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Advance in the Management of Sepsis-Induced Coagulopathy and Disseminated Intravascular Coagulation
Coagulopathy commonly occurs in sepsis as a critical host response to infection that can progress to disseminated intravascular coagulation (DIC) with an increased mortality. Recent studies have further defined factors responsible for the thromboinflammatory response and intravascular thrombosis, in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572234/ https://www.ncbi.nlm.nih.gov/pubmed/31121897 http://dx.doi.org/10.3390/jcm8050728 |
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author | Iba, Toshiaki Levy, Jerrold H. Raj, Aditya Warkentin, Theodore E. |
author_facet | Iba, Toshiaki Levy, Jerrold H. Raj, Aditya Warkentin, Theodore E. |
author_sort | Iba, Toshiaki |
collection | PubMed |
description | Coagulopathy commonly occurs in sepsis as a critical host response to infection that can progress to disseminated intravascular coagulation (DIC) with an increased mortality. Recent studies have further defined factors responsible for the thromboinflammatory response and intravascular thrombosis, including neutrophil extracellular traps, extracellular vesicles, damage-associated molecular patterns, and endothelial glycocalyx shedding. Diagnosing DIC facilitates sepsis management, and is associated with improved outcomes. Although the International Society on Thrombosis and Haemostasis (ISTH) has proposed criteria for diagnosing overt DIC, these criteria are not suitable for early detection. Accordingly, the ISTH DIC Scientific Standardization Committee has proposed a new category termed “sepsis-induced coagulopathy (SIC)” to facilitate earlier diagnosis of DIC and potentially more rapid interventions in these critically ill patients. Therapy of SIC includes both treatment of the underlying infection and correcting the coagulopathy, with most therapeutic approaches focusing on anticoagulant therapy. Recently, a phase III trial of recombinant thrombomodulin was performed in coagulopathic patients. Although the 28-day mortality was improved by 2.6% (absolute difference), it did not reach statistical significance. However, in patients who met entry criteria for SIC at baseline, the mortality difference was approximately 5% without increased risk of bleeding. In this review, we discuss current advances in managing SIC and DIC. |
format | Online Article Text |
id | pubmed-6572234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65722342019-06-18 Advance in the Management of Sepsis-Induced Coagulopathy and Disseminated Intravascular Coagulation Iba, Toshiaki Levy, Jerrold H. Raj, Aditya Warkentin, Theodore E. J Clin Med Review Coagulopathy commonly occurs in sepsis as a critical host response to infection that can progress to disseminated intravascular coagulation (DIC) with an increased mortality. Recent studies have further defined factors responsible for the thromboinflammatory response and intravascular thrombosis, including neutrophil extracellular traps, extracellular vesicles, damage-associated molecular patterns, and endothelial glycocalyx shedding. Diagnosing DIC facilitates sepsis management, and is associated with improved outcomes. Although the International Society on Thrombosis and Haemostasis (ISTH) has proposed criteria for diagnosing overt DIC, these criteria are not suitable for early detection. Accordingly, the ISTH DIC Scientific Standardization Committee has proposed a new category termed “sepsis-induced coagulopathy (SIC)” to facilitate earlier diagnosis of DIC and potentially more rapid interventions in these critically ill patients. Therapy of SIC includes both treatment of the underlying infection and correcting the coagulopathy, with most therapeutic approaches focusing on anticoagulant therapy. Recently, a phase III trial of recombinant thrombomodulin was performed in coagulopathic patients. Although the 28-day mortality was improved by 2.6% (absolute difference), it did not reach statistical significance. However, in patients who met entry criteria for SIC at baseline, the mortality difference was approximately 5% without increased risk of bleeding. In this review, we discuss current advances in managing SIC and DIC. MDPI 2019-05-22 /pmc/articles/PMC6572234/ /pubmed/31121897 http://dx.doi.org/10.3390/jcm8050728 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Iba, Toshiaki Levy, Jerrold H. Raj, Aditya Warkentin, Theodore E. Advance in the Management of Sepsis-Induced Coagulopathy and Disseminated Intravascular Coagulation |
title | Advance in the Management of Sepsis-Induced Coagulopathy and Disseminated Intravascular Coagulation |
title_full | Advance in the Management of Sepsis-Induced Coagulopathy and Disseminated Intravascular Coagulation |
title_fullStr | Advance in the Management of Sepsis-Induced Coagulopathy and Disseminated Intravascular Coagulation |
title_full_unstemmed | Advance in the Management of Sepsis-Induced Coagulopathy and Disseminated Intravascular Coagulation |
title_short | Advance in the Management of Sepsis-Induced Coagulopathy and Disseminated Intravascular Coagulation |
title_sort | advance in the management of sepsis-induced coagulopathy and disseminated intravascular coagulation |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572234/ https://www.ncbi.nlm.nih.gov/pubmed/31121897 http://dx.doi.org/10.3390/jcm8050728 |
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