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Activity of temocillin against ESBL-, AmpC-, and/or KPC-producing Enterobacterales isolated in Poland.
Kuch, Alicja; Zieniuk, Bartlomiej; Zabicka, Dorota; Van de Velde, Sebastien; Literacka, Elzbieta; Skoczynska, Anna; Hryniewicz, Waleria.
Afiliação
  • Kuch A; Department of Epidemiology and Clinical Microbiology, National Medicines Institute, Chelmska 30/34, 00-725, Warsaw, Poland.
  • Zieniuk B; Department of Epidemiology and Clinical Microbiology, National Medicines Institute, Chelmska 30/34, 00-725, Warsaw, Poland.
  • Zabicka D; Department of Epidemiology and Clinical Microbiology, National Medicines Institute, Chelmska 30/34, 00-725, Warsaw, Poland. d.zabicka@nil.gov.pl.
  • Van de Velde S; Eumedica S.A., Chemin de Nauwelette 1, 7170, Manage, Belgium.
  • Literacka E; Department of Epidemiology and Clinical Microbiology, National Medicines Institute, Chelmska 30/34, 00-725, Warsaw, Poland.
  • Skoczynska A; Department of Epidemiology and Clinical Microbiology, National Medicines Institute, Chelmska 30/34, 00-725, Warsaw, Poland.
  • Hryniewicz W; Department of Epidemiology and Clinical Microbiology, National Medicines Institute, Chelmska 30/34, 00-725, Warsaw, Poland.
Eur J Clin Microbiol Infect Dis ; 39(6): 1185-1191, 2020 Jun.
Article em En | MEDLINE | ID: mdl-32096107
ABSTRACT
We evaluated the in vitro effectiveness of temocillin and several commonly used antimicrobials against Enterobacterales bacteria in isolates from Polish patients. We tested 400 isolates 260 extended-spectrum ß-lactamase (ESBL)- and/or ampC ß-lactamase (AmpC)-producing isolates; 40 Klebsiella pneumoniae carbapenemase (KPC)-producing isolates; and 100 ESBL-, AmpC-, and KPC-negative isolates. The minimal inhibitory concentrations (MICs) of temocillin and 16 other antimicrobials were determined by reference microdilution. We also determined the activities of fosfomycin and ceftazidime/avibactam in KPC-producing isolates. The antibiotic sensitivities were interpreted according to EUCAST, BSAC, and CLSI criteria. Overall, 91% of the isolates were susceptible to temocillin using the urinary tract infection breakpoint (≤ 32 mg/L), and 61.8% were susceptible using the systemic infection breakpoint (≤ 8 mg/L). Meropenem and imipenem were the most active drugs (MIC50 values of 0.06 and 0.5 mg/L, respectively). Colistin and ertapenem (both MIC50 = 0.12 mg/L) were less active than meropenem or imipenem, but some strains were 77% susceptible to each of them. Among the KPC-producing isolates, 42.5% had MIC values of ≤ 32 mg/L (urinary tract infection breakpoint), but 100% were resistant to temocillin (systemic infection breakpoint). Ceftazidime/avibactam was active against 100% of the KPC-producing isolates, and fosfomycin was active against 40%. The empirical susceptibility rate observed among the urinary isolates suggests that temocillin may be considered as an alternative to carbapenems in the absence of KPC-producing bacteria. With regard to isolates from other sources, temocillin might be useful as a documented therapy agent or an empirical treatment in hospitals with a low prevalence of ESBL/AmpC-producing strains.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Penicilinas / Beta-Lactamases / Gammaproteobacteria / Antibacterianos Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Penicilinas / Beta-Lactamases / Gammaproteobacteria / Antibacterianos Idioma: En Ano de publicação: 2020 Tipo de documento: Article