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Advances in Pediatric Therapeutic Drug Monitoring
Sarah A Coggins1,2, Kelly C Wade1,2, Kevin J Downes2,3
1Division of Neonatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Pediatric therapeutic drug monitoring (TDM) is advancing, particularly for vancomycin. Shifting from trough to AUC-based monitoring improves efficacy and reduces toxicity in children and neonates.
Area of Science:
- Pharmacology
- Pediatric Infectious Diseases
- Clinical Pharmacy
Background:
- Therapeutic drug monitoring (TDM) is crucial for drugs with narrow therapeutic indices to balance efficacy and toxicity.
- Pediatric TDM innovation lags due to data scarcity and logistical challenges.
- Vancomycin, a key antibiotic for gram-positive infections, has historically relied on trough concentration monitoring in children.
Purpose of the Study:
- To review advancements in pediatric TDM, focusing on vancomycin as a model.
- To highlight the shift from trough-based to AUC-based vancomycin monitoring in pediatric populations.
- To discuss the implications of AUC-guided TDM for neonates and children.
Main Methods:
- Review of recent literature on vancomycin TDM in pediatric populations.
- Comparison of TDM approaches in infectious diseases.
- Analysis of pharmacokinetic (PK) modeling and flexible sampling strategies.
Main Results:
- Emerging data indicate vancomycin troughs are unreliable for predicting efficacy or toxicity.
- Trough-based vancomycin monitoring is linked to increased nephrotoxicity without clinical benefit.
- Area under the concentration-time curve (AUC) is the preferred metric for vancomycin exposure.
Conclusions:
- Consensus guidelines recommend transitioning to AUC-guided vancomycin monitoring for all age groups, including neonates and children.
- AUC-guided TDM offers optimal vancomycin exposure assessment, improving outcomes.
- Implementation of AUC-guided TDM in pediatrics presents opportunities and challenges.
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