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PMID: 11926786 Published · ppublish English Clinical Trial Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Combination therapy with oral sildenafil and inhaled iloprost for severe pulmonary hypertension.

Annals of internal medicine ·Vol. 136 ·No. 7 ·2002-04-02 ·Pages 515-22

Ghofrani HA, Wiedemann R, Rose F, Olschewski H, Schermuly RT, Weissmann N, Seeger W, Grimminger F

Abstract

Inhalation of the stable prostacyclin analogue iloprost is being studied for treatment of pulmonary hypertension. The selective phosphodiesterase-5 inhibitor sildenafil has been reported to cause pulmonary vasodilatation. To evaluate the safety and effectiveness of oral sildenafil, alone and in combination with inhaled iloprost, for treatment of pulmonary hypertension. Randomized, controlled, open-label trial. Intensive care unit. 30 patients with severe pulmonary arterial hypertension (n = 16), chronic thromboembolic pulmonary hypertension (n = 13), or pulmonary hypertension due to aplasia of the left pulmonary artery (n = 1), all classified as New York Heart Association class III or IV. All patients received inhaled nitric oxide and aerosolized iloprost (inhaled dose, 2.8 microg). They were then randomly assigned to receive 12.5 mg of oral sildenafil, 50 mg of sildenafil, 12.5 mg of sildenafil plus inhaled iloprost, or 50 mg of sildenafil plus inhaled iloprost. Systemic and pulmonary arterial pressure, pulmonary arterial occlusion pressure, cardiac output, central venous pressure, peripheral arterial oxygen saturation, and arterial and mixed venous blood gases were measured during right-heart catheterization by using a Swan-Ganz catheter. In rank order of pulmonary vasodilatory potency (maximum reduction of pulmonary vascular resistance and increase in cardiac index), 50 mg of sildenafil plus iloprost was most effective, followed by 12.5 mg of sildenafil plus iloprost. Iloprost alone and 50 mg of sildenafil were almost equally effective but were less potent than the combination regimens, and the least potent treatments were 12.5 mg of sildenafil and nitric oxide. In patients who received 50 mg of sildenafil plus iloprost, the maximum change in pulmonary vasodilatory potency was -44.2% (95% CI, -49.5% to -38.8%), compared with -14.1% (CI, -19.1% to -9.2%) in response to nitric oxide. With administration of 50 mg of sildenafil plus iloprost, the area under the curve for reduction in pulmonary vasodilatory resistance surpassed that of administration of 50 mg of sildenafil alone and iloprost alone combined, the vasodilatory effect lasted longer than 3 hours, and systemic arterial pressure and arterial oxygenation were maintained. No serious adverse events occurred. Although limited by the small sample and lack of long-term observations, the study shows that oral sildenafil is a potent pulmonary vasodilator that acts synergistically with inhaled iloprost to cause strong pulmonary vasodilatation in both severe pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension.

MeSH Terms
3',5'-Cyclic-GMP Phosphodiesterases/antagonists & inhibitors Administration, Oral Analysis of Variance Area Under Curve Dose-Response Relationship, Drug Drug Synergism Drug Therapy, Combination Female Hemodynamics/drug effects Humans Hypertension, Pulmonary/drug therapy,physiopathology Iloprost/administration & dosage,pharmacokinetics Male Phosphodiesterase Inhibitors/administration & dosage,pharmacokinetics Piperazines/administration & dosage,pharmacokinetics Purines Sildenafil Citrate Sulfones Vasodilator Agents/administration & dosage,pharmacokinetics
Chemicals
Phosphodiesterase Inhibitors Piperazines Purines Sulfones Vasodilator Agents Sildenafil Citrate 3',5'-Cyclic-GMP Phosphodiesterases Iloprost
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Ghofrani Hossein Ardeschir
Department of Internal Medicine, University Hospital, Justus-Liebig-University, Klinikstrasse 36, 35392 Giessen, Germany. [email protected]
Wiedemann Ralph
Rose Frank
Olschewski Horst
Schermuly Ralph Theo
Weissmann Norbert
Seeger Werner
Grimminger Friedrich
Article Info
Journal
Annals of internal medicine
Abbr.
Ann Intern Med
ISSN
1539-3704
Published
2002-04-02
Pages
515-22
Language
English
Region
United States
NLM ID
0372351
Subset
IM
Corrections
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