Clinical aspects of portopulmonary hypertension

Respir Med. 2014 Jul;108(7):943-54. doi: 10.1016/j.rmed.2014.04.004. Epub 2014 Apr 29.

Abstract

Portopulmonary hypertension (PoPH) is an often neglected form of pulmonary hypertension where pulmonary hypertension occurs in the presence of portal hypertension. PoPH is important to diagnose and treat as it may improve the patient's quality of life and improve the outcome after liver transplantation. In this review, we discuss the clinical aspects of PoPH including its pathophysiology, diagnosis, treatment, and prognosis.

Keywords: PAH; PoPH; Portopulmonary hypertension.

Publication types

  • Review

MeSH terms

  • Genetic Predisposition to Disease
  • Humans
  • Hypertension, Portal / diagnosis*
  • Hypertension, Portal / etiology
  • Hypertension, Portal / physiopathology
  • Hypertension, Portal / therapy*
  • Hypertension, Pulmonary / diagnosis*
  • Hypertension, Pulmonary / etiology
  • Hypertension, Pulmonary / physiopathology
  • Hypertension, Pulmonary / therapy*
  • Liver Transplantation
  • Prognosis
  • Vasodilator Agents / therapeutic use

Substances

  • Vasodilator Agents