Key result
Digoxin use in HFrEF is linked to ~76% higher mortality and increased re-hospitalization.
Why the study?
The impact of digoxin use on HFrEF outcomes and its interaction with atrial fibrillation or guideline-recommended treatments in real-world China remained to be determined.
Does digoxin use improve mortality and re-hospitalization outcomes in patients with HFrEF?
Observational (n=882)
Yes
Does digoxin use improve mortality and re-hospitalization outcomes in patients with HFrEF?
Effect estimate: HR 1.76 (95% CI 1.27-2.44)
p-value: p=0.001
In a real-world Chinese registry of HFrEF patients, digoxin use was independently associated with increased risks of all-cause mortality and all-cause re-hospitalization.
AIMS: The aim of this study was to investigate the impact of digoxin use on the outcomes of patients with heart failure with reduced ejection fraction (HFrEF) and its possible interaction with atrial fibrillation or use of currently guideline-recommended treatments in the real world in China. METHODS AND RESULTS: Patients hospitalized with HFrEF from 45 hospitals participating in the China National Heart Failure Registration Study (CN-HF) were enrolled to assess the all-cause mortality, HF mortality, all-cause re-hospitalization, and HF re-hospitalization associated with digoxin use. Eight hundred eighty-two eligible HFrEF patients in the CN-HF registry were included: 372 patients with digoxin and 510 patients without digoxin. Among them, 794 (90.0%) patients were followed up for the endpoint events, with a median follow-up of 28.6 months. Kaplan-Meier survival analysis showed that the all-cause mortality (P < 0.001) and all-cause re-hospitalization (P = 0.020) were significantly higher in digoxin group than non-digoxin group, while HF mortality (P = 0.232) and HF re-hospitalization (P = 0.098) were similar between the two groups. The adjusted Cox proportional-hazards regression analysis demonstrated that digoxin use remained as an independent risk factor for increased all-cause mortality [hazard ratio (HR) 1.76; 95% confidence interval (CI) 1.27-2.44; P = 0.001] and all-cause re-hospitalization (HR 1.27; 95% CI 1.03-1.57; P = 0.029) in HFrEF patients and the predictive value of digoxin for all-cause mortality irrespective of rhythm or in combination with other guideline-recommended therapies. CONCLUSIONS: Digoxin use is independently associated with increased risk of all-cause mortality and all-cause re-hospitalization in HFrEF patients.
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Zhou et al. (2020) conducted an observational in Heart failure with reduced ejection fraction (HFrEF) (n=882). Digoxin vs. No digoxin was evaluated on All-cause mortality (HR 1.76, 95% CI 1.27-2.44, p=0.001). Digoxin use in HFrEF patients was independently associated with an increased risk of all-cause mortality (HR 1.76; 95% CI 1.27-2.44; P=0.001) and all-cause re-hospitalization.
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