Laurito C E, Baughman V L, Becker G L, DeSilva T W, Carranza C J
Department of Anesthesiology, Michael Reese Hospital and Medical Center, Chicago, IL 60616.
J Clin Anesth. 1991 May-Jun;3(3):186-93. doi: 10.1016/0952-8180(91)90157-i.
To determine the effects of oral clonidine premedication on sedative, anxiolytic, and hemodynamic responses during the immediate preoperative period, laryngoscopy/intubation, and postanesthetic recovery.
Randomized double-blind assignment to one of four treatment groups (clonidine 0.1 mg, clonidine 0.2 mg, triazolam 0.25 mg, or placebo); n = 10 per group.
Inpatient surgery in a university-staffed tertiary center.
Forty ASA physical status I and II adults of both sexes scheduled for a variety of procedures requiring general anesthesia.
Anxiety and sedation scored on ordinal scale at time of treatment and 90 minutes later, just prior to anesthetic induction. Standardized induction protocol with automated hemodynamic monitoring at 1-minute intervals and a 45-second laryngoscopy to ensure a vigorous stress response.
Triazolam and both doses of clonidine increased sedation at 90 minutes both absolutely and compared with a placebo. Clonidine 0.2 mg decreased anxiety absolutely at 90 minutes but no more than a placebo. Clonidine 0.2 mg decreased systolic, mean, and diastolic blood pressures (BPs) but not heart rate (HR) at 90 minutes. Clonidine 0.2 mg also blunted the increase in systolic blood pressure (SP) [but not in diastolic blood pressure (DP) or HR] that accompanied laryngoscopy. There were no treatment differences in postanesthetic hemodynamics or duration of recovery.
Oral clonidine 0.2 mg was effective in reducing the level of behavioral and hemodynamic responses preoperatively and in blunting systolic hypertension produced by prolonged laryngoscopy.
确定术前即刻、喉镜检查/插管及麻醉后恢复期间口服可乐定预处理对镇静、抗焦虑及血流动力学反应的影响。
随机双盲分为四个治疗组之一(可乐定0.1毫克、可乐定0.2毫克、三唑仑0.25毫克或安慰剂);每组n = 10。
大学附属三级中心的住院手术。
40名美国麻醉医师协会(ASA)身体状况为I级和II级的成年男女,计划进行各种需要全身麻醉的手术。
治疗时及90分钟后、麻醉诱导前,采用序数量表对焦虑和镇静程度进行评分。采用标准化诱导方案,每隔1分钟进行自动血流动力学监测,并进行45秒的喉镜检查,以确保出现强烈的应激反应。
与安慰剂相比,三唑仑和两种剂量的可乐定在90分钟时均绝对增加了镇静程度。可乐定0.2毫克在90分钟时绝对降低了焦虑程度,但降幅不超过安慰剂。可乐定0.2毫克在90分钟时降低了收缩压、平均动脉压和舒张压,但未降低心率。可乐定0.2毫克还减弱了喉镜检查时伴随的收缩压升高(但舒张压和心率未升高)。麻醉后血流动力学或恢复持续时间方面无治疗差异。
口服可乐定0.2毫克可有效降低术前行为和血流动力学反应水平,并减弱长时间喉镜检查引起的收缩期高血压。