Derived from the foxglove plant (Digitalis spp), digoxin is a cardiac glycoside that was historically used for "dropsy" (edema) and is currently used as an inotrope to improve systolic dysfunction in patients with congestive heart failure (CHF) and as an atrioventricular nodal blocking agent for managing atrial tachydysrhythmias. Digoxin may improve the quality of life in CHF patients, but it does not provide a mortality benefit. Digoxin toxicity can present acutely, by an intentional or accidental overdose, or chronically, such as when patients on digoxin develop worsening renal function. Similar toxicity can occur after exposure to cardioactive steroids in plants such as oleander, red squill, or dogbane or from animals such as Bufo toads.
Digoxin exhibits its therapeutic and toxic effects by poisoning the sodium-potassium ATPase. The subsequent increase in intracellular sodium leads to increased intracellular calcium by decreasing calcium expulsion through the sodium-calcium, cation exchanger. Higher intracellular calcium increases inotropy which can be of symptomatic benefit in CHF. At toxic levels, automaticity can be increased as well. Digoxin also increases vagal tone by decreasing dromotropy at the AV node. This can be used to control atrial tachydysrhythmias.
Approximately 1% of CHF patients treated with digoxin develop toxicity. Additionally, 1% of adverse drug effects in patients greater than age 40 are due to digoxin toxicity; the incidence rises to greater than 3% in patients over age 85. Plant ingestions account for 80% of pediatric exposure; the remaining 20% of pediatric ingestions arise from medications. In general, ventricular dysrhythmias are more common in the elderly whereas supraventricular dysrhythmias are more common in children.
Increased intracellular calcium from the poisoning of the Na-K transporter and AV nodal blockade from increased vagal tone are the primary causes of digoxin toxicity. The former leads to increased automaticity and inotropy; the latter leads to decreased dromotropy. Hyperkalemia can be a marker of severe toxicity in acute poisoning. The role of potassium is less clear in chronic toxicity, although it has been linked to higher mortality despite traditional teaching that hypokalemia worsens the dysfunction at the Na-K transporter.
Digoxin's therapeutic half-life is between 30 to 40 hours, but this may change in overdose. Digoxin excretion is primarily renal, and for this reason, patients with poor or worsening renal function, such as patients who are elderly or have CKD, are more likely to develop toxicity. Digoxin levels start to plateau at 6 hours, which is after tissue redistribution has occurred; earlier levels may thus be misleadingly high. Cardiovascular toxicity may have delayed manifestation of up to 8 to 12 hours post ingestion.
Gastrointestinal upset is the most common symptom of digoxin toxicity. Patients also may report visual symptoms, which classically present as a yellow-green discoloration, and cardiovascular symptoms, such as palpitations, dyspnea, and syncope. Elderly patients frequently will present with vague symptoms, such as dizziness and fatigue. The most important historical detail in evaluating a random digoxin level is the time of the last dose.
For patients with acute digoxin toxicity, it is critical to obtain an ECG, a basic metabolic panel, and digoxin levels on arrival. These tests should be repeated at 6 hours post ingestion. Digoxin effect on the ECG is characterized by diffuse scooping of the ST segments which can be seen with therapeutic levels and is not associated with toxicity. The most common ECG abnormality is frequent PVCs, although the "pathognomonic" ECG finding is bidirectional ventricular tachycardia. However, this has been reported in aconitine poisoning.
In the setting of acute overdose, acetaminophen and aspirin levels can help screen for occult overdose.
In chronic toxicity, the cause of toxicity should be sought. Common causes include infection, renal failure, and accidental overdose. Serum digoxin levels do not always correlate with toxicity given variable tissue levels and other factors affecting digoxin's toxicodynamic effects.
Digoxin-specific antibody antigen-binding fragments (DSFab), brand name Digibind or Digifab, are an effective antidote that directly binds digoxin.
DSFab is indicated for life-threatening toxicity including:
Empiric dosing of DSFab can be given at a dose of ten to 20 vials for critically ill patients after acute overdose, three to six vials for chronic toxicity in adults, or one to two vials for chronic toxicity in children.
DSFab also can be dosed as follows:
(0.8 times the ingested dose)/0.5 = Number of vials of DSFab for acute overdose
(Digoxin level (steady state) x Weight (kg))/100 = Number vials of DSFab for acute or chronic overdose
DSFab fragments also can be given for poisoning with natural toxins, but the dosing is unclear.
The typical DSFab infusion is over 30 minutes, but it may be given as a bolus for critical patients. The onset of effect is approximately 20 minutes, with complete effect usually seen within 90 minutes.
Care should be taken to completely reverse digoxin in patients who are chronically taking digoxin, as reversal may exacerbate their underlying disease. These patients should be closely monitored afterward for the same reasons.
If DSFab is not available, then treatments such multidose-activated charcoal, atropine, and antidysrhythmics such as phenytoin or lidocaine may be employed. Cardioversion and pacing may induce dysrhythmias and are typically not used, but they may be needed in patients without other therapeutic options.
Dialysis also may be indicated in the patient with acute renal failure or refractory hyperkalemia; however, it is not useful as a treatment for digoxin toxicity itself.
Disposition depends on the patient's symptoms and stability as well as their potassium and digoxin levels.
Many analyzers cannot measure free digoxin concentrations, and in this setting, digoxin levels should not be followed after administration of DSFab.
In patients with the end-stage renal disease, dissociation of the DSFab-digoxin complex may occur and cause recurrent toxicity.
Calcium is traditionally considered contraindicated in hyperkalemic patients with digoxin toxicity for fear of 'stone heart syndrome,' an irreversible state of global myocardial contraction. This is based on animal evidence and case report, but more recent literature found no evidence of increased mortality with calcium administration. In general, hyperkalemia in the setting of digoxin toxicity should be treated primarily with DSFab fragments if available.
A classic but uncommon side effect of digoxin is the appearance of yellow halos around lights, called xanthopsia, and altered color vision, called chromatopsia. This may have influenced the work of Dutch impressionist painter Vincent Van Gogh in paintings such as "The Starry Night" as he reportedly used foxglove for the treatment of his 'dropsy' which is an old term for edema due to CHF.