Sear J W
Nuffield Department of Anaesthetics, John Radcliffe Hospital, Headington, Oxford, England.
Drugs. 1992 Jan;43(1):54-68. doi: 10.2165/00003495-199243010-00006.
General anaesthesia is the reversible depression of central nervous system function. There is still no agreement over what constitutes depth of anaesthesia, and the clinical anaesthetist must thus titrate drug input according to clinical signs (heart rate, blood pressure, somatic movement, autonomic responses). The potency of inhalational agents may be expressed in terms of the MAC (minimum alveolar concentration); comparable end-points (including blood concentrations) have been proposed for the intravenous agents. Kinetic infusion regimens can be constructed for the intravenous agents to achieve the ED95 concentrations required to provide clinically adequate anaesthesia. However, because of individual differences in drug kinetics and dynamics, as well as the influences of disease states and intercurrent therapy, the clinician will titrate the dose according to response. Administration of volatile or intravenous anaesthetics by fixed regimens may result in either overdosage or the risk of patient awareness. The choice of anaesthetic drug is usually based on the nonhypnotic side effects of the different agents--including their central and regional cardiovascular effects, the speed and completeness of recovery, and the need to provide intraoperative analgesia. In addition, special techniques and drugs are often needed for neurosurgical, cardiothoracic and obstetric anaesthesia. All anaesthetic agents (inhalation and intravenous) have other side effects (such as cardiorespiratory depression and organ toxicity related to the liver or kidney). Both halothane and enflurane may be responsible for postoperative hepatic dysfunction, while the metabolism of enflurane can also result in nephrotoxicity in patients with pre-existing renal dysfunction. Isoflurane has been reported to cause 'coronary steal' in patients with ischaemic heart disease through its coronary vasodilator properties.(ABSTRACT TRUNCATED AT 250 WORDS)
全身麻醉是中枢神经系统功能的可逆性抑制。目前对于麻醉深度的构成仍未达成共识,因此临床麻醉医生必须根据临床体征(心率、血压、躯体运动、自主反应)来调整药物输入量。吸入性麻醉药的效能可以用MAC(最低肺泡浓度)来表示;对于静脉麻醉药也提出了类似的终点指标(包括血药浓度)。可以为静脉麻醉药构建动力学输注方案,以达到提供临床充分麻醉所需的ED95浓度。然而,由于药物动力学和药效学的个体差异,以及疾病状态和并发治疗的影响,临床医生会根据反应来调整剂量。采用固定方案给予挥发性或静脉麻醉药可能会导致用药过量或患者术中知晓的风险。麻醉药物的选择通常基于不同药物的非催眠副作用——包括它们对中枢和局部心血管的影响、恢复的速度和完全程度,以及提供术中镇痛的需求。此外,神经外科、心胸外科和产科麻醉通常还需要特殊技术和药物。所有麻醉药(吸入性和静脉性)都有其他副作用(如心肺抑制以及与肝或肾相关的器官毒性)。氟烷和恩氟烷都可能导致术后肝功能障碍,而恩氟烷的代谢在已有肾功能不全的患者中还可能导致肾毒性。据报道,异氟烷因其冠状动脉扩张特性可导致缺血性心脏病患者出现“冠状动脉窃血”。(摘要截选于250词)