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Primary pulmonary hypertension is generally classified as a disease of the lung, related to high blood-pressure. Essentially, the increased pressure causes some pulmonary arteries and veins to work at drastically different rates than others, creating an imbalance that can cause fatigue, shortness of breath, fainting, and a persistent cough.

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Why does Pulmonary Arterial Hypertension develop?

Pulmonary Arterial Hypertension (PAH) develops due to the narrowing of the small arteries in the lungs, leading to increased resistance to blood flow. This increased resistance causes the right side of the heart to work harder to pump blood through the lungs, eventually leading to the thickening and stiffening of the pulmonary arteries. The exact cause of PAH can vary and may include genetic factors, underlying medical conditions, or exposure to certain toxins or drugs. Early detection and management of PAH are crucial to prevent further complications and improve quality of life for affected individuals.


What are the dangers of arterial hypertension?

The danger of arterial hypertension is high blood pressure in the lungs. It can worsen over time and become life-threatening because of the pressure in the pulmonary arteries rising to a dangerously high levels and puts a strain on the heart.


What is Viagra?

Viagra is used to treat male Impotence also known as Erectile Dysfunction. Also, it has been approved by US FDA for treating pulmonary arterial hypertension.


What did evil cannieval die from?

Idiopathic pulmonary fibrosis


What is the medical term meaning idiopathic high blood pressure?

An idiopathic condition is a real condition with no known medical explanation. This is not to be mixed up with psychosomatic conditions, with the patient creating the condition.


What is Remodulin used to treat?

Remodulin has two main uses, both of which are related to individuals who suffer from pulmonary arterial hypertension. The first use of Remodulin is to reduce hypertension symptoms while the patient is exercising. The second use is to treat hypertension patients who can no longer take the drug Flolan.


What is the difference between pulmonary hypertension and regular hypertension?

Blood pressure (BP) is the pressure exerted by circulating blood upon the walls of blood vessel, and is one of the principal vital signs. Arterial hypertension or hypertension or high BP can be an indicator of other problems and may have long-term adverse effects. Sometimes it can be an acute problem, for example hypertensive emergency. Types of hypertension usually are primary and secondary, in that alcohol induced, medication induced, pregnancy induced, isolated systolic, isolated diastolic, white coat hypertension (BP due to stress) and malignant hypertension or hypertension emergency are present. In medicine, pulmonary hypertension (PH or PHT) is an increase in blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, together known as the lung vasculature, leading to SOB, dizziness, fainting, and other symptoms, all of which are exacerbated by exertion. Pulmonary hypertension can be a severe disease with a markedly decreased exercise tolerance and heart failure. So both are different terms.


What is the difference between unspecified Hypertension and benign hypertension?

these are misnomers actually,when there is no evident cause of hypertension then it is called idiopathic/benign/primary/unspecified hypertension. http://treathypertension.blogspot.com/


Is Viagra a stimulant?

Sildenafil citrate, sold as Viagra, Revatioand under various other trade names, is a drug used to treat erectile dysfunction and pulmonary arterial hypertension (PAH).Viagra is neither a hallucinogen, depressant, nor is it a stimulant.


Who found how to prevent idiopathic intercranial hypertension?

dr Daniel jame gray.


What is Bosentan used to treat?

Bosentan is used in the treatment of pulmonary arterial hypertension (PAH) and usually comes in pill form. Bosentan treatment is used to control symptoms of PAH, not the cause or as a cure.


Is alpha 1 anTitrypsin deficiency the same as idiopathic pulmonary fibrosis?

no