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High vancomycin minimum inhibitory concentration and clinical outcomes in adults with methicillin-resistant
Jesse T Jacob1, Carlos A DiazGranados
1Division of Infectious Diseases, Emory University School of Medicine, Orr Building, Suite 1020, 550 Peachtree Street NE, Atlanta, GA 30308, USA. jtjacob@emory.edu
Background:
Patients with methicillin-resistant Staphylococcus aureus (MRSA) infections caused by isolates with a high but 'susceptible' minimum inhibitory concentration (MIC) to vancomycin may suffer poor outcomes. The aim of this study was to determine the association of high compared to low vancomycin MICs and clinical outcomes (treatment failure and mortality) in patients with MRSA infections.
Methods:
PubMed, the Cochrane Library, and electronic abstracts from meetings were queried from January 2000 to July 2010. Two reviewers independently screened titles and abstracts of studies evaluating outcomes of patients with MRSA infections, using broth microdilution (BMD) or the Etest to determine MIC, for full-text review. Patients participating in included studies were classified into two mutually exclusive groups: high MIC or low MIC. High MIC was defined as MIC ≥1mg/l by BMD or ≥1.5mg/l by Etest. Study-defined failure and mortality were assessed in each group.
Results:
Fourteen publications and six electronic abstracts met the inclusion criteria, with 2439 patients (1492 high MIC and 947 low MIC). There was no evidence of publication bias or heterogeneity. An increased risk of failure was observed in the high MIC group compared to the low MIC group (summary risk ratio (RR) 1.40, 95% confidence interval (CI) 1.15-1.71). The overall mortality risk was greater in the high MIC group than in the low MIC group (summary RR 1.42, 95% CI 1.08-1.87). Sensitivity analyses showed similar findings for failure (summary RR 1.37, 95% CI 1.09-1.73) and mortality (summary RR 1.46, 95% CI 1.06-2.01) for patients with bacteremia. The study quality was poor-to-moderate, and study-defined endpoints were variable.
Conclusions:
A susceptible but high MIC to vancomycin is associated with increased mortality and treatment failure among patients with MRSA infections.
Insights
High vancomycin minimum inhibitory concentration (MIC) in methicillin-resistant Staphylococcus aureus (MRSA) infections is linked to worse patient outcomes. This includes increased treatment failure and higher mortality rates, even with susceptible MIC levels.
Area of Science:
- Infectious Diseases
- Clinical Microbiology
- Pharmacology
Background:
- Methicillin-resistant Staphylococcus aureus (MRSA) infections pose significant treatment challenges.
- Vancomycin is a key antibiotic for MRSA, but rising minimum inhibitory concentrations (MICs) are a concern.
- Patients with MRSA isolates exhibiting high, yet susceptible, vancomycin MICs may experience poorer clinical outcomes.
Purpose of the Study:
- To investigate the association between high vancomycin MICs and clinical outcomes in patients with MRSA infections.
- To compare treatment failure and mortality rates in patients with high versus low vancomycin MICs.
Main Methods:
- A systematic literature search of PubMed, Cochrane Library, and conference abstracts (2000-2010).
- Inclusion of studies using broth microdilution (BMD) or Etest for vancomycin MIC determination in MRSA infections.
- Classification of patients into high MIC (≥1 mg/L by BMD or ≥1.5 mg/L by Etest) and low MIC groups for outcome assessment.
Main Results:
- Analysis of 14 publications and 6 abstracts, encompassing 2439 patients (1492 high MIC, 947 low MIC).
- Significantly increased risk of treatment failure (RR 1.40) and mortality (RR 1.42) in the high vancomycin MIC group.
- Consistent findings in sensitivity analyses, including for patients with bacteremia, despite variable study quality and endpoints.
Conclusions:
- A high, but susceptible, vancomycin MIC is associated with increased treatment failure and mortality in MRSA infections.
- These findings highlight the clinical relevance of monitoring vancomycin MICs in MRSA infections.
- Further research may be warranted to optimize treatment strategies for MRSA with high vancomycin MICs.
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