首页> 外文期刊>British journal of ophthalmology >Bevacizumab for Coats' disease with exudative retinal detachment and risk of vitreoretinal traction
【24h】

Bevacizumab for Coats' disease with exudative retinal detachment and risk of vitreoretinal traction

机译:贝伐单抗用于伴有渗出性视网膜脱离和玻璃体视网膜牵引风险的Coats病

获取原文
获取原文并翻译 | 示例
       

摘要

Aim: To evaluate the effect of supplemental intravitreal bevacizumab for management of Coats' disease. Methods: Retrospective analysis of eight patients with Coats' disease manifesting total or partial exudative retinal detachment where the retinal telangiectasia was treated with standard laser photocoagulation and/or cryotherapy plus additional intravitreal bevacizumab (1.25 mg/0.05 ml). Results: The mean patient age was 88 (range 7-240) months and 63% were male. Coats' disease was classified as stage 2 (n=1, 12%), 3a (n=3, 38%) and 3b (n=4, 50%). Features included retinal detachment (n=8, 100% with mean detachment extent involving 8 clock hours), telangiectasia (n=8, 100% with mean extent of 8 clock hours), peripheral retinal ischaemia on fluorescein angiography (n=7, 88%) and no evidence of neovascularisation. Treatment consisted of cryotherapy (n=8, 100%), laser photocoagulation (n=4, 50%) and bevacizumab intravitreal injection (n=8) with median number of one injection per eye (mean 1.75, and range 1-4 injections). After a mean follow-up of 8.5 months, resolution of retinopathy (n=8, 100%), Coats'-related subretinal fluid (n=8, 100%) and retinal exudation (n=6, 75%) was noted. However, vitreous fibrosis developed (n=4, 50%) at a mean of 5 months following a mean of 1.75 bevacizumab injections with three (38%) evolving into traction retinal detachment. Conclusion: Coats' disease treated with intravitreal bevacizumab in addition to standard therapy can develop to vitreoretinal fibrosis and potentially traction retinal detachment. These tractional features are not often found in Coats' disease treated with standard measures without bevacizumab. Caution is advised in the use of bevacizumab for patients with Coats' disease.
机译:目的:评估补充玻璃体内贝伐单抗治疗高士氏病的效果。方法:回顾性分析8例Coats病患者,表现为全部或部分渗出性视网膜脱离,其中视网膜毛细血管扩张用标准激光光凝和/或冷冻疗法加玻璃体内贝伐单抗(1.25 mg / 0.05 ml)治疗。结果:患者平均年龄为88(7-240)个月,男性为63%。高士氏病分为2期(n = 1,12%),3a(n = 3,38%)和3b(n = 4,50%)。特征包括视网膜脱离(n = 8,100%,平均脱离程度为8个时钟小时),毛细血管扩张(n = 8,100%,平均程度为8个时钟小时),荧光素血管造影的周围性视网膜缺血(n = 7,88) %),没有新血管形成的证据。治疗包括冷冻疗法(n = 8,100%),激光光凝术(n = 4、50%)和贝伐单抗玻璃体内注射(n = 8),每只眼睛中位数为一次注射(平均1.75,范围为1-4次注射) )。平均随访8.5个月后,观察到视网膜病变的消退(n = 8,100%),Coats相关的视网膜下液(n = 8,100%)和视网膜渗出(n = 6,75%)。然而,在平均1.75贝伐单抗注射后3个月(38%)演变为牵引性视网膜脱离,平均5个月后出现玻璃体纤维化(n = 4,50%)。结论:除标准治疗外,玻璃体内贝伐单抗治疗的大衣病可发展为玻璃体视网膜纤维化和潜在的视网膜脱离。在没有贝伐单抗的标准方法治疗的高士氏病中,这些牵引特征并不常见。建议对患有Coats病的患者使用贝伐单抗要谨慎。

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