Loading…

Prothrombotic changes in patients with COVID‐19 are associated with disease severity and mortality

Patients with severe coronavirus disease 2019 (COVID‐19) are at significant risk of thrombotic complications. However, their prothrombotic state is incompletely understood. Therefore, we measured in vivo activation markers of hemostasis, plasma levels of hemostatic proteins, and functional assays of...

Full description

Saved in:
Bibliographic Details
Published in:Research and Practice in Thrombosis and Haemostasis 2021-01, Vol.5 (1), p.132-141
Main Authors: von Meijenfeldt, Fien A., Havervall, Sebastian, Adelmeijer, Jelle, Lundström, Annika, Rudberg, Ann‐Sofie, Magnusson, Maria, Mackman, Nigel, Thalin, Charlotte, Lisman, Ton
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Request full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c7922-dcfbc272b40831f7043a41067024bff971ddf43fcab513c595e5199535d82db3
cites cdi_FETCH-LOGICAL-c7922-dcfbc272b40831f7043a41067024bff971ddf43fcab513c595e5199535d82db3
container_end_page 141
container_issue 1
container_start_page 132
container_title Research and Practice in Thrombosis and Haemostasis
container_volume 5
creator von Meijenfeldt, Fien A.
Havervall, Sebastian
Adelmeijer, Jelle
Lundström, Annika
Rudberg, Ann‐Sofie
Magnusson, Maria
Mackman, Nigel
Thalin, Charlotte
Lisman, Ton
description Patients with severe coronavirus disease 2019 (COVID‐19) are at significant risk of thrombotic complications. However, their prothrombotic state is incompletely understood. Therefore, we measured in vivo activation markers of hemostasis, plasma levels of hemostatic proteins, and functional assays of coagulation and fibrinolysis in plasma from patients with COVID‐19 and determined their association with disease severity and 30‐day mortality. We included 102 patients with COVID‐19 receiving various levels of respiratory support admitted to general wards, intermediate units, or intensive care units and collected plasma samples shortly after hospital admission. Patients with COVID‐19 with higher respiratory support had increased in vivo activation of coagulation and fibrinolysis, as reflected by higher plasma levels of d‐dimer, thrombin‐antithrombin, and plasmin‐antiplasmin complexes as compared to patients with no to minimal respiratory support and healthy controls. Moreover, the patients with COVID‐19 with higher respiratory support exhibited substantial ex vivo thrombin generation and lower ex vivo fibrinolytic capacity, despite higher doses of anticoagulant therapy compared to less severely ill patients. Fibrinogen, factor VIII, and von Willebrand factor levels increased, and ADAMTS13 levels decreased with increasing respiratory support in patients with COVID‐19. Low platelet count; low levels of prothrombin, antithrombin, and ADAMTS13; and high levels of von Willebrand factor were associated with short‐term mortality. Severe COVID‐19 is associated with prothrombotic changes with increased in vivo activation of coagulation and fibrinolysis, despite anticoagulant therapy.
