首页> 外文期刊>Folia medica >Comparison of the Safety and Efficacy of Intravitreal Ranibizumab with or without Laser Photocoagulation Versus Dexamethasone Intravitreal Implant with or without Laser Photocoagulation for Macular Edema Secondary to Branch Retinal Vein Occlusion
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Comparison of the Safety and Efficacy of Intravitreal Ranibizumab with or without Laser Photocoagulation Versus Dexamethasone Intravitreal Implant with or without Laser Photocoagulation for Macular Edema Secondary to Branch Retinal Vein Occlusion

机译:玻璃体腔内雷珠单抗联合或不联合激光光凝治疗与地塞米松玻璃体内植入物联合或不联合激光光凝治疗黄斑水肿继发视网膜静脉阻塞的安全性和有效性比较

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Background: There is an ambiguity regarding the therapy of choice for patients with macular edema following branch retinal vein occlusion (BRVO). Aim: The purpose of the study was to compare the efficacy and safety of ranibizumab (3 injections 0.5 mg) versus ranibizumab (1 injection 0.5 mg) with laser photocoagulation (LP) versus dexamethamethasone intravitreal (IVT) implant (0.7 mg) with or without LP in patients with macular edema following BRVO. Materials and methods: 60 eyes of 60 patients were divided into 4 groups. Group 1 received IVT ranibizumab (3 injections 0.5 mg), Group 2 received IVT ranibizumab (1 injection 0.5 mg) + LP, Group 3 received dexamethasone IVT implant (0.7 mg), and Group 4 received dexamethasone IVT implant (0.7 mg) + LP. The endpoints were the difference in mean changes in best corrected visual acuity (BCVA), central macular thickness (CMT), and inter-group differences in contrast sensitivity (CS), retinal sensitivity (RS), and intraocular pressure (IOP). Results: BCVA gains in Group 1 (18.00±8.51) patients were significantly (p < 0.05) higher than patients in Groups 2 (10.00±10.26), 3 (9.50±9.60), and 4 (10.50±10.97), after 6 months of therapy. No significant inter-group variation was found in the CMT, CS, and RS. Conclusions: Ranibizumab (3 injections 0.5 mg) showed significantly higher BCVA gains at 6 months post-therapy. Improvements in the BCVA, CMT, CS, and RS were comparable initially in all the therapies.
机译:背景:对于视网膜分支静脉闭塞(BRVO)后黄斑水肿的患者选择的治疗方法存在歧义。目的:本研究的目的是比较雷尼珠单抗(3针0.5 mg)与雷尼单抗(1针0.5 mg)激光光凝术(LP)与地塞米松玻璃体内注射(IVT)植入物(0.7 mg)有无的疗效和安全性。 BRVO后黄斑水肿患者的LP。材料与方法:将60例患者的60只眼分为4组。第1组接受IVT雷尼单抗(3针0.5毫克),第2组接受IVT雷尼单抗(1针0.5毫克)+ LP,第3组接受地塞米松IVT植入物(0.7 mg),第4组接受地塞米松IVT植入物(0.7 mg)+ LP 。终点为最佳矫正视力(BCVA),中央黄斑厚度(CMT),组间对比敏感度(CS),视网膜敏感度(RS)和眼内压(IOP)的平均变化之差。结果:六个月后,第1组(18.00±8.51)患者的BCVA增益显着(p <0.05)高于第2组(10.00±10.26),3(9.50±9.60)和4组(10.50±10.97)的患者。治疗。在CMT,CS和RS中未发现明显的组间差异。结论:雷尼单抗(3针0.5 mg)在治疗后6个月显示BCVA明显升高。最初,在所有疗法中,BCVA,CMT,CS和RS的改善都是可比的。

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