16)General anaesthesia Flashcards

1
Q

General Anaesthesia

A
  • State characterised by ⇢ Unconsciousness, analgesia, amnesia, skeletal muscle relaxation + loss of reflexes

Balanced anaesthesia:

  • Produced by mixture of drugs often including both inhaled + IV agents
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2
Q

Preanesthetic medication

A
  • Anticholinergic drugs ⇢ Atropine
  • Antihistamines ⇢ Promethazine
  • Benzodiazepines ⇢ Diazepam/Lorazepam
  • Neuromuscular blockers ⇢ Pancuronium bromide
  • Hydrogen blockers ⇢ Famotidine
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3
Q

Mechanism of action

A
  • Excitatory NTs ⇢ Glutamate, ACh, serotonin ⇢ inhibited by GA
  • Inhibitory NTs ⇢ GABA + Glycine ⇢ Potentiated by GA
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4
Q

Classification - Inhalation

A

N2O - nitrous oxide

Volatile liquids:

  • Halothane
  • Enflurane
  • Isoflurane
  • Desflurane
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5
Q

Classification - IV anaesthetics

A
  • Barbiturates
  • Dissociative anaesthetics
  • Propofol
  • Benzodiazepine’s
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6
Q

Minimal alveolar concentration

A

Alveolar anaesthetic conc at which 50% of patients fail to respond to standard surgical stimuli

  • Indicated potency of an anaesthetic
  • Important for inhaled anaesthetics
  • N2O MAC > 100%
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7
Q

N2O

A
  • Low potency ⇢ must be combined
  • Rapid induction + recovery
  • Good analgesic properties
  • ⇣ Toxicity

Side effects

  • Post-operative nausea + vomiting
  • Prolonged exposure of N2O ⇢ Oxidises vitamin B12Reversible anaemia
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8
Q

Halothane

A
  • Widely used agent w/potent anaesthetic activity
  • No analgesic properties

Side effects:

  • Hypotension
  • 30% metabolised in liver ⇢ Repeated use = hepatotoxicity
  • Bradycardia
  • Cardiac arrhythmias
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9
Q

Barbiturates/Thiopental

A
  • Ultra-short acting
  • High lipid solubility
  • Rapid action
  • Accumulates in fat
  • No analgesic properties
  • Narrow therapeutic stage
  • Bind to B-subunit of GABAa receptor + potentiates inhibitory action of GABA
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10
Q

Propofol

A
  • Rapidly metabolised
  • ⇣ Blood pressure
  • Used for day-case surgery
  • FOS-propofol = water soluble derivative
  • Propofol interacts w/ beta-containing GABAa-ergic receptors
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