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Browsing by Author "Liu, Xiaofei (57194779909)"

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    Publication
    DIGitoxin to Improve ouTcomes in patients with advanced chronic Heart Failure (DIGIT-HF): Baseline characteristics compared to recent randomized controlled heart failure trials
    (2025)
    Bavendiek, Udo (6603181145)
    ;
    Thomas, Nele Henrike (57462387700)
    ;
    Berliner, Dominik (35763672200)
    ;
    Liu, Xiaofei (57194779909)
    ;
    Schwab, Johannes (7103000098)
    ;
    Rieth, Andreas (56671124800)
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    Maier, Lars S. (7006758541)
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    Schallhorn, Sven (57208665843)
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    Angelini, Eleonora (57208630137)
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    Soltani, Samira (57221604303)
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    Rathje, Fabian (57196454880)
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    Sandu, Mircea-Andrei (59522326400)
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    Geller, Welf (57219306461)
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    Gaspar, Thomas (35242589300)
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    Hambrecht, Rainer (55270627500)
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    Zdravkovic, Marija (24924016800)
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    Philipp, Sebastian (7005290672)
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    Kosevic, Dragana (15071017200)
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    Nickenig, Georg (55618199500)
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    Scheiber, Daniel (57188684210)
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    Winkler, Sebastian (35761822300)
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    Becher, Peter Moritz (25025631600)
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    Lurz, Philipp (35810676500)
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    Hülsmann, Martin (7006719269)
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    von Karpowitz, Maria (57218118768)
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    Schröder, Christoph (57196280792)
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    Neuhaus, Barbara (57204459000)
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    Seltmann, Anika (59522013000)
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    von der Leyen, Heiko (6604097968)
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    Veltmann, Christian (8866550200)
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    Störk, Stefan (6603842450)
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    Böhm, Michael (35392235500)
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    Koch, Armin (7403037285)
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    Großhennig, Anika (26025890500)
    ;
    Bauersachs, Johann (7004626054)
    Aims: This report presents the baseline characteristics of patients enrolled in the DIGIT-HF trial and compares them with participants from recent trials with improved outcomes in patients with heart failure (HF) and a reduced ejection fraction (HFrEF). Methods and results: DIGIT-HF, a randomized, double-blind, placebo-controlled, multicentre trial enrolling patients with symptomatic HFrEF (New York Heart Association [NYHA] functional class II and left ventricular ejection fraction [LVEF] ≤30%, or NYHA class III–IV and LVEF ≤40%), compares the efficacy and safety of digitoxin versus placebo in addition to standard treatment. Most baseline characteristics of the intention-to-treat population (1212 patients, mean age 66 ± 11 years, 20% women, mean LVEF 29 ± 7%) were similar to those in recent HFrEF trials. The distribution of NYHA class II, III, and IV was 30%, 66% and 4%, respectively, and indicates that the patients were sicker than in comparator HFrEF trials. Less patients had atrial fibrillation (27%) than those in recent HFrEF trials, but prescription rates of background therapy with beta-blockers (96%), angiotensin-converting enzyme inhibitors/angiotensin receptor blockers/angiotensin receptor–neprilysin inhibitors (95%), mineralocorticoid receptor antagonists (76%), and diuretics (87%) were high and similar. Overall, 40% of patients were on angiotensin receptor–neprilysin inhibitors, 19% on sodium–glucose cotransporter 2 inhibitors, and 9% on ivabradine. Rates of implantable cardioverter-defibrillator (ICD, 64%) and cardiac resynchronization therapy (CRT, 25%) devices were much higher than in recent HFrEF trials. Conclusions: Patients included in DIGIT-HF display a more severe HF symptom burden and higher rates of ICD/CRT implants compared to participants in recent HFrEF trials, while pharmacotherapy was largely similar. Clinical Trial Registration: EudraCT (2013–005326-38). © 2025 The Author(s). European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

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