Comparison of EEG Burst Suppression and Hemodynamic Effects Between Remimazolam Tosilate and Etomidate During General Anesthesia Induction: A Retrospective Analysis.

IF 5.1 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-09-03 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S528483
Ying Cao, Mi Gan, Linling Wan, Jun Lu, Ting Liu, Meiyan Liu, Di Wang, Sen Hong, Lin Zhou, Luying Deng, Zijun Wang, Jingjie Wang, Changyu Sun, Yang Liu, Yanqiu Liu, Meiwu Zhou
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引用次数: 0

Abstract

Background: Remimazolam tosilate, a novel ultra-short-acting benzodiazepine, demonstrates promising safety profiles in clinical settings. While both remimazolam tosilate and etomidate provide hemodynamic stability during anesthesia induction, limited research has directly compared their effects on electroencephalogram (EEG) burst suppression (periods of transient brain wave silence), a potential predictor of adverse neurological outcomes. This study aims to compare the incidence rate of EEG burst suppression (ESR) with remimazolam tosilate versus etomidate by reviewing the drug regimens used by different anesthesiologists in clinical practice.

Methods: This single-center retrospective study analyzed clinical anesthesia induction data from 161 patients from October 2023 to July 2024. Patients received either remimazolam tosilate (0.2 mg/kg, n=86, Group R) or etomidate (0.3 mg/kg, n=75, Group E) for general anesthesia induction. Primary outcomes included ESR and its duration during induction. Second outcomes comprised hemodynamic parameters: systolic blood pressure, diastolic blood pressure mean arterial pressure, and heart rate, measured at baseline (T0), 3 minutes post-induction (T1), immediately after intubation (T2), 5 minutes post-intubation (T3), 10 minutes post-intubation (T4), and adverse events occurrence.

Results: Baseline characteristics were comparable except ASA classification (higher ASA III proportion in Group R: 24.4% vs 2.7%, P<0.001). No ESR occurred in Group R versus 29.34% in Group E (P<0.01). Group R had a significantly lower incidence of intubation-related hypertension (10.5% vs 42.7%, P<0.001) and maintained stable blood pressure and HR throughout induction, whereas Group E exhibited marked MAP and HR fluctuations. Other adverse events showed no significant inter-group differences.

Conclusion: Remimazolam tosilate demonstrated notable differences compared to etomidate during general anesthesia induction, including the absence of ESR and different hemodynamic response patterns. While these findings suggest potential advantages for certain patient populations, the retrospective design and ASA classification imbalance limit definitive conclusions, warranting prospective validation studies.

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全麻诱导时雷马唑仑与依托咪酯对脑电图爆发抑制及血流动力学影响的回顾性分析。
背景:托silate Remimazolam是一种新型超短效苯二氮卓类药物,在临床环境中显示出良好的安全性。虽然雷马唑仑和依咪酯在麻醉诱导过程中都能提供血流动力学稳定性,但有限的研究直接比较了它们对脑电图(EEG)爆发抑制(短暂脑电波沉默期)的影响,这是不良神经系统预后的潜在预测指标。本研究旨在通过回顾不同麻醉医师在临床实践中使用的药物方案,比较雷马唑仑与依托咪酯的脑电图爆发抑制(ESR)发生率。方法:本研究为单中心回顾性研究,分析2023年10月至2024年7月161例患者的临床麻醉诱导资料。患者接受雷马唑仑(0.2 mg/kg, n=86, R组)或依托咪酯(0.3 mg/kg, n=75, E组)全麻诱导。主要结局包括ESR及其诱导持续时间。第二个结果包括血流动力学参数:收缩压、舒张压、平均动脉压和心率,分别在基线(T0)、诱导后3分钟(T1)、插管后立即(T2)、插管后5分钟(T3)、插管后10分钟(T4)和不良事件发生时测量。结果:除ASA分类(R组ASA III比例较高:24.4% vs 2.7%)外,基线特征具有可比性。结论:在全麻诱导过程中,雷马唑仑与乙咪酯相比存在显著差异,包括无ESR和不同的血流动力学反应模式。虽然这些发现表明对某些患者群体有潜在的优势,但回顾性设计和ASA分类不平衡限制了明确的结论,需要前瞻性验证研究。
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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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