Rapid sequence induction and intubation with a divided dose of mivacurium compared with rocuronium: a non-inferiority clinical trial |
Received:February 13, 2022 Revised:April 03, 2023 Click here to download the full text |
Citation of this paper:LI Yu-xin,MA Yi-mei,DU Fang,SHI Yun-cen,CANG Jing,MIAO Chang-hong,ZHANG Xiao-guang.Rapid sequence induction and intubation with a divided dose of mivacurium compared with rocuronium: a non-inferiority clinical trial[J].Chinese Journal of Clinical Medicine,2023,30(3):414-420 |
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Author Name | Affiliation | E-mail | LI Yu-xin | Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai 200032, China | | MA Yi-mei | Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai 200032, China | | DU Fang | Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai 200032, China | | SHI Yun-cen | Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai 200032, China | | CANG Jing | Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai 200032, China | | MIAO Chang-hong | Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai 200032, China | | ZHANG Xiao-guang | Department of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai 200032, China Department of Anesthesiology, Jinshan Hospital, Fudan University, Shanghai 201508, China | zhang.xiaoguang@zs-hospital.sh.cn |
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Abstract:Objective To compare endotracheal intubation condition and hemodynamics during rapid sequence induction and intubation (RSII) with mivacurium in divided doses and rocuronium in routine dose, and to optimize the application of mivacurium in RSII regimen. Methods A total of 158 patients receiving elective surgery in Zhongshan Hospital, Fudan University were randomized to mivacurium group (group M, n=79) or rocuronium group (group R, n=79). Anesthesia was induced with mivacurium 0.25 mg/kg in divided doses or rocuronium 0.9 mg/kg combined with propofol, lidocaine, remifentanil, and ephedrine. The primary outcome was the excellent tracheal intubation condition rate evaluated by Cooper's scale, and the excellent rate difference was compared with the non-inferior cut-off value (-10%). The secondary outcome were changes of mean arterial pressure (MAP) and heart rate (HR) before and 10 minutes after induction (T0-10) and incidences of adverse events. Results The difference of excellent tracheal intubation condition rate was-5.06% (94.94% vs 100%; one-sided 97.5% CI-9.96%-∞), the lower limit of CI was higher than the non-inferiority margin (-10%), which satisfied the non-inferiority hypothesis (P=0.024). The MAP at T3 and the HR at T10 in group M were significantly lower than those in group R (P<0.05), but there was no significant difference in MAP and HR at other time points. Upper chest flushing occurred in 18 patients (22.8%) in group M, which was significantly higher than that in group R (2[2.5%], P<0.001). Conclusions The intubation condition under 0.25 mg/kg of mivacurium in divided doses in RSII regimen is not inferior to that under 0.9 mg/kg rocuronium, and can provide stable hemodynamic environment. |
keywords:mivacurium rocuronium rapid sequence induction and intubation neuromuscular blocking agent |
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