International Epidemiology of Carbapenemase-Producing Escherichia coli
| dc.contributor.author | Boutzoukas, Angelique E. | |
| dc.contributor.author | Komarow, Lauren | |
| dc.contributor.author | Chen, Liang | |
| dc.contributor.author | Hanson, Blake M. | |
| dc.contributor.author | Kanj, Souha S. | |
| dc.contributor.author | Liu, Zhengyin | |
| dc.contributor.author | Salcedo-Mendoza, Soraya | |
| dc.contributor.author | Ordóñez, Karen Melissa | |
| dc.contributor.author | Wang, Minggui | |
| dc.contributor.author | Paterson, David L. | |
| dc.contributor.author | Evans, Scott R. | |
| dc.contributor.author | Ge, Lizhao | |
| dc.contributor.author | Giri, Abhigya | |
| dc.contributor.author | Hill, Carol B. | |
| dc.contributor.author | Baum, Keri R. | |
| dc.contributor.author | Bonomo, Robert A. | |
| dc.contributor.author | Kreiswirth, Barry N. | |
| dc.contributor.author | Patel, Robin | |
| dc.contributor.author | Arias, Cesar A. | |
| dc.contributor.author | Chambers, Henry F. | |
| dc.contributor.author | Fowler, Vance G. | |
| dc.contributor.author | Van Duin, David Van | |
| dc.contributor.department | Internal Medicine | |
| dc.contributor.department | Division of Infectious Diseases | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T11:45:03Z | |
| dc.date.available | 2025-01-24T11:45:03Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Background: Carbapenemase-producing (CP) Escherichia coli (CP-Ec) are a global public health threat. We aimed to describe the clinical and molecular epidemiology and outcomes of patients from several countries with CP-Ec isolates obtained from a prospective cohort. Methods: Patients with CP-Ec were enrolled from 26 hospitals in 6 countries. Clinical data were collected, and isolates underwent whole-genome sequencing. Clinical and molecular features and outcomes associated with isolates with or without metallo-β-lactamases (MBLs) were compared. The primary outcome was desirability of outcome ranking (DOOR) at 30 days after the index culture. Results: Of the 114 CP-Ec isolates in Consortium on resistance against carbapenems in Klebsiella and other Enterobacterales-2 (CRACKLE-2), 49 harbored an MBL, most commonly blaNDM-5 (38/49, 78%). Strong regional variations were noted with MBL-Ec predominantly found among patients in China (23/49). Clinically, MBL-Ec were more often from urine sources (49% vs 29%), less often met criteria for infection (39% vs 58%, P =. 04), and had lower acuity of illness when compared with non-MBL-Ec. Among patients with infection, the probability of a better DOOR outcome for a randomly selected patient with MBL-Ec as compared with non-MBL-Ec was 62% (95% CI: 48.2-74.3%). Among infected patients, non-MBL-Ec had increased 30-day (26% vs 0%; P =. 02) and 90-day (39% vs 0%; P =. 001) mortality compared with MBL-Ec. Conclusions: Emergence of CP-Ec was observed with important geographic variations. Bacterial characteristics, clinical presentations, and outcomes differed between MBL-Ec and non-MBL-Ec. Mortality was higher among non-MBL isolates, which were more frequently isolated from blood, but these findings may be confounded by regional variations. © 2023 The Author(s). Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. | |
| dc.identifier.doi | https://doi.org/10.1093/cid/ciad288 | |
| dc.identifier.eid | 2-s2.0-85168786187 | |
| dc.identifier.pmid | 37154071 | |
| dc.identifier.uri | http://hdl.handle.net/10938/30524 | |
| dc.language.iso | en | |
| dc.publisher | Oxford University Press | |
| dc.relation.ispartof | Clinical Infectious Diseases | |
| dc.source | Scopus | |
| dc.subject | Carbapenem resistance | |
| dc.subject | E. coli | |
| dc.subject | Multidrug resistance | |
| dc.subject | Anti-bacterial agents | |
| dc.subject | Bacterial proteins | |
| dc.subject | Beta-lactamases | |
| dc.subject | Carbapenem-resistant enterobacteriaceae | |
| dc.subject | Escherichia coli | |
| dc.subject | Humans | |
| dc.subject | Microbial sensitivity tests | |
| dc.subject | Prospective studies | |
| dc.subject | Carbapenem derivative | |
| dc.subject | Carbapenemase | |
| dc.subject | Metallo beta lactamase | |
| dc.subject | Antiinfective agent | |
| dc.subject | Bacterial protein | |
| dc.subject | Beta lactamase | |
| dc.subject | Adult | |
| dc.subject | Article | |
| dc.subject | Bacterium culture | |
| dc.subject | Bacterium isolate | |
| dc.subject | Carbapenemase producing enterobacteriaceae | |
| dc.subject | China | |
| dc.subject | Cohort analysis | |
| dc.subject | Controlled study | |
| dc.subject | Crackle | |
| dc.subject | Enterobacterales | |
| dc.subject | Female | |
| dc.subject | Human | |
| dc.subject | Human tissue | |
| dc.subject | Klebsiella | |
| dc.subject | Male | |
| dc.subject | Molecular epidemiology | |
| dc.subject | Mortality | |
| dc.subject | Multicenter study | |
| dc.subject | Nonhuman | |
| dc.subject | Outcome assessment | |
| dc.subject | Probability | |
| dc.subject | Prospective study | |
| dc.subject | Randomized controlled trial | |
| dc.subject | Whole genome sequencing | |
| dc.subject | Genetics | |
| dc.subject | Microbial sensitivity test | |
| dc.title | International Epidemiology of Carbapenemase-Producing Escherichia coli | |
| dc.type | Article |
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