Serum cystatin C for acute kidney injury evaluation in children treated with aminoglycosides
Autor: | Lorraine Lau, Michael Zappitelli, Michael Pizzi, Zubaida Al-Ismaili, Theresa Mottes, Stuart L. Goldstein, Jillian Caldwell, Maya Harel-Sterling, Michael R. Bennett, Prasad Devarajan, Larry C. Lands, Melissa Piccioni |
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Rok vydání: | 2016 |
Předmět: |
Male
Nephrology medicine.medical_specialty Pathology Adolescent 030232 urology & nephrology Renal function Pilot Projects urologic and male genital diseases behavioral disciplines and activities Gastroenterology Article Cohort Studies 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Predictive Value of Tests Internal medicine medicine Humans Prospective Studies Cystatin C Child Prospective cohort study Creatinine urogenital system business.industry Incidence Area under the curve Acute kidney injury 030208 emergency & critical care medicine Bacterial Infections Acute Kidney Injury medicine.disease female genital diseases and pregnancy complications Anti-Bacterial Agents Aminoglycosides Treatment Outcome chemistry Area Under Curve Child Preschool Pediatrics Perinatology and Child Health Biomarker (medicine) Female business Biomarkers Kidney disease |
Zdroj: | Pediatric Nephrology. 32:163-171 |
ISSN: | 1432-198X 0931-041X |
DOI: | 10.1007/s00467-016-3450-1 |
Popis: | Serum cystatin C (CysC) is a more accurate glomerular filtration rate marker than serum creatinine (SCr) and may rise more quickly with acute kidney injury (AKI). We performed a prospective cohort study of 81 non-critically ill children during 110 aminoglycoside (AG) treatments. We calculated area under the curve (AUC) for CysC to diagnose SCr-defined AKI and predict persistent AKI. SCr-AKI definition was based on the Kidney Disease: Improving Global Outcomes (≥stage 1: ≥50 % or 26.5 μmol/l SCr rise from baseline; stage 2: SCr doubling); CysC-AKI was based on a modified version using CysC rise. SCr-AKI and CysC-AKI developed in 45 and 48 % treatments, respectively. CysC rise predicted stage 1 (AUC = 0.75, 95 % CI 0.60–0.90) and 2 (AUC = 0.85, 95 % CI 0.75–0.95) SCr-AKI 2 days before SCr-AKI attainment. The best combined sensitivity/specificity for percent CysC rise to predict stage 1 SCr-AKI was with a 44 % CysC rise (sensitivity = 65 %, specificity = 83 %). CysC rise on day of SCr-AKI development was associated with SCr-AKI ≥48 h (AUC = 0.73, 95 % CI 0.56–0.90) and ≥50 % persistent SCr rise at treatment end (AUC = 0.76, 95 % CI 0.61–0.90). CysC is as an early AKI biomarker and predictive of persistent AKI on aminoglycoside treatment. |
Databáze: | OpenAIRE |
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