EFFECTS OF INTRAVITREAL BEVACIZUMAB THERAPY ON GLOMERULAR FILTRATION RATES IN PATIENTS TREATED FOR PROLIFERATIVE DIABETIC RETINOPATHY.

David A Camp, David A Price, Ashley E Neiweem, Denis Jusufbegovic
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引用次数: 1

Abstract

Purpose: To assess whether the repeated use of intravitreal bevacizumab injections in treatment of proliferative diabetic retinopathy is associated with a long-term decline in the glomerular filtration rate (GFR).

Methods: Three hundred charts were retrospectively reviewed, of which 60 patients met the criteria for inclusion. The criteria were as follows: reception of at least one bevacizumab injection, baseline GFR before initial bevacizumab injection, and end GFR 6 to 24 months after baseline. Analysis controlled for time between baseline and end GFR measurements, blood pressure, hemoglobin A1C, race, sex, age, and use of an angiotensin-converting enzyme inhibitor or angiotensin receptor blocker. Significance testing was performed with step-wise multiple linear regression. The significance threshold was 5%, and all tests were two-sided.

Results: Patients received a range of 1 to 17 injections (average 3.6). The average baseline GFR was 76 ± 38 mL/minute, and the end GFR was 63 ± 39 mL/min. The number of injections patients received was not associated with end GFR ( P = 0.72), GFR reduction ( P = 0.88), or percent GFR reduction ( P = 0.49).

Conclusion: Increased number of intravitreal bevacizumab injections at therapeutic dosage was not associated with reduced GFR in patients with proliferative diabetic retinopathy. This study supports that intravitreal antivascular endothelial growth factor agents are renally safe.

玻璃体内贝伐单抗治疗对增生性糖尿病视网膜病变患者肾小球滤过率的影响。
目的:评估反复使用玻璃体内注射贝伐单抗治疗增殖性糖尿病视网膜病变是否与肾小球滤过率(GFR)的长期下降有关。方法:回顾性分析300份病历,其中60例符合纳入标准。标准如下:接受至少一次贝伐单抗注射,初始贝伐单抗注射前的基线GFR,基线后6至24个月的结束GFR。分析控制了基线和终末GFR测量、血压、血红蛋白A1C、种族、性别、年龄和使用血管紧张素转换酶抑制剂或血管紧张素受体阻滞剂之间的时间。采用逐步多元线性回归进行显著性检验。显著性阈值为5%,所有检验均为双侧检验。结果:患者接受1 ~ 17次注射,平均3.6次。平均基线GFR为76±38 mL/min,结束GFR为63±39 mL/min。患者接受注射的次数与终GFR (P = 0.72)、GFR降低(P = 0.88)或GFR降低百分比(P = 0.49)无关。结论:在增殖性糖尿病视网膜病变患者中,增加治疗剂量的玻璃体内贝伐单抗注射次数与GFR降低无关。本研究支持玻璃体内抗血管内皮生长因子药物是肾脏安全的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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