Increase in progenitor endothelial cells associated to right heart failure in pediatric patients with secondary pulmonary arterial hypertension
Background: Pulmonary arterial hypertension (PAH) is a serious condition that causes right heart failure. A persistent inflammatory process is present in the vascular endothelial...
Analysis of risk assessment tools in the REPLACE study
Purpose: The REPLACE study showed that PAH patients treated with phosphodiesterase-5 inhibitors (PDE5i) still at intermediate risk could achieve clinical improvement when...
Effect of digoxin use on mortality in pulmonary arterial hypertension: A single center experience
Background: Digoxin increases cardiac output modestly in acute settings in patients with pulmonary arterial hypertension (PAH) and right ventricular failure; however, very little...
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