首页> 外文期刊>Retina >Changes in retinal sensitivity in patients with neovascular age-related macular degeneration after systemic bevacizumab (avastin) therapy.
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Changes in retinal sensitivity in patients with neovascular age-related macular degeneration after systemic bevacizumab (avastin) therapy.

机译:系统性贝伐单抗(avastin)治疗后与新生血管性年龄相关性黄斑变性患者的视网膜敏感性变化。

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OBJECTIVE: To evaluate changes in central retinal sensitivity in patients with neovascular age-related macular degeneration after systemic bevacizumab (Avastin; Genentech, Inc., South San Francisco, CA) therapy. METHODS: For all eyes, the central 12 x 12 degrees visual field was recorded using the MP 1 Microperimeter (Nidek, Gamagori, Japan) at baseline and 1 week, 1 month, 3 months, and 6 months after initial treatment. Patients received systemic anti-vascular endothelial growth factor (VEGF) therapy with three initial bevacizumab infusions at 2-week intervals. Retreatment during follow-up was performed only in cases of choroidal neovascularization recurrence. Seven patients (12 eyes) received bevacizumab infusions at a dose of 5 mg/kg, and 7 patients (9 eyes), at a dose of 2.5 mg/kg. RESULTS: Of 41 stimulation points, a mean absolute scotoma of 15 missed stimulation points was measured at baseline, which decreased to 10 missed stimulation points at month 3 (-5; P = 0.005) and to 11 stimulation pointsat month 6 (-4; P = 0.106). The mean absolute scotoma size (in % of total tested area) decreased from 33% to 22% (-11%; P = 0.011) at month 3 and to 23% (-10%, P 0.123) at month 6. Mean differential light threshold increased significantly throughout the observation period from 3.8 dB at baseline to 5.5 dB (+1.7 dB; P = 0.012) at month 6. CONCLUSIONS: Systemic bevacizumab therapy induced a significant increase in mean retinal sensitivity at month 6 of follow-up and a significant decrease of mean absolute scotoma size at month 3. The MP 1 Microperimeter proved to be a valuable tool in the evaluation of functional benefits and retinal safety of anti-VEGF therapy with systemic bevacizumab.
机译:目的:评估系统性贝伐单抗(Avastin; Genentech,Inc。,南旧金山,加利福尼亚州)治疗后新血管性年龄相关性黄斑变性患者中央视网膜敏感性的变化。方法:对于所有眼睛,在基线时以及初次治疗后1周,1个月,3个月和6个月,使用MP 1微型视野仪(Nidek,日本蒲郡,日本)记录中心12 x 12度视野。患者接受系统性抗血管内皮生长因子(VEGF)治疗,每两周间隔三次初始贝伐单抗输注。仅在脉络膜新生血管复发的情况下进行随访期间的再治疗。 7名患者(12眼)以5 mg / kg的剂量接受贝伐单抗输注,7名患者(9眼)以2.5 mg / kg的剂量接受输注。结果:在41个刺激点中,在基线测量了15个遗漏刺激点的平均绝对红点,在第3个月减少至10个遗漏刺激点(-5; P = 0.005),在第6个月减少了11个刺激点(-4; P = 0.005)。 P = 0.106)。平均绝对葡萄球菌大小(以总测试面积的百分比表示)从第3个月的33%降至22%(-11%; P = 0.011),并在第6个月降至23%(-10%,P 0.123)。平均差异在整个观察期间,光阈值从基线时的3.8 dB显着提高到第6个月的5.5 dB(+1.7 dB; P = 0.012)。结论:系统性贝伐单抗治疗在随访的第6个月和第6个月引起平均视网膜敏感性显着提高。在第3个月时,平均绝对葡萄球菌大小显着减少。MP 1微孔镜被证明是评估全身性贝伐单抗抗VEGF治疗的功能益处和视网膜安全性的有价值的工具。

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