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Effectiveness of ranibizumab intravitreal injections for exudative age-related macular degeneration treatment: 12-month outcomes

机译:雷珠单抗玻璃体内注射治疗渗出性年龄相关性黄斑变性的疗效:12个月的结果

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Background:The aim of this paper was to evaluate functional and anatomical results of intravitreal ranibizumab injections and the course of exudative age-related macular degeneration (AMD) treatment over a 12-month observation period.Material/Methods:In 25 patients with active dominantly classic exudative AMD, treatment was performed according to the following schedule: 3 intravitreal injections of 0.5 mg ranibizumab at monthly intervals (saturation phase); further injections were based on activity of the neovascular process. Changes in VA and central retinal thickness (CRT) during treatment were evaluated with ANOVA testing.Results:Mean pre-treatment best corrected visual acuity was 0.73±0.27 logMAR. After the third ranibizumab injection the best results, 0.54±0.27 logMAR, were seen; 12-month results were 0.58±0.26 logMAR. Patients had a mean improvement of 10.6 letters at 12 months. In 92% of patients stabilization or improvement of vision was observed. The mean number of injections in the 12-month period was 6.Baseline mean CRT was 351.12±74.15 μm. After the first ranibizumab injection it decreased significantly to 221.96±60.85 μm, after the third injection it was 200.80±47.63 μm, and after 12 months it was 213.16±44.37 μm. Mean correlations between baseline average CRT and baseline average VA measured in ETDRS letters (p=0.017) and in logMAR scale (p=0.033) and between average CRT after the third injection and average VA in logMAR scale after the third injection (p=0.047) were noted.Conclusions:Treatment with intravitreal ranibizumab injections according to the presented scheme provides AMD patients with a chance of stabilization and improvement of the topical state, with a lower number of injections and preserved topical and general safety. Our results suggest that regular monthly controls are necessary to be able react rapidly to the smallest signs of deterioration, not only in visual acuity, but also in OCT images.
机译:背景:本研究旨在评估玻璃体内雷珠单抗注射液的功能和解剖学结果,以及在12个月的观察期内对渗出性年龄相关性黄斑变性(AMD)治疗的过程。材料/方法:在25例活动为主的患者中经典的渗出性AMD,按照以下时间表进行治疗:每月3次(饱和期)玻璃体内注射0.5 mg雷珠单抗。进一步的注射是基于新血管过程的活性。应用方差分析(ANOVA)评估治疗过程中VA和视网膜中央厚度(CRT)的变化。结果:治疗前最佳矫正视力的平均值为0.73±0.27 logMAR。在第三次兰尼单抗注射后,观察到最佳结果为0.54±0.27 logMAR。 12个月结果为0.58±0.26 logMAR。患者在12个月时平均改善了10.6个字母。在92%的患者中,观察到视力稳定或改善。 12个月期间的平均注射次数为6。基线平均CRT为351.12±74.15μm。第一次雷珠单抗注射后,其显着下降至221.96±60.85μm,第三次注射后为200.80±47.63μm,而在12个月后为213.16±44.37μm。以ETDRS字母(p = 0.017)和logMAR量表(p = 0.033)测得的基线平均CRT与基线平均VA之间的平均相关性,以及第三次注射后的logMAR量表中的平均VA与第三次注射后的平均VA之间的相关性(p = 0.047)结论:根据提出的方案玻璃体内注射兰尼单抗治疗可以为AMD患者提供稳定和改善局部状态的机会,减少了注射次数并保持了局部和一般安全性。我们的结果表明,有必要定期进行每月控制,以便能够对最小的退化迹象迅速做出反应,不仅在视敏度上,而且在OCT图像中也是如此。

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