Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/173595
Title: Efficacy and safety of intermittent intravenous outpatient administration of levosimendan in patients with advanced heart failure: the LION-HEART multicentre randomised trial
Author: Comín Colet, Josep
Manito Lorite, Nicolás
Segovia Cubero, Javier
Delgado, Juan
García Pinilla, José Manuel
Almenar, Luis
Crespo Leiro, María G.
Sionis, Alessandro
Blasco, Teresa
Pascual Figal, Domingo
Gonzalez Vilchez, Francisco
Lambert Rodríguez, José Luis
Grau, María
Bruguera, Jordi
LION- HEART Study Investigators
Keywords: Malalties del cor
Insuficiència cardíaca
Heart diseases
Heart failure
Issue Date: 1-Jul-2018
Publisher: Oxford University Press
Abstract: Aims. The LION‐HEART study was a multicentre, double‐blind, randomised, parallel‐group, placebo‐controlled trial evaluating the efficacy and safety of intravenous administration of intermittent doses of levosimendan in outpatients with advanced chronic heart failure. Methods and results. Sixty‐nine patients from 12 centres were randomly assigned at a 2:1 ratio to levosimendan or placebo groups, receiving treatment by a 6‐hour intravenous infusion (0.2 μg/kg/min without bolus) every 2 weeks for 12 weeks. The primary endpoint was the effect on serum concentrations of N‐terminal pro‐B‐type natriuretic peptide (NT‐proBNP) throughout the treatment period in comparison with placebo. Secondary endpoints included evaluation of safety, clinical events and health‐related quality of life (HRQoL). The area under the curve (AUC, pg.day/mL) of the levels of NT‐proBNP over time for patients who received levosimendan was significantly lower than for the placebo group (344 × 103 [95% Confidence Interval (CI) 283 × 103−404 × 103] vs. 535 × 103 [443 × 103−626 × 103], p = 0.003). In comparison with the placebo group, the patients on levosimendan experienced a reduction in the rate of heart failure hospitalisation (hazard ratio 0.25; 95% CI 0.11-0.56; P = 0.001). Patients on levosimendan were less likely to experience a clinically significant decline in HRQoL over time (P = 0.022). Adverse event rates were similar in the two treatment groups. Conclusions. In this small pilot study, intermittent administration of levosimendan to ambulatory patients with advanced systolic heart failure reduced plasma concentrations of NT‐proBNP, worsening of HRQoL and hospitalisation for heart failure. The efficacy and safety of this intervention should be confirmed in larger trials.
Note: Versió postprint del document publicat a: https://doi.org/10.1002/ejhf.1145
It is part of: European Journal of Heart Failure, 2018, vol. 20, num. 7, p. 1128-1136
URI: http://hdl.handle.net/2445/173595
Related resource: https://doi.org/10.1002/ejhf.1145
ISSN: 1388-9842
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Ciències Clíniques)
Articles publicats en revistes (Medicina)

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