Diagnostic Microbiology & Infectious Disease
Volume 67, Issue 3 , Pages 251-260, July 2010

Comparative in vitro activity of cefditoren and other antimicrobials against Enterobacteriaceae causing community-acquired uncomplicated urinary tract infections in women: a Spanish nationwide multicenter study

  • Oscar Cuevas

      Affiliations

    • Servicio de Microbiología y Enfermedades Infecciosas, Hospital General Universitario Gregorio Marañón, Universidad Complutense, Madrid, Spain
  • ,
  • Emilia Cercenado

      Affiliations

    • Servicio de Microbiología y Enfermedades Infecciosas, Hospital General Universitario Gregorio Marañón, Universidad Complutense, Madrid, Spain
    • Corresponding Author InformationCorresponding author. Servicio de Microbiología, Hospital General Universitario Gregorio Marañón, Dr Esquerdo 46, 28007 Madrid, Spain. Tel.: +34-91-586-8459; fax: +34-91-504-4906.
  • ,
  • Mercedes Gimeno

      Affiliations

    • Scientific Department, Tedec-Meiji Farma, Madrid, Spain
  • ,
  • Mercedes Marín

      Affiliations

    • Servicio de Microbiología y Enfermedades Infecciosas, Hospital General Universitario Gregorio Marañón, Universidad Complutense, Madrid, Spain
  • ,
  • Pilar Coronel

      Affiliations

    • Scientific Department, Tedec-Meiji Farma, Madrid, Spain
  • ,
  • Emilio Bouza

      Affiliations

    • Servicio de Microbiología y Enfermedades Infecciosas, Hospital General Universitario Gregorio Marañón, Universidad Complutense, Madrid, Spain
  • ,
  • Spanish Urinary Tract Infection Study Group (SUTIS)

      Affiliations

    • Members of the SUTIS group are listed in the Acknowledgements.

Received 18 December 2009; accepted 14 February 2010.

Abstract 

Cefditoren is a third-generation orally administered cephalosporin with a broad spectrum of activity against Gram-positive and Gram-negative bacterial species. After an oral 400-mg single dose, the mean concentrations in urine are 186.5 mg/L at 2 to 4 h and 12.7 mg/L at 8 to 12 h, and it is a potential drug to be used in the treatment of urinary tract infection (UTI). We performed a multicenter nationwide study in Spain in order to determine the in vitro activity of cefditoren and other comparative agents against Enterobacteriaceae causing community-acquired uncomplicated UTI in women. From June 2008 to March 2009, 89 institutions participated in the study. A total of 2152 Enterobacteriaceae were collected and sent to a coordinating laboratory where identification and antimicrobial susceptibility testing was performed against 20 antimicrobials using an automated microdilution method (MicroScan; Siemens, Sacramento, CA). Cefditoren MICs were determined by the broth microdilution method (Clinical and Laboratory Standards Institute guidelines) using the same inoculum. Microorganisms isolated were Escherichia coli (81.8%), Klebsiella pneumoniae (7.9%), Proteus mirabilis (5.2%), and others (5.1%). A total of 51 isolates (2.4%) were extended-spectrum β-lactamase (ESBL) producers, 3 (0.1%) produced plasmidic AmpC enzymes, and 64 (2.9%) produced chromosomal AmpC. The MIC50/MIC90 (mg/L) of cefditoren against all isolates was 0.12/0.5. Cefditoren inhibited 96.5% of isolates at 1 mg/L and was uniformly active against all isolates with the exception of strains producing ESBLs or AmpC enzymes. The MIC50/MIC90 of other antimicrobials were ampicillin (AMP) >16/>16, amoxicillin/clavulanic acid (A/C) ≤8/4/16/8, cefuroxime (FUR) ≤4/8, cefotaxime ≤1/≤1, ciprofloxacin (CIP) ≤0.12/>2, trimethoprim/sulfamethoxazole (SxT) ≤2/38/>4/76, and fosfomycin (FOS) ≤16/≤16. The respective percentages of resistance were 61%, 17.2%, 5.5%, 2.3%, 20.2%, 27.4%, and 4.8%. The activity of cefditoren against Enterobacteriaceae producing community-acquired uncomplicated UTI in women was superior to that of AMP, A/C, FUR, CIP, and SxT and similar to that of FOS.

Keywords: Uncomplicated urinary tract infection, Cystitis, Pyelonephritis, Cefditoren, Surveillance, Urinary pathogens

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PII: S0732-8893(10)00049-0

doi:10.1016/j.diagmicrobio.2010.02.013

Diagnostic Microbiology & Infectious Disease
Volume 67, Issue 3 , Pages 251-260, July 2010