MedicalResearch.com Interview with: Raymond L. Benza, MD, FACC, FAHA, FACP Primary Study Investigator and Professor of Medicine at The Ohio State University MedicalResearch.com: What is the background for this study? Would you briefly explain the significance of Pulmonary Arterial Hypertension? Response: Pulmonary arterial hypertension (PAH) is a silently progressive disease with no known cure and is often fatal. It’s a specific form of pulmonary hypertension (PH) that causes the walls of the pulmonary arteries to become thick and stiff, narrowing the space for blood to flow, and causing an increased blood pressure to develop within the lungs. PAH has a variety of etiologies and long-term impact on patients' functioning as well as their physical, psychological and social wellbeing. Assessing a patient's risk of 1-year mortality is a crucial component to the management and treatment of PAH, as the main treatment goal is for patients to achieve a low-risk status. Given the severity of the disease, physicians need to be able to risk stratify patients in order to characterize their disease better, know how to intelligently implement their medications, and when to refer them for lung transplantation. There are different approaches to assessing risk in PAH, including the use of variables, equations, and calculator tools; however, real-world evidence indicates risk assessment in the clinical setting is suboptimal. This is why we conducted an analysis to determine the validity of the Registry to Evaluate Early and Long-Term PAH Disease Management (REVEAL) Lite 2 risk calculator, an abridged version of the REVEAL 2.0 risk calculator, in patients with PAH.  (more…)