Pulmonary hypertension (PH) is the elevation of mean pulmonary arterial pressure (mPAP) of >20 mmHg, accompanied by a pulmonary vascular resistance (PVR) of ≥3 Wood Units.(1) The World Symposium on Pulmonary Hypertension has categorized PH into five groups, according to characteristic pathophysiology, etiologies, clinical presentation, hemodynamic
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