...
首页> 外文期刊>Graefe's archive for clinical and experimental ophthalmology: Albrecht von Graefes Archiv fur klinische und experimentelle Opthalmologie >Prognostic factors for visual outcome after intravitreal bevacizumab for macular edema due to branch retinal vein occlusion.
【24h】

Prognostic factors for visual outcome after intravitreal bevacizumab for macular edema due to branch retinal vein occlusion.

机译:玻璃体腔注射贝伐单抗治疗后因视网膜分支静脉阻塞引起的黄斑水肿的视觉预后。

获取原文
获取原文并翻译 | 示例

摘要

PURPOSE: To evaluate the prognostic factors for visual outcome after intravitreal bevacizumab injection to treat macular edema due to branch retinal vein occlusion (BRVO). METHODS: Fifty eyes of 50 consecutive patients treated with intravitreal bevacizumab for macular edema due to BRVO with minimum follow-up of 3 months were retrospectively reviewed. Patients were categorized into two groups according to the final visual acuity. Group 1 consisted of eyes with 5 or more ETDRS letters gain, and group 2 consisted of eyes with less than 5 letters improvement or which had worsened at last follow-up visit. Comparative clinical and fluorescein angiographic characteristics were analyzed between the two groups. RESULTS: Of 50 eyes, 28 (56%) had improved vision after intravitreal bevacizumab injections and were categorized as group 1; 22 eyes (44%) were categorized as group 2. The number of early VA gainers, who showed visual improvement at 1 month after bevacizumab injection, was significantly higher in group 1(P < 0.001, chi-square test). The early gainers tend to maintain significantly better visual outcome until last follow-up. The number of eyes with angiographically documented macular ischemia was significantly higher in group 2 (P < 0.001). In group 2, the decrease in central macular thickness was not accompanied by visual acuity improvement. CONCLUSION: Preoperative presence of macular ischemia can be useful in predicting the outcome of visual acuity after intravitreal bevacizumab for macular edema due to BRVO. The early gainers who favorably responded to the initial intravitreal bevacizumab injection are most likely to benefit from the bevacizumab treatment.
机译:目的:评估玻璃体内注射贝伐单抗注射治疗因视网膜分支静脉阻塞(BRVO)引起的黄斑水肿后视觉效果的预后因素。方法:回顾性分析了连续50例接受玻璃体腔注射贝伐单抗治疗的BRVO引起的黄斑水肿的50眼,至少随访3个月。根据最终视力将患者分为两组。第1组由具有5个或更多ETDRS字母增加的眼睛组成,第2组由具有不到5个字母改善或在上次随访时变差的眼睛组成。比较两组之间的临床和荧光素造影比较特征。结果:50只眼中,有28只(56%)在玻璃体内注射贝伐单抗注射后视力得到改善,被归为第1组。第2组被分类为22只眼(44%)。在第一组中,VA早期获得者的数量在注射贝伐单抗后1个月时显示出视觉改善,数量明显更高(P <0.001,卡方检验)。早起者倾向于保持明显更好的视觉效果,直到最后一次随访。在第2组中,具有血管造影记录的黄斑缺血的眼睛数量明显更高(P <0.001)。在第二组中,黄斑中央厚度的减少并没有伴随视力的改善。结论:术前存在黄斑缺血可用于预测玻璃体内贝伐单抗治疗BRVO引起的黄斑水肿后的视敏度。对最初的玻璃体内贝伐单抗注射剂反应良好的早期获益者最有可能从贝伐单抗治疗中受益。

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