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Experimental Endocarditis Model of Methicillin Resistant Staphylococcus aureus (MRSA) in Rat
Published on: June 4, 2012
Costs of treating infections caused by methicillin-resistant staphylococci and vancomycin-resistant enterococci
1Hôpital Bichat-Claude Bernard, Médecine Interne, Paris, France.
Abstract:
Infection with methicillin-resistant Staphylococcus aureus (MRSA) or vancomycin-resistant Enterococcus faecium (VREF) increases the risk of mortality and results in prolonged hospitalization and high utilization of costly treatment modalities. Measures to prevent the spread of MRSA (and possibly VREF) include patient isolation and decontamination, hygiene measures, ward closure, and screening of patients and staff for carriage. In seriously ill patients, the increased use of vancomycin for the treatment of MRSA can lead to the emergence of VREF colonization/infection. Quinupristin/dalfopristin is effective in the treatment of MRSA infections, including nosocomial pneumonia, skin and soft tissue infection, and septicaemia. In the treatment of nosocomial pneumonia, clinical success rates were equivalent between quinupristin/dalfopristin and vancomycin. In the context of a hospital policy which emphasizes effective hygiene measures and the prudent use of antibacterials, quinupristin/dalfopristin is an effective antimicrobial that can help to control the high costs associated with multiresistant MRSA and VREF infections.
Insights
Methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus faecium (VREF) infections pose significant risks. Quinupristin/dalfopristin offers an effective treatment option, aiding in cost control for these multidrug-resistant infections.
Area of Science:
- Infectious Diseases
- Clinical Pharmacology
- Hospital Epidemiology
Background:
- Healthcare-associated infections caused by multidrug-resistant organisms like methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus faecium (VREF) are associated with increased mortality, prolonged hospital stays, and high treatment costs.
- The widespread use of vancomycin for MRSA infections can inadvertently lead to the emergence of VREF colonization and infections, complicating patient care.
- Preventive strategies for MRSA and VREF include isolation, decontamination, stringent hygiene, ward closures, and screening of patients and healthcare personnel.
Purpose of the Study:
- To evaluate the efficacy of quinupristin/dalfopristin in treating infections caused by MRSA and VREF.
- To compare the clinical success rates of quinupristin/dalfopristin with vancomycin in treating nosocomial pneumonia.
- To assess the role of quinupristin/dalfopristin in managing costs associated with multidrug-resistant infections within a hospital setting.
Main Methods:
- Clinical efficacy of quinupristin/dalfopristin was assessed in patients with MRSA infections, including pneumonia, skin and soft tissue infections, and septicemia.
- Comparative analysis of clinical success rates between quinupristin/dalfopristin and vancomycin for nosocomial pneumonia.
- Evaluation of cost-effectiveness in the context of hospital infection control policies.
Main Results:
- Quinupristin/dalfopristin demonstrated effectiveness in treating various MRSA infections.
- Clinical success rates for quinupristin/dalfopristin were comparable to vancomycin in the treatment of nosocomial pneumonia.
- The implementation of quinupristin/dalfopristin, alongside hygiene and prudent antibiotic use, contributed to controlling costs associated with MRSA and VREF infections.
Conclusions:
- Quinupristin/dalfopristin is a viable therapeutic option for MRSA infections, including nosocomial pneumonia.
- This agent can be used effectively as an alternative to vancomycin, particularly when VREF emergence is a concern.
- Integrating quinupristin/dalfopristin into hospital antimicrobial stewardship programs can help mitigate the economic burden of multidrug-resistant bacterial infections.
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