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Intravenous levosimendan vs. dobutamine in acute decompensated heart failure patients on beta-blockers
AIMS: The aim of this study is to compare the effects of a 24 h intravenous infusion of levosimendan and a 48 h infusion of dobutamine on invasive haemodynamics in patients with acutely decompensated chronic NYHA class III–IV heart failure. All patients were receiving optimal oral therapy including...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2844760/ https://www.ncbi.nlm.nih.gov/pubmed/20335355 http://dx.doi.org/10.1093/eurjhf/hfq032 |
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author | Bergh, Claes-Håkan Andersson, Bert Dahlström, Ulf Forfang, Kolbjorn Kivikko, Matti Sarapohja, Toni Ullman, Bengt Wikström, Gerhard |
author_facet | Bergh, Claes-Håkan Andersson, Bert Dahlström, Ulf Forfang, Kolbjorn Kivikko, Matti Sarapohja, Toni Ullman, Bengt Wikström, Gerhard |
author_sort | Bergh, Claes-Håkan |
collection | PubMed |
description | AIMS: The aim of this study is to compare the effects of a 24 h intravenous infusion of levosimendan and a 48 h infusion of dobutamine on invasive haemodynamics in patients with acutely decompensated chronic NYHA class III–IV heart failure. All patients were receiving optimal oral therapy including a β-blocker. METHODS AND RESULTS: This was a multinational, randomized, double-blind, phase IV study in 60 patients; follow-up was 1 month. There was a significant increase in cardiac index and a significant decrease in pulmonary capillary wedge pressure (PCWP) at 24 and 48 h for both dobutamine and levosimendan. The improvement in cardiac index with levosimendan was not significantly different from dobutamine at 24 h (P = 0.07), but became significant at 48 h (0.44 ± 0.56 vs. 0.66 ± 0.63 L/min/m(2); P = 0.04). At 24 h, the reduction in the mean change in PCWP from baseline was similar for levosimendan and dobutamine, however, at 48 h the difference was more marked for levosimendan (−3.6 ± 7.6 vs. −8.3 ± 6.7 mmHg; P = 0.02). No difference was observed between the groups for change in NYHA class, β-blocker use, hospitalizations, treatment discontinuations or rescue medication use. Reduction in B-type natriuretic peptide (BNP) was significantly greater with levosimendan at 48 h (P = 0.03). According to physician's assessment, the improvement in fatigue (P = 0.01) and dyspnoea (P = 0.04) was in favour of dobutamine treatment, and hypotension was significantly more frequent with levosimendan (P = 0.007). No increase in atrial fibrillation or ventricular tachycardia was seen in either group. CONCLUSION: A 24 h levosimendan infusion achieved haemodynamic and neurohormonal improvement that was at least comparable at 24 h and superior at 48 h to a 48 h dobutamine infusion. |
format | Text |
id | pubmed-2844760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28447602010-03-25 Intravenous levosimendan vs. dobutamine in acute decompensated heart failure patients on beta-blockers Bergh, Claes-Håkan Andersson, Bert Dahlström, Ulf Forfang, Kolbjorn Kivikko, Matti Sarapohja, Toni Ullman, Bengt Wikström, Gerhard Eur J Heart Fail Clinical Trial AIMS: The aim of this study is to compare the effects of a 24 h intravenous infusion of levosimendan and a 48 h infusion of dobutamine on invasive haemodynamics in patients with acutely decompensated chronic NYHA class III–IV heart failure. All patients were receiving optimal oral therapy including a β-blocker. METHODS AND RESULTS: This was a multinational, randomized, double-blind, phase IV study in 60 patients; follow-up was 1 month. There was a significant increase in cardiac index and a significant decrease in pulmonary capillary wedge pressure (PCWP) at 24 and 48 h for both dobutamine and levosimendan. The improvement in cardiac index with levosimendan was not significantly different from dobutamine at 24 h (P = 0.07), but became significant at 48 h (0.44 ± 0.56 vs. 0.66 ± 0.63 L/min/m(2); P = 0.04). At 24 h, the reduction in the mean change in PCWP from baseline was similar for levosimendan and dobutamine, however, at 48 h the difference was more marked for levosimendan (−3.6 ± 7.6 vs. −8.3 ± 6.7 mmHg; P = 0.02). No difference was observed between the groups for change in NYHA class, β-blocker use, hospitalizations, treatment discontinuations or rescue medication use. Reduction in B-type natriuretic peptide (BNP) was significantly greater with levosimendan at 48 h (P = 0.03). According to physician's assessment, the improvement in fatigue (P = 0.01) and dyspnoea (P = 0.04) was in favour of dobutamine treatment, and hypotension was significantly more frequent with levosimendan (P = 0.007). No increase in atrial fibrillation or ventricular tachycardia was seen in either group. CONCLUSION: A 24 h levosimendan infusion achieved haemodynamic and neurohormonal improvement that was at least comparable at 24 h and superior at 48 h to a 48 h dobutamine infusion. Oxford University Press 2010-04 2010-02-10 /pmc/articles/PMC2844760/ /pubmed/20335355 http://dx.doi.org/10.1093/eurjhf/hfq032 Text en Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2010. For permissions please email: journals.permissions@oxfordjournals.org. http://creativecommons.org/licenses/by-nc/2.0/uk/ The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that the original authorship is properly and fully attributed; the Journal, Learned Society and Oxford University Press are attributed as the original place of publication with correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org |
spellingShingle | Clinical Trial Bergh, Claes-Håkan Andersson, Bert Dahlström, Ulf Forfang, Kolbjorn Kivikko, Matti Sarapohja, Toni Ullman, Bengt Wikström, Gerhard Intravenous levosimendan vs. dobutamine in acute decompensated heart failure patients on beta-blockers |
title | Intravenous levosimendan vs. dobutamine in acute decompensated heart failure patients on beta-blockers |
title_full | Intravenous levosimendan vs. dobutamine in acute decompensated heart failure patients on beta-blockers |
title_fullStr | Intravenous levosimendan vs. dobutamine in acute decompensated heart failure patients on beta-blockers |
title_full_unstemmed | Intravenous levosimendan vs. dobutamine in acute decompensated heart failure patients on beta-blockers |
title_short | Intravenous levosimendan vs. dobutamine in acute decompensated heart failure patients on beta-blockers |
title_sort | intravenous levosimendan vs. dobutamine in acute decompensated heart failure patients on beta-blockers |
topic | Clinical Trial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2844760/ https://www.ncbi.nlm.nih.gov/pubmed/20335355 http://dx.doi.org/10.1093/eurjhf/hfq032 |
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