Thomson I R, MacAdams C L, Hudson R J, Rosenbloom M
Department of Anesthesia, St. Boniface General Hospital, University of Manitoba, Winnipeg, Canada.
Anesthesiology. 1992 Jun;76(6):922-9. doi: 10.1097/00000542-199206000-00008.
Induction of anesthesia with synthetic opioids is occasionally accompanied by undesirable hemodynamic changes such as tachycardia and hypertension, or bradycardia and hypotension. We hypothesized that drug interactions cause many of these adverse responses. Therefore, we conducted a randomized double-blind study to investigate the interactive effect of premedication and muscle relaxants on the hemodynamic response to induction with intravenous (iv) sufentanil 10 micrograms.kg-1. Eighty patients with left ventricular ejection fraction greater than or equal to 0.40, undergoing elective coronary artery surgery, were premedicated with either morphine 0.1 mg.kg-1 and scopolamine 6 micrograms.kg-1 intramuscularly, or lorazepam 60 micrograms.kg-1 orally, and paralyzed with either pancuronium 0.1 mg.kg-1 or vecuronium 0.1 mg.kg-1 iv. The four treatment groups were SP (morphine-scopolamine + pancuronium), LP (lorazepam + pancuronium), SV (morphine-scopolamine + vecuronium), and LV (lorazepam + vecuronium). Hemodynamics were recorded at three time periods: 1) control, 2) induction, and 3) intubation. Premedication-relaxant interactions significantly affected hemodynamics. In group SP, mean heart rate (HR) increased significantly on induction (56 +/- 11 to 69 +/- 13 beats.min-1), while mean arterial pressure (MAP) and cardiac index (CI) were unchanged. HR, MAP, and CI were significantly higher after induction in group SP compared to the other three groups. In group LP, mean HR increased less than in group SP (56 +/- 8 to 62 +/- 14 beats.min-1), whereas MAP and CI declined significantly. In group SV, HR and CI were unchanged, but MAP declined significantly. In group LV, HR was stable, whereas both MAP and CI declined significantly. The incidence of pharmacologic interventions during the study period also differed significantly among groups.(ABSTRACT TRUNCATED AT 250 WORDS)
使用合成阿片类药物诱导麻醉时,偶尔会伴随不良的血流动力学变化,如心动过速和高血压,或心动过缓和低血压。我们推测药物相互作用会导致许多此类不良反应。因此,我们进行了一项随机双盲研究,以调查术前用药和肌肉松弛剂对静脉注射10微克·千克-1舒芬太尼诱导的血流动力学反应的交互作用。80例左心室射血分数大于或等于0.40、接受择期冠状动脉手术的患者,术前分别接受肌内注射吗啡0.1毫克·千克-1和东莨菪碱6微克·千克-1,或口服劳拉西泮60微克·千克-1,并分别静脉注射泮库溴铵0.1毫克·千克-1或维库溴铵0.1毫克·千克-1使其麻痹。四个治疗组分别为SP(吗啡-东莨菪碱+泮库溴铵)、LP(劳拉西泮+泮库溴铵)、SV(吗啡-东莨菪碱+维库溴铵)和LV(劳拉西泮+维库溴铵)。在三个时间段记录血流动力学:1)对照,2)诱导,3)插管。术前用药-松弛剂相互作用显著影响血流动力学。在SP组,诱导时平均心率(HR)显著增加(从56±11次/分钟增至69±13次/分钟),而平均动脉压(MAP)和心脏指数(CI)未改变。与其他三组相比,SP组诱导后HR、MAP和CI显著更高。在LP组,平均HR的增加少于SP组(从56±8次/分钟增至62±14次/分钟),而MAP和CI显著下降。在SV组,HR和CI未改变,但MAP显著下降。在LV组,HR稳定,而MAP和CI均显著下降。研究期间药物干预的发生率在各组之间也有显著差异。(摘要截短于250字)