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Pulmonary Arterial Hypertension

What is primary pulmonary hypertension?

Primary pulmonary hypertension is now known as (PAH). The name was changed in 1998 because it was determined to be more descriptive of the condition.

PAH is a disorder characterized by an abnormal increase in pulmonary artery pressure, normal pulmonary capillary wedge pressure, and increased pulmonary vascular resistance. A gradual increase of pulmonary artery pressure can lead to eventual right-heart failure and death. Increases in pulmonary arterial pressure are the most important indicators of PAH.

Imaging tests are used to look inside the body for a diagnosis. Enlarged arteries or damage to the heart are sure signs of PAH. Medications are used to slow heart damage and deal with symptoms.

Even with treatment, about one-third of people with PAH will die of diagnosis. Thanks to new treatments, this number is an improvement from the 50 percent who used to die within 3 years. The medical community hopes to find a cure to stop the damage of PAH.

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Causes

Causes of pulmonary arterial hypertension

The cause of PAH can be either idiopathic (IPAH) or familial (FPAH). Idiopathic diseases arise spontaneously, and their causes are unknown. Familial diseases are genetically passed down through families.

Environmental factors and medications are believed to be possible causes of IPAH.

Possible causes of IPAH:

  • appetite suppressants (aminorex, fenfluramine, dexfenfluramine, etc.)
  • hormone therapy (which may explain why more women than men have the disease)

Most cases of FPAH arise from a mutation in the BMPR2 gene. Severe cases are generally linked to the presence of the mutation. Although the mutation may be present at birth, the disease may take months or years to appear.

Symptoms

Symptoms of pulmonary arterial hypertension

The characteristic symptom of PAH is an increase in pulmonary vascular resistance. This causes an increase in pressure on the right ventricle of the heart. That problem leads to trouble in filling the left part of the heart. Eventually, the heart fails as a result.

Common symptoms of PAH are:

  • difficult or labored breathing on exertion
  • fatigue, caused by the heart having to pump harder and harder
  • nearly fainting
  • fainting

Read more: The symptoms of pulmonary arterial hypertension »

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Risks

Risk factors of pulmonary arterial hypertension

PAH is still not well understood. Research has found certain diseases that may make a person more likely to develop PAH:

  • The exact link is unknown, but the rate for developing PAH among people with human immunodeficiency virus (HIV) is 0.5 percent, which is than in the general population.
  • In of FPAH, the person has a mutation in the 2(BNP2) gene.
  • PAH is noted in of people with portal hypertension (increased pressure in the veins that carry blood from the gastrointestinal tract and organs to the liver).
  • Certain unrepaired, congenital heart abnormalities also may make someone more likely to develop PAH.

Diagnosis

Diagnosis of pulmonary arterial hypertension

Diagnosis isn’t easy, because damage inside the heart can’t be seen during a routine examination. Doctors try to rule out all other causes of pulmonary hypertension before a diagnosis is made. Your doctor may order some or all of the following tests:

  • electrocardiogram to look for proof of right ventricle damage or strain
  • chest X-ray to look for enlarged arteries from the overworking heart
  • computed tomography (CT) scan to see enlarged pulmonary arteries and the right ventricle
  • transthoracic echocardiography to look at the size and motion of the heart, function of the heart valves, etc. (essential for diagnosis)
  • 6-minute test to assess exercise endurance by having the person being tested be physically active for 6 minutes
  • lung biopsy, done only if PAH is not assumed to be your primary disease
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Treatment

Treatment of pulmonary arterial hypertension

Treatments for PAH are meant to reduce symptoms and prolong life. Doctors often begin treatments late in the disease, because it’s hard to detect.

The FDA has approved several medications for PAH. They can ease symptoms and improve physical function. None of the medications can completely relieve the symptoms of PAH and some are extremely expensive, costing .

Medications

  • prostacyclins, the first new treatment for pulmonary hypertension
  • endothelial receptor antagonists, which relax blood vessels
  • phosphodiesterase inhibitors, which relax the muscles of the arterial walls to widen blood vessels

Other treatment

  • heart-lung transplantation, although this is only done in certain cases
  • restriction of physical activity
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Outlook

Outlook for pulmonary arterial hypertension

Although modern treatment has come a long way, one-third of all people with PAH will die within three years of diagnosis.

Death is an expectation and a common occurrence with PAH, because no cure or effective treatment exists. The medications that are available to treat symptoms can extend life for a while, but they can’t stop eventual terminal heart failure.

Keep reading: Pulmonary arterial hypertension: Prognosis and life expectancy »

  • Are there any steps someone can take to prevent developing PAH?
  • Pulmonary arterial hypertension cannot always be prevented. However, some conditions that can lead to PAH can be prevented or controlled to reduce the risk of developing PAH. These conditions include coronary artery disease, hypertension, chronic liver disease (most often related to fatty liver, alcohol, and viral hepatitis), HIV, and chronic lung disease, especially related to smoking and environmental exposures.

    - Graham Rogers, MD
  • Answers represent the opinions of our medical experts. All content is strictly informational and should not be considered medical advice.
Article resources
  • Barst, R. J., Ertel, S. I., Beghetti, M., & Ivy, D. D. (2011). Pulmonary arterial hypertension: A comparison between children and adults. European Respiratory Journal, 37(3): 665-677. Retrieved from
  • Brown, L. M., Chen, H., Halpern, S., Taichman, D., McGoon, M. D., Farber, H. W., . . . Frost, A. E. (2011). Delay in recognition of pulmonary arterial hypertension: Factors identified from the REVEAL Registry. Chest, 140: 19-26. Retrieved from
  • Loyd, J. E. (2011). Pulmonary arterial hypertension: Insights from genetic studies. Proceedings of the American Thoracic Society, 8(2): 154-157. Retrieved from
  • Natarajan, R. (2011). Recent trends in pulmonary arterial hypertension. Lung India, 28(1): 39-48. Retrieved from
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