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Pulmonary arterial hypertension is a condition characterized by high blood pressure in the lungs. This condition is different from regular hypertension (raised blood pressure). In pulmonary arterial hypertension, the arteries going from the heart towards the lungs get narrow or obstructed, therefore, causing hindrance in the flow of blood that results in increased blood pressure in the lungs.
Causes of pulmonary arterial hypertension can be classified as idiopathic (no known cause) and pulmonary arterial hypertension caused by an underlying disease. Idiopathic pulmonary arterial hypertension can be linked to genetics in some cases. Diseases that can cause pulmonary arterial hypertension include:
Sometimes, the cause of High blood pressure in lungs is difficult to be determined and doctors term this idiopathic pulmonary hypertension where family (genetic) history might be a factor.
Few factors are known to increase the risk of this condition:
Symptoms of pulmonary arterial hypertension include:
A person with the complaint of shortness of breath will see a doctor who makes a diagnosis by taking a detailed history of smoking and drug usage, heart and lung disease in a family, the severity of chest pain and suffocation and factors that increase these symptoms.
He will further perform these tests:
Treatment for pulmonary hypertension is aimed at the cause of the disease.
You should consult a doctor if your condition worsens, there is no improvement in your condition, you start experiencing new side effects because of the medicines, your symptoms start hampering your daily life, and there is a general feeling of discomfort.
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