Overview
Overview
  • Alpha-2 agonist with sedative and analgesic effects
  • Produces sedation without significant effect on respiratory drive
  • Used for multiple indications across anaesthesia, critical care and pain management
  • An older drug which has been superseded by dexmedetomidine for some indications
  • Alpha-2 agonist with sedative and analgesic effects
  • Produces sedation without significant effect on respiratory drive
  • Used for multiple indications across anaesthesia, critical care and pain management
  • An older drug which has been superseded by dexmedetomidine for some indications
Indications & Dosing
Indications & Dosing

Sedation on critical care

  • Sedation of intubated and mechanically ventilated patients as an adjunct to other sedatives
  • Treatment of agitated and delirious patients
  • Must be weaned gradually
IV infusion: 0.5-1.0 mcg/kg/hr
IV/PO: 50-200 mcg QDS

Adjunct to anaesthesia

  • Reduces MAC of volatile agents
IV: 1–2 mcg/kg

Adjunct to perioperative analgesia

IV: 1–2 mcg/kg

Adjunct to regional anaesthesia

  • Prolongs duration of effect
  • Useful in peripheral nerve, epidural, caudal and spinal blocks

Anxiolysis (Premedication)

  • May be a useful in both children and adults (though onset is slow)
PO: 4 mcg/kg

Antihypertensive

  • Medical use is limited by severe rebound hypertension following discontinuation
  • May be useful for hypotensive anaesthesia

Alcohol & opiate withdrawal

PO: 0.6-1.2 mg/day in divided doses

Postoperative shivering

IV/PO: up to 0.5 mcg/kg (low dose)

Migraine prophylaxis

PO: low dose
Contraindications
Contraindications
  • No definitive contraindications
  • Extreme caution should be exercised in patients with:
    • Heart block
    • Bradycardia
    • Hypotension or hypovolaemia
    • Severe ventricular dysfunction
    • Peripheral vascular disease
    • Concomitant use of:
      • Beta-blockers (bradycardia)
      • Tricyclic antidepressants (counteract effect)
      • Digoxin (bradycardia)
      • Haloperidol (prolongation of QT interval)
  • Sudden withdrawal should be avoided due to the risk of rebound hypertension
  • No definitive contraindications
  • Extreme caution should be exercised in patients with:
    • Heart block
    • Bradycardia
    • Hypotension or hypovolaemia
    • Severe ventricular dysfunction
    • Peripheral vascular disease
    • Concomitant use of:
      • Beta-blockers (bradycardia)
      • Tricyclic antidepressants (counteract effect)
      • Digoxin (bradycardia)
      • Haloperidol (prolongation of QT interval)
  • Sudden withdrawal should be avoided due to the risk of rebound hypertension
Formulation
Formulation
Intravenous
150mcg in 1ml vial
Oral
25 – 150 mcg tablets
Transdermal
100-300 mcg/24hrs patches
Preparation
Preparation
  • IV Injection:
    • May be given undiluted or diluted to aid slow administration
  • IV infusion:
    • Suggested standard infusion in critical care
    • Dilute to 15mcg/ml or 30mcg/ml
    • Sodium chloride 0.9% or glucose 5% can be used
  • IV Injection:
    • May be given undiluted or diluted to aid slow administration
  • IV infusion:
    • Suggested standard infusion in critical care
    • Dilute to 15mcg/ml or 30mcg/ml
    • Sodium chloride 0.9% or glucose 5% can be used