Department of Perioperative Services, Intensive Care and Pain Medicine, Turku University Hospital, Turku, Finland.
Anaesthesia. 2015 Feb;70(2):190-204. doi: 10.1111/anae.12868. Epub 2014 Sep 29.
Although electroencephalogram reactivity (i.e. transient changes in electrical brain activity following external stimulus) might be useful in depth-of-anaesthesia monitoring, it has not been systematically examined with different anaesthetics at doses titrated to unresponsiveness. Three 10-subject groups of healthy volunteers received dexmedetomidine, propofol or sevoflurane in escalating pseudo-steady-state concentrations at 10-min intervals until they did not open their eyes to command. The electroencephalogram was continuously recorded and spectral variables were calculated with short-time Fourier transform and time-varying autoregressive modelling. Electroencephalogram reactivity was most prominent in the midfrontal derivations (termed F3 and F4). During drug-induced unresponsiveness, electroencephalogram reactivity was still present in all drug groups. Dexmedetomidine, propofol and sevoflurane induced distinct suppression patterns on the electroencephalogram reactivity at the same clinical endpoint (unresponsiveness). Reactivity was best maintained with propofol, while only minimally preserved with dexmedetomidine and sevoflurane. Thus, it may be difficult to harness reactivity for depth-of-anaesthesia monitoring.
虽然脑电图反应性(即外部刺激后脑电活动的短暂变化)在麻醉深度监测中可能有用,但它尚未在不同剂量滴定至无反应的麻醉药物下进行系统检查。三组 10 名健康志愿者分别接受右美托咪定、丙泊酚或七氟醚,以 10 分钟的间隔递增伪稳态浓度,直到他们不能根据指令睁眼。连续记录脑电图,并使用短时傅里叶变换和时变自回归模型计算频谱变量。脑电图反应性在前额中部导联(称为 F3 和 F4)最为明显。在药物诱导的无反应性期间,所有药物组的脑电图反应性仍然存在。右美托咪定、丙泊酚和七氟醚在相同的临床终点(无反应性)下诱导出不同的脑电图反应性抑制模式。丙泊酚能最好地维持反应性,而右美托咪定和七氟醚则只能最小程度地维持反应性。因此,利用反应性进行麻醉深度监测可能很困难。