Park G R, Navapurkar V, Ferenci P
John Farman Intensive Care Unit, Addenbrooke's NHS Trust Hospital, Cambridge, UK.
Acta Anaesthesiol Scand Suppl. 1995;108:23-34. doi: 10.1111/j.1399-6576.1995.tb04376.x.
Flumazenil is a specific benzodiazepine antagonist. It competitively inhibits the action of benzodiazepines at gamma aminobutyric acid (GABA) receptors in the central nervous system and thus reverses the sedative effects of benzodiazepines. Usually, it is given intravenously as a bolus dose or as an infusion. It has a short duration of action. Flumazenil is extensively metabolized to compounds that have minimal benzodiazepine antagonistic properties. Reversal of sedation can be useful in many conditions that are often encountered in the critically ill. The adverse effects of its use are usually predictable and, with sufficient clinical monitoring, are usually avoidable. These properties make it a useful and safe drug when used appropriately.
氟马西尼是一种特异性苯二氮䓬拮抗剂。它在中枢神经系统中竞争性抑制苯二氮䓬类药物在γ-氨基丁酸(GABA)受体上的作用,从而逆转苯二氮䓬类药物的镇静作用。通常,它通过静脉推注或输注给药。其作用持续时间短。氟马西尼会广泛代谢为苯二氮䓬拮抗特性极小的化合物。在危重症患者中经常遇到的许多情况下,逆转镇静作用可能会很有用。使用它的不良反应通常是可预测的,并且通过充分的临床监测,通常是可以避免的。这些特性使其在适当使用时成为一种有用且安全的药物。