Current and emerging drug treatment strategies to tackle invasive community-associated methicillin-resistant Staphylococcus aureus (MRSA) infection: what are the challenges?

Expert Opin Pharmacother. 2023 Feb;24(3):331-346. doi: 10.1080/14656566.2022.2161885. Epub 2023 Jan 3.

Abstract

Introduction: Community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) infections represent a leading cause of purulent skin and soft tissue infections in some geographical regions. Traditionally, 'old antibiotics' such as trimethoprim-sulfamethoxazole, tetracyclines, clindamycin, chloramphenicol,vancomycin, and teicoplanin have been used to treat these infections, but these were often associated with low efficacy and excessive side effects and toxicity, especially nephrotoxicity. Along with the development of new compounds, the last decade has seen substantial improvements in the management of CA-MRSA infections.

Areas covered: In this review, the authors discuss the current and emerging drug treatment strategies to tackle invasive CA-MRSA infections. Articles reported in this review were selected from through literature searches using the PubMed database.

Expert opinion: The availability of new drugs showing a potent in vitro activity against CA-MRSA represents a unique opportunity to face the threat of resistance while potentially reducing toxicity. All these compounds represent promising options to enhance our antibiotic armamentarium. However, data regarding the use of these new drugs in real-life studies are limited and their best placement in therapy and in terms of optimization of medical resources and balance of cost-effectiveness requires further investigation.

Keywords: MRSA; PVL; cephalosporins; community-acquired; fluoroquinolones; lefamulin; lipoglycopeptides; oxazolidinones; tetracyclines.

Publication types

  • Review

MeSH terms

  • Anti-Bacterial Agents / adverse effects
  • Clindamycin / therapeutic use
  • Community-Acquired Infections* / drug therapy
  • Humans
  • Methicillin-Resistant Staphylococcus aureus*
  • Staphylococcal Infections* / drug therapy

Substances

  • Anti-Bacterial Agents
  • Clindamycin