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Target concentration of propofol required to insert the laryngeal mask airway in children
X Viviand1, L Berdugo, C Aubry De La Noé
1Department of Anaesthesia, Hôpital Nord, Marseille Cedex, France. xviviand@aphm.fr
Insights
This study determined propofol target concentration curves for laryngeal mask airway insertion in children. The target-controlled infusion technique proved safe and effective for anesthesia induction.
Area of Science:
- Anesthesiology
- Pharmacokinetics
- Pediatric Anesthesia
Background:
- Laryngeal mask airway (LMA) insertion requires precise anesthetic dosing.
- Determining target concentration (CPRED) curves for propofol is crucial for pediatric LMA procedures.
Purpose of the Study:
- To establish target concentration (CPRED) curves for laryngeal mask airway (LMA) insertion in pediatric patients.
- To evaluate the safety and efficacy of target-controlled infusion (TCI) for anesthesia induction and LMA placement in children.
Main Methods:
- Prospective study involving 72 unpremedicated children (3-10 years, ASA I).
- Propofol CPRED for LMA insertion determined using sequential allocation.
- Insertion conditions assessed as satisfactory, excellent, or unacceptable.
Main Results:
- CPRED50 and CPRED90 values varied based on pharmacokinetic models (Kataria, Marsh, Schüttler).
- Satisfactory LMA insertion CPRED50 was 7.86 µg/mL (Kataria), increasing with pharmacokinetic model adjustments.
- Excellent insertion conditions required higher propofol concentrations across all models.
Conclusions:
- Target-controlled infusion (TCI) is a safe and effective method for anesthesia induction.
- TCI facilitates successful laryngeal mask airway insertion in pediatric patients.
- Established CPRED curves provide valuable guidance for pediatric anesthesia.
Background:
The aim of this prospective study was to determine the target concentration (CPRED) curves for laryngeal mask airway (LMA) insertion in children.
Methods:
The CPRED of propofol required for insertion of the LMA was determined in 72 unpremedicated children, aged 3-10 years, ASA physical status I. CPRED was reached in 2 min according to a sequential allocation. LMA insertion was then performed by an experienced anaesthetist who was unaware of the concentration. Insertion conditions were noted as satisfactory (jaw relaxed, no coughing, gagging, swallowing or laryngeal spasm, minimal limb movement), excellent (no movement at all) or unacceptable if otherwise.
Results:
The CPRED50 and CPRED90 were 7.86 microg.ml(-l)[95% confidence interval (CI) 6.46-9.26] and 10.71 microg.ml(-l) (95% CI 9.31-12.12), respectively, in the satisfactory group and 10.86 microg.ml(-l) (95% CI 10.14-11.57) and 13.71 microg.ml(-l) (95% CI 12.99-14.42) in the excellent group when calculations were based on Kataria's pharmacokinetics. These figures were increased 1.5-fold when calculations were based on Marsh's pharmacokinetics. With Schüttler's pharmacokinetics, CPRED50 were 4.62 microg.ml(-l) and 13.66 microg.ml(-l) for satisfactory and excellent groups, respectively.
Conclusions:
The target-controlled infusion technique for anaesthesia induction and insertion of the LMA was a safe and effective technique in our study.
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