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Real-Life Management of Diabetic Macular Edema with Dexamethasone Intravitreal Implant: A Retrospective Analysis of Long-Term Clinical Outcomes

机译:糖尿病性黄斑水肿的现实生活管理与地塞米松玻璃体内植入物:长期临床结果的回顾性分析

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Purpose. Inflammation plays a key role in the pathogenesis of diabetic macular edema (DME), and intravitreal corticosteroids are among the recommended therapies. The goal of this retrospective analysis was to describe outcomes with dexamethasone intravitreal implant (DEX implant) in real life. Methods. Medical digital records of DME patients treated with DEX implant and followed up for 3 years were analyzed. Treatment with DEX implant was started either as first-line therapy in pseudophakic patients and in patients with cardiovascular comorbidities or as second-line therapy in patients refractory to the inhibitor of the vascular endothelial growth factor (anti-VEGF) therapy. Analyzed outcomes included central macular thickness (CMT) and best-corrected visual acuity (BCVA). Mean number of implant injections per patient and mean duration of the interval between injections were also estimated. Results. Seventy-five patients (mean age 65.7 (±12.3) years; 53 phakic and 22 pseudophakic) with DME were included. Overall, 84 eyes were treated. Mean CMT improved from 380.1 (±100.3) μm at baseline to 306.8 (±77.0) μm at 36 months (p=0.0003). Mean BCVA improved for up to 6 months (p=0.08) and then started to decrease reaching values lower than baseline after 24 months. In pseudophakic patients, BCVA improvements were more pronounced and sustained up to 36 months (p=0.6). Over 36 months, each patient received on average 2.4 (±1.6) intravitreal injections of DEX implant. The time interval between consecutive injections was included between 180 and 240 days. No unexpected safety issues were reported. Conclusions. With fewer than 3 injections per patient over a 3-year period, DEX implant was able to improve anatomic outcomes in DME patients. Only pseudophakic eyes showed also a long lasting functional benefit at 36 months.
机译:目的。炎症在糖尿病黄斑水肿(DME)的发病机制中起关键作用,玻璃体内皮质类固醇是推荐的疗法。该回顾性分析的目标是在现实生活中描述用地塞米松含有地甲基喹啉植入物(DEX植入物)的结果。方法。分析了DME患者的医疗数字记录,并进行了DEX植入物,随访3年。用Dex植入物治疗初始治疗伪疗效,并且在心血管患者患者中或作为患者抑制血管内皮生长因子(抗VEGF)治疗的抑制剂的二线治疗。分析结果包括中央黄斑厚度(CMT)和最佳校正的视力(BCVA)。还估计了每位患者的平均植入物植入物的数量,并且注射之间的间隔的平均持续时间。结果。七十五名患者(平均年龄为65.7(±12.3)岁; 53个phakic和22伪)被包括DME。总体而言,治疗了84只眼睛。平均CMT在36个月的基线下以380.1(±100.3)μm改善为306.8(±77.0)μm(p = 0.0003)。平均BCVA改善长达6个月(P = 0.08),然后开始减少24个月后基线低于基线的值。在假脂疗患者中,BCVA改善更加明显并持续36个月(P = 0.6)。超过36个月,每个患者平均接受2.4(±1.6)玻璃体内注射DEX植入物。连续注射之间的时间间隔包括在180到240天之间。没有报告意外的安全问题。结论。在3年内,每位患者少于3个注射,Dex植入物能够改善DME患者的解剖结果。仅在36个月内才显示出持久的功能效益较长。

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