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Review
.2021 Aug 20;10(8):1012.
doi: 10.3390/antibiotics10081012.

The Revival of Aztreonam in Combination with Avibactam against Metallo-β-Lactamase-Producing Gram-Negatives: A Systematic Review of In Vitro Studies and Clinical Cases

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Review

The Revival of Aztreonam in Combination with Avibactam against Metallo-β-Lactamase-Producing Gram-Negatives: A Systematic Review of In Vitro Studies and Clinical Cases

Carola Mauri et al. Antibiotics (Basel)..

Abstract

Infections caused by metallo-β-lactamase (MBL)-producingEnterobacterales andPseudomonas are increasingly reported worldwide and are usually associated with high mortality rates (>30%). Neither standard therapy nor consensus for the management of these infections exist. Aztreonam, an old β-lactam antibiotic, is not hydrolyzed by MBLs. However, since many MBL-producing strains co-produce enzymes that could hydrolyze aztreonam (e.g., AmpC, ESBL), a robust β-lactamase inhibitor such as avibactam could be given as a partner drug. We performed a systematic review including 35 in vitro and 18 in vivo studies on the combination aztreonam + avibactam for infections sustained by MBL-producing Gram-negatives. In vitro data on 2209 Gram-negatives were available, showing the high antimicrobial activity of aztreonam (MIC ≤ 4 mg/L when combined with avibactam) in 80% of MBL-producingEnterobacterales, 85% ofStenotrophomonas and 6% of MBL-producingPseudomonas. Clinical data were available for 94 patients: 83% of them had bloodstream infections. Clinical resolution within 30 days was reported in 80% of infected patients. Analyzing only patients with bloodstream infections (64 patients), death occurred in 19% of patients treated with aztreonam + ceftazidime/avibactam. The combination aztreonam + avibactam appears to be a promising option against MBL-producing bacteria (especiallyEnterobacterales, much less forPseudomonas) while waiting for new antimicrobials.

Keywords: Enterobacterales; Pseudomonas; Stenotrophomonas; antibiotic combination; avibactam; aztreonam; ceftazidime/avibactam; last resource antibiotic; metallo-β-lactamase; old antibiotic.

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Conflict of interest statement

All the authors declare no conflict of interest.

Figures

Figure 1
Figure 1
β-lactam antibiotic targets of MBL enzymatic activity.
Figure 2
Figure 2
Literature search strategy.
Figure 3
Figure 3
Forest plot of the 30-day mortality odds ratio between CZA plus ATM and other regimens against infections by MBL-producing strains. ATM, aztreonam; CZA, ceftazidime/avibactam; OAA, other active agent.
See this image and copyright information in PMC

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References

    1. Tan X., Kim H.S., Baugh K., Huang Y., Kadiyala N., Wences M., Singh N., Wenzler E., Bulman Z.P. Therapeutic Options for Metallo-β-Lactamase-Producing Enterobacterales. Infect. Drug Resist. 2021;14:125–142. doi: 10.2147/IDR.S246174. - DOI - PMC - PubMed
    1. Khan A.U., Maryam L., Zarrilli R. Structure, genetics and worldwide spread of New Delhi metallo-β-lactamase (NDM): A threat to public health. BMC Microbiol. 2017;17:101–112. doi: 10.1186/s12866-017-1012-8. - DOI - PMC - PubMed
    1. Snyder B.M., Montague B.T., Anandan S., Madabhushi A.G., Pragasam A.K., Verghese V.P., Balaji V., Simões E.A.F. Risk factors and epidemiologic predictors of bloodstream infections with New Delhi metallo-β-lactamase (NDM-1) producing Enterobacteriaceae. Epidemiol. Infect. 2019;147:1–9. doi: 10.1017/S0950268819000256. - DOI - PMC - PubMed
    1. Falcone M., Tiseo G., Antonelli A., Giordano C., Di Pilato V., Bertolucci P., Parisio E.M., Leonildi A., Aiezza N., Baccani I., et al. Clinical features and outcomes of bloodstream infections caused by New Delhi metallo-β-lactamase-producing Enterobacterales during a regional outbreak. Open Forum Infect. Dis. 2020;7:1–5. doi: 10.1093/ofid/ofaa011. - DOI - PMC - PubMed
    1. Spyropoulou A., Bartzavali C., Vamvakopoulou S., Marangos M., Anastassiou E.D., Spiliopoulou I., Christofidou M. The first NDM metallo-β-lactamase producing Klebsiella pneumoniae isolate in a university hospital of southwestern Greece. J. Chemother. 2016;28:350–351. doi: 10.1179/1973947815Y.0000000003. - DOI - PubMed

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