%的患者则减少了2-3行。在52%的患者中,中央凹厚度较基线降低了200微米以上,其中28%的患者降低了100-200微米,而20%的患者降低了100微米以下。讨论:大约10%的ARMD患者表现出该疾病的新血管形式。 12周)。我们的研究表明,一年结束时80%的患者中央凹厚度较基线降低了100微米以上。 Snellen视力表中有85%的患者从基线获得了2条或更多条线。没有患者出现任何严重的局部或全身不良反应。本研究的局限性是患者数量少,ICG未完成,未与其他抗凝剂比较-vegf药物。结论:玻璃体内贝伐单抗是治疗新生血管性年龄相关性黄斑变性的安全有效药物,无任何严重的全身或局部不良反应

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号