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. 2020 Jan-Mar;32(1):123–132. doi: 10.5935/0103-507X.20200018

Table 3.

Comparison between biomarkers, prediction models, and combined models for early acute kidney injury diagnosis in adult intensive care units

Characteristic Characteristic sub-groups Malhotra et al.(25) Flechet et al.*(26) Deng et al.(28) Chiofolo et al.(29) Zimmerman et al.(30)
Biomarkers used for comparison   Not applicable sNGAL sCysC and uNAG Not applicable Not applicable
Discrimination of biomarkers (AUROC)   Not applicable For NGAL in validation NGAL cohort: 0.74 (0.74 - 0.74) 0.756 (0.723 - 0.789) Not applicable Not applicable
Discrimination of prediction models (AUROC) Development cohort Not reported 0.86 (0.86 - 0.86) 0.821 (0.792 - 0.850) 0.949 (0.943 - 0.954) Not reported
Internal validation cohort 0.792 (0.697 - 0.887) 0.86 (0.86 - 0.86) 0.821 (0.792 - 0.850) 0.882 (0.867 - 0.897) 0.78
External validation cohort 0.81 (0.78 - 0.83) 0.81 (0.81 - 0.81) Not applicable Not applicable Not applicable
Discrimination of prediction models with biomarkers (AUROC)   Not applicable For combined model in validation NGAL cohort: 0.80 (0.80 - 0.80) 0.836 (0.808 - 0.864) Not applicable Not applicable

sNGAL - serum neutrophil gelatinase-associated lipocalin; sCysC - serum cystatin C; uNAG - urinary N-acetyl-β-D-glucosaminidase; AUROC - area under the receiver operating characteristics; NGAL - neutrophil gelatinase-associated lipocalin.

*

Data from Flechet et al. are only reported for the prediction model for any acute kidney injury on the first day;

data from Deng et al. are only reported for the prediction model for any acute kidney injury;

data for Zimmerman et al. are only reported for the multivariate logistic regression model derived with backward selection.