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A scoring system based on novel biomarkers and clinical risk factors to predict invasive candidiasis in immunocompetent critically ill patients

BACKGROUND: Delayed diagnosis further increases the mortality of invasive candidiasis (IC) in intensive care unit (ICU) patients. This study aimed to develop and validate a score based on novel serological biomarkers and clinical risk factors for predicting IC in immunocompetent ICU patients. METHOD...

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Autores principales: Li, Wen, Chen, Gang, Lin, Fengyu, Yang, Hang, Cui, Yanhui, Lu, Rongli, Song, Chao, Li, Haitao, Li, Yi, Pan, Pinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033536/
https://www.ncbi.nlm.nih.gov/pubmed/36970699
http://dx.doi.org/10.3389/fmicb.2023.1097574
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author Li, Wen
Chen, Gang
Lin, Fengyu
Yang, Hang
Cui, Yanhui
Lu, Rongli
Song, Chao
Li, Haitao
Li, Yi
Pan, Pinhua
author_facet Li, Wen
Chen, Gang
Lin, Fengyu
Yang, Hang
Cui, Yanhui
Lu, Rongli
Song, Chao
Li, Haitao
Li, Yi
Pan, Pinhua
author_sort Li, Wen
collection PubMed
description BACKGROUND: Delayed diagnosis further increases the mortality of invasive candidiasis (IC) in intensive care unit (ICU) patients. This study aimed to develop and validate a score based on novel serological biomarkers and clinical risk factors for predicting IC in immunocompetent ICU patients. METHODS: We retrospectively collected clinical data and novel serological markers on admission to ICU. Multivariate logistic regression was used to identify the risk factors associated with IC, which were adopted to establish a scoring system. RESULTS: Patients with IC had a higher C-reactive protein-to-albumin ratio (CAR) and neutrophil-to-lymphocyte ratio (NLR) and lower prognostic nutritional index than those without IC. The NLR, CAR, sepsis, total parenteral nutrition, 1,3-β-D-glucan (BDG)-positivity, and Sequential Organ Failure Assessment score were identified as independent risk factors for IC by multivariate logistic regression analysis and entered into the final scoring system. The area under receiver operating characteristic curve of the score were 0.883 and 0.892, respectively, in the development and validation cohort, higher than Candida score (0.883 vs.0.730, p < 0.001). CONCLUSION: We established a parsimonious score based on NLR, CAR, BDG-positivity, and clinical risk factors, which can accurately identify IC in ICU patients to give treatment on time and reduce mortality.
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spelling pubmed-100335362023-03-24 A scoring system based on novel biomarkers and clinical risk factors to predict invasive candidiasis in immunocompetent critically ill patients Li, Wen Chen, Gang Lin, Fengyu Yang, Hang Cui, Yanhui Lu, Rongli Song, Chao Li, Haitao Li, Yi Pan, Pinhua Front Microbiol Microbiology BACKGROUND: Delayed diagnosis further increases the mortality of invasive candidiasis (IC) in intensive care unit (ICU) patients. This study aimed to develop and validate a score based on novel serological biomarkers and clinical risk factors for predicting IC in immunocompetent ICU patients. METHODS: We retrospectively collected clinical data and novel serological markers on admission to ICU. Multivariate logistic regression was used to identify the risk factors associated with IC, which were adopted to establish a scoring system. RESULTS: Patients with IC had a higher C-reactive protein-to-albumin ratio (CAR) and neutrophil-to-lymphocyte ratio (NLR) and lower prognostic nutritional index than those without IC. The NLR, CAR, sepsis, total parenteral nutrition, 1,3-β-D-glucan (BDG)-positivity, and Sequential Organ Failure Assessment score were identified as independent risk factors for IC by multivariate logistic regression analysis and entered into the final scoring system. The area under receiver operating characteristic curve of the score were 0.883 and 0.892, respectively, in the development and validation cohort, higher than Candida score (0.883 vs.0.730, p < 0.001). CONCLUSION: We established a parsimonious score based on NLR, CAR, BDG-positivity, and clinical risk factors, which can accurately identify IC in ICU patients to give treatment on time and reduce mortality. Frontiers Media S.A. 2023-03-09 /pmc/articles/PMC10033536/ /pubmed/36970699 http://dx.doi.org/10.3389/fmicb.2023.1097574 Text en Copyright © 2023 Li, Chen, Lin, Yang, Cui, Lu, Song, Li, Li and Pan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Li, Wen
Chen, Gang
Lin, Fengyu
Yang, Hang
Cui, Yanhui
Lu, Rongli
Song, Chao
Li, Haitao
Li, Yi
Pan, Pinhua
A scoring system based on novel biomarkers and clinical risk factors to predict invasive candidiasis in immunocompetent critically ill patients
title A scoring system based on novel biomarkers and clinical risk factors to predict invasive candidiasis in immunocompetent critically ill patients
title_full A scoring system based on novel biomarkers and clinical risk factors to predict invasive candidiasis in immunocompetent critically ill patients
title_fullStr A scoring system based on novel biomarkers and clinical risk factors to predict invasive candidiasis in immunocompetent critically ill patients
title_full_unstemmed A scoring system based on novel biomarkers and clinical risk factors to predict invasive candidiasis in immunocompetent critically ill patients
title_short A scoring system based on novel biomarkers and clinical risk factors to predict invasive candidiasis in immunocompetent critically ill patients
title_sort scoring system based on novel biomarkers and clinical risk factors to predict invasive candidiasis in immunocompetent critically ill patients
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033536/
https://www.ncbi.nlm.nih.gov/pubmed/36970699
http://dx.doi.org/10.3389/fmicb.2023.1097574
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