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General anaesthesia and relaxation

Ideal inhalational anaesthetic agent

  • The ideal inhalational anaesthetic agent should have several properties 
  • In its preparation is should be
    • Easily administered
    • Boiling point above ambient temperature
    • Low latent heat of vaporization
    • Chemically stable with long shelf-life
    • Compatible with soda-lime, metals and plastics
    • Non-flammable
    • Cheap
  • Pharmacokinetic
    • Low solubility
    • Rapid onset, rapid offset, adjustable depth
    • Minimal metabolism
    • Predictable in all age groups
  • Pharmacodynamic
    • High potency - allows high FiO2
    • High therapeutic index
    • Analgesic
  • Adverse actions
    • Minimal toxicity
    • Minimal unwanted effects - nausea, vomiting, cardiac arrhythmias
    • No toxicity with chronic low-level exposure of staff

Maintenance of anaesthesia

  • Balanced anaesthesia has three aspects to it

    • Hypnosis = suppression of consciousness
    • Analgesia = suppression of physiological responses to stimuli
    • Relaxation = suppression of muscle tone and relaxation
  • Anaesthesia is normally maintained with inhaled volatile gases
  • They are lipid soluble hydrocarbons
  • They have high saturated vapour pressures
  • Modern agents are potent, non-inflammable and non-explosive
  • MAC = Minimum alveolar concentration
  • It is the alveolar concentration required to keep 50% of population unresponsive

Adverse effects of inhalational anaesthetic agents

Cardiovascular

  • Decreased myocardial contractility
  • Reduced cardiac output
  • Hypotension
  • Arrhythmias
  • Increased myocardial sensitivity to catecholamines

Respiratory

  • Depress ventilation
  • Laryngospasm and airway obstruction
  • Decreased ventilatory response to hypoxia and hypercapnia
  • Bronchodilatation

Central nervous system

  • Increased cerebral blood flow
  • Reduced cerebral metabolic rate
  • Increased risk of epilepsy
  • Increased intracranial pressure

Others

  • Decreased renal blood flow
  • Stimulate nausea and vomiting
  • Precipitate hepatitis

Specific anaesthetic agents

Halothane

  • Potent anaesthetic but poor analgesic agent (MAC = 0.75)
  • Can be used for gaseous induction in children
  • 20% is metabolised in the liver and can cause hepatic dysfunction
  • Occasionally causes severe hepatitis that can progress to liver necrosis
  • Depressed myocardial contractility and can induce arrhythmias

Isoflurane

  • Potent anaesthetic but poor analgesic agent (MAC = 1.05)
  • Less cardiotoxic but causes greater respiratory depression
  • Reduces peripheral resistance and cause a 'coronary steal'
  • Few adverse effects have been reported

Nitrous oxide

  • Weak anaesthetic agent (MAC = 103)
  • Can not be used as an anaesthetic agent alone without causing hypoxia
  • Very potent analgesic agent
  • Used as 50% N2O / 50% O2 mixture = 'Entonox'
  • Used in anaesthesia mainly for its analgesic properties

Muscle relaxants

Muscle relaxants are either depolarising or non-depolarising agents

Depolarising agents

  • For example - suxamethonium
  • Act rapidly within seconds and last for approximately 5 minutes
  • Used during induction of anaesthesia
  • Side effects:
    • Histamine release producing a 'scoline rash'
    • Bradycardia
    • Somatic pain resulting from fasciculation
    • Hyperkalaemia
    • Persistent neuromuscular blockade = 'scoline apnoea'
      • Affects 1:7000 of population
      • Due to pseudocholinesterase deficiency
    • Malignant hyperpyrexia
      • Affects 1:100,000 of population
      • Due to increased calcium influx and uncontrolled metabolism
      • Rapid increase in body temperature with increased PaCO2
    • Increased intra-ocular pressure
    • Increased gastric pressure

Non-depolarising agents

  • For example - vecuronium
  • Act over 2-3 minutes and effects last for 30 minutes to one hour
  • Competitive antagonism of acetylcholine receptor
  • Used for muscle relaxation

Bibliography

Campagna J A,  Miller K W,  Forman S A.  Mechanism of action of inhaled anesthetics.  N Eng J Med 2003;  348:  2110-2124.

Fox A J,  Rowbotham D J.  Anaesthesia.  Br Med J 1999;  319:  557-560.

Heggie J E.   Malignant hyperthermia:  considerations for the general surgeon.  Can J Surg 2002;  45:  369-372.

Hopkins P M.  Malignant hyperthermia:  advances in clinical management and diagnosis.  Br J Anaesth 2000;  85:  118-128.

Wapper F.  Malignant hyperthermia.  Eur J Anaesthesiol 2001;  18:  632-652.

 

 
 

Last updated: 05 January 2008

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