The Save Sight Institute, University of Sydney, Australia.
Macula Research Group, Save Sight and Eye Health Institute, University of Sydney, 8 Macquarie Street, Sydney, NSW 2000, Australia.
Ther Adv Chronic Dis. 2015 Sep;6(5):234-45. doi: 10.1177/2040622315590319.
Diabetic macular oedema (DMO) is the most common cause of visual loss in the working age population. Intravitreal therapy has superseded macular laser as the first-line treatment for the management of centre-involving DMO in most patients. As well as the proven efficacy of intravitreal anti-vascular endothelial growth factor (anti-VEGF) agents, phase II and III clinical trials of Ozurdex intravitreal dexamethasone implants for DMO have also demonstrated a mean increase in visual acuity and corresponding mean reduction in central macular thickness, particularly in pseudophakic eyes. Because of the risk of visual loss from cataract, glaucoma and intraocular infection with the use of intravitreal steroids, Ozurdex tends to be reserved for use in patients unresponsive to anti-VEGF therapy for centre-involving DMO. Situations where Ozurdex may be considered a first-line treatment option for eyes with centre-involving DMO include pseudophakia, impending cataract surgery, or in the context of a recent arterial thromboembolic event. Because of their stable pharmacokinetics, Ozurdex slow-release implants may also be considered in vitrectomized eyes.
糖尿病性黄斑水肿(DMO)是工作年龄人群视力丧失的最常见原因。在大多数患者中,玻璃体内治疗已取代黄斑激光成为治疗中心性 DMO 的一线治疗方法。除了已证明的玻璃体内抗血管内皮生长因子(anti-VEGF)药物的疗效外,Ozurdex 玻璃体内地塞米松植入物治疗 DMO 的 II 期和 III 期临床试验还表明,视力平均提高,中央黄斑厚度相应平均降低,尤其是在人工晶状体眼。由于玻璃体内类固醇使用引起白内障、青光眼和眼内感染导致视力丧失的风险,Ozurdex 倾向于保留用于对中心性 DMO 的抗 VEGF 治疗无反应的患者。Ozurdex 可能被视为中心性 DMO 眼的一线治疗选择的情况包括:人工晶状体眼、即将进行白内障手术或近期动脉血栓栓塞事件。由于其稳定的药代动力学,Ozurdex 缓释植入物也可考虑用于玻璃体切割眼。