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Levosimendan in patients with left ventricular systolic dysfunction undergoing cardiac surgery on cardiopulmonary bypass: Rationale and study design of the Levosimendan in Patients with Left Ventricular Systolic Dysfunction Undergoing Cardiac Surgery Requiring Cardiopulmonary Bypass (LEVO-CTS) trial.
- Source :
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American heart journal [Am Heart J] 2016 Dec; Vol. 182, pp. 62-71. Date of Electronic Publication: 2016 Sep 09. - Publication Year :
- 2016
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Abstract
- Background: Low cardiac output syndrome is associated with increased mortality and occurs in 3% to 14% of patients undergoing cardiac surgery on cardiopulmonary bypass (CPB). Levosimendan, a novel calcium sensitizer and K <subscript>ATP</subscript> channel activator with inotropic, vasodilatory, and cardioprotective properties, has shown significant promise in reducing the incidence of low cardiac output syndrome and related adverse outcomes in patients undergoing cardiac surgery on CPB.<br />Methods: LEVO-CTS is a phase 3 randomized, controlled, multicenter study evaluating the efficacy, safety, and cost-effectiveness of levosimendan in reducing morbidity and mortality in high-risk patients with reduced left ventricular ejection fraction (≤35%) undergoing cardiac surgery on CPB. Patients will be randomly assigned to receive either intravenous levosimendan (0.2 μg kg <superscript>-1</superscript> min <superscript>-1</superscript> for the first hour followed by 0.1 μg/kg for 23hours) or matching placebo initiated within 8hours of surgery. The co-primary end points are (1) the composite of death or renal replacement therapy through day 30 or perioperative myocardial infarction, or mechanical assist device use through day 5 (quad end point tested at α<.01), and (2) the composite of death through postoperative day 30 or mechanical assist device use through day 5 (dual end point tested at α<.04). Safety end points include new atrial fibrillation and death through 90days. In addition, an economic analysis will address the cost-effectiveness of levosimendan compared with placebo in high-risk patients undergoing cardiac surgery on CPB. Approximately 880 patients will be enrolled at approximately 60 sites in the United States and Canada between July 2014 and September 2016, with results anticipated in January 2017.<br />Conclusion: LEVO-CTS, a large randomized multicenter clinical trial, will evaluate the efficacy, safety, and cost-effectiveness of levosimendan in reducing adverse outcomes in high-risk patients undergoing cardiac surgery on CPB.<br />Clinical Trial Registration: ClinicalTrials.gov (NCT02025621).<br /> (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Subjects :
- Administration, Intravenous
Adult
Cardiopulmonary Bypass methods
Cardiovascular Agents administration & dosage
Cardiovascular Agents adverse effects
Dose-Response Relationship, Drug
Drug Monitoring methods
Female
Humans
Male
Middle Aged
Simendan
Stroke Volume
Treatment Outcome
Ventricular Dysfunction, Left diagnosis
Ventricular Dysfunction, Left physiopathology
Cardiac Surgical Procedures adverse effects
Cardiac Surgical Procedures methods
Hydrazones administration & dosage
Hydrazones adverse effects
Postoperative Complications mortality
Postoperative Complications prevention & control
Pyridazines administration & dosage
Pyridazines adverse effects
Ventricular Dysfunction, Left therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1097-6744
- Volume :
- 182
- Database :
- MEDLINE
- Journal :
- American heart journal
- Publication Type :
- Academic Journal
- Accession number :
- 27914501
- Full Text :
- https://doi.org/10.1016/j.ahj.2016.09.001