titrated to the minimum dose that achieves the desired ventricular rate control without causing
undesirable side effects.
Dose Adjustments
If patients are switched from intravenous to oral formulations, allowances must be made for
differences in bioavailability when calculating maintenance dosages. When changing from oral
formulations to IM or IV therapy, dosage should be reduced by 20% to 25%.
Lanoxicaps (gelatin capsules) have greater bioavailability than standard tablets, and the
recommended oral doses are only 80% of those for tablets and elixir. Therefore, the 0.2 mg
capsule is equivalent to 0.25 mg tablets; the 0.1 mg capsule is equivalent to 0.125 mg tablets; and
the 0.05 mg capsule is equivalent to 0.0625 mg. Divided dosage of the capsule formulation is
preferred in patients that require a daily dose greater than 300 mcg, those with a previous history
of digitalis toxicity, and in patients who may be more likely to become toxic.
Hyperthyroid patients generally require a slightly higher loading dose (10%). Hypothyroid
patients generally require a slightly lower loading dose (10%).
Dialysis
Digoxin is not removed by hemo- or peritoneal dialysis.
Other Comments
Calculated doses should be based on lean body weight.
While most patients with signs and symptoms of toxicity have serum digoxin levels greater than
2.0 ng/mL, there is a somewhat poor correlation between levels, effect and toxicity. Therefore,
serum level monitoring is usually only recommended to assess patient compliance, to evaluate
clinical deterioration following an initially good response, to evaluate unsuspected toxicity, and
to assess patients who are at a higher risk of toxicity. Such patients may include individuals with
underlying renal or cardiopulmonary disease, thyroid disease, and electrolyte imbalances such as
hypokalemia, hypomagnesemia, or hypercalcemia. Patients > 65 years of age are also at higher
risk for toxicity. The best time to sample a trough serum digoxin level is just before a dose 7 to
14 days after initiation of therapy. If the patient is also taking quinidine when serum digoxin
levels are needed, the blood sample may be drawn just before both drugs are given. A common
mistake is checking serum digoxin levels immediately after a loading or maintenance dose.
Because digoxin distributes slowly into peripheral tissues over at least 6 hours, assays performed
before this period do not indicate steady-state levels.
Intramuscular injection is extremely painful and offers no advantages unless other routes of
administration are contraindicated.
A post-hoc analysis of a large study (DIG trial) involving patients with chronic heart failure (HF)
receiving long-term digoxin therapy, revealed that discontinuation of digoxin was associated
with a significant increase in all-cause hospitalization and hospitalization for HF, but had no
effect on all-cause mortality. In contrast, continuation of digoxin at low serum concentrations
(0.5 to 0.9 ng/mL) was associated with a reduction in all-cause mortality, all-cause
hospitalizations, and hospitalizations for HF. In addition, heart failure guideline
recommendations include that if a patient with HF is already receiving digoxin but not an ACEI
or beta-blocker, treatment with digoxin should not be discontinued.