An agent-based model on antimicrobial de-escalation in intensive care units: Implications on clinical trial design

PLoS One. 2024 Apr 16;19(4):e0301944. doi: 10.1371/journal.pone.0301944. eCollection 2024.

Abstract

Antimicrobial de-escalation refers to reducing the spectrum of antibiotics used in treating bacterial infections. This strategy is widely recommended in many antimicrobial stewardship programs and is believed to reduce patients' exposure to broad-spectrum antibiotics and prevent resistance. However, the ecological benefits of de-escalation have not been universally observed in clinical studies. This paper conducts computer simulations to assess the ecological effects of de-escalation on the resistance prevalence of Pseudomonas aeruginosa-a frequent pathogen causing nosocomial infections. Synthetic data produced by the models are then used to estimate the sample size and study period needed to observe the predicted effects in clinical trials. Our results show that de-escalation can reduce colonization and infections caused by bacterial strains resistant to the empiric antibiotic, limit the use of broad-spectrum antibiotics, and avoid inappropriate empiric therapies. Further, we show that de-escalation could reduce the overall super-infection incidence, and this benefit becomes more evident under good compliance with hand hygiene protocols among health care workers. Finally, we find that any clinical study aiming to observe the essential effects of de-escalation should involve at least ten arms and last for four years-a size never attained in prior studies. This study explains the controversial findings of de-escalation in previous clinical studies and illustrates how mathematical models can inform outcome expectations and guide the design of clinical studies.

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Anti-Bacterial Agents / therapeutic use
  • Anti-Infective Agents* / therapeutic use
  • Clinical Trials as Topic
  • Humans
  • Intensive Care Units
  • Pseudomonas Infections* / drug therapy

Substances

  • Anti-Bacterial Agents
  • Anti-Infective Agents

Grants and funding

XH was partially supported by the National Science Foundation (DMS-1853622 and DMS-2052648) and the College of Arts and Sciences at the University of Miami. This report is solely the responsibility of the authors and does not necessarily represent the official views of the National Science Foundation and the University of Miami.