Effect of different doses of dexmedetomidine on the median effective
concentration of propofol during gastrointestinal endoscopy:a
randomized controlled trial
Abstract
Background: Dexmedetomidine could be an ideal adjuvant to propofol
during gastrointestinal endoscopy because it provides both analgesia and
sedation without respiratory depression. This study investigates the
effect of different doses of dexmedetomidine on the median effective
concentration of propofol during gastrointestinal endoscopy. Methods: 90
adult patients were randomly assigned to Group Control , Group DEX0.5
(0.5 μg/kg dexmedetomidine), or Group DEX1.0 (1.0 μg/kg dexmedetomidine)
. Anaesthesia during endoscopy was implemented by plasma
target-controlled infusion (TCI) of propofol with different doses of
dexmedetomidine. TCI concentration of the first patient for each group
was 2.5 μg/ml and the consecutive adjacent concentration gradient was
0.5 μg/mL. EC50 of TCI propofol for gastrointestinal endoscopy was
determined by using the modified Dixon’s up-and-down method.
Cardiovascular variables were also measured. Results: EC50 of TCI
propofol and 95% confidence interval (CI) for gastrointestinal
endoscopy were, 3.77 (3.48-4.09), 2.51 (2.27-2.78) and 2.10 (1.90-2.33)
μg/mL in Group Control, Group DEX0.5 and Group DEX1.0. The average
percent change from baseline in HR was 2.8 (8.9), -7.4 (7.7) and -10.5
(8.8) (P<0.001), and the average percent change from baseline in MAP
was -10.6 [-24.7; 3.5], -9.5 [-29.2; 11.4] and -4.0 [-27.3;
15.5] (P = 0.034) in Group Control, Group DEX0.5 and Group DEX1.0,
respectively. Conclusions: Dexmedetomidine reduced the EC50 of TCI
propofol. A 0.5-1 μg/kg dexmedetomidine caused a decrease in HR without
bradycardia. The decrease in dosage of propofol with increasing doses of
dexmedetomidine caused more stable MAP. Dexmedetomidine is an ideal
adjuvant drug to propofol during gastrointestinal endoscopy.