Department of Ophthalmology, Trabzon Kanuni Training and Research Hospital, University of Health Sciences, Trabzon, Turkey.
Department of Ophthalmology, Istanbul Faculty of Medicine, Istanbul University Istanbul, Turkey.
Arq Bras Oftalmol. 2023 Oct 20;87(6):e20220228. doi: 10.5935/0004-2749.2022-0228. eCollection 2023.
To evaluate early changes after the first antivascular endothelial growth factor injection for macular edema secondary to diabetic retinopathy and retinal vein occlusion and the relationship between longterm outcomes.
The study enrolled patients who received anti-vascular endothelial growth factor injections for treatment-naive macular edema due to retinal vein occlusion and diabetic retinopathy. The central macular thickness was measured at baseline, post-injection day 1, week 2, and month 1, and at the last visit using spectral-domain optical coherence tomography. A good response was defined as a central macular thickness reduction of ≥10% on post-injection day 1. Patients were reassessed at the last visit with regard to treatment response on post-injection day 1 based on the favorable anatomic outcome defined as a central macular thickness <350 µm.
In total, 26 (44.8%) patients had macular edema-retinal vein occlusion and 32 (55.2%) had macular edema-diabetic retinopathy. The mean follow-up time was 24.0 (SD 8.5) months. A statistically significant decrease in the central macular thickness was observed in both patients with macular edema-retinal vein occlusion and macular edema-diabetic retinopathy after antivascular endothelial growth factor injection therapy (p<0.001 for both). All patients with macular edema-retinal vein occlusion were good responders at post-injection day 1. All nongood responders at post-injection day 1 belong to the macular edema-diabetic retinopathy group (n=16.50%). The rate of hyperreflective spots was higher in nongood responders than in good responders of the macular edema-diabetic retinopathy group (p=0.03). Of 42 (2.4%) total good responders, one had a central macular thickness >350 µm, whereas 5 (31.2%) of 16 total nongood responders had a central macular thickness >350 µm at the last visit (p=0.003).
The longterm anatomical outcomes of macular edema secondary to retinal vein occlusion and diabetic retinopathy may be predicted by treatment response 1 day after antivascular endothelial growth factor injection.
评估首次抗血管内皮生长因子注射治疗糖尿病视网膜病变和视网膜静脉阻塞继发黄斑水肿的早期变化及其与长期疗效的关系。
本研究纳入了因视网膜静脉阻塞和糖尿病视网膜病变而接受抗血管内皮生长因子注射治疗的初治黄斑水肿患者。使用频域光相干断层扫描仪在基线、注射后第 1 天、第 2 周和第 1 个月以及最后一次就诊时测量中心黄斑厚度。将注射后第 1 天中央黄斑厚度减少≥10%定义为良好反应。最后一次就诊时,根据定义为中心黄斑厚度<350 µm的有利解剖结局,根据注射后第 1 天的良好治疗反应对患者进行重新评估。
共有 26 例(44.8%)患者为黄斑水肿-视网膜静脉阻塞,32 例(55.2%)患者为黄斑水肿-糖尿病视网膜病变。平均随访时间为 24.0(8.5)个月。在接受抗血管内皮生长因子注射治疗后,黄斑水肿-视网膜静脉阻塞和黄斑水肿-糖尿病视网膜病变患者的中央黄斑厚度均有统计学显著下降(均为 p<0.001)。注射后第 1 天,所有黄斑水肿-视网膜静脉阻塞患者均为良好反应者。注射后第 1 天所有非良好反应者均属于黄斑水肿-糖尿病视网膜病变组(n=16.50%)。非良好反应者的高反射斑点发生率高于黄斑水肿-糖尿病视网膜病变组的良好反应者(p=0.03)。在 42 例(2.4%)总良好反应者中,有 1 例患者的中心黄斑厚度>350 µm,而在 16 例总非良好反应者中,有 5 例(31.2%)患者的中心黄斑厚度>350 µm(p=0.003)。
通过抗血管内皮生长因子注射治疗后 1 天的治疗反应,可预测视网膜静脉阻塞和糖尿病视网膜病变继发黄斑水肿的长期解剖结局。