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Intravitreal bevacizumab for extrafoveal choroidal neovascularization secondary to pathologic myopia

机译:玻璃体腔注射贝伐单抗治疗继发于病理性近视的小凹前脉络膜新生血管

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Purpose: To assess the effects of intravitreal bevacizumab injections in the treatment of extrafoveal choroidal neovascularization (CNV) associated with pathologic myopia. METHODS:: Patients diagnosed with pathologic myopia complicated by extrafoveal CNV were considered in this prospective, open-label interventional study. All patients underwent a complete ophthalmologic examination, including Early Treatment Early of Diabetic Retinopathy Study (ETDRS) visual acuity measurement, optical coherence tomography, and fluorescein angiography. The protocol treatment included a first injection, followed by repeated injections over a 24-month follow-up period on the basis of optical coherence tomography and angiographic features, monitored monthly. Primary outcomes were the mean changes in best-corrected visual acuity and the proportion of eyes gaining at least 15 letters at the 24-month examination. Secondary outcomes included central macular thickness, size of the CNV, and extension to the fovea. RESULTS:: Fifteen patients were included in the study. Mean best-corrected visual acuity changed from 0.47 logarithm of the minimum angle of resolution (20/60 Snellen equivalent) at baseline to 0.22 logarithm of the minimum angle of resolution (20/30 Snellen equivalent) at the 24-month examination. An improvement of at least 3 ETDRS lines was achieved by 7 eyes (46.6%) at the 24-month examination. Mean central macular thickness changed from 313 ??m to 254 ??m at the 24-month examination (P = 0.008). Mean CNV size decreased from 348 ??m to 251 ??m at 24 months (P = 0.029). CONCLUSION:: Intravitreal bevacizumab injection is a beneficial treatment for extrafoveal CNV associated with pathologic myopia.
机译:目的:评估玻璃体内贝伐单抗注射液治疗与病理性近视相关的中央凹脉络膜新生血管(CNV)的效果。方法:这项前瞻性开放性干预研究考虑了诊断为病理性近视并发中心凹CNV的患者。所有患者均接受了完整的眼科检查,包括糖尿病视网膜病变研究的早期治疗早期(ETDRS)视敏度测量,光学相干断层扫描和荧光素血管造影。方案治疗包括第一次注射,然后在光学相干断层扫描和血管造影特征的基础上,每月监测一次,在24个月的随访期内重复注射。主要结局是经过24个月检查的最佳矫正视力的平均变化以及获得至少15个字母的眼睛比例。次要结果包括中央黄斑厚度,CNV大小和中央凹延伸。结果:15名患者被纳入研究。平均最佳矫正视力从基线时的最小分辨角的0.47对数(20/60 Snellen当量)更改为在24个月检查时最小分辨角的0.22对数(20/30 Snellen当量)。在24个月的检查中,有7眼(46.6%)改善了至少3条ETDRS系。在24个月的检查中,平均黄斑中心厚度从313?m变为254?m(P = 0.008)。在24个月时,平均CNV大小从348?m降至251?m(P = 0.029)。结论:玻璃体腔注射贝伐单抗是治疗与病理性近视相关的小凹CNV的有益方法。

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