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Detomidine

Alpha-2 adrenergic agonist

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Detomidine

Detomidine is an alpha2-adrenergic agonist used predominantly in horses for sedation and analgesia. It facilitates standing examinations and minor procedures and is used as an adjunct to general anesthesia. Injectable and oromucosal formulations have different clinical applications, with oromucosal gel used mainly for sedation during handling and husbandry procedures.

Group

Alpha-2 adrenergic agonist

Mechanism of Action

Detomidine activates central alpha2-adrenergic receptors, reducing norepinephrine release and sympathetic neurotransmission. Suppression of arousal pathways produces sedation, while effects in spinal and supraspinal pain pathways reduce nociceptive transmission and provide analgesia. The depth and duration of these effects are dose dependent. Peripheral alpha2-receptor activation also influences vascular tone and other autonomic functions.

Dose Rates

Dog

Use / stageDoseRouteScheduleInstructions
Sedation5 mcg/kgIVDo not use in: Shock or severe cardiovascular compromise
Sedation10–20 mcg/kgIMDo not use in: Shock or severe cardiovascular compromise
SedationReference onlyOTMDo not use in: Shock or severe cardiovascular compromise; Gel: 0.5 mg/m² for mild sedation, 1 mg/m² for greater sedation, or 2–4 mg/m² for profound sedation; apply to upper gingiva. BSA calculation required. Reversal: atipamezole 0.1 mg/kg IM.

Cat

Use / stageDoseRouteScheduleInstructions
Sedation with ketamineReference onlyOTMDo not use in: Shock or severe cardiovascular compromise; Injectable detomidine 0.5 mg/kg plus ketamine 10 mg/kg sprayed into the mouth. Combination protocol.
SedationReference onlyOTMDo not use in: Shock or severe cardiovascular compromise; Gel 2–4 mg/m²; vomiting is common. BSA calculation required. Reversal: atipamezole 0.1 mg/kg IM.

Horse

Use / stageDoseRouteScheduleInstructions
Sedation20–40 mcg/kgIV, IMDo not use in: Shock or severe cardiovascular compromise
Sedation — Initial10–20 mcg/kgIV, IMDo not use in: Shock or severe cardiovascular compromise; Lower initial regimen; repeat according to effect. Doses as low as 5 mcg/kg have been used in draft horses.
Analgesia20 mcg/kgIV, IMDo not use in: Shock or severe cardiovascular compromise; A 40 mcg/kg dose may prolong analgesia.
Sedation40 mcg/kgOTMDo not use in: Shock or severe cardiovascular compromise; Sublingual gel.
Sedation infusionReference onlyIVDo not use in: Shock or severe cardiovascular compromise; 10 mcg/kg IV loading bolus, then 0.5 mcg/kg/min for 15 minutes; progressively reduce toward 0.1 mcg/kg/min according to effect.
Analgesia30–40 mcg/kgIV
Caudal epidural analgesia0.06 mg/kgEPIDURALInjection at S4–S5; reported analgesia 2–3 hours.
Combined epidural analgesiaReference onlyEPIDURALDetomidine 0.03 mg/kg plus morphine 0.2 mg/kg; the source prints an anatomically inconsistent S1–L6 injection site, which must be resolved before procedural use. Reported duration exceeds 6 hours.
Sedation0.06 mg/kgPOAlternative when injection is impractical; onset may take approximately 45 minutes.
Standing restraint infusion alternativesReference onlyIVAlternative A: load 7.5 mcg/kg, infuse 0.6 mcg/kg/min for 15 minutes, then halve the rate every 15 minutes. Alternative B: load 8.4 mcg/kg, then 0.5 mcg/kg/min for 15 minutes, 0.3 for 15 minutes, and 0.15 thereafter. Additional local analgesia or butorphanol may be needed.

Cattle

Use / stageDoseRouteScheduleInstructions
SedationReference onlyIVDo not use in: Shock or severe cardiovascular compromise; The source gives 2–10 mcg/kg but an inconsistent parenthetical conversion of 0.002–0.1 mg/kg. Resolve the endpoint before calculation.
Sedation5–40 mcg/kgIMDo not use in: Shock or severe cardiovascular compromise
Calf sedation30 mcg/kgIVDo not use in: Shock or severe cardiovascular compromise; Calves.
Calf sedation80 mcg/kgOTMDo not use in: Shock or severe cardiovascular compromise; Calves; equine oral mucosal gel.
Sedation30–60 mcg/kgIV, IM
Analgesia10 mcg/kgIVReported duration approximately 30 minutes.

Sheep

Use / stageDoseRouteScheduleInstructions
Anesthesia with propofolReference onlyIMDetomidine 0.01 mg/kg IM followed by propofol 3–5 mg/kg IV.
AnalgesiaReference onlyIV, IMThe source gives 0.005–0.05 mg/kg IV or IM but combines “every 3–6 hours” with “once”; the repeat schedule is contradictory.

Goat

Use / stageDoseRouteScheduleInstructions
Anesthesia with propofolReference onlyIMDetomidine 0.01 mg/kg IM followed by propofol 3–5 mg/kg IV.
AnalgesiaReference onlyIV, IMThe source gives 0.005–0.05 mg/kg IV or IM but combines “every 3–6 hours” with “once”; the repeat schedule is contradictory.

Llama

Use / stageDoseRouteScheduleInstructions
AnalgesiaReference onlyIV, IMThe source gives 0.005–0.05 mg/kg IV or IM but combines “every 3–6 hours” with “once”; the repeat schedule is contradictory.

Alpaca

Use / stageDoseRouteScheduleInstructions
AnalgesiaReference onlyIV, IMThe source gives 0.005–0.05 mg/kg IV or IM but combines “every 3–6 hours” with “once”; the repeat schedule is contradictory.

Bird

Use / stageDoseRouteScheduleInstructions
Sedation and analgesia0.3 mg/kgIMLimited information on duration and adverse effects.

Indications

Contraindications

Interactions

Adverse effects

Preparations

PreparationFormStrengthRoute
Detomidine injection 10 mg/mLInjection10 mg / mLIV, IM
Detomidine oral mucosal gel 7.6 mg/mLOral Gel7.6 mg / mLOTM

Monitoring and Administration

Monitor ECG, heart rate, blood pressure and respiration. Routine atropine treatment of alpha-2-associated bradycardia is not indicated.

Apply oral gel to the mucosa; onset is slower than injection. Atipamezole can reverse effects in small animals.

Intravaginal equine gel administration has been studied at 40 mcg/kg; this route is not supported by the app.

Veterinary use

For veterinary reference. Confirm the indication, dose, route, interval, product strength and any applicable withdrawal period before administration.