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首页> 外文期刊>Retina >Macular functional changes evaluated with MP-1 microperimetry after intravitreal bevacizumab for subfoveal myopic choroidal neovascularization: one-year results.
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Macular functional changes evaluated with MP-1 microperimetry after intravitreal bevacizumab for subfoveal myopic choroidal neovascularization: one-year results.

机译:玻璃体腔注射贝伐单抗治疗小凹下近视脉络膜新生血管后的黄斑功能改变(MP-1显微视野测定法):一年结果。

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摘要

PURPOSE: The purpose of this study was to evaluate 1-year functional and structural effects of intravitreal bevacizumab for subfoveal choroidal neovascularization secondary to pathologic myopia (myopic choroidal neovascularization). METHODS: Fifteen eyes with myopic choroidal neovascularization participated in this prospective interventional, noncomparative case series. All patients were treated with one intravitreal injection of 1.25 mg bevacizumab. Retreatments were performed in case of persistent or recurrent leakage on fluorescein angiography and/or intraretinal fluid on optical coherence tomography. Evaluation of best-corrected visual acuity using Early Treatment of Diabetic Retinopathy Study criteria, MP-1 microperimetry, optical coherence tomography, and fluorescein angiography were performed before treatment and 1 month, 3 months, 6 months, and 1 year after treatment. RESULTS: After a follow-up of 12 months, best-corrected visual acuity improved on average of 0.23 logarithm of the minimum angle of resolution. Mean macular sensitivity within the central 8 degrees increased on average of 2.62 dB at 12-month postinjection. The mean number of measurement points within the central absolute scotoma reduced significantly from 12.47 before treatment to 6.27 at 1-year follow-up. An improvement of fixation stability from baseline was observed in 9 patients (60%). No treatment adverse events were evidenced. CONCLUSION: Improvement of macular sensitivity and fixation stability 1 year after intravitreal bevacizumab for myopic choroidal neovascularization suggest a stable and progressive macular function recovery. The mean treatment session was 1.53, with 53.3% of patients needing only a single intravitreal bevacizumab injection, supporting a potential long-lasting efficacy of intravitreal bevacizumab treatment.
机译:目的:本研究的目的是评估玻璃体内贝伐单抗治疗继发于病理性近视的小凹下脉络膜新生血管(近视脉络膜新生血管)的一年功能和结构作用。方法:15眼近视脉络膜新生血管参与了该前瞻性介入,非对照病例系列。所有患者均接受玻璃体内注射1.25 mg贝伐单抗治疗。在荧光血管造影和/或光学相干断层扫描的视网膜内液持续或反复渗漏的情况下进行再治疗。使用糖尿病性视网膜病的早期治疗评估最佳矫正视力在治疗前以及治疗后1个月,3个月,6个月和1年进行了研究标准,MP-1显微视野测定,光学相干断层扫描和荧光素血管造影。结果:经过12个月的随访,经过最佳矫正的视力平均提高了最小分辨角的0.23对数。注射后12个月,中心8度内的平均黄斑敏感度平均增加2.62 dB。中心绝对性黑质瘤中的平均测量点数从治疗前的12.47显着降低到1年随访时的6.27。 9名患者(60%)观察到固定稳定性较基线有所改善。没有治疗不良事件的证据。结论:玻璃体内贝伐单抗治疗近视脉络膜新生血管后1年,黄斑区敏感性和固定稳定性得到改善,提示黄斑功能恢复稳定且逐步进行。平均治疗时间为1.53,其中53.3%的患者仅需单次玻璃体内贝伐单抗注射,支持玻璃体内贝伐单抗的潜在长期疗效。

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