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Systematic assessment of venous thromboembolism in COVID-19 patients receiving thromboprophylaxis: incidence and role of D-dimer as predictive factors.

Identifieur interne : 000530 ( Main/Exploration ); précédent : 000529; suivant : 000531

Systematic assessment of venous thromboembolism in COVID-19 patients receiving thromboprophylaxis: incidence and role of D-dimer as predictive factors.

Auteurs : Mathieu Artifoni [France] ; Gwenvael Danic [France] ; Giovanni Gautier [France] ; Pascal Gicquel [France] ; David Boutoille [France] ; François Raffi [France] ; Antoine Néel [France] ; Raphaël Lecomte [France]

Source :

RBID : pubmed:32451823

Descripteurs français

English descriptors

Abstract

Coagulopathy in COVID-19 is a burning issue and strategies to prevent thromboembolic events are debated and highly heterogeneous. The objective was to determine incidence and risk factors of venous thromboembolism (VTE) in COVID-19 inpatients receiving thromboprophylaxis. In this retrospective French cohort study, patients hospitalized in medical wards non-ICU with confirmed COVID-19 and adequate thromboprophylaxis were included. A systematic low limb venous duplex ultrasonography was performed at hospital discharge or earlier if deep venous thrombosis (DVT) was clinically suspected. Chest angio-CT scan was performed when pulmonary embolism (PE) was suspected. Of 71 patients, 16 developed VTE (22.5%) and 7 PE (10%) despite adequate thromboprophylaxis. D-dimers at baseline were significantly higher in patients with DVT (p < 0.001). Demographics, comorbidities, disease manifestations, severity score, and other biological parameters, including inflammatory markers, were similar in patients with and without VTE. The negative predictive value of a baseline D-dimer level < 1.0 µg/ml was 90% for VTE and 98% for PE. The positive predictive value for VTE was 44% and 67% for D-dimer level ≥ 1.0 µg/ml and ≥ 3 µg/ml, respectively. The association between D-dimer level and VTE risk increased by taking into account the latest available D-dimer level prior to venous duplex ultrasonography for the patients with monitoring of D-dimer. Despite thromboprophylaxis, the risk of VTE is high in COVID-19 non-ICU inpatients. Increased D-dimer concentrations of more than 1.0 μg/ml predict the risk of venous thromboembolism. D-dimer level-guided aggressive thromboprophylaxis regimens using higher doses of heparin should be evaluated in prospective studies.

