Structure/Class |
- Volatile fluorinated hydrocarbon anaesthetic agent
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Pharmacokinetics |
- Very soluble agent
- Blood gas partition coefficient of 10-14. Also very soluble in fatty tissues.
- Hence, very slow onset and offset if used as induction agent (and therefore should not be used as such).
- Metabolism
- 50-70% metabolised in the liver to free fluoride and oxalic acid à causes dose related nephrotoxicity
- 20% excreted in air.
- 30% excreted in urine.
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Pharmacodynamics |
- Powerful analgesic at sub-anaesthetic doses.
- Organ system effects
- CVS effects
- Has myocardial depressant properties: may cause bradycardia, hypotension and reduced contractility.
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Indications |
- Prehospital analgesia in the conscious and haemodynamically stable patient.
- Relief of pain in conscious patients undergoing short procedures (e.g. dressing change)
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Contraindications |
- Renal failure
- Previous hypersensitivity to fluorinated anaesthetics
- CVS instability
- Respiratory depression
- Severe head injury or LoC
- Inducing anaesthesia
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Special precautions |
- Elderly patients or those with DM à increased risk of nephrotoxicity
- Nor for daily use
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Interactions |
- Tetracyclines – fatal nephrotoxicity
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Adverse events |
- CNS (common) – drowsiness, disorientation, coughing, dislike of odor and headache.
- Less common – hypotension, bradycardia and nephrotoxicity
- Rare – Respiratory distress, bronchospasm, laryngospasm, malignant hyperthermia, hepatitis.
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Dosing/administration |
- 3ml at a time via Penthrox inhaler. Maximum of 6ml/day.
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Toxicology |
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Withdrawal syndrome |
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Special notes |
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