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Risk factors of septic shock development and thirty-day mortality with a predictive model in adult candidemia patients in intensive care units.

Authors :
Suh, Jin Woong
Kim, Min Ja
Kim, Jong Hun
Source :
Infectious Diseases. Nov/Dec 2021, Vol. 53 Issue 12, p908-919. 12p. 4 Charts, 4 Graphs.
Publication Year :
2021

Abstract

This study aimed to investigate factors associated with septic shock development and 30-day mortality outcome with a prediction model among adult candidemia patients in the intensive care unit (ICU). A retrospective study was conducted among patients admitted to the ICU from 2009 to 2018 at a tertiary care medical centre. The study subjects included adult patients ≥ 19 years with candidemia treated with antifungal agent for ≥ 3 days. Clinical variables were collected and analysed. A total of 126 patients were included in the study. Of these patients, 32 patients (25.4%) had septic shock. Multivariate logistic regression analysis revealed that chronic liver disease was associated with septic shock (odds ratio [OR] 3.372, 95% confidence interval [CI] 1.057 − 10.057). The rate of 30-day mortality was 35.7% and the associated mortality risk factors were malignancy (OR 8.251, 95% CI 2.227 − 30.573), chronic liver disease (OR 3.605, 95% CI 0.913 − 14.227), haemodialysis (OR 8.479, 95% CI 1.801 − 39.924), mycological failure (OR 29.675, 95% CI 7.012 − 125.578), and septic shock (OR 3.980, 95% CI 1.238 − 12.796). A predictive model for 30-day mortality was created based on the mortality risk factor scores, which had an area of 0.862 under the receiver operating characteristic curve. Adult candidemia patients in the ICU who have chronic liver disease may be at higher risk of developing septic shock. Furthermore, our predictive model for 30-day mortality based on the mortality risk factors may be useful for clinical assessment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23744235
Volume :
53
Issue :
12
Database :
Academic Search Index
Journal :
Infectious Diseases
Publication Type :
Academic Journal
Accession number :
153219065
Full Text :
https://doi.org/10.1080/23744235.2021.1959052