Buccal, Sublingual Acute agitation associated with bipolar I or II disorder, Acute agitation associated with schizophrenia
Adult: Mild to moderate agitation: Initially, 120 mcg. If agitation persists, may give additional 2 doses of 60 mcg at least 2 hours apart. Max: 240 mcg daily. Severe agitation: Initially, 180 mcg. If agitation persists, may give additional 2 doses of 90 mcg at least 2 hours apart. Max: 360 mcg daily. Elderly: >65 years Initially, 120 mg. If agitation persists, may give additional 2 doses of 60 mcg at least 2 hours apart Max: 240 mcg daily.
Intravenous Sedation in critical care
Adult: Initially, 1 mcg/kg infused over 10 minutes followed by maintenance infusion of 0.2-0.7 mcg/kg/hour to achieve desired level of sedation. Max infusion duration: 24 hours. Elderly: >65 years Dose reduction may be needed.
Intravenous Sedation in minor surgical and medical procedures
Adult: Initially, 0.5-1 mcg/kg infused over 10 minutes followed by continuous infusion of 0.2-1 microgram/kg/hour; titrate dose to desired level of sedation. Elderly: >65 years Initially, 0.05 mcg/kg infused over 10 minutes.
Hepatic Impairment
Intravenous:
Dose reduction may be needed.
Sublingual/Buccal:
Mild to moderate (Child-Pugh Class A or B): Initially, 90 mcg (mild to moderate agitation); 120 mcg (severe agitation). If agitation persists, may give additional 2 doses of 60 mcg at least 2 hours apart. Max: 210 mcg (mild to moderate agitation); 240 mcg daily (severe agitation). Severe impairment (Child-Pugh Class C): Initially, 60 mcg (mild to moderate agitation); 90 mcg (severe agitation). If agitation persists, may give additional 2 doses of 60 mcg at least 2 hours apart. Max: 180 mcg (mild to moderate agitation); 210 mcg daily (severe agitation).
Reconstitution
Dilute vial labelled as containing 100 mcg/mL in NaCl 0.9% solution for inj to a final concentration of 4 mcg/mL.
This drug may occasionally cause dizziness or drowsiness, if affected, do not drive or operate machinery for at least 8 hours after administration.
Monitoring Parameters
Monitor cardiac and respiratory function, level of sedation, blood pressure, pain control.
Overdosage
Symptoms: Bradycardia, hypertension (more prominent), hypotension, oversedation, somnolence, first degree atrioventricular block, second degree heart block, cardiac arrest. Management: Symptomatic treatment. Treat sinus arrest with atropine and glycopyrrolate.
Drug Interactions
Enhanced pharmacologic effects with anaesthetics, sedatives, hypnotics, opioids.
Action
Description: Mechanism of Action: Dexmedetomidine is a selective α2-adrenoceptor agonist with anxiolytic, anaesthetic, and sedative properties. Its action is thought to be due to the activation of G-proteins by α2a-adrenoceptors in the brainstem, resulting in inhibition of norepinephrine release in the sympathetic nerve endings. Onset: 5-10 minutes. Duration: 60-240 minutes. Pharmacokinetics: Distribution: Crosses the placenta, enters breast milk. Volume of distribution: Approx 118 L. Plasma protein binding: Approx 94%, mainly to albumin. Metabolism: Almost completely metabolised in the liver by CYP2A6 enzyme via direct N-glucuronidation, N-methylation, and oxidation. Excretion: Via urine (95%) and faeces (4%), mainly as metabolites. Terminal elimination half-life: Approx 2 hours.
N05CM18 - dexmedetomidine ; Belongs to the class of other hypnotics and sedatives.
References
Anon. Dexmedetomidine. AHFS Clinical Drug Information [online]. Bethesda, MD. American Society of Health-System Pharmacists, Inc. https://www.ahfscdi.com. Accessed 04/03/2023.Anon. Dexmedetomidine. Lexicomp Online. Hudson, Ohio. Wolters Kluwer Clinical Drug Information, Inc. https://online.lexi.com. Accessed 04/03/2023.Buckingham R (ed). Dexmedetomidine Hydrochloride. Martindale: The Complete Drug Reference [online]. London. Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 04/03/2023.Dexmedetomidine 4 micrograms/mL Solution for Infusion (Altan Pharma Ltd). MHRA. https://products.mhra.gov.uk. Accessed 04/03/2023.Dexmedetomidine Hydrochloride Injection, Solution, Concentrate (Akorn). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed. Accessed 04/03/2023.Igalmi Sublingual Film for Sublingual or Buccal Use (BioXcel Therapeutics, Inc.). U.S. FDA. https://www.fda.gov. Accessed 16/05/2023.Joint Formulary Committee. Dexmedetomidine. British National Formulary [online]. London. BMJ Group and Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 04/03/2023.Pfizer New Zealand Limited. Precedex 100 micrograms/mL Concentrate for Infusion data sheet 28 October 2022. Medsafe. http://www.medsafe.govt.nz. Accessed 04/03/2023.Precedex Injection (Hospira Malaysia Sdn Bhd). National Pharmaceutical Regulatory Agency - Ministry of Health Malaysia. https://www.npra.gov.my. Accessed 04/03/2023.