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Mortality and morbidity of heart failure treated with digoxin. A propensity-matched study
J L Andrey1, S Romero, A García-Egido
1Department of Medicine, Hospital Universitario Puerto Real, University of Cadiz, School of Medicine, Spain.
Insights
Digoxin treatment in heart failure (HF) patients is linked to better survival and fewer hospitalizations. This study confirms digoxin
Area of Science:
- Cardiology
- Clinical Pharmacology
- Heart Failure Management
Background:
- The prognostic impact of digoxin in heart failure (HF) patients is not well-established.
- Existing research presents conflicting evidence regarding digoxin's benefits in HF management.
Purpose of the Study:
- To investigate the association between initiating digoxin treatment (CTDig) and patient outcomes in heart failure.
- To evaluate the impact of CTDig on all-cause mortality, cardiovascular mortality, and morbidity events.
Main Methods:
- A prospective, 8-year study involving 4467 heart failure patients.
- Propensity score-matching was used to compare 1421 patients who commenced digoxin treatment with 1421 similar patients who did not.
- Outcomes analyzed included all-cause and cardiovascular mortality, hospitalizations, and healthcare visits.
Main Results:
- Commencing digoxin treatment was associated with significantly lower all-cause mortality (HR=0.90) and cardiovascular mortality (HR=0.87).
- Digoxin use correlated with reduced hospitalizations (HR=0.91), 30-day HF readmissions (HR=0.88), and healthcare visits (HR=0.94).
- These benefits were consistent across different patient subgroups, including women and those with non-systolic heart failure.
Conclusions:
- Digoxin therapy appears to improve both mortality and morbidity in heart failure patients.
- The positive effects of digoxin were observed independently of patient gender or HF type (systolic vs. non-systolic).
- These findings support the continued use of digoxin in selected heart failure populations.
Background:
The role of digoxin in the prognosis of patients with heart failure (HF) remains unclear.
Aims:
To evaluate the relationship of commencing treatment with digoxin (CTDig) with the mortality and the morbidity of patients with HF.
Methods:
Prospective study over 8 years on 4467 patients with HF. Main outcomes were all-cause and cardiovascular mortality, hospitalisations and visits. We analyse the independent relationship of CTDig, with the mortality and the morbidity, stratifying patients for cardiovascular comorbidity, after propensity score-matching for potential confounders (1421 patients who CTDig vs. another 1421 patients non-exposed to digoxin).
Results:
During a median follow up of 46.1 months, 1872 patients (65.9%) died, and 2203 (77.5%) were hospitalised. CTDig was associated with a lower all-cause mortality (HR = 0.90 [95% CI, 0.84-0.97]), and cardiovascular mortality (HR = 0.87 [0.81-0.96]), hospitalisation (HR = 0.91 [0.86-0.97]), 30-day readmission for HF (HR = 0.88 [0.79-0.95]), and visits (HR = 0.94 [0.90-0.98]) (p < 0.001 in all cases), after adjustment for the propensity to take digoxin, other medications, and other potential confounders. These effects of digoxin were independent of gender, or type of HF (systolic or non-systolic).
Conclusion:
The data suggest that therapy with digoxin is associated with an improved mortality and morbidity of HF, including women and patients with non-systolic HF.
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