Maleki Alireza, Nezamdust Zahra, Salari Amirmasoud, Ahmadi Seyed Sajad, Sabbaghi Hamideh, Bagherzadeh Omid, Ataollahi Alireza, Yaseri Mehdi
Department of Ophthalmology, Alzahra Eye Hospital, Zahedan University of Medical Sciences, Zahedan, Iran.
Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Med Hypothesis Discov Innov Ophthalmol. 2018 Winter;7(4):176-182.
The aim of this study was to investigate the efficacy of Intravitreal Injection of Bevacizumab (IVB) in patients with Central Serous Chorioretinopathy (CSC) compared to the control group, after four months of injection. In this study, 30 eyes of 30 patients with CSC, who were in the age range of 23 to 50 years old (70% male subject) were included. Eligible patients were randomly allocated to the intervention (n = 15) and control groups (n = 15). Patients in the intervention group received a single dose injection of bevacizumab (1.25 mg in 0.05 mL), while patients in the control group were followed-up during the same time interval, without any medical interventions. Corrected Distance Visual Acuity (CDVA) and Central Macular Thickness (CMT) were evaluated as the primary outcome measures at the four-month follow-up. There was no statistically significant difference between the intervention and control groups regarding their baseline characteristics. Corrected Distance Visual Acuity was improved significantly in the intervention group (P < 0.001), while this improvement was not observed in the control group. Furthermore, greater improvement of CDVA was detected in the IVB group compared to the patients without injection (P = 0.018). The CMT findings were in line with CDVA changes in both groups, revealing a significant reduction of CMT only in the intervention group (P < 0.001). Also, thinner central retina was found in the intervention group compared to the comparison group, at the four-month follow-up (P < 0.001). Based on the findings, bevacizumab could be effective for improvement of both anatomical and functional outcomes in patients with CSC.
本研究旨在探讨玻璃体内注射贝伐单抗(IVB)对中心性浆液性脉络膜视网膜病变(CSC)患者的疗效,并与对照组进行比较,观察注射四个月后的情况。本研究纳入了30例年龄在23至50岁之间的CSC患者的30只眼(70%为男性)。符合条件的患者被随机分配到干预组(n = 15)和对照组(n = 15)。干预组患者接受单次剂量的贝伐单抗注射(0.05 mL中含1.25 mg),而对照组患者在相同时间间隔内进行随访,不进行任何医学干预。在四个月的随访中,将矫正远视力(CDVA)和中心黄斑厚度(CMT)作为主要观察指标进行评估。干预组和对照组在基线特征方面无统计学显著差异。干预组的矫正远视力有显著改善(P < 0.001),而对照组未观察到这种改善。此外,与未注射的患者相比,IVB组的CDVA改善更明显(P = 0.018)。两组的CMT结果与CDVA变化一致,仅干预组的CMT有显著降低(P < 0.001)。同样,在四个月的随访中,干预组的中央视网膜比对照组更薄(P < 0.001)。基于这些发现,贝伐单抗可能对改善CSC患者的解剖和功能结局有效。