Abstract

Objective. The incidence of propofol injection pain during induction of general anesthesia varies from 28% to 90%. This prospective, randomized, double-blind, placebo-controlled study evaluated the effect of dexmedetomidine (DEX) for reducing the incidence and severity of propofol injection pain.Methods. Patients undergoing elective surgical procedures were randomly allocated into seven groups of 30 patients each. Experimental treatments were intravenously administered over 10 min (total volume 10 mL) prior to intravenous propofol injection, as follows: group I, the control group, was given isotonic saline. Patients in groups II, III, and IV received DEX 0.25 µg/kg, 0.5 µg/kg, or 1.0 µg/kg, respectively, mixed with isotonic saline immediately before propofol injection. Patients in groups V, VI, and VII received DEX as above, but 5 minutes before propofol injection. Propofol consisted of 1% long-chain triglyceride propofol (2.5 mg/kg) injected at 1 mL/s.Results. Median propofol injection pain score was 0.00 (IQR 0.00–3.00) in patients who received 1.0 µg/kg DEX 5 min before the propofol injection (group VII), and only 1 patient (of 30) in this group received a pain score >2. The median pain score and number of patients with pain scores >2 in group VII were both significantly less than in the control (group I; p = 0.000, both). There were no differences in either mean arterial pressure or heart rate at any time point after DEX injection among the groups.Conclusions. Pretreatment with intravenous DEX 1 µg/kg 5 min prior to injection of long-chain triglyceride propofol is effective and safe in reducing the incidence and severity of pain due to propofol injection.

Highlights

  • Propofol is widely administered during anesthetic induction

  • There was no difference in median propofol injection pain scores among groups I (3.00 (IQR 2.00– 4.00)), II, III, V, and VI

  • There were no differences between the groups as regards Mean arterial pressure (MAP) and heart rate (HR) at any time point after DEX injection (p > 0.05, detailed data not shown). This prospective, randomized, double-blind, placebo-controlled study was carried out in order to evaluate the effect of DEX for reducing the incidence and severity of propofol injection pain

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Summary

Introduction

Propofol is widely administered during anesthetic induction. the pain of injection is undesirable, and may cause hand withdrawal and dislodging of the venous cannula [1,2]. The incidence of propofol injection pain varies from 28% to 90% [3]. Many methods have been used to relieve the pain of propofol injection, such as pretreatment with lidocaine, ondansetron, and methylene blue, but the effectiveness of these methods remains uncertain [4,5,6,7,8]. The alpha-2 adrenoceptor agonist clonidine was found to alleviate the pain of injected propofol effectively [9]. Dexmedetomidine (DEX; Jiangsu Singch Pharmaceutical, Lianyungang, Jiangsu province, China) is an alpha-2 adrenoceptor agonist, but is more selective than clonidine and has analgesic and sedative properties [2]. DEX has been evaluated for reducing the incidence and intensity of propofol-induced pain, but reported results are inconsistent [1,2]

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