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Review
. 2021 Jun 3;11(6):519.
doi: 10.3390/life11060519.

Emerging Treatment Options for Multi-Drug-Resistant Bacterial Infections

Affiliations
Review

Emerging Treatment Options for Multi-Drug-Resistant Bacterial Infections

Roberto Giurazza et al. Life (Basel). .

Abstract

Antimicrobial resistance (AMR) remains one of the top public health issues of global concern. Among the most important strategies for AMR control there is the correct and appropriate use of antibiotics, including those available for the treatment of AMR pathogens. In this article, after briefly reviewing the most important and clinically relevant multi-drug-resistant bacteria and their main resistance mechanisms, we describe the emerging antimicrobial options for both MDR Gram-positive cocci and Gram-negative bacilli, including recently marketed agents, molecules just approved or under evaluation and rediscovered older antibiotics that have regained importance due to their antimicrobial spectrum. Specifically, emerging options for Gram-positive cocci we reviewed include ceftaroline, ceftobiprole, tedizolid, dalbavancin, and fosfomycin. Emerging treatment options for Gram-negative bacilli we considered comprise ceftolozane-tazobactam, ceftazidime-avibactam, meropenem-vaborbactam, imipenem-relebactam, aztreonam-avibactam, minocycline, fosfomycin, eravacycline, plazomicin, and cefiderocol. An exciting scenario is opening today with the long awaited growing availability of novel molecules for the treatment of AMR bacteria. Knowledge of mechanisms of action and resistance patterns allows physicians to increasingly drive antimicrobial treatment towards a precision medicine approach. Strict adherence to antimicrobial stewardship practices will allow us to preserve the emerging antimicrobials for our future.

Keywords: antimicrobial resistance; brand-new antibiotics; drug therapy; emerging infectious diseases; extensively drug resistant; old revived antibiotics; place in therapy; resistance mechanisms.

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Conflict of interest statement

E.D.-M. received research funding to his Institution from MSD and Pfizer and personal fees for advisory board participation or meeting presentations from Roche, Genentech, Pfizer, MSD, Angelini, Nordic pharma, Correvio/Advanz Pharma, Bio-Merieux, Abbvie, Sanofi-Aventis, Medtronic, and DiaSorin. The other authors have no conflicts of interest relevant to the content of this article.

Figures

Figure 1
Figure 1
Chemical structure of the antimicrobial agents discussed in this article.

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