DOI: 10.1007/s11239-020-02146-z
PubMed: 32451823
PubMed Central: PMC7246965


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<div type="abstract" xml:lang="en">Coagulopathy in COVID-19 is a burning issue and strategies to prevent thromboembolic events are debated and highly heterogeneous. The objective was to determine incidence and risk factors of venous thromboembolism (VTE) in COVID-19 inpatients receiving thromboprophylaxis. In this retrospective French cohort study, patients hospitalized in medical wards non-ICU with confirmed COVID-19 and adequate thromboprophylaxis were included. A systematic low limb venous duplex ultrasonography was performed at hospital discharge or earlier if deep venous thrombosis (DVT) was clinically suspected. Chest angio-CT scan was performed when pulmonary embolism (PE) was suspected. Of 71 patients, 16 developed VTE (22.5%) and 7 PE (10%) despite adequate thromboprophylaxis. D-dimers at baseline were significantly higher in patients with DVT (p < 0.001). Demographics, comorbidities, disease manifestations, severity score, and other biological parameters, including inflammatory markers, were similar in patients with and without VTE. The negative predictive value of a baseline D-dimer level < 1.0 µg/ml was 90% for VTE and 98% for PE. The positive predictive value for VTE was 44% and 67% for D-dimer level ≥ 1.0 µg/ml and ≥ 3 µg/ml, respectively. The association between D-dimer level and VTE risk increased by taking into account the latest available D-dimer level prior to venous duplex ultrasonography for the patients with monitoring of D-dimer. Despite thromboprophylaxis, the risk of VTE is high in COVID-19 non-ICU inpatients. Increased D-dimer concentrations of more than 1.0 μg/ml predict the risk of venous thromboembolism. D-dimer level-guided aggressive thromboprophylaxis regimens using higher doses of heparin should be evaluated in prospective studies.</div>
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<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">32451823</PMID>
<DateCompleted>
<Year>2020</Year>
<Month>06</Month>
<Day>19</Day>
</DateCompleted>
<DateRevised>
<Year>2020</Year>
<Month>09</Month>
<Day>22</Day>
</DateRevised>
<Article PubModel="Print">
<Journal>
<ISSN IssnType="Electronic">1573-742X</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>50</Volume>
<Issue>1</Issue>
<PubDate>
<Year>2020</Year>
<Month>Jul</Month>
</PubDate>
</JournalIssue>
<Title>Journal of thrombosis and thrombolysis</Title>
<ISOAbbreviation>J. Thromb. Thrombolysis</ISOAbbreviation>
</Journal>
<ArticleTitle>Systematic assessment of venous thromboembolism in COVID-19 patients receiving thromboprophylaxis: incidence and role of D-dimer as predictive factors.</ArticleTitle>
<Pagination>
<MedlinePgn>211-216</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1007/s11239-020-02146-z</ELocationID>
<Abstract>
<AbstractText>Coagulopathy in COVID-19 is a burning issue and strategies to prevent thromboembolic events are debated and highly heterogeneous. The objective was to determine incidence and risk factors of venous thromboembolism (VTE) in COVID-19 inpatients receiving thromboprophylaxis. In this retrospective French cohort study, patients hospitalized in medical wards non-ICU with confirmed COVID-19 and adequate thromboprophylaxis were included. A systematic low limb venous duplex ultrasonography was performed at hospital discharge or earlier if deep venous thrombosis (DVT) was clinically suspected. Chest angio-CT scan was performed when pulmonary embolism (PE) was suspected. Of 71 patients, 16 developed VTE (22.5%) and 7 PE (10%) despite adequate thromboprophylaxis. D-dimers at baseline were significantly higher in patients with DVT (p < 0.001). Demographics, comorbidities, disease manifestations, severity score, and other biological parameters, including inflammatory markers, were similar in patients with and without VTE. The negative predictive value of a baseline D-dimer level < 1.0 µg/ml was 90% for VTE and 98% for PE. The positive predictive value for VTE was 44% and 67% for D-dimer level ≥ 1.0 µg/ml and ≥ 3 µg/ml, respectively. The association between D-dimer level and VTE risk increased by taking into account the latest available D-dimer level prior to venous duplex ultrasonography for the patients with monitoring of D-dimer. Despite thromboprophylaxis, the risk of VTE is high in COVID-19 non-ICU inpatients. Increased D-dimer concentrations of more than 1.0 μg/ml predict the risk of venous thromboembolism. D-dimer level-guided aggressive thromboprophylaxis regimens using higher doses of heparin should be evaluated in prospective studies.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Artifoni</LastName>
<ForeName>Mathieu</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Service de Médecine Interne, CHU de Nantes, 44093, Nantes, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Danic</LastName>
<ForeName>Gwenvael</ForeName>
<Initials>G</Initials>
<AffiliationInfo>
<Affiliation>Service de Médecine Interne, CHU de Nantes, 44093, Nantes, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gautier</LastName>
<ForeName>Giovanni</ForeName>
<Initials>G</Initials>
<AffiliationInfo>
<Affiliation>Service de Médecine Interne, CHU de Nantes, 44093, Nantes, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gicquel</LastName>
<ForeName>Pascal</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>Service de Médecine Polyvalente, CH de Châteaubriant, 44110, Châteaubriant, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Boutoille</LastName>
<ForeName>David</ForeName>
<Initials>D</Initials>
<AffiliationInfo>
<Affiliation>Service de Maladies Infectieuses et Tropicales, CHU de Nantes, 44093, Nantes, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>CIC UIC 1413 INSERM, CHU de Nantes, 44093, Nantes, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Raffi</LastName>
<ForeName>François</ForeName>
<Initials>F</Initials>
