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The inflammatory basis of pulmonary arterial hypertension
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This resource is a video abstract of a research paper created by Research Square on behalf of its authors. It provides a synopsis that's easy to understand, and can be used to introduce the topics it covers to students, researchers, and the general public. The video's transcript is also provided in full, with a portion provided below for preview:

"Pulmonary arterial hypertension is a relatively rare but serious condition – in fact, 60 percent of patients don’t live more than 5 years after diagnosis. Most treatment of the disease involves dilating the arteries to lower pressure. But increasingly, research suggests inflammation may be behind the condition – and newer therapies are on the horizon. A review of pulmonary arterial hypertension from this immunological perspective -- including specialized information for anesthesiologists -- is now available from the journal Anesthesiology. Pulmonary hypertension is defined as a resting mean pulmonary artery pressure of 25 millimeters of mercury or higher. Pulmonary arterial hypertension is a type of pulmonary hypertension that mainly affects the blood vessels in the lung. Cases can be idiopathic, hereditary, or associated with infections or a variety of autoimmune or other systemic conditions. The disease is progressive and cannot be cured..."

The rest of the transcript, along with a link to the research itself, is available on the resource itself.

Subject:
Applied Science
Health, Medicine and Nursing
Material Type:
Diagram/Illustration
Reading
Provider:
Research Square
Provider Set:
Video Bytes
Date Added:
09/27/2019