Conscious sedation with remifentanil and midazolam during brief painful procedures in children
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Published on: July 30, 2009
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.
Objective:
To test the hypothesis that remifentanil, because of its favorable pharmacokinetic properties, would be advantageous to use in combination with midazolam to provide analgesia and sedation during brief painful procedures.
Design:
Prospective observation and data collection.
Setting:
University hospital.
Patients:
Seventeen children aged 2 to 12 years, who underwent 20 brief, painful procedures.
Interventions:
Administration of intravenous midazolam hydrochloride, 0.05 mg/kg, and remifentanil hydrochloride, 1 microg/kg, followed by a remifentanil infusion at 0.1 microg x kg(-1) x min(-1). The dose was titrated at 5-minute intervals to levels of sedation and analgesia.
Main Outcome Measures:
Successful remifentanil doses, times to discharge readiness, side effects, complications, and requirement for additional medications.
Results:
The technique was successful in 17 of 20 procedures. The mean +/- SD successful dose was 0.4 +/- 0.2 microg x kg(-1) x min(-1). Four children developed hypoxemia that abated with mild stimulation; 1 child became unresponsive and required positive-pressure ventilation. The mean +/- SD time to reach discharge criteria was 9.5 +/- 4.3 minutes. Hypoxemia was avoided in 10 of 13 patients by continuous stimulation throughout the procedure.
Conclusion:
The use of remifentanil and midazolam during brief, painful procedures results in rapid times to discharge but is complicated by a high incidence of life-threatening respiratory depression at subtherapeutic levels.
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