Mnemonic

Amiodarone Monitoring

A memory aid for the organ toxicity and monitoring of amiodarone.

Expansion

Lungs, liver, thyroid, eyes, skin and nerves

Expansion

Toxicity by organ

  • Lungs: pulmonary fibrosis and pneumonitis, the most feared
  • Liver: hepatitis, deranged transaminases
  • Thyroid: both hypo- and hyperthyroidism, because the molecule contains iodine
  • Eyes: corneal microdeposits, almost universal, usually asymptomatic and reversible; optic neuropathy is rare but serious
  • Skin: photosensitivity and a slate grey discolouration
  • Nerves: peripheral neuropathy
  • Heart: bradycardia, heart block, QT prolongation

Monitoring

  • Before starting: thyroid function, liver function, urea and electrolytes, chest radiograph, and lung function tests where feasible
  • Every 6 months: thyroid and liver function
  • Annually: chest radiograph
  • Ophthalmology review if visual symptoms develop

“Half life of 50 days” governs everything else: it takes months to reach steady state, which is why loading is needed; interactions and toxicity persist for months after stopping; and thyroid dysfunction can appear long after discontinuation.

Interactions: it inhibits CYP enzymes and P-glycoprotein, so it raises digoxin levels (halve the digoxin dose), potentiates warfarin, and adds to the QT prolongation of many drugs.

Amiodarone induced thyrotoxicosis has two types: type 1 in pre-existing thyroid disease, treated with carbimazole; type 2, a destructive thyroiditis, treated with steroids.