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Case Series on Initial Responses to Intravitreal Brolucizumab in Patients with Recalcitrant Chronic Wet Age-Related Macular Degeneration

机译:案例系列关于含有顽固性慢性湿期年龄相关性黄斑变性患者玻璃体内玻璃纤维蛋白的初始反应

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Purpose: To report a case series of initial responses to intravitreal brolucizumab in patients already undergoing anti-VEGF therapy for wet age-related macular degeneration. Case Series: Six eyes (6 patients) with a history of wet age-related macular degeneration presented with either decline in vision or no improvement while undergoing treatment with anti-VEGF therapy – aflibercept or bevacizumab. Patients were switched to intravitreal brolucizumab. Four weeks post-injection, there was no significant change in visual acuity. Optical coherence tomography scans were taken and improved IRF/SRF, central macular thickness and average pericentral thickness were observed in all 6 patients. No serious adverse reactions were observed, including signs of vasculitis or increase in anterior chamber cell count at the 4-week follow-up for all 6 patients. Conclusion: Intravitreal brolucizumab appears to be a safe and limitedly effective option for patients with recalcitrant CNV from wet AMD.
机译:目的:在已经接受抗VEGF治疗的患者中向湿法年龄相关性黄斑变性的患者报告对玻璃体内玻璃杆菌的病例系列次要反应。案例系列:六只眼(6名患者)患有湿龄相关的黄斑变性历史,随着抗VEGF治疗的治疗而呈现出视力下降或没有改善 - AFLIBERCEPT或BEVACIZUAB。患者切换到玻璃体玻璃纤维蛋白。注射后四周,视力没有显着变化。采用光学相干断层扫描扫描,并改善了IRF / SRF,在所有6名患者中观察到中央黄斑厚度和平均围流厚度。没有观察到严重的不良反应,包括血管炎的迹象或在所有6名患者的4周随访中占前房细胞计数的迹象。结论:玻璃体内玻璃纤维素似乎是从湿AMD顽固的CNV患者安全且有限有效的选择。

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