Douvali Maria, Chatziralli Irini P, Theodossiadis Panagiotis G, Chatzistefanou Klio I, Giannakaki Emmanouella, Rouvas Alexandros A
2nd Department of Ophthalmology, Attikon Hospital, Athens, Greece.
Ophthalmologica. 2014;232(3):136-43. doi: 10.1159/000360909. Epub 2014 Aug 27.
To evaluate the impact of macular ischemia on the functional and anatomical outcome after intravitreal injections of ranibizumab for the treatment of diabetic macular edema (DME).
Participants were 49 patients with diabetes mellitus, divided into two groups based on the presence of ischemia on fluorescein angiography: (i) nonischemic group (n = 32) and (ii) ischemic group (n = 17). All patients were treated with intravitreal ranibizumab and were followed up for 6 months. The main outcome measures were changes in visual acuity (VA) and central foveal thickness (CFT).
There was a statistically significant improvement in VA and CFT between baseline and the end of the follow-up in the nonischemic group, while in the ischemic group there was no significant difference in VA but CFT differed significantly at the 6-month follow-up.
Macular ischemia may have a negative impact on functional outcomes 6 months after intravitreal ranibizumab treatment in patients with DME but has no effect on anatomical outcomes.
评估黄斑缺血对玻璃体内注射雷珠单抗治疗糖尿病性黄斑水肿(DME)后功能和解剖学结局的影响。
参与者为49例糖尿病患者,根据荧光素血管造影检查有无缺血分为两组:(i)非缺血组(n = 32)和(ii)缺血组(n = 17)。所有患者均接受玻璃体内雷珠单抗治疗,并随访6个月。主要结局指标为视力(VA)和中心凹厚度(CFT)的变化。
非缺血组基线与随访结束时VA和CFT有统计学意义的改善,而缺血组VA无显著差异,但在6个月随访时CFT有显著差异。
黄斑缺血可能对DME患者玻璃体内注射雷珠单抗治疗6个月后的功能结局有负面影响,但对解剖学结局无影响。