Sergio Caravita, Mauro Gori, Andrea Garascia, Claudia Baratto, Nino Camassa, Samuela Carigi, Luisa De Gennaro, Renata De Maria, Iolanda Enea, Piero Gentile, Francesca Giordana, Giuseppe Leonardi, Francesco Lo Giudice, Francesco Orso, Antonella Romaniello, Loris Roncon, Maria Denitza Tinti, Marco Vatrano, Maria Cristina Vedovati, Marco Marini, Claudio Picariello
Pulmonary hypertension (PH) is a common complication of diseases affecting the left heart, mostly found in patients suffering from heart failure. Left atrial hypertension is the initial driver of post-capillary PH. However, several mechanisms may lead in a subset of patients to structural changes in the pulmonary vessels with development of a pre-capillary component. The right ventricle may be frequently affected, leading to right ventricular failure and a worse outcome. The differential diagnosis of PH associated with left heart disease vs pulmonary arterial hypertension (PAH) is challenging in patients with cardiovascular comorbidities, risk factors for PAH and/or a preserved left ventricular ejection fraction...
February 2024: Giornale Italiano di Cardiologia