Digoxin: Difference between revisions
(Fix SMW query: replace link=subject with mainlabel=- to fix broken subobject fragment links) |
(Switch SMW query from broadtable to table format for better layout with TOC) |
||
| Line 59: | Line 59: | ||
|?Has Route=Route | |?Has Route=Route | ||
|?Has Population=Population | |?Has Population=Population | ||
|format= | |format=table | ||
|headers=plain | |headers=plain | ||
|mainlabel=- | |mainlabel=- | ||
Latest revision as of 21:56, 20 March 2026
General
- Type: Cardiac glycoside; CHF medications
- Mechanism of action- Inhibits Na+/K+ ATPase, leading to an increase in intracellular sodium that can increase cardiac contractility
- Dosage Forms: PO, IV, IM
- Common Trade Names: Digitek, Digox, Lanoxin
Adult Dosing
- Loading dose = 0.25mg IV q2hr until effect (max total = 1.5mg)
- in acute atrial fibrillation with RVR with heart failure = 0.5mg IV, then 0.25mg IV q4hr until effect or max 1.5mg
Pediatric Dosing
Special Populations
- Pregnancy Rating: C
- Lactation risk:
- Renal Dosing
- Adult
- Pediatric
- Hepatic Dosing
- Adult
- Pediatric
Indications
- RVR control in a-fib/flutter, PSVT
Contraindications
- Allergy to class/drug
- WPW
- Increases conduction velocity in atrial tissue
Adverse Reactions
- GI: nausea and vomiting, diarrhea, abdominal pain
- CV: Bradycardia, SA/AV block, ventr arrhythmias
- Neuro: altered mental status, visual disturbances (yellow-tinted vision)
Pharmacology
- Onset of action
- IV = 5-30 minutes
- PO = 0.5-2 hours
- Half-life: 36-48 hours (may be increased with renal impairment)
- Absorption: 60-80% absorption after oral administration
- Metabolism: ~16% is converted to metabolites
- Excretion: Almost entirely by the kidneys
Mechanism of Action
- Inhibits Na+/K+ ATPase in the myocardium[1]
- Causes increase in intracellular sodium levels
- Results in reversal of sodium-calcium exchanger
- Normally imports three extracellular sodium ions into the cardiac myocyte in exchange for one intracellular calcium being exported
- Sodium accumulates intracellularly and is exchanged for Calcium.
- Causes an increase in the intracellular calcium concentration increasing contractility
- Also a lengthening of phase 4 and phase 0 of the cardiac action potential which ultimately decreases heart rate
- Summary
- Inhibits NaK pump
- Positive inotropy
- Negative chronotropy/dromotropy
- Indirect vagal stimulator
- Inhibits NaK pump
Comments
Indications by Condition
The following table is automatically generated from disease/condition pages across WikEM.
| Indication | Dose | Context | Route | Population |
|---|---|---|---|---|
| Atrial fibrillation (main) | 500 mcg IV, then 250 mcg q4h x2 (total 1000 mcg digitizing dose) | Rate control (if hypotensive or advanced HF) | IV | Adult |
See Also
References
- ↑ Gheorghiade M. et al. Digoxin in the Management of Cardiovascular Disorders. Circulation. 2004; 109: 2959-2964