doi_str_mv 10.1002/rth2.12462
format article
fullrecord <record><control><sourceid>proquest_COVID</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_bdc4ab05fd334b419099c41a75635090</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S2475037922013139</els_id><doaj_id>oai_doaj_org_article_bdc4ab05fd334b419099c41a75635090</doaj_id><sourcerecordid>2486466724</sourcerecordid><originalsourceid>FETCH-LOGICAL-c7922-dcfbc272b40831f7043a41067024bff971ddf43fcab513c595e5199535d82db3</originalsourceid><addsrcrecordid>eNqdkt2KEzEUxwdR3GXdGx9ABrwRoWs-J5MbQbrqFhZWpHgbMsmZNnU6qUna0jsfwWf0SUx3dpdWZC-EhHz9zj_JOf-ieInRBUaIvAtpTi4wYRV5UpwSJvgIUSGfHsxPivMYFyjDiOTGnxcnlHIqcjst7Jfg0zz4ZeOTM6WZ634GsXR9udLJQZ9iuXVpXo5vvk0uf__8hWWpA5Q6Rm-cTmCHY-si6AhlhA0El3al7m259CHpLq9eFM9a3UU4vxvPiumnj9Px1ej65vNk_OF6ZIQkZGRN2xgiSMNQTXErEKOaYVQJRFjTtlJga1tGW6MbjqnhkgPHUnLKbU1sQ8-KySBrvV6oVXBLHXbKa6duN3yYKR3yLztQjTVMN4i3llLWMCyRlIZhLXhFOZIoa8lBK25htW6O1FbBW3W3_93tu4qgyH1S_yMWs7rCFSd1jn0_xGZgCdbkCgTdHUscnfRurmZ-o0TNeE5bFnhzJxD8jzXEpJYuGug63YNfR0XyVayqBGEZff0XuvDr0OcK7SnCmci5fZyqhBB1JXGm3g6UCT7GAO3DkzFSe6OqvVHVrVEz_Orwkw_oQQbxAGxdB7tHpNTX6RW5F2VDDGSHbRwEFU02sAHrApiUPeD-9ZY_rQ8F_Q</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2467778691</pqid></control><display><type>article</type><title>Prothrombotic changes in patients with COVID‐19 are associated with disease severity and mortality</title><source>Coronavirus Research Database</source><creator>von Meijenfeldt, Fien A. ; Havervall, Sebastian ; Adelmeijer, Jelle ; Lundström, Annika ; Rudberg, Ann‐Sofie ; Magnusson, Maria ; Mackman, Nigel ; Thalin, Charlotte ; Lisman, Ton</creator><creatorcontrib>von Meijenfeldt, Fien A. ; Havervall, Sebastian ; Adelmeijer, Jelle ; Lundström, Annika ; Rudberg, Ann‐Sofie ; Magnusson, Maria ; Mackman, Nigel ; Thalin, Charlotte ; Lisman, Ton</creatorcontrib><description>Patients with severe coronavirus disease 2019 (COVID‐19) are at significant risk of thrombotic complications. However, their prothrombotic state is incompletely understood. Therefore, we measured in vivo activation markers of hemostasis, plasma levels of hemostatic proteins, and functional assays of coagulation and fibrinolysis in plasma from patients with COVID‐19 and determined their association with disease severity and 30‐day mortality. We included 102 patients with COVID‐19 receiving various levels of respiratory support admitted to general wards, intermediate units, or intensive care units and collected plasma samples shortly after hospital admission. Patients with COVID‐19 with higher respiratory support had increased in vivo activation of coagulation and fibrinolysis, as reflected by higher plasma levels of d‐dimer, thrombin‐antithrombin, and plasmin‐antiplasmin complexes as compared to patients with no to minimal respiratory support and healthy controls. Moreover, the patients with COVID‐19 with higher respiratory support exhibited substantial ex vivo thrombin generation and lower ex vivo fibrinolytic capacity, despite higher doses of anticoagulant therapy compared to less severely ill patients. Fibrinogen, factor VIII, and von Willebrand factor levels increased, and ADAMTS13 levels decreased with increasing respiratory support in patients with COVID‐19. Low platelet count; low levels of prothrombin, antithrombin, and ADAMTS13; and high levels of von Willebrand factor were associated with short‐term mortality. Severe COVID‐19 is associated with prothrombotic changes with increased in vivo activation of coagulation and fibrinolysis, despite anticoagulant therapy.</description><identifier>ISSN: 2475-0379</identifier><identifier>EISSN: 2475-0379</identifier><identifier>DOI: 10.1002/rth2.12462</identifier><identifier>PMID: 33537537</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Anticoagulants ; Blood ; Body mass index ; coagulation ; Coronaviruses ; COVID-19 ; Cytokine storm ; Diabetes ; Drug dosages ; fibrinolysis ; hemostasis ; Intensive care ; Intubation ; Laboratories ; Medicin och hälsovetenskap ; Mortality ; Original ; Original ‐ Thrombosis ; Patients ; Plasma ; Severe acute respiratory syndrome ; Severe acute respiratory syndrome coronavirus 2 ; Thromboembolism ; thrombosis ; Variables</subject><ispartof>Research and Practice in Thrombosis and Haemostasis, 2021-01, Vol.5 (1), p.132-141</ispartof><rights>2020 Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis.