Pulmonary Arterial Hypertension
Pulmonary hypertension - UF Health
Unknown cause, called idiopathic pulmonary arterial hypertension · Changes in gene passed through families · Autoimmune or connective tissue ...
Pulmonary Arterial Hypertension (PAH) - UCLA Health
PAH is defined as elevated blood pressure in the lungs, which leads to enlargement of the right side of the heart and, if untreated, heart failure and death.
Pulmonary Hypertension - Merck Manual Professional Edition
Pulmonary hypertension is currently classified into 5 groups (see table Classification of Pulmonary Hypertension) based on a number of pathologic, physiologic, ...
Pulmonary Hypertension - Brigham and Women's Hospital
Connective tissue disease, particularly scleroderma; Liver disease; HIV; Valvular or hypertensive (caused by high blood pressure) heart disease; Lung disease ...
Idiopathic Pulmonary Arterial Hypertension - Medscape Reference
Primary pulmonary hypertension (PPH) is a rare disease characterized by elevated pulmonary artery pressure with no apparent cause.
Idiopathic pulmonary arterial hypertension - BMJ Best Practice
Idiopathic pulmonary arterial hypertension (IPAH) is a rare, frequently fatal disease. Presenting symptoms and signs are nonspecific and ...
Pulmonary Arterial Hypertension (PAH) - Yale Medicine
As the only accredited pulmonary hypertension program in the state, we offer patient- and family-centered care to patients from throughout the Northeast. Our ...
Pulmonary arterial hypertension in children
This review of pulmonary arterial hypertension will highlight the key features of pulmonary hypertension in infants and children
Welcome to the Pulmonary Hypertension Association
Founded in 1991, the Pulmonary Hypertension Association is dedicated to extending and improving the lives of those affected by pulmonary hypertension.
Pulmonary Hypertension | Patient Information Series
What are the different groups of pulmonary hypertension? There are 5 different groups, based on their causes: Group 1—Pulmonary arterial hypertension (PAH).
Pulmonary Arterial Hypertension - Causes, Symptoms & Signs
Pulmonary arterial hypertension is a form of high blood pressure where small arteries in the lungs become narrow or blocked.
Pulmonary Hypertension - Boston Children's Hospital
Group 1: Pulmonary arterial hypertension (PAH) ... PAH causes the right side of the heart to work harder to pump blood because pulmonary arteries are narrowed or ...
Pulmonary Arterial Hypertension Information - Piedmont Healthcare
What is the treatment? The treatment depends on what is causing the pulmonary hypertension and is directed at managing that condition. There are treatment ...
Pulmonary Hypertension in Children | Johns Hopkins Medicine
Pulmonary arterial hypertension (PAH). PAH occurs when the arteries in the lungs become thickened, narrow or stiff. “This causes the right side of the heart to ...
Mechanisms and treatment of pulmonary arterial hypertension - Nature
Substantial progress has been made in the management of pulmonary arterial hypertension (PAH) in the past 25 years, but the disease remains ...
Treating Pulmonary Arterial Hypertension - WebMD
Sildenafil (Revatio). Small studies suggest this drug can improve blood flow in your lungs. The recommended dose is a 20-milligram pill taken ...
Pulmonary Arterial Hypertension - American Journal of Managed Care
The AJMC® Pulmonary Arterial Hypertension compendium is a comprehensive resource for clinical news and expert insights for the progressive disorder, ...
Pulmonary hypertension is defined by high blood pressure in the blood vessels of the lungs. There are many different types pulmonary hypertension.
Pulmonary Arterial Hypertension | New England Journal of Medicine
Pulmonary arterial hypertension is defined as a sustained elevation of pulmonary arterial pressure to more than 25 mm Hg at rest or to more than ...
Pulmonary Arterial Hypertension (PAH) - Jefferson Health
PAH is a rare, progressive condition that causes shortness of breath, chest pain, and can lead to heart failure.