Title of article :
Bosentan for Treatment of Inoperable Chronic Thromboembolic Pulmonary Hypertension: BENEFiT (Bosentan Effects in iNopErable Forms of chronIc Thromboembolic pulmonary hypertension), a Randomized, Placebo-Controlled Trial Original Research Article
Author/Authors :
Xavier Jais، نويسنده , , Andrea M. DʹArmini، نويسنده , , Pavel Jansa، نويسنده , , Adam Torbicki، نويسنده , , Marion Delcroix، نويسنده , , Hossein A. Ghofrani، نويسنده , , Marius M. Hoeper، نويسنده , , Irene M. Lang، نويسنده , , Eckhard Mayer، نويسنده , , Joanna Pepke-Zaba، نويسنده , , Loïc Perchenet، نويسنده , , Adele Morganti، نويسنده , , Gerald Simonneau، نويسنده , , Lewis J. Rubin and BENEFiT Study Group، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
8
From page :
2127
To page :
2134
Abstract :
Objectives Our goal was to investigate the effect of treatment with the oral dual endothelin receptor antagonist bosentan on the hemodynamics and exercise capacity of patients with chronic thromboembolic pulmonary hypertension (CTEPH). Background CTEPH is characterized by vascular obstruction and remodeling, leading to increased pulmonary vascular resistance (PVR). Although pulmonary endarterectomy (PEA) is potentially curative, medical therapy is needed in patients with inoperable disease or persistent/recurrent pulmonary hypertension after PEA. Methods The BENEFiT (Bosentan Effects in iNopErable Forms of chronIc Thromboembolic pulmonary hypertension) study was a double-blind, randomized, placebo-controlled study in CTEPH including patients with either inoperable CTEPH or persistent/recurrent pulmonary hypertension after PEA (>6 months after PEA). Independent coprimary end points were change in PVR as a percentage of baseline and change from baseline in 6-min walk distance after 16 weeks of treatment with bosentan or placebo. Secondary end points included change from baseline in World Health Organization functional class and other hemodynamic parameters. Results One hundred fifty-seven patients were enrolled and randomized: 80 to placebo, 77 to bosentan. A statistically significant treatment effect (TE) of bosentan over placebo on PVR was demonstrated: −24.1% of baseline (95% confidence interval [CI]: −31.5% to −16.0%; p < 0.0001). Total pulmonary resistance (TE: −193 dyn·s·cm−5; 95% CI: −283 to −104 dyn·s·cm−5; p < 0.0001) and cardiac index (TE: 0.3 l·min−1·m−2; 95% CI: 0.14 to 0.46 l·min−1·m−2; p = 0.0007) improved. Mean TE on 6-min walk distance was +2.2 m (95% CI: −22.5 to 26.8 m; p = 0.5449). Bosentan treatment was well tolerated. Conclusions This study demonstrated a positive TE of bosentan on hemodynamics in this patient population. No improvement was observed in exercise capacity. Further trials are needed to define the role of medical therapy in patients with CTEPH (Bosentan Effects in Inoperable Forms of Chronic Thromboembolic Pulmonary Hypertension; NCT00313222).
Keywords :
hemodynamics , Operability , pulmonary endarterectomy , bosentan
Journal title :
JACC (Journal of the American College of Cardiology)
Serial Year :
2008
Journal title :
JACC (Journal of the American College of Cardiology)
Record number :
473749
Link To Document :
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