Yonekawa Yoshihiro, Modi Yasha S, Kim Leo A, Skondra Dimitra, Kim Judy E, Wykoff Charles C
Mid Atlantic Retina, Wills Eye Hospital, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA.
Department of Ophthalmology, New York University School of Medicine, New York, NY.
J Vitreoretin Dis. 2020 Mar 1;4(2):125-135. doi: 10.1177/2474126419893829. Epub 2020 Jan 6.
Nonproliferative (NPDR) and proliferative diabetic retinopathy (PDR) without diabetic macular edema (DME) affect millions of individuals living with diabetes throughout the world. There is increasing data on various management strategies for such patients, but there is limited consensus on how the data should be adopted into clinical practice.
This literature review and editorial presents and synthesizes the current evidence for various management paradigms for NPDR and PDR without DME.
Retina specialists are an integral member of the diabetes management team, and should encourage patients on the importance of glycemic and cardiovascular optimization for both systemic and retinopathy risk factor reduction. The diabetic retinopathy severity scale (DRSS) is now an approvable endpoint for clinical trials in the United States, therefore becoming more clinically relevant. For PDR without DME, the Diabetic Retinopathy Study (DRS) and the Early Treatment Diabetic Retinopathy Study (ETDRS) established the standard of care with panretinal photocoagulation (PRP). Laser parameters have since evolved to include less intense and earlier intervention. Studies have recently demonstrated that anti-vascular endothelial growth factor (VEGF) treatment of PDR is effective at regressing neovascularization and improving DRSS levels in many patients. Further evidence is required to determine optimal treatment frequency, duration, and retreatment criteria, in the real world. There are concerns for adverse events in patients being lost to follow up during anti-VEGF treatment. For NPDR without DME, the standard of care has been a wait-and-watch approach. Data within the DRS and the ETDRS suggest that PRP for severe NPDR can be an option for select patients as well. Multiple clinical trials have now demonstrated that anti-VEGF treatment can improve the DRSS score in NPDR. Further studies are required to assess whether this positively affects long-term visual outcomes, and whether the benefits outweigh the risks in the real world for routine use.
There is cumulative evidence demonstrating the efficacy of various treatment options for NPDR and PDR without DME. Currently, patients would most likely benefit from thoughtful management strategies that are tailored to the individual patient.
非增殖性糖尿病视网膜病变(NPDR)和无糖尿病性黄斑水肿(DME)的增殖性糖尿病视网膜病变(PDR)影响着全球数百万糖尿病患者。关于此类患者的各种管理策略的数据越来越多,但对于如何将这些数据应用于临床实践,人们的共识有限。
本综述和社论展示并综合了目前关于NPDR和无DME的PDR的各种管理模式的证据。
视网膜专科医生是糖尿病管理团队不可或缺的成员,应鼓励患者认识到血糖和心血管系统优化对于降低全身和视网膜病变风险因素的重要性。糖尿病视网膜病变严重程度量表(DRSS)现在是美国临床试验的一个可批准终点,因此在临床上更具相关性。对于无DME的PDR,糖尿病视网膜病变研究(DRS)和早期治疗糖尿病视网膜病变研究(ETDRS)确立了全视网膜光凝(PRP)的治疗标准。此后激光参数不断发展,包括强度更低和更早干预。最近的研究表明,抗血管内皮生长因子(VEGF)治疗PDR在使许多患者新生血管消退和改善DRSS水平方面是有效的。在现实世界中,还需要进一步的证据来确定最佳治疗频率、持续时间和再次治疗标准。人们担心抗VEGF治疗期间失访患者的不良事件。对于无DME的NPDR,治疗标准一直是观察等待方法。DRS和ETDRS的数据表明,对于严重NPDR患者,PRP也可以是一种选择。多项临床试验现已证明,抗VEGF治疗可改善NPDR患者的DRSS评分。还需要进一步研究来评估这是否对长期视力结果有积极影响,以及在现实世界中常规使用时益处是否大于风险。
有越来越多的证据表明各种治疗方案对无DME的NPDR和PDR有效。目前,患者最有可能从针对个体患者量身定制的周到管理策略中获益。