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Published on: May 4, 2020
Safety and Tolerability of Continuous Inhaled Iloprost Therapy for Severe Pulmonary Hypertension in Neonates and
Amit V Krishnan1, Victoria Freniere2, Rakesh Sahni3
1Department of Pediatrics (Cardiology), Columbia University Irving Medical Center, New York, NY 10932, USA.
Insights
Continuous inhaled iloprost is safe and well-tolerated as rescue therapy for critically ill infants with pulmonary hypertension (PH). This treatment shows promise in improving oxygenation and reducing the need for extracorporeal membrane oxygenation (ECMO).
Area of Science:
- Neonatal Medicine
- Pediatric Critical Care
- Pharmacology
Background:
- Pulmonary hypertension (PH) poses a significant risk to critically ill neonates and infants.
- Refractory PH often requires rescue therapy, but options for this vulnerable population are limited.
- Continuous inhaled iloprost has emerged as a potential rescue therapy.
Purpose of the Study:
- To assess the safety and tolerability of continuous inhaled iloprost.
- To evaluate iloprost as rescue therapy for refractory PH in critically ill neonates and infants.
- To determine the impact of iloprost on key physiological parameters and clinical outcomes.
Main Methods:
- Single-center retrospective study involving 58 infants with refractory PH.
- Data collected at multiple time points after iloprost initiation (baseline to 72 hours).
- Analysis of primary outcomes (heart rate, FiO2, MAP, BP, OI) and secondary outcomes (ECMO use, mortality).
Main Results:
- Significant decreases observed in fraction of inspired oxygen (FiO2) and oxygenation index (OI) (p < 0.001, p = 0.01).
- No significant changes noted in mean airway pressures (MAP), blood pressure (BP), or heart rate (HR).
- 47% of patients recovered without ECMO; 23% died. Seven patients were bridged off ECMO with iloprost.
Conclusions:
- Continuous inhaled iloprost demonstrates an acceptable safety and tolerability profile.
- Iloprost serves as a viable add-on therapy for refractory PH in critically ill infants in the NICU.
- Further large-scale prospective multicenter studies are needed to validate these findings in neonatal ICUs.
Abstract:
This is a single-center retrospective study to assess the safety and tolerability of continuous inhaled iloprost use as rescue therapy for refractory pulmonary hypertension (PH) in critically ill neonates and infants. A retrospective chart review was performed on 58 infants and data were collected at baseline, 1, 6, 12, 24, 48 and 72 h of iloprost initiation. Primary outcomes were change in heart rate (HR), fraction of inspired oxygen (FiO2), mean airway pressures (MAP), blood pressure (BP) and oxygenation index (OI). Secondary outcomes were need for extracorporeal membrane oxygenation (ECMO) and death. 51 patients treated for >6 h were analyzed in 2 age groups, neonate (≤28 days: n = 32) and infant (29-365 days: n = 19). FiO2 (p < 0.001) and OI (p = 0.01) decreased, while there were no significant changes in MAP, BP and HR. Of the fifteen patients placed on ECMO, seven were bridged off ECMO on iloprost and eight died. Twenty-four out of fifty-one patients (47%) recovered without requiring ECMO, while twelve (23%) died. Iloprost as add-on therapy for refractory PH in critically ill infants in the NICU has an acceptable tolerability and safety profile. Large prospective multicenter studies using iloprost in the neonatal ICU are necessary to validate these results.
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