Failure to Complete Induction in Anti-VEGF Therapy for Neovascular Age-Related Macular Degeneration

H. Joel, S ComaneshterDoron, V. Shlomo
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引用次数: 1

Abstract

Purpose: To evaluate the proportion and characteristics of patients diagnosed with neovascular age-related macular degeneration (AMD) who do not complete the loading dose of bevacizumab, given as first line agent. Methods: Using the electronic medical records of all patients affiliated to the largest health maintenance organization in Israel who received intravitreal injections of bevacizumab between September 2008 and October 2014, we isolated patients aged of 60 years or more treated for neovascular age-related macular degeneration. We considered patients with less than three injections and those having completed the initial course within 100 days as two separate groups. We then compared patients living at the end of follow-up in terms of demographics and baseline conditions. Results: 22.3% of all patients started with bevacizumab did not fulfill the loading dose within 100 days. Mortality was higher in patients not achieving induction (32.5% vs. 20.2%, OR = 2.39, CI: 2.04 2.80, p < 0.001). When considering patients living at the end of the follow-up, 13.7% did not receive the loading dose. We found a larger proportion of rural residents in patients who failed induction than in those who received three injections or more (OR = 1.54, 95% CI: 1.23 1.92, p < 0.001). Patients, living at the end of follow-up, who failed to complete the loading dose were relatively younger than patients with three or more injections (79.6 vs. 80.7 vs. years, p < 0.001). No other demographic variable and no specific medical condition was found to be associated with failure to complete induction. Conclusions: In this nationwide retrospective study, we report that a large number of patients do not comply with treatment guidelines. Since the area of residence was identified as the main risk factor for failing to receive the loading dose, we think distance to anti-VEGF delivering facilities should be seriously taken into account when defining global policies relating to retinal care.
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抗vegf治疗新生血管性年龄相关性黄斑变性的诱导失败
目的:评估未完成贝伐单抗负荷剂量的新生血管性年龄相关性黄斑变性(AMD)患者的比例和特征,贝伐单抗是一线药物。方法:利用2008年9月至2014年10月期间以色列最大的健康维护组织所有接受玻璃体内注射贝伐单抗的患者的电子病历,我们分离出年龄在60岁及以上的新生血管性年龄相关性黄斑变性患者。我们将注射少于三次的患者和在100天内完成初始疗程的患者分为两组。然后,我们比较了随访结束时患者的人口统计学和基线条件。结果:在所有开始使用贝伐单抗的患者中,有22.3%的患者在100天内没有完成负荷剂量。未实现诱导的患者死亡率更高(32.5% vs. 20.2%, OR = 2.39, CI: 2.04 2.80, p < 0.001)。在随访结束时,13.7%的患者没有接受负荷剂量。我们发现,在诱导失败的患者中,农村居民的比例大于接受三次或三次以上注射的患者(or = 1.54, 95% CI: 1.23 1.92, p < 0.001)。随访结束时未能完成负荷剂量的患者相对于接受三次或三次以上注射的患者年轻(79.6 vs. 80.7 vs.年,p < 0.001)。没有发现其他人口统计学变量和特定的医疗状况与诱导失败有关。结论:在这项全国性的回顾性研究中,我们报告了大量患者不遵守治疗指南。由于居住区域被确定为未能接受加载剂量的主要风险因素,我们认为在制定与视网膜护理相关的全球政策时,应认真考虑到与抗vegf输送设施的距离。
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