A Predictive Model to Identify Complicated Clostridiodes difficile Infection
Author
Berinstein, J.A.Steiner, C.A.
Rifkin, S.
Alexander, Perry, D.
Micic, D.
Shirley, D.
Higgins, P.D.R.
Young, V.B.
Lee, A.
Rao, K.
Affiliation
Division of Infectious Diseases, University of ArizonaIssue Date
2023-02-02
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Oxford University PressCitation
Jeffrey A Berinstein, Calen A Steiner, Samara Rifkin, D Alexander Perry, Dejan Micic, Daniel Shirley, Peter D R Higgins, Vincent B Young, Allen Lee, Krishna Rao, A Predictive Model to Identify Complicated Clostridiodes difficile Infection, Open Forum Infectious Diseases, Volume 10, Issue 2, February 2023, ofad049, https://doi.org/10.1093/ofid/ofad049Journal
Open Forum Infectious DiseasesRights
© The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Background: Clostridioides difficile infection (CDI) is a leading cause of health care-Associated infection and may result in organ dysfunction, colectomy, and death. Published risk scores to predict severe complications from CDI demonstrate poor performance upon external validation. We hypothesized that building and validating a model using geographically and temporally distinct cohorts would more accurately predict risk for complications from CDI. Methods: We conducted a multicenter retrospective cohort study of adults diagnosed with CDI. After randomly partitioning the data into training and validation sets, we developed and compared 3 machine learning algorithms (lasso regression, random forest, stacked ensemble) with 10-fold cross-validation to predict disease-related complications (intensive care unit admission, colectomy, or death attributable to CDI) within 30 days of diagnosis. Model performance was assessed using the area under the receiver operating curve (AUC). Results: A total of 3646 patients with CDI were included, of whom 217 (6%) had complications. All 3 models performed well (AUC, 0.88-0.89). Variables of importance were similar across models, including albumin, bicarbonate, change in creatinine, non-CDI-related intensive care unit admission, and concomitant non-CDI antibiotics. Sensitivity analyses indicated that model performance was robust even when varying derivation cohort inclusion and CDI testing approach. However, race was an important modifier, with models showing worse performance in non-White patients. Conclusions: Using a large heterogeneous population of patients, we developed and validated a prediction model that estimates risk for complications from CDI with good accuracy. Future studies should aim to reduce the disparity in model accuracy between White and non-White patients and to improve performance overall. © 2023 The Author(s). Published by Oxford University Press on behalf of Infectious Diseases Society of America.Note
Open access journalISSN
2328-8957Version
Final Published Versionae974a485f413a2113503eed53cd6c53
10.1093/ofid/ofad049
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Except where otherwise noted, this item's license is described as © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/).