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Updated: Jul 2, 2025

Intravenous Injections in Neonatal Mice
Published on: November 11, 2014
Applied pharmacokinetics to improve pharmacotherapy in neonatal and paediatric intensive care units: focus on correct
Dotan Shaniv1,2, Karel Allegaert3,4,5
1Pharmacy Services, Kaplan Medical Center, Clalit Health Services, Rehovot, Israel.
Insights
Drug dosing in neonatal and paediatric intensive care units (NICU/PICU) requires careful adjustment due to maturational and non-maturational factors. Precision dosing strategies, including therapeutic drug monitoring, are recommended for optimizing drug exposure in critically ill children.
Area of Science:
- Pharmacology
- Clinical Pharmacy
- Pediatrics
Background:
- Drug dosing in children is influenced by maturational changes (weight, age, body surface area).
- Neonatal and Paediatric Intensive Care Units (NICU/PICU) introduce non-maturational factors impacting drug exposure, such as sepsis, cardiac failure, acute kidney injury, extracorporeal circuits, and drug-drug interactions (DDIs).
- These factors can lead to significant intrapatient and interpatient drug exposure variability, necessitating individual dosage adjustments.
Purpose of the Study:
- To highlight the complexities of drug dosing in NICU/PICU settings.
- To emphasize the need for individualized dosage adjustments for both loading and maintenance doses.
- To provide recommendations for optimizing drug dose selection in critically ill pediatric populations.
Main Methods:
- Review of factors affecting drug pharmacokinetics in NICU/PICU patients.
- Illustration of dosing challenges using phenobarbital and vancomycin as examples.
- Discussion of strategies for optimizing dose selection.
Main Results:
- Maturational and non-maturational factors significantly alter drug pharmacokinetics in pediatric intensive care.
- Individual dosage adjustments are often required to manage drug exposure variability.
- Phenobarbital and vancomycin dosing serve as case studies for these complexities.
Conclusions:
- Optimizing drug dose selection in NICU/PICU settings requires a multifaceted approach.
- Integration of therapeutic drug monitoring with model-informed precision dosing is recommended.
- Utilizing paediatric drug formularies and DDI databases, with guidance from paediatric clinical pharmacologists and pharmacists, is crucial for safe and effective drug therapy.
Abstract:
Drug dosing and exposure throughout childhood are constantly affected by maturational changes like weight, age or body surface area. In neonatal and paediatric intensive care units (NICU and PICU, respectively), drug dosing and exposure are further impacted by non-maturational changes. These changes are related to factors such as sepsis, cardiac failure, acute kidney injury, extracorporeal circuits or drug-drug interactions (DDIs) resulting from polypharmacy.This potentially complex situation may alter drug pharmacokinetics to result in greater-than-usual intrapatient and interpatient drug exposure variability. These effects may call for individual dosage adjustments. Dosage adjustments may apply to both loading doses or maintenance doses, which should be used as appropriate, depending on the specific characteristics of a given drug. Phenobarbital and vancomycin dosing are hereby used as illustrations.To optimise dose selection in NICU/PICU settings, we suggest to consider therapeutic drug monitoring integrated in model-informed precision dosing, and to familiarise oneself with existing paediatric drug formularies as well as DDI databases/search engines. Paediatric clinical pharmacologists and pharmacists can hereby guide clinicians with no prior experience on how to properly apply these data sources to day-to-day practice in individual patients or specific subpopulations of NICU or PICU patients.
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