Biomarker Rule-in or Rule-out in Patients With Acute Diseases for Validation of Acute Kidney Injury in the Emergency Department (BRAVA): A Multicenter Study Evaluating Urinary TIMP-2/IGFBP7

Urine tissue inhibitor of metalloproteinases-2/insulin-like growth factor-binding protein 7 (TIMP-2/IGFBP7) (NephroCheck, Ortho Clinical Diagnostics, Raritan, NJ, USA) is a US Food and Drug Administration-approved biomarker for risk assessment of acute kidney injury (AKI) in critically ill adult pat...

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Published inAnnals of laboratory medicine Vol. 42; no. 2; pp. 178 - 187
Main Authors Yang, Hyun Suk, Hur, Mina, Lee, Kyeong Ryong, Kim, Hanah, Kim, Hahn Young, Kim, Jong Won, Chua, Mui Teng, Kuan, Win Sen, Chua, Horng Ruey, Kitiyakara, Chagriya, Phattharapornjaroen, Phatthranit, Chittamma, Anchalee, Werayachankul, Thiyapha, Anandh, Urmila, Herath, Sanjeeva, Endre, Zoltan, Horvath, Andrea Rita, Antonini, Paola, Di Somma, Salvatore
Format Journal Article
LanguageEnglish
Published Korea (South) Korean Society for Laboratory Medicine 01.03.2022
대한진단검사의학회
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ISSN2234-3806
2234-3814
2234-3814
DOI10.3343/alm.2022.42.2.178

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Summary:Urine tissue inhibitor of metalloproteinases-2/insulin-like growth factor-binding protein 7 (TIMP-2/IGFBP7) (NephroCheck, Ortho Clinical Diagnostics, Raritan, NJ, USA) is a US Food and Drug Administration-approved biomarker for risk assessment of acute kidney injury (AKI) in critically ill adult patients in intensive care units; however, its clinical impact in the emergency department (ED) remains unproven. We evaluated the utility of NephroCheck for predicting AKI development and short-term mortality in the ED. This was a prospective, observational, five-center international study. We consecutively enrolled ED patients admitted with ≥30% risk of AKI development (assessed by ED physician: ED score) or acute diseases. Serum creatinine was tested on ED arrival (T0), day 1, and day 2 (T48); urine for NephroCheck was collected at T0 and T48. We performed ROC curve and reclassification analyses. Among the 529 patients enrolled (213 females; median age, 65 years), AKI developed in 59 (11.2%) patients. The T0 NephroCheck value was higher in the AKI group than in the non-AKI group (median 0.77 vs. 0.29 (ng/m) /1,000, P=0.001), and better predicted AKI development than the ED score (area under the curve [AUC], 0.64 vs. 0.53; =0.04). In reclassification analyses, adding NephroCheck to the ED score improved the prediction of AKI development ( <0.05). The T0 NephroCheck value predicted 30-day mortality (AUC, 0.68; <0.001). NephroCheck can predict both AKI development and short-term mortality in at-risk ED patients. NephroCheck would be a useful biomarker for early ruling-in or ruling-out of AKI in the ED.
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ISSN:2234-3806
2234-3814
2234-3814
DOI:10.3343/alm.2022.42.2.178