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Comparative study of 1+PRN ranibizumab versus bevacizumab in the clinical setting

机译:1 + PRN雷珠单抗与贝伐单抗在临床中的比较研究

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Purpose: We compared the efficacy of intravitreal ranibizumab and bevacizumab for treating neovascular age-related macular degeneration using an on-demand regimen.Methods: A total of 186 wet age-related macular degeneration eyes of 186 treatment-na?ve patients were compared retrospectively (67 eyes treated with ranibizumab with 91 treated with bevacizumab). At baseline, mean age, best corrected visual acuity, and angiographic lesion types were similar in both groups. Best corrected visual acuity and ocular coherence tomography were evaluated.Results: Sixty eyes treated with ranibizumab and 85 eyes treated with bevacizumab completed a 12-month evaluation. At 12 months, mean best corrected visual acuity increased by +6.65 letters with ranibizumab treatment and by +5.59 with bevacizumab treatment (P = 0.64). Visual acuity improved by ≥15 letters in 15 eyes treated with ranibizumab and in 21 eyes treated with bevacizumab (P = 0.75). An overall reduction in ocular coherence tomography central thickness occurred for all time points. The mean number of injections per eye was 5.97 with ranibizumab and 5.92 with bevacizumab (P = 0.90).Conclusion: Intravitreal therapies with ranibizumab or bevacizumab have similar visual and anatomical results. These results confirm those of comparison of Age-Related Macular Degeneration Treatment Trials in as-needed cohorts in clinical practice. Randomized long-term clinical trials are necessary to examine the systemic safety of these treatments.
机译:目的:我们比较了按需方案玻璃体内雷珠单抗和贝伐单抗治疗新生血管性年龄相关性黄斑变性的方法。方法:回顾性比较了186例初治患者的186例与年龄相关的湿性黄斑变性眼。 (使用兰尼单抗治疗的67只眼和使用贝伐单抗治疗的91只眼)。在基线时,两组的平均年龄,最佳矫正视力和血管造影病变类型相似。结果:兰尼单抗治疗60眼,贝伐单抗治疗85眼,完成了为期12个月的评估。在12个月时,兰尼单抗治疗的平均最佳矫正视力提高了+6.65个字母,贝伐单抗治疗的平均矫正视力提高了+5.59(P = 0.64)。雷珠单抗治疗的15只眼和贝伐单抗治疗的21只眼的视力提高≥15个字母(P = 0.75)。在所有时间点都发生了眼相干断层扫描中心厚度的总体下降。雷尼单抗的平均每眼注射数为5.97,贝伐单抗的平均注射数为5.92(P = 0.90)。结论:兰尼单抗或贝伐单抗的玻璃体内治疗具有相似的视觉和解剖结果。这些结果证实了在临床实践中根据需要对年龄相关的黄斑变性治疗试验进行比较的结果。随机长期临床试验对于检查这些治疗方法的系统安全性是必要的。

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