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.

PubMed

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.

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