Pulmonary Hypertension (PH) is a significant clinical concern due to its complex pathophysiology and potentially fatal outcomes.
PH is characterized by elevated pulmonary arterial pressure, primarily due to vasoconstriction, vascular remodeling, and thrombosis.
Diagnosis involves echocardiography, right heart catheterization, and lung function tests.
Treatment strategies include vasodilators, anticoagulants, and in severe cases, lung transplantation.
Understanding PH is crucial for timely diagnosis and effective treatment, ultimately improving patient outcomes.
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