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Relationship between vancomycin exposure and outcomes among patients with MRSA bloodstream infections with vancomycin
D M Martirosov1, M R Bidell1, M P Pai1
1Albany College of Pharmacy and Health Sciences, 106 New Scotland Ave, Albany, NY 12008, USA.
Abstract:
Data suggest that vancomycin is less effective for methicillin-resistant Staphylococcus aureus (MRSA) bloodstream infection (BSI) with vancomycin Etest® MIC (MICEtest) ≥1.5 mg/L. No published studies have evaluated the relationship between vancomycin exposure and outcomes among patients with MRSA BSIs vancomycin MICEtest ≥1.5 mg/L. This study was a retrospective cohort of 71 hospitalized, adult, non-dialysis patients with MRSA BSIs treated with vancomycin. All but three patients had a vancomycin MICEtest of 1.5 mg/L. Achievement of CART-derived AUC24-48h of at least 550 mg*h/L (AUC24-48h/MIC of 366 mg*h/L) was associated with a lower incidence of treatment failure. In multivariate analyses, the risk ratio was 0.45 for the CART-derived AUC24-48h threshold, indicating that achievement of the CART-derived AUC24-48h threshold of 550 was associated with a 2-fold decrease in treatment failure. These findings suggest a potential association between vancomycin exposure and outcomes in patients with MRSA BSIs with MICEtest ≥1.5 mg/L. As this study was retrospective, these findings provide the basis for a future large-scale, multi-center prospective study.
Insights
For methicillin-resistant Staphylococcus aureus (MRSA) bloodstream infections with vancomycin MIC ≥1.5 mg/L, achieving adequate vancomycin exposure (AUC/MIC) is linked to reduced treatment failure. This suggests optimizing vancomycin dosing may improve outcomes in these challenging infections.
Area of Science:
- Infectious Diseases
- Pharmacokinetics
- Antimicrobial Stewardship
Background:
- Methicillin-resistant Staphylococcus aureus (MRSA) bloodstream infections (BSIs) pose significant treatment challenges.
- Vancomycin efficacy may be reduced in MRSA infections with elevated vancomycin minimum inhibitory concentrations (MICs).
- Limited data exist on the relationship between vancomycin exposure and outcomes in MRSA BSIs with vancomycin MIC ≥1.5 mg/L.
Purpose of the Study:
- To investigate the association between vancomycin exposure and treatment outcomes in hospitalized adult patients with MRSA BSIs and vancomycin MIC ≥1.5 mg/L.
- To determine if achieving a specific vancomycin exposure threshold (AUC/MIC) is associated with lower treatment failure rates.
Main Methods:
- Retrospective cohort study of 71 adult, non-dialysis patients with MRSA BSIs treated with vancomycin.
- Vancomycin minimum inhibitory concentrations (MICs) were determined using Etest®.
- Area under the concentration-time curve (AUC) was estimated, and achievement of a CART-derived AUC24-48h threshold of 550 mg*h/L (AUC/MIC of 366 mg*h/L) was assessed.
Main Results:
- Most patients (68/71) had a vancomycin MICEtest of 1.5 mg/L.
- Achievement of the CART-derived vancomycin AUC24-48h threshold of 550 mg*h/L was associated with a lower incidence of treatment failure.
- Multivariate analysis indicated a risk ratio of 0.45 for achieving this threshold, suggesting a 2-fold decrease in treatment failure risk.
Conclusions:
- Vancomycin exposure, specifically achieving an AUC24-48h of at least 550 mg*h/L, may be associated with improved outcomes in patients with MRSA BSIs and vancomycin MIC ≥1.5 mg/L.
- These findings support the potential benefit of optimizing vancomycin dosing in this patient population.
- Further prospective studies are warranted to confirm these results.
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