Pulmonary Artery Hypertension

Pulmonary Artery Hypertension

Pulmonary Artery Hypertension is a type of high blood pressure in the arteries of the lungs, where the pulmonary arteries become narrowed or stiff, making it hard for the blood to flow through the lungs. This increases the pressure in the lung arteries and puts strain on the right side of the heart. It is a progressive and potentially fatal disease if left untreated.

Causes of Pulmonary Arterial Hypertension

PAH can be idiopathic or associated with other conditions:

Symptoms of PAH

These symptoms often develop slowly and may be missed early.

Diagnosis

Treatment

General

PAH-specific Drugs

Advanced

Frequently Asked Questions (FAQs)

No, PAH affects only the arteries in the lungs, while regular BP affects the whole body.

No cure exists, but early diagnosis and proper treatment can control symptoms and slow the progression.

PAH is a chronic and potentially life – threatening disease, especially without the treatment. It can lead to right heart failure over time.

Yes, if you take early treatment and with careful monitoring, many people with PAH can live productive lives, but the activity may be limited.

Make An Appointment