Dynamic coagulofibrinolytic responses under long-term VV-ECMO management without anticoagulation in a COVID-19-ARDS patient: A case report
Venovenous extracorporeal membrane oxygenation (ECMO) is recommended for the treatment of critically ill patients with acute respiratory distress syndrome due to coronavirus disease 2019 (COVID-19). However, ECMO management can cause both bleeding and thrombotic complications. There are insufficient...
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Veröffentlicht in: | Medicine (Baltimore) 2023-01, Vol.102 (4), p.e32817-e32817 |
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creator | Matsumoto, Hironori Kikuchi, Satoshi Murata, Satoru Ohshita, Muneaki Harima, Yutaka Annen, Suguru Mukai, Naoki Nakabayashi, Yuki Ogawa, Shirou Okita, Mitsuo Takeba, Jun Sato, Norio |
description | Venovenous extracorporeal membrane oxygenation (ECMO) is recommended for the treatment of critically ill patients with acute respiratory distress syndrome due to coronavirus disease 2019 (COVID-19). However, ECMO management can cause both bleeding and thrombotic complications. There are insufficient coagulofibrinolytic data for appropriate ECMO management in patients with COVID-19.
A 48-year-old man with severe COVID-19-acute respiratory distress syndrome underwent long-term venovenous ECMO management for 48 days. Refractory oronasal bleeding developed on day 13, so the administration of unfractionated heparin was ceased for 29 days.
The patient showed dynamic coagulofibrinolytic responses associated with ECMO management, as shown by fibrin/fibrinogen degradation products, soluble fibrin, thrombin-antithrombin complex, and plasmin-α2-plasmin inhibitor complex elevations, suggesting the development of ECMO-induced coagulopathy.
We assessed coagulofibrinolytic markers to decide the appropriate timing for controlling excessive activation of coagulation by exchanging ECMO circuits. Moreover, viscoelastic hemostatic assays were used for adequate transfusion of blood products.
Safe long-term ECMO management was completed, which was withdrawn on day 48. The patient was weaned off mechanical ventilation on day 57 and was transferred to another hospital for rehabilitation.
Monitoring the coagulofibrinolytic status using markers and viscoelastic hemostatic assays may be effective for safe long-term ECMO management even without anticoagulant therapy. |
doi_str_mv | 10.1097/MD.0000000000032817 |
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A 48-year-old man with severe COVID-19-acute respiratory distress syndrome underwent long-term venovenous ECMO management for 48 days. Refractory oronasal bleeding developed on day 13, so the administration of unfractionated heparin was ceased for 29 days.
The patient showed dynamic coagulofibrinolytic responses associated with ECMO management, as shown by fibrin/fibrinogen degradation products, soluble fibrin, thrombin-antithrombin complex, and plasmin-α2-plasmin inhibitor complex elevations, suggesting the development of ECMO-induced coagulopathy.
We assessed coagulofibrinolytic markers to decide the appropriate timing for controlling excessive activation of coagulation by exchanging ECMO circuits. Moreover, viscoelastic hemostatic assays were used for adequate transfusion of blood products.
Safe long-term ECMO management was completed, which was withdrawn on day 48. The patient was weaned off mechanical ventilation on day 57 and was transferred to another hospital for rehabilitation.
