Pulmonary arterial hypertension (PAH) is hemodynamically defined by elevated pressure in the pulmonary vascular circulation. It was long considered a “model disease” because it often affected young women with no relevant preexisting conditions. However, many patients today are older at the time of diagnosis, have concomitant cardiovascular diseases, or exhibit a cardiopulmonary phenotype characterized by impaired diffusion capacity and a history of smoking.
Autoren
- Jens Dehn
Publikation
- InFo PNEUMOLOGIE & ALLERGOLOGIE
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