Valašková J, Popov I, Krásnik V
Cesk Slov Oftalmol. 2018 Spring;73(5-6):183-188.
functional and anatomical results after combination of intravitreal dexamethasone implant with anti-VEGF bevacizumab in macular edema secondary to retinal vein occlusion.
Retrospective analysis of 50 patients, average age 72 years, 15 men and 35 women. Inclusion criteria for treatment were retinal vein occlusion, best corrected visual acuity (BCVA) more than 20/200 and macular edema more than 250 μm. Algorithm of treatment was dexamethason, anti-VEGF (bevacizumab), dexamethason. Application of anti-VEGF bevacizumab was in interval between two applications of dexamethasone, for the first time in every patient. If there were nonperfusion areas on fluoresceine angiography (FA), or ischemia on slit lamp, repeatedly. Patients observed for 12 months at least. This cohort included patients with branch retinal vein occlusion together with central retinal vein occlusion. This is an evaluation of nonperfusion areas based on FA, BCVA, macular edema on optical coherence tomography (OCT) and number of reapplication of anti-VEGF bevacizumab. Observed adverse effects are elevation of intraocular pressure and number of patients who underwent cataract surgery.
The gain of 8 letters in 1st month after 1st application of dexamethasone, central retinal thickness (CRT) reduced from 512 μm to 318 μm in average. 33 patients get 1, 3 patients get 2 and 14 patients 3 injections of bevacizumab. On the day of 2nd application of dexamethasone, in 7th month in average, the CRT increased on 465 μm, and 1th month after, the gain from the baseline was 10 letters and CRT reduced on 380 μm. All the patients were phackic at the baseline, 18 (36 %) patients underwent cataract surgery with intraocular lens implantation. Transient elevation of intraocular pressure in 15 (30 %) eyes, treated by local therapy.
Combination of intravitreal dexamethasone implant with anti-VEGF bevacizumab is functionally and anatomically effective. Key words: retinal vein occlusion, macular edema, dexamethasone, bevacizumab.
探讨玻璃体内注射地塞米松植入剂联合抗血管内皮生长因子(VEGF)药物贝伐单抗治疗视网膜静脉阻塞继发黄斑水肿的功能及解剖学疗效。
回顾性分析50例患者,平均年龄72岁,男性15例,女性35例。治疗纳入标准为视网膜静脉阻塞、最佳矫正视力(BCVA)高于20/200且黄斑水肿厚度超过250μm。治疗方案为地塞米松、抗VEGF(贝伐单抗)、地塞米松。抗VEGF药物贝伐单抗在两次地塞米松注射间隔期应用,每位患者首次使用。若荧光素血管造影(FA)显示有非灌注区,或裂隙灯检查发现缺血,则重复使用。患者至少观察12个月。该队列包括视网膜分支静脉阻塞和视网膜中央静脉阻塞患者。评估指标包括基于FA的非灌注区、BCVA、光学相干断层扫描(OCT)显示的黄斑水肿情况以及抗VEGF药物贝伐单抗的重复使用次数。观察到的不良反应为眼压升高及接受白内障手术的患者数量。
首次注射地塞米松后第1个月视力平均提高8行,中央视网膜厚度(CRT)平均从512μm降至318μm。33例患者接受1次、3例患者接受2次、14例患者接受3次贝伐单抗注射。平均在第7个月第二次注射地塞米松时,CRT增加至465μm,之后第1个月,相对于基线视力提高10行,CRT降至380μm。所有患者基线时均为晶状体在位,18例(36%)患者接受了白内障摘除联合人工晶状体植入术。15只眼(30%)出现眼压短暂升高,经局部治疗后缓解。
玻璃体内注射地塞米松植入剂联合抗VEGF药物贝伐单抗在功能及解剖学上均有效。关键词:视网膜静脉阻塞;黄斑水肿;地塞米松;贝伐单抗