- Inotropic agent for treatment of congestive heart failure
- Antiarrhythmic for treatment of supraventricular arrhythmias such as atrial fibrillation, atrial flutter and paroxysmal atrial tachycardia
- Available as 50 mcg/mL (0.05 mg/mL). Stable at room temperature. Protect from light
- Diluted solutions stable 48 hours at room temperature or in fridge
- Solutions Compatible: dextrose up to D10W, NS, Sterile Water for Injection, ringer's lactate
- Additives/Above Cassette Compatible: furosemide
-Y-site Compatible: KCl (up to 40 mmol/mL), morphine, TPN (amino acids/dextrose), heparin, meropenem
-Incompatible: dobutamine, propofol, fluconazole
(For approved routes of administration by nursing personnel, refer to Policy for the Administration of Intravenous Medications.)
SC | NO |
IM | NO, very painful |
IV Direct |
NO |
IV Intermittent Infusion |
YES |
IV Continuous Infusion | NO |
(For neonatal dosages, refer to Neonatal IV Drug Manual.)
DIGITALIZING DOSE: (3 doses- 1st stat; 2nd in 6 hrs; 3rd in another 6 hrs)
- Term infants-2 years: 12 mcg/kg/dose IV
- >2 years: 10 mcg/kg/dose IV
- Maximum total digitalizing dose: 1 mg
MAINTENANCE DOSE: Start 12 hours after last digitalizing dose
- Term infants-2 years: 7 mcg/kg/day IV divided Q12H
- >2-10 years: 6 mcg/kg/day IV once daily or divided Q12H
- >10 years: 2-3 mcg/kg/day IV once daily
- Maximum maintenance dose: 250 mcg/day
DOSAGE ADJUSTMENT IN RENAL IMPAIRMENT:
- Total digitalizing dose: reduce by 50% in end-stage renal disease
- Maintenance dose:
- CrCl 10-50 mL/min: Administer 25-75% of normal daily dose (divided and given at normal intervals) or administer normal dose every 36 hours
- CrCl < 10 mL/min: Administer 10-25% of normal daily dose (divided and given at normal intervals) or administer normal dose every 48 hours
- IM injections may cause pain and muscle spasm, erratic absorption and crystal deposition in the muscle
- Extravasation may cause local irritation and sloughing
- Non-cardiac symptoms of digoxin toxicity hard to evaluate in children; usual toxic effects reported in infants are:
- Gastrointestinal: feeding intolerance/diminished appetite, persistent vomiting
- Cardiac effects: the diagnosis of digoxin toxicity in neonates and infants usually
rests on ECG abnormalities, arrhythmias, first degree AV block, PVC's, bigeminy
PAT with block; sinus node bradycardia is the major cardiac manifestation in low
birth weight infants.
- Monitor heart rate and rhythm, serum potassium, magnesium, calcium, ECG
- IV dose = oral dose × 0.7
- Oral dose = IV dose × 1.4
Treatment of overdose:
- Discontinue drug
- Administer potassium salts and other cardiac drugs for treating arrhythmias
- Possibility of digitalis toxicity greater in patients who are hypokalemic, hypo or hypermagnesemic, hypercalcemic, have decreased renal function, are in premature age category, had a loading dose
- DIGIBIND may be used as an antidote. One vial of Digibind neutralizes 0.5 mg digoxin.
Drug levels:
- Therapy should be monitored by clinical effect rather than serum level; useful when toxicity suspected
- "Therapeutic" serum level 1.3-2.7 nmol/L (correlation with therapeutic effect not clearly defined)
- Draw blood for digoxin at least 8 hrs post dose or preferably prior to next scheduled dose
- Levels may be elevated in neonates due to endogenous digoxin-like substances
- When administering digoxin, nurses first take the heart rate. If the heart rate is lower than indicated below, the medication is held and the physician is notified:
Age
Heart Rate
Birth- 6 months
95 beats/minute
6 months-18 months
80 beats/minute
>18 months
65 beats/minute