</rights><rights>The Authors. 2020 published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis.</rights><rights>The Authors. 2020 Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis.</rights><rights>2020. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c7922-dcfbc272b40831f7043a41067024bff971ddf43fcab513c595e5199535d82db3</citedby><cites>FETCH-LOGICAL-c7922-dcfbc272b40831f7043a41067024bff971ddf43fcab513c595e5199535d82db3</cites><orcidid>0000-0002-3503-7140</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2482547953/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2467778691?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,38516,43895,44590,46052,46476,53791,53793,74412,75126</link.rule.ids><linktorsrc>$$Uhttps://www.proquest.com/docview/2467778691?pq-origsite=primo$$EView_record_in_ProQuest$$FView_record_in_$$GProQuest</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33537537$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:148616528$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:233537537$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>von Meijenfeldt, Fien A.</creatorcontrib><creatorcontrib>Havervall, Sebastian</creatorcontrib><creatorcontrib>Adelmeijer, Jelle</creatorcontrib><creatorcontrib>Lundström, Annika</creatorcontrib><creatorcontrib>Rudberg, Ann‐Sofie</creatorcontrib><creatorcontrib>Magnusson, Maria</creatorcontrib><creatorcontrib>Mackman, Nigel</creatorcontrib><creatorcontrib>Thalin, Charlotte</creatorcontrib><creatorcontrib>Lisman, Ton</creatorcontrib><title>Prothrombotic changes in patients with COVID‐19 are associated with disease severity and mortality</title><title>Research and Practice in Thrombosis and Haemostasis</title><addtitle>Res Pract Thromb Haemost</addtitle><description>Patients with severe coronavirus disease 2019 (COVID‐19) are at significant risk of thrombotic complications. However, their prothrombotic state is incompletely understood. Therefore, we measured in vivo activation markers of hemostasis, plasma levels of hemostatic proteins, and functional assays of coagulation and fibrinolysis in plasma from patients with COVID‐19 and determined their association with disease severity and 30‐day mortality. We included 102 patients with COVID‐19 receiving various levels of respiratory support admitted to general wards, intermediate units, or intensive care units and collected plasma samples shortly after hospital admission. Patients with COVID‐19 with higher respiratory support had increased in vivo activation of coagulation and fibrinolysis, as reflected by higher plasma levels of d‐dimer, thrombin‐antithrombin, and plasmin‐antiplasmin complexes as compared to patients with no to minimal respiratory support and healthy controls. Moreover, the patients with COVID‐19 with higher respiratory support exhibited substantial ex vivo thrombin generation and lower ex vivo fibrinolytic capacity, despite higher doses of anticoagulant therapy compared to less severely ill patients. Fibrinogen, factor VIII, and von Willebrand factor levels increased, and ADAMTS13 levels decreased with increasing respiratory support in patients with COVID‐19. Low platelet count; low levels of prothrombin, antithrombin, and ADAMTS13; and high levels of von Willebrand factor were associated with short‐term mortality. Severe COVID‐19 is associated with prothrombotic changes with increased in vivo activation of coagulation and fibrinolysis, despite anticoagulant therapy.