Basic Pharmacology Flashcards
Atracurium - Mechanism of action
Atracurium is a benzylisoquinolinium non-depolarising neuromuscular blocking drug. It competes with acetylcholine for motor end-plate cholinergic receptors and blocks neuromuscular transmission. This leads to skeletal muscle relaxation.
Atracurium - Preparation and Dose range
10mg/mL Initially 400-500mcg/kg Maintenance IV injection: 100-200mcg/kg as required IV infusion: 300-600mcg/kg/hr
Atracurium - ADRs
Hypotension
Tachycardia
Bronchospasm
Skin flushing
Rocuronium - Mechanism of action
Rocuronium is an aminosteroid non-depolarising neuromuscular blocking drug. It competes with acetylcholine for motor end-plate cholinergic receptors and blocks neuromuscular transmission. This leads to skeletal muscle relaxation.
Rocuronium - Preparation and Dose range
10mg/mL
Initially 600mcg/kg
Maintenance
IV injection: 150mcg/kg (elderly 75-100mcg/kg)
IV infusion: 300-600mcg/kg/hr (elderly up to 400mcg/kg/hr)
Rocuronium - ADRs
Hypotension
Tachycardia
Bronchospasm
Skin flushing
Vecuronium - Mechanism of action
Vecuronium is an aminosteroid non-depolarising neuromuscular blocking drug. It competes with acetylcholine for motor end-plate cholinergic receptors and blocks neuromuscular transmission. This leads to skeletal muscle relaxation.
Vecuronium - Preparation and Dose range
10mg powder
Initially 80-100mcg/kg
Maintenance
IV injection: 20-30mcg/kg, adjusted to response (max 100mcg/kg in C-section)
IV infusion: 0.8-1.4mcg/kg/minute (48-84mcg/kg/hr)
Vecuronium - ADRs
Hypotension
Tachycardia
Bronchospasm
Skin flushing
Atracurium - Onset and Duration of action
Onset of action: 2-2.5 minutes
Duration of action: 35-45 minutes (regain 25% of control)
Rocuronium - Onset and Duration of action
Onset of action: 45-120 seconds
Duration of action: 30-90 minutes
Vecuronium - Onset and Duration of action
Onset of action: 90-120 seconds
Duration of action: 25-30 minutes
Suxamethonium - Mechanism of action
Suxamethonium is a depolarising neuromuscular blocker that binds to cholinergic receptors at the motor end-plate. Initially depolarisation causes skeletal muscle fasciculation. The action of acetylcholine is then blocked preventing neural transmission and producing muscle relaxation.
Suxamethonium - Preparation and Dose range
50mg/mL
0.6mg/kg in adults (range 0.3-1.1mg/kg)
1-2mg/kg in children
Administered IV over 10-30 seconds
Suxamethonium - Onset and Duration of action
Onset of action: 60 seconds
Duration of action: 4-6 minutes
Suxamethonium - ADRs
Hypotension Myalgia Rash Malignant hyperthermia Rhabdomyolysis Transient ocular hypertension
Morphine - Mechanism of action
Morphine is a full opioid agonist. Opioid agonists bind to opiate receptors in the brain and spinal cord resulting in inhibition of the ascending pain pathways thus altering the perception and response to pain. Morphine reduces breathlessness and respiratory effort by reducing ventilatory drive in hypoxic and hypercapnic states. The sedating effect may also reduce anxiety associated with breathlessness. Cough suppression results from direct central action on the cough centre in the medulla.
Morphine - Preparations and Dose range
Oral: Controlled release - M-Eslon (sulfate); Immediate release - Sevredol (sulfate), elixir (hydrochloride)
SC/IM/IV: Morphine sulfate, multiple dose preparations
IT: Morphine sulfate (200mcg in 0.4mL; 300mcg in 0.3mL)
Morphine - ADRs
Sedation
Respiratory depression
Nausea/vomiting
Constipation