Su Peng, Li Zheng, Jia Xiaoqian, Peng Xiaoling, Liu Daiqiang, Xiao Jing, Tu Ye, Gao Feng
Department of Anesthesiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Department of Anesthesiology, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Chengdu, China.
Dose Response. 2022 Apr 9;20(2):15593258221092367. doi: 10.1177/15593258221092367. eCollection 2022 Apr-Jun.
Dexmedetomidine combined with opioids has been extensively used to blunt cardiovascular responses to endotracheal intubation. To determine their interaction, we aimed to develop a response surface model between dexmedetomidine and sufentanil.
One hundred and twenty patients undergoing scheduled gynaecological surgery were recruited. According to a simulation of slice design, patients received different dose pairs of dexmedetomidine (0 to 1.1 μg/kg) and sufentanil (.1 to .5 μg/kg). The mean arterial blood pressure and heart rate of patients were recorded just before endotracheal intubation, immediately after intubation, and during the first 3 min after intubation. The primary outcomes were haemodynamic changes. The full dose-response relationship between dexmedetomidine and sufentanil was analysed using a logit model.
This response surface model revealed that the interaction between dexmedetomidine and sufentanil was additive. The dose pairs that could effectively attenuate the haemodynamic response to endotracheal intubation primarily ranged from .3 to .4 μg/kg and .5 to 1.1 μg/kg for sufentanil and dexmedetomidine, respectively.
When used propofol as the main hypnotic drug during anaesthesia induction, dexmedetomidine could effectively reduce the requirement of sufentanil in an additive manner. However, it is not an effective drug for ablating the cardiovascular response to endotracheal intubation when used alone. The clinical trial registry. The trial registry name: Chinese Clinical Trial Registry. Registration number: ChiCTR1800015273. URL:http://www.chictr.org.cn.
右美托咪定联合阿片类药物已被广泛用于减轻气管插管引起的心血管反应。为确定它们之间的相互作用,我们旨在建立右美托咪定和舒芬太尼之间的反应表面模型。
招募120例行择期妇科手术的患者。根据模拟的析因设计,患者接受不同剂量组合的右美托咪定(0至1.1μg/kg)和舒芬太尼(0.1至0.5μg/kg)。在气管插管前、插管后即刻以及插管后最初3分钟记录患者的平均动脉血压和心率。主要结局是血流动力学变化。使用logit模型分析右美托咪定和舒芬太尼之间的完整剂量反应关系。
该反应表面模型显示右美托咪定和舒芬太尼之间的相互作用是相加性的。能有效减轻气管插管血流动力学反应的剂量组合,舒芬太尼主要为0.3至0.4μg/kg,右美托咪定主要为0.5至1.1μg/kg。
在麻醉诱导期间以丙泊酚作为主要催眠药物时,右美托咪定可通过相加的方式有效降低舒芬太尼的用量。然而,单独使用时它并不是减轻气管插管心血管反应的有效药物。临床试验注册。试验注册名称:中国临床试验注册中心。注册号:ChiCTR1800015273。网址:http://www.chictr.org.cn