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Intravitreal anti-VEGF therapy for choroidal neovascularisation secondary to pathological myopia: 4-year outcome

机译:玻璃体腔内抗VEGF治疗病理性近视继发的脉络膜新生血管:4年结局

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摘要

OBJECTIVE:To report the visual outcome after 4-year follow-up in a series of highly myopic eyes with choroidal neovascularisation (CNV) treated with antivascular endothelial growth factor (anti-VEGF) drugs.METHODS:A retrospective, non-randomised, multicentre, consecutive, interventional case series study was performed. 92 highly myopic eyes with subfoveal CNV were treated with intravitreal injection (IVI) of anti-VEGF. The initial protocol (1 vs 3 injections) was dictated by surgeons' preferences and followed by an as-needed monthly regime. Best-corrected visual acuity (BCVA) was evaluated at baseline and then monthly. The primary aim was to analyse BCVA changes. The effect of age, spherical equivalent (SE) and treating drug were evaluated as secondary objectives.RESULTS:The mean age of the patients was 57 years (SD 14, range 30-93). The mean number of letters read was 46.1 (SD 16.8, range 5-70) at baseline, 55.5 (SD 18.6, range 10-85) at 12 months, 50.1 (SD 20.1, range 5-82) at 24 months, 54.2 (SD 21.9, range 2-85) at 36 months and 53.1 (SD 22.5, range 1-83) at 48 months (p=0.000, initial vs 12, 24 and 36 months; p=0.01 initial vs 48 months; Student t test for paired data). The mean total number of IVI was 4.9 (SD 5.4, range 1-29). SE and treating drug had no influence on the final visual outcome and number of injections required.CONCLUSIONS:Intravitreal bevacizumab and ranibizumab are effective therapies and show similar clinical effects in highly myopic CNV. Visual acuity gain is maintained at 4-year follow-up.
机译:目的:报告在接受抗血管内皮生长因子(anti-VEGF)药物治疗的高度近视眼的脉络膜新生血管(CNV)系列的近视眼四年后的视觉结果。方法:回顾性,非随机,多中心进行了连续的干预性病例系列研究。用玻璃体内注射抗VEGF治疗92只高度近视的小凹下CNV眼。最初的方案(1 vs 3注射)是由外科医生的偏好决定的,随后是按需的每月方案。在基线时评估最佳矫正视力(BCVA),然后每月进行评估。主要目的是分析BCVA变化。次要目标是评估年龄,球等效量(SE)和治疗药物的影响。结果:患者的平均年龄为57岁(SD 14,范围30-93)。基线平均阅读字母数为46.1(SD 16.8,范围5-70),12个月为55.5(SD 18.6,范围10-85),24个月为50.1(SD 20.1,范围5-82),54.2( 36个月时为SD 21.9,范围2-85),48个月时为53.1(SD 22.5,范围1-83)(初始= 12、24和36个月,p = 0.000;初始= 48个月,p = 0.01); Student t检验用于配对数据)。 IVI的平均总数为4.9(SD 5.4,范围1-29)。 SE和治疗药物对最终的视觉结果和所需的注射次数没有影响。结论:玻璃体内贝伐单抗和兰尼单抗是有效的疗法,在高度近视CNV中显示出相似的临床效果。在4年的随访中保持视力增加。

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