Levosimendan in the treatment of patients with acute cardiac conditions: an expert opinion of the Association of Intensive Cardiac Care of the Polish Cardiac Society.

Ewa Kucewicz-Czech, Janina Stępińska, Robert Zymliński, Barbara Zawiślak, Katarzyna Wilk, Ewa Straburzyńska-Migaj, Bożena Sobkowicz, Joanna Płonka, Przemysław Leszek, Agnieszka Tycińska, Jacek Kubica, Jarosław D Kasprzak, Grzegorz Grześk, Marcin Gruchała, Rafał Depukat, Marek Deja, Jarosław Bugajski, Marek Gierlotka

Journal: Kardiologia polska 2021;78(7-8):825-834

PMID: 32788567

Abstract

Levosimendan is a new inodilator which involves 3 main mechanisms: increases the calcium sensitivity of cardiomyocytes, acts as a vasodilator due to the opening of potassium channels, and has a cardioprotective effect. Levosimendan is mainly used in the treatment of acute decompensated heart failure (class IIb recommendation according to the European Society of Cardiology guidelines). However, numerous clinical trials indicate the validity of repeated infusions of levosimendan in patients with stable heart failure as a bridge therapy to heart transplantation, and in patients with accompanying right ventricular heart failure and pulmonary hypertension. Due to the complex mechanism of action, including the cardioprotective and anti- -aggregating effect, the use of levosimendan may be particularly beneficial in acute coronary syndromes, preventing the occurrence of acute heart failure. There are data indicating that levosimendan administered prior to cardiac surgery may improve outcomes in patients with severely impaired left ventricular function. The multidirectional mechanism of action also affects other organs and systems. The positive effect of levosimendan in the treatment of cardiorenal and cardiohepatic syndromes has been shown. It has a safe and predictable profile of action, does not induce tolerance, and shows no adverse effects affecting patients survival or prognosis. However, with inconclusive results of previous studies, there is aneed for awell-designed multicenter randomized placebo-‑controlled study, including an adequately large group of outpatients with chronic advanced systolic heart failure.

Address: Department of Cardiology, Medical University of Białystok, Białystok, Poland. [email protected]; Department of Cardiology, University Hospital in Opole, Institute of Medical Sciences, University of Opole, Opole, Poland; Department of Cardiac Surgery, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland; Department of Cardiology and Cardiovascular Interventions, University Hospital, Kraków, Poland; 1st Department of Cardiology, Medical University of Gdańsk, Gdańsk, Poland; Department of Cardiology and Clinical Pharmacology, Faculty of Health Sciences Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland; I Department and Chair of Cardiology, Bieganski Hospital, Medical University of Lodz, Łódź, Poland; Department of Cardiology and Internal Medicine, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland; Department of Cardiac Anaesthesiology and Intensive Therapy, Medical University of Silesia, Katowice, Poland; Department of Heart Failure and Transplantology, National Institute of Cardiology, Warsaw, Poland; Department of Cardiology, Medical University of Białystok, Białystok, Poland; 1st Department of Cardiology, University of Medical Sciences in Poznan, University Hospital of Lord’s Transfiguration, Poznań, Poland; Intensive Cardiac Care Unit, University Hospital, Kraków, Poland; Department of Heart Diseases, Wroclaw Medical University, Wrocław, Poland; Centre for Heart Diseases, University Hospital, Wrocław, Poland; Department of Intensive Cardiac Therapy, National Institute of Cardiology, Warsaw, Poland
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