首页> 外文期刊>Acta ophthalmologica >Diabetic macular oedema treated with intravitreal anti‐vascular endothelial growth factor – 2–4?years follow‐up of visual acuity and retinal thickness in 566 patients following Danish national guidelines
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Diabetic macular oedema treated with intravitreal anti‐vascular endothelial growth factor – 2–4?years follow‐up of visual acuity and retinal thickness in 566 patients following Danish national guidelines

机译:糖尿病黄斑水肿用玻璃体抗血管内皮生长因子治疗 - 2-4岁,在丹麦国家指南后566名患者的视力和视网膜厚度随访

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Abstract Purpose To investigate long‐term functional and anatomical outcomes, discontinuation patterns, drug switching and rates of nonimprovement in patients treated with ranibizumab pro re nata ( PRN ) regimen for diabetic macular oedema ( DME ) according to the Danish national guidelines. Methods Retrospective cohort study of 566 eyes in 566 patients with centre‐involved DME who started intravitreal treatment with ranibizumab between January 2011 and December 2013 in the Greater Copenhagen region. Data were retrieved from a database and patient records between January 2011 and March 2016 and analysed using mixed‐model statistics. Results At the conclusion of follow‐up, 24.6% were in active ranibizumab follow‐up, 25.4% had switched to other intravitreal pharmacotherapy, 31.6% had been discontinued because of disease stability, 13.8% had been lost to follow‐up, 1.4% had been discontinued because of low visual acuity (VA), and 3.2% had died. At baseline, mean best‐corrected visual acuity ( BCVA) and mean central subfield thickness (CST) were 64.9 (±15.0) letters and 400.2 (±120.3)? μ m. Mean change in BCVA and mean change in CST from baseline to 3, 12, 24, 36 and 48?months of follow‐up were +3.9, +3.5, +2.7, +1.8, +2.3 letters and ?97.4, ?102.6, ?106.9, ?105.9, ?131.6? μ m, respectively. Mean number of injections was 6.1 in year 1 and 1.8 in year 4. In 93 patients, drug switching to aflibercept showed no difference between the two drugs on BCVA or CST . In 79 patients, CST decreased 10% compared to baseline during the first year. Conclusion In a single‐centre clinical setting, 566 patients treated for DME with ranibizumab according to the Danish national guidelines were followed for up to 4?years. Best‐corrected visual acuity (BCVA) outcomes are in the low end of clinical studies, but studied on a wider population and achieved with fewer injections.
机译:摘要目的是调查丹麦国家指南糖尿病蛋白质(PRN)治疗患者的长期功能和解剖结果,停止模式,药物切换和非患者的非预防率的率。方法回顾性队列566眼中的566名中枢中心DME患者的研究,他在2011年1月至2013年1月和2013年12月在大哥本哈根地区开始含有Ranibizumab。从2011年1月至2016年1月至2016年3月之间的数据库和患者记录中检索数据,并使用混合模型统计分析。结果在随访结束时,24.6%处于活跃的Ranibizumab随访中,25.4%已切换到其他玻璃体内药物疗法,31.6%由于疾病稳定而停产,随访13.8%已损失,1.4%由于低视力(VA),已停止,3.2%已死亡。在基线时,平均最佳校正的视力(BCVA)和平均中央子场厚度(CST)为64.9(±15.0)字母,400.2(±120.3)? μm。 BCVA的平均变化与CST的平均变化从基线到3,12,24,36和48?几个月的后续时间为+ 3.9,+ 3.5,+ 2.7,+1.8,+ 2.3字母和?97.4,?102.6, ?106.9,?105.9,?131.6?分别为μm。 1年级的注射次数为6.1,4.8岁,4.8岁,在93名患者中,对AfliBercept的药物切换在BCVA或CST上的两种药物之间没有差异。在79名患者中,与第一年的基线相比,CST减少了10%。结论在单中心临床环境中,根据丹麦国家指南对DME治疗DME治疗的566名患者最多4年。最佳纠正的视力(BCVA)结果是临床研究的低端,但在更广泛的人口上研究并通过较少的注射来实现。

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