scholarly journals Efficacy of Ceftazidime-Avibactam against Multi-Drug Resistant Enterobacteriaceae and Pseudomonas aeruginosa from the Phase 3 Clinical Trial Program

2016 ◽  
Vol 3 (suppl_1) ◽  
Author(s):  
Gregory G. Stone ◽  
Leanne Gasink ◽  
Paul Newell ◽  
Helen Broadhurst ◽  
Angela Wardman ◽  
...  
2018 ◽  
Vol 124 (1) ◽  
pp. 27-38 ◽  
Author(s):  
Janet Thomas ◽  
Harvey Levy ◽  
Stephen Amato ◽  
Jerry Vockley ◽  
Roberto Zori ◽  
...  

2018 ◽  
Vol 62 (7) ◽  
pp. e02584-17 ◽  
Author(s):  
Gregory G. Stone ◽  
Paul Newell ◽  
Patricia A. Bradford

ABSTRACT The increasing prevalence of multidrug-resistant Gram-negative pathogens has generated a requirement for new treatment options. Avibactam, a novel non-β-lactam–β-lactamase inhibitor, restores the activity of ceftazidime against Ambler class A, C, and some class D β-lactamase-producing strains of Enterobacteriaceae and Pseudomonas aeruginosa. The in vitro activities of ceftazidime-avibactam versus comparators were evaluated against 1,440 clinical isolates obtained in a phase 3 clinical trial in patients with complicated intra-abdominal infections (cIAI; ClinicalTrials.gov identifier NCT01499290). Overall, in vitro activities were determined for 803 Enterobacteriaceae, 70 P. aeruginosa, 304 Gram-positive aerobic, and 255 anaerobic isolates obtained from 1,066 randomized patients at baseline. Susceptibility was determined by broth microdilution. The most commonly isolated Gram-negative, Gram-positive, and anaerobic pathogens were Escherichia coli (n = 549), Streptococcus anginosus (n = 130), and Bacteroides fragilis (n = 96), respectively. Ceftazidime-avibactam was highly active against isolates of Enterobacteriaceae, with an overall MIC90 of 0.25 mg/liter. In contrast, the MIC90 for ceftazidime alone was 32 mg/liter. The MIC90 value for ceftazidime-avibactam (4 mg/liter) was one dilution lower than that of ceftazidime alone (8 mg/liter) against isolates of Pseudomonas aeruginosa. The ceftazidime-avibactam MIC90 for 109 ceftazidime-nonsusceptible Enterobacteriaceae isolates was 2 mg/liter, and the MIC range for 6 ceftazidime-nonsusceptible P. aeruginosa isolates was 8 to 32 mg/liter. The MIC90 values were within the range of susceptibility for the study drugs permitted per the protocol in the phase 3 study to provide coverage for aerobic Gram-positive and anaerobic pathogens. These findings demonstrate the in vitro activity of ceftazidime-avibactam against bacterial pathogens commonly observed in cIAI patients, including ceftazidime-nonsusceptible Enterobacteriaceae. (This study has been registered at ClinicalTrials.gov under identifier NCT01499290.)


2020 ◽  
pp. AAC.02461-20
Author(s):  
Mariana Castanheira ◽  
Matthew G. Johnson ◽  
Brian Yu ◽  
Jennifer A. Huntington ◽  
Patricia Carmelitano ◽  
...  

We evaluated β-lactam-resistant Enterobacterales species and Pseudomonas aeruginosa baseline lower respiratory tract isolates collected during the ASPECT-NP phase 3 clinical trial evaluating the safety and efficacy of ceftolozane-tazobactam compared with meropenem for treatment of ventilated nosocomial pneumonia in adults. Isolates were subjected to whole genome sequencing, quantitative real-time PCR for quantification of the expression levels of β-lactamase and efflux genes, and Western blot analysis for detection of OprD (P. aeruginosa only). ESBL genes were detected in 168 of 262 Enterobacterales isolates and among these blaCTXM-15 was the most common, detected in 125 isolates. Sixty-one Enterobacterales carried genes encoding carbapenemases while 33 isolates did not carry ESBLs or carbapenemases. Carbapenemase-producing isolates carried mainly NDM and OXA-48 variants, with ceftolozane-tazobactam MIC values ranging from 4 to 128 μg/mL. Most ceftolozane-tazobactam-nonsusceptible Enterobacterales isolates that did not carry carbapenemases were K. pneumoniae that exhibited disrupted OmpK35, specific mutations in OmpK36, and, in some isolates, elevated expression of blaCTXM-15. Among 89 P. aeruginosa isolates, carbapenemases and ESBL-encoding genes were observed among 12 and 22 isolates, respectively. P. aeruginosa isolates without acquired β-lactamases displaying elevated expression of AmpC (14 isolates), elevated expression of efflux pumps (11 isolates), and/or decrease or loss of OprD (22 isolates) were susceptible to ceftolozane-tazobactam. Ceftolozane-tazobactam was active against >75% of the Enterobacterales isolates from the ASPECT-NP trial that did not carry carbapenemases. K. pneumoniae resistant to ceftolozane-tazobactam might represent a challenge for treatment due to its multiple resistance mechanisms. Ceftolozane-tazobactam was among the agents displaying the greatest activity against P. aeruginosa isolates.


HemaSphere ◽  
2019 ◽  
Vol 3 (S1) ◽  
pp. 306
Author(s):  
J. Bussel ◽  
D. Arnold ◽  
R. Boccia ◽  
M. Boxer ◽  
N. Cooper ◽  
...  

2019 ◽  
Vol 94 (5) ◽  
pp. 546-553 ◽  
Author(s):  
James B. Bussel ◽  
Donald M. Arnold ◽  
Michael A. Boxer ◽  
Nichola Cooper ◽  
Jiri Mayer ◽  
...  

Author(s):  
James F. Donohue ◽  
Sanjay Sethi ◽  
Craig N. Barnes ◽  
Edmund J. Moran ◽  
Srikanth Pendyala ◽  
...  

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