New drugs for difficult bugs: management of multidrug-resistant gram-negative infections in solid organ transplant

Stephanie M Pouch1

  • 1Emory University School of Medicine, Atlanta, Georgia, USA.

Abstract

Insights

Multidrug-resistant Gram-negative infections pose a significant threat to solid organ transplant (SOT) recipients. This review highlights novel antimicrobial agents and therapeutic strategies for managing these challenging infections in SOT patients.

Area of Science:

  • Infectious Diseases
  • Transplantation Medicine
  • Pharmacology

Background:

  • Multidrug-resistant Gram-negative bacteria (MDRGN) present a critical challenge to patient and allograft survival in solid organ transplant (SOT) recipients.
  • The limited antimicrobial pipeline and lack of systematic evaluation of novel agents in SOT populations complicate infection management.

Purpose of the Study:

  • To review current therapeutic options for MDRGN infections in SOT recipients.
  • To summarize the role of recently approved antimicrobial agents in managing difficult-to-treat Gram-negative infections in this vulnerable patient group.

Main Methods:

  • Literature review focusing on antimicrobial therapies for MDRGN infections.
  • Analysis of novel agents including second-generation β-lactam/β-lactamase inhibitors, cefiderocol, plazomicin, and eravacycline.
  • Emphasis on evidence and recommendations specific to the SOT population.

Main Results:

  • Novel antimicrobials offer new hope but have specific niches requiring further study in SOT recipients.
  • Therapeutic strategies are discussed for extended-spectrum β-lactamase-producing Enterobacterales, carbapenem-resistant Enterobacterales, and difficult-to-treat resistant *Pseudomonas aeruginosa*.
  • Recently approved agents are highlighted for their potential in combating MDRGN infections.

Conclusions:

  • Effective management of MDRGN infections in SOT recipients necessitates a thorough understanding of novel antimicrobial agents and their appropriate use.
  • Continued research and systematic evaluation of these agents in the transplant population are crucial for optimizing patient and allograft outcomes.

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