纤维蛋白原与白蛋白比值预测药物洗脱支架植入后非st段抬高急性冠脉综合征患者造影术后急性肾损伤

IF 2.1 4区 医学 Q3 PERIPHERAL VASCULAR DISEASE
Yong Qiao, Mingkang Li, Linqing Li, Chengchun Tang
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引用次数: 1

摘要

背景:造影剂后急性肾损伤(PC-AKI)是碘造影剂的不良反应。在这项研究中,我们研究了使用纤维蛋白原与白蛋白比(FAR)作为一种新的炎症标志物来跟踪非st段抬高急性冠脉综合征(NSTE-ACS)患者在植入药物洗脱支架(DESs)后PC-AKI的发生和进展。方法:共纳入872例NSTE-ACS患者。当暴露于碘化造影剂48-72小时内血清肌酐(SCr)水平升高>26.5 mol/L (0.3 mg/dL)或1.5倍于基线水平时,诊断为PC-AKI。采用单变量回归分析评估不同变量对PC-AKI的影响。采用多因素logistic回归分析确定PC-AKI的独立预测因素。通过估算受试者工作特征(ROC)曲线下面积来评估FAR的预测价值。结果:114例(13.1%)患者发生PC-AKI。与非PC-AKI患者相比,PC-AKI患者白蛋白水平较低(40.5±3.4比39.0±3.5,P < 0.001),纤维蛋白原水平较高(3.7±0.6比4.1±0.5,P < 0.001), FAR水平较高(9.2±1.7比10.5±1.7,P < 0.001)。两组患者术前SCr水平无显著差异。在校正混杂因素后,发现FAR是PC-AKI的独立预测因子(OR = 1.478, 95% CI = 1.298-1.684, P < 0.001)。ROC分析显示,对于PC-AKI预测,FAR的曲线下面积为0.702。FAR的最佳临界值为10.0,灵敏度为64.9%,特异性为69.8%。此外,FAR对PC-AKI的预测价值高于Mehran评分(0.702比0.645)。结论:我们的研究表明,NSTE-ACS患者植入DESs后,术前FAR升高与PC-AKI的发生密切相关。因此,监测FAR可作为预防措施的指导,以避免PC-AKI的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fibrinogen-to-Albumin Ratio Predicts Postcontrast Acute Kidney Injury in Patients with Non-ST Elevation Acute Coronary Syndrome after Implantation of Drug-Eluting Stents.

Fibrinogen-to-Albumin Ratio Predicts Postcontrast Acute Kidney Injury in Patients with Non-ST Elevation Acute Coronary Syndrome after Implantation of Drug-Eluting Stents.

Fibrinogen-to-Albumin Ratio Predicts Postcontrast Acute Kidney Injury in Patients with Non-ST Elevation Acute Coronary Syndrome after Implantation of Drug-Eluting Stents.

Fibrinogen-to-Albumin Ratio Predicts Postcontrast Acute Kidney Injury in Patients with Non-ST Elevation Acute Coronary Syndrome after Implantation of Drug-Eluting Stents.

Background: Postcontrast acute kidney injury (PC-AKI) is an adverse reaction to iodinated contrast agents. In this study, we investigated the use of fibrinogen-to-albumin ratio (FAR) as a novel inflammatory marker to track the development and progression of PC-AKI in patients with non-ST elevation acute coronary syndrome (NSTE-ACS) after the implantation of drug-eluting stents (DESs).

Methods: A total of 872 patients with NSTE-ACS were enrolled in this study. PC-AKI was identified when serum creatinine (SCr) levels increased >26.5 mol/L (0.3 mg/dL) or was 1.5 times the baseline level within 48-72 h of exposure to an iodinated contrast agent. The effects of different variables on PC-AKI were evaluated using univariate regression analysis. Multivariate logistic regression analysis was used to determine the independent predictors of PC-AKI. The predictive value of FAR was assessed by estimating the area under the receiver operating characteristic (ROC) curve.

Results: In total, 114 (13.1%) patients developed PC-AKI. The patients with PC-AKI had lower albumin levels (40.5 ± 3.4 vs. 39.0 ± 3.5, P < 0.001), higher fibrinogen levels (3.7 ± 0.6 vs. 4.1 ± 0.5, P < 0.001), and higher FAR levels (9.2 ± 1.7 vs. 10.5 ± 1.7, P < 0.001) than those with non-PC-AKI. There were no significant differences in the preoperative SCr levels between the two groups. After adjusting for confounding factors, FAR was found to be an independent predictor of PC-AKI (OR = 1.478, 95% CI = 1.298-1.684, P < 0.001). ROC analysis revealed that for PC-AKI prediction, the area under the curve for FAR was 0.702. The optimum cut-off value of FAR was 10.0, with a sensitivity of 64.9% and a specificity of 69.8%. Moreover, FAR had a higher predictive value for PC-AKI than the Mehran score (0.702 vs. 0.645).

Conclusion: Our study showed that elevated preoperative FAR was closely associated with the development of PC-AKI in patients with NSTE-ACS after implantation of DESs. Therefore, it may be worth monitoring FAR as a guide for using preventive measures to avoid the development of PC-AKI.

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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
16
审稿时长
6-12 weeks
期刊介绍: JRAAS is a peer-reviewed, open access journal, serving as a resource for biomedical professionals, primarily with an active interest in the renin-angiotensin-aldosterone system in humans and other mammals. It publishes original research and reviews on the normal and abnormal function of this system and its pharmacology and therapeutics, mostly in a cardiovascular context but including research in all areas where this system is present, including the brain, lungs and gastro-intestinal tract.
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