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Precision dosing of vancomycin: in defence of AUC-guided therapy in children
Mark E Murphy1,2, Sonya Tang Girdwood2,3,4, Jennifer L Goldman5,6,7
1Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Insights
New guidelines recommend AUC24 monitoring for vancomycin in children, moving beyond trough levels. This approach optimizes dosing to reduce vancomycin-associated nephrotoxicity and improve outcomes in high-risk pediatric patients.
Area of Science:
- Pharmacology
- Pediatric Infectious Diseases
- Clinical Pharmacy
Background:
- Vancomycin dosing guidelines shifted in 2020 to AUC24 monitoring.
- Debate exists regarding the resources and benefits of AUC24 monitoring versus traditional trough monitoring.
- A recent review questioned the data supporting AUC24 monitoring in pediatrics.
Purpose of the Study:
- To provide supporting arguments for AUC24-guided vancomycin monitoring in pediatric patients.
- To address concerns about the transition to AUC24 monitoring.
- To advocate for optimized vancomycin therapy in children.
Main Methods:
- This article presents a supportive argument based on existing literature and clinical reasoning.
- It critically evaluates the limitations of trough-based monitoring.
- It highlights the clinical implications of vancomycin dosing in pediatric populations.
Main Results:
- Trough vancomycin levels are insufficient surrogates for AUC24.
- Vancomycin-associated nephrotoxicity has serious consequences necessitating optimized dosing.
- A significant number of children are at high risk for adverse outcomes with vancomycin therapy.
- Limited efficacy data for AUC24 does not justify reverting to less supported methods.
Conclusions:
- AUC24 monitoring is superior to trough monitoring for vancomycin in children.
- Optimizing vancomycin dosing through AUC24 monitoring is crucial for mitigating nephrotoxicity and improving outcomes.
- Continued adoption of AUC24-guided monitoring in pediatric patients is warranted.
Abstract:
In 2020, new vancomycin guidelines were released, recommending the transition from trough-based to AUC24 monitoring for adult and paediatric patients. Given the resources required to achieve this transition, there has been debate about the costs and benefits of AUC24-based monitoring. A recent narrative review of vancomycin therapeutic drug monitoring in paediatrics claims to have uncovered the methodological weaknesses of the data that informed the guidelines and advises against premature adoption of AUC24-guided monitoring. In this article, we present supporting arguments for AUC24-guided monitoring in children, which include that: (i) troughs alone are inadequate surrogates for AUC24; (ii) vancomycin-associated nephrotoxicity has significant consequences that warrant optimization of dosing; (iii) a substantial portion of children receiving vancomycin are at high risk for poor outcomes and deserve targeted monitoring; and (iv) limited efficacy data in support of AUC24 is not a justification to revert to a less supported monitoring approach.
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