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Combination therapy of bosentan and ambrisentan for portopulmonary hypertension

✍ Scribed by Muraoka, Hironori; Hatano, Masaru; Fujino, Takeo; Minatsuki, Shun; Imamura, Teruhiko; Inaba, Toshiro; Maki, Hisataka; Yao, Atsushi; Kinugawa, Koichiro; Komuro, Issei

Book ID
122170634
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
47 KB
Volume
93
Category
Article
ISSN
0024-3205

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Portopulmonary hypertension (PPHTN) represents a constrictive pulmonary vasculopathy in patients with portal hypertension. Liver transplantation (LT) may be curative and is usually restricted to patients with mild-to-moderate disease severity characterized by a mean pulmonary artery pressure (mPAP <