Monitoring the coagulofibrinolytic status using markers and viscoelastic hemostatic assays may be effective for safe long-term ECMO management even without anticoagulant therapy.</description><identifier>ISSN: 0025-7974</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000032817</identifier><identifier>PMID: 36705388</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins</publisher><subject>Anticoagulants ; Clinical Case Report ; COVID-19 - complications ; COVID-19 - therapy ; Extracorporeal Membrane Oxygenation - adverse effects ; Fibrin Fibrinogen Degradation Products ; Hemorrhage - etiology ; Hemostatics ; Heparin ; Humans ; Male ; Middle Aged ; Respiratory Distress Syndrome - etiology ; Respiratory Distress Syndrome - therapy</subject><ispartof>Medicine (Baltimore), 2023-01, Vol.102 (4), p.e32817-e32817</ispartof><rights>Lippincott Williams & Wilkins</rights><rights>Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc.</rights><rights>Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4504-fecdf10c62e4464c5e8b415cc48c35afa38f33be42549837fe1e4a0fb5cb4e123</citedby><cites>FETCH-LOGICAL-c4504-fecdf10c62e4464c5e8b415cc48c35afa38f33be42549837fe1e4a0fb5cb4e123</cites><orcidid>0000-0002-6728-4605</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9875986/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9875986/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36705388$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matsumoto, Hironori</creatorcontrib><creatorcontrib>Kikuchi, Satoshi</creatorcontrib><creatorcontrib>Murata, Satoru</creatorcontrib><creatorcontrib>Ohshita, Muneaki</creatorcontrib><creatorcontrib>Harima, Yutaka</creatorcontrib><creatorcontrib>Annen, Suguru</creatorcontrib><creatorcontrib>Mukai, Naoki</creatorcontrib><creatorcontrib>Nakabayashi, Yuki</creatorcontrib><creatorcontrib>Ogawa, Shirou</creatorcontrib><creatorcontrib>Okita, Mitsuo</creatorcontrib><creatorcontrib>Takeba, Jun</creatorcontrib><creatorcontrib>Sato, Norio</creatorcontrib><title>Dynamic coagulofibrinolytic responses under long-term VV-ECMO management without anticoagulation in a COVID-19-ARDS patient: A case report</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>Venovenous extracorporeal membrane oxygenation (ECMO) is recommended for the treatment of critically ill patients with acute respiratory distress syndrome due to coronavirus disease 2019 (COVID-19). However, ECMO management can cause both bleeding and thrombotic complications. There are insufficient coagulofibrinolytic data for appropriate ECMO management in patients with COVID-19.
A 48-year-old man with severe COVID-19-acute respiratory distress syndrome underwent long-term venovenous ECMO management for 48 days. Refractory oronasal bleeding developed on day 13, so the administration of unfractionated heparin was ceased for 29 days.
The patient showed dynamic coagulofibrinolytic responses associated with ECMO management, as shown by fibrin/fibrinogen degradation products, soluble fibrin, thrombin-antithrombin complex, and plasmin-α2-plasmin inhibitor complex elevations, suggesting the development of ECMO-induced coagulopathy.
We assessed coagulofibrinolytic markers to decide the appropriate timing for controlling excessive activation of coagulation by exchanging ECMO circuits. Moreover, viscoelastic hemostatic assays were used for adequate transfusion of blood products.
Safe long-term ECMO management was completed, which was withdrawn on day 48. The patient was weaned off mechanical ventilation on day 57 and was transferred to another hospital for rehabilitation.
