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Response to pulmonary vasodilators in infants with congenital diaphragmatic hernia
Vasantha H S Kumar1,2, Rita Dadiz3, Jamie Koumoundouros4
1Department of Pediatrics, University at Buffalo, Buffalo, NY, USA. vkumar3@buffalo.edu.
Insights
Inhaled nitric oxide (iNO) and milrinone are pulmonary vasodilators for congenital diaphragmatic hernia (CDH). Response to iNO with milrinone may improve oxygenation and survival in CDH infants after ECMO.
Area of Science:
- Neonatalogy
- Pediatric Cardiology
- Pulmonology
Background:
- Congenital diaphragmatic hernia (CDH) causes lung hypoplasia, cardiac dysfunction, and pulmonary hypertension.
- Inhaled nitric oxide (iNO) and milrinone are common pulmonary vasodilators for CDH.
- This study investigated the hemodynamic effects of iNO and milrinone in infants with CDH.
Purpose of the Study:
- To evaluate the hemodynamic and oxygenation effects of iNO and milrinone in infants with CDH.
- To determine if response to iNO influences outcomes with milrinone therapy.
- To assess the impact of these vasodilators on survival in CDH patients.
Main Methods:
- Retrospective chart review of CDH infants from two perinatal centers.
- Infants categorized into No-iNO, iNO-responder, and iNO-nonresponder groups.
- Assessment of oxygenation via blood gases and hemodynamics via echocardiography.
Main Results:
- 54% of CDH infants received iNO; 31% showed a complete oxygenation response.
- iNO response did not correlate with reduced right ventricular pressures (RVP) or ECMO use.
- Milrinone, used in both iNO groups, lowered RVP and improved ejection fraction (EF).
- iNO responders receiving milrinone had improved oxygenation and higher survival post-ECMO (67% vs. 20% in nonresponders).
Conclusions:
- Response to iNO in CDH infants may predict improved outcomes with milrinone.
- Combined iNO and milrinone therapy shows potential for enhancing oxygenation.
- This combination therapy might be associated with better survival rates following ECMO in CDH patients.
Background:
Congenital diaphragmatic hernia (CDH) is associated with lung hypoplasia, cardiac dysfunction and pulmonary hypertension. Inhaled nitric oxide (iNO) and milrinone are commonly used pulmonary vasodilators in CDH. We studied the hemodynamic effects of iNO and milrinone in infants with CDH.
Methods:
A retrospective chart review was performed of all CDH infants admitted to two regional perinatal centers and infants classified into three groups: No-iNO group; iNO-responders and iNO-nonresponders. Oxygenation and hemodynamic effects of iNO and milrinone were assessed by blood gases and echocardiography.
Results:
Fifty-four percent (39/72) of infants with CDH received iNO and 31% of these infants (12/39) had complete oxygenation response to iNO. Oxygenation response to iNO was not associated with a decrease in right ventricular pressures (RVP) or ECMO use. Four infants (33%) in the iNO-responder group and eight infants (30%) in the iNO-nonresponder group received milrinone. Milrinone lowered RVP and improved ejection fraction (EF). Response to iNO was associated with improved oxygenation to milrinone and increased survival following ECMO (67 vs. 20% among nonresponders).
Conclusions:
Response to inhaled nitric oxide in combination with milrinone may be associated with improved oxygenation and better survival after ECMO in infants with CDH.
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