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Clinical relevance of increasing glycopeptide MICs against Staphylococcus aureus
1Department of Medical Microbiology, Aberdeen Royal Infirmary, Foresterhill, Aberdeen, UK.
Abstract:
Glycopeptides are among the most widely used agents for the treatment of serious infections caused by Gram-positive bacteria, with vancomycin recommended for the treatment of infections caused by beta-lactam-resistant Staphylococcus aureus (MRSA). However, the utility of glycopeptides against MRSA has come into question owing to their poor tissue penetration, slow bactericidal activity and the emergence of strains with reduced susceptibility. A number of single-centre studies have demonstrated incremental increases in glycopeptide MICs for S. aureus strains over time - a phenomenon known as glycopeptide creep. High MICs have long been known to correlate with poorer clinical outcomes, but recent studies have shown that even small increases in MIC below the susceptibility breakpoint can affect the clinical efficacy of glycopeptides. The accurate measurement and ongoing surveillance of glycopeptide MICs at individual sites is therefore recommended to assist clinicians in their choice of empiric therapy for suspected serious S. aureus infections.
Insights
Glycopeptide antibiotics are crucial for treating Gram-positive bacterial infections, but rising minimum inhibitory concentrations (MICs) in Staphylococcus aureus strains, including MRSA, are concerning. Continuous MIC surveillance is vital for effective empiric therapy selection.
Area of Science:
- Microbiology
- Infectious Diseases
- Pharmacology
Background:
- Glycopeptides, including vancomycin, are frontline treatments for Gram-positive bacterial infections, particularly methicillin-resistant Staphylococcus aureus (MRSA).
- Concerns exist regarding glycopeptide efficacy against MRSA due to poor tissue penetration, slow bacterial killing, and increasing resistance.
- Glycopeptide creep, characterized by incremental increases in MICs for S. aureus, has been observed in single-center studies.
Purpose of the Study:
- To highlight the growing challenge of glycopeptide resistance in Staphylococcus aureus.
- To emphasize the clinical implications of increasing minimum inhibitory concentrations (MICs) for glycopeptides.
- To advocate for accurate MIC measurement and surveillance in clinical practice.
Main Methods:
- Review of existing literature on glycopeptide susceptibility trends in Staphylococcus aureus.
- Analysis of the correlation between elevated MICs and clinical outcomes.
- Discussion of the phenomenon of glycopeptide creep.
Main Results:
- Single-center studies indicate a trend of increasing glycopeptide MICs for S. aureus over time (glycopeptide creep).
- Elevated MICs, even below established susceptibility breakpoints, are associated with reduced clinical efficacy.
- Poor tissue penetration and slow bactericidal activity of glycopeptides contribute to treatment challenges.
Conclusions:
- Accurate and ongoing surveillance of glycopeptide MICs is essential for effective treatment of serious S. aureus infections.
- Clinicians should be aware of potential decreases in glycopeptide susceptibility when selecting empiric therapy.
- Monitoring MIC trends can guide therapeutic choices and antimicrobial stewardship efforts.
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