Arıkan Yorgun Mücella, Toklu Yasin, Mutlu Melek
Department of Ophthalmology, Ankara Atatürk Education and Research Hospital, Yıldırım Beyazıt University, Ankara, Turkey.
Int Ophthalmol. 2017 Feb;37(1):185-196. doi: 10.1007/s10792-016-0251-2. Epub 2016 May 12.
The purpose of the study is to evaluate the efficacy and safety of as-needed dexamethasone (DEX) retreatment compared with standard DEX retreatment combined with PRN ranibizumab injections among patients with persistent diabetic macular edema (DME). Twenty-eight patients with persistent macular edema having recurrence earlier than 6 months after initial DEX implantation were included in this retrospective study. Group I consisted of 13 patients retreated using monthly PRN ranibizumab injections combined with standard 6-monthly DEX implantation; Group II consisted of 15 patients retreated with DEX implantation earlier than 6 months on an "as-needed" basis. There was no significant difference between the groups with regarding to age, gender, HbA1C levels, duration of diabetes, duration of macular edema, baseline central macular thickness (CMT), best-corrected visual acuity (BCVA), and intraocular pressure (IOP) values (p > 0.05). The mean follow-up time of the whole study population was 10.13 ± 1.75 months (range 9-15). The mean CMT values were significantly decreased in both groups compared to baseline values except for the 6th-month CMT in Group I (p < 0.05). The mean logMAR BCVA values were not statistically different between groups during the follow-up compared to baseline BCVA values (p > 0.05). However, a significant change in mean BCVA from baseline was seen at 4th, 6th, and 9th months in Group II (p ≤ 0.05). The mean number of total intravitreal treatments was 3.50 ± 0.77 in Group I and 2.53 ± 0.51 in Group II (p = 0.001). During the follow-up period, one patient in Group I and five patients in Group II had increased IOP (≥25 mmHg). Early DEX retreatment improved vision with superior anatomical improvement at 6th month and with fewer intravitreal treatments in eyes with DME. However, improvement in visual acuity is similar with standard DEX retreatment combined with PRN ranibizumab group.
本研究的目的是评估按需使用地塞米松(DEX)再治疗与标准DEX再治疗联合按需注射雷珠单抗相比,在持续性糖尿病性黄斑水肿(DME)患者中的疗效和安全性。本回顾性研究纳入了28例初始DEX植入后6个月内复发的持续性黄斑水肿患者。第一组由13例患者组成,采用每月按需注射雷珠单抗联合标准的每6个月一次DEX植入进行再治疗;第二组由15例患者组成,在“按需”基础上于6个月前进行DEX植入再治疗。两组在年龄、性别、糖化血红蛋白水平、糖尿病病程、黄斑水肿病程、基线中心黄斑厚度(CMT)、最佳矫正视力(BCVA)和眼压(IOP)值方面无显著差异(p>0.05)。整个研究人群的平均随访时间为10.13±1.75个月(范围9 - 15个月)。与基线值相比,两组的平均CMT值均显著降低,但第一组的第6个月CMT除外(p<0.05)。随访期间,两组的平均logMAR BCVA值与基线BCVA值相比无统计学差异(p>0.05)。然而,第二组在第4、6和9个月时,平均BCVA较基线有显著变化(p≤0.05)。第一组玻璃体内治疗的总平均次数为3.50±0.77次,第二组为2.53±0.51次(p = 0.001)。随访期间,第一组有1例患者和第二组有5例患者眼压升高(≥25 mmHg)。早期DEX再治疗可改善视力,在第个月时解剖学改善更优,且DME患者的玻璃体内治疗次数更少。然而,视力改善与标准DEX再治疗联合按需注射雷珠单抗组相似。
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