Feng Lin, Zeng Liang, Zhou Xuelei, Guo Yiping, Liu Xianchun, Zhang Longyi, Zhang Ting, Li Linji, Zhao Li
Department of Anesthesiology, The Second Clinical Medical College, North Sichuan Medical College, Beijing Anzhen Nanchong Hospital of Capital Medical University & Nanchong Central Hospital, Nanchong, China.
Nanchong Center for Disease Control and Prevention, Nanchong, China.
Sci Rep. 2025 Jul 2;15(1):23635. doi: 10.1038/s41598-025-08907-1.
To determine the median effective dose (ED50) and 95% effective dose (ED95) of sufentanil combined with remimazolam for inhibiting the tracheal intubation response in patients undergoing general anesthesia and to evaluate the hemodynamic stability and adverse events associated with this drug combination. This prospective dose-finding study used Dixon's up-and-down sequential allocation method. A total of 36 patients undergoing general anesthesia surgery between April 2024 and June 2024 were enrolled. Patients were administered remimazolam for induction, followed by sufentanil at an initial dose of 0.4 µg/kg, with subsequent doses adjusted based on the presence or absence of an intubation response. The primary outcome was the ED50 of sufentanil combined with remimazolam, and the secondary outcomes included patient baseline characteristics, hemodynamic parameters, and adverse events. The ED50 and ED95 of sufentanil for inhibiting tracheal intubation response were 0.374 µg/kg (95% CI: 0.342-0.402 µg/kg) and 0.436 µg/kg (95% CI: 0.406-0.586 µg/kg), respectively. Patients with a positive tracheal intubation response had significantly higher heart rates and mean arterial pressures and a higher incidence of hypertension. The ED50 and ED95 of sufentanil combined with remimazolam for inhibiting the tracheal intubation response in patients undergoing general anesthesia were 0.374 and 0.436 µg/kg, respectively. This study provides valuable insights into the dosing of these drugs for effective anesthesia induction and hemodynamic control during tracheal intubation.
确定舒芬太尼联合瑞马唑仑抑制全身麻醉患者气管插管反应的半数有效剂量(ED50)和95%有效剂量(ED95),并评估该药物组合相关的血流动力学稳定性和不良事件。这项前瞻性剂量探索研究采用了狄克逊上下序贯分配法。纳入了2024年4月至2024年6月期间接受全身麻醉手术的36例患者。患者先接受瑞马唑仑诱导,随后给予初始剂量为0.4μg/kg的舒芬太尼,后续剂量根据是否存在插管反应进行调整。主要结局是舒芬太尼联合瑞马唑仑的ED50,次要结局包括患者基线特征、血流动力学参数和不良事件。舒芬太尼抑制气管插管反应的ED50和ED95分别为0.374μg/kg(95%CI:0.342 - 0.402μg/kg)和0.436μg/kg(95%CI:0.406 - 0.586μg/kg)。气管插管反应阳性的患者心率和平均动脉压显著更高,高血压发生率也更高。舒芬太尼联合瑞马唑仑抑制全身麻醉患者气管插管反应的ED50和ED95分别为0.374和0.