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Effects of aggregate and individual antibiotic exposure on vancomycin MICs for Staphylococcus aureus isolates
Lucia Rose1, Shannon Chan, Jobayer Hossain
1Department of Pharmacy Practice, Western New England University College of Pharmacy, Springfield, Massachusetts, USA.
Abstract:
We evaluated the evolution of vancomycin MICs for Staphylococcus aureus and their relationship with vancomycin use among hospitalized children. S. aureus isolates recovered from sterile sites were prospectively tested for vancomycin susceptibility using the Etest between 1 April 2000 and 31 March 2008. Vancomycin MICs were grouped into three categories: ≤ 1, 1.5, and 2 μg/ml. The association between vancomycin MICs and aggregate vancomycin use and individual patient vancomycin exposure 6 months prior to the documented infection was assessed. The geometric mean values for vancomycin MICs for S. aureus fluctuated over time without a significant trend (P = 0.146). Of the 436 patients included in the study, 363 (83%) had methicillin-susceptible S. aureus (MSSA) and 73 (17%) had methicillin-resistant S. aureus (MRSA) infections. The rate of isolates with a vancomycin MIC of 2 μg/ml increased from 4% (2 of 46) in 2000 to 2001 to 24% (11 of 46) in 2007 to 2008, despite a decrease in vancomycin use (r = -0.11; P = 0.825). The percentage of isolates with a vancomycin MIC of 2 μg/ml was higher for MRSA (15%; 11 of 73) than for MSSA strains (5.2%; 19 of 363) (χ(2) = 9.2; P = 0.01). Individual patient vancomycin exposure was not associated with a higher vancomycin MIC. In the unadjusted model, in which we compared patients with S. aureus infections with MICs of ≤ 1 μg/ml, the odds ratios of exposure rates for patients with isolates with MICs of 1.5 μg/ml and 2 μg/ml were 1.02 (P = 0.929) and 1.13 (P = 0.767), respectively. In our experience, the geometric means of vancomycin MICs from S. aureus isolates recovered from hospitalized children oscillated over time and were not associated with previous individual patient vancomycin exposure or aggregate vancomycin use.
Insights
Vancomycin MICs in Staphylococcus aureus among children fluctuated without a clear trend, despite changes in antibiotic use. Methicillin-resistant S. aureus showed higher MICs, but individual vancomycin exposure didn
Area of Science:
- Clinical Microbiology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Vancomycin is a critical antibiotic for treating serious Staphylococcus aureus infections.
- Monitoring vancomycin Minimum Inhibitory Concentrations (MICs) is essential for tracking antimicrobial resistance trends.
- Understanding the relationship between vancomycin use and evolving resistance in pediatric populations is crucial.
Purpose of the Study:
- To evaluate the trends in vancomycin MICs for Staphylococcus aureus isolates from hospitalized children.
- To assess the association between vancomycin MICs and both aggregate vancomycin use and individual patient exposure.
- To differentiate resistance patterns between methicillin-susceptible S. aureus (MSSA) and methicillin-resistant S. aureus (MRSA).
Main Methods:
- Prospective surveillance of S. aureus isolates from sterile sites in hospitalized children from 2000 to 2008.
- Vancomycin susceptibility testing using Etest, with MICs categorized as ≤1, 1.5, or 2 μg/ml.
- Statistical analysis to correlate vancomycin MICs with historical vancomycin usage data.
Main Results:
- Geometric mean vancomycin MICs for S. aureus fluctuated over time without a significant trend (P = 0.146).
- The proportion of isolates with vancomycin MIC of 2 μg/ml increased from 4% to 24% despite decreased vancomycin use.
- Higher vancomycin MICs (2 μg/ml) were observed more frequently in MRSA (15%) compared to MSSA (5.2%) isolates (P = 0.01).
Conclusions:
- Vancomycin MICs in pediatric S. aureus isolates showed temporal oscillations unrelated to overall vancomycin consumption.
- Increased vancomycin MICs were significantly associated with MRSA strains.
- Individual patient vancomycin exposure history did not correlate with elevated vancomycin MICs in this cohort.
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