What is the recommended dose of digoxin (digitalis glycoside) for controlling heart rate in atrial fibrillation?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: September 15, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Digoxin Dosing for Heart Rate Control in Atrial Fibrillation

For heart rate control in atrial fibrillation, the recommended digoxin dose is 0.25 mg PO every 2 hours up to 1.5 mg total for loading, followed by a maintenance dose of 0.125-0.375 mg daily, with adjustments based on renal function, age, and body weight. 1

Initial Dosing Strategy

Loading Dose (for rapid rate control)

  • Intravenous: 0.25 mg IV every 2 hours, up to a total loading dose of 1.5 mg 1
  • Oral: 0.25 mg PO every 2 hours, up to a total loading dose of 1.5 mg 1
  • Onset of action: Approximately 2 hours 1

Maintenance Dose

  • Standard range: 0.125-0.375 mg daily 1, 2
  • Typical starting dose: 0.125-0.25 mg daily 2, 3

Dose Adjustments

Patient Factors Requiring Lower Doses (0.125 mg daily or less)

  • Age >70 years 2
  • Impaired renal function 2, 3
  • Low lean body weight 2, 3

Renal Function Adjustments

Renal Function eGFR Recommended Dose
Normal >60 mL/min 0.25 mg daily
Mild impairment 45-59 mL/min 0.125 mg daily
Moderate impairment 30-44 mL/min 0.125 mg daily or every other day
Severe impairment <30 mL/min 0.0625-0.125 mg every other day

Monitoring and Target Levels

Target Heart Rate

  • Resting heart rate: 60-80 bpm 1
  • Exercise heart rate: 90-115 bpm 1

Therapeutic Serum Levels

  • Target serum concentration: 0.5-0.9 ng/mL 2
  • Check levels 5-7 days after initiation 2
  • Toxicity risk increases with levels >2 ng/mL 4

Important Considerations

Efficacy Limitations

  • Digoxin alone is often insufficient for rate control during exercise 5
  • Consider combination therapy with beta-blockers or non-dihydropyridine calcium channel blockers for better rate control 1, 6

Contraindications

  • Wolff-Parkinson-White syndrome with pre-excited AF (Class III: Harm) 1
  • Significant AV block without pacemaker 2
  • Sinus node dysfunction without pacemaker 2

Drug Interactions

  • Amiodarone, verapamil, quinidine, and other medications can increase digoxin levels 2
  • Reduce digoxin dose by 30-50% when these medications are initiated 2

Monitoring for Toxicity

  • Signs of toxicity: confusion, nausea, anorexia, visual disturbances, cardiac arrhythmias 2
  • Monitor serum potassium and magnesium levels (hypokalemia and hypomagnesemia increase toxicity risk) 2

Clinical Recommendations

  1. In patients with AF and heart failure with reduced ejection fraction (HFrEF), digoxin is effective for controlling resting heart rate (Class I recommendation) 1

  2. For patients with AF and normal heart function, beta-blockers or calcium channel blockers are preferred first-line agents, with digoxin as an adjunct 1

  3. Combination therapy with digoxin plus a beta-blocker (or non-dihydropyridine calcium channel antagonist in patients with preserved ejection fraction) is reasonable to control both resting and exercise heart rate (Class IIa recommendation) 1

  4. Higher doses of digoxin (>0.25 mg daily) for rate control in AF are not recommended 4

  5. For acute rate control in critically ill patients, a median total loading dose of 750 mcg (approximately 11 mcg/kg) distributed over six-hour intervals may be considered 7

Remember that digoxin has a narrow therapeutic window, and careful dosing and monitoring are essential to maximize benefits while minimizing toxicity risks.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.