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Pulmonary Arterial Hypertension PAH or PH

Treatments

Pulmonary arterial hypertension (PAH) is a serious condition where the blood pressure in the pulmonary artery becomes abnormally high. This occurs when the tiny arteries in the lungs narrow, increasing the workload of the heart. Causes include congestive heart failure, blood clots in the lungs, HIV, liver diseases, inborn heart defects, sleep apnea, autoimmune diseases, and lung conditions such as emphysema and pulmonary fibrosis. In some cases, the cause remains unknown, termed idiopathic PAH.

Symptoms of pulmonary arterial hypertension (PAH) can be subtle and easily mistaken for other conditions, including chest pain, breathing difficulties, dry or bloody cough, dizziness, fainting, fatigue, nausea, vomiting, wheezing, and swelling in the ankles or arms. Ignoring these symptoms can lead to complications such as anaemia, arrhythmias, blood clots, lung bleeding, heart failure, liver damage, and pregnancy complications.

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