Key result
Intravenous fentanyl 2 micrograms kg-1 attenuated increases in heart rate and blood pressure during tracheal extubation more effectively than 1 microgram kg-1 or saline.
Why the study?
Does intravenous fentanyl attenuate cardiovascular responses during tracheal extubation in patients undergoing elective gynecological surgery?
RCT (n=60)
Double-blind
randomized
Does intravenous fentanyl attenuate cardiovascular responses during tracheal extubation in patients undergoing elective gynecological surgery?
A bolus dose of intravenous fentanyl 2 micrograms kg-1 at peritoneal closure effectively attenuates cardiovascular changes during tracheal extubation without prolonging recovery.
Supports 2 μg/kg fentanyl at peritoneal closure to blunt extubation hemodynamics without delaying recovery; extends RCT evidence on opioid dosing for airway management.
We carried out a controlled, randomized, double-blind study to examine the effects of intravenous fentanyl (1 or 2 micrograms kg-1) on hemodynamic changes during tracheal extubation and emergence from anesthesia in 60 ASA physical status I or II patients undergoing elective gynecological surgery. Anesthesia was maintained with 0.5%-1.5% isoflurane and 60% nitrous oxide (N2O) in oxygen. Muscle relaxation was achieved with vecuronium. The patients were randomly assigned to three group (each, n = 20), and fentanyl (1 or 2 micrograms kg-1), or saline (as a control) was given at the time of peritoneal closure. Changes in heart rate (HR) and blood pressure (BP) were measured during and after tracheal extubation. Adverse effects, including postoperative sedation and respiratory depression, were also assessed. The HR, systolic BP, and diastolic BP increased significantly during tracheal extubation in the control group (P < 0.05). Fentanyl 2 micrograms kg-1 attenuated the increases in these variables more effectively than fentanyl 1 microgram kg-1. The time interval from the study drug to extubation was similar in each group. Postoperative somnolence and respiratory depression were not observed in any patients in any of the three groups. We concluded that a bolus dose of intravenous fentanyl 2 micrograms kg-1 given at the time of peritoneal closure was of value in attenuating the cardiovascular changes associated with tracheal extubation and emergence from anesthesia, and that this treatment did not prolong the recovery. However, further studies are required to assess this technique in patients with cardiovascular or cerebrovascular diseases.
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Nishina et al. (1995) conducted an RCT in Elective gynecological surgery (n=60). Intravenous fentanyl vs. Saline was evaluated on Changes in heart rate (HR) and blood pressure (BP) during and after tracheal extubation (p=<0.05). Intravenous fentanyl 2 micrograms kg-1 attenuated increases in heart rate and blood pressure during tracheal extubation more effectively than 1 microgram kg-1 or saline.
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