Anderson J A
Anesth Prog. 1988 Mar-Apr;35(2):43-7.
This paper reviews the use of prototypic drugs for reversal of the effects produced by anesthetic and sedative agents. Efficacy and toxicity information is presented for naloxone (as used to reverse opioids), physostigmine (as used for reversal of sedatives), and Flumazenil (a new specific benzodiazepine receptor antagonist). Naloxone is very useful and specific for reversing adverse and life-threatening respiratory depression caused by narcotic drugs and should be used in these situations. Physostigmime has been advocated in incremental doses for reversing sedative effects in patients who are obtunded or depressed after having received benzodiazepines, droperidol, scopolamine, opioids, and phenothiazines. Flumazenil has been shown to readily antagonize the sedative, respiratory depressant, anxiolytic, muscle relaxant, anticonvulsant, amnestic, and anesthetic effects of the benzodiazepines; it appears to have tremendous potential for use in anesthesia, conscious sedation, and emergency medicine when available.
本文综述了原型药物用于逆转麻醉药和镇静药所产生效应的情况。文中给出了纳洛酮(用于逆转阿片类药物作用)、毒扁豆碱(用于逆转镇静药作用)和氟马西尼(一种新型特异性苯二氮䓬受体拮抗剂)的疗效及毒性信息。纳洛酮对于逆转由麻醉药物引起的不良和危及生命的呼吸抑制非常有用且具有特异性,应在这些情况下使用。有人主张使用递增剂量的毒扁豆碱来逆转在接受苯二氮䓬类药物、氟哌利多、东莨菪碱、阿片类药物和吩噻嗪类药物后出现意识模糊或抑郁的患者的镇静作用。已证明氟马西尼能迅速拮抗苯二氮䓬类药物的镇静、呼吸抑制、抗焦虑、肌肉松弛、抗惊厥、遗忘和麻醉作用;当有氟马西尼可用时,它在麻醉、清醒镇静和急诊医学中似乎具有巨大的应用潜力。