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Published on: April 8, 2013
Levosimendan in patients with low-output heart failure: lessons from the LIDO trial
1Department of Internal Medicine, University Hospital, Ramistrasse 100, 8091 Zurich, Switzerland. ferenc.follath@usz.ch
Abstract:
The novel calcium sensitizer levosimendan improves myocardial contractility without causing an increase in intracellular calcium and cyclic adenosine monophosphate concentrations. It also has a vasodilator action due to an opening of the adenosine triphosphate-sensitive potassium channels. In a double-blind clinical trial levosimendan was compared with dobutamine in 203 patients with severe low-output congestive heart failure. A 24-hour infusion of these inotropic drugs was administered to increase the cardiac output by at least 30% together with a decrease in the pulmonary capillary wedge pressure by > or = 25%. The pre-defined hemodynamic improvement was achieved in 28% of patients receiving levosimendan compared to only 15% with dobutamine (p = 0.022). Levosimendan also reduced the 1- and 6-month mortality more than dobutamine (7.8 vs 17%, p = 0.045 and 26 vs 38%, p = 0.029, respectively). Levosimendan produced less myocardial ischemia and cardiac arrhythmias than dobutamine. Calcium sensitizers offer a new therapeutic possibility in patients with decompensated low-output heart failure.
Insights
Levosimendan, a novel calcium sensitizer, effectively treats severe low-output heart failure by improving cardiac function and reducing mortality compared to dobutamine. This drug offers a promising new therapeutic option for patients with decompensated heart failure.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Severe low-output congestive heart failure requires effective inotropic support.
- Current treatments like dobutamine have limitations.
Purpose of the Study:
- To compare the efficacy and safety of levosimendan versus dobutamine in patients with severe low-output congestive heart failure.
Main Methods:
- A double-blind clinical trial involving 203 patients.
- 24-hour infusion of levosimendan or dobutamine.
- Primary endpoint: achieving at least 30% increase in cardiac output and 25% decrease in pulmonary capillary wedge pressure.
Main Results:
- Hemodynamic improvement achieved in 28% of levosimendan patients vs. 15% of dobutamine patients (p=0.022).
- Levosimendan significantly reduced 1- and 6-month mortality (p=0.045 and p=0.029, respectively).
- Fewer instances of myocardial ischemia and cardiac arrhythmias with levosimendan.
Conclusions:
- Levosimendan demonstrates superior hemodynamic efficacy and improved survival in severe low-output heart failure compared to dobutamine.
- Levosimendan offers a favorable safety profile with reduced adverse cardiac events.
- Calcium sensitizers represent a new therapeutic avenue for decompensated heart failure.
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