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Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory
Coronavirus disease 2019 (COVID-19) is associated with extreme inflammatory response, disordered hemostasis and high thrombotic risk. A high incidence of thromboembolic events has been reported despite thromboprophylaxis, raising the question of a more effective anticoagulation. First-line hemostasi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7474970/ https://www.ncbi.nlm.nih.gov/pubmed/32922211 http://dx.doi.org/10.1186/s12959-020-00230-1 |
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author | Hardy, M. Lecompte, T. Douxfils, J. Lessire, S. Dogné, J. M. Chatelain, B. Testa, S. Gouin-Thibault, I. Gruel, Y. Medcalf, R. L. ten Cate, H. Lippi, G. Mullier, F. |
author_facet | Hardy, M. Lecompte, T. Douxfils, J. Lessire, S. Dogné, J. M. Chatelain, B. Testa, S. Gouin-Thibault, I. Gruel, Y. Medcalf, R. L. ten Cate, H. Lippi, G. Mullier, F. |
author_sort | Hardy, M. |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19) is associated with extreme inflammatory response, disordered hemostasis and high thrombotic risk. A high incidence of thromboembolic events has been reported despite thromboprophylaxis, raising the question of a more effective anticoagulation. First-line hemostasis tests such as activated partial thromboplastin time, prothrombin time, fibrinogen and D-dimers are proposed for assessing thrombotic risk and monitoring hemostasis, but are vulnerable to many drawbacks affecting their reliability and clinical relevance. Specialized hemostasis-related tests (soluble fibrin complexes, tests assessing fibrinolytic capacity, viscoelastic tests, thrombin generation) may have an interest to assess the thrombotic risk associated with COVID-19. Another challenge for the hemostasis laboratory is the monitoring of heparin treatment, especially unfractionated heparin in the setting of an extreme inflammatory response. This review aimed at evaluating the role of hemostasis tests in the management of COVID-19 and discussing their main limitations. |
format | Online Article Text |
id | pubmed-7474970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74749702020-09-08 Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory Hardy, M. Lecompte, T. Douxfils, J. Lessire, S. Dogné, J. M. Chatelain, B. Testa, S. Gouin-Thibault, I. Gruel, Y. Medcalf, R. L. ten Cate, H. Lippi, G. Mullier, F. Thromb J Review Coronavirus disease 2019 (COVID-19) is associated with extreme inflammatory response, disordered hemostasis and high thrombotic risk. A high incidence of thromboembolic events has been reported despite thromboprophylaxis, raising the question of a more effective anticoagulation. First-line hemostasis tests such as activated partial thromboplastin time, prothrombin time, fibrinogen and D-dimers are proposed for assessing thrombotic risk and monitoring hemostasis, but are vulnerable to many drawbacks affecting their reliability and clinical relevance. Specialized hemostasis-related tests (soluble fibrin complexes, tests assessing fibrinolytic capacity, viscoelastic tests, thrombin generation) may have an interest to assess the thrombotic risk associated with COVID-19. Another challenge for the hemostasis laboratory is the monitoring of heparin treatment, especially unfractionated heparin in the setting of an extreme inflammatory response. This review aimed at evaluating the role of hemostasis tests in the management of COVID-19 and discussing their main limitations. BioMed Central 2020-09-07 /pmc/articles/PMC7474970/ /pubmed/32922211 http://dx.doi.org/10.1186/s12959-020-00230-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Hardy, M. Lecompte, T. Douxfils, J. Lessire, S. Dogné, J. M. Chatelain, B. Testa, S. Gouin-Thibault, I. Gruel, Y. Medcalf, R. L. ten Cate, H. Lippi, G. Mullier, F. Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory |
title | Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory |
title_full | Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory |
title_fullStr | Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory |
title_full_unstemmed | Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory |
title_short | Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory |
title_sort | management of the thrombotic risk associated with covid-19: guidance for the hemostasis laboratory |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7474970/ https://www.ncbi.nlm.nih.gov/pubmed/32922211 http://dx.doi.org/10.1186/s12959-020-00230-1 |
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