Dexmedetomidine


Thông tin thuốc gốc
Chỉ định và Liều dùng
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 mcg/kg/hour; titrate dose to desired level of sedation.
Elderly: >65 years Initially, 0.05 mcg/kg infused over 10 minutes.
Suy gan
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).
Hướng dẫn pha thuốc
Dilute vial labelled as containing 100 mcg/mL in NaCl 0.9% solution for inj to a final concentration of 4 mcg/mL.
Tương kỵ
Incompatible with amphotericin B and diazepam.
Chống chỉ định
Grade 2 or 3 advanced heart block (unless paced), uncontrolled hypotension, acute cerebrovascular disorders.
Thận trọng
Patient with severe neurological disorders, bradycardia, ischaemic heart disease, peripheral autonomic activity, chronic hypertension, severe ventricular dysfunction, hypovolaemia, diabetes mellitus. Avoid abrupt withdrawal after prolonged use. Renal and hepatic impairment. Elderly. Pregnancy and lactation.
Tác dụng không mong muốn
Significant: Hyperthermia or pyrexia, tolerance, tachyphylaxis, withdrawal syndrome, transient hypertension, sinus arrest.
Cardiac disorders: Tachycardia, atrial fibrillation.
Gastrointestinal disorders: Oral hypoaesthesia, constipation, nausea, vomiting.
Metabolism and nutrition disorders: Hypo- or hyperglycaemia.
Nervous system disorders: Agitation, anxiety, drowsiness, dizziness, paraesthesia.
Respiratory, thoracic and mediastinal disorders: Hypoxia, bradypnoea, respiratory depression.
Potentially Fatal: Hypotension, bradycardia.
Thông tin tư vấn bệnh nhân
This drug may occasionally cause dizziness or drowsiness, if affected, do not drive or operate machinery for at least 8 hours after administration.
Chỉ số theo dõi
Monitor cardiac and respiratory function, level of sedation, blood pressure, pain control.
Quá liều
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.
Tương tác
Enhanced pharmacologic effects with anaesthetics, sedatives, hypnotics, opioids.
Tác dụng
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.
Đặc tính

Chemical Structure Image
Dexmedetomidine

Source: National Center for Biotechnology Information. PubChem Compound Summary for CID 5311068, Dexmedetomidine. https://pubchem.ncbi.nlm.nih.gov/compound/Dexmedetomidine. Accessed Oct. 25, 2023.

Bảo quản
Store between 20-25°C.
Phân loại MIMS
Thuốc ngủ & thuốc an thần
Phân loại ATC
N05CM18 - dexmedetomidine ; Belongs to the class of other hypnotics and sedatives.
Tài liệu tham khảo
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.

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