Monoamine oxidase inhibitors (MAOI) - NYSORA

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Monoamine oxidase inhibitors (MAOI)

Learning objectives

  • Describe the side effects and anesthetic consequences of patients on monoamine oxidase inhibitors (MAOI)

Definition and mechanisms

  • Monoamine oxidase inhibitors (MAOI) inhibit the activity of one or both monoamine oxidase enzymes A and B, thus preventing the breakdown of monoamine neurotransmitters serotonin and norepinephrine and thereby increasing their availability
    • MAO type A has a preference for norepinephrine and serotonin
    • MAO type B deaminates tyramine and phenylethylamine 
  • Risk of hypertensive crisis with norepinephrine release
  • MAOIs are effective antidepressants and are used in the treatment of:
    • Panic disorder
    • Atypical depression
    • Anxiety disorder
    • Depression
    • Bulimia
    • Post-traumatic stress disorder
    • Borderline personality disorder
    • Obsessive Compulsive Disorder
    • Bipolar depression
  • Be cautious of withdrawal symptoms and recurrence of the psychiatric illness if the psychoactive drug is stopped 
  • MAOIs interact severely with commonly used anesthetic agents 
    • MAOIs inhibit the metabolism of indirectly acting sympathomimetics resulting in the potentiation of their action
    • Where necessary, direct sympathomimetics are preferable 

Side effects

  • Dry mouth
  • Nausea, diarrhea, or constipation
  • Headache
  • Drowsiness
  • Insomnia
  • Dizziness or lightheadedness
  • Skin reaction at the patch site
  • Involuntary muscle jerks
  • Low blood pressure
  • Reduced sexual desire or difficulty reaching orgasm
  • Weight gain
  • Difficulty starting a urine flow
  • Muscle cramps
  • Prickling or tingling sensation in the skin (paresthesia)

Management

Monoamine oxidase inhibitors, MAOI, hypertensive crisis, tyramine, direct-acting sympathomimetics, meperidine, pancuronium, ephedrine

Suggested reading

  • Peck T, Wong A, Norman E. 2010. Anaesthetic implications of psychoactive drugs. Continuing Education in Anaesthesia Critical Care & Pain.10;(6); 177-181. 

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