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ARMD-Predict: multi-site machine learning to predict antibiotic resistance before culture results

Fateme Nateghi Haredasht, Nicholas P. Marshall, Wenyuan Chen, Lauren N. Cooper, Ziming Wei, Harrison Konsker, Jacob S. Chen, Michael Klompas, Cara McKenna, Richard J. Medford, Sanjat Kanjilal, Austin J. Schoeffler, Stephen P. Ma, Niaz Banaei, Steven M. Asch, Amy Chang, Stanley C. Deresinski, Mary K. Goldstein, Robert Tibshirani, Jonathan H. Chen

Preprint source: arXiv: Quantitative Methods

Abstract

Clinicians select empiric antibiotics before culture susceptibility results are available. Electronic health record (EHR) models could inform that choice, but most are developed at a single hospital and transport poorly to others. We developed ARMD-Predict using 7.5 million culture-antibiotic observations from four academic medical centers. One set of models estimates susceptibility to individual antibiotics; a second, hierarchical set predicts the infecting organism and then organism-specific resistance phenotypes. Across 23 pooled susceptibility models evaluated in same-period, patient-grouped test partitions, median area under the receiver operating characteristic curve (AUROC) was 0.77 for inpatient urine and 0.70 for inpatient blood cultures; chronological retraining reduced AUROC by approximately 0.04. At an exploratory threshold with 95% positive predictive value, derived and evaluated on the same test observations, the model identified 55% of ceftriaxone-susceptible inpatient urine observations as suitable for narrower therapy and flagged 60% of ceftriaxone-resistant observations for broader coverage. Organism classifiers achieved top-3 accuracy of 51.3-83.3%; phenotype AUROCs were conditional on the observed organism. Research applications are available at https://armd-predict.stanford.edu. Independent calibration, threshold and end-to-end prospective validation are required before clinical use.

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