Previous Antibiotic Exposure Increases Risk of Infection with Extended-Spectrum-β-Lactamase- and AmpC-Producing Escherichia coli and Klebsiella pneumoniae in Pediatric Patients

Author:

Zerr Danielle M.12,Miles-Jay Arianna3,Kronman Matthew P.12,Zhou Chuan12,Adler Amanda L.2,Haaland Wren2,Weissman Scott J.12,Elward Alexis45,Newland Jason G.67,Zaoutis Theoklis89,Qin Xuan102

Affiliation:

1. Department of Pediatrics, University of Washington, Seattle, Washington, USA

2. Seattle Children's Research Institute, Seattle, Washington, USA

3. Department of Epidemiology, University of Washington, Seattle, Washington, USA

4. Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA

5. St. Louis Children's Hospital, St. Louis, Missouri, USA

6. Department of Pediatrics, University of Missouri—Kansas City, Kansas City, Missouri, USA

7. Children's Mercy Hospital and Clinics, Kansas City, Missouri, USA

8. Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA

9. The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA

10. Department of Laboratory Medicine, University of Washington, Seattle, Washington, USA

Abstract

ABSTRACT The objective of this study was to determine whether antibiotic exposure is associated with extended-spectrum-beta-lactamase- or AmpC-producing Escherichia coli or Klebsiella pneumoniae infections in children. We collected extended-spectrum-beta-lactamase- or AmpC-producing E. coli or K. pneumoniae isolates and same-species susceptible controls from normally sterile sites of patients aged ≤21 years, along with associated clinical data, at four free-standing pediatric centers. After controlling for potential confounders, the relative risk of having an extended-spectrum-beta-lactamase-producing isolate rather than a susceptible isolate was 2.2 times higher (95% confidence interval [CI], 1.49 to 3.35) among those with antibiotic exposure in the 30 days prior to infection than in those with no antibiotic exposure. The results were similar when analyses were limited to exposure to third-generation cephalosporins, other broad-spectrum beta-lactams, or trimethoprim-sulfamethoxazole. Conversely, the relative risk of having an AmpC-producing versus a susceptible isolate was not significantly elevated with any antibiotic exposure in the 30 days prior to infection (adjusted relative risk ratio, 1.12; 95% CI, 0.65 to 1.91). However, when examining subgroups of antibiotics, the relative risk of having an AmpC-producing isolate was higher for patients with exposure to third-generation cephalosporins (adjusted relative risk ratio, 4.48; 95% CI, 1.75 to 11.43). Dose-response relationships between antibiotic exposure and extended-spectrum-beta-lactamase-producing or AmpC-producing isolates were not demonstrated. These results reinforce the need to study and implement pediatric antimicrobial stewardship strategies, and they indicate that epidemiological studies of third-generation cephalosporin-resistant E. coli and K. pneumoniae isolates should include resistance mechanisms when possible.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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