Pulmonary hypertension can occur primarily with an unknown aetiology or sec
ondary in association with cardiac or pulmonary disorders such as congenita
l diaphragmatic hernia, idiopathic respiratory distress syndrome, acute res
piratory distress syndrome (ARDS), congenital heart disease with malformati
on of the pulmonary blood vessels, chronic obstructive lung disease and fol
lowing cardiac surgery. Prostacyclin (PGI(2)), an arachidonic acid metaboli
te, has been evaluated for its efficacy in the treatment of pulmonary hyper
tension and for its use in assessing the reversibility of the disorder prio
r to surgical interventions. While the intravenous application of PGI(2) ca
n cause a decrease not only of the pulmonary but also of the systemic vascu
lar tone, aerosolised PGI(2) results in a selective pulmonary vasodilation
without affecting the systemic blood pressure. Furthermore, aerosolised PGI
(2) can improve gas exchange and pulmonary shunt in clinical settings of im
paired ventilation/perfusion ratio such as ARDS, due to the redistribution
of pulmonary blood flow from nonventilated to ventilated, aerosol-accessibl
e lung regions.
Conclusion Aerosolised prostacyclin can be a valuable tool in the treatment
and diagnostic evaluation of elevated pulmonary vascular resistance and im
paired pulmonary gas exchange. Reservations must be made for its long-term
use, as its short half-life necessitates continuous inhalation.