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Using Genetic Distance from Archived Samples for the Prediction of Antibiotic Resistance in Escherichia coli.
MacFadden, Derek R; Coburn, Bryan; Brinda, Karel; Corbeil, Antoine; Daneman, Nick; Fisman, David; Lee, Robyn S; Lipsitch, Marc; McGeer, Allison; Melano, Roberto G; Mubareka, Samira; Hanage, William P.
Afiliação
  • MacFadden DR; Division of Infectious Diseases, University of Toronto, Toronto, Canada derek.macfadden@mail.utoronto.ca whanage@hsph.harvard.edu.
  • Coburn B; Harvard T. H. Chan School of Public Health, Boston, Massachusetts, USA.
  • Brinda K; Ottawa Hospital Research Institute, Ottawa, Canada.
  • Corbeil A; Division of Infectious Diseases, University of Toronto, Toronto, Canada.
  • Daneman N; University Health Network, Toronto, Canada.
  • Fisman D; Harvard T. H. Chan School of Public Health, Boston, Massachusetts, USA.
  • Lee RS; Harvard Medical School, Boston, Massachusetts, USA.
  • Lipsitch M; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
  • McGeer A; Division of Infectious Diseases, University of Toronto, Toronto, Canada.
  • Melano RG; Division of Infectious Diseases, University of Toronto, Toronto, Canada.
  • Mubareka S; Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.
  • Hanage WP; Harvard Medical School, Boston, Massachusetts, USA.
Article em En | MEDLINE | ID: mdl-32152083
ABSTRACT
The rising rates of antibiotic resistance increasingly compromise empirical treatment. Knowing the antibiotic susceptibility of a pathogen's close genetic relative(s) may improve empirical antibiotic selection. Using genomic and phenotypic data for Escherichia coli isolates from three separate clinically derived databases, we evaluated multiple genomic methods and statistical models for predicting antibiotic susceptibility, focusing on potentially rapidly available information, such as lineage or genetic distance from archived isolates. We applied these methods to derive and validate the prediction of antibiotic susceptibility to common antibiotics. We evaluated 968 separate episodes of suspected and confirmed infection with Escherichia coli from three geographically and temporally separated databases in Ontario, Canada, from 2010 to 2018. Across all approaches, model performance (area under the curve [AUC]) ranges for predicting antibiotic susceptibility were the greatest for ciprofloxacin (AUC, 0.76 to 0.97) and the lowest for trimethoprim-sulfamethoxazole (AUC, 0.51 to 0.80). When a model predicted that an isolate was susceptible, the resulting (posttest) probabilities of susceptibility were sufficient to warrant empirical therapy for most antibiotics (mean, 92%). An approach combining multiple models could permit the use of narrower-spectrum oral agents in 2 out of every 3 patients while maintaining high treatment adequacy (∼90%). Methods based on genetic relatedness to archived samples of E. coli could be used to predict antibiotic resistance and improve antibiotic selection.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Farmacorresistência Bacteriana / Escherichia coli Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País como assunto: America do norte Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Farmacorresistência Bacteriana / Escherichia coli Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País como assunto: America do norte Idioma: En Ano de publicação: 2020 Tipo de documento: Article