🚨 Digoxin-specific antibody fragments, also called digoxin immune Fab or DigiFab®, are the antidote for life-threatening digoxin or cardiac glycoside toxicity.
They bind free digoxin in the blood, forming complexes that are then renally cleared.
Always check the BNF digoxin-specific antibody fragments monograph, local policy and TOXBASE/NPIS before prescribing where possible.
ℹ️ About
- Drug: digoxin-specific antibody fragments.
- Brand: DigiFab®.
- Class: antidote; ovine Fab immunoglobulin fragments.
- Use: treatment of known or strongly suspected life-threatening digoxin or cardiac glycoside toxicity.
- Formulation: 40 mg vial for solution for infusion.
- Key fact: one 40 mg vial binds approximately 0.5 mg digoxin.
- Specialist advice: discuss with TOXBASE/NPIS, senior clinician, cardiology, ICU or toxicology as appropriate.
🧬 Mode of Action
- Digoxin inhibits the sodium-potassium ATPase pump, increasing intracellular sodium and calcium.
- This increases vagal tone and myocardial automaticity, causing bradyarrhythmias, AV block and ventricular arrhythmias.
- Digoxin-specific Fab fragments bind free digoxin with high affinity.
- The bound digoxin becomes pharmacologically inactive and is eliminated mainly by the kidneys.
- Clinical improvement is often rapid, sometimes within 30–60 minutes, but monitoring must continue because rebound toxicity can occur.
⚠️ When to Suspect Severe Digoxin Toxicity
- 🤢 Nausea, vomiting, abdominal pain, anorexia or diarrhoea.
- 👁 Visual symptoms: yellow-green vision, blurred vision or halos.
- 🧠 Confusion, delirium, weakness or dizziness.
- 🐢 Bradycardia, AV block or slow atrial fibrillation.
- ⚡ Ventricular ectopics, bidirectional VT, VT or VF.
- 🧪 Hyperkalaemia, especially in acute poisoning.
- 🫘 Risk factors: renal impairment, older age, dehydration, hypokalaemia, hypercalcaemia, interacting drugs.
🚨 Indications for Digoxin-Specific Antibody Fragments
- Cardiac arrest or peri-arrest rhythm due to suspected digoxin/cardiac glycoside toxicity.
- Life-threatening ventricular arrhythmias, including VT or VF.
- Severe bradyarrhythmia, severe sinus bradycardia, or second-/third-degree AV block not responding to atropine.
- Haemodynamic instability with suspected digoxin toxicity.
- Hyperkalaemia in acute digoxin toxicity, especially potassium >5.0 mmol/L.
- Very high serum digoxin concentration after acute ingestion or in chronic toxicity, interpreted with timing, renal function and clinical features.
- Large acute ingestion, especially in adults, children, renal impairment or underlying cardiac disease.
⚠️ Do not treat the number alone.
Serum digoxin concentrations are difficult to interpret if taken too early after ingestion, because distribution into tissues takes time.
A result taken before at least 6 hours post-ingestion may overestimate clinically relevant tissue toxicity.
The patient’s ECG, potassium, renal function, haemodynamics and symptoms are often more important than the serum concentration alone.
💊 Dose - Always Check BNF / TOXBASE / Local Policy
| Clinical Situation |
Example Initial Dose |
Route |
Key Notes |
| 🚨 Cardiac arrest / life-threatening toxicity |
Often 10–20 vials depending on severity and advice |
IV infusion |
Give urgently with resuscitation, senior and toxicology/cardiology input. Do not delay in peri-arrest toxicity. |
| ⚡ Acute severe toxicity |
Dose may be calculated from ingested dose or serum concentration if reliable; partial neutralisation may be used in some cases |
IV infusion |
Discuss with TOXBASE/NPIS. Potassium >5.0 mmol/L in acute poisoning is a serious marker. |
| 🕰 Chronic toxicity |
Often smaller initial doses are used and repeated according to response |
IV infusion |
Chronic toxicity is common in older adults and renal impairment. Avoid excessive reversal if digoxin is needed for rate control, but treat life-threatening toxicity promptly. |
🧮 Dose Calculation Principles
- One 40 mg vial neutralises approximately 0.5 mg digoxin.
