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Intravitreal bevacizumab (avastin) treatment of retinal angiomatous proliferation.

机译:玻璃体内贝伐单抗(avastin)治疗视网膜血管瘤增生。

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PURPOSE: To report our short-term experience with intravitreal bevacizumab treatment of retinal angiomatous proliferation (RAP) in neovascular age-related macular degeneration (AMD). METHODS: A retrospective, interventional case series was performed that included 13 patients who received intravitreal injection of bevacizumab (1.25 mg) for treatment of RAP and completed 12 weeks of follow-up. Ophthalmic assessment included determination of best-corrected Snellen visual acuity (BCVA), complete ocular examination, fluorescein angiography, and optical coherence tomography (OCT). Injections were repeated if no further improvement or worsening was observed after an initial favorable functional and/or anatomical response. Main outcome measures were BCVA and central macular thickness (CMT) measured by OCT. RESULTS: Twelve eyes (92.3%) had stable or improved BCVA, and 8 eyes (61.5%) had at least 2 lines of vision improvement. The average BCVA improved from 20/203 at baseline to 20/113 at 12 weeks (P = 0.001). Average CMT improved from 369 mum at baseline to 216 microm (P = 0.016) and 315 microm (P = 0.020) at 8 weeks and 12 weeks, respectively. Six eyes underwent fluorescein angiography at the 12-week follow-up visit; 3 (50%) of these eyes had decreased leakage compared with baseline. Both stabilization of vision and improved CMT were maintained for at least 8 weeks after a single injection in almost all eyes. No significant side effects were observed. CONCLUSION: These short-term data suggest that bevacizumab is a viable treatment option for RAP in AMD. The initial treatment effect appears to be maintained for at least 8 weeks.
机译:目的:报告我们在玻璃体内贝伐单抗治疗新生血管性年龄相关性黄斑变性(AMD)中视网膜血管瘤增殖(RAP)的短期经验。方法:回顾性介入病例系列研究,包括13例接受玻璃体内注射贝伐单抗(1.25 mg)治疗RAP的患者,并完成了12周的随访。眼科评估包括确定最佳矫正的Snellen视力(BCVA),完整的眼科检查,荧光素血管造影和光学相干断层扫描(OCT)。如果最初的良好功能和/或解剖反应未观察到进一步改善或恶化,则重复注射。主要结局指标是BCVA和OCT测量的中央黄斑厚度(CMT)。结果:12眼(92.3%)的BCVA稳定或改善,8眼(61.5%)的视力至少改善2条。平均BCVA从基线的20/203改善到12周的20/113(P = 0.001)。在第8周和第12周,平均CMT从基线的369微米分别提高到216微米(P = 0.016)和315微米(P = 0.020)。在12周的随访中,六只眼接受了荧光素血管造影;与基线相比,其中3眼(50%)的渗漏减少。几乎所有眼睛单次注射后,视力稳定和CMT改善均维持至少8周。没有观察到明显的副作用。结论:这些短期数据表明贝伐单抗是AMD RAP的可行治疗选择。初始治疗效果似乎可以维持至少8周。

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