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静脉造影对比剂肾病争议:风险有多大?

The Controversy of Contrast-Induced Nephropathy With Intravenous Contrast: What Is the Risk?

机构信息

Division of Nephrology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.

Division of Nephrology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.

出版信息

Am J Kidney Dis. 2020 Jan;75(1):105-113. doi: 10.1053/j.ajkd.2019.05.022. Epub 2019 Aug 28.

Abstract

Contrast-induced nephropathy (CIN) has long been observed in both experimental and clinical studies. However, recent observational studies have questioned the prevalence and severity of CIN following intravenous contrast exposure. Initial studies of acute kidney injury following intravenous contrast were limited by the absence of control groups or contained control groups that did not adjust for additional acute kidney injury risk factors, including prevalent chronic kidney disease, as well as accepted prophylactic strategies. More contemporary use of propensity score-adjusted models have attempted to minimize the risk for selection bias, although bias cannot be completely eliminated without a prospective randomized trial. Based on existing data, we recommend the following CIN risk classification: patients with estimated glomerular filtration rates (eGFRs) ≥ 45mL/min/1.73m are at negligible risk for CIN, while patients with eGFRs<30mL/min/1.73m are at high risk for CIN. Patients with eGFRs between 30 and 44mL/min/1.73m are at an intermediate risk for CIN unless diabetes mellitus is present, which would further increase the risk. In all patients at any increased risk for CIN, the risk for CIN needs to be balanced by the risk of not performing an intravenous contrast-enhanced study.

摘要

对比剂肾病(CIN)在实验和临床研究中均已长期观察到。然而,最近的观察性研究对静脉内应用对比剂后 CIN 的发生率和严重程度提出了质疑。静脉内应用对比剂后急性肾损伤的最初研究受到缺乏对照组或包含未调整其他急性肾损伤危险因素(包括普遍存在的慢性肾脏病以及公认的预防性策略)的对照组的限制。更现代的使用倾向评分调整模型已试图最小化选择偏倚的风险,但如果没有前瞻性随机试验,偏倚就不能完全消除。基于现有数据,我们建议以下 CIN 风险分类:估算肾小球滤过率(eGFR)≥45mL/min/1.73m 的患者发生 CIN 的风险可忽略不计,而 eGFR<30mL/min/1.73m 的患者发生 CIN 的风险很高。eGFR 在 30 至 44mL/min/1.73m 之间的患者发生 CIN 的风险处于中等水平,除非存在糖尿病,这会进一步增加风险。对于任何发生 CIN 风险增加的患者,均需要权衡进行静脉内增强研究的风险和发生 CIN 的风险。

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