Comparison of anti-VEGF results between non-ischemic branch retinal vein occlusion and ischemic branch retinal vein occlusion with early sector panretinal photocoagulation

Retinal vein occlusion (RVO) is among the leading causes of visual impairment in vascular diseases [1]. Branch retinal vein occlusion (BRVO) is the most common RVO type with an incidence of 4.4-16/1000 persons/year [2], [3]. BRVO is a venous occlusion at any branch of the central retinal vein. It occurs at arteriovenous crossing sites that share a common adventitia [4], [5]. BRVO has many known ophthalmic and systemic risk factors, including age, hypertension, hyperlipidemia, ocular hypertension, and glaucoma [1], [6], [7]. The typical funduscopic examination consists of flame hemorrhages, dot and blot hemorrhages, cotton wool spots, hard exudates, retinal edema, and dilated tortuous veins [8]. BRVO can be divided into ischemic and nonischemic subtypes according to the area of capillary nonperfusion, and this distinction affects the clinical approach [8]. The BRVO is generally considered ischemic whenever there is an area of retinal capillary non-perfusion of five-disc areas or greater on fundus fluorescein angiography (FFA) [9].

One major complication of BRVO is the development of ME in more than 90% of the eyes affected, which can cause severe visual disturbance and vision loss [10]. Today optic coherence tomography (OCT) is the best way to diagnose and evaluate ME secondary to BRVO [11]. It is especially helpful in monitoring and evaluating the treatment response [11], [12]. The ME is closely associated with increased vascular endothelial growth factor (VEGF) [13]. Anti-VEGF agents are commonly used to treat the ME, reduce the severity of anterior segment neovascularization, and lower the risk of ocular angiogenesis [14], [15]. Laser photocoagulation is a procedure that ablates nonperfusion areas [16]. One may hypothesize that coagulating nonperfused retinal areas can reduce the release of new VEGF and other factors causing a breakdown in the blood-retinal barrier, thereby reducing the need for anti-VEGF [16], [17]. Data on early laser photocoagulation in BRVO are limited.

In the current study, we planned to investigate the relationship between the treatment of peripheral non-perfused retina with early peripheral photocoagulation and the number of needed intravitreal injections in patients with BRVO with ME.

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