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Sökning: onr:"swepub:oai:DiVA.org:uu-533290" > Repetitive levosime...

Repetitive levosimendan infusions for patients with advanced chronic heart failure in the vulnerable post-discharge period : The multinational randomized LeoDOR trial

Poelzl, Gerhard (författare)
Med Univ Innsbruck, Dept Internal Med 3, A-6020 Innsbruck, Austria.;Med Univ Innsbruck, Dept Internal Med 3, Anichstr 35, A-6020 Innsbruck, Austria.
Altenberger, Johann (författare)
Paracelsus Med Private Univ, Teaching Hosp, Cardiac Rehabil Ctr Grossgmain, Pensionsversicherungsanstalt, Salzburg, Austria.
Comin-Colet, Josep (författare)
Bellvitge Univ Hosp, Dept Cardiol, Barcelona, Spain.;Univ Barcelona Hospitalet Llobregat, IDIBELL, CIBER CV, Barcelona, Spain.
visa fler...
Delgado, Juan F. (författare)
Univ Hosp 12 Octubre, Dept Cardiol, CIBERCV, Madrid, Spain.
Fedele, Francesco (författare)
Sapienza Univ Rome, Dept Cardiovasc Resp Nephrol Anesthesiol & Geriat, Rome, Italy.
Garcia-Gonzalez, Martin Jesus (författare)
Univ Hosp Canarias, Anaesthesiol Dept, Santa Cruz De Tenerife, Spain.
Gustafsson, Finn (författare)
Copenhagen Univ Hosp, Dept Cardiol, Copenhagen, Denmark.
Masip, Josep (författare)
Univ Barcelona, Consorci Sanit Integral, Res Direct, Barcelona, Spain.
Papp, Zoltan (författare)
Univ Debrecen, Fac Med, Dept Cardiol, Div Clin Physiol, Debrecen, Hungary.
Stoerk, Stefan (författare)
Univ Hosp Wurzburg, Comprehens Heart Failure Ctr, D-97080 Wurzburg, Germany.;Univ Hosp Wurzburg, Dept Internal Med 1, Wurzburg, Germany.
Ulmer, Hanno (författare)
Med Univ Innsbruck, Inst Med Stat & Informat, Innsbruck, Austria.
Maier, Sarah (författare)
Med Univ Innsbruck, Inst Med Stat & Informat, Innsbruck, Austria.
Vrtovec, Bojan (författare)
Univ Med Ctr Ljubljana, Dept Cardiol, Ljubljana, Slovenia.
Wikström, Gerhard (författare)
Uppsala universitet,Kardiologi
Zima, Endre (författare)
Semmelweis Univ, Heart & Vasc Ctr, Cardiac Intens Care Unit, Budapest, Hungary.
Bauer, Axel (författare)
Med Univ Innsbruck, Dept Internal Med 3, A-6020 Innsbruck, Austria.
visa färre...
Med Univ Innsbruck, Dept Internal Med 3, A-6020 Innsbruck, Austria;Med Univ Innsbruck, Dept Internal Med 3, Anichstr 35, A-6020 Innsbruck, Austria. Paracelsus Med Private Univ, Teaching Hosp, Cardiac Rehabil Ctr Grossgmain, Pensionsversicherungsanstalt, Salzburg, Austria. (creator_code:org_t)
John Wiley & Sons, 2023
2023
Engelska.
Ingår i: European Journal of Heart Failure. - : John Wiley & Sons. - 1388-9842 .- 1879-0844. ; 25:11, s. 2007-2017
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Aim The LeoDOR trial explored the efficacy and safety of intermittent levosimendan therapy in the vulnerable phase following a hospitalization for acute heart failure (HF) Methods and results In this prospective multicentre, double-blind, two-armed trial, patients with advanced HF were randomized 2:1 at the end of an index hospitalization for acute HF to intermittent levosimendan therapy or matching placebo for 12weeks. All patients had left ventricular ejection fraction (LVEF) =30% during index hospitalization. Levosimendan was administered according to centre preference either as 6 h infusion at a rate of 0.2 mu g/kg/min every 2weeks, or as 24 h infusion at a rate of 0.1 mu g/kg/min every 3weeks. The primary efficacy assessment after 14weeks was based on a global rank score consisting of three hierarchical groups. Secondary clinical endpoints included the composite risk of tiers 1 and 2 at 14 and 26weeks, respectively. Due to the COVID-19 pandemic, the planned number of patients could not be recruited. The final modified intention-to-treat analysis included 145 patients (93 in the combined levosimendan arm, 52 in the placebo arm), which reduced the statistical power to detect a 20% risk reduction in the primary endpoint to 60%. Compared with placebo, intermittent levosimendan had no significant effect on the primary endpoint: the mean rank score was 72.55 for the levosimendan group versus 73.81 for the placebo group (p= 0.863). However, there was a signal towards a higher incidence of the individual clinical components of the primary endpoint in the levosimendan group versus the placebo group both after 14weeks (hazard ratio [HR] 2.94, 95% confidence interval [CI] 1.12- 7.68; p= 0.021) and 26weeks (HR 1.64, 95% CI 0.87- 3.11; p= 0.122). Among patients recently hospitalized with HF and reduced LVEF, intermittent levosimendan therapy did not improve post-hospitalization clinical stability. [GRAPHICS.]

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

Levosimendan
Acute heart failure
Randomised controlled trial
Hospitalization
N-terminal pro-B-type natriuretic peptide
Global rank endpoint

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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