Simple algorithm to narrow down the candidates to receive echocardiography in patients with chronic liver disease for suspected pulmonary hypertension

AIMS: Portopulmonary hypertension (PoPH) is a subtype of pulmonary arterial hypertension related to portal hypertension. The definitive diagnosis of PoPH is made by invasive right heart catheterization. Alternatively, pulmonary arterial hypertension may be recognized noninvasively from the tricuspid...

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Detalles Bibliográficos
Autores principales: Yamashita, Koji, Kurosaki, Masayuki, Nakanishi, Hiroyuki, Tanaka, Yuki, Ishido, Shun, Inada, Kento, Kirino, Sakura, Hayakawa, Yuka, Matsumoto, Hiroaki, Nobusawa, Tsubasa, Kakegawa, Tatsuya, Higuchi, Mayu, Takaura, Kenta, Tanaka, Shohei, Maeyashiki, Chiaki, Kaneko, Shun, Tamaki, Nobuharu, Yasui, Yutaka, Tsuchiya, Kaoru, Takahashi, Yuka, Miyazaki, Ryoichi, Ashikaga, Takashi, Enomoto, Nobuyuki, Izumi, Namiki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667407/
https://www.ncbi.nlm.nih.gov/pubmed/36406650
http://dx.doi.org/10.1002/jgh3.12821

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667407/
https://www.ncbi.nlm.nih.gov/pubmed/36406650
http://dx.doi.org/10.1002/jgh3.12821

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