</description><subject>Anticoagulants</subject><subject>Blood</subject><subject>Body mass index</subject><subject>coagulation</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Cytokine storm</subject><subject>Diabetes</subject><subject>Drug dosages</subject><subject>fibrinolysis</subject><subject>hemostasis</subject><subject>Intensive care</subject><subject>Intubation</subject><subject>Laboratories</subject><subject>Medicin och hälsovetenskap</subject><subject>Mortality</subject><subject>Original</subject><subject>Original ‐ Thrombosis</subject><subject>Patients</subject><subject>Plasma</subject><subject>Severe acute respiratory syndrome</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Thromboembolism</subject><subject>thrombosis</subject><subject>Variables</subject><issn>2475-0379</issn><issn>2475-0379</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqdkt2KEzEUxwdR3GXdGx9ABrwRoWs-J5MbQbrqFhZWpHgbMsmZNnU6qUna0jsfwWf0SUx3dpdWZC-EhHz9zj_JOf-ieInRBUaIvAtpTi4wYRV5UpwSJvgIUSGfHsxPivMYFyjDiOTGnxcnlHIqcjst7Jfg0zz4ZeOTM6WZ634GsXR9udLJQZ9iuXVpXo5vvk0uf__8hWWpA5Q6Rm-cTmCHY-si6AhlhA0El3al7m259CHpLq9eFM9a3UU4vxvPiumnj9Px1ej65vNk_OF6ZIQkZGRN2xgiSMNQTXErEKOaYVQJRFjTtlJga1tGW6MbjqnhkgPHUnLKbU1sQ8-KySBrvV6oVXBLHXbKa6duN3yYKR3yLztQjTVMN4i3llLWMCyRlIZhLXhFOZIoa8lBK25htW6O1FbBW3W3_93tu4qgyH1S_yMWs7rCFSd1jn0_xGZgCdbkCgTdHUscnfRurmZ-o0TNeE5bFnhzJxD8jzXEpJYuGug63YNfR0XyVayqBGEZff0XuvDr0OcK7SnCmci5fZyqhBB1JXGm3g6UCT7GAO3DkzFSe6OqvVHVrVEz_Orwkw_oQQbxAGxdB7tHpNTX6RW5F2VDDGSHbRwEFU02sAHrApiUPeD-9ZY_rQ8F_Q</recordid><startdate>202101</startdate><enddate>202101</enddate><creator>von Meijenfeldt, Fien A.</creator><creator>Havervall, Sebastian</creator><creator>Adelmeijer, Jelle</creator><creator>Lundström, Annika</creator><creator>Rudberg, Ann‐Sofie</creator><creator>Magnusson, Maria</creator><creator>Mackman, Nigel</creator><creator>Thalin, Charlotte</creator><creator>Lisman, Ton</creator><general>Elsevier Inc</general><general>John Wiley &amp; Sons, Inc</general><general>Elsevier Limited</general><general>John Wiley and Sons Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>COVID</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3503-7140</orcidid></search><sort><creationdate>202101</creationdate><title>Prothrombotic changes in patients with COVID‐19 are associated with disease severity and mortality</title><author>von Meijenfeldt, Fien A. ; Havervall, Sebastian ; Adelmeijer, Jelle ; Lundström, Annika ; Rudberg, Ann‐Sofie ; Magnusson, Maria ; Mackman, Nigel ; Thalin, Charlotte ; Lisman, Ton</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c7922-dcfbc272b40831f7043a41067024bff971ddf43fcab513c595e5199535d82db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anticoagulants</topic><topic>Blood</topic><topic>Body mass index</topic><topic>coagulation</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>Cytokine storm</topic><topic>Diabetes</topic><topic>Drug dosages</topic><topic>fibrinolysis</topic><topic>hemostasis</topic><topic>Intensive care</topic><topic>Intubation</topic><topic>Laboratories</topic><topic>Medicin och hälsovetenskap</topic><topic>Mortality</topic><topic>Original</topic><topic>Original ‐ Thrombosis</topic><topic>Patients</topic><topic>Plasma</topic><topic>Severe acute respiratory syndrome</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Thromboembolism</topic><topic>thrombosis</topic><topic>Variables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>von Meijenfeldt, Fien A.</creatorcontrib><creatorcontrib>Havervall, Sebastian</creatorcontrib><creatorcontrib>Adelmeijer, Jelle</creatorcontrib><creatorcontrib>Lundström, Annika</creatorcontrib><creatorcontrib>Rudberg, Ann‐Sofie</creatorcontrib><creatorcontrib>Magnusson, Maria</creatorcontrib><creatorcontrib>Mackman, Nigel</creatorcontrib><creatorcontrib>Thalin, Charlotte</creatorcontrib><creatorcontrib>Lisman, Ton</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Wiley-Blackwell Open Access Titles(OpenAccess)</collection><collection>Wiley-Blackwell Open Access Backfiles (Open Access)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Coronavirus Research Database</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Research and Practice in Thrombosis and Haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>von Meijenfeldt, Fien A.