![]() Survival of PoPH has remained poor compared to IPAH and other forms of PAH. Significant strides in elucidating the pathogenesis, effective screening algorithms, accurate diagnoses, and treatment options have been made in past 20 years. PoPH is a cause of significant morbidity and mortality in patients with portal hypertension with or without liver disease. Portopulmonary hypertension (PoPH) is defined as pulmonary arterial hypertension (PAH) associated with portal hypertension and is a subset of Group 1 pulmonary hypertension (PH). ![]() ![]()
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