{Reference Type}: Journal Article
{Title}: Pulmonary Complications of Portal Hypertension.
{Author}: Bommena S;Fallon MB;
{Journal}: Clin Liver Dis
{Volume}: 28
{Issue}: 3
{Year}: 2024 Aug
{Factor}: 6.265
{DOI}: 10.1016/j.cld.2024.03.005
{Abstract}: Portopulmonary hypertension (POPH), hepatopulmonary syndrome, and hepatic hydrothorax constitute significant complications of portal hypertension, with important implications for management and liver transplantation (LT) candidacy. POPH is characterized by obstruction and remodeling of the pulmonary resistance arterial bed. Hepatopulmonary syndrome is the most common pulmonary vascular disorder, characterized by intrapulmonary vascular dilatations causing impaired gas exchange. LT may improve prognosis in select patients with POPH. LT is the only effective treatment of hepatopulmonary syndrome. Hepatic hydrothorax is defined as transudative pleural fluid accumulation that is not explained by primary cardiopulmonary or pleural disease. LT is the definitive cure for hepatic hydrothorax.