利多卡因、艾司洛尔及其他:喉镜检查和插管过程中的血流动力学压力综合分析

S. A. Aasim, I.Raj Kumar Reddy, Kayyam Kiran, N. Trivikram, J.Rohith Varma
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引用次数: 0

摘要

目的:评估在喉镜检查和插管过程中利多卡因和艾司洛尔联合使用与利多卡因或艾司洛尔单独使用的血流动力学应激反应:本研究包括 60 名获得书面许可并符合纳入和排除标准的患者。根据计算机生成的随机数,选定的患者被随机分配到三组中的一组:利多卡因 1.5 毫克/千克(40 人)、艾司洛尔 2 毫克/千克(40 人)或利多卡因 1 毫克/千克和艾司洛尔 1 毫克/千克(40 人)。研究对象为年龄在20至42岁之间、在全身麻醉下进行择期手术且ASA为I级和II级的患者。患者有使用β受体阻滞剂的禁忌症,如支气管哮喘、慢性阻塞性肺病、基础心率每分钟 60 次、呼吸系统受损以及对局部麻醉剂有反应的记录:两组患者的年龄、术前心率和血压没有明显差异。男性和女性在所有组别中的分布大致相同。给药后,三组患者的心率均大幅下降(E 组 61.23±3.64,L 组 73.25±5.36,LE 组 72.23±5.36)(P<0.001)。四名 E 组患者出现心动过缓。(心率<60)。虽然 LE 组和 L 组都显示出接近基线的数值,但 L 组在第三分钟前显示出接近基线的数值,而 LE 组则显示出心率率持续下降。30 分钟后,所有三组的心率在统计学上均无差别。诱导和服用试验药物后,所有三组的收缩压、舒张压以及平均动脉血压都逐渐降低(P<0.001)。(这是收缩压)。E 组 97.36±5.69,L 组 125.39±6.36,LE 组 116.78±4.78)。E 组 60.034.69,L 组 82.935.36,LE 组 72.034.78)(E 组 72.10±3.69,L 组 96.90±3.85,LE 组 86.44±2.87)插管前,E 组患者的收缩压、舒张压和平均动脉血压均大幅下降(低于基线的 20%)。插管后,LE 组患者的血压水平在第 30 分钟前一直接近基线(P<0.001)。E 组在插管后直到第 5 分钟,三个血压读数均持续下降。第 15 分钟和第 30 分钟,E 组的血压同样接近基线。直到第 15 分钟,L 组的三项血压读数均大幅上升:因此,艾司洛尔和利多卡因合用是一种安全有效的策略,可最大限度地减少喉镜对插管和拔管的反应,降低心肌耗氧量和全身麻醉下心肌缺血的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lidocaine, Esmolol, and Beyond: A Comprehensive Analysis of Hemodynamic Stress during Laryngoscopy and Intubation
Aim: To evaluate the haemodynamic stress response  in combination of lidocaine and esmolol versus lidocaine or esmolol alone during laryngoscopy and intubation Methods: This research comprised 60 patients who provided written permission and met the inclusion and exclusion criteria. Selected patients were randomly assigned to one of three groups based on a computer-generated random number: lignocaine 1.5 mg/kg (n=40), esmolol 2mg/kg (n=40), or lignocaine 1mg/kg and esmolol 1mg/kg (n=40). This research comprised patients aged 20 to 42 who had elective procedures under general anaesthetic and had ASA I and II. Patients with contraindications to beta blockers, such as bronchial asthma, COPD, a basal heart rate of 60 beats per minute, respiratory impairment, and documented reactions to local anaesthetics. Results: There were no significant variations in age, preoperative heart rate, or blood pressure between the groups. Males and females were approximately equally dispersed throughout all groupings. Following the delivery of the test medicines, all three groups saw a substantial drop in heart rate (Group E 61.23±3.64, Group L 73.25±5.36, Group LE 72.23±5.36) (p<0.001). Four Group E patients developed bradycardia. (HR <60). Although both Group LE and Group L showed near baseline values, Group L showed near baseline values until the third minute, whereas Group LE showed a continuous reduction in heart rate rates. After 30 minutes, all three groups' heart rates were statistically insignificant. Following induction and administration of the test medicines, systolic, diastolic, and hence mean arterial blood pressure lowers gradually in all three groups (p<0.001). (This is for systolic blood pressure.). Group E 97.36±5.69, Group L 125.39±6.36, Group LE 116.78±4.78) Group E 60.034.69, Group L 82.935.36, Group LE 72.034.78) (Group E 72.10±3.69, Group L 96.90±3.85, Group LE 86.44±2.87) Before intubation, patients in Group E experienced substantial decreases in systolic, diastolic, and mean arterial blood pressure (less than 20% of baseline). Following intubation, blood pressure levels in Group LE were near baseline until the 30th minute (p<0.001). Group E had a consistent fall in all three blood pressure readings following intubation until the fifth minute. Group E's blood pressures were likewise around baseline at the 15th and 30th minutes. Until the 15th minute, Group L had a considerable rise in all three blood pressures. Conclusion: As a result, esmolol and lidocaine together are a safe and effective strategy to minimise laryngoscopy responses to intubation and extubation, lowering myocardial oxygen consumption and the risk of myocardial ischemia under general anaesthesia.
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