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Updated: May 3, 2026

Multiplex Therapeutic Drug Monitoring by Isotope-dilution HPLC-MS/MS of Antibiotics in Critical Illnesses
Published on: August 30, 2018
[Pharmacokinetics of vancomycin in children hospitalized in a critical care unit]
Insights
Many children in the Pediatric Intensive Care Unit (PICU) may not receive adequate vancomycin doses. Monitoring pharmacokinetic/pharmacodynamic (PK/PD) parameters is crucial for optimizing vancomycin therapy in pediatric patients.
Area of Science:
- Pediatric Intensive Care
- Pharmacokinetics and Pharmacodynamics
- Antimicrobial Therapy
Context:
- Vancomycin is a critical antibiotic for treating staphylococcal infections in children.
- Optimizing vancomycin dosing in pediatric patients is essential for effective treatment and minimizing resistance.
- Current monitoring strategies may not adequately capture therapeutic efficacy in critically ill children.
Purpose:
- To evaluate the pharmacokinetic/pharmacodynamic (PK/PD) parameters of vancomycin in children admitted to the Pediatric Intensive Care Unit (PICU).
- To assess the achievement of therapeutic targets, specifically the area under the curve of drug exposure over the 24-hour period divided by the minimum inhibitory concentration (ABC 24 h/MIC), in this pediatric population.
- To determine the proportion of children achieving optimal vancomycin exposure based on PK/PD targets.
Summary:
- Eighty-four children receiving vancomycin (40 mg/kg/day) in the PICU were studied retrospectively.
- While 49% had basal vancomycin levels within the therapeutic range (5-15 μg/mL), only 54% achieved the target ABC 24 h/MIC of > 400 mg*h/L.
- A significant proportion of children may be exposed to sub-therapeutic vancomycin doses, highlighting potential limitations in standard dosing and monitoring.
Impact:
- The findings suggest that standard vancomycin dosing may be insufficient for achieving therapeutic targets in critically ill children.
- Implementing tailored antimicrobial treatment strategies based on PK/PD monitoring is recommended for optimizing vancomycin therapy in pediatric patients.
- This study underscores the importance of individualized vancomycin dosing and therapeutic drug monitoring in the PICU setting to improve patient outcomes.
Introduction:
Monitoring PK/PD of vancomycin with basal and peak serum levels and the area under the curve of drug exposure 24 h/MIC (ABC 24 h/MIC) could optimize the management of children.
Objective:
To study the PK of vancomycin in children hospitalized in the Pediatric Intensive Care Unit (PICU), assessing PK/PD parameters withABC24 h/MIC.
Methods:
Retrospective, descriptive study in the PICU (Hospital Luis Calvo Mackenna) between January 2008-March 2010. We included children < 18 years who required antimicrobial treatment with vancomycin for suspected/confirmed staphylococcal infection using a dose of 40 mg/k/day. Plasmatic levels were performed one hour postinfusion and 30 min prior to the next dose. The following PK/PD parameters were calculated: vancomycin clearance, elimination rate constant, volume of distribution, half-life (T1/2) and ABC 24 h/ MIC.
Results:
We enrolled eighty-four children. According to ABC 24 h/MIC obtained, 54% (45/84) of children reached an optimal level (> 400 mg*hr/L). Based on the traditional PK/PD parameters, 49% of cases (41/84) presented a basal level of vancomycin in the therapeutic range (5-15 μg/mL) and of those, only 39% (16/41) had a ABC 24 h/MIC over 400 mg*h/L.
Discussion:
Based on our results, children admitted to PICU could be exposed to sub therapeutic doses of vancomycin. We recommend to implement tailored antimicrobial treatment monitoring vancomycin PK/PD parameters.
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