Circulation Journal
Online ISSN : 1347-4820
Print ISSN : 1346-9843
Pulmonary Circulation
Safety and Efficacy of Epoprostenol Therapy in Pulmonary Veno-Occlusive Disease and Pulmonary Capillary Hemangiomatosis
Aiko OgawaKatsumasa MiyajiIchiro YamadoriYoko ShinnoAya MiuraKengo F. KusanoHiroshi ItoHiroshi DateHiromi Matsubara
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Volume 76 (2012) Issue 7 Pages 1729-1736

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Abstract

Background: Pulmonary veno-occlusive disease (PVOD) and pulmonary capillary hemangiomatosis (PCH) are rare causes of pulmonary hypertension. There is no proven medical therapy to treat these diseases, and lung transplantation is thought to be the only cure. Administration of vasodilators including epoprostenol sometimes causes massive pulmonary edema and could be fatal in these patients. Methods and Results: Eight patients were treated with epoprostenol for 387.3±116.3 days (range, 102-1,063 days), who were finally diagnosed with PVOD or PCH by pathological examination. The maximum dose of epoprostenol given was 55.3±10.7ng·kg-1·min-1 (range, 21.0-110.5ng·kg-1·min-1). With careful management, epoprostenol therapy significantly improved the 6-min walk distance (97.5±39.2 to 329.4±34.6m, P<0.001) and plasma brain natriuretic peptide levels (381.3±136.8 to 55.2±14.4pg/ml, P<0.05). The cardiac index significantly increased from 2.1±0.1 to 2.9±0.3L·min-1·m-2 (P<0.05). However, pulmonary artery pressure and pulmonary vascular resistance were not significantly reduced. For 4 patients, epoprostenol therapy acted as a bridge to lung transplantation. For the other patients who had no chance to undergo lung transplantation, epoprostenol therapy was applied for 528.0±216.6 days and the maximum dose was 63.9±19.0ng·kg-1·min-1. Conclusions: This study data suggest that cautious application of epoprostenol can be considered as a therapeutic option in patients with PVOD and PCH.  (Circ J 2012; 76: 1729–1736)

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© 2012 THE JAPANESE CIRCULATION SOCIETY
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