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右美托咪定:现状与未来方向。

Dexmedetomidine: present and future directions.

机构信息

Department of Anesthesiology and Pain Medicine, Chonnam National University Medical School & Hospital, Gwangju, Korea.

出版信息

Korean J Anesthesiol. 2019 Aug;72(4):323-330. doi: 10.4097/kja.19259. Epub 2019 Jun 21.

Abstract

Dexmedetomidine is a potent, highly selective α-2 adrenoceptor agonist, with sedative, analgesic, anxiolytic, sympatholytic, and opioid-sparing properties. Dexmedetomidine induces a unique sedative response, which shows an easy transition from sleep to wakefulness, thus allowing a patient to be cooperative and communicative when stimulated. Dexmedetomidine may produce less delirium than other sedatives or even prevent delirium. The analgesic effect of dexmedetomidine is not strong; however, it can be administered as a useful analgesic adjuvant. As an anesthetic adjuvant, dexmedetomidine decreases the need for opioids, inhalational anesthetics, and intravenous anesthetics. The sympatholytic effect of dexmedetomidine may provide stable hemodynamics during the perioperative period. Dexmedetomidine-induced cooperative sedation with minimal respiratory depression provides safe and acceptable conditions during neurosurgical procedures in awake patients and awake fiberoptic intubation. Despite the lack of pediatric labelling, dexmedetomidine has been widely studied for pediatric use in various applications. Most adverse events associated with dexmedetomidine occur during or shortly after a loading infusion. There are some case reports of dexmedetomidine-related cardiac arrest following severe bradycardia. Some extended applications of dexmedetomidine discussed in this review are promising, but still limited, and further research is required. The pharmacological properties and possible adverse effects of dexmedetomidine should be well understood by the anesthesiologist prior to use. Moreover, it is necessary to select patients carefully and to determine the appropriate dosage of dexmedetomidine to ensure patient safety.

摘要

右美托咪定是一种强效、高选择性的α-2 肾上腺素受体激动剂,具有镇静、镇痛、抗焦虑、交感神经抑制和阿片类药物节约作用。右美托咪定诱导出一种独特的镇静反应,表现为易于从睡眠向清醒状态过渡,从而使患者在受到刺激时能够合作和交流。与其他镇静剂相比,右美托咪定可能产生更少的谵妄,甚至可以预防谵妄。右美托咪定的镇痛作用不强;然而,它可以作为一种有用的镇痛辅助剂使用。作为麻醉辅助剂,右美托咪定减少了对阿片类药物、吸入性麻醉剂和静脉麻醉剂的需求。右美托咪定的交感神经抑制作用可在围手术期提供稳定的血流动力学。右美托咪定诱导的合作性镇静作用伴有最小的呼吸抑制,为清醒患者的神经外科手术和清醒纤维支气管镜检查提供了安全可接受的条件。尽管缺乏儿科标签,但右美托咪定已广泛研究用于各种儿科应用。与右美托咪定相关的大多数不良事件发生在负荷输注期间或之后不久。有一些关于右美托咪定相关心搏骤停的病例报告,这些病例与严重心动过缓有关。右美托咪定的一些扩展应用在本文中进行了讨论,这些应用具有很大的前景,但仍有限,需要进一步研究。在使用之前,麻醉师应该充分了解右美托咪定的药理学特性和可能的不良反应。此外,有必要仔细选择患者,并确定右美托咪定的适当剂量,以确保患者的安全。

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