• Renal impairment
  • Preparation/Dilution IV CHECK PRODUCT SELECTION CAREFULLY. Dilution only applies to Lanoxin Infant Injection.
  • Administration
  • Neonatal Intensive Care Drug Manual




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    Infants aged 2–24 months:

    PO:         Loading dose 10 microgram/kg/dose 8-hourly for 2–3 doses, followed by

    Maintenance dose: 8–10 microgram/kg/dose daily or in 2 divided doses.

    IV:          Loading and maintenance doses are 75% of oral dose.


    Doses should be titrated to the lowest dose needed to achieve effect.
    Renal impairment: Predominantly renally cleared (about 70%); reduce dose by at least half in renal impairment.
    When switching from oral to IV therapy, reduce the digoxin dosage by 20–25%.

    Maximum daily dose

    250 microgram daily.

    Route

    Oral

    Intravenous



    Preparation/Dilution

    IV

    CHECK PRODUCT SELECTION CAREFULLY. Dilution only applies to Lanoxin Infant Injection.
    Lanoxin Infant Injection:

    Add 2 mL (50 microgram) of digoxin to 8 mL of sodium chloride 0.9% or glucose 5% to make a 5 microgram/mL solution.



    Administration

    ORAL: May be taken with or without food.32 However, administer consistently at the same time with respect to meals to avoid day to day variation.33

    IV: Give over at least 10 minutes.

    IM: Do not give IM (unpredictable absorption, local irritation).


    Monitoring

    Check renal function and electrolyte concentrations before starting digoxin.

    For intravenous infusion, continuous cardiac monitoring is recommended. It may not be necessary when IV injection is used to temporarily replace oral dosing in a patient stabilised on digoxin. Check local guidelines.

    The onset of effect is approximately 5 to 10 minutes, with a maximum effect being achieved after 2 hours.

    Take drug levels at least 6 hours after the dose is given.

    For oral treatment without loading dose, steady state is reached after about 7 days if renal function is normal (half-life is 36 hours); this may be prolonged in renal impairment.

    The therapeutic range for those with atrial tachyarrhythmias is 0.5 to 2 microgram/L (0.6 to 2.6 nmol/L) as toxicity is more common at digoxin concentrations >2 microgram/L. However, toxic effects can occur at lower concentrations, particularly in the elderly or in those with electrolyte disturbance, hypoxia or hypothyroidism. GI symptoms (e.g. nausea, anorexia) may precede cardiac symptoms (e.g. arrhythmias).

    Heart failure: Consider maintaining lower concentrations of 0.5 to 0.8 microgram/L (0.6 to 1 nmol/L) in patients with heart failure who are in sinus rhythm.

    Therapeutic drug monitoring for digoxin should be performed using an assay free from interference with digoxin-like immunoreactive factors, spironolactone, canrenoate, digoxin metabolites and steroids.




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    Neonatal Intensive Care Drug Manual

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