首页> 外文期刊>International ophthalmology >Visual and morphological outcomes of bevacizumab (Avastin?) versus ranibizumab (Lucentis?) treatment for retinal angiomatous proliferation.
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Visual and morphological outcomes of bevacizumab (Avastin?) versus ranibizumab (Lucentis?) treatment for retinal angiomatous proliferation.

机译:贝伐单抗(Avastin?)与兰尼单抗(Lucentis?)治疗视网膜血管瘤增生的视觉和形态学结果。

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Retinal angiomatous proliferation (RAP) is a variant of exudative age-related macular degeneration with particularly bad prognosis. The purpose of this work is to describe the long-term functional and morphological outcome of patients treated with intravitreal bevacizumab and ranibizumab. Retrospective case series of 16 eyes treated with bevacizumab and 19 eyes treated with ranibizumab. All patients received initially three intravitreal injections of bevacizumab (1.25 mg/0.05 ml) or ranibizumab (0.5 mg/0.05 ml) every 4 weeks. Follow-up ranged from 1 to 7 months after the third injection. Complete ophthalmologic examination including best-corrected visual acuity (VA), optical coherence tomography, fluorescein angiography, and in selected cases, indocyanine green angiography was performed. Triple intravitreal injections resulted in improvement of VA in bevacizumab-treated as well as in ranibizumab-treated patients; logarithm of the minimal angle of resolution (logMAR) 0.84 before treatment and 0.67 at month 9, and logMAR 0.75 before treatment and 0.59 at month 9, respectively. Central macular thickness (CMT) in the bevacizumab group improved from 363.67 ± 47.4 μm at baseline to 328 ± 49.77 μm at month 6 (p = 0.03) and 301 ± 129.69 at month 9 (p = 0.35). CMT in the ranibizumab group improved from 545.62 ± 167.39 μm at baseline to 395.88 ± 169.37 μm at month 6 and 411.83 ± 212.41 μm at month 9 (p = 0.03, p = 0.05, respectively). Patients with RAP might benefit from both intravitreal bevacizumab and ranibizumab treatments with stabilization of VA over a longer period of time. Close follow-up should nevertheless be performed in this special subgroup because of the high recurrence rate.
机译:视网膜血管瘤增生(RAP)是渗出的年龄相关性黄斑变性的一种变体,预后特别差。这项工作的目的是描述接受玻璃体内贝伐单抗和兰尼单抗治疗的患者的长期功能和形态学结果。回顾性病例系列分析:贝伐单抗治疗16眼,兰尼单抗治疗19眼。所有患者最初每4周接受3次玻璃体内注射贝伐单抗(1.25 mg / 0.05 ml)或兰尼单抗(0.5 mg / 0.05 ml)注射。第三次注射后的随访时间为1到7个月。完整的眼科检查包括最佳矫正视力(VA),光学相干断层扫描,荧光素血管造影,在某些情况下,进行吲哚菁绿血管造影。玻璃体内注射三次可改善贝伐单抗和兰尼单抗治疗患者的视力;最小分辨角(logMAR)的对数在治疗前为0.84,在第9个月为0.67,logMAR 0.75在治疗前和第9个月为0.59。贝伐单抗组的中央黄斑厚度(CMT)从基线时的363.67±47.4μm改善到第6个月的328±49.77μm(p = 0.03)和第9个月的301±129.69(p = 0.35)。雷珠单抗组的CMT从基线时的545.62±167.39μm改善至第6月的395.88±169.37μm和第9月的411.83±212.41μm(分别为p = 0.03,p = 0.05)。 RAP患者可能会从玻璃体内贝伐单抗和兰尼单抗治疗中受益,并在更长的时间内稳定VA。但是,由于高复发率,应该在这个特殊的亚组中进行密切随访。

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