Early Multicenter Experience With Imipenem-Cilastatin-Relebactam for Multidrug-Resistant Gram-Negative Infections

Nicholas Rebold1, Taylor Morrisette1,2,3, Abdalhamid M Lagnf1

  • 1Anti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, Michigan, USA.

Insights

This study evaluated imipenem-cilastatin-relebactam for treating multidrug-resistant infections, primarily caused by Pseudomonas aeruginosa. The treatment showed a 67% 30-day survival rate in patients with severe infections.

Area of Science:

  • Infectious Diseases
  • Antimicrobial Resistance
  • Clinical Pharmacology

Background:

  • Multidrug-resistant (MDR) infections pose a significant global health threat.
  • Pseudomonas aeruginosa is a common cause of difficult-to-treat hospital-acquired infections.
  • Novel antibiotic combinations are crucial for combating resistant bacterial strains.

Purpose of the Study:

  • To assess the clinical outcomes of imipenem-cilastatin-relebactam in patients with serious infections.
  • To evaluate the efficacy of this combination against multidrug-resistant Pseudomonas aeruginosa.

Main Methods:

  • A multicenter case series involving 21 patients treated with imipenem-cilastatin-relebactam.
  • Analysis of infection sources, primary pathogens, and antimicrobial susceptibility.
  • Evaluation of 30-day survival and adverse events.

Main Results:

  • Pulmonary infections were the most common source (52%).
  • Pseudomonas aeruginosa was the primary pathogen (76%), with 94% of isolates being multidrug-resistant.
  • Thirty-day survival was observed in 67% of patients (14/21).
  • Two patients experienced adverse effects.

Conclusions:

  • Imipenem-cilastatin-relebactam demonstrated potential in treating complex infections caused by multidrug-resistant pathogens.
  • Further investigation is warranted to establish its role in clinical practice.
  • The safety profile appears manageable in this case series.