Bloodstream infections caused by Escherichia coli producing AmpC β-lactamases: epidemiology and clinical features
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  • 作者:V. Pascual ; N. Alonso ; M. Simó ; G. Ortiz…
  • 刊名:European Journal of Clinical Microbiology & Infectious Diseases
  • 出版年:2016
  • 出版时间:December 2016
  • 年:2016
  • 卷:35
  • 期:12
  • 页码:1997-2003
  • 全文大小:
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Medical Microbiology; Internal Medicine;
  • 出版者:Springer Berlin Heidelberg
  • ISSN:1435-4373
  • 卷排序:35
文摘
The aim of the study was to investigate the epidemiology and clinical features of bloodstream infections due to Escherichia coli producing AmpC β-lactamases (AmpC-Ec-BSI). In a multi-centre case–control study, all third-generation-cephalosporin-resistant Escherichia coli BSI (3GC-Ec-BSI) isolates were analysed. Acquired blaAmpC (blaac-AmpC) detection was done by polymerase chain reaction (PCR) and sequencing. Chromosomal blaAmpC (blac-AmpC) expression was quantified by real-time PCR. Cases were patients with AmpC-Ec-BSI. Controls were patients with cephalosporin-susceptible E. coli BSI, matched 1:1 by sex and age. Demographics, comorbidities, intrinsic and extrinsic risk factors for antimicrobial resistance, clinical presentation and outcomes were investigated. Among 841 E. coli BSI, 17 were caused by AmpC-Ec (2 %). Eleven isolates (58.8 %) had blaac-AmpC and six were blac-AmpC overproducers. The mean age of cases was 66.2 years and 71 % were men. Cases were more frequently healthcare-related (82 vs. 52 % controls, p < 0.05) and presented more intrinsic and extrinsic risk factors. At least one risk factor was present in 94.1 % of cases vs. 41.7 % of controls (p = 0.002). Severity and length of stay (LOS) were higher among cases (mean Pitt Score 2.6 vs. 0.38 in controls, p = 0.03; LOS 17.5 days vs. 6 in controls, p = 0.02). Inappropriate empirical therapy (IET) was administered to 70.6 % of cases and 23.5 % of controls (p < 0.003). No differences were found in terms of cure rate at the 14th day and mortality. Bloodstream infections due to AmpC-Ec (mostly plasmid-mediated) are infrequent in our area. AmpC-Ec-BSI affects mainly patients with intrinsic risk factors and those with previous antibiotic exposure. A high proportion received IET.
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