Efficacy of Ceftazidime-avibactam Plus Aztreonam in Patients With Bloodstream Infections Caused by Metallo-β-lactamase–Producing Enterobacterales

Author:

Falcone Marco1,Daikos George L2,Tiseo Giusy1,Bassoulis Dimitrios2,Giordano Cesira3,Galfo Valentina1,Leonildi Alessandro3,Tagliaferri Enrico1,Barnini Simona3,Sani Spartaco4,Farcomeni Alessio5,Ghiadoni Lorenzo6,Menichetti Francesco1

Affiliation:

1. Department of Clinical and Experimental Medicine, Infectious Diseases Unit, University of Pisa, Pisa, Italy

2. First Department of Medicine, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece

3. Microbiology Unit, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy

4. Infectious Disease Unit, Livorno Hospital, Livorno, Italy

5. Department of Economics and Finance, University of Rome “Tor Vergata,” Rome, Italy

6. Emergency Medicine Department, Azienda Ospedaliera Universitaria Pisana, University of Pisa, Pisa, Italy

Abstract

Abstract Background In vitro data support the use of combination of aztreonam (ATM) with ceftazidime-avibactam (CAZ-AVI), but clinical studies are lacking. The aim of our study was to compare the outcome of patients with bloodstream infections (BSIs) due to metallo-β-lactamase (MBL)–producing Enterobacterales treated either with CAZ-AVI plus ATM or other active antibiotics (OAAs). Methods This was a prospective observational study including patients admitted to 3 hospitals in Italy and Greece. The primary outcome measure was 30-day all-cause mortality. Secondary outcomes were clinical failure at day 14 and length of stay after BSI diagnosis. Cox regression analysis including a propensity score (PS) for receiving CAZ-AVI + ATM was performed to evaluate primary and secondary outcomes. A PS-based matched analysis was also performed. Results We enrolled 102 patients with BSI; 82 had infections caused by NDM-producing (79 Klebsiella pneumoniae and 3 Escherichia coli) and 20 by VIM-producing (14 K. pneumoniae, 5 Enterobacter species, 1 Morganella morganii) strains. The 30-day mortality rate was 19.2% in the CAZ-AVI + ATM group vs 44% in the OAA group (P = .007). The PS-adjusted analysis showed that the use of CAZ-AVI + ATM was associated with lower 30-day mortality (hazard ratio [HR], 0.37 [95% confidence interval {CI}, .13–.74]; P = .01), lower clinical failure at day 14 (HR, 0.30 [95% CI, .14–.65]; P = .002), and shorter length of stay (subdistributional HR, 0.49 [95% CI, .30–.82]; P = .007). The PS-matched analysis confirmed these findings. Conclusions The CAZ-AVI + ATM combination offers a therapeutic advantage compared to OAAs for patients with BSI due to MBL-producing Enterobacterales. Further studies are warranted.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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