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Published on: January 23, 2026
Vancomycin dosing and target attainment in children
David Hwang1, Nan-Chang Chiu2, Lung Chang3
1Department of Pediatrics, Mackay Memorial Hospital, Taipei, Taiwan.
Insights
A 15 mg/kg dose of vancomycin every 6 hours is more effective than 10 mg/kg for achieving therapeutic vancomycin trough concentrations and AUC/MIC goals in children.
Area of Science:
- Pediatric pharmacology
- Infectious disease pharmacokinetics
- Antibiotic dosing optimization
Background:
- Vancomycin is a critical antibiotic for treating serious Gram-positive infections.
- Optimizing vancomycin dosing in children is essential for efficacy and safety.
- Understanding the relationship between vancomycin exposure and clinical outcomes is crucial.
Purpose of the Study:
- To determine the optimal vancomycin dosing strategy in pediatric patients.
- To examine factors influencing vancomycin pharmacokinetics.
- To correlate vancomycin area under the curve (AUC) values with trough concentrations.
Main Methods:
- Retrospective analysis of 218 children (3 months to 18 years) receiving vancomycin.
- Calculation of vancomycin clearance (CL) using a validated model.
- Determination of AUC and AUC/MIC ratios based on dosing regimens.
Main Results:
- Vancomycin trough concentrations moderately correlated with AUC values (r² = 0.232, p < 0.01).
- A 15 mg/kg dose every 6 hours (q6h) resulted in significantly higher AUC and trough concentrations compared to 10 mg/kg q6h.
- 54.3% of children on 15 mg/kg q6h achieved the target AUC/MIC (≥400), versus 9.5% on 10 mg/kg q6h.
Conclusions:
- A vancomycin dosing regimen of 15 mg/kg/dose q6h is superior to 10 mg/kg/dose q6h in pediatric patients.
- The higher dose regimen increases the likelihood of achieving target trough concentrations (15-20 μg/mL) and AUC/MIC goals.
- This finding supports optimizing vancomycin dosing for improved therapeutic outcomes in children.
Background/Purpose:
The aim of this study is to determine the best dosing strategy for vancomycin by studying the associated factors and examining correlations between the area under the plasma concentration-time curve (AUC) values and trough concentrations in children.
Methods:
Children aged 3 months to 18 years were included if they received vancomycin for more than three doses between January 1, 2010 and December 31, 2012 and had one or more serum vancomycin trough concentrations. Vancomycin clearance (CL) was calculated using the following model: CL = 0.248*Wt0.75*(0.48/serum creatinine)0.361*[ln (age)/7.8]0.995. The AUC (mg-h/L) was calculated by 24-hour dose (mg/kg/d)/CL(L/h). The value of AUC divided by the minimum inhibitory concentration (MIC) of vancomycin was AUC/MIC.
Results:
A total of 218 children were included. The mean age was 6.0 ± 5.1 years and the mean body weight was 20 ± 11.7 kg. Vancomycin trough concentrations were moderately correlated with AUC values (r2 = 0.232, p < 0.01). Dosing of 15 mg/kg/dose q6h produced significantly higher AUC values (p < 0.001) and vancomycin trough concentrations (p < 0.001) compared to dosing of 10 mg/kg/dose q6h. In children receiving a 10-mg/kg/dose q6h, 5.6% (5/90) achieved the target trough concentrations of 15-20 μg/mL and 9.5% (5/90) achieved the goal AUC/MIC ≥ 400. In children receiving a 15-mg/kg/dose q6h, 13% (6/46) achieved the target trough concentrations of 15-20 μg/mL, whereas 54.3% (25/46) achieved the goal AUC/MIC ≥ 400.
Conclusion:
A 15-mg/kg/dose q6h compared to a 10-mg/kg/dose q6h is more likely to achieve target trough concentrations of 15-20 μg/mL and the goal AUC/MIC ≥ 400.
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