Background: Nephrocheck ® was approved for acute kidney injury (AKI) risk assessment in critically illness. However, new studies suggest that urinary concentration affects Nephrocheck ® and previous studies did not provide data on urinary output (UO) at the time of measurement.
Methods:We performed a prospective cohort study of the Nephrocheck ® in intensive care unit patients fulfilling standard inclusion criteria. The primary outcome was Stage 2 or 3 AKI defined by both UO and creatinine Kidney Disease Improving Global Outcomes (KDIGO) criteria in the subsequent 12 h. The secondary outcome was the relationship of UO with Nephrocheck ® measurement.Results: Among 98 patients, the primary outcome occurred in 53 (54.1%) overall, but in 23 (23.5%) by creatinine criteria alone. The median (interquartile range) Nephrocheck ® in patients with subsequent Stage 2 or 3 AKI was greater than in Stage 1 or no-AKI patients (0.97 [0.48-1.99] vs. 0.46 [0.22-1.17]; p = .005). However, its area under the receiver characteristic curve was 0.66 (95% confidence interval [CI], 0.56-0.77). Moreover, Nephrocheck ® was significantly and inversely correlated with UO (ρ = À.46, p < .001) at the time of measurement and, on a multivariable logistic regression, Nephrocheck ® was not associated with subsequent Stage 2 or 3 AKI (OR 1.06 [95% CI,], p = .73). In contrast, the UO had an OR of 0.98 for each ml/h increase (95% CI, 0.97-1.00, p = .007).Conclusion: Nephrocheck ® 's predictive performance was limited and its value was inversely correlated with UO. Nephrocheck ® had no independent relationship with outcome once UO at measurement was considered.