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Prospective clinical assessment of patients with pulmonary arterial hypertension switched from bosentan to macitentan (POTENT)

Abstract Even though pulmonary arterial hypertension (PAH) remains an incurable disease, the combination of PAH‐specific therapies allowed treatment strategies to evolve from symptom‐based ones to others that aim to move patients to low‐risk conditions. Endothelin‐1 (ET‐1) receptor antagonists emerg...

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Bibliografische Detailangaben
Hauptverfasser: Abdullah M. Aldalaan, Sarfraz A. Saleemi, Ihab Weheba, Abeer Abdelsayed, Maha M. Aleid, Fatima Alzubi, Hamdeia Zaytoun, Nadeen Alharbi
Format: Artigo
Sprache:Inglês
Veröffentlicht: Wiley 2022-04-01
Schriftenreihe:Pulmonary Circulation
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Online-Zugang:https://doi.org/10.1002/pul2.12083
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