Digitalis Toxicity

Etiology

Digitalis use was first described in 1785 and was derived from the foxglove plant. Poisoning with digitalis can occur with acute over-ingestion of medication or as chronic toxicity most commonly due to decreased renal clearance. Some metabolic disturbances such as hypokalemia and hypercalcemia can make one more prone to toxicity as well as some drug interactions. Chronic toxicity is more common than acute intoxication.[3]

The most common trigger of digoxin toxicity is hypokalemia, which may occur as a result of diuretic therapy. Dosing errors are also a common cause of toxicity in the younger population.

Factors that increase the risk of digoxin toxicity include:

• Hypothyroidism/hyperthyroidism
• Advanced age
• MI
• Renal insufficiency
• Hypercalcemia
• Alkalosis
• Hypoxemia
• Acidosis

Medications that are associated with digoxin toxicity include?

• Diuretics
• Amiodarone
• Beta-blockers
• Benzodiazepines
• Calcium channel blockers
• Macrolide antibiotics
• Propylthiouracil
• Amphotericin

Epidemiology

Over time, the use of digoxin has become less common, and as a result, the incidence of digoxin toxicity has also been on the decline. This can also be attributed to improved technology in the detection of digoxin levels as well as increased knowledge of various drug interactions. Nevertheless, digoxin use is prevalent enough with a narrow therapeutic window, and toxicity continues to be a significant problem. In 2011 as per United States poison control, 2513 cases of digitalis toxicity were reported of those 27 resulted in death.[4][5]

Pathophysiology

The main mechanism of action of digitalis is on the sodium-potassium ATPase of the myocyte. It reversibly inhibits the ATPase resulting in increased intracellular sodium levels. The build-up of intracellular sodium leads to a shift of sodium extracellularly through another channel in exchange for calcium ions. This influx of intracellular calcium assists with myocyte contractility. Digoxin also has direct effects on conduction through increased vagal tone. Digoxin stimulates the vagus nerve leading to prolonged conduction through the sinuatrial (SA) and atrioventricular (AV) nodes. Overall, digoxin slows the conduction and increases the refractory period in cardiac tissue by enhancing vagal tone. These actions of digoxin can result in almost every type of arrhythmia possible such as:

• Extrasystole
• Nonparoxysmal junctional tachycardia
• Ventricular fibrillation
• Premature ventricular contractions
• Atrial fibrillation and flutter
• Bidirectional ventricular tachycardia
• SA and AV node block

The major electrolyte complication in acute digoxin toxicity is hyperkalemia.

Toxicokinetics

Distribution of digoxin to various tissues normally takes several hours; therefore, levels of digoxin should me measured six hours after last ingestion for the most accurate measurement. A steady-state of dioxin can take up to seven days with a half-life of digoxin being anywhere between 36 to 48 hours. Increased intracellular calcium seen with digitalis use may lead to premature contractions of the myocytes. Repolarization time for both the atria and ventricles are reduced. This decreased refractory period leads to increased automaticity and makes the myocytes more prone to the induction of arrhythmias. Digoxin is primarily renally excreted with chronic toxicity commonly seen in those with renal impairment. Many drug interactions lead to decreased clearance of digoxin. Well-known offenders include verapamil, macrolides, and antifungals. There is very little difference between sub-therapeutic and toxic levels of digoxin. The therapeutic window for digoxin is narrow and difficult to determine. The accepted range is between 0.5 ng/mL to 0.9 ng/mL. What is important to consider is that concentration does not necessarily correlate with toxicity. There have been documented cases of clinical toxicity with digoxin levels in the therapeutic range. Electrolyte disturbances such as hypomagnesemia, hypercalcemia, and hypokalemia lead to increased sensitivity to digoxin making toxicity more likely even with a lower concentration of serum digoxin. This makes diagnosis difficult and has led to the declining use of digoxin over the last several years. Diagnosis is primarily based on clinical presentation in the setting of suspected digoxin intoxication.

History and Physical

History of exposure is necessary to determine if poisoning is acute or chronic. Most reported poisonings result from chronic toxicity. Clinical signs of toxicity include gastrointestinal, neurological and the most concerning cardiac. Most symptoms are non-specific findings and include a headache, malaise, insomnia, altered mental status, abdominal pain, nausea, and vomiting. Of note visual changes especially changes involving colors such as seeing a yellow hue are better known and specifically seen in digitalis toxicity. Cardiac manifestations include arrhythmias and rhythm disturbances. Other visual problems include photophobia, photopsia and diminished visual acuity.

