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Examines the prognostic utility of echocardiography in pulmonary arterial hypertension, highlighting right ventricular failure driven by vascular remodeling.
Pulmonary Arterial Hypertension (PAH) represents a rare but devastating disease due to small pulmonary arterial vessels remodelling and increased pulmonary vascular resistance leading to right ventricular dysfunction, right heart failure and death.
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Demerouti et al. (2022) studied this question.
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