What it isNa-K ATPase inhibitor raising intracellular calcium; rate control in atrial fibrillation and symptom control in heart failure.
Why this oneIt slows the ventricular rate without lowering blood pressure, so it suits hypotensive patients whom beta blockers and diltiazem cannot.
What limits itNarrow therapeutic index with level monitoring. Renally cleared, and hypokalemia worsens toxicity; amiodarone and verapamil raise levels through P-gp.
Oral loading dose (rapid titration; HF / AF rate control)
Adults & pediatric >10 y
10–15 mcg/kg total: ½ initially, then ¼ q6–8h ×2
Oral loading dose (rapid titration)
Children 5–10 y
20–45 mcg/kg total: ½ initially, then ¼ q6–8h ×2
Maintenance dosing
Adults & pediatric >10 y
Individualized to lean body weight, renal function, age, and concomitant drugs
Renal Renally eliminated; consider renal function in dosage selection and reduce dose accordingly.
Hepatic Undefined
Toxic levels are only slightly higher than therapeutic; monitor serum concentrations and for signs of toxicity.
Instructions
Use digoxin oral solution for infants, young children, or very low body weight to obtain the appropriate dose
Give loading as ½ the total dose initially, then ¼ q6–8h ×2, assessing response/toxicity before each dose
Consider dose interruption or reduction before electrical cardioversion
Available strengths
tab 62.5, 125, 250 mcg
inj 0.1, 0.25 mg/mL
sol 0.05 mg/mL
Contraindications
Ventricular fibrillation
Cautions
Ventricular fibrillation risk in Wolff-Parkinson-White / accessory AV pathway with atrial fibrillation
Severe sinus bradycardia, SA block, or advanced/complete heart block in sinus node or AV conduction disease (consider pacemaker first)
Digoxin toxicity (anorexia, nausea, vomiting, visual changes, arrhythmias); predisposed by advanced age, low body weight, renal impairment, electrolyte abnormalities
Ventricular arrhythmias during electrical cardioversion
Not recommended in acute myocardial infarction; avoid in myocarditis
Adverse reactions
Cardiac arrhythmias
Digoxin toxicity
GI disturbances (anorexia, nausea, vomiting)
CNS and visual disturbances
Pregnancy No identified drug-associated risk; requirements may increase during pregnancy and decrease postpartum — monitor levels; monitor neonate for toxicity.