Old antibiotics for multidrug-resistant pathogens: from in vitro activity to clinical outcomes

Keith S Kaye1, Ana C Gales2, Grégory Dubourg3

  • 1University of Michigan Health System, Department of Medicine, Division of Infectious Diseases, Ann Arbor, MI, USA.

Insights

Antimicrobial resistance is a growing global threat, limiting treatment options. Research should re-evaluate older antimicrobial drugs for treating multidrug-resistant bacteria, especially in complex patient groups.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Pharmacology

Background:

  • Antimicrobial resistance (AMR) poses a significant global health challenge.
  • Development of new antimicrobials lags behind the emergence of resistant pathogens.
  • Limited treatment options exist for multidrug-resistant (MDR) bacteria.

Purpose of the Study:

  • To highlight the increasing reliance on older antimicrobial agents for MDR infections.
  • To underscore the scarcity of clinical data on the efficacy of older agents against MDR pathogens.
  • To advocate for focused research on evaluating older antimicrobials in MDR infections and complex patient populations.

Main Methods:

  • Review of existing literature on older antimicrobial agents and their in vitro activity.
  • Analysis of clinical data, where available, for the treatment of MDR pathogens.
  • Identification of knowledge gaps concerning pharmacokinetic/pharmacodynamic properties and toxicities of older agents.

Main Results:

  • Some older antimicrobials retain potent in vitro activity against highly resistant bacteria.
  • Clinical data on the use of older agents for MDR infections are generally limited.
  • Unfavorable pharmacokinetic/pharmacodynamic profiles and toxicities can restrict the use of some older agents.

Conclusions:

  • Older antimicrobial agents represent a valuable, albeit underutilized, resource in combating MDR pathogens.
  • Further clinical investigation is crucial to establish the safety and efficacy of older antimicrobials.
  • Research should prioritize evaluating these agents in diverse and complex patient populations, including those with comorbidities.

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