ISSN: 2041-6792

Clinical Investigation

Pulmonary Hypertension Impact Factor

Pulmonary arterial hypertension (PAH) is a social movement disease affecting the arteries of the lungs. The pulmonary arteries carry blood from the right side of the heart via the lungs. The definition requires specific hemodynamic parameters (body measure the measurements of the forces involved in the circulation of blood) be measured and met. Normally hypertension otherwise known as high blood pressure, pulmonary arterial hypertension (PAH) cannot be easily measured with a blood pressure cuff. There are different tests such as echocardiograms that may point towards a diagnosis of pulmonary arterial hypertension (PAH) but right heart catheterization is the only way to definitively measure the required hemodynamics necessary to make the diagnosis. A normal pulmonary artery pressure for a healthy patient is 12-16 mmHg and a normal wedge pressure is 6-12 mmHg. Normally, the pressures in the right side of the heart and the pulmonary arteries are elevated while the pressures in the left side of the heart are normal. These specific pressures can only be measured accurately through right heart catheterization. Pulmonary hypertension varies from person to person, so your treatment plan are going to be specific to your needs. First, your doctor will treat the explanation for your condition. For example, if emphysema is causing the matter , you will need to treat that to enhance your pulmonary hypertension.Most people also get treatment to enhance their breathing, which makes it easier to be active and do daily tasks.

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