Pulmonary Hypertention Hero

About PAH

What is PAH?


PAH is a rare, life-threatening disease in which chronically elevated pressure in the pulmonary arteries causes progressive strain on the right ventricle of the heart. PAH causes narrowing of the smallest pulmonary arteries, elevating blood pressure within them to dangerously high levels.2

PAH is defined by a mean pulmonary artery pressure at rest ≥25 mm Hg in the presence of a pulmonary capillary wedge pressure ≤15 mm Hg.3 To eliminate the confounding effects of cardiac output and left ventricular end-diastolic pressure, pulmonary vascular resistance >3 Wood units should also be present.4

PAH Initiative

According to today’s treatment recommendations, patients with pulmonary arterial hypertension (PAH) should receive an objective, multiparameter risk assessment (opens in new tab) at diagnosis and follow-up risk assessments as often as every 3 months thereafter.5,6

These risk calculation tools can help you quickly calculate your patient’s risk score with point-and-click ease. You can choose from among 5 calculators.

View Risk Calculators (opens in new tab)
The PAH Initiative logo

Visit pahinitiative.com(opens in new tab) to learn more, explore risk calculators, and download helpful resources.

Give patients peace of mind with the Patient Info Sheet

This document includes some of the most important information you should know about ADCIRCA, how to take ADCIRCA properly, common side effects, and more.

Resources


Here you will find additional resources on pulmonary arterial hypertension (PAH), including PAH organizations and community groups, and downloadable resources to support your treatment with ADCIRCA.

ADCIRCA® (tadalafil) is a phosphodiesterase 5 inhibitor (PDE-5i) indicated for the treatment of pulmonary arterial hypertension (PAH) (WHO Group 1) to improve exercise ability. Studies establishing effectiveness included predominately patients with NYHA Functional Class II–III symptoms and etiologies of idiopathic or heritable PAH (61%) or PAH associated with connective tissue diseases (23%).

References

  1. Data on file, June 2016.
  2. Badesch DB, Abman SH, Simonneau G, Rubin LJ, McLaughlin VV. Medical therapy for pulmonary arterial hypertension: updated ACCP evidence-based clinical practice guidelines. Chest.
    2007;131(6):1917-1928.
  3. Hoeper MM. Definition, classification, and epidemiology of pulmonary arterial hypertension.Semin Respir Crit Care Med. 2009;30(4):369-375.
  4. Archer SL, Michelakis ED. An evidence-based approach to the management of pulmonary arterial hypertension. Curr Opin Cardiol. 2006;21(4):385-392.
  5. Humbert M, et al. Eur Heart J. 2022;43(38):3618-3731.
  6. Dardi F, et al. Eur Respir J. 2024;64(4):2401323.