Tracheal intubating conditions using propofol and remifentanil target-controlled infusion: a comparison of remifentanil EC50 for Glidescope and Macintosh

被引:24
作者
Ithnin, F. [1 ]
Ma, Y. Li [1 ]
Shah, M. [1 ]
Shen, L. [2 ]
Sia, A. T. H. [1 ]
机构
[1] KK Womens & Childrens Hosp, Dept Womens Anaesthesia, Singapore 229899, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Level Clin Res Ctr MD 11 2, Singapore 117595, Singapore
关键词
endotracheal intubation; Glidescope; muscle relaxants; opioids; remifentanil; HEMODYNAMIC-RESPONSES; VIDEO LARYNGOSCOPE; ALFENTANIL; INDUCTION; VIDEOLARYNGOSCOPE; PHARMACOKINETICS; ANESTHESIA; SYSTEM; ADULTS; EASE;
D O I
10.1097/EJA.0b013e328324b4fc
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background and objective The combination remifentanil-propofol was used for tracheal intubation without muscle relaxant in patients with anticipated difficult airway. Using a target-controlled infusion, we compared the remifentanil concentrations required for intubation with the Macintosh laryngoscope and the Glidescope, at a constant plasma concentration of propofol without muscle relaxant. Methods Sixty ASA I or II patients were randomly assigned to either the Macintosh or Glidescope group (30 per group). A target-controlled infusion of propofol was used to maintain a predetermined effect-site concentration of 3 mu g ml(-1). The target concentration of remifentanil for each patient in a group was determined by the response of the previous patient, using increments or decrements of 0.5 ng ml(-1). Intubation was attempted at 4 min following induction to allow for equilibration between the blood and the effect site. The intubation response was graded as successful or failure by the Helbo-Hansen scoring system. The median effective concentration of remifentanil for tracheal intubation was determined using the probit regression model. Results The median effective concentration of remifentanil required for intubation with the Macintosh laryngoscope was 4.41 ng ml(-1) (3.13-5.27; 95% confidence interval) and that of the Glidescope was 5.45 ng ml(-1) (4.45-6.45; 95% confidence interval; P=0.083). There was no difference in the total intubation scores. No patients showed signs of muscle rigidity. Arterial pressures or heart rate did not differ between the groups. Conclusion There is no strong evidence that the target remifentanil concentrations required for adequate intubating conditions differed according to the technique used for intubation in the nonparalysed patient. We did not detect any major complications using this technique for either method. Eur J Anaesthesiol 26:223-228 (C) 2009 European Society of Anaesthesiology.
引用
收藏
页码:223 / 228
页数:6
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