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Is digoxin an independent risk factor for long-term mortality after acute myocardial infarction?
L Køber1, C Torp-Pedersen, N Gadsbøll
1Department of Medicine C, Glostrup Hospital, University of Copenhagen, Denmark.
Insights
Digoxin treatment in acute myocardial infarction survivors is associated with increased mortality. This study found digoxin significantly increased the risk of death, even after accounting for other risk factors.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Acute myocardial infarction (MI) survivors face long-term risks.
- Digoxin is a medication sometimes used in post-MI care.
- The safety of digoxin in this population requires further investigation.
Purpose of the Study:
- To investigate the safety and impact of digoxin treatment on mortality in hospital survivors of acute myocardial infarction.
Main Methods:
- A cohort of 584 MI survivors was followed for a median of 6.2 years.
- Patients were assessed for left ventricular ejection fraction (LVEF) via radionuclide ventriculography.
- Mortality data was collected, and a proportional hazard model was used to analyze risk factors.
Main Results:
- Digoxin-treated patients were older, had lower LVEF, and higher rates of diabetes and heart failure.
- 1- and 5-year mortality rates were significantly higher in the digoxin group (38% and 74%) compared to the non-digoxin group (8% and 26%).
- Digoxin was independently associated with an increased risk of death (relative risk 1.8).
Conclusions:
- Digoxin administration may be harmful in hospital survivors of acute myocardial infarction.
- The increased mortality risk associated with digoxin persisted across various patient subgroups.
- Further research into safer therapeutic options for post-MI patients is warranted.
Abstract:
The safety of treatment with digoxin in patients with acute myocardial infarction (MI) was investigated in 584 hospital survivors of MI. All patients were examined by radionuclide ventriculography, with determination of left ventricular ejection fraction (LVEF), close to the time of discharge. Clinical data were collected on admission. All patients were followed up with regard to death (median 6.2 years, range 3.9-7.8 years). Patients treated with digoxin (N = 172 (29%) were older (median 66 vs 59 years; (P < 0.001), had a higher incidence of diabetes (13% vs 7%; P = 0.025), and a lower LVEF (0.33 vs 0.49; P < 0.001). As expected, clinical heart failure was more frequent among them (84% vs 14%; P < 0.001), than in patients not receiving digoxin. The 1- and 5-year mortality of patients treated with digoxin was 38% and 74% compared to 8% and 26% in patients not receiving digoxin (P < 0.001). The increased risk associated with digoxin therapy remained statistically significant when patients were stratified according to the presence or absence of heart failure or atrial fibrillation/flutter during hospitalization, or to LVEF above or below 0.45 at discharge. In a proportional hazard model including age, LVEF, diabetes mellitus, heart failure, atrial fibrillation or flutter, ventricular fibrillation, gender, dose of furosemide at discharge and calcium antagonists and digoxin treatment as covariates, digoxin was independently associated with an increased risk of death (relative risk 1.8 (95% confidence limit 1.2-2.5)). We conclude that administration of digoxin may be harmful in hospital survivors of MI.
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