Ihmsen H, Saari T I
Anästhesiologische Klinik, Universitätsklinikum Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Krankenhausstr. 12, 91054 Erlangen, Deutschland.
Anaesthesist. 2012 Dec;61(12):1059-66. doi: 10.1007/s00101-012-2114-1.
Dexmedetomidine is a highly selective, potent α₂-adrenoceptor agonist which was approved in 2011 by the European Medicines Agency for sedation of patients in intensive care units (ICU). Dexmedetomidine exhibits sedative as well as analgesic and anxiolytic effects. Recent studies suggest that dexmedetomidine may be an alternative to midazolam in long-term ICU sedation. This review summarizes the pharmacokinetics and pharmacodynamics of dexmedetomidine particularly in ICU patients and with special regard to covariate effects. Although dexmedetomidine is currently approved only for use in adults the pharmacokinetics and pharmacodynamics in children will also be addressed as there are numerous studies on this off-label use.
右美托咪定是一种高度选择性、强效的α₂肾上腺素能受体激动剂,于2011年获欧洲药品管理局批准用于重症监护病房(ICU)患者的镇静。右美托咪定具有镇静、镇痛和抗焦虑作用。近期研究表明,在ICU长期镇静中,右美托咪定可能是咪达唑仑的替代药物。本综述总结了右美托咪定的药代动力学和药效学,尤其在ICU患者中的情况,并特别关注协变量效应。尽管右美托咪定目前仅被批准用于成人,但鉴于有大量关于其超说明书使用于儿童的研究,也将探讨其在儿童中的药代动力学和药效学。