<AffiliationInfo>
<Affiliation>Service de Maladies Infectieuses et Tropicales, CHU de Nantes, 44093, Nantes, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>CIC UIC 1413 INSERM, CHU de Nantes, 44093, Nantes, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Néel</LastName>
<ForeName>Antoine</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Service de Médecine Interne, CHU de Nantes, 44093, Nantes, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Faculté de Médecine, Université de Nantes, 44093, Nantes, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Lecomte</LastName>
<ForeName>Raphaël</ForeName>
<Initials>R</Initials>
<Identifier Source="ORCID">http://orcid.org/0000-0003-2144-9221</Identifier>
<AffiliationInfo>
<Affiliation>Service de Maladies Infectieuses et Tropicales, CHU de Nantes, 44093, Nantes, France. raphael.lecomte@chu-nantes.fr.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>CIC UIC 1413 INSERM, CHU de Nantes, 44093, Nantes, France. raphael.lecomte@chu-nantes.fr.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D016448">Multicenter Study</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo>
<Country>Netherlands</Country>
<MedlineTA>J Thromb Thrombolysis</MedlineTA>
<NlmUniqueID>9502018</NlmUniqueID>
<ISSNLinking>0929-5305</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D000925">Anticoagulants</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D017984">Enoxaparin</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D005338">Fibrin Fibrinogen Degradation Products</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C036309">fibrin fragment D</NameOfSubstance>
</Chemical>
</ChemicalList>
<SupplMeshList>
<SupplMeshName Type="Disease" UI="C000657245">COVID-19</SupplMeshName>
</SupplMeshList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000925" MajorTopicYN="N">Anticoagulants</DescriptorName>
<QualifierName UI="Q000627" MajorTopicYN="Y">therapeutic use</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018352" MajorTopicYN="N">Coronavirus Infections</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D017984" MajorTopicYN="N">Enoxaparin</DescriptorName>
<QualifierName UI="Q000627" MajorTopicYN="Y">therapeutic use</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005338" MajorTopicYN="N">Fibrin Fibrinogen Degradation Products</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005602" MajorTopicYN="N" Type="Geographic">France</DescriptorName>
<QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D015994" MajorTopicYN="N">Incidence</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D058873" MajorTopicYN="N">Pandemics</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D011024" MajorTopicYN="N">Pneumonia, Viral</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D012189" MajorTopicYN="N">Retrospective Studies</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D054556" MajorTopicYN="N">Venous Thromboembolism</DescriptorName>
<QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName>
<QualifierName UI="Q000453" MajorTopicYN="Y">epidemiology</QualifierName>
<QualifierName UI="Q000517" MajorTopicYN="N">prevention & control</QualifierName>
<QualifierName UI="Q000821" MajorTopicYN="N">virology</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">COVID-19</Keyword>
<Keyword MajorTopicYN="N">D-dimer</Keyword>
<Keyword MajorTopicYN="N">Pulmonary embolism</Keyword>
<Keyword MajorTopicYN="N">Venous thromboembolism</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="pubmed">
<Year>2020</Year>
<Month>5</Month>
<Day>27</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2020</Year>
<Month>6</Month>
<Day>20</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2020</Year>
<Month>5</Month>
<Day>27</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">32451823</ArticleId>
<ArticleId IdType="doi">10.1007/s11239-020-02146-z</ArticleId>
<ArticleId IdType="pii">10.1007/s11239-020-02146-z</ArticleId>
<ArticleId IdType="pmc">PMC7246965</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations>
<list>
<country>
<li>France</li>
</country>
<region>
<li>Pays de la Loire</li>
</region>
<settlement>
<li>Châteaubriant</li>
<li>Nantes</li>
</settlement>
<orgName>
<li>Université de Nantes</li>
</orgName>
</list>
<tree>
<country name="France">
<region name="Pays de la Loire">
<name sortKey="Artifoni, Mathieu" sort="Artifoni, Mathieu" uniqKey="Artifoni M" first="Mathieu" last="Artifoni">Mathieu Artifoni</name>
</region>
<name sortKey="Boutoille, David" sort="Boutoille, David" uniqKey="Boutoille D" first="David" last="Boutoille">David Boutoille</name>
<name sortKey="Boutoille, David" sort="Boutoille, David" uniqKey="Boutoille D" first="David" last="Boutoille">David Boutoille</name>
<name sortKey="Danic, Gwenvael" sort="Danic, Gwenvael" uniqKey="Danic G" first="Gwenvael" last="Danic">Gwenvael Danic</name>
<name sortKey="Gautier, Giovanni" sort="Gautier, Giovanni" uniqKey="Gautier G" first="Giovanni" last="Gautier">Giovanni Gautier</name>
<name sortKey="Gicquel, Pascal" sort="Gicquel, Pascal" uniqKey="Gicquel P" first="Pascal" last="Gicquel">Pascal Gicquel</name>
<name sortKey="Lecomte, Raphael" sort="Lecomte, Raphael" uniqKey="Lecomte R" first="Raphaël" last="Lecomte">Raphaël Lecomte</name>
<name sortKey="Lecomte, Raphael" sort="Lecomte, Raphael" uniqKey="Lecomte R" first="Raphaël" last="Lecomte">Raphaël Lecomte</name>
<name sortKey="Neel, Antoine" sort="Neel, Antoine" uniqKey="Neel A" first="Antoine" last="Néel">Antoine Néel</name>
<name sortKey="Neel, Antoine" sort="Neel, Antoine" uniqKey="Neel A" first="Antoine" last="Néel">Antoine Néel</name>
<name sortKey="Raffi, Francois" sort="Raffi, Francois" uniqKey="Raffi F" first="François" last="Raffi">François Raffi</name>
<name sortKey="Raffi, Francois" sort="Raffi, Francois" uniqKey="Raffi F" first="François" last="Raffi">François Raffi</name>
</country>
</tree>
</affiliations>
</record>

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