Digoxin 0.25mg Tablet Dosage for Heart Failure
For most adult patients with heart failure and normal renal function under age 70, initiate digoxin at 0.25 mg daily without a loading dose, targeting serum concentrations of 0.5-1.0 ng/mL. 1
Standard Dosing Algorithm
Initial Dose Selection Based on Patient Characteristics
- Patients under 70 years with normal renal function: Start with 0.25 mg daily 1, 2
- Patients over 70 years, impaired renal function, or low lean body mass: Start with 0.125 mg daily 1, 2
- Marked renal impairment (CrCl <30 mL/min): Start with 0.0625 mg daily 3
- Dialysis-dependent patients: Use 0.0625 mg daily or every other day 3
Loading Doses Are Not Recommended
There is no reason to use loading doses of digoxin to initiate therapy in patients with heart failure. 1, 3 The ACC/AHA guidelines explicitly state that loading doses should be avoided, as steady-state concentrations will be achieved in approximately 1-3 weeks depending on renal function, and this gradual accumulation is safer than rapid loading. 1, 3
Target Therapeutic Range
Aim for serum digoxin concentrations of 0.5-1.0 ng/mL (specifically 0.5-0.9 ng/mL), which is lower than historically recommended levels. 1, 3 Retrospective analysis of the Digitalis Investigation Group trial demonstrated that risk-adjusted mortality increased when plasma concentrations exceeded 1.0 ng/mL, and lower concentrations (0.5-0.9 ng/mL) provided equivalent prevention of worsening heart failure. 1
Monitoring Requirements
- Check digoxin levels early during chronic therapy in all patients, with sampling done just before the next scheduled dose or at least 6-8 hours after the last dose 3, 2
- Serial monitoring of serum electrolytes and renal function is mandatory 3
- Routine digoxin level monitoring is not beneficial in stable patients, but should be checked for suspected toxicity, significant changes in renal function, or initiation of interacting medications 3
Critical Dose Adjustments for Drug Interactions
Reduce the digoxin dose by approximately 50% when initiating the following medications, as they significantly increase serum digoxin concentrations: 1, 3, 4
- Amiodarone (consider 0.0625 mg daily if N-desethylamiodarone >600 ng/mL) 5
- Clarithromycin or erythromycin
- Verapamil or diltiazem
- Quinidine
- Itraconazole
- Cyclosporine
- Propafenone
- Dronedarone
Common Pitfalls to Avoid
Electrolyte Disturbances
**Toxicity may occur even with therapeutic digoxin levels if hypokalemia (K+ <4.0 mEq/L), hypomagnesemia, or hypothyroidism coexist.** 1, 4 Maintain potassium >4.0 mEq/L to minimize toxicity risk. 4
Higher Doses Are Rarely Needed
Higher doses (0.375-0.50 mg daily) are rarely used or needed in heart failure management and increase toxicity risk without superior outcomes. 1 The European Society of Cardiology guidelines specify that the usual daily dose is 0.125-0.25 mg for patients with normal serum creatinine. 1
Acute Decompensation
Digoxin is not indicated as primary therapy for stabilization of patients with acute exacerbation of heart failure symptoms. 1 Such patients should first receive appropriate treatment with intravenous medications; digoxin may be initiated after stabilization. 1
Contraindications
Do not administer digoxin to patients with: 1
- Significant sinus or atrioventricular block (unless treated with permanent pacemaker)
- Bradycardia
- Sick sinus syndrome
- Carotid sinus syndrome
- Wolff-Parkinson-White syndrome
- Hypertrophic obstructive cardiomyopathy
- Severe hypokalemia or hyperkalemia
Maintenance Dosing Calculation
For patients requiring precise dose calculation, the FDA label provides a formula based on creatinine clearance: 2
Maintenance Dose = Peak Body Stores × % Daily Loss/100
Where: % Daily Loss = 14 + (CrCl/5)
This formula accounts for the fact that digoxin elimination is primarily renal, and steady-state will be achieved in 1-3 weeks depending on renal function. 2
Signs of Toxicity Requiring Immediate Action
Overt digoxin toxicity is commonly associated with serum levels >2 ng/mL but may occur at lower levels. 1, 4 Manifestations include: 4
- Cardiac: ventricular tachycardia (especially fascicular or bidirectional), enhanced automaticity with AV block
- Gastrointestinal: anorexia, nausea, vomiting
- Neurological: visual disturbances (blurred or yellow vision), confusion, disorientation
For life-threatening toxicity with serious arrhythmias or hyperkalemia, administer digoxin-specific Fab antibody fragments immediately. 3, 4