Wallsh Josh, Sharareh Behnam, Gallemore Ron
Retina Macula Institute, Torrance, CA, USA.
Clin Ophthalmol. 2016 May 25;10:947-54. doi: 10.2147/OPTH.S105412. eCollection 2016.
To test the efficacy of the intravitreal dexamethasone (DEX) implant in patients with retinal vein occlusions (RVOs) who have failed multiple anti-vascular endothelial growth factor (anti-VEGF) treatments.
A randomized exploratory study of ten patients with branch RVO or central RVO who received at least two previous anti-VEGF treatments and had persistent or unresponsive cystoid macular edema. Treatment with the DEX implant was either every 4 months or pro re nata (PRN) depending on their group assignment for 1 year. Multifocal electroretinography and microperimetry were the primary end points, with high-resolution optical coherence tomography and best-corrected visual acuity as the secondary end points.
All patients in both the every 4 month and PRN cohorts who completed the study received the three maximal injections of DEX; therefore, the data from both cohorts were combined and reported as a case series. On average, the multifocal electroretinography amplitude increased significantly from 5.11±0.66 to 24.19±5.30 nV/deg2 at 12 months (P<0.005), mean macular sensitivity increased from 7.67±2.10 to 8.01±1.98 dB at 4 months (P=0.32), best-corrected visual acuity increased significantly from 51.0±5.1 to 55.4±5.1 early treatment of diabetic retinopathy study letters at 2 months (P<0.05), and central retinal thickness decreased from 427.6±39.5 to 367.1±37.8 μm at 4 months (P<0.05). Intraocular pressure increased significantly in one patient, with that patient requiring an additional glaucoma medication for management. Additionally, cataract progression increased significantly (P<0.05) in this patient population and partially limited analysis of other end points.
DEX should be considered as a treatment option in patients with RVOs who have failed anti-VEGF therapy, as the results of this study demonstrated an improvement in retinal morphology and macular function. Cataract progression did occur following multiple consecutive injections; however, steroid-induced glaucoma was not a limiting factor.
测试玻璃体内地塞米松(DEX)植入物对多次抗血管内皮生长因子(抗VEGF)治疗失败的视网膜静脉阻塞(RVO)患者的疗效。
一项随机探索性研究,纳入10例分支RVO或中央RVO患者,这些患者此前至少接受过两次抗VEGF治疗且存在持续性或反应性不佳的黄斑囊样水肿。根据分组情况,DEX植入物治疗每4个月进行一次或按需(PRN)进行,为期1年。多焦视网膜电图和微视野检查为主要终点,高分辨率光学相干断层扫描和最佳矫正视力为次要终点。
完成研究的每4个月治疗组和PRN组的所有患者均接受了3次最大剂量的DEX注射;因此,将两组的数据合并并作为病例系列报告。平均而言,多焦视网膜电图振幅在12个月时从5.11±0.66显著增加至24.19±5.30 nV/deg2(P<0.005),黄斑平均敏感度在4个月时从7.67±2.10增加至8.01±1.98 dB(P=0.32),最佳矫正视力在2个月时从51.0±5.1显著提高至55.4±5.1糖尿病视网膜病变早期治疗研究字母(P<0.05),视网膜中央厚度在4个月时从427.6±39.5降至367.1±37.8μm(P<0.05)。1例患者眼压显著升高,该患者需要额外使用青光眼药物进行治疗。此外,该患者群体中白内障进展显著增加(P<0.05),部分限制了对其他终点的分析。
对于抗VEGF治疗失败的RVO患者,应考虑将DEX作为一种治疗选择,因为本研究结果表明视网膜形态和黄斑功能有所改善。连续多次注射后确实出现了白内障进展;然而,类固醇性青光眼并非限制因素。