Development and external validation of a model to predict multidrug-resistant bacterial infections in patients with cirrhosis

With the increasing rate of infections caused by multidrug-resistant organisms (MDRO), selecting appropriate empiric antibiotics has become challenging. We aimed to develop and externally validate a model for predicting the risk of MDRO infections in patients with cirrhosis. We included patients wit...

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Published in:Liver international Vol. 44; no. 11; pp. 2915 - 2928
Main Authors: Marciano, Sebastián, Piano, Salvatore, Singh, Virendra, Caraceni, Paolo, Maiwall, Rakhi, Alessandria, Carlo, Fernandez, Javier, Kim, Dong Joon, Kim, Sung Eun, Soares, Elza, Marino, Mónica, Vorobioff, Julio, Merli, Manuela, Elkrief, Laure, Vargas, Victor, Krag, Aleksander, Singh, Shivaram, Elizondo, Martín, Anders, Maria M, Dirchwolf, Melisa, Mendizabal, Manuel, Lesmana, Cosmas R A, Toledo, Claudio, Wong, Florence, Durand, Francois, Gadano, Adrián, Giunta, Diego H, Angeli, Paolo
Format: Journal Article
Language:English
Published: United States Wiley Subscription Services, Inc 01-11-2024
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Summary:With the increasing rate of infections caused by multidrug-resistant organisms (MDRO), selecting appropriate empiric antibiotics has become challenging. We aimed to develop and externally validate a model for predicting the risk of MDRO infections in patients with cirrhosis. We included patients with cirrhosis and bacterial infections from two prospective studies: a transcontinental study was used for model development and internal validation (n = 1302), and a study from Argentina and Uruguay was used for external validation (n = 472). All predictors were measured at the time of infection. Both culture-positive and culture-negative infections were included. The model was developed using logistic regression with backward stepwise predictor selection. We externally validated the optimism-adjusted model using calibration and discrimination statistics and evaluated its clinical utility. The prevalence of MDRO infections was 19% and 22% in the development and external validation datasets, respectively. The model's predictors were sex, prior antibiotic use, type and site of infection, MELD-Na, use of vasopressors, acute-on-chronic liver failure, and interaction terms. Upon external validation, the calibration slope was 77 (95% CI .48-1.05), and the area under the ROC curve was .68 (95% CI .61-.73). The application of the model significantly changed the post-test probability of having an MDRO infection, identifying patients with nosocomial infection at very low risk (8%) and patients with community-acquired infections at significant risk (36%). This model achieved adequate performance and could be used to improve the selection of empiric antibiotics, aligning with other antibiotic stewardship program strategies.
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ISSN:1478-3223
1478-3231
1478-3231
DOI:10.1111/liv.16063