Levosimendan Efficacy and Safety: 20 Years of SIMDAX in Clinical Use

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3021031 48 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Levosimendan Efficacy and Safety: 20 Years of SIMDAX in Clinical Use
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Levosimendan was first approved for clinical use in 2000, when authorization was granted by Swedish regulatory authorities for the hemodynamic stabilization of patients with acutely decompensated chronic heart failure (HF). In the ensuing 20 years, this distinctive inodilator, which enhances cardiac contractility through calcium sensitization and promotes vasodilatation through the opening of adenosine triphosphate-dependent potassium channels on vascular smooth muscle cells, has been approved in more than 60 jurisdictions, including most of the countries of the European Union and Latin America. Areas of clinical application have expanded considerably and now include cardiogenic shock, takotsubo cardiomyopathy, advanced HF, right ventricular failure, pulmonary hypertension, cardiac surgery, critical care, and emergency medicine. Levosimendan is currently in active clinical evaluation in the United States. Levosimendan in IV formulation is being used as a research tool in the exploration of a wide range of cardiac and noncardiac disease states. A levosimendan oral form is at present under evaluation in the management of amyotrophic lateral sclerosis. To mark the 20 years since the advent of levosimendan in clinical use, 51 experts from 23 European countries (Austria, Belgium, Croatia, Cyprus, Czech Republic, Estonia, Finland, France, Germany, Greece, Hungary, Italy, the Netherlands, Norway, Poland, Portugal, Russia, Slovenia, Spain, Sweden, Switzerland, the United Kingdom, and Ukraine) contributed to this essay, which evaluates one of the relatively few drugs to have been successfully introduced into the acute HF arena in recent times and charts a possible development trajectory for the next 20 years. © 2020 Lippincott Williams and Wilkins. All rights reserved.
Έτος δημοσίευσης:
2020
Συγγραφείς:
Papp, Z.
Agostoni, P.
Alvarez, J.
Bettex, D.
Bouchez, S.
Brito, D.
Černý, V.
Comin-Colet, J.
Crespo-Leiro, M.G.
Delgado, J.F.
Édes, I.
Eremenko, A.A.
Farmakis, D.
Fedele, F.
Fonseca, C.
Fruhwald, S.
Girardis, M.
Guarracino, F.
Harjola, V.-P.
Heringlake, M.
Herpain, A.
Heunks, L.M.A.
Husebye, T.
Ivancan, V.
Karason, K.
Kaul, S.
Kivikko, M.
Kubica, J.
Masip, J.
Matskeplishvili, S.
Mebazaa, A.
Nieminen, M.S.
Oliva, F.
Papp, J.G.
Parissis, J.
Parkhomenko, A.
Põder, P.
Pölzl, G.
Reinecke, A.
Ricksten, S.-E.
Riha, H.
Rudiger, A.
Sarapohja, T.
Schwinger, R.H.G.
Toller, W.
Tritapepe, L.
Tschöpe, C.
Wikström, G.
Lewinski, D.V.
Vrtovec, B.
Pollesello, P.
Περιοδικό:
Journal of Cardiovascular Pharmacology
Εκδότης:
Lippincott Williams and Wilkins
Τόμος:
76
Αριθμός / τεύχος:
1
Σελίδες:
4-22
Λέξεις-κλειδιά:
cardiovascular agent; levosimendan; neurohormone; cardiotonic agent; simendan; vasodilator agent, acute heart failure; amyotrophic lateral sclerosis; Austria; Belgium; cardiogenic shock; clinical effectiveness; clinical outcome; critical illness; Croatia; Cyprus; Czech Republic; drug efficacy; drug metabolism; drug safety; drug use; Estonia; Finland; France; Germany; Greece; heart right ventricle failure; heart surgery; hemodynamics; hospitalization; human; Hungary; Italy; kidney function; medical expert; mortality; motor neuron disease; Netherlands; nonhuman; Norway; Poland; Portugal; priority journal; pulmonary hypertension; respiratory function; Review; Russian Federation; Slovenia; Spain; Sweden; Switzerland; takotsubo cardiomyopathy; Ukraine; United Kingdom; drug effect; heart contraction; heart failure; pathophysiology; patient safety; treatment outcome; vasodilatation, Cardiotonic Agents; Heart Failure; Humans; Myocardial Contraction; Patient Safety; Simendan; Treatment Outcome; Vasodilation; Vasodilator Agents
Επίσημο URL (Εκδότης):
DOI:
10.1097/FJC.0000000000000859
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