</au><au>Havervall, Sebastian</au><au>Adelmeijer, Jelle</au><au>Lundström, Annika</au><au>Rudberg, Ann‐Sofie</au><au>Magnusson, Maria</au><au>Mackman, Nigel</au><au>Thalin, Charlotte</au><au>Lisman, Ton</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prothrombotic changes in patients with COVID‐19 are associated with disease severity and mortality</atitle><jtitle>Research and Practice in Thrombosis and Haemostasis</jtitle><addtitle>Res Pract Thromb Haemost</addtitle><date>2021-01</date><risdate>2021</risdate><volume>5</volume><issue>1</issue><spage>132</spage><epage>141</epage><pages>132-141</pages><issn>2475-0379</issn><eissn>2475-0379</eissn><abstract>Patients with severe coronavirus disease 2019 (COVID‐19) are at significant risk of thrombotic complications. However, their prothrombotic state is incompletely understood. Therefore, we measured in vivo activation markers of hemostasis, plasma levels of hemostatic proteins, and functional assays of coagulation and fibrinolysis in plasma from patients with COVID‐19 and determined their association with disease severity and 30‐day mortality. We included 102 patients with COVID‐19 receiving various levels of respiratory support admitted to general wards, intermediate units, or intensive care units and collected plasma samples shortly after hospital admission. Patients with COVID‐19 with higher respiratory support had increased in vivo activation of coagulation and fibrinolysis, as reflected by higher plasma levels of d‐dimer, thrombin‐antithrombin, and plasmin‐antiplasmin complexes as compared to patients with no to minimal respiratory support and healthy controls. Moreover, the patients with COVID‐19 with higher respiratory support exhibited substantial ex vivo thrombin generation and lower ex vivo fibrinolytic capacity, despite higher doses of anticoagulant therapy compared to less severely ill patients. Fibrinogen, factor VIII, and von Willebrand factor levels increased, and ADAMTS13 levels decreased with increasing respiratory support in patients with COVID‐19. Low platelet count; low levels of prothrombin, antithrombin, and ADAMTS13; and high levels of von Willebrand factor were associated with short‐term mortality. Severe COVID‐19 is associated with prothrombotic changes with increased in vivo activation of coagulation and fibrinolysis, despite anticoagulant therapy.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>33537537</pmid><doi>10.1002/rth2.12462</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-3503-7140</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier ISSN: 2475-0379
ispartof Research and Practice in Thrombosis and Haemostasis, 2021-01, Vol.5 (1), p.132-141
issn 2475-0379
2475-0379
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_bdc4ab05fd334b419099c41a75635090
source Coronavirus Research Database
subjects Anticoagulants
Blood
Body mass index
coagulation
Coronaviruses
COVID-19
Cytokine storm
Diabetes
Drug dosages
fibrinolysis
hemostasis
Intensive care
Intubation
Laboratories
Medicin och hälsovetenskap
Mortality
Original
Original ‐ Thrombosis
Patients
Plasma
Severe acute respiratory syndrome
Severe acute respiratory syndrome coronavirus 2
Thromboembolism
thrombosis
Variables
title Prothrombotic changes in patients with COVID‐19 are associated with disease severity and mortality
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T03%3A52%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_COVID&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Prothrombotic%20changes%20in%20patients%20with%20COVID%E2%80%9019%20are%20associated%20with%20disease%20severity%20and%20mortality&rft.jtitle=Research%20and%20Practice%20in%20Thrombosis%20and%20Haemostasis&rft.au=von%20Meijenfeldt,%20Fien%20A.&rft.date=2021-01&rft.volume=5&rft.issue=1&rft.spage=132&rft.epage=141&rft.pages=132-141&rft.issn=2475-0379&rft.eissn=2475-0379&rft_id=info:doi/10.1002/rth2.12462&rft_dat=%3Cproquest_COVID%3E2486466724%3C/proquest_COVID%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c7922-dcfbc272b40831f7043a41067024bff971ddf43fcab513c595e5199535d82db3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2467778691&rft_id=info:pmid/33537537&rfr_iscdi=true