Pulmonary Hypertension


Pulmonary Hypertension (PH or PHTN) is a condition of high blood pressure in the arteries of the lungs. Symptoms include shortness of breath, fainting, tiredness, chest pain, leg swelling, and heart palpitations. This condition can make it difficult to exercise. The onset is usually gradual. It is a form of high blood pressure that affects the lungs arteries and the right side of the coronary heart. In one form of pulmonary high blood pressure, tiny arteries in the lungs known as pulmonary arterioles and capillaries become narrowed, blocked, or destroyed. This makes it harder for blood to flow to the lungs and increases pressure in the arteries of the lungs. As stress builds up, the heart's own lower chamber (native ventricle) must work hard to pump blood through the lungs, which ultimately leads to weakening and failure of the coronary heart muscle. Pulmonary hypertension is a pathophysiological disease with many possible causes. Indeed, this condition often accompanies severe heart or lung disease .Each form of pulmonary hypertension is different, so it is important for newly diagnosed patients to find a pulmonary hypertension specialist who can pinpoint the cause of their pulmonary hypertension and develop a treatment plan that is appropriate for that pulmonary hypertension as quickly as possible as far as it is possible. Every person with pulmonary hypertension is different, and new studies are being conducted every day to improve the prognosis for people living with the disease. After the treatment of pulmonary hypertension has been treated and treated appropriately, people with pulmonary hypertension can remain in it for many years.



 


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