Key result
Digoxin use in hospitalized patients with HFrEF receiving β-blockers was associated with a lower risk of 30-day all-cause readmission (15% vs 27%; HR 0.51; 95% CI 0.31-0.83; P=0.007).
Why the study?
Does digoxin reduce 30-day all-cause readmission in older patients with HFrEF receiving beta-blockers?
Cohort (n=334)
Does digoxin reduce 30-day all-cause readmission in older patients with HFrEF receiving beta-blockers?
In older patients with HFrEF on beta-blockers, adding digoxin at discharge is associated with a significantly lower risk of 30-day all-cause readmission.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for digoxin addition in older HFrEF on beta-blockers; prospective trials needed before clinical adoption.
BACKGROUND: Digoxin use has been associated with a lower risk of 30-day all-cause admission and readmission in patients with heart failure and reduced ejection fraction (HFrEF). HYPOTHESIS: Digoxin use will be associated with improved outcomes in patients with HFrEF receiving β-blockers. METHODS: Of the 3076 hospitalized Medicare beneficiaries with HFrEF (EF <45%), 1046 received a discharge prescription for β-blockers, of which 634 were not on digoxin. Of the 634, 204 received a new discharge prescription for digoxin. Propensity scores for digoxin use, estimated for each of the 634 patients, were used to assemble a matched cohort of 167 pairs of patients receiving and not receiving digoxin, balanced on 30 baseline characteristics. Matched patients (n = 334) had a mean age of 74 years and were 46% female and 30% African American. RESULTS: 30-day all-cause readmission occurred in 15% and 27% of those receiving and not receiving digoxin, respectively (hazard ratio [HR]: 0.51, 95% confidence interval [CI]: 0.31-0.83, P = 0.007). This beneficial association persisted during 4 years of follow-up (HR: 0.72, 95% CI: 0.57-0.92, P = 0.008). Digoxin use was also associated with a lower risk of the combined endpoint of all-cause readmission or all-cause mortality at 30 days (HR: 0.54, 95% CI: 0.34-0.86, P = 0.009) and at 4 years (HR: 0.76, 95% CI: 0.61-0.96, P = 0.020). CONCLUSIONS: In hospitalized patients with HFrEF receiving β-blockers, digoxin use was associated with a lower risk of 30-day all-cause readmission but not mortality, which persisted during longer follow-up.
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Lam et al. (2018) conducted a cohort in Heart failure and reduced ejection fraction (HFrEF) (n=334). Digoxin vs. No digoxin was evaluated on 30-day all-cause readmission (HR 0.51, 95% CI 0.31-0.83, p=0.007). Digoxin use in hospitalized patients with HFrEF receiving β-blockers was associated with a lower risk of 30-day all-cause readmission (15% vs 27%; HR 0.51; 95% CI 0.31-0.83; P=0.007).
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