|Trade names||Precedex, Dexdor, Dexdomitor, Sileo|
|Metabolism||Near complete hepatic metabolism to inactive metabolites|
|Biological half-life||2 hours|
|Chemical and physical data|
|Molar mass||200.28 g/mol|
|3D model (JSmol)|
Dexmedetomidine, sold under the trade names Precedex among others, is an anxiety reducing, sedative, and pain medication. Dexmedetomidine is notable for its ability to provide sedation without risk of respiratory depression (unlike other commonly used sedatives such as propofol, fentanyl, and midazolam) and can provide cooperative or semi-arousable sedation.
Similar to clonidine, it is an agonist of α2-adrenergic receptors in certain parts of the brain. Dexmedetomidine hydrochloride is also used in veterinary medicine for dogs and cats. The drug was developed by Orion Pharma.
Intensive care unit sedation
Dexmedetomidine is most often used in the intensive care setting for light to moderate sedation. It is not recommended for long term deep sedation. A unique feature of dexmedetomidine is that it has analgesic properties in addition to its role as a hypnotic, but is opioid sparing, and is therefore not associated with significant respiratory depression (unlike propofol).
Many studies suggest dexmedetomidine for sedation in mechanically ventilated adults may reduce time to extubation and ICU stay. People on dexmedetomidine are arousable and cooperative, and as such are able to actively cooperate with various procedures.
Compared with other sedatives, some studies suggest dexmedetomidine may be associated with less delirium. However, this finding is not consistent across multiple studies. At the very least, when aggregating many study results together, usage of dexmedetomidine appears to be associated with less neurocognitive dysfunction compared to other sedatives. Whether this has beneficial psychological impact is unclear. From an economic perspective, dexmedetomidine is associated with lower ICU costs. These decreased costs are largely due to a shorter time to extubation.
Dexmedetomidine can also be used as sedoanalgesic for procedural sedation, such as during colonoscopy. It can be used as an adjunct with other sedatives like benzodiazepines, opioids, and propofol to enhance sedation and help maintain hemodynamic stability by decreasing the requirement of other sedatives. Dexmedetomidine is also used for procedural sedation in children.
Dosage and administration
Intravenous infusion of dexmedetomidine is commonly initiated with a loading dose followed by a maintenance infusion. There may be great individual variability in the hemodynamic effects (especially on heart rate and blood pressure), as well as the sedative effects of this drug. For this reason, the dose must be carefully adjusted to achieve the desired clinical effect.
There are no absolute contraindications to the use of dexmedetomidine. Dexmedetomidine has a biphasic effect on blood pressure with decreased blood pressure observed at lower concentrations and elevated blood pressure at higher concentrations. Rapid IV administration or bolus has been associated with slow heart rate (bradycardia) and low blood pressure (hypotension) due to peripheral α2-receptor stimulation.
Dexmedetomidine may enhance the effects of other sedatives and anesthetics when co-administered. Similarly, drugs that lower blood pressure and heart rate, such as beta blockers, may also have enhanced effects when co-administered with dexmedetomidine.
Dexmedetomidine is a highly selective α2-adrenergic agonist. Unlike opioids and other sedatives such as propofol, dexmedetomidine is able to achieve its effects without causing respiratory depression. Dexmedetomidine induces sedation by decreasing activity of noradrenergic neurons in the locus ceruleus in the brain stem, thereby increasing the activity of inhibitory gamma-aminobutyric acid neurons in the ventrolateral preoptic nucleus. In contrast[clarification needed], other sedatives like propofol and benzodiazepines directly increase activity of gamma-aminobutyric acid neurons. Sedation by dexemeditomidine mirrors natural sleep. As such, dexmedetomidine provides less amnesia than benzodiazepines. Dexmedetomidine also has analgesic effects at the spinal cord level and other supraspinal sites. Thus, unlike other hypnotic agents like propofol, dexmedetomidine can be used as an adjunct medication to help decrease the opioid requirements of people in pain while still providing similar analgesia.
Intravenous dexmedetomidine exhibits linear pharmacokinetics with a rapid distribution half-life of approximately 6 minutes and a terminal elimination half-life of approximately 2 hours. Plasma protein binding of dexemedotomindine is ~94% (mostly albumin).
The majority of metabolized dexmedetomidine is excreted in the urine ~95%.
Dexmedetomidine was approved in 1999 by the Food and Drug Administration (FDA) as a short term sedative and analgesic (<24 hours) for critically ill or injured people on mechanical ventilation in the intensive care unit (ICU). The rationale for its use short term was due to concerns over withdrawal side effects, such as rebound high blood pressure. These withdrawal side effects have not been consistently observed in research studies, however. More recently, in 2008 the FDA expanded its indication to include nonintubated people requiring sedation for surgical or non-surgical procedures, such as colonoscopy.
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For the treatment of noise aversion in dogs