TABLE 2.
Summary of baseline aerobic Gram-negative pathogens recovered from each patient in the ME population in the cUTI trials for ceftazidime-avibactama
| Pathogen(s) in each patient (no. of patients) | Result (no. [%] of isolates)b |
|---|---|
| E. coli (55) | Screen negative (34 [61.8]) |
| Screen positive (21 [38.2]) | |
| CTX-M-14 (2) | |
| CTX-M-15c (11) | |
| CTX-M-15 + OXA-1/30 (8) | |
| E. cloacae (1) | AmpC overexpression (1) |
| E. coli-C. koseri (1) | Screen negative for E. coli (1) and C. koseri (1) |
| E. coli-P. mirabilis (1) | CTX-M-15 for E. coli (1) and screen negative for P. mirabilis (1) |
| P. mirabilis (1) | Screen negative (1) |
| P. aeruginosa (1) | Screen negative (1) |
| P. aeruginosa-E. coli (2) | Screen negative for P. aeruginosa (1) and E. coli (1) |
| Screen negative for P. aeruginosa (1) and CTX-M-15 + OXA-1/30 for E. coli (1) |
The cUTI trial results shown represent 62 ME patients.
Screen negative, isolates that did not meet the MIC-based screening criteria; screen positive, isolates that met the screening criteria (i.e., ceftriaxone and/or ceftazidime MICs of ≥2 μg/ml, NF-GNB with ceftazidime MICs of ≥16 μg/ml, and Enterobacteriaceae and NF-GNB isolates exhibiting imipenem and meropenem MICs of ≥2 and ≥16 μg/ml, respectively). All Enterobacteriaceae and NF-GNB isolates had imipenem MICs of ≤0.25 and ≤2 μg/ml, respectively.
Hyperproduction of the intrinsic AmpC enzyme was detected in one blaCTX-M-15-carrying isolate.