Pulmonary Hypertension (PH) is a complex and often misunderstood disorder, characterized by elevated pulmonary artery pressure.
PH is primarily caused by constriction or blockage in the pulmonary arteries, leading to increased workload for the heart.
Patients often present with dyspnea, fatigue, and syncope. Diagnosis is typically confirmed through echocardiography and right heart catheterization.
Treatment strategies include vasodilators, endothelin receptor antagonists, and phosphodiesterase inhibitors.
Understanding the fundamentals of PH aids in early detection and effective management, ultimately improving patient outcomes.
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