Key result
Composite uNGAL/pCysC strongly predicts severe post-CPB pediatric AKI, outperforming standard creatinine changes.
Why the study?
Increases in serum creatinine signify AKI but provide limited information on its characteristics, and combining AKI biomarkers may improve prognostic precision.
Does a composite of functional and tubular damage biomarkers improve prediction of acute kidney injury characteristics compared to serum creatinine in children after cardiopulmonary bypass?
Observational (n=345)
Does a composite of functional and tubular damage biomarkers improve prediction of acute kidney injury characteristics compared to serum creatinine in children after cardiopulmonary bypass?
Effect estimate: +LR 34.2 (95% CI 13.0-94.0)
A composite of functional (pCysC) and tubular damage (uNGAL) biomarkers measured 2 hours after cardiopulmonary bypass provides superior prediction of severe and persistent acute kidney injury compared to serum creatinine in children.
May aid early severe AKI risk stratification after pediatric CPB; leaves open whether biomarker-guided care improves outcomes.
BACKGROUND Increases in serum creatinine (ΔSCr) from baseline signify acute kidney injury (AKI) but offer little granular information regarding its characteristics. The 10th Consensus Conference of the Acute Dialysis Quality Initiative (ADQI) suggested that combining AKI biomarkers would provide better precision for AKI course prognostication. OBJECTIVES This study investigated the value of combining a functional damage biomarker (plasma cystatin C [pCysC]) with a tubular damage biomarker (urine neutrophil gelatinase-associated lipocalin [uNGAL]), forming a composite biomarker for prediction of discrete characteristics of AKI. METHODS Data from 345 children after cardiopulmonary bypass (CPB) were analyzed. Severe AKI was defined as Kidney Disease Global Outcomes Initiative stages 2 to 3 (>100% ΔSCr) within 7 days of CPB. Persistent AKI lasted >2 days. SCr in reversible AKI returned to baseline ≤48 h after CPB. The composite of uNGAL (>200 ng/mg urine Cr = positive [+]) and pCysC (>0.8 mg/l = positive [+]), uNGAL+/pCysC+, measured 2 h after CPB initiation, was compared to ΔSCr increases of ≤50% for correlation with AKI characteristics by using predictive probabilities, likelihood ratios (LR), and area under the curve receiver operating curve (AUC-ROC) values. RESULTS Severe AKI occurred in 18% of patients. The composite uNGAL+/pCysC+ demonstrated a greater likelihood than ΔSCr for severe AKI (+LR: 34.2 [13.0:94.0] vs. 3.8 [1.9:7.2]) and persistent AKI (+LR: 15.6 [8.8:27.5] versus 4.5 [2.3:8.8]). In AKI patients, the uNGAL−/pCysC+ composite was superior to ΔSCr for prediction of transient AKI. Biomarker composites carried greater probability for specific outcomes than ΔSCr strata. CONCLUSIONS Composites of functional and tubular damage biomarkers are superior to ΔSCr for predicting discrete characteristics of AKI.
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Basu et al. (2014) conducted an observational in Acute kidney injury after cardiopulmonary bypass (n=345). Composite of uNGAL+/pCysC+ vs. Increases in serum creatinine (ΔSCr) was evaluated on Severe acute kidney injury (>100% ΔSCr) within 7 days of CPB (+LR 34.2, 95% CI 13.0-94.0). A composite biomarker of uNGAL+/pCysC+ was superior to ΔSCr for predicting severe acute kidney injury (+LR 34.2; 95% CI 13.0-94.0) in children after cardiopulmonary bypass.
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