Epidemiology of carbapenemase-producing Enterobacterales carriage in a paediatric tertiary health care centre of Ontario, Canada

Author:

Blanchard Ana C1,Zahradnik Stephanie2,Isabel Sandra2,Mehta Kayur2,Ali Mohsin2,Airo Adriana3,Streitenberger Laurie24,Freeman Renee24,Yau Yvonne CW3,Campigotto Aaron3,Tadros Manal3,Science Michelle245

Affiliation:

1. Division of Infectious Diseases, Department of Paediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, Quebec, Canada

2. Division of Infectious Diseases, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

3. Division of Microbiology, Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

4. Infection Prevention & Control Program, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

5. Correspondence: Michelle Science, Division of Infectious Diseases, Department of Paediatrics, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada. Telephone: 416-813-7654, ext. 201157.

Abstract

Introduction: The epidemiology of carbapenemase-producing Enterobacterales (CPE) in hospitalized children in low endemicity settings is not well known. We aim to describe it in a large tertiary paediatric health care centre in Canada. Methods: A repeated point-prevalence study including all inpatients was conducted at the Hospital for Sick Children, Toronto, for surveillance purposes over 3 days serially in April 2017, April 2019, and April 2022. Patients in the emergency department and medical day units were excluded. Stools or rectal swabs were analyzed for CPE identification, with confirmatory testing at the provincial reference laboratory. Results: We detected CPE colonization in 0.4% (1/242), 0.7% (2/278), and 0.9% (2/220) of inpatients in 2017, 2019, and 2022, respectively. Identified CPE included OXA-48-like and NDM beta-lactamases in Escherichia coli and Klebsiella pneumoniae. All patients with CPE colonization had a history of travel or hospitalization outside of Canada, including in the Middle East and Asia. Discussion: CPE colonization in children hospitalized in this Canadian hospital was detected. A history of prolonged travel or hospitalization outside of Canada are risk factors that should be considered in targeted screening programs.

Publisher

University of Toronto Press Inc. (UTPress)

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