TY - JOUR
T1 - Rationale and design of the hemodynamic, echocardiographic and neurohormonal effects of istaroxime, a novel intravenous inotropic and lusitropic agent
T2 - A randomized controlled trial in patients hospitalized with heart failure (horizon-hf) trial
AU - Blair, John E.A.
AU - Macarie, Cezar
AU - Ruzyllo, Witold
AU - Bacchieri, Antonella
AU - Valentini, Giovanni
AU - Bianchetti, Maria
AU - Pang, Peter S.
AU - Harinstein, Matthew E.
AU - Sabbah, Hani N.
AU - Filippatos, Gerasimos S.
AU - Gheorghiade, Mihai
PY - 2008/5/1
Y1 - 2008/5/1
N2 - Background: Current inotropes have inodilator properties and, although are frequently used in acute heart failure syndromes, do not improve outcomes, likely from reduction in systolic blood pressure and increasing in arrhythmias, causing worsened myocardial ischemia and end-organ damage. Istaroxime is a novel agent that, in animal models, has both inotropic (inhibition of the Na/ K ATPase channel) and lusitropic (stimulation of sarcoplasmic reticulum calcium ATPase activity) effects. HORIZON-HF is designed to test the hypothesis that istaroxime is effective in improving central hemodynamics and left ventricular (LV) function, without lowering systolic blood pressure, increasing heart rate, and worsening renal function or myocardial necrosis. Methods and Results: This was a phase 2, randomized, double-blind, placebo-controlled, multicenter dose escalation exploratory study comparing 3 different doses of istaroxime to placebo in patients with LV systolic dysfunction (LV ejection fraction ≤ 35%) admitted to the hospital with worsening HF. Three cohorts of 40 patients each were randomized after an initial stabilization period of <48 h 3:1 to istaroxime 0.5,1.0, or 1.5 μg/kg/min versus placebo infused over 6 h, with increasing doses after each cohort. The primary endpoint was change in pulmonary capillary wedge pressure from baseline, whereas secondary endpoints were improvement in other hemodynamic parameters, changes in echocardiographic assessment of LV systolic and diastolic function, neurohonal activation, renal function, and myocardial integrity. Pharmacokinetics and safety were also recorded. Conclusions: The novel inotropic and lusitropic agent, istaroxime, was tested in acute heart failure syndromes using a comprehensive assessment of cardiovascular function in addition to hemodynamic measurements.
AB - Background: Current inotropes have inodilator properties and, although are frequently used in acute heart failure syndromes, do not improve outcomes, likely from reduction in systolic blood pressure and increasing in arrhythmias, causing worsened myocardial ischemia and end-organ damage. Istaroxime is a novel agent that, in animal models, has both inotropic (inhibition of the Na/ K ATPase channel) and lusitropic (stimulation of sarcoplasmic reticulum calcium ATPase activity) effects. HORIZON-HF is designed to test the hypothesis that istaroxime is effective in improving central hemodynamics and left ventricular (LV) function, without lowering systolic blood pressure, increasing heart rate, and worsening renal function or myocardial necrosis. Methods and Results: This was a phase 2, randomized, double-blind, placebo-controlled, multicenter dose escalation exploratory study comparing 3 different doses of istaroxime to placebo in patients with LV systolic dysfunction (LV ejection fraction ≤ 35%) admitted to the hospital with worsening HF. Three cohorts of 40 patients each were randomized after an initial stabilization period of <48 h 3:1 to istaroxime 0.5,1.0, or 1.5 μg/kg/min versus placebo infused over 6 h, with increasing doses after each cohort. The primary endpoint was change in pulmonary capillary wedge pressure from baseline, whereas secondary endpoints were improvement in other hemodynamic parameters, changes in echocardiographic assessment of LV systolic and diastolic function, neurohonal activation, renal function, and myocardial integrity. Pharmacokinetics and safety were also recorded. Conclusions: The novel inotropic and lusitropic agent, istaroxime, was tested in acute heart failure syndromes using a comprehensive assessment of cardiovascular function in addition to hemodynamic measurements.
KW - Acute heart failure syndromes
KW - Diastolic function
KW - Echocardiography
KW - Hemodynamics
KW - Inotropes
KW - Lusitropic agents
KW - Myocardial integrity
KW - Neurohormones
KW - Renal function
KW - Systolic function
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UR - http://www.scopus.com/inward/citedby.url?scp=45949093312&partnerID=8YFLogxK
U2 - 10.1097/MJT.0b013e31816d9186
DO - 10.1097/MJT.0b013e31816d9186
M3 - Article
C2 - 18496261
AN - SCOPUS:45949093312
SN - 1075-2765
VL - 15
SP - 231
EP - 240
JO - American journal of therapeutics
JF - American journal of therapeutics
IS - 3
ER -