Idiopathic Pulmonary Arterial Hypertension

Idiopathic Pulmonary Artery Hypertension - StatPearls - NCBI

The criteria for testing positive is a fall in pulmonary artery pressure to more than 10 mmHg with an increase or no change in cardiac output. Although first- ...

Pulmonary hypertension - Symptoms and causes - Mayo Clinic

In one form of pulmonary hypertension, called pulmonary arterial hypertension (PAH), blood vessels in the lungs are narrowed, blocked or ...

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 - Symptoms, Causes, Treatment

Pulmonary arterial hypertension (PAH) is a rare, progressive disorder characterized by high blood pressure (hypertension) in the arteries of the lungs.

Pulmonary Arterial Hypertension (PAH): Symptoms and Treatment

Pulmonary arterial hypertension (PAH) is a condition in which the small blood vessels in your lungs become narrow.

Idiopathic pulmonary arterial hypertension - Orphanet

IPAH is a sporadic form of pulmonary arterial hypertension (PAH, see this term) characterized by elevated pulmonary arterial resistance leading to right heart ...

Pulmonary Arterial Hypertension: Symptoms, Causes, and Treatments

Chest pain · Fatigue; Passing out; Swelling in your ankles and legs. Getting a Diagnosis. If you have shortness of breath and see your doctor, ...

Pulmonary Arterial Hypertension Symptoms and Diagnosis

Edema, or swelling of the feet, legs and eventually the abdomen and neck; Dizziness and fainting spells; Chest pain; Heart palpitations (racing or pounding) ...

Pulmonary Hypertension - Symptoms and Causes - Penn Medicine

In this case, the condition is called idiopathic pulmonary arterial hypertension (IPAH). Idiopathic means the cause of a disease is not known. IPAH affects more ...

The prognostic impact of follow-up assessments in patients with ...

Idiopathic pulmonary arterial hypertension (IPAH) is a rare chronic disease characterised by progressive remodelling of the pulmonary vasculature which ...

Pulmonary arterial hypertension - Genetics - MedlinePlus

Pulmonary arterial hypertension is a progressive disorder characterized by abnormally high blood pressure (hypertension) in the pulmonary artery.

Types of PH - Pulmonary Hypertension Association

Pulmonary arterial hypertension (PAH) is a chronic and currently incurable disease that causes the walls of the arteries of the lungs to tighten ...

Idiopathic pulmonary arterial hypertension (Concept Id - NCBI

Idiopathic pulmonary arterial hypertension (IPAH) is a sporadic form of pulmonary arterial hypertension (PAH, see this term) characterized by elevated ...

Pulmonary hypertension - Diagnosis and treatment - Mayo Clinic

Lung or heart-lung transplant. Sometimes, a lung or heart-lung transplant may be needed, especially for younger people who have idiopathic ...

Idiopathic Pulmonary Arterial Hypertension Workup

European guidelines recommend first evaluating for significant group 2 or 3 disease by ordering a TTE, pulmonary function tests with arterial blood gas ...

Pulmonary hypertension - Wikipedia

The pathogenesis of pulmonary arterial hypertension (WHO Group I) involves the · Persistent pulmonary hypertension of the newborn occurs when the circulatory ...

Biological heterogeneity in idiopathic pulmonary arterial ... - Nature

Idiopathic pulmonary arterial hypertension (IPAH) is a rare but fatal disease diagnosed by right heart catheterisation and the exclusion of ...

Idiopathic pulmonary arterial hypertension phenotypes determined ...

This cluster analysis identified distinct phenotypes, which differed in clinical presentation, response to therapy, and survival.

Long-Term Response to Calcium Channel Blockers in Idiopathic ...

Pulmonary arterial hypertension (PAH) is a disease of the small pulmonary arteries characterized by a progressive increase in pulmonary vascular ...