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Published on: April 18, 2019
Case Commentary: Imipenem/Cilastatin and Fosfomycin for Refractory Methicillin-Resistant Staphylococcus aureus
1Division of Host-Microbe Systems & Therapeutics, Center for Immunity, Infection & Inflammation, Collaborative to Halt Antimicrobial Resistant Microbes, University of California-San Diego School of Medicine, La Jolla, California, USA george.sakoulas@sharp.com.
Abstract:
Given that it is unlikely that randomized clinical trials will yield answers for treating the most challenging bacteremic infections caused by methicillin-resistant Staphylococcus aureus, clinicians, microbiologists, and pharmacists will have to cooperate to discover novel ways to select successful individualized antimicrobial therapy for these patients. An example of such a strategy was demonstrated in the identification and utilization of imipenem/cilastatin plus fosfomycin to treat a particularly recalcitrant MRSA bacteremia and spinal abscess.
Insights
Treating difficult methicillin-resistant Staphylococcus aureus bacteremia requires collaboration. A successful strategy involved using imipenem/cilastatin plus fosfomycin for a challenging MRSA infection.
Area of Science:
- Infectious Diseases
- Pharmacology
- Clinical Microbiology
Background:
- Randomized clinical trials are unlikely to provide solutions for complex methicillin-resistant Staphylococcus aureus (MRSA) bacteremic infections.
- Effective treatment of recalcitrant MRSA infections necessitates innovative therapeutic approaches.
Purpose of the Study:
- To highlight the need for interdisciplinary collaboration in developing individualized antimicrobial therapies for challenging MRSA infections.
- To present a case study demonstrating a successful novel treatment strategy for MRSA bacteremia and spinal abscess.
Main Methods:
- Literature review on challenges in treating MRSA bacteremia.
- Case report detailing the clinical course and treatment of a patient with MRSA bacteremia and spinal abscess.
- Antimicrobial susceptibility testing and pharmacokinetic/pharmacodynamic considerations for combination therapy.
Main Results:
- Identification of a treatment regimen combining imipenem/cilastatin with fosfomycin.
- Successful resolution of a particularly recalcitrant MRSA bacteremia and associated spinal abscess.
- Demonstration of a viable individualized therapeutic strategy for complex MRSA infections.
Conclusions:
- Interprofessional collaboration between clinicians, microbiologists, and pharmacists is crucial for managing difficult MRSA infections.
- Combination therapy with imipenem/cilastatin and fosfomycin can be effective against recalcitrant MRSA bacteremia.
- Individualized antimicrobial selection is a key strategy for treating challenging Gram-positive bacterial infections.
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