Intrapulmonary vascular dilatations are common in portopulmonary hypertension and may be associated with decreased survival
Lynn A. Fussner, Vivek N. Iyer, Rodrigo Cartin‐Ceba, Grace Lin, Kymberly D. Watt, Michael J. Krowka – 16 June 2015 – Hepatopulmonary syndrome (HPS) and portopulmonary hypertension (POPH) are pulmonary vascular complications of portal hypertension with divergent clinicopathologic features and management. The presence of intrapulmonary vascular dilatations (IPVDs), detected by agitated saline contrast‐enhanced transthoracic echocardiography (cTTE), is an essential feature of HPS but is not typically characteristic of POPH.