- If the amount ingested is known, dose can be estimated from the ingested digoxin dose.
- If a reliable serum concentration is available, dose can be estimated from serum digoxin concentration and body weight.
- In emergency practice, dose is often guided by clinical severity and TOXBASE/NPIS advice.
- Repeat dosing may be required if toxicity persists or recurs.
💉 Administration
- Route: intravenous infusion.
- DigiFab® is reconstituted with water for injections, then diluted in sodium chloride 0.9% according to product information/local policy.
- Manufacturer information commonly advises infusion over about 30 minutes.
- In cardiac arrest or immediately life-threatening toxicity, more rapid administration may be considered under expert/resuscitation guidance.
- Use aseptic preparation and monitor continuously during administration.
🔎 Monitoring
- Continuous ECG monitoring.
- Heart rate, blood pressure, oxygen saturations and conscious level.
- Serum potassium frequently - hypokalaemia can occur after Fab treatment.
- U&E and creatinine because Fab–digoxin complexes are renally cleared.
- Magnesium and calcium.
- Clinical response: rhythm, perfusion, symptoms and haemodynamics.
- Do not rely on total serum digoxin concentration after Fab treatment, as assays may measure bound digoxin and appear falsely high.
⚠️ Cautions
- Previous allergy to sheep protein, papaya/papain or Fab products may increase hypersensitivity risk.
- Renal impairment may delay clearance of Fab–digoxin complexes and increase rebound risk.
- Hypokalaemia may develop as digoxin effect is reversed, so potassium must be monitored closely.
- Reversal of digoxin may worsen heart failure or allow recurrence of rapid atrial fibrillation in patients dependent on digoxin for rate control.
- Pregnancy, children and complex poisoning require specialist toxicology advice.
⛔ Contraindications
- There are no absolute contraindications in immediately life-threatening digoxin toxicity.
- Known severe hypersensitivity to digoxin-specific antibody fragments is a major caution, but life-saving treatment may still be required with senior specialist input.
⚕️ Side Effects
- Hypokalaemia.
- Hypotension during or after infusion.
- Allergic reactions, including urticaria, angioedema, bronchospasm or anaphylaxis.
- Febrile reactions.
- Serum sickness, usually delayed.
- Worsening heart failure after reversal of digoxin effect.
- Rapid ventricular response in atrial fibrillation if digoxin effect is reversed.
- Rebound digoxin toxicity, especially in renal impairment.
🚫 Important Pitfalls
- Do not delay Fab in unstable life-threatening toxicity while waiting for a serum digoxin concentration.
- Do not interpret early post-ingestion digoxin concentrations without considering timing.
- Do not use serum digoxin levels after Fab treatment to guide immediate clinical response.
- Do not forget potassium: hyperkalaemia suggests severe acute toxicity; hypokalaemia may follow treatment.
- Do not give routine calcium for hyperkalaemia in digoxin toxicity without senior/toxicology advice because of historical concern about arrhythmia risk.
- Do not perform electrical cardioversion unless immediately necessary, as digoxin-toxic myocardium may be very irritable.
📝 Exam Pearls
- 🚨 Digoxin toxicity can cause both bradyarrhythmias and ventricular arrhythmias.
- 🧪 Hyperkalaemia in acute digoxin poisoning is a marker of severe toxicity.
- 💊 Digoxin-specific Fab is the antidote for life-threatening toxicity.
- 🧮 One 40 mg vial binds about 0.5 mg digoxin.
- 📈 Digoxin level after Fab can be misleading because bound digoxin may still be measured.
- 🫘 Chronic toxicity is common in older patients with renal impairment or interacting drugs.
- 📞 In the UK, check TOXBASE/NPIS and local policy early.
🧠 Teaching Note
Digoxin toxicity is dangerous because it creates a combination of increased automaticity and impaired AV conduction.
That is why the ECG can show apparently contradictory rhythms: ventricular ectopics or VT alongside bradycardia or AV block.
In acute poisoning, hyperkalaemia reflects severe sodium-potassium ATPase inhibition and is a major warning sign.
Fab fragments work by pulling free digoxin out of the circulation, shifting the equilibrium away from tissue binding and rapidly reducing toxicity.
📚 References