Development of a prediction model for the acquisition of extended spectrum beta-lactam-resistant organisms in U.S. international travellers

Author:

Brown David Garrett1ORCID,Worby Colin J2,Pender Melissa A1,Brintz Ben J3,Ryan Edward T4567,Sridhar Sushmita467,Oliver Elizabeth6,Harris Jason B68,Turbett Sarah E469ORCID,Rao Sowmya R10,Earl Ashlee M2,LaRocque Regina C4567,Leung Daniel T111ORCID

Affiliation:

1. University of Utah School of Medicine Division of Infectious Diseases, , Salt Lake City, UT , USA

2. Broad Institute of MIT and Harvard Infectious Disease and Microbiome Program, , Cambridge, MA , USA

3. University of Utah School of Medicine Division of Epidemiology, , Salt Lake City, UT , USA

4. Harvard Medical School , Boston, MA , USA

5. Massachusetts General Hospital Travelers’ Advice and Immunization Center, , Boston, MA , USA

6. Massachusetts General Hospital Division of Infectious Diseases, , Boston, MA , USA

7. Massachusetts General Hospital Department of Medicine, , Boston, MA , USA

8. Harvard Medical School, Boston Department of Pediatrics, , MA , USA

9. Massachusetts General Hospital Department of Pathology, , Boston, MA , USA

10. Boston University School of Public Health Department of Global Health, , Boston, MA , USA

11. University of Utah School of Medicine Division of Microbiology & Immunology, , Salt Lake City, UT , USA

Abstract

Abstract Background Extended spectrum beta-lactamase producing Enterobacterales (ESBL-PE) present a risk to public health by limiting the efficacy of multiple classes of beta-lactam antibiotics against infection. International travellers may acquire these organisms and identifying individuals at high risk of acquisition could help inform clinical treatment or prevention strategies. Methods We used data collected from a cohort of 528 international travellers enrolled in a multicentre US-based study to derive a clinical prediction rule (CPR) to identify travellers who developed ESBL-PE colonization, defined as those with new ESBL positivity in stool upon return to the United States. To select candidate features, we used data collected from pre-travel and post-travel questionnaires, alongside destination-specific data from external sources. We utilized LASSO regression for feature selection, followed by random forest or logistic regression modelling, to derive a CPR for ESBL acquisition. Results A CPR using machine learning and logistic regression on 10 features has an internally cross-validated area under the receiver operating characteristic curve (cvAUC) of 0.70 (95% confidence interval 0.69–0.71). We also demonstrate that a four-feature model performs similarly to the 10-feature model, with a cvAUC of 0.68 (95% confidence interval 0.67–0.69). This model uses traveller’s diarrhoea, and antibiotics as treatment, destination country waste management rankings and destination regional probabilities as predictors. Conclusions We demonstrate that by integrating traveller characteristics with destination-specific data, we could derive a CPR to identify those at highest risk of acquiring ESBL-PE during international travel.

Funder

National Center for Advancing Translational Sciences of the National Institutes of Health

National Institutes of Health

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services

Centers for Disease Control and Prevention

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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