Inhaled Iloprost To Treat Severe Pulmonary Hypertension: An Uncontrolled Trial
- 21 March 2000
- journal article
- clinical trial
- Published by American College of Physicians in Annals of Internal Medicine
- Vol. 132 (6), 435-443
- https://doi.org/10.7326/0003-4819-132-6-200003210-00003
Abstract
Inhaled aerosolized iloprost, a stable prostacyclin analogue, has been considered a selective pulmonary vasodilator in the management of pulmonary hypertension. To assess the efficacy of inhaled iloprost in the treatment of life-threatening pulmonary hypertension. Open, uncontrolled, multicenter study. Intensive care units and pulmonary hypertension clinics at six university hospitals in Germany. 19 patients who had progressive right-heart failure despite receiving maximum conventional therapy (12 with primary pulmonary hypertension, 3 with pulmonary hypertension related to collagen vascular disease without lung fibrosis, and 4 with secondary pulmonary hypertension). Inhaled iloprost, 6 to 12 times daily (50 to 200 µg/d). Right-heart catheterization and distance walked in 6 minutes at baseline and after 3 months of therapy. During the first 3 months of therapy, New York Heart Association functional class improved in 8 patients and was unchanged in 7 patients. Four patients died, 3 of right-heart failure and 1 of sepsis. The acute hemodynamic response to inhaled iloprost was predominant pulmonary vasodilatation with little systemic effect at baseline and at 3 months (data available for 12 patients). Hemodynamic variables were improved at 3 months, and the distance walked in 6 minutes improved by 148 m (95% CI, 4.5 to 282 m; P = 0.048). Of the 15 patients who continued to use inhaled iloprost, 8 stopped: Four had lung transplantation, 1 switched to intravenous prostacyclin therapy, and 3 died. Seven patients are still receiving inhaled iloprost [mean ±SD] duration of therapy, 536 ± 309 days; mean dosage, 164 ± 38 µg/d). Inhaled iloprost may offer a new therapeutic option for improvement of hemodynamics and physical function in patients with life-threatening pulmonary hypertension and progressive right-heart failure that is refractory to conventional therapy. *For additional members of the German PPH Study Group, see the Appendix.Keywords
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