Key result
Clinically acceptable intubating conditions were achieved in 95% of patients receiving 2 or 3 μg/kg of remifentanil with propofol, compared to only 55% in those receiving 1 μg/kg (P < 0.05).
Why the study?
Does a higher dose of remifentanil (3-4/kg) combined with propofol improve intubating conditions without muscle relaxants compared to a lower dose (2/kg) in healthy premedicated patients?
RCT (n=60)
Randomized
Does a higher dose of remifentanil (3-4/kg) combined with propofol improve intubating conditions without muscle relaxants compared to a lower dose (2/kg) in healthy premedicated patients?
Absolute Event Rate: 95% vs 55%
p-value: p=<0.05
Remifentanil at doses of 3-4/kg combined with propofol provides reliable and clinically acceptable conditions for tracheal intubation without the use of neuromuscular blocking drugs.
Supports 2-3 μg/kg remifentanil with propofol for intubation without relaxants; extends dose-response evidence for opioid-only airway management.
Background: Using alfentanil followed by an anesthetic induction dose of propofol provides adequate conditions for tracheal intubation without neuromuscular blocking drugs in most patients. Providing an option for intense opioid effect without compromising recovery after short operations, remifentanil might offer benefits over alfentanil. In this study intubating conditions after remifentanil-propofol were evaluated. Methods: Sixty healthy premedicated patients were divided randomly into 3 groups. Anesthesia was intravenously induced with propofol (4/ml) followed by remifentanil. Group , , received 2, 3, 4/kg remifentanil, respectively. Ninety seconds after the administration of remifentanil, laryngoscopy and intubation were attempted. Intubation conditions were assessed as excellent, good or poor. The hemodynamic changes were measured at preinduction (base), preintubation, postintubation (immediately, 3 minute, 5 minute after intubation). Results: Clinically acceptable intubating conditions were observed in 65%, 95%, and 95% of patients in the , , and groups, respectively. Clinically acceptable intubating conditions were significantly (P < 0.05) less likely to occur in Group c. The mean arterial pressure decreased immediately after induction in all groups. There was no significant elevation in heart rate after tracheal intubation in all groups. There were no significant differences among groups. Conclusions: Healthy, premedicated patients with favorable airway anatomy can be reliably intubated with good or excellent conditions 90 seconds after the administrations of remifentanil 3-4/kg and propofol.
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Jung et al. (2006) conducted an RCT in Healthy patients requiring tracheal intubation (n=60). Remifentanil vs. Remifentanil 1 μg/kg (with propofol) was evaluated on Clinically acceptable intubating conditions (p=<0.05). Clinically acceptable intubating conditions were achieved in 95% of patients receiving 2 or 3 μg/kg of remifentanil with propofol, compared to only 55% in those receiving 1 μg/kg (P < 0.05).
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