An international, double-blind, placebo-controlled trial suggested that digitoxin modestly lowered the combined risk of death from any cause or hospital admission for worsening heart failure (HF) than placebo in patients with advanced HF receiving modern therapy. The trial evaluated digitoxin in 1,240 patients with chronic HF and reduced ejection fraction (≤40% with New York Heart Association [NYHA] III–IV or ≤30% with NYHA II). Patients were randomized 1:1 to digitoxin (at a starting dose of 0.07 mg daily) or placebo in addition to guideline-directed medical therapy and followed for a median of 36 months. In the modified intention-to-treat population (n=1,212), digitoxin reduced the composite risk of death or first hospitalization for worsening HF compared with placebo (39.5% vs. 44.1%). Death from any cause occurred in 27.2% vs. 29.5% (HR 0.86) and first hospitalization in 28.1% vs. 30.4% (HR 0.85). Serious adverse events were more frequent in the digitoxin group (4.7% vs. 2.8%). Cardiac glycosides such as digitoxin actions as positive inotropic agents and modulators of atrioventricular conduction. Source: https://www.nejm.org/
A secondary MRI analysis of the US POINTER randomized clinical trial found that a structured…
Dementia risk factors vary substantially across countries, but they frequently cluster together in similar patterns…
A systematic review and network meta-analysis of 262 randomized trials involving 99,791 participants found that…
Approximately 21% of patients with phenotypically mild hypertrophic cardiomyopathy (HCM) experienced major adverse cardiovascular events…
A Danish randomized crossover trial found that a single session of high-intensity interval exercise (HIIE)…
Baseline use of proton pump inhibitors (PPIs) and, to a lesser extent, antibiotics was associated…
This website uses cookies.