Sirakaya Ender, Kilic Deniz, Aslan Sirakaya Hatice
Department of Ophthalmology, Health Science University, The Kayseri City Hospital, Kayseri, Turkey.
Department of Internal Medicine, Health Science University, The Kayseri City Hospital, Kayseri, Turkey.
Eur J Ophthalmol. 2023 May;33(3):1459-1466. doi: 10.1177/11206721221144797. Epub 2022 Dec 8.
To compare the effects of ranibizumab, aflibercept and bevacizumab treatments in treatment-naive diabetic macular edema(DME) patients with serous retinal detachment(SRD).
This is a retrospective, comparative study. In a sample of 86 eyes of 86 untreated DME patients with accompanying SRD, 23 patients were treated with ranibizumab (IVR), 28 patients with aflibercept (IVA), and 35 patients with bevacizumab (IVB). All were injected intravitreally once a month for a 3-month loading dose. Subsequently, all participants were evaluated every months and if neccessary they received additional intravitreal treatments.Mean changes in best corrected visual acuity (BCVA), central retinal thickness (CRT), and SRD height over the 6-months study period were compared.
At baseline, the groups did not differ in mean BCVA,CRT and SRD height. During the first 3 months, in IVA group the mean decrease in CRT and SRD height were significantly more than in the other two groups (< 0.05 for all). However, these differences disappeared at 6 months.The number of injections was similar between the groups during the study period.
In patients with DME accompanied by SRD, IVA is a more advantageous option in terms of reduction in CRT and SRD height from baseline to 3 months. In the 6-month period of treatment, IVR, IVA and IVB therapies areanatomically and functionally similar and significant effective modalities.
比较雷珠单抗、阿柏西普和贝伐单抗治疗初治的伴有浆液性视网膜脱离(SRD)的糖尿病性黄斑水肿(DME)患者的疗效。
这是一项回顾性比较研究。在86例未经治疗的伴有SRD的DME患者的86只眼中,23例患者接受雷珠单抗治疗(玻璃体内注射雷珠单抗,IVR),28例患者接受阿柏西普治疗(玻璃体内注射阿柏西普,IVA),35例患者接受贝伐单抗治疗(玻璃体内注射贝伐单抗,IVB)。所有患者每月玻璃体腔内注射一次,共注射3个月作为负荷剂量。随后,每月对所有参与者进行评估,必要时给予额外的玻璃体腔内治疗。比较了6个月研究期内最佳矫正视力(BCVA)、中心视网膜厚度(CRT)和SRD高度的平均变化。
基线时,各组在平均BCVA、CRT和SRD高度方面无差异。在最初3个月内,IVA组CRT和SRD高度的平均降低幅度显著大于其他两组(均P<0.05)。然而,这些差异在6个月时消失。研究期间各组的注射次数相似。
对于伴有SRD的DME患者,从基线到3个月,就降低CRT和SRD高度而言,IVA是更有利的选择。在6个月的治疗期内,IVR、IVA和IVB疗法在解剖学和功能上相似,都是有效的治疗方式。