2005
DOI: 10.1097/01.aco.0000174958.05383.d5
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Dexmedetomidine in anaesthesia

Abstract: Dexmedetomidine offers beneficial pharmacological properties, providing dose-dependent sedation, analgesia, sympatholysis and anxiolysis without relevant respiratory depression. The side-effects are predictable from the pharmacological profile of (2-adrenoceptor agonists. In particular, the unique sedative properties of dexmedetomidine resulted in several interesting applications in anaesthesia practice, promising benefits in the perioperative use of this compound. However, dexmedetomidine was approved for sed… Show more

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Cited by 191 publications
(134 citation statements)
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“…Dexmedetomidine is a relatively new drug which has potent sympatholytic, analgesic, and sedative properties mediated through α 2-adrenoceptors in the central and peripheral nervous systems (Bekker and Sturaitis 2005;Paris and Tonner 2005). It has become increasingly popular among anesthesiologists and intensive care physicians as an adjuvant to the classical regimen of anesthesia techniques (Paris and Tonner 2005).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Dexmedetomidine is a relatively new drug which has potent sympatholytic, analgesic, and sedative properties mediated through α 2-adrenoceptors in the central and peripheral nervous systems (Bekker and Sturaitis 2005;Paris and Tonner 2005). It has become increasingly popular among anesthesiologists and intensive care physicians as an adjuvant to the classical regimen of anesthesia techniques (Paris and Tonner 2005).…”
Section: Discussionmentioning
confidence: 99%
“…It has become increasingly popular among anesthesiologists and intensive care physicians as an adjuvant to the classical regimen of anesthesia techniques (Paris and Tonner 2005). Also, it has been shown to reduce the anesthetic and analgesic requirements in animals and humans (Khan et al 1999;Dutta et al 2001).…”
Section: Discussionmentioning
confidence: 99%
“…Dexmedetomidine is one of the most frequently applied intravenous pharmacs used for sedation in ICUs. It is a non-benzodiazepine, highly selective alpha 2 -adrenergic agonist which links itself to the transmembrane g protein alpha 2a, alpha 2b and alpha 2c of the peripheral, cerebral and spinal adrenoreceptors [33]. Unlike other sedatives dexmedetomidine, by acting on the alpha 2 receptors of locus coeruleus [34], causes an-algesia [35] without the risk of breathing depression [36,37].…”
Section: Discussionmentioning
confidence: 99%
“…However, dexmedetomidine was approved for sedation in the Intensive care unit in the USA in 1999 and administration in anaesthesia practice remains an 'offlabel' use. Further studies are needed to establish the role of dexmedetomidine in the perioperative period [16].…”
Section: Discussionmentioning
confidence: 99%