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Published on: August 30, 2018
Vancomycin therapeutic drug monitoring in paediatrics
Joanne Patel1,2, Catherine J Lucas1,2, Jessica Ryan1,2,3,4
1School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia.
Insights
Vancomycin therapeutic drug monitoring (TDM) in children shows poor adherence to guidelines, with low trough concentrations often unaddressed. Optimizing vancomycin dosing and monitoring is crucial for effective treatment and preventing resistance.
Area of Science:
- Pharmacology
- Pediatric Infectious Diseases
- Clinical Pharmacy
Background:
- Vancomycin therapeutic drug monitoring (TDM) guidelines aim to optimize efficacy and minimize toxicity and resistance.
- Target trough concentrations are used for convenience but poorly correlate with the desired area under the concentration-time curve (AUC)/minimum inhibitory concentration (MIC) ratio > 400 in children.
Purpose of the Study:
- To audit the performance of vancomycin TDM against current guidelines in pediatric inpatients.
- To identify necessary changes for optimizing vancomycin monitoring in children.
Main Methods:
- Retrospective collection of vancomycin prescriptions in patients under 18 years.
- Primary outcomes: initial vancomycin dose and timing/result of first trough concentration.
- Secondary outcomes: achievement of target concentrations and appropriateness of dose adjustments.
Main Results:
- Only 25% of vancomycin courses had trough concentrations measured at the recommended time.
- The mean trough concentration was 11.6 mg/L, with significant variability.
- Half of patients with low trough concentrations did not have their vancomycin dose adjusted.
Conclusions:
- A poor correlation exists between prescribed vancomycin doses and achieved trough concentrations in pediatric patients.
- Current trough concentration monitoring recommendations are poorly adhered to, necessitating a strategic plan for improvement.
Aim:
Vancomycin guidelines for therapeutic drug monitoring (TDM) aim to maximise efficacy while minimising toxicity and resistance. Vancomycin is effective against Staphylococcus aureus when it achieves area under the concentration-time curve (AUC)/minimum inhibitory concentration (MIC) > 400. Studies in children have shown that target trough concentrations poorly correlate to AUC/MIC > 400; however, they are used in practice for clinical convenience. This review in paediatric inpatients aims to audit performance against TDM guidelines and consider what changes are needed to optimise vancomycin monitoring.
Methods:
Vancomycin prescriptions in patients younger than 18 years old were collected over a 15-month period. Primary outcome measures were vancomycin initial dose (mg/kg/day) and the timing and result of first trough concentration (mg/L). Secondary outcome measures were the numbers achieving recommended targets and whether appropriate dose adjustments were made in response to TDM.
Results:
A total of 133 courses reached the time when TDM should occur. Average patient age was 6.5 years, and the average initial dose was 52.55 mg/kg/day (range 19.05-86.54 mg/kg). Only 25% of courses (n = 34) had a trough concentration measured at the recommended time. The mean trough concentration was 11.6 mg/L (range < 2.0-39.7). Of 40 patients with a low trough concentration, 50% continued without dose adjustment.
Conclusion:
As shown in the literature, there is a poor correlation between the vancomycin dose given and the trough concentration achieved. Given that recommendations for trough concentration monitoring are designed to simplify the process yet are poorly adhered to, a strategic plan to address these issues is needed.
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