About PAH
Pulmonary arterial hypertension (PAH) is a devastating disease. Before the introduction of modern therapies, on average, patients survived only 2.5 years.1 Fortunately, treatment options have expanded over the last decade and now include 6 FDA-approved medications. With these expanded treatment options, the prognosis is improving2 and patients are living longer than historical predictions indicated. PAH therapies, including Ventavis® (iloprost), have had a positive impact on clinical status, exercise capacity, functional class, and hemodynamics.
Pulmonary Arterial Hypertension Defined
Mean pulmonary artery pressure (mPAP) ≥ 25 mm Hg with a pulmonary capillary wedge pressure ≤ 15 mm Hg measured by cardiac catheterization1
Read more about Ventavis:
Disease Classification
|
 |