Choudhary Annu, Singh Swati, Singh Swati, Alam Faseehullah, Kumar Harsh
Department of Anaesthesiology, Indira Gandhi Institute of Medical Sciences, Patna, Bihar, India.
Department of Anaesthesiology, CISRO Hospital, Patna, Bihar, India.
Indian J Anaesth. 2024 Apr;68(4):334-339. doi: 10.4103/ija.ija_884_23. Epub 2024 Mar 13.
Laryngoscopy and tracheal intubation require an adequate depth of anaesthesia. The study's primary objective was to compare the time needed to achieve the bispectral index (BIS)-guided adequate depth of anaesthesia for endotracheal intubation using fentanyl and dexmedetomidine.
After institutional ethics committee clearance and written informed consent, this randomised study was conducted on 140 patients of either gender between 18 and 60 years who were scheduled for elective surgeries under general anaesthesia. Patients were randomised to intravenous dexmedetomidine 1 μg/kg (Group D) or fentanyl 2 μg/kg (Group F). The drugs were given as an intravenous infusion over 10 min before induction of anaesthesia. The primary outcome was the time required to achieve BIS 50. Normally distributed variables were compared using Student's test, and non-normally distributed variables were compared using the Mann-Whitney U test. Qualitative data were analysed using Chi-square/Fisher's exact test. A value <0.05 was considered significant.
The time to achieve BIS 50 was lesser in Group F, 1546 (27) as compared to Group D, 1558 (11) s [mean difference (95% confidence interval (CI) 12[5.11, 18.89]), < 0.001]. Haemodynamic parameters were comparable at all time points between both the groups, except heart rate, which was significantly lower. Propofol consumption was significantly less in group D than in group F [125.9 (25.36) versus 157.3 (42.80) mg, respectively, mean difference (95% CI) 31.4 (-44.16 to -20.63) < 0.001)].
Dexmedetomidine achieves BIS 50 faster and has a propofol-sparing effect as compared to fentanyl.
喉镜检查和气管插管需要足够的麻醉深度。本研究的主要目的是比较使用芬太尼和右美托咪定达到双谱指数(BIS)引导下气管插管所需的足够麻醉深度的时间。
经机构伦理委员会批准并获得书面知情同意后,对140例年龄在18至60岁之间、计划接受全身麻醉下择期手术的患者进行了这项随机研究。患者被随机分为静脉注射右美托咪定1μg/kg组(D组)或芬太尼2μg/kg组(F组)。在麻醉诱导前10分钟内通过静脉输注给予药物。主要结局是达到BIS 50所需的时间。使用学生检验比较正态分布变量,使用曼-惠特尼U检验比较非正态分布变量。使用卡方/费舍尔精确检验分析定性数据。P值<0.05被认为具有统计学意义。
F组达到BIS 50的时间较短,为1546(27)秒,而D组为1558(11)秒[平均差异(95%置信区间(CI))为12[5.11, 18.89],P<0.001]。除心率显著较低外,两组在所有时间点的血流动力学参数均具有可比性。D组丙泊酚消耗量显著低于F组[分别为125.9(25.36)mg和157.3(42.80)mg,平均差异(95%CI)为31.4(-44.16至-20.63),P<0.001]。
与芬太尼相比,右美托咪定能更快达到BIS 50,且具有节省丙泊酚的作用。