Pulmonary arterial hypertension can be treated in a variety of ways (PAH). The kind of PAH you have and the severity of your symptoms will determine the treatment or combination of medications you receive. Pulmonary arterial hypertension (PAH) is a rare but potentially life-threatening condition characterized by high blood pressure in the arteries that supply blood to the lungs. Pulmonary Arterial Hypertension Drug can lead to serious complications, including heart failure and death. Fortunately, there are several drugs available to treat PAH. In this article, we will discuss how these drugs work and the mechanisms behind their effectiveness.
First, let's take a look at the pathophysiology of PAH. PAH occurs when the blood vessels in the lungs become narrow and thickened, leading to increased resistance to blood flow. This increased resistance causes the right side of the heart to work harder to pump blood to the lungs, which can eventually lead to heart failure. PAH can be caused by a variety of factors, including genetic mutations, chronic lung disease, and exposure to certain drugs and toxins.
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