Janik R, Dick W
Klinik für Anaesthesiologie, Johannes Gutenberg-Universität Mainz.
Anaesthesist. 1989 Dec;38(12):673-80.
A lack of uniform methodology used in the assessment of moderate doses of sufentanil in combination with non-depolarizing neuromuscular blocking drugs formed the basis of the current study which compared under randomized conditions the effects of sufentanil-pancuronium versus sufentanil-vecuronium on hemodynamics, intubating conditions and chest wall rigidity during induction of anesthesia. MATERIAL and METHODS. One hundred and twenty ASA physical status I and II patients aged between 20 and 40 years of age who were undergoing elective urological surgery were included in the study. Premedication consisted of 0.15 mg kg-1 diazepam, given orally 60 min prior to induction of anesthesia. Patients were randomly divided into eight groups of 15 each to receive 0.5 microgram kg-1 sufentanil or placebo in combination with pancuronium (groups I-IV) or vecuronium (groups V-VIII) Within each group, patients were randomly allocated to receive the relaxant either as a single bolus dose of 0.095 mg kg-1 pancuronium or 0.1 mg kg-1 vecuronium, or in divided doses (the priming principle), the smaller priming dose (0.015 mg kg-1 pancuronium or 0.015 mg kg-1 vecuronium) being administered 2 min before induction of anesthesia with 5 mg kg-1 thiopentone, followed by the second intubating dose of 0.080 mg kg-1 pancuronium or 0.085 mg kg-1 vecuronium. To maintain blind study conditions in the groups, the patients given the relaxants in one dose were given an equivalent volume of saline 2 min prior before 5 mg kg-1 thiopentone. Intubating was attempted 60 s after administration of the main dose of the relaxant, and conditions were assessed on a four-point scale: excellent, satisfactory, fair, or poor. Neuromuscular transmission was monitored with the Datex Relaxograph, a neuromuscular transmission analyzer, that utilizes the integration of the EMG response. Producing train-of-four (TOF) stimuli, with a pulse width of 100 microseconds and a frequency of 2 Hz every 20 s the following parameters were recorded by the Datex Relaxograph: The percentage of first twitch amplitude compared with the reference (T1), and the train-of-four (TOF) ratio, i.e., the ratio of last twitch height to first height. Measurements were taken after premedication in the operating room, the value which served as a baseline (t0), 1 min after sufentanil or placebo (t1), 1 min after priming or placebo (t2), 1 min after thiopentone (t3), and 1 min after intubation (t4).(ABSTRACT TRUNCATED AT 400 WORDS)
在评估中等剂量舒芬太尼与非去极化神经肌肉阻滞药物联合使用时,缺乏统一的方法,这构成了本研究的基础。本研究在随机条件下比较了舒芬太尼 - 潘库溴铵与舒芬太尼 - 维库溴铵在麻醉诱导期间对血流动力学、插管条件和胸壁强直的影响。材料与方法。本研究纳入了120例年龄在20至40岁之间、美国麻醉医师协会(ASA)身体状况为I级和II级、正在接受择期泌尿外科手术的患者。麻醉前用药为术前60分钟口服0.15mg/kg地西泮。患者被随机分为8组,每组15人,分别接受0.5μg/kg舒芬太尼或安慰剂与潘库溴铵(I - IV组)或维库溴铵(V - VIII组)联合使用。在每组中,患者被随机分配接受0.095mg/kg潘库溴铵或0.1mg/kg维库溴铵的单次推注剂量,或采用分次给药(预注原则),较小的预注剂量(0.015mg/kg潘库溴铵或0.015mg/kg维库溴铵)在使用5mg/kg硫喷妥钠诱导麻醉前2分钟给药,随后给予第二次插管剂量0.080mg/kg潘库溴铵或0.085mg/kg维库溴铵。为保持各组的盲法研究条件,单次给药组的患者在使用5mg/kg硫喷妥钠前2分钟给予等量的生理盐水。在给予主要剂量的松弛剂后60秒尝试插管,并根据四点量表评估插管条件:优、良、中、差。使用Datex Relaxograph(一种神经肌肉传递分析仪)监测神经肌肉传递,该仪器利用肌电图反应的积分。每20秒产生一次四个成串刺激(TOF),脉冲宽度为100微秒,频率为2Hz,Datex Relaxograph记录以下参数:与参考值相比的第一个颤搐幅度百分比(T1)以及四个成串刺激(TOF)比值,即最后一个颤搐高度与第一个高度的比值。在手术室进行麻醉前用药后、舒芬太尼或安慰剂给药后1分钟(t1)、预注或安慰剂给药后1分钟(t2)、硫喷妥钠给药后1分钟(t3)以及插管后1分钟(t4)进行测量。(摘要截断于400字)