Vancomycin MIC Does Not Predict 90-Day Mortality, Readmission, or Recurrence in a Prospective Cohort of Adults with

Sanjiv M Baxi1, Angelo Clemenzi-Allen2, Alice Gahbauer3

  • 1Department of Medicine, Division of Infectious Diseases, University of California, San Francisco, San Francisco, California, USA School of Public Health, Division of Epidemiology, University of California, Berkeley, Berkeley, California, USA sanjiv.baxi@ucsf.edu.

Insights

This study found that vancomycin minimum inhibitory concentration (MIC) levels of 2 μg/ml did not increase mortality or adverse outcomes in patients with Staphylococcus aureus bacteremia (SAB). These findings suggest vancomycin remains a viable treatment option for SAB.

Area of Science:

  • Infectious Diseases
  • Clinical Microbiology
  • Pharmacology

Background:

  • Staphylococcus aureus bacteremia (SAB) poses a significant health challenge.
  • Previous research on vancomycin minimum inhibitory concentration (MIC) and SAB outcomes has yielded inconclusive results.
  • Understanding the impact of vancomycin MIC on patient prognosis is crucial for effective treatment strategies.

Purpose of the Study:

  • To evaluate the association between vancomycin MIC values and 30- or 90-day mortality in patients diagnosed with SAB.
  • To investigate the relationship between vancomycin MIC and secondary outcomes such as recurrence, readmission, or a composite of these events.

Main Methods:

  • A prospective cohort study was conducted involving adult patients with a first episode of SAB between 2008 and 2013.
  • Vancomycin MIC was determined using MicroScan, with a focus on MICs of 2 μg/ml compared to <2 μg/ml.
  • Propensity-adjusted Cox proportional-hazards models were employed to analyze 30- and 90-day mortality and composite outcomes, controlling for covariates.

Main Results:

  • Out of 418 analyzed SAB episodes, 19.9% had a vancomycin MIC of 2 μg/ml.
  • A vancomycin MIC of 2 μg/ml was not significantly associated with increased 30- or 90-day mortality.
  • No significant association was found between vancomycin MIC of 2 μg/ml and the composite outcome of mortality, readmission, or recurrence at 30 or 90 days.

Conclusions:

  • In patients with SAB, a vancomycin MIC of 2 μg/ml does not appear to be associated with increased mortality.
  • The study suggests that vancomycin remains an effective treatment option for SAB, even with MICs of 2 μg/ml.
  • Further research may explore optimal vancomycin dosing strategies based on MIC values and patient-specific factors.

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