Development and validation of machine learning models to predict MDRO colonization or infection on ICU admission by using electronic health record data
- PMID: 38971777
- PMCID: PMC11227715
- DOI: 10.1186/s13756-024-01428-y
Development and validation of machine learning models to predict MDRO colonization or infection on ICU admission by using electronic health record data
Abstract
Background: Multidrug-resistant organisms (MDRO) pose a significant threat to public health. Intensive Care Units (ICU), characterized by the extensive use of antimicrobial agents and a high prevalence of bacterial resistance, are hotspots for MDRO proliferation. Timely identification of patients at high risk for MDRO can aid in curbing transmission, enhancing patient outcomes, and maintaining the cleanliness of the ICU environment. This study focused on developing a machine learning (ML) model to identify patients at risk of MDRO during the initial phase of their ICU stay.
Methods: Utilizing patient data from the First Medical Center of the People's Liberation Army General Hospital (PLAGH-ICU) and the Medical Information Mart for Intensive Care (MIMIC-IV), the study analyzed variables within 24 h of ICU admission. Machine learning algorithms were applied to these datasets, emphasizing the early detection of MDRO colonization or infection. Model efficacy was evaluated by the area under the receiver operating characteristics curve (AUROC), alongside internal and external validation sets.
Results: The study evaluated 3,536 patients in PLAGH-ICU and 34,923 in MIMIC-IV, revealing MDRO prevalence of 11.96% and 8.81%, respectively. Significant differences in ICU and hospital stays, along with mortality rates, were observed between MDRO positive and negative patients. In the temporal validation, the PLAGH-ICU model achieved an AUROC of 0.786 [0.748, 0.825], while the MIMIC-IV model reached 0.744 [0.723, 0.766]. External validation demonstrated reduced model performance across different datasets. Key predictors included biochemical markers and the duration of pre-ICU hospital stay.
Conclusions: The ML models developed in this study demonstrated their capability in early identification of MDRO risks in ICU patients. Continuous refinement and validation in varied clinical contexts remain essential for future applications.
Keywords: Infection; Intensive care unit; Machine learning; Multidrug-resistant organisms; Predictive modeling.
© 2024. The Author(s).
Conflict of interest statement
The authors declare no competing interests.
Figures




Similar articles
-
Predicting infections with multidrug-resistant organisms (MDROs) in neurocritical care patients with hospital-acquired pneumonia (HAP): development of a novel multivariate prediction model.Microbiol Spectr. 2025 Jun 3;13(6):e0246024. doi: 10.1128/spectrum.02460-24. Epub 2025 May 15. Microbiol Spectr. 2025. PMID: 40372026 Free PMC article.
-
Resistance patterns and outcomes in intensive care unit (ICU)-acquired pneumonia. Validation of European Centre for Disease Prevention and Control (ECDC) and the Centers for Disease Control and Prevention (CDC) classification of multidrug resistant organisms.J Infect. 2015 Mar;70(3):213-22. doi: 10.1016/j.jinf.2014.10.004. Epub 2014 Oct 27. J Infect. 2015. PMID: 25445887
-
Development and Validation of a Dynamic Real-Time Risk Prediction Model for Intensive Care Units Patients Based on Longitudinal Irregular Data: Multicenter Retrospective Study.J Med Internet Res. 2025 Apr 23;27:e69293. doi: 10.2196/69293. J Med Internet Res. 2025. PMID: 40266658 Free PMC article.
-
Gut colonization with multidrug resistant organisms in the intensive care unit: a systematic review and meta-analysis.Crit Care. 2024 Jun 28;28(1):211. doi: 10.1186/s13054-024-04999-9. Crit Care. 2024. PMID: 38943133 Free PMC article.
-
An integrative review of infection prevention and control programs for multidrug-resistant organisms in acute care hospitals: a socio-ecological perspective.Am J Infect Control. 2011 Jun;39(5):368-378. doi: 10.1016/j.ajic.2010.07.017. Epub 2011 Mar 23. Am J Infect Control. 2011. PMID: 21429622 Review.
Cited by
-
The role of artificial intelligence and machine learning in predicting and combating antimicrobial resistance.Comput Struct Biotechnol J. 2025 Jan 18;27:423-439. doi: 10.1016/j.csbj.2025.01.006. eCollection 2025. Comput Struct Biotechnol J. 2025. PMID: 39906157 Free PMC article. Review.
-
Artificial Intelligence in Bacterial Infections Control: A Scoping Review.Antibiotics (Basel). 2025 Mar 2;14(3):256. doi: 10.3390/antibiotics14030256. Antibiotics (Basel). 2025. PMID: 40149067 Free PMC article. Review.
-
Multidrug-Resistant Infections and Metabolic Syndrome: An Overlooked Bidirectional Relationship.Biomedicines. 2025 May 30;13(6):1343. doi: 10.3390/biomedicines13061343. Biomedicines. 2025. PMID: 40564061 Free PMC article. Review.
-
Machine Learning-Based Prediction Model for Multidrug-Resistant Organisms Infections: Performance Evaluation and Interpretability Analysis.Infect Drug Resist. 2025 May 6;18:2255-2269. doi: 10.2147/IDR.S459830. eCollection 2025. Infect Drug Resist. 2025. PMID: 40353201 Free PMC article.
-
The Synergy of Machine Learning and Epidemiology in Addressing Carbapenem Resistance: A Comprehensive Review.Antibiotics (Basel). 2024 Oct 21;13(10):996. doi: 10.3390/antibiotics13100996. Antibiotics (Basel). 2024. PMID: 39452262 Free PMC article. Review.
References
-
- Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, Harbarth S, Hindler JF, Kahlmeter G, Olsson-Liljequist B, et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012;18(3):268–81. doi: 10.1111/j.1469-0691.2011.03570.x. - DOI - PubMed
-
- Serra-Burriel M, Keys M, Campillo-Artero C, Agodi A, Barchitta M, Gikas A, Palos C, López-Casasnovas G. Impact of multi-drug resistant bacteria on economic and clinical outcomes of healthcare-associated infections in adults: systematic review and meta-analysis. PLoS ONE. 2020;15(1):e0227139. doi: 10.1371/journal.pone.0227139. - DOI - PMC - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources