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Hepatic Failure

The progression of liver disease can cause several physiologic derangements that may precipitate hepatic failure and require admission to an intensive care unit. The underlying pathology may be acute, acute-on chronic, or chronic in nature. Liver failure may manifest with a variety of clinical signs...

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Detalles Bibliográficos
Autores principales: Rueda, Mario, Lipsett, Pamela A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7123541/
http://dx.doi.org/10.1007/978-3-319-33341-0_18
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author Rueda, Mario
Lipsett, Pamela A.
author_facet Rueda, Mario
Lipsett, Pamela A.
author_sort Rueda, Mario
collection PubMed
description The progression of liver disease can cause several physiologic derangements that may precipitate hepatic failure and require admission to an intensive care unit. The underlying pathology may be acute, acute-on chronic, or chronic in nature. Liver failure may manifest with a variety of clinical signs and symptoms that need prompt attention. The compromised synthetic and metabolic activity of the failing liver affects all organ systems, from neurologic to integumentary. Supportive care and specific therapies should be instituted in order to improve outcome and minimize time of recovery. In this chapter we will discuss the definition, clinical manifestations, workup, and management of acute and chronic liver failure and the general principles of treatment of these patients. Management of liver failure secondary to certain common etiologies will also be presented. Finally, liver transplantation and alternative therapies will also be discussed.
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spelling pubmed-71235412020-04-06 Hepatic Failure Rueda, Mario Lipsett, Pamela A. Principles of Adult Surgical Critical Care Article The progression of liver disease can cause several physiologic derangements that may precipitate hepatic failure and require admission to an intensive care unit. The underlying pathology may be acute, acute-on chronic, or chronic in nature. Liver failure may manifest with a variety of clinical signs and symptoms that need prompt attention. The compromised synthetic and metabolic activity of the failing liver affects all organ systems, from neurologic to integumentary. Supportive care and specific therapies should be instituted in order to improve outcome and minimize time of recovery. In this chapter we will discuss the definition, clinical manifestations, workup, and management of acute and chronic liver failure and the general principles of treatment of these patients. Management of liver failure secondary to certain common etiologies will also be presented. Finally, liver transplantation and alternative therapies will also be discussed. 2016-10-09 /pmc/articles/PMC7123541/ http://dx.doi.org/10.1007/978-3-319-33341-0_18 Text en © Springer International Publishing Switzerland 2016 Open Access This chapter is licensed under the terms of the Creative Commons Attribution-NonCommercial 2.5 International License (http://creativecommons.org/licenses/by-nc/2.5/), which permits any noncommercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license and indicate if changes were made. The images or other third party material in this chapter are included in the chapter's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the chapter's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
spellingShingle Article
Rueda, Mario
Lipsett, Pamela A.
Hepatic Failure
title Hepatic Failure
title_full Hepatic Failure
title_fullStr Hepatic Failure
title_full_unstemmed Hepatic Failure
title_short Hepatic Failure
title_sort hepatic failure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7123541/
http://dx.doi.org/10.1007/978-3-319-33341-0_18
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