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Primary Pulmonary Hypertension: Conditions
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Primary Pulmonary Hypertension, better known as "PPH," is a little known medical condition, but it's an extremely serious infliction that's affecting more and more people every day. PPH can ... be deadly, and at this point, there is no known singular cause for the development of this condition. However, PPH has been linked to several products, and if you have been diagnosed with PPH, you should contact a PPH lawyer at Williams Kherkher in order to schedule a free initial consultation.
Pulmonary embolism ... leads to pulmonary hypertension, acutely as well as chronically (WHO Group IV). Treatments for these two conditions are vastly different. Schistosomiasis is a very common cause of pulmonary hypertension in endemic areas such as the Nile river due to obstruction of pulmonary vessels with the parasite.
The estimated incidence of primary pulmonary hypertension is 1 to 2 cases per 1 million persons in the general population. During childhood, the condition affects both genders equally; after puberty, it is more common in women than in men (ratio: 1.7 to 1). Primary pulmonary hypertension is most prevalent in persons 20 to 40 years of age. The condition has no racial predilection.1
Source:
Studies estimate that approximately 100,000 people in the U.S. and Europe are afflicted with either primary pulmonary arterial hypertension or secondary forms of the disease related to conditions or tissue disorders that affect the lungs. One available treatment option for pulmonary arterial hypertension involves use of IV medication that must be administered 24 hours a day and seven days a week via a central intravenous catheter.
There is extremely wide variability in the severity of pulmonary hypertension among various patients. Evaluating, accurately diagnosing and treating the condition is ... very complex. For these reasons, patients with symptoms that suggest pulmonary hypertension require thorough evaluation at a medical center with expertise and experience in pulmonary hypertension.
Diagnosis of PAH requires the presence of pulmonary hypertension with two other conditions. Pulmonary artery occlusion pressure (PAOP or PCWP) must be less than 15 mm Hg (2000 Pa) and pulmonary vascular resistance (PVR) must be greater than 3 Wood units (240 dyn•s•cm-5 or 2.4 mN•s•cm-5).
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