Pulmonary Arterial Hypertension
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When the lungs come under pressure
German scientists have found a way of treating pulmonary arterial hypertension.
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Heart drugs ineffective in treating pulmonary arterial hypertension
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In medicine, pulmonary hypertension (PH) is an increase in blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, together known as the lung vasculature, leading to shortness of breath, 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. It was first identified by Dr. Ernst von Romberg in 1891. According to the most recent classification, it can be one of five different types: arterial, venous, hypoxic, thromboembolic or miscellaneous.
This text uses material from Wikipedia and is available under the GNU Free Documentation License.
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