4.7 Article

In Vitro Activity Comparison of Ceftazidime-Avibactam and Aztreonam-Avibactam Against Bloodstream Infections With Carbapenem-Resistant Organisms in China

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2021.780365

关键词

carbapenem-resistant Enterobacterales (CRE); Pseudomonas aeruginosa; carbapenemase; avibactam; bloodstream infections

资金

  1. Key Research and Development Program of Zhejiang Province [2021C03068]
  2. Youth Program of National Natural Science Foundation of China [81803589]

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The study found that in vitro activity of aztreonam-avibactam was superior to ceftazidime-avibactam against carbapenem-resistant Escherichia coli and Klebsiella pneumoniae, while ceftazidime-avibactam showed better effect against carbapenem-resistant Pseudomonas aeruginosa.
Objectives: The aim of this work was to investigate the activity of ceftazidime-avibactam (CZA) and aztreonam-avibactam (AZA) against bloodstream infections caused by carbapenem-resistant organisms (CROs). Methods: Non-duplicate CROs, including 56 carbapenem-resistant Escherichia coil (CREco), 318 carbapenem-resistant Kiebsiella pneumoniae (CR-Kpn), and 65 carbapenem-resistant Pseudomonas aeruginosa (CR-Pae), were collected using the Blood Bacterial Resistant Investigation Collaborative System (BRICS) program in China. The minimum inhibitory concentrations (MICs) of 24 antibiotics were tested. Carbapenemase genes were amplified for CZA-resistant CROs by PCR. The MICs of CZA and AZA were further determined with avibactam at 8 and 16 mg/L, respectively. Results: The resistance rate of polymyxin B against CROs was less than 5%. Only one CR-Kpn was resistant to tigecycline. The resistance rates of CZA against CR-Eco, CR-Kpn, and CR-Pae were 75.0%, 12.6%, and 18.5%, respectively. The MIC, 0 values of AZA against CR-Eco, CR-Kpn, and CR-Pae were 2/4, 1/4, and 64/4 mg/L, respectively. Among the CZA-resistant CROs, 42 (100%) CR-Eco, 24 (60%) CR-Kpn, and 1 (8.3%) CR-Pae isolates harbored metallo-13-lactamase genes. The increase of avibactam concentration enhanced the susceptibility of CZA and AZA against CROs, especially for CR-Eco and CR-Kpn. Conclusions: The in vitro activity of AZA was superior to that of CZA against CR-Eco and CR-Kpn, whereas CZA showed better effect against CR-Pae.

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