Table 4.
Reference | Study place, year | Study design | Patients, number | Infection foci | Organism(s)/β-lactamase types | Antibiotic(s) | Clinical outcomes | Remarks |
---|---|---|---|---|---|---|---|---|
van Duin et al., 2018 | United States, 8 sites, 2011–2015 | Prospective | 137 | BSI (n = 63; 46%) and pneumonia (n = 30, 22%) | 97% (133/137) were K. pneumoniae | CAZ/AVI (n = 38) vs. colistin (n = 99) | Adjusted all-cause mortality was significantly lower in the CAZ/AVI group (9% vs. 32%, P = 0.001) | Prospective, observational study on the use of CAZ/AVI compared to colistin specifically for infections due to CRE, including 30 (22%) patients with pneumonia |
Castón et al., 2017 | Spain, Israel, multicenter, 2012–2016 | Retrospective | 31, all with hematologic malignancy | Primary BSI (n = 14, 45.2%) | 80.6% (25/31) were K. pneumoniae | CAZ/AVI (n = 8) vs. others (n = 23) | 14-day clinical cure rate was higher in the CAZ/AVI group (85.7% [6/8] vs. 34.8% [8/23], P = 0.031) | Small case numbers; no difference in crude mortality |
Shields et al., 2017b | United States, single site, 2009-2017 | Retrospective | 109 | Secondary bacteremia resulted from abdominal (46%, 50/109) | 97% (106/109) of K. pneumoniae harbored blaKPC | CAZ/AVI (n = 13) vs. others (n = 96) | CAZ/AVI group had higher clinical success rates (85% [11/13] vs. 40.6% [39/96], P = 0.003) | Small case numbers with CAZ/AVI treatment; bias in selection of therapy |
CAZ/AVI, ceftazidime/avibactam; BSI, bloodstream infection.