4.7 Article

In Vitro Activity of Cefepime-Zidebactam, Ceftazidime-Avibactam, and Other Comparators against Clinical Isolates of Enterobacterales, Pseudomonas aeruginosa, and Acinetobacter baumannii: Results from China Antimicrobial Surveillance Network (CHINET) in 2018

期刊

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.01726-20

关键词

Enterobacterales; Pseudomonas aeruginosa; Acinetobacter baumannii; cefepime-zidebactam; ceftazidime-avibactam; bla(KPC); bla(NDM); bla(OXA-48)

资金

  1. National Mega-project for Innovative Drugs [2019ZX09721001-006-004]
  2. National Natural Science Foundation of China [81871690, 81902100, 81902101]
  3. Science and Technology Innovation Action Plan of Shanghai Science and Technology Committee [17DZ1910403]
  4. Shanghai Antimicrobial Surveillance Network [3030231003]
  5. China Antimicrobial Surveillance Network [WI207259]

向作者/读者索取更多资源

The study found that cefepime-zidebactam exhibited potent activity against almost all Enterobacterales and good activity against P. aeruginosa, while ceftazidime-avibactam showed good in vitro activity against Enterobacterales and P. aeruginosa but less activity against Acinetobacter baumannii. Most of the carbapenem-resistant Enterobacteriaceae isolates were susceptible to cefepime-zidebactam and ceftazidime-avibactam showed good activity against bla(KPC-2)-positive Enterobacterales and carbapenem-resistant P. aeruginosa.
This study evaluated the in vitro activity of cefepime-zidebactam in comparison with that of ceftazidime-avibactam and other comparators against clinically significant Gram-negative bacillus isolates. A total of 3,400 nonduplicate Gram-negative clinical isolates were collected from 45 medical centers across China in the CHINET Program in 2018, including Enterobacterales (n = 2,228), Pseudomonas aeruginosa (n = 657), and Acinetobacter baumannii (n = 515). The activities of cefepime-zidebactam and 20 comparators were determined by broth microdilution as recommended by the Clinical and Laboratory Standards Institute. Cefepime-zidebactam demonstrated potent activity against almost all Enterobacterales (MIC50/90, 0.125/ 1 mg/liter) and good activity against P. aeruginosa (MIC50/90, 2/8 mg/liter). Among the 373 carbapenem-resistant Enterobacteriaceae isolates, 57.3% (213/373) and 15.3% (57/373) were positive for bla(KPC-2) and bla(NDM), respectively. Cefepime-zidebactam showed a MIC of <= 2 mg/liter for 92.0% (196/213) of bla(KPC-2) producers and 79.7%(47/59) of bla(NDM) producers. Ceftazidime-avibactam showed good in vitro activity against Enterobacterales (MIC50/90, 0.25/2 mg/liter; 94.0% susceptible) and P. aeruginosa (MIC50/90, 4/16 mg/liter; 86.9% susceptible). Ceftazidime-avibactam was active against 9.1% of carbapenem-resistant Escherichia coli isolates (63.6% were bla(NDM) producers) and 84.6% of Klebsiella pneumoniae isolates (74.3% were bla(KPC) producers). Most (90.1%) bla(KPC-2) producers were susceptible to ceftazidime-avibactam. Cefepime-zidebactam demonstrated limited activity (MIC50/90, 16/32 mg/liter) against the 515 A. baumannii isolates (79.2% were carbapenem resistant), and ceftazidime-avibactam was less active (MIC50/90, 64/>64 mg/liter). Cefepime-zidebactam was highly active against clinical isolates of Enterobacterales and P. aeruginosa, including bla(KPC-2)-positive Enterobacterales and bla(NDM)-positive Enterobacterales and carbapenem-resistant P. aeruginosa. And ceftazidime-avibactam was highly active against bla(KPC-2)-positive Enterobacterales and carbapenem-resistant P. aeruginosa.

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