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Korean Circ J. 2009 Aug;39(8):343-345. English. Case Report. https://doi.org/10.4070/kcj.2009.39.8.343
Hwang SK , O YC , Kim NS , Park HK , Yum MK .
Department of Pediatrics, College of Medicine, Hanyang University, Seoul, Korea. namsukim@hanyang.ac.kr
Abstract

Pulmonary artery hypertension is a common cardiovascular complication in preterm infants with bronchopulmonary dysplasia which is associated with increased morbidity and mortality. Inhaled iloprost is used as a therapeutic option in pulmonary hypertension, especially in adults. There have been but a few reports on the use of iloprost for neonates and infants. We report the case of a 5 month-old-male infant who received neonatal intensive care for 4 months due to respiratory distress syndrome and prematurity, during which he developed bronchopulmonary dysplasia. Echocardiography showed severe pulmonary hypertension. The initial treatment included respiratory support with high frequency oscillatory ventilation (HFOV); however, his clinical condition did not improve. Inhaled iloprost with sildenafil, an oral phosphodiesterase-5 inhibitor, was thus used. With the administration of iloprost and sildenafil, his condition improved and he was weaned from oxygen. Our clinical experience suggests that iloprost is a promising therapy for pulmonary hypertension, especially when inhaled nitric oxide is unavailable.

Copyright © 2019. Korean Association of Medical Journal Editors.