Levosimendan, a calcium-sensitizer, is prescribed for the short-term management of acute decompensated congestive heart failure.
Levosimendan exert positive inotropic effect by activation of ATP-dependent potassium channels. Levosimendan promotes cardioprotective and vasodilatation effects. Levosimendan directly acts on the molecular cascade of myocardial infarction pathogenesis. Levosimendan increase the calcium affinity towards cardiac Troponin C proteins and stabilize calcium-dependent conformational changes. Levosimendan enhances myocardial performance rate without increasing myocardial oxygen demand. Levosimendan induces vascular smooth muscle cells and promotes vasodilatation.
After intravenous administration, the drug is metabolized into two metabolites. The plasma half-life of Levosimendan is about one hour. The terminal half-life of the metabolites is 70-80 hours.
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Levosimendan can cause hypotension and headache
Levosimendan is contraindicated in patients with renal and/or hepatic impairment, severe hypotension, history of torsades de pointes, severe ventricular filling, obstruction of ventricular outflow and tachycardia.
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Levosimendan may interact with nitrates, ACE-II inhibitors, norepinephrine, beta blockers and dobutamine.
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Consider administration of 6-24 µg kg-1 min-1 over 10-20 minutes. The maintenance dose should be 0.05–0.2 µg kg-1 min-1. The infusions should not be administered more than 24 hours.
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USFDA Pregnancy category is unknown. However, Levosimendan should be avoided during pregnancy.
No adequate clinical studies to demonstrate the safety of Levosimendan in nursing mothers. Breastfeeding mothers should be avoided while taking Levosimendan.
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