Amiodarone (Cordarone)

  • Description and indication for use

    Amiodarone is a Class III anti-arrhythmic agent, prolonging the action potential duration and hence refractory period of atrial, nodal and ventricular tissues.  Amiodarone has a very broad spectrum of activity, and is also a potent vasodilator. 

    It is indicated in severe cases of tachyarrhythmias, supraventricular nodal and ventricular tachycardias, and atrial flutter.  Due to frequent and severe toxicity, amiodarone should be used only in the treatment of life-threatening arrhythmias.

    Dose

    IV:

    2.5 mg/kg 6 hourly, extending the interval over time.

    Dose must be titrated against therapeutic effect.

    Reconstitution/Dilution

    Ampoule = 150 mg in 3 mL (50 mg/mL).     Not Ward Stock.

    For IV use:

    Withdraw 0.2 mL of 50 mg/mL solution and add to 0.8 mL of Glucose 5% in a second 1 mL syringe = 10 mg/mL.

    Take 1 mL of this solution and add 4 mL of Glucose 5% in a 5 mL syringe = 10 mg in 5 mL = 2 mg/mL.

    Discard excess volume to obtain required dose or withdraw required dose using another 10 mL syringe.

    Route and method of administration

    IV:

    Give as an infusion over 1 hour - via infusion syringe pump.

    **Draw up an additional syringe of glucose 5% (3 mL) in a 10 mL syringe for a flush.

    After infusion completed, change to syringe of glucose 5% and infuse (2 mL) at same rate as the Amiodarone was infusing (set appropriate volume limit).

    Discard syringes and line following completion of drug and flush.

    If repeated doses are anticipated, where possible, administration via central venous catheter (CVC) is recommended due to peripheral administration causing inflammation of the vein.

    Not for IM use.

    Side effects

    Hypotension, bradycardia, atypical ventricular tachycardia.

    Hot flushes, sweating.

    Nausea, constipation.

    Hepatotoxicity, abnormal liver function tests.

    Nephrotoxicity, raised serum creatinine.

    Abnormal thyroid function tests, hyperthyroidism/hypothyroidism.

    Hyperglycaemia.

    Pulmonary toxicity with long term use.

    Thrombophlebitis.

    Photosensitivity.

    Blue-grey discoloration of skin.

    Special precautions

    CAUTION in patients with left ventricular dysfunction.

    CAUTION in patients with hypotension.

    CAUTION in patients with thyroid dysfunction.

    Marked cardiomegaly is a relative contra-indication.

    Incompatibilities

    Amiodarone is incompatible with many drugs.

    Amiodarone must not be diluted with sodium chloride 0.9%.

    Do not administer with TPN solution or Intralipid.

    Recommended to be administered alone or contact Pharmacy for further information.

    Drug interactions

    Digoxin Plasma levels of digoxin are increased.  A reduced dose of digoxin is recommended. 
    Phenytoin Plasma levels of phenytoin are increased.  Recommended that phenytoin levels be closely monitored.  Effectiveness of amiodarone may also be reduced. 
    Sotalol, betablockers Can result in symptomatic bradycardia and sinus arrest.  Hypotension as a side effect can be severe when the combination is used. 
    Theophylline Plasma levels of theophylline may be increased.  Theophylline levels should be monitored. 

    Nursing responsibilities

    Continuous cardiorespiratory monitoring.

    Monitor blood pressure.


Disclaimer:  This Drug information was designed for use by PIPER Neonatal. Whilst great care has been taken to check the information is accurate, it is possible that errors may have been missed. Furthermore, dosage schedules are continually being revised and new side effects recognised. For these reasons, the reader is strongly advised to consult the drug companies' printed information before administering any of the drugs recommended in this book.
Most drugs in this document are appropriate only for specialist use in hospitals.  A number of drugs should only be used in consultation with the appropriate Paediatric subspecialist. 

Note: The electronic version of this guideline is the version currently in use.  Any printed version cannot be assumed to be current. Printed copies of this document are valid for