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Primary Pulmonary Hypertension: Lungs
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Primary pulmonary hypertension (PPH) is a rare cause of high blood pressure in the lungs. Blood, after giving up its oxygen to the body tissues, is returned through the veins to the right lower heart chamber (right ventricle). The right ventricle then pumps the blood through the lungs to pick up a new supply of oxygen. Blood pressure in the lungs and the right ventricle is normally about one-fifth as much as elsewhere in the body.
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Primary Pulmonary Hypertension, commonly referred to as PPH, is caused by an increased pressure within the pulmonary arteries which carry blood from your heart to your lungs. This eventually leads to the thickening of the arteries and narrowing of the arterial passageways, which further obstruct the flow of blood. In an effort to compensate for poor circulation, the right side of your heart becomes enlarged, and the extra work the heart must do can eventually cause right-sided heart failure. Primary Pulmonary Hypertension complications can occur in the form of liver failure, kidney failure, or heart failure.
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Primary pulmonary hypertension (PPH) is a rare, serious, and life threatening condition in which the blood pressure in the arteries of the lung is extremely high excluding other diseases of the heart or lungs. There is no known cause of PPH but it is linked to the use of fen-phen. PPH develops in response to increased resistance to blood flow and the increased workload that is caused by the resistance causes the right side of the heart to become enlarged. This condition can eventually lead to progressive heart failure, a disorder where the heart loses the ability to efficiently pump blood.
Primary pulmonary hypertension (PPH) is a rare disease that causes high blood pressure in the blood vessels of the lungs. A person with PPH has extra muscle in the walls of these blood vessels. That extra muscle makes it more difficult for blood to flow through them. So, the right side of the heart, which pumps blood to the lungs, has to work harder. This additional strain can eventually lead to heart failure.
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Primary Pulmonary Hypertension is an incurable condition that progresses over time, causing insurmountable pressure in the pulmonary artery connecting the lungs to the heart. Eventually the pressure buildup causes the heart major stress, and the capillaries and arteries will fatally shut. Even with early diagnosis, there is no cure for PPH. The only therapy available merely controls the PPH side effect of high blood pressure, and does not save the patient from eventual fatal heart valve damage. The most viable treatment option remains a single or bilateral lung transplant.
Primary or unexplained pulmonary hypertension (PPH) is a rare lung disorder in which the blood pressure in the pulmonary artery rises far above normal levels for no apparent reason. The pulmonary artery is a blood vessel carrying oxygen-poor blood from the right ventricle (one of the heart's pumping chambers) to the lungs. In the lungs, the blood picks up oxygen, then flows to the heart's left side, where the left ventricle pumps it to the rest of the body through the aorta.
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