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Updated: May 16, 2026

Guidelines for Elective Pediatric Fiberoptic Intubation
Published on: January 17, 2011
[Update on propofol TCI in children]
I Constant1, A Rigouzzo, N Louvet
1Département d'anesthésie-réanimation chirurgicale, hôpital Armand Trousseau, AP-HP, UPMC, 26, avenue du Docteur-A.-Netter, 75012 Paris, France. isabelle.constant@trs.aphp.fr
Insights
Propofol total intravenous anaesthesia (TIVA) offers advantages in pediatric care. Tailored pharmacokinetic (PK) models are crucial for accurate propofol TCI dosing in children, considering factors beyond weight.
Area of Science:
- Anesthesiology
- Pharmacokinetics
- Pediatric Pharmacology
Context:
- Total intravenous anesthesia (TIVA) using propofol offers advantages in pediatric anesthesia.
- Current pharmacokinetic (PK) models for TCI in children are limited, often relying solely on weight and exhibiting high variability.
- Physiological covariates like age and lean body mass are increasingly recognized as important for pediatric PK/PD models.
Purpose:
- To review the challenges and advancements in developing pediatric pharmacokinetic (PK) and pharmacodynamic (PD) models for propofol TCI.
- To evaluate the potential adaptation of adult models, such as Schnider et al.'s, for use in pediatric populations over 5 years old.
- To highlight the need for PK/PD models specifically validated for pediatric anesthesia.
Summary:
- Existing pediatric propofol PK models, primarily weight-based, show significant interindividual variability.
- Incorporating physiological covariates is essential for accurate modeling during pediatric growth and maturation.
- No definitive PK/PD model currently exists for pediatric anesthesia, though adult models may be adaptable for older children.
Impact:
- Improved accuracy in propofol dosing for pediatric patients undergoing TIVA.
- Enhanced understanding of propofol's PK/PD in children, leading to safer anesthesia practices.
- Potential for reduced interindividual variability in anesthetic response through model refinement and pharmacodynamic monitoring.
Abstract:
For several years, total intravenous anaesthesia (TIVA) has demonstrated many advantages that allow considering propofol anaesthesia as an interesting alternative in pediatric anaesthesia. TCI in children requires calculation and validation of pharmacokinetic (PK) models specifically adapted to the paediatric population. Several PK models based on a 3-compartement approach have been proposed in children: all these models, which integrate only weight as covariable, show increased distribution volumes with a wide interindividual variability. The particular importance to include physiological covariables, as age and lean body mass, to describe metabolic processes during growth and maturation in pediatric PKPD models is in agreement with recent allometric scaling works in children. However, as pharmacodynamic (PD) parameters are still debated in children, there is up to now, no PKPD model currently available for paediatric anaesthesia. Schnider et al.'s model, a model described in adults that includes numerous covariables, may be adapted and more efficient than the classical paediatric models to describe propofol-PKPD relationship in children over 5years. Whatever the model, a pharmacodynamic feedback such as the bispectral index may be useful to counteract interindividual variability in the paediatric population.
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