: Aztreonam-avibactam (ATM-AVI) and ceftazidime-avibactam plus aztreonam (CAZ/AVI-ATM) represent therapeutic strategies for infections caused by metallo-β-lactamase (MBL)-producing Enterobacterales. This perspective synthesizes mechanistic rationale, microbiologic determinants of activity, pharmacokinetic/pharmacodynamic principles, and available clinical outcomes to compare these regimens and identify knowledge gaps. Both approaches are expected to provide activity against MBL-producing organisms; however, important distinctions exist. ATM-AVI ensures fixed and predictable co-exposure of aztreonam and avibactam, minimizing the risk of pharmacokinetic asynchrony inherent to administering CAZ/AVI with separate aztreonam. The efficacy of ATM-AVI may nevertheless be influenced by organism-specific resistance mechanisms and pharmacologic variables. CAZ/AVI-ATM offers a pragmatic alternative but introduces logistical complexity and potential variability in inhibitor exposure. Observational data appear more favorable for ATM-AVI, although direct comparisons are not available. In the absence of direct comparative trials, regimen selection should consider renal function, infection syndrome, and the feasibility of sustaining adequate inhibitor exposure.

A Comparative Evaluation of Aztreonam-Avibactam and Ceftazidime-Avibactam Plus Aztreonam for Infections Due to MBL-Producing Enterobacterales

Moreal, Chiara;Tascini, Carlo
2026-01-01

Abstract

: Aztreonam-avibactam (ATM-AVI) and ceftazidime-avibactam plus aztreonam (CAZ/AVI-ATM) represent therapeutic strategies for infections caused by metallo-β-lactamase (MBL)-producing Enterobacterales. This perspective synthesizes mechanistic rationale, microbiologic determinants of activity, pharmacokinetic/pharmacodynamic principles, and available clinical outcomes to compare these regimens and identify knowledge gaps. Both approaches are expected to provide activity against MBL-producing organisms; however, important distinctions exist. ATM-AVI ensures fixed and predictable co-exposure of aztreonam and avibactam, minimizing the risk of pharmacokinetic asynchrony inherent to administering CAZ/AVI with separate aztreonam. The efficacy of ATM-AVI may nevertheless be influenced by organism-specific resistance mechanisms and pharmacologic variables. CAZ/AVI-ATM offers a pragmatic alternative but introduces logistical complexity and potential variability in inhibitor exposure. Observational data appear more favorable for ATM-AVI, although direct comparisons are not available. In the absence of direct comparative trials, regimen selection should consider renal function, infection syndrome, and the feasibility of sustaining adequate inhibitor exposure.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11390/1328524
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