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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.
Abstract:
A multicenter case series of 21 patients were treated with imipenem-cilastatin-relebactam. There were mixed infection sources, with pulmonary infections (11/21,52%) composing the majority. The primary pathogen was Pseudomonas aeruginosa (16/21, 76%), and 15/16 (94%) isolates were multidrug-resistant. Thirty-day survival occurred in 14/21 (67%) patients. Two patients experienced adverse effects.
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.
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