What is Pulmonary Hypertension?

Pulmonary Hypertension

Pulmonary hypertension or pulmonary hypertension is a disease complex and often misunderstood. Pulmonary hypertension is a condition where there is high blood pressure in the lungs. Pulmonary hypertension is different from normal blood pressure. In hypertension Regular (also known as hypertension), in the arteries of a person in the whole body contract. In pulmonary hypertension, the blood vessels to constrict the lungs and the heart must work harder to pump blood through them. HP can also be caused by multiple blood clots, diseases that the failure of the lungs or heart damage. Early symptoms are often nonspecific and the diagnosis is often delayed.

Hypertension is known to affect people of all ages. The most common symptoms are heavy physical activity, fatigue, dizziness and sometimes fainting. Because these symptoms can be caused by a number of other problems, diagnosis of pulmonary arterial hypertension may be difficult and requires a specialist. When pulmonary hypertension is diagnosed, however, treatment can start immediately.

Pulmonary arterial hypertension

Pulmonary hypertension One way is called pulmonary arterial hypertension (PAH). In PAH, the blood vessels that carry blood to the lungs (known as pulmonary arteries) narrow, thick and hard. For this reason, the pressure in the arteries becomes abnormally high. This means that the right side of the heart must pump harder to circulate blood.

Types of pulmonary hypertension

There are several types of pulmonary arterial hypertension. In what is called idiopathic pulmonary arterial hypertension (PAH). The cause of pulmonary arterial hypertension is not known. In what is known as familial pulmonary arterial hypertension (PAH family), the disease is hereditary, meaning that another member or members of the family of the patient was diagnosed with pulmonary hypertension. pulmonary arterial hypertension can also be associated with other medical conditions such as connective tissue diseases (scleroderma and lupus, for example), chronic liver disease, congenital heart disease, and sickle cell anemia and HIV infection. PAH can be associated with drug use in the past or present, such as methamphetamine or any diet pills.

Symptoms of pulmonary hypertension

Some patients with pulmonary hypertension also have other special problems. There may be other diseases of the heart on the left (for example, people who have had heart attacks, high blood pressure or heart valve disease), thrombosis, chronic obstructive pulmonary disease (COPD) and emphysema, thromboembolic disease (chronic blood in the lungs).

P is a serious disease and without treatment, symptoms can only worsen, leading to heart failure and death. Therefore it is important that patients follow the advice of your doctor. pulmonary arterial hypertension, such as PD itself are rare and the signs and symptoms are vague and often confused with other disorders. Diagnosis and treatment are crucial.

Public awareness of pulmonary arterial hypertension (and PH) will help patients to seek treatment earlier, which could lead to better long-term health. Although no cure has yet to be found for pulmonary hypertension, a search has resulted in new drugs and better treatment and allowing patients to live longer PH, more complete, with the disease much less interference.

Treatment for pulmonary Hypertension

Treatment for Pulmonary Hypertension generally includes therapeutic strategies such as vasodilators that includes calcium channel blockers and prostacycline, anticoagulation, treatment of right heart failure and most common transplantation. Other therapeutic strategic includes counseling on smoke termination, oxegen therapy in hypoxemic patients and avoiding conditions that can increase pulmonary artery pressure. Also drugs that depress cardiac output should be decreased. Pulmonary hypertension is highly contraindication to pregnant lady and patient needs to practice birth control without contraceptives is preferred as it may increase pulmonary hypertension.

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