The use of levosimendan in comparison and in combination with dobutamine in the treatment of decompensated heart failure
- PMID: 17376021
- DOI: 10.1517/14656566.8.5.665
The use of levosimendan in comparison and in combination with dobutamine in the treatment of decompensated heart failure
Abstract
Levosimendan is a new calcium sensitizer with inotropic and vasodilatory actions mediated by the sensitization of contractile proteins to calcium, opening of potassium channels and inhibition of phosphodiesterase-3. Its alternative mechanisms of action to those of other traditional inotropes provide a new approach in the management of decompensated heart failure. In contrast to dobutamine, levosimendan does not increase myocardial oxygen demand and, therefore, it is thought to have a lower potential to induce increases in myocardial ischemia and cardiac arrhythmias. The commonly used inotropic agent dobutamine increases myocardial contractility at the expense of increased myocardial oxygen consumption and, therefore, it can result in poor outcomes. Although dobutamine may also have favorable hemodynamic and symptomatic effects, levosimendan has been shown to be superior to dobutamine in increasing cardiac output and decreasing pulmonary capillary wedge pressure in patients with decompensated heart failure. In the presence of concomitant beta-blocker therapy, these favorable effects were present or even more pronounced during treatment with levosimendan, but not dobutamine. However, the mortality benefit of levosimendan observed in earlier trials has not been confirmed in recent, larger clinical trials. A distinct advantage of levosimendan over dobutamine is its prolonged hemodynamic effects, which last for up to 7-9 days. There are more data on the safety of levosimendan in ischemic patients than with any other inotropic drug and, therefore, levosimendan seems to be safe and effective in patients with ischemic heart disease when used at the recommended doses. Despite advances in heart failure therapy, many patients experience clinical deterioration, or do not respond to a single inotropic drug. Increasing evidence suggests the use of levosimendan in combination with dobutamine in patients with decompensated heart failure that is refractory to dobutamine alone.
Similar articles
-
Levosimendan: a new inodilatory drug for the treatment of decompensated heart failure.Curr Pharm Des. 2005;11(4):435-55. doi: 10.2174/1381612053382043. Curr Pharm Des. 2005. PMID: 15725064 Review.
-
Levosimendan: a review of its use in the management of acute decompensated heart failure.Drugs. 2003;63(23):2651-71. doi: 10.2165/00003495-200363230-00009. Drugs. 2003. PMID: 14636085 Review.
-
Levosimendan: from basic science to clinical practice.Heart Fail Rev. 2009 Dec;14(4):265-75. doi: 10.1007/s10741-008-9128-4. Epub 2008 Dec 20. Heart Fail Rev. 2009. PMID: 19101796
-
Levosimendan, a new calcium-sensitizing inotrope for heart failure.Pharmacotherapy. 2004 Oct;24(10):1366-84. doi: 10.1592/phco.24.14.1366.43145. Pharmacotherapy. 2004. PMID: 15628834 Review.
-
Levosimendan: beyond its simple inotropic effect in heart failure.Pharmacol Ther. 2007 May;114(2):184-97. doi: 10.1016/j.pharmthera.2007.01.008. Epub 2007 Feb 16. Pharmacol Ther. 2007. PMID: 17363065 Review.
Cited by
-
Effect of levosimendan combined with recombinant human brain natriuretic peptide on diuretic resistance.Libyan J Med. 2021 Dec;16(1):1973762. doi: 10.1080/19932820.2021.1973762. Libyan J Med. 2021. PMID: 34493175 Free PMC article.
-
Diagnosis and management of acute heart failure.Anatol J Cardiol. 2015 Nov;15(11):860-89. doi: 10.5152/AnatolJCardiol.2015.6567. Anatol J Cardiol. 2015. PMID: 26574757 Free PMC article.
-
The effects of levosimendan and dobutamine in experimental bupivacaine-induced cardiotoxicity.BMC Anesthesiol. 2013 Oct 3;13(1):28. doi: 10.1186/1471-2253-13-28. BMC Anesthesiol. 2013. PMID: 24088357 Free PMC article.
-
The Early Pharmacological Strategy with Inodilator, bEta-blockers, Mineralocorticoid Receptor Antagonists, Sodium-glucose coTransporter-2 Inhibitors and Angiotensin Receptor-neprylisin Inhibitors in Acute Heart Failure (PENTA-HF).Curr Vasc Pharmacol. 2025;23(3):213-223. doi: 10.2174/0115701611334141241217044516. Curr Vasc Pharmacol. 2025. PMID: 39844570
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical