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In vitro interaction of ceftazidime–avibactam in combination with different antimicrobials against KPC-producing Klebsiella pneumoniae clinical isolates

•In vitro synergistic activity of ceftazidime–avibactam (CAZ–AVI) in combination with different antimicrobials was evaluated against KPC-producing K. pneumoniae (KPC-Kp).•CAZ–AVI in combination with meropenem and imipenem was synergistic against both CAZ–AVI -susceptible and -resistant KPC-Kp clinic...

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Bibliographic Details
Published in:International journal of infectious diseases 2017-12, Vol.65, p.1-3
Main Authors: Gaibani, Paolo, Lewis, Russell E., Volpe, Silvia L., Giannella, Maddalena, Campoli, Caterina, Landini, Maria Paola, Viale, PierLuigi, Re, Maria Carla, Ambretti, Simone
Format: Article
Language:English
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Summary:•In vitro synergistic activity of ceftazidime–avibactam (CAZ–AVI) in combination with different antimicrobials was evaluated against KPC-producing K. pneumoniae (KPC-Kp).•CAZ–AVI in combination with meropenem and imipenem was synergistic against both CAZ–AVI -susceptible and -resistant KPC-Kp clinical isolates.•CAZ–AVI restored meropenem and imipenem susceptibility against CAZ–AVI -susceptible KPC-3 producers.•Combination of CAZ–AVI with imipenem exerted higher susceptible breakpoint indices (SBPIs) against CAZ–AVI -susceptible and -resistant KPC-Kp isolates. Combination therapy has been recommended when using ceftazidime–avibactam (CAZ–AVI) for the treatment of KPC-producing Klebsiella pneumoniae (KPC-Kp), but the optimal combination is unknown. Six common antimicrobial agents (ertapenem, imipenem, meropenem, gentamicin, tigecycline, and ciprofloxacin) were evaluated for synergy with the recently approved cephalosporin–β-lactamase inhibitor combination CAZ–AVI in this study. Different antimicrobial combinations were tested against 13 KPC-Kp, including CAZ–AVI-susceptible (n=11) and resistant (n=2) clinical isolates. In vitro interactions of CAZ–AVI with different antimicrobials were tested using the gradient synergy test. Changes in the minimum inhibitory concentration (MIC) value were interpreted using the fractional inhibitory concentration (FIC) index and susceptible breakpoint index (SBPI). The combination of CAZ–AVI with gentamicin or ciprofloxacin displayed no synergism against any of the KPC-Kp isolates, whereas synergistic activity was observed with imipenem and meropenem against all KPC-Kp isolates. Notably, CAZ–AVI reduced MICs for meropenem and imipenem below the resistance breakpoints against all strains. The SBPI analysis showed that CAZ–AVI in combination with imipenem achieved higher SBPI values than other CAZ–AVI-based combinations. These data suggest that combinations of CAZ–AVI with imipenem may be considered a useful therapeutic option for the treatment of KPC-Kp infections.
ISSN:1201-9712
1878-3511
DOI:10.1016/j.ijid.2017.09.017