Comparison of the bispectral indices of patients receiving remimazolam and propofol for general anesthesia: a randomized crossover trial

医学 异丙酚 脑电双频指数 麻醉 养生 交叉研究 随机对照试验 临床终点 无意识 血压 麻醉药 外科 内科学 替代医学 病理 安慰剂
作者
Chen Yang,Jing Jiao,Yuyan Nie,Wenyu Shao,Hongwei Zhang,Shaoqiang Huang
出处
期刊:Anaesthesia, critical care & pain medicine [Elsevier]
卷期号:43 (3): 101377-101377
标识
DOI:10.1016/j.accpm.2024.101377
摘要

Remimazolam is a safe and effective new benzodiazepine sedative that has unique advantages in anesthesia induction and maintenance. The differences in the electroencephalogram bispectral index (BIS) during general anesthesia between propofol and remimazolam deserve further exploration. Single-center randomized crossover study. Patients who required multiple hysteroscopic surgery were randomly assigned to use remimazolam (0.27 mg/kg for induction and 1 mg/kg/h for maintenance) first and then propofol (2.0 mg/kg for induction and 6 mg/kg/h for maintenance) during hysteroscopic surgery again 3 months later, or in the opposite order. Both drugs were used at the latest ED95 for unconsciousness. The BIS values (primary endpoint), intraoperative conditions, and incidence of adverse reactions (secondary endpoints) were compared at each time point. BIS values were analyzed with a mixed model of repeated measurements (MMRM). Seventeen patients completed the study. The lowest BIS value in the remimazolam regimen was significantly higher than that in the propofol regimen (p = 0.001). The MMRM analysis of the BIS values revealed significant differences between the regimens at each time point (p < 0.001). The intraoperative diastolic blood pressure and heart rate changes were smaller, the recovery was faster, and there were fewer adverse reactions and less injection pain, but a greater incidence of intraoperative body movement and hiccups, in the remimazolam regimen. The trial indicated that remimazolam maintained a higher BIS level than propofol. The correlation between the BIS and the depth of anesthesia induced by remimazolam needs to be further studied. This trial is registered at ClinicalTrials.gov: ChiCTR2200064551
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