Koyner Jay L, Davison Danielle L, Brasha-Mitchell Ermira, Chalikonda Divya M, Arthur John M, Shaw Andrew D, Tumlin James A, Trevino Sharon A, Bennett Michael R, Kimmel Paul L, Seneff Michael G, Chawla Lakhmir S
Section of Nephrology, Department of Medicine, University of Chicago, Chicago, Illinois;
Department of Anesthesiology and Critical Care Medicine and.
J Am Soc Nephrol. 2015 Aug;26(8):2023-31. doi: 10.1681/ASN.2014060535. Epub 2015 Feb 5.
Clinicians have access to limited tools that predict which patients with early AKI will progress to more severe stages. In early AKI, urine output after a furosemide stress test (FST), which involves intravenous administration of furosemide (1.0 or 1.5 mg/kg), can predict the development of stage 3 AKI. We measured several AKI biomarkers in our previously published cohort of 77 patients with early AKI who received an FST and evaluated the ability of FST urine output and biomarkers to predict the development of stage 3 AKI (n=25 [32.5%]), receipt of RRT (n=11 [14.2%]), or inpatient mortality (n=16 [20.7%]). With an area under the curve (AUC)±SEM of 0.87±0.09 (P<0.0001), 2-hour urine output after FST was significantly better than each urinary biomarker tested in predicting progression to stage 3 (P<0.05). FST urine output was the only biomarker to significantly predict RRT (0.86±0.08; P=0.001). Regardless of the end point, combining FST urine output with individual biomarkers using logistic regression did not significantly improve risk stratification (ΔAUC, P>0.10 for all). When FST urine output was assessed in patients with increased biomarker levels, the AUC for progression to stage 3 improved to 0.90±0.06 and the AUC for receipt of RRT improved to 0.91±0.08. Overall, in the setting of early AKI, FST urine output outperformed biochemical biomarkers for prediction of progressive AKI, need for RRT, and inpatient mortality. Using a FST in patients with increased biomarker levels improves risk stratification, although further research is needed.
临床医生可用于预测哪些早期急性肾损伤(AKI)患者会进展到更严重阶段的工具有限。在早期AKI中,速尿应激试验(FST)后的尿量可预测3期AKI的发生,该试验包括静脉注射速尿(1.0或1.5mg/kg)。我们在先前发表的77例接受FST的早期AKI患者队列中测量了几种AKI生物标志物,并评估了FST尿量和生物标志物预测3期AKI(n = 25 [32.5%])、接受肾脏替代治疗(RRT)(n = 11 [14.2%])或住院死亡率(n = 16 [20.7%])的能力。FST后2小时尿量的曲线下面积(AUC)±标准误为0.87±0.09(P<0.0001),在预测进展到3期方面显著优于所测试的每种尿液生物标志物(P<0.05)。FST尿量是唯一能显著预测RRT的生物标志物(0.86±0.08;P = 0.001)。无论终点如何,使用逻辑回归将FST尿量与单个生物标志物相结合并不能显著改善风险分层(所有ΔAUC,P>0.10)。当在生物标志物水平升高的患者中评估FST尿量时,进展到3期的AUC提高到0.90±0.06,接受RRT的AUC提高到0.91±0.08。总体而言,在早期AKI的情况下,FST尿量在预测进展性AKI、RRT需求和住院死亡率方面优于生化生物标志物。在生物标志物水平升高的患者中使用FST可改善风险分层,尽管还需要进一步研究。