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Updated: Feb 28, 2026

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Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
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agr functionality affects clinical outcomes in patients with persistent methicillin-resistant Staphylococcus aureus
Summary
Persistent methicillin-resistant Staphylococcus aureus bacteremia (pMRSAB) is linked to higher mortality. Accessory gene regulator (agr) dysfunction and non-eradicated infection foci are key independent risk factors for in-hospital death in pMRSAB patients.
Area of Science:
- Infectious Diseases
- Clinical Microbiology
- Epidemiology
Background:
- Methicillin-resistant Staphylococcus aureus bacteremia (MRSAB) can persist despite treatment, leading to poor outcomes.
- Microbiological factors influencing persistent MRSAB (pMRSAB) and associated mortality remain incompletely understood.
Purpose of the Study:
- To identify clinical and microbiological risk factors for in-hospital mortality in patients with pMRSAB.
Main Methods:
- Prospective analysis of 152 pMRSAB cases (MRSAB ≥5 days despite effective antibiotics) from 11 Korean hospitals (2009-2016).
- Microbiological testing included SCCmec type, Spa type, agr type, PVL, PSM-mec genes, vancomycin MIC, vancomycin heteroresistance, and agr functionality.
- Clinical data included comorbidity scores (CCWI, Pitt, SOFA), septic shock, pneumonia, and infection foci.
Main Results:
- Univariable analysis identified CCWI, Pitt bacteremia score, SOFA score, septic shock, pneumonia, agr dysfunction, and vancomycin heteroresistance as mortality-associated factors.
- Bone and joint infections were associated with lower mortality.
- Multivariable analysis revealed CCWI score, Pitt bacteremia score, non-eradicated foci of infection, and agr dysfunction as independent predictors of in-hospital mortality.
Conclusions:
- Accessory gene regulator (agr) dysfunction is an independent risk factor for in-hospital mortality in persistent MRSAB.
- Clinical severity scores and uncontrolled infection sources also significantly contribute to mortality in pMRSAB.
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