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Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory.

Identifieur interne : 000B43 ( Main/Exploration ); précédent : 000B42; suivant : 000B44

Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory.

Auteurs : M. Hardy [Belgique] ; T. Lecompte ; J. Douxfils [Belgique] ; S. Lessire [Belgique] ; J M Dogné [Belgique] ; B. Chatelain [Belgique] ; S. Testa [Italie] ; I. Gouin-Thibault [France] ; Y. Gruel [France] ; R L Medcalf ; H. Ten Cate [Pays-Bas] ; G. Lippi [Italie] ; F. Mullier [Belgique]

Source :

RBID : pubmed:32922211

Abstract

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.

DOI: 10.1186/s12959-020-00230-1
PubMed: 32922211
PubMed Central: PMC7474970


Affiliations:


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<div type="abstract" xml:lang="en">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.</div>
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<ISOAbbreviation>Thromb J</ISOAbbreviation>
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<ArticleTitle>Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory.</ArticleTitle>
<Pagination>
<MedlinePgn>17</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1186/s12959-020-00230-1</ELocationID>
<Abstract>
<AbstractText>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.</AbstractText>
<CopyrightInformation>© The Author(s) 2020.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Hardy</LastName>
<ForeName>M</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Université catholique de Louvain, CHU UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), Hematology Laboratory, Yvoir, Belgium.</Affiliation>
<Identifier Source="GRID">grid.7942.8</Identifier>
<Identifier Source="ISNI">0000 0001 2294 713X</Identifier>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Université catholique de Louvain, CHU UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), Anesthesiology Department, Yvoir, Belgium.</Affiliation>
<Identifier Source="GRID">grid.7942.8</Identifier>
<Identifier Source="ISNI">0000 0001 2294 713X</Identifier>
</AffiliationInfo>
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<AffiliationInfo>
<Affiliation>Département de Médecine, Hôpitaux Universitaires de Genève, service d'angiologie et d'hémostase et Faculté de Médecine Geneva Platelet Group (GpG), Université de Genève, Geneva, Suisse Switzerland.</Affiliation>
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<Affiliation>Pharmacy Department, University of Namur, Namur Thrombosis and Hemostasis Center (NTHC), Namur, Belgium.</Affiliation>
<Identifier Source="GRID">grid.6520.1</Identifier>
<Identifier Source="ISNI">0000 0001 2242 8479</Identifier>
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<AffiliationInfo>
<Affiliation>Qualiblood s.a, Namur, Belgium.</Affiliation>
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<LastName>Lessire</LastName>
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<AffiliationInfo>
<Affiliation>Université catholique de Louvain, CHU UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), Anesthesiology Department, Yvoir, Belgium.</Affiliation>
<Identifier Source="GRID">grid.7942.8</Identifier>
<Identifier Source="ISNI">0000 0001 2294 713X</Identifier>
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<Identifier Source="GRID">grid.6520.1</Identifier>
<Identifier Source="ISNI">0000 0001 2242 8479</Identifier>
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<Affiliation>Université catholique de Louvain, CHU UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), Hematology Laboratory, Yvoir, Belgium.</Affiliation>
<Identifier Source="GRID">grid.7942.8</Identifier>
<Identifier Source="ISNI">0000 0001 2294 713X</Identifier>
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<Affiliation>Haemostasis and Thrombosis Center, Cremona Hospital, Cremona, Italy.</Affiliation>
<Identifier Source="GRID">grid.419450.d</Identifier>
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<AffiliationInfo>
<Affiliation>Département d'Hématologie Biologique, INSERM, CIC 1414 (Centre d'Investigation Clinique de Rennes), Université de Rennes, CHU de Rennes, Rennes, France.</Affiliation>
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<Affiliation>Laboratoire d'Hématologie-Hémostase, CHRU de Tours, Hôpital Trousseau, Tours, France.</Affiliation>
<Identifier Source="GRID">grid.411167.4</Identifier>
<Identifier Source="ISNI">0000 0004 1765 1600</Identifier>
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<Affiliation>Australian Centre for Blood Diseases, Monash University, Melbourne, Victoria Australia.</Affiliation>
<Identifier Source="GRID">grid.1002.3</Identifier>
<Identifier Source="ISNI">0000 0004 1936 7857</Identifier>
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<Affiliation>Department of Internal Medicine, Cardiovascular Research Institute (CARIM), Maastricht University Medical Center, Maastricht, the Netherlands.</Affiliation>
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<Affiliation>Section of Clinical Biochemistry, University of Verona, Verona, Italy.</Affiliation>
<Identifier Source="GRID">grid.5611.3</Identifier>
<Identifier Source="ISNI">0000 0004 1763 1124</Identifier>
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<Identifier Source="ORCID">0000-0001-6947-6099</Identifier>
<AffiliationInfo>
<Affiliation>Université catholique de Louvain, CHU UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), Hematology Laboratory, Yvoir, Belgium.</Affiliation>
<Identifier Source="GRID">grid.7942.8</Identifier>
<Identifier Source="ISNI">0000 0001 2294 713X</Identifier>
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<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D016454">Review</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2020</Year>
<Month>09</Month>
<Day>07</Day>
</ArticleDate>
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<MedlineJournalInfo>
<Country>England</Country>
<MedlineTA>Thromb J</MedlineTA>
<NlmUniqueID>101170542</NlmUniqueID>
<ISSNLinking>1477-9560</ISSNLinking>
</MedlineJournalInfo>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Anticoagulation</Keyword>
<Keyword MajorTopicYN="N">COVID-19</Keyword>
<Keyword MajorTopicYN="N">Coagulopathy</Keyword>
<Keyword MajorTopicYN="N">D-dimers</Keyword>
<Keyword MajorTopicYN="N">Fibrinolysis</Keyword>
<Keyword MajorTopicYN="N">Hemostasis</Keyword>
<Keyword MajorTopicYN="N">Heparin</Keyword>
<Keyword MajorTopicYN="N">Thrombin generation</Keyword>
<Keyword MajorTopicYN="N">Thrombosis</Keyword>
<Keyword MajorTopicYN="N">Viscoelastic tests</Keyword>
</KeywordList>
<CoiStatement>Competing interestsThe authors declare no competing interest.</CoiStatement>
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