Aerosolized iloprost in the treatment of pulmonary hypertension in extremely preterm infants: a pilot study
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F Eifinger1, N Sreeram, K Mehler
1Klinik und Poliklinik für Kinderheilkunde, Abteilung für Neonatologie, Klinikum der Universität zu Köln. frank.eifinger@uk-koeln.de
Insights
Aerosolized iloprost improved oxygenation in premature infants with persistent pulmonary hypertension. This treatment may help extremely low-birthweight neonates with breathing difficulties after prolonged rupture of membranes.
Area of Science:
- Neonatal Medicine
- Pediatric Pulmonology
- Pharmacology
Background:
- Persistent pulmonary hypertension is a significant cause of mortality in premature infants with prolonged rupture of membranes.
- Current treatments for this condition in extremely low-birthweight neonates are limited.
Purpose of the Study:
- To evaluate the efficacy of aerosolized iloprost in treating persistent pulmonary hypertension in extremely low-birthweight neonates.
- To assess the safety and impact of iloprost inhalation on oxygenation and pulmonary resistance.
Main Methods:
- Four extremely low-birthweight neonates (23-25 weeks' gestation) with pulmonary hypertension due to prolonged rupture of fetal membranes received aerosolized iloprost.
- Treatment involved 44-65 inhalations of 2 microg/kg b.w. iloprost within the first hour of life over several days, with single inhalations lasting 5 minutes.
Main Results:
- Following the first iloprost inhalation, the PaO2/FiO2 ratio significantly increased from a mean of 65 to 194 mmHg.
- Oxygenation requirements decreased within 7 days, and echocardiography demonstrated a reduction in pulmonary resistance.
- No severe side effects on blood pressure or prolonged bleeding were observed.
Conclusions:
- Aerosolized iloprost shows promise as an adjunctive treatment for improving oxygenation in extremely low-birthweight infants with persistent pulmonary hypertension under spontaneous breathing.
- Further randomized clinical trials are necessary to confirm the role of iloprost in managing this critical condition.
Background:
In premature infants with preterm prolonged rupture of membranes, death after birth is often due to persistent pulmonary hyper-tension.
Patients:
Aerosolized iloprost was used to treat pulmonary hypertension due to prolonged preterm rupture of fetal membranes (7-56 days) in four extremely low-birthweight neonates (23-25 weeks' gestation, weight 448-645 g) under spontaneous breathing supported by nasal continuous positive airway pressure.
Method:
Inhalation dose was 2 microg/kg b.w. and between 44 and 65 inhalations were performed in each patient starting within the first hour of life over a total of several days. Single inhalations lasted 5 min and were not repeated until 60 min had elapsed.
Results:
After the first inhalation, the PaO2/FiO2 mean ratio increased from 65 (range 35-114) to 194 (148-250) mmHg and oxygenation requirements decreased within the next 7 days. Echocardiography similarly showed reduction in pulmonary resistance. We observed no severe side effects on blood pressure or prolonged bleeding time during inhalation.
Conclusions:
Iloprost inhalation might therefore be an additional treatment for improving oxygenation in cases of persistent pulmonary hypertension in extremely low-birthweight infants under spontaneous breathing. Further randomized clinical studies are required to establish the role of iloprost in this setting.
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