Milrinone Dosing Recommendations
The recommended dose of milrinone for patients with heart failure is a loading dose of 50 mcg/kg administered over 10 minutes, followed by a continuous infusion of 0.375-0.75 mcg/kg/min, with dosage adjustments based on hemodynamic response and renal function. 1, 2
Standard Dosing Protocol
Loading Dose
- 50 mcg/kg administered slowly over 10 minutes 1
- May be given undiluted or diluted to a total volume of 10 or 20 mL for easier visualization of injection rate 1
- In patients with hypotension, consider starting without the loading dose to avoid further blood pressure reduction 2, 3
Maintenance Infusion
Preparation for Infusion
- Dilute milrinone with compatible solutions:
- 0.45% Sodium Chloride Injection
- 0.9% Sodium Chloride Injection
- 5% Dextrose Injection 1
- Target concentration: 200 mcg/mL 1
Dosage Adjustment for Renal Impairment
Milrinone is primarily cleared by renal excretion, requiring dose adjustment in patients with renal dysfunction 3, 1:
| Creatinine Clearance (mL/min/1.73m²) | Recommended Infusion Rate (mcg/kg/min) |
|---|---|
| 5 | 0.2 |
| 10 | 0.23 |
| 20 | 0.28 |
| 30 | 0.33 |
| 40 | 0.38 |
| 50 | 0.43 |
Clinical Indications
Milrinone is indicated for:
- Acute decompensated heart failure with documented severe systolic dysfunction 3
- Low cardiac output states with evidence of end-organ hypoperfusion 3, 2
- Patients with systolic blood pressure >90 mmHg 3
- Patients on concomitant beta-blocker therapy who may have inadequate response to dobutamine 2, 3
Monitoring and Titration
- Titrate dose based on hemodynamic response (cardiac output, pulmonary capillary wedge pressure) 2, 1
- Continuous ECG monitoring and frequent blood pressure assessment are essential 3
- Monitor for signs of hypotension, especially during loading dose administration 3, 4
- Maximum daily dose should not exceed 1.13 mg/kg/day 1
Precautions and Contraindications
- Avoid or use extreme caution in patients with:
- Thrombocytopenia is an uncommon but recognized adverse effect (0.4%) 2
- Studies with oral milrinone have shown increased arrhythmias and mortality; therefore, intravenous use should be limited to short-term therapy 3
Advantages Over Other Inotropes
- Maintains effectiveness during beta-blocker therapy 2, 3
- Causes less tachycardia than dobutamine 2, 3
- Has more pronounced vasodilatory effects than pure inotropes 2
- Hemodynamic profile intermediate between pure vasodilators and predominant inotropic agents 2
Common Pitfalls to Avoid
- Administering loading dose to hypotensive patients - Consider starting without a bolus in patients with borderline blood pressure 2, 4
- Failure to adjust dose in renal impairment - Terminal elimination half-life is significantly increased in renal dysfunction 1, 5
- Prolonged use beyond short-term therapy - Increased risk of arrhythmias and potential mortality with extended use 3
- Using in hypovolemic patients - Correct volume status before administration to prevent severe hypotension 3
- Inadequate monitoring - Continuous hemodynamic monitoring is essential during initiation and dose adjustments 3
By following these evidence-based recommendations, milrinone can be effectively and safely used to improve cardiac output and reduce pulmonary capillary wedge pressure in appropriately selected patients with heart failure.