Erstad Brian L, Patanwala Asad E
Department of Pharmacy Practice & Science, College of Pharmacy, University of Arizona, 1295 N Martin Ave, PO Box 210202, Tucson, AZ, USA.
Department of Pharmacy Practice & Science, College of Pharmacy, University of Arizona, 1295 N Martin Ave, PO Box 210202, Tucson, AZ, USA.
J Crit Care. 2016 Oct;35:145-9. doi: 10.1016/j.jcrc.2016.05.016. Epub 2016 May 25.
The purpose of this narrative review is to provide practical and useful guidance for clinicians considering the use of intravenous ketamine for its analgosedative properties in adult, critically ill patients.
MEDLINE was searched from inception until January 2016. Articles related to the pharmacological properties of ketamine were retrieved. Information pertaining to pharmacology, pharmacokinetics, dosing regimens, adverse effects, and outcomes was obtained from relevant studies.
Although the primary mechanism for ketamine's pharmacological effects is N-methyl-d-aspartate blockade, there are several potential mechanisms of action. It has a very large volume of distribution due to its lipophilicity, which can lead to drug accumulation with sustained infusions. Ketamine has several advantages compared with conventional sedatives such as preserving pharyngeal and laryngeal protective reflexes, lowering airway resistance, increasing lung compliance, and being less likely to produce respiratory depression. It causes sympathetic stimulation, which is also unlike other sedatives and analgesics. There are psychotomimetic effects, which are a concern in terms of delirium. Dosing and monitoring recommendations are provided.
Ketamine has a unique pharmacological profile compared with more traditional agents such as opioids, which makes it an appealing alternative agent for analgosedation in the intensive care unit setting.
本叙述性综述的目的是为临床医生在考虑对成年重症患者使用静脉注射氯胺酮发挥其镇痛镇静特性时提供实用且有用的指导。
检索MEDLINE自创建至2016年1月的文献。检索了与氯胺酮药理特性相关的文章。从相关研究中获取了有关药理学、药代动力学、给药方案、不良反应和结果的信息。
尽管氯胺酮药理作用的主要机制是N-甲基-D-天冬氨酸受体阻断,但存在几种潜在的作用机制。由于其亲脂性,它具有非常大的分布容积,这可能导致持续输注时药物蓄积。与传统镇静剂相比,氯胺酮有几个优点,如保留咽和喉的保护性反射、降低气道阻力、增加肺顺应性以及不太可能产生呼吸抑制。它会引起交感神经兴奋,这也与其他镇静剂和镇痛药不同。存在拟精神病效应,这在谵妄方面是一个问题。提供了给药和监测建议。
与阿片类等更传统的药物相比,氯胺酮具有独特的药理学特征,这使其成为重症监护病房环境中镇痛镇静的一种有吸引力的替代药物。