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Hepatopulmonary syndrome

Hepatopulmonary syndrome (HPS) is a pulmonary vascular complication of liver disease, which adversely affects prognosis. The disease is characterised by intrapulmonary vascular dilatations and shunts, resulting in impaired gas exchange. A complex interaction between the liver, the gut and the lungs,...

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Detalles Bibliográficos
Autores principales: Raevens, Sarah, Boret, Maxine, Fallon, Michael B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403489/
https://www.ncbi.nlm.nih.gov/pubmed/36035361
http://dx.doi.org/10.1016/j.jhepr.2022.100527
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author Raevens, Sarah
Boret, Maxine
Fallon, Michael B.
author_facet Raevens, Sarah
Boret, Maxine
Fallon, Michael B.
author_sort Raevens, Sarah
collection PubMed
description Hepatopulmonary syndrome (HPS) is a pulmonary vascular complication of liver disease, which adversely affects prognosis. The disease is characterised by intrapulmonary vascular dilatations and shunts, resulting in impaired gas exchange. A complex interaction between the liver, the gut and the lungs, predominately impacting pulmonary endothelial cells, immune cells and respiratory epithelial cells, is responsible for the development of typical pulmonary alterations seen in HPS. Liver transplantation is the only therapeutic option and generally reverses HPS. Since the implementation of the model for end-stage liver disease (MELD) standard exception policy, outcomes in patients with HPS have been significantly better than they were in the pre-MELD era. This review summarises current knowledge and highlights what’s new regarding the diagnosis and management of HPS, and our understanding of pathogenesis based on experimental models and translational studies.
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spelling pubmed-94034892022-08-26 Hepatopulmonary syndrome Raevens, Sarah Boret, Maxine Fallon, Michael B. JHEP Rep Review Hepatopulmonary syndrome (HPS) is a pulmonary vascular complication of liver disease, which adversely affects prognosis. The disease is characterised by intrapulmonary vascular dilatations and shunts, resulting in impaired gas exchange. A complex interaction between the liver, the gut and the lungs, predominately impacting pulmonary endothelial cells, immune cells and respiratory epithelial cells, is responsible for the development of typical pulmonary alterations seen in HPS. Liver transplantation is the only therapeutic option and generally reverses HPS. Since the implementation of the model for end-stage liver disease (MELD) standard exception policy, outcomes in patients with HPS have been significantly better than they were in the pre-MELD era. This review summarises current knowledge and highlights what’s new regarding the diagnosis and management of HPS, and our understanding of pathogenesis based on experimental models and translational studies. Elsevier 2022-07-04 /pmc/articles/PMC9403489/ /pubmed/36035361 http://dx.doi.org/10.1016/j.jhepr.2022.100527 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Raevens, Sarah
Boret, Maxine
Fallon, Michael B.
Hepatopulmonary syndrome
title Hepatopulmonary syndrome
title_full Hepatopulmonary syndrome
title_fullStr Hepatopulmonary syndrome
title_full_unstemmed Hepatopulmonary syndrome
title_short Hepatopulmonary syndrome
title_sort hepatopulmonary syndrome
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403489/
https://www.ncbi.nlm.nih.gov/pubmed/36035361
http://dx.doi.org/10.1016/j.jhepr.2022.100527
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