Pulmonary Arterial Hypertension
Pulmonary Arterial Hypertension (PAH) is a serious condition that affects the blood vessels in the lungs. In PAH, the small arteries that carry blood from the heart to the lungs become narrow or blocked, making it harder for blood to flow. This leads to increased pressure in these arteries and can strain the heart. Symptoms often include shortness of breath, fatigue, and chest pain. If left untreated, PAH can lead to severe complications, but there are treatments available to help manage the condition and improve quality of life.
Additional Insights
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Pulmonary arterial hypertension (PAH) is a serious condition where the blood pressure in the arteries that supply the lungs becomes too high. This increased pressure makes it harder for the heart to pump blood through the lungs, which can lead to symptoms like shortness of breath, fatigue, and chest pain. PAH can be caused by various factors, including genetic conditions, certain medical disorders, or can occur without an obvious cause. Treatment typically involves medications to lower blood pressure in the lungs, improve blood flow, and help manage symptoms, though it can be a progressive and challenging condition.
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Pulmonary arterial hypertension (PAH) is a serious condition characterized by high blood pressure in the arteries that supply blood to the lungs. It makes it harder for the heart to pump blood through these narrowed or blocked blood vessels, leading to symptoms like shortness of breath, fatigue, and chest pain. PAH can be caused by various factors, including heart problems, lung diseases, or genetic conditions. While there is no cure, treatments are available to help manage symptoms and improve quality of life, making it essential for those affected to work closely with their healthcare providers.