Department of Ophthalmology and Visual Sciences, University of Alberta, Edmonton, Alberta, Canada.
McMaster University, Department of Surgery, Division of Ophthalmology, Hamilton, Ontario, Canada.
Surv Ophthalmol. 2022 Sep-Oct;67(5):1346-1363. doi: 10.1016/j.survophthal.2022.04.003. Epub 2022 Apr 25.
Anti-vascular endothelial growth factor (Anti-VEGF) agents are the standard of care for diabetic macular edema (CI-DME) with vision loss. They are commonly administered using several treatment protocols, including fixed, pro re nata (PRN) and treat-and-extend (T&E) regimens. Because of the lack of evidence defining an ideal treatment paradigm, we systematically compared T&E with fixed or PRN regimens. Visual acuity improvement was similar when comparing T&E to fixed or PRN dosing at 12 and 24 months. Regarding anatomic outcomes, no significant difference was found between T&E and fixed regimens for central retinal thickness or central subfoveal thickness at 12 and 24 months. Similarly, no significant difference was found for central retinal thickness at 12 months for T&E versus PRN regimen. Regarding total number of injections, no significant difference existed between T&E versus fixed regimens at 12 months. PRN regimens delivered fewer injections compared to T&E regimens at 12 months. The results of this analysis support that visual acuity and anatomic outcomes at 12 and 24 months are similar between T&E with either fixed or PRN regimens. More head-to-head trials comparing T&E versus fixed and PRN dosing are needed to provide visual and functional outcome data beyond year 2. PROSPERO Registration: CRD42021249362.
抗血管内皮生长因子(Anti-VEGF)药物是治疗伴有视力丧失的糖尿病黄斑水肿(CI-DME)的标准治疗方法。它们通常通过几种治疗方案进行给药,包括固定剂量、按需治疗(PRN)和治疗-扩展(T&E)方案。由于缺乏定义理想治疗模式的证据,我们系统地比较了 T&E 与固定或 PRN 方案。在 12 个月和 24 个月时,比较 T&E 与固定或 PRN 剂量,视力改善情况相似。在 12 个月和 24 个月时,比较 T&E 与固定方案,在视网膜中心厚度或中心下黄斑厚度方面,解剖学结果没有显著差异。同样,在 12 个月时,T&E 与 PRN 方案相比,在视网膜中心厚度方面也没有显著差异。关于总注射次数,在 12 个月时,T&E 与固定方案之间没有显著差异。与 T&E 方案相比,PRN 方案在 12 个月时注射次数更少。这项分析的结果支持在 12 个月和 24 个月时,T&E 与固定或 PRN 方案的视力和解剖学结果相似。需要更多的头对头试验来比较 T&E 与固定和 PRN 剂量,以提供超过 2 年的视觉和功能结果数据。PROSPERO 注册号:CRD42021249362。