From the Guidelines
Milrinone is a phosphodiesterase-3 inhibitor used to treat heart failure, whereas "obtained" is a verb with no medical significance. The primary use of milrinone is to increase cardiac output in patients with heart failure by enhancing the contractility of the heart muscle and causing vasodilation, which reduces the workload on the heart 1. Milrinone is typically administered intravenously in hospital settings for acute decompensated heart failure, cardiogenic shock, or as a bridge therapy for patients awaiting heart transplantation. The typical dosing involves a loading dose followed by a continuous infusion of 0.125–0.75 mcg/kg/min, adjusted based on clinical response 1. In contrast, "obtained" is simply a verb meaning to acquire, get, or receive something, with no medical relevance. These terms belong to entirely different categories of words - one being a specific cardiovascular medication and the other being a common English verb with no medical relevance. Key considerations for the use of milrinone include its potential to cause hypotension, particularly in patients with low filling pressures, and the need for careful monitoring of kidney function and liver function tests due to its potential for accumulation in renal failure 1. Overall, the decision to use milrinone should be based on a thorough assessment of the patient's clinical condition and the potential benefits and risks of treatment, with careful consideration of the most recent and highest quality evidence available 1.
Some of the key points to consider when using milrinone include:
- The medication is a phosphodiesterase-3 inhibitor used to treat heart failure
- It works by increasing the contractility of the heart muscle and causing vasodilation
- Typical dosing involves a loading dose followed by a continuous infusion of 0.125–0.75 mcg/kg/min
- Careful monitoring of kidney function and liver function tests is necessary due to its potential for accumulation in renal failure
- The potential for hypotension, particularly in patients with low filling pressures, should be carefully considered.
It is also important to note that the use of milrinone should be guided by the most recent and highest quality evidence available, and that the medication should only be used under the close supervision of a qualified healthcare professional 1.
From the FDA Drug Label
The FDA drug label does not answer the question.
From the Research
Difference between Milrinone and Dobutamine
- Milrinone and dobutamine are both used to treat heart failure, but they have different mechanisms of action and effects on the body 2, 3, 4, 5, 6.
- Milrinone is a phosphodiesterase III inhibitor, which means it works by increasing the levels of cyclic AMP in the heart, leading to increased contractility and relaxation of the heart muscle 6.
- Dobutamine, on the other hand, is a beta-adrenergic agonist, which means it works by stimulating the beta-adrenergic receptors in the heart, leading to increased contractility and heart rate 2, 5.
Hemodynamic Effects
- Both milrinone and dobutamine have been shown to improve hemodynamic parameters, such as cardiac index, pulmonary capillary wedge pressure, and systemic vascular resistance, in patients with heart failure 2, 3, 5.
- However, milrinone has been shown to have a more sustained effect on these parameters, with a greater reduction in pulmonary capillary wedge pressure and a more prolonged increase in cardiac index 2, 6.
- Dobutamine, on the other hand, has been shown to have a more rapid effect on heart rate and contractility, but its effects may be shorter-lived 5, 6.
Safety and Tolerability
- Both milrinone and dobutamine have been shown to be generally well-tolerated, but they have different side effect profiles 3, 5.
- Milrinone has been associated with a lower risk of arrhythmias and hypotension, but a higher risk of thrombocytopenia 3, 4.
- Dobutamine, on the other hand, has been associated with a higher risk of arrhythmias and hypotension, but a lower risk of thrombocytopenia 3, 5.
Clinical Outcomes
- The clinical outcomes of milrinone and dobutamine have been compared in several studies, with mixed results 2, 3, 4.
- One study found that milrinone was associated with a lower risk of mortality in patients with acute decompensated heart failure, but another study found no difference in mortality between the two drugs 3, 4.
- A meta-analysis of several studies found that milrinone was associated with a marginal benefit in terms of mortality and clinical outcomes, but the results were not statistically significant 4.