Detailed Information on Publication Record
2018
Prediction of major adverse kidney events in critically ill burn patients
DEPRET, F., L. BOUTIN, Jiří JARKOVSKÝ, M. CHAUSSARD, S. SOUSSI et. al.Basic information
Original name
Prediction of major adverse kidney events in critically ill burn patients
Authors
DEPRET, F. (250 France), L. BOUTIN (250 France), Jiří JARKOVSKÝ (203 Czech Republic, belonging to the institution), M. CHAUSSARD (250 France), S. SOUSSI (250 France), A. BATAILLE (250 France), H. OUESLATI (250 France), N. MORENO (250 France), C. de TYMOWSKI (250 France), Jiří PAŘENICA (203 Czech Republic, belonging to the institution), Klára BENEŠOVÁ (203 Czech Republic, belonging to the institution), T. VAUCHEL (250 France), A. FERRY (250 France), M. BENYAMINA (250 France), A. CUPACIU (250 France), M. COUTROT (250 France), J.P. GARNIER (250 France), K. SERROR (250 France), M. CHAOUAT (250 France), A. MEBAZAA (250 France) and M. LEGRAND (250 France, guarantor)
Edition
Burns, OXFORD, ELSEVIER SCI LTD, 2018, 0305-4179
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30212 Surgery
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.247
RIV identification code
RIV/00216224:14110/18:00104900
Organization unit
Faculty of Medicine
UT WoS
000451331200004
Keywords in English
Plasmatic Neutrophil Gelatinase-Associated Lipocain; Acute kidney injury; Burn patients; Major adverse kidney event
Tags
International impact, Reviewed
Změněno: 23/4/2024 10:05, Mgr. Michal Petr
Abstract
V originále
Objective: We aimed at assessing the predictive value of plasmatic Neutrophil Gelatinase Associated Lipocalin (pNGAL) at admission and severity scores to predict major adverse kidney events (MAKE, defined as death and/or need for renal replacement therapy (RRT) and/or non-renal recovery at day 90) in critically ill burn patients. Material and methods: Single-center cohort study in a burn critical care unit in a tertiary center, including all consecutive severely burn patients (total burned body surface >20%) from January 2012 until January 2015 with a pNGAL dosage at admission. Reclassification of patients was assessed by Integrated Discrimination Improvement (IDI). Measurements and results: 87 patients were included. Mean age was 47.7 (IQ 25-75: 33.4-65.2) years; total burn body surface area was 40 (IQ 25-75: 30-55) % and ICU mortality 36%. 39(44.8%) patients presented a MAKE, 32(88.9%) patients died at day 90. pNGAL was higher in the MAKE group (423 [IQ25-75: 327-518] pg/mL vs 184 [IQ25-75: 147-220] pg/mL, p<0.001). In multivariate analysis, pNGAL and abbreviated burn severity index (ABSI) remained associated with MAKE (OR 1.005 [CI 95% 1.0005-1.009], p=0.03 and OR 1.682 [CI95%1.038-2.726], p=0.035 respectively). Adding pNGAL to abbreviated burn severity index, simplified organ failure assessment and the simplified acute physiology score 2 did outperform clinical scores for the prediction of MAKE and AKI and for most severe forms of AKI and allowed a statistically significant reclassification of patients compared to ABSI for MAKE, RRT, AKI at Day 7 and AKI during hospitalization with a number of patients needed to screen to detect one extra episode of MAKE was 44, 13 for severe AKI and 15 for AKI. Conclusions: pNGAL at admission is associated with the risk of MAKE in this population, and outperform severity scores when associated. Interventional studies are now needed to assess if impact of biomarkers-guided strategies would improve outcome. (C) 2018 Elsevier Ltd and ISBI. All rights reserved.