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Intravenous Versus Inhaled Milrinone in Patients with Known Pulmonary Hypertension Undergoing Cardiac Surgery: A
Thomas Kavanagh1, Thomas Kilpatrick1, Ben Hardy2
1Anaesthetic Department, Royal Sussex County Hospital, University Hospitals Sussex, United Kingdom.
Inhaled milrinone showed no significant benefit over intravenous milrinone for mean pulmonary artery pressure in cardiac surgery patients with pulmonary hypertension (PH). However, it improved oxygenation and maintained mean arterial pressure.
Area of Science:
- Cardiology
- Anesthesiology
- Pharmacology
Background:
- Pulmonary hypertension (PH) poses significant risks during cardiac surgery.
- Milrinone is used to manage hemodynamic instability in these patients.
- Evidence comparing inhaled and intravenous milrinone for PH in cardiac surgery is limited.
Purpose of the Study:
- To evaluate the hemodynamic effects and vasopressor needs of adult cardiac surgery patients with PH treated with inhaled versus intravenous milrinone.
- To synthesize evidence from prospective studies and randomized controlled trials (RCTs).
Main Methods:
- Pooled analysis of 5 prospective studies, including 4 RCTs, with a total of 400 patients.
- Comparison of hemodynamic parameters between inhaled and intravenous milrinone groups.
Main Results:
- No significant difference in mean pulmonary artery pressure (MPAP) between groups (MD: -4.80).
- Inhaled milrinone showed increased systemic vascular resistance index (SVRI) (MD: 259.21) and reduced pulmonary capillary wedge pressure (MD: -4.64).
- No differences observed in mean arterial pressure, pulmonary vascular resistance, cardiac index, or central venous pressure. Risk of bias was moderate/some concern.
Conclusions:
- Inhaled milrinone did not demonstrate significant advantages over intravenous milrinone for MPAP and SVR in PH patients undergoing cardiac surgery.
- Inhaled milrinone may offer benefits in maintaining mean arterial pressure and improving oxygenation.
- Further well-powered RCTs are needed due to study limitations and variability in drug administration.
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