scholarly journals MONITORING OF SERUM DIGOXIN CONCENTRATION AND SAFETY OF THERAPY WITH DIGOXIN IN PATIENTS WITH ATRIAL FIBRILLATION

2018 ◽  
Vol 14 (2) ◽  
pp. 197-203
Author(s):  
S. F. Zadvorev ◽  
A. A. Yakovlev ◽  
A. S. Pushkin ◽  
S. A. Rukavishnikova ◽  
A. E. Filippov ◽  
...  
1997 ◽  
Vol 31 (4) ◽  
pp. 438-440 ◽  
Author(s):  
Christopher P Alderman ◽  
Peter D Allcroft

Objective To document a case in which the administration of itraconazole was associated with an apparent decrease in digoxin clearance, resulting in an increase in the serum digoxin concentration. Case Summary A man receiving digoxin for atrial fibrillation was concurrently treated with itraconazole 200 mg/d for esophageal candidiasis. The estimated urinary digoxin clearance was decreased during this combination therapy. Discussion Digoxin is primarily cleared by the kidneys, and the mechanism of renal clearance involves both glomerular filtration and tubular secretion. We postulate that itraconazole or a metabolite of this compound may have resulted in decreased tubular secretion of digoxin, accounting for decreased urinary digoxin clearance. Conclusions Monitoring of serum digoxin concentrations should be performed if patients taking digoxin are treated with itraconazole. Further investigation is necessary to elucidate the nature of the interaction between digoxin and itraconazole.


1979 ◽  
Vol 17 (13) ◽  
pp. 49-51

Digoxin is widely used to treat heart failure and atrial fibrillation. Toxicity from the drug is common1 2 and dangerous, and it is therefore important to consider whether it can be avoided by careful prescribing and a knowledge of the serum digoxin concentration.


1973 ◽  
Vol 3 (6) ◽  
pp. 606-613 ◽  
Author(s):  
G. J. Schapel ◽  
B. P. McGrath ◽  
K. D. G. Edwards ◽  
M. R. Hawkins ◽  
A. S. Mitchell

2016 ◽  
Vol 18 (8) ◽  
pp. 1072-1081 ◽  
Author(s):  
Kirkwood F. Adams ◽  
Javed Butler ◽  
J. Herbert Patterson ◽  
Wendy Gattis Stough ◽  
Jerry L. Bauman ◽  
...  

1997 ◽  
Vol 31 (7-8) ◽  
pp. 864-866 ◽  
Author(s):  
James J. Nawarskas ◽  
David M. McCarthy ◽  
Sarah A. Spinier

OBJECTIVE: To report a case of digoxin toxicity thought to be secondary to clarithromycin therapy. CASE SUMMARY: A 78-year-old white woman with congestive heart failure taking digoxin 0.25 mg po qd presented to our hospital with nausea, vomiting, and diarrhea. She had taken clarithromycin 500 mg po bid for 3 days, and a serum digoxin concentration obtained the day of admission was 4.4 μg/L. An electrocardiogram (ECG) done on admission revealed ST segment changes consistent with digoxin effect and later asymptomatic, nonsustained ventricular tachycardia (NSVT). Clarithromycin was discontinued and digoxin was withheld at admission, resulting in the resolution of symptoms, ECG abnormalities, and NSVT on day 3 of hospitalization. On day 5 her serum digoxin concentration was 1.5 μg/L and digoxin therapy was reinstituted at a dose of 0.125 mg/d po. DISCUSSION: This is the fourth published case implicating clarithromycin as the cause of digoxin toxicity. This interaction is most likely due to clarithromycin eradication of digoxinmetabolizing gut flora, thereby increasing digoxin bioavailability. CONCLUSIONS: Approximately 10% of patients are thought to be extensive presystemic metabolizers of digoxin and may therefore be most susceptible to a drug interaction with clarithromycin. Serum digoxin concentrations in such patients should be monitored closely during clarithromycin therapy.


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