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385: Successful liver transplantation following vasodilator therapy for portopulmonary hypertension: Single center series

✍ Scribed by V. Kaza; N. Sussman; C. O’Mahoney; J. Goss; R.J. Stribling; A.E. Frost


Book ID
116519297
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
67 KB
Volume
25
Category
Article
ISSN
1557-3117

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Pulmonary arterial hypertension (PAH) associated with portal hypertension [portopulmonary hypertension (PPHTN)] occurs in 2% to 10% of patients with advanced liver disease and carries a very poor prognosis without treatment. Most hepatic transplantation centers consider moderate to severe PPHTN to b