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比较在新生血管性年龄相关性黄斑变性中从玻璃体内注射贝伐单抗转换为雷珠单抗治疗后的结局。

Comparison of outcomes after switching treatment from intravitreal bevacizumab to ranibizumab in neovascular age-related macular degeneration.

机构信息

Department of Ophthalmology, University of Western Ontario, London, Ontario, Canada.

出版信息

Can J Ophthalmol. 2012 Apr;47(2):159-64. doi: 10.1016/j.jcjo.2012.01.003.

Abstract

OBJECTIVE

To compare visual acuity and central retinal thickness in patients initially treated with bevacizumab (Avastin) and switched to ranibizumab (Lucentis) for neovascular age-related macular degeneration (AMD).

DESIGN

A retrospective chart review.

PARTICIPANTS

This study included 87 eyes from 80 patients over the age of 65 with neovascular AMD.

METHODS

Patients were initially treated with bevacizumab injections every 6 weeks and then switched to ranibizumab every 4 weeks when it became publicly funded by the Ontario government. Outcomes include comparison of visual acuity and central retinal thickness after bevacizumab treatment, and after switching to ranibizumab.

RESULTS

Visual acuity improved significantly versus initial baseline values following a treatment course of 3 or more injections of bevacizumab (0.58 logMar, SD = 0.30 vs 0.73 logMar, SD = 0.41; p = 0.0007). Patients then showed a further significant improvement in visual acuity after switching and receiving a course of ranibizumab (0.51 logMar, SD = 0.32) (p = 0.0122). Mean central retinal thickness as measured by optical coherence tomography significantly decreased after a course of bevacizumab (p = 0.0158), and a further decrease was noted after a subsequent course of ranibizumab (p < 0.0001).

CONCLUSIONS

There was a significant improvement in visual acuity and central retinal thickness in patients with neovascular AMD initially treated with bevacizumab. When these patients were uniformly switched to ranibizumab there was a further significant improvement in visual acuity and a reduction of retinal thickness. It appears that ranibizumab can maintain, or improve the effect achieved after an initial course of bevacizumab.

摘要

目的

比较初始接受贝伐单抗(阿瓦斯汀)治疗并转为雷珠单抗(Lucentis)治疗的新生血管性年龄相关性黄斑变性(AMD)患者的视力和中心视网膜厚度。

设计

回顾性图表审查。

参与者

这项研究包括 80 名 65 岁以上患有新生血管性 AMD 的患者的 87 只眼。

方法

患者最初每 6 周接受贝伐单抗注射治疗,然后在安大略省政府将其纳入公共资助范围后,每 4 周转换为雷珠单抗治疗。结果包括贝伐单抗治疗后和转换为雷珠单抗后的视力和中心视网膜厚度比较。

结果

与初始基线值相比,3 次或更多次贝伐单抗治疗后视力显著提高(0.58 logMAR,SD=0.30 与 0.73 logMAR,SD=0.41;p=0.0007)。患者随后在转换并接受雷珠单抗治疗后视力进一步显著提高(0.51 logMAR,SD=0.32)(p=0.0122)。经光学相干断层扫描测量的中心视网膜厚度在贝伐单抗治疗后显著降低(p=0.0158),随后接受雷珠单抗治疗后进一步降低(p<0.0001)。

结论

初始接受贝伐单抗治疗的新生血管性 AMD 患者的视力和中心视网膜厚度均显著改善。当这些患者统一转换为雷珠单抗治疗时,视力进一步显著改善,视网膜厚度降低。雷珠单抗似乎可以维持或改善初始贝伐单抗治疗后的效果。

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