Follow-up
Further Inpatient Care
- Postimmunotherapy treatment
- After treatment with Fab fragments, the serum digoxin level will rise considerably. Digoxin level cannot be used as a guide to treatment after administration of Fab fragments
- Free digoxin levels can be used, but most hospitals do not have this assay available. The elimination half-life of digoxin Fab complex is 20-30 hours, although clearance is related directly to the glomerular filtration rate and consequently is prolonged in renal insufficiency. Recrudescence of digoxin toxicity is possible because the Fab complex is eliminated more rapidly than digoxin is released from tissue-binding sites.
- Significantly, in a long-term digoxin user who requires Fab treatment for digitalis toxicity, administration can precipitate worsening heart failure by removing the beneficial inotropic activity of digoxin, causing hypokalemia and atrial arrhythmia with rapid ventricular response. Hypokalemia occurred in patients who were treated with standard therapy as well as Fab fragments. Clinically adverse phenomena have occurred in fewer than 10% of patients treated with immunotherapy.
- Other untoward effects of Digibind include anaphylaxis and serum sickness because it is a foreign protein; these reactions are uncommon. Allergy to Fab fragments is associated with patients who have multiple allergies.
- Hemodialysis
- Hemodialysis (HD) and activated charcoal hemoperfusion (HP) have no role in the management of digitalis intoxication. Without the use of Fab, these procedures are not indicated because the molecular weight of digoxin is too large for HD to be successful. In addition, the volume of distribution of digoxin is too large to make either approach feasible. Hemodialysis is superfluous after administration of Fab and HP.
- Digoxin-specific antibody fragments are effective even in anephric patients, although symptoms may recur 7–14 days later, possibly indicating the need for another dose of Fab.
- Hemoperfusion through columns with antidigoxin antibodies bound to agarose polyacrolein microsphere beads has been accomplished, but the availability of Fab in the United States makes this modality outdated.
- Continuous arteriovenous hemofiltration in an experimental model has failed to remove the digoxin-Fab complex.
Further Outpatient Care
- Patients with accidental exposure and no sign of toxicity after 12 hours can be discharged home with appropriate follow-up. Observe patients for at least 6 hours on a cardiac monitor, and lab results should be normalized.
- Suicidal, depressed patients should be cleared by a psychiatry consult for prevention of repeated toxic ingestion before discharge.
Transfer
Transfer hemodynamically unstable patients to a tertiary care center equipped with medical intensive care unit/critical care unit (MICU/CCU) capabilities. Notifying of the and discussing the treatment of the poisoning with the regional poison center also is important.
Deterrence/Prevention
- Dosage adjustment with frequent laboratory monitoring, especially if the patient has chronic renal failure
- Adequate hydration
- Supplementation of potassium chloride in patients with diuretic therapy
Prognosis
Prognosis is poor with increasing age and associated comorbid conditions.
Patient Education
- Increase patient awareness about the symptoms of digitalis toxicity.
- Educate patients about drug interactions.
- Educate patients about maintaining adequate hydration.
- For excellent patient education resources, visit eMedicine's Drug Overdose Center, Poisoning - First Aid and Emergency Center and Mental Health and Behavior Center. Also, see eMedicine's patient education articles Poisoning, Drug Overdose, Activated Charcoal, and Poison Proofing Your Home.
Miscellaneous
Medicolegal Pitfalls
Failure to provide psychiatric follow-up with suicidal ingestion is a potential pitfall. Others are failure to follow up on digitalis level with new medication prescription, a hospitalized elderly patient with recent normal outpatient digitalis level on "same" dose, regular rhythm in a patient with chronic atrial fibrillation, and teenager drug overdose.
Special Concerns
- Digoxin in pregnancy
- Digoxin is used widely in the acute management and prophylaxis of fetal paroxysmal supraventricular tachycardia (SVT), as well as in rate control of atrial fibrillation. It is a category C drug. Increased digoxin dosage may be necessary during pregnancy because of enhanced renal clearance and expanded blood volume.
- No series has been published regarding toxicity in the pregnant woman. Digoxin-specific Fab fragments can be used in pregnancy with the caveat that careful monitoring of the fetus must be maintained.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous author Thomas P Smith Jr, MD to the development and writing of this article.
More on Digitalis Toxicity |
| Overview: Digitalis Toxicity |
| Differential Diagnoses & Workup: Digitalis Toxicity |
| Treatment & Medication: Digitalis Toxicity |
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References
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Hoffman BF, Bigger T Jr. Digitalis and allied cardiac glycosides. In: Gilman AG, Rall TW, Nies AS, Taylor P, eds. Goodman and Gilman's The Pharmacological Basis of Therapeutics. 8th ed. New York, NY: Pergamon Press; 1990:814-39.
Howland MA. Prescription medications, digoxin-specific antibody fragments. In: Goldfrank LR, Flomenbaum NE, Lewin NA, Weis, eds. Goldfrank's Toxicologic Emergencies. 6th ed. Norwalk, Conn: Appleton & Lange; 1998:48:801-807.
Lewin NA. Prescription medications, cardiac glycosides. In: Goldfrank LR, Flomenbaum NE, Lewin NA, Weis, eds. Goldfrank's Toxicologic Emergencies. 6th ed. Appleton & Lange; 1998:791-800.
Roberts DJ. Common cardiovascular drugs. In: Rosen P, ed. Emergency Medicine, Concepts and Clinical Practice. 2nd ed. St Louis, Mo: Mosby; 1992:1307-12.
Smith TW, Antman EM, Friedman PL, et al. Digitalis glycosides: mechanisms and manifestations of toxicity. Part I. Prog Cardiovasc Dis. Mar-Apr 1984;26(5):413-58. [Medline].
Further Reading
Keywords
digitalis toxicity, atrial fibrillation, cardiac glycoside, congestive heart failure, CHF, digitoxin, digoxin, inotropic agent, inotropy, Digitalis purpurea, Thevetia peruviana, depletion of potassium stores, myocardial infarction, myocardial ischemia, hypothyroidism, hypercalcemia, renal insufficiency
Follow-up: Digitalis Toxicity