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Levosimendan improves exercise performance in patients with advanced chronic heart failure

AIMS: Cardiopulmonary exercise test (CPET) provides parameters such as peak VO(2) and ventilation/CO(2) production (VE/VCO(2)) slope, which are strong prognostic predictors in patients with stable advanced chronic heart failure (ADHF). The study aim was to evaluate the effects of the inodilator levo...

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Detalles Bibliográficos
Autores principales: Mushtaq, Saima, Andreini, Daniele, Farina, Stefania, Salvioni, Elisabetta, Pontone, Gianluca, Sciomer, Susanna, Volpato, Valentina, Agostoni, Piergiuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042087/
https://www.ncbi.nlm.nih.gov/pubmed/27708855
http://dx.doi.org/10.1002/ehf2.12047
Descripción
Sumario:AIMS: Cardiopulmonary exercise test (CPET) provides parameters such as peak VO(2) and ventilation/CO(2) production (VE/VCO(2)) slope, which are strong prognostic predictors in patients with stable advanced chronic heart failure (ADHF). The study aim was to evaluate the effects of the inodilator levosimendan on CPET in patients with ADHF under stable clinical conditions. METHODS AND RESULTS: We enrolled patients with ADHF (peak VO(2) < 12 mL/min/kg) in a double‐blind, placebo‐controlled protocol. Patients were randomly assigned to i.v. infusion of placebo (500 mL 5% glucose; n = 19) or levosimendan (in 500 mL 5% glucose; n = 23). Before and 24 h after the end of the infusion, patients underwent determination of New York Heart Association class, B‐type natriuretic peptide (BNP), haemoglobin, serum creatinine, and blood urea nitrogen levels, as well as CPET, standard spirometry, and alveolar capillary gas diffusion. BNP showed no change with placebo (1042 ± 811 to 1043 ± 867 pg/mL), but it was decreased with levosimendan (1163 ± 897 to 509 ± 543 pg/mL, P < 0.001). No changes were observed for haemoglobin, creatinine, and blood urea nitrogen in either group. With levosimendan, a minor improvement was observed in spirometry measurements, but not in alveolar capillary gas diffusion. Peak VO(2) showed a small, non‐significant increase with placebo (9.5 ± 1.7 to 10.0 ± 2.1 mL/kg/min, P = 0.12), and a greater increase with levosimendan (9.8 ± 1.7 to 11.0 ± 1.9 mL/kg/min, P < 0.005). The VE/VCO(2) slope showed no change (44.0 ± 11 vs. 43.4 ± 10.3, P = 0.44), and a decrease (41.9 ± 10 vs. 36.6 ± 6.4, P < 0.001) in the placebo and in the levosimendan group, respectively. CONCLUSION: Levosimendan treatment significantly improves peak VO(2) and reduces VE/VCO(2) slope and BNP in patients with ADHF.