Introduction Pulmonary arterial hypertension (PAH) is a rare, progressive, and life-threatening condition characterized by elevated pulmonary arterial pressure, increased pulmonary vascular resistance, and right heart failure (1). The disease affects the small pulmonary arteries, leading to vascular remodeling, vasoconstriction, and thrombosis (1).
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ACC, AHA and ESC Recommendations for Heart Failure Management
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