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Low cardiac output syndrome after cardiac surgery is associated with poor outcomes. Prior small trials have suggested that the inotrope and calcium sensitizer levosimendan, which has not been FDA-approved, may be beneficial. In a manufacturer-sponsored trial (NCT02025621), 882 patients (median age, 65; 20% women) with left ventricular ejection fraction (LVEF) ≤35%, who were scheduled to undergo cardiac surgery with cardiopulmonary bypass, were randomized to receive levosimendan or placebo. Administration started preoperatively and continued for 24 hours.
The primary combined endpoint (death within 30 days; renal replacement therapy within 30 days; perioperative myocardial infarction within 5 days; or use of mechanical cardiac assist device w…