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Optimal rocuronium dose for intubation during inhalation induction with sevoflurane in children

M Eikermann1, I Hunkemöller, L Peine

  • 1Abteilung für Anästhesiologie und Intensivmedizin, Universität Essen, Hufelandstr. 55, D-45122 Essen, Germany.

Insights

Rocuronium at 0.29 mg/kg optimizes intubation conditions for children during sevoflurane inhalation induction. This dose provides a 95% probability of acceptable intubation, crucial for pediatric anesthesia.

Area of Science:

  • Pediatric Anesthesiology
  • Pharmacology
  • Neuromuscular Blockade

Background:

  • Inhalation induction with sevoflurane is common in pediatric anesthesia.
  • Optimizing neuromuscular blockade is essential for successful intubation.
  • Rocuronium's optimal dose for intubation during sevoflurane induction in children requires definition.

Purpose of the Study:

  • To determine the rocuronium dose providing a 95% probability of acceptable intubation conditions (ED95TI).
  • To evaluate rocuronium's efficacy during inhalation induction with sevoflurane in children aged 2-7 years.

Main Methods:

  • Prospective, randomized, assessor-blinded study of 120 children.
  • Inhalation induction with sevoflurane followed by varying rocuronium doses or placebo.
  • Neuromuscular function assessed via accelerometry; intubation conditions evaluated 2 minutes post-injection.

Main Results:

  • Rocuronium doses of 0.24 mg/kg and 0.29 mg/kg provided 90% and 95% probability of acceptable intubation, respectively.
  • Acceptable intubation conditions were achieved in 97% of children when thumb acceleration decreased by ≥50%.
  • Recovery of neuromuscular function (train-of-four ratio to 0.8) varied by dose, averaging 12-50 minutes.

Conclusions:

  • Rocuronium 0.29 mg/kg is the optimal dose (ED95) for intubation during sevoflurane inhalation induction in children.
  • This dose ensures optimal intubating conditions for short-duration pediatric surgical procedures.
  • The study provides critical data for safe and effective pediatric anesthesia.
Abstract

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