External validation of urinary C-C motif chemokine ligand 14 (CCL14) for prediction of persistent acute kidney injury

被引:44
作者
Bagshaw, Sean M. [1 ]
Al-Khafaji, Ali [2 ]
Artigas, Antonio [3 ]
Davison, Danielle [4 ]
Haase, Michael [5 ,6 ]
Lissauer, Matthew [7 ]
Zacharowski, Kai [8 ]
Chawla, Lakhmir S. [9 ]
Kwan, Thomas [10 ]
Kampf, J. Patrick [10 ]
McPherson, Paul [10 ]
Kellum, John A. [2 ]
机构
[1] Univ Alberta, Fac Med & Dent, Dept Crit Care Med, 2-124 Clin Sci Bldg,8440-112 ST NW, Edmonton, AB T6G 2B7, Canada
[2] Univ Pittsburgh, Ctr Crit Care Nephrol, Dept Crit Care Med, 3550 Terrace St,Scaife Hall,Suite 600, Pittsburgh, PA 15213 USA
[3] Univ Autonoma Barcelona, Corp Sanitaria Univ Parc Tauli, CIBER Enfermedades Resp, Crit Care Dept, Parc Tauli, E-08193 Barcelona, Spain
[4] George Washington Univ, Dept Anesthesiol, Crit Care Med, Sch Med & Hlth Sci, 900 23rd St, Washington, DC 20037 USA
[5] Otto Von Guericke Univ, Diaverum Renal Care Ctr, 14469 Potsdam, D-39120 Magdeburg, Germany
[6] Otto Von Guericke Univ, Fac Med, Leipziger Str 44, D-39120 Magdeburg, Germany
[7] Rutgers Robert Wood Johnson Med Sch, Dept Surg, Div Acute Care Surg, 125 Patterson St, New Brunswick, NJ 07746 USA
[8] Goethe Univ, Univ Hosp Frankfurt, Intens Care Med & Pain Therapy, Dept Anesthesiol, Theodor Stern Kai 7, D-60590 Frankfurt, Germany
[9] Vet Affairs Med Ctr, 3350 Jolla Village Dr, San Diego, CA 92161 USA
[10] Astute Med Inc, 3550 Gen Atom Ct, San Diego, CA 92121 USA
关键词
Acute kidney injury; Prediction; Validation; Renal replacement therapy; Mortality; RENAL-REPLACEMENT THERAPY; RECOVERY; RISK; AKI;
D O I
10.1186/s13054-021-03618-1
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BackgroundPersistent acute kidney injury (AKI) portends worse clinical outcomes and remains a therapeutic challenge for clinicians. A recent study found that urinary C-C motif chemokine ligand 14 (CCL14) can predict the development of persistent AKI. We aimed to externally validate urinary CCL14 for the prediction of persistent AKI in critically ill patients.MethodsThis was a secondary analysis of the prospective multi-center SAPPHIRE study. We evaluated critically ill patients with cardiac and/or respiratory dysfunction who developed Kidney Disease: Improving Global Outcomes (KDIGO) stage 2-3 AKI within one week of enrollment. The main exposure was the urinary concentration of CCL14 measured at the onset of AKI stage 2-3. The primary endpoint was the development of persistent severe AKI, defined as >= 72 h of KDIGO stage 3 AKI or death or renal-replacement therapy (RRT) prior to 72 h. The secondary endpoint was a composite of RRT and/or death by 90 days. We used receiver operating characteristic (ROC) curve analysis to assess discriminative ability of urinary CCL14 for the development of persistent severe AKI and multivariate analysis to compare tertiles of urinary CCL14 and outcomes.ResultsWe included 195 patients who developed KDIGO stage 2-3 AKI. Of these, 28 (14%) developed persistent severe AKI, of whom 15 had AKI >= 72 h, 12 received RRT and 1 died prior to >= 72 h of KDIGO stage 3 AKI. Persistent severe AKI was associated with chronic kidney disease, diabetes mellitus, higher non-renal APACHE III score, greater fluid balance, vasopressor use, and greater change in baseline serum creatinine. The AUC for urinary CCL14 to predict persistent severe AKI was 0.81 (95% CI, 0.72-0.89). The risk of persistent severe AKI increased with higher values of urinary CCL14. RRT and/or death at 90 days increased within tertiles of urinary CCL14 concentration.ConclusionsThis secondary analysis externally validates urinary CCL14 to predict persistent severe AKI in critically ill patients.
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