There is no specific arrhythmia for digoxin toxicity rather a range of arrhythmias can be present such as various degrees of AV block, premature ventricular contractions, bradycardia, and even ventricular tachycardia. Cardiac arrhythmias are the main cause of death for those with digoxin toxicity.

Some patients may have hemodynamic instability depending on the type of arrhythmia and others may have dyspnea and altered mental status.

Evaluation

The difference between toxicity and therapeutic range is small for digoxin and is determined to be between 0.5-2 ng/mL. Diagnosis is difficult and usually made clinically, as levels of digoxin in the blood do not necessarily correlate with toxicity. Digoxin is primarily cleared by the kidneys and declining renal function is a common cause of chronic toxicity. Therefore, renal function must be assessed. Electrolytes must also be evaluated; hypokalemia, hypercalcemia, and hypomagnesemia are known to worsen the effects of toxicity. The inhibition of the sodium-potassium ATPase leads to hyperkalemia and can be used as a marker of toxicity severity.  Serial electrocardiograms should be performed and the use of continuous cardiac monitoring may be considered as fluctuation in rhythms is commonly seen. EKG findings sometimes referred to as the digitalis effect may be seen. These changes commonly involve the T wave and include flattening, inversion, scooped appearance of ST-segment and ST depression in the lateral leads.[6][7]

It is important to know that endogenous digoxin like immunoreactive proteins can result in a false-positive result. This is more likely to occur in patients with:

• Liver or renal disease
• Chronic heart failure
• Subarachnoid hemorrhage
• Acromegaly
• Diabetes
• Pregnancy

The other problem is that there are several types of assays to measure digoxin and its metabolites, but these assays do vary in sensitivity. Further, the tests are hampered by cross-reaction with steroids and cholesterol-like substances.

Treatment / Management

Treatment involves early recognition and the administration of antibodies specifically against digoxin also known as Fab fragments. Digoxin concentration does not necessarily correlate with clinical symptoms of toxicity however digoxin concentrations may be used for calculating the amount of antidote therapy. Although guidelines are unclear, treatment with digoxin immune Fab is also known by the trade name Digibind, is considered first-line therapy for dysrhythmias including AV block and ventricular tachycardia caused by suspected digoxin toxicity.   Fab fragments are highly effective in binding the digoxin molecule with minimal detrimental side effects.  The antibody fragments form complexes and are secreted via the urine. Empiric treatment consists of 10 vials of Fab fragments for adults and five vials for children. Treatment with digoxin-specific antibodies will lead to hypokalemia, and serum potassium should be monitored frequently. Activated charcoal can be considered in the treatment of acute ingestion within two hours. Further treatment is supportive.  More research is needed for optimal dosing and whether or not the use of digoxin-specific antibodies are cost-effective for use in non-life threatening toxicities. [8][9]

Hydration, oxygenation, and close monitoring are necessary. The ECG has to be continuously monitored for dysrhythmias. All electrolyte disturbances need to be corrected.

One should remember that if digoxin is neutralized with antibodies, the patient may develop heart failure and lead to worsening of the arrhythmias. Other issues related to the antibody include serum sickness and anaphylaxis.

Supraventricular need to be managed with short-acting beta-blockers. Phenytoin as been shown to suppress digoxin induced tachyarrhythmias. Another option is lidocaine when managing ventricular arrhythmias. Atropine may be used to managed bradycardia. The use of magnesium is not recommended as it can worsen bradycardia or an AV block. Cardioversion is not recommended as it can precipitate ventricular arrhythmias; instead, defibrillation may be used according to ACLS protocol.

Differential Diagnosis

• Acute kidney injury

• Beta-blocker toxicity

• Calcium channel blocker toxicity

• Hypercalcemia

• Hyperkalemia

• Hypernatremia

• Hypoglycemia

• Hypokalemia

• Hyponatremia

Prognosis

The prognosis depends on the time of presentation, age and associated comorbidity. The mortality is usually increased when the toxicity is associated with a heart block or a new arrhythmia. Deaths may occur in 1-5% of patients despite optimal care.

Complications

• Heart failure
• Nodal block
• Anaphylaxis associated with digibind