Conscious sedation with remifentanil and midazolam during brief painful procedures in children

R S Litman1

  • 1Department of Anesthesiology, University of Rochester School of Medicine and Dentistry, NY, USA. Ronald_Litman@urmc.rochester.edu

Insights

Remifentanil and midazolam offer rapid discharge after painful procedures but carry a high risk of serious respiratory depression in children. Continuous stimulation may mitigate hypoxemia risks.

Area of Science:

  • Pediatric Anesthesiology
  • Pharmacology
  • Critical Care Medicine

Background:

  • Brief, painful procedures in children often require effective analgesia and sedation.
  • Remifentanil, an ultra-short-acting opioid, possesses favorable pharmacokinetic properties for procedural sedation.
  • Midazolam is commonly used for procedural sedation in pediatric patients.

Purpose of the Study:

  • To evaluate the efficacy and safety of combining remifentanil and midazolam for analgesia and sedation during brief, painful pediatric procedures.
  • To assess pharmacokinetic advantages of remifentanil in this setting.

Main Methods:

  • Prospective observational study in a university hospital setting.
  • Seventeen children (aged 2-12 years) undergoing 20 procedures received intravenous midazolam (0.05 mg/kg) and remifentanil (1 microg/kg), followed by a remifentanil infusion (0.1 microg x kg(-1) x min(-1)).
  • Doses were titrated every 5 minutes, monitoring sedation, analgesia, and adverse events.

Main Results:

  • The combination was successful in 17 of 20 procedures, with a mean successful remifentanil dose of 0.4 +/- 0.2 microg x kg(-1) x min(-1).
  • Mean discharge readiness time was 9.5 +/- 4.3 minutes.
  • Four children experienced hypoxemia (resolved with stimulation), and one required positive-pressure ventilation. Continuous stimulation helped avoid hypoxemia in 10 of 13 patients.

Conclusions:

  • Remifentanil and midazolam facilitate rapid discharge after pediatric procedures.
  • However, this combination is associated with a significant incidence of life-threatening respiratory depression, even at subtherapeutic doses.
  • Careful monitoring and potential interventions like continuous stimulation are crucial when using this regimen.
Abstract

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