Monitoring the coagulofibrinolytic status using markers and viscoelastic hemostatic assays may be effective for safe long-term ECMO management even without anticoagulant therapy.</description><subject>Anticoagulants</subject><subject>Clinical Case Report</subject><subject>COVID-19 - complications</subject><subject>COVID-19 - therapy</subject><subject>Extracorporeal Membrane Oxygenation - adverse effects</subject><subject>Fibrin Fibrinogen Degradation Products</subject><subject>Hemorrhage - etiology</subject><subject>Hemostatics</subject><subject>Heparin</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Respiratory Distress Syndrome - etiology</subject><subject>Respiratory Distress Syndrome - therapy</subject><issn>0025-7974</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUtvEzEUhS0EoqHwC5CQl2xc_BzPsECKMgUqNYrEI1vL49xJBmbs1J4hyl_gV-M2pTy8sXTvOd-50kHoJaMXjFb6zbK-oH-e4CXTj9CMKVEQVRXyMZpRyhXRlZZn6FlK3yhlQnP5FJ2JQlMlynKGftZHb4fOYRfsdupD2zWx86E_jnkWIe2DT5Dw5DcQcR_8lowQB7xek8vFcoUH6-0WBvAjPnTjLkwjtj5b72B27ILHnccWL1brq5qwisw_1Z_xPm-y5S2eY2cT5Jx9iONz9KS1fYIX9_85-vr-8sviI7lefbhazK-Jk4pK0oLbtIy6goOUhXQKykYy5ZwsnVC2taJshWhAciWrUugWGEhL20a5RgLj4hy9O3H3UzPAxuVLou3NPnaDjUcTbGf-3fhuZ7bhh6lKraqyyIDX94AYbiZIoxm65KDvrYcwJcO1poxVUt9miZPUxZBShPYhhlFz26JZ1ub_FrPr1d8XPnh-15YF8iQ4hD73kb730wGi2YHtx90dT-mKE065oIxrSvJESvELH0WqAQ</recordid><startdate>20230127</startdate><enddate>20230127</enddate><creator>Matsumoto, Hironori</creator><creator>Kikuchi, Satoshi</creator><creator>Murata, Satoru</creator><creator>Ohshita, Muneaki</creator><creator>Harima, Yutaka</creator><creator>Annen, Suguru</creator><creator>Mukai, Naoki</creator><creator>Nakabayashi, Yuki</creator><creator>Ogawa, Shirou</creator><creator>Okita, Mitsuo</creator><creator>Takeba, Jun</creator><creator>Sato, Norio</creator><general>Lippincott Williams & Wilkins</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6728-4605</orcidid></search><sort><creationdate>20230127</creationdate><title>Dynamic coagulofibrinolytic responses under long-term VV-ECMO management without anticoagulation in a COVID-19-ARDS patient: A case report</title><author>Matsumoto, Hironori ; Kikuchi, Satoshi ; Murata, Satoru ; Ohshita, Muneaki ; Harima, Yutaka ; Annen, Suguru ; Mukai, Naoki ; Nakabayashi, Yuki ; Ogawa, Shirou ; Okita, Mitsuo ; Takeba, Jun ; Sato, Norio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4504-fecdf10c62e4464c5e8b415cc48c35afa38f33be42549837fe1e4a0fb5cb4e123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Anticoagulants</topic><topic>Clinical Case Report</topic><topic>COVID-19 - complications</topic><topic>COVID-19 - therapy</topic><topic>Extracorporeal Membrane Oxygenation - adverse effects</topic><topic>Fibrin Fibrinogen Degradation Products</topic><topic>Hemorrhage - etiology</topic><topic>Hemostatics</topic><topic>Heparin</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Respiratory Distress Syndrome - etiology</topic><topic>Respiratory Distress Syndrome - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsumoto, Hironori</creatorcontrib><creatorcontrib>Kikuchi, Satoshi</creatorcontrib><creatorcontrib>Murata, Satoru</creatorcontrib><creatorcontrib>Ohshita, Muneaki</creatorcontrib><creatorcontrib>Harima, Yutaka</creatorcontrib><creatorcontrib>Annen, Suguru</creatorcontrib><creatorcontrib>Mukai, Naoki</creatorcontrib><creatorcontrib>Nakabayashi, Yuki</creatorcontrib><creatorcontrib>Ogawa, Shirou</creatorcontrib><creatorcontrib>Okita, Mitsuo</creatorcontrib><creatorcontrib>Takeba, Jun</creatorcontrib><creatorcontrib>Sato, Norio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsumoto, Hironori</au><au>Kikuchi, Satoshi</au><au>Murata, Satoru</au><au>Ohshita, Muneaki</au><au>Harima, Yutaka</au><au>Annen, Suguru</au><au>Mukai, Naoki</au><au>Nakabayashi, Yuki</au><au>Ogawa, Shirou</au><au>Okita, Mitsuo</au><au>Takeba, Jun</au><au>Sato, Norio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamic coagulofibrinolytic responses under long-term VV-ECMO management without anticoagulation in a COVID-19-ARDS patient: A case report</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>2023-01-27</date><risdate>2023</risdate><volume>102</volume><issue>4</issue><spage>e32817</spage><epage>e32817</epage><pages>e32817-e32817</pages><issn>0025-7974</issn><eissn>1536-5964</eissn><abstract>Venovenous extracorporeal membrane oxygenation (ECMO) is recommended for the treatment of critically ill patients with acute respiratory distress syndrome due to coronavirus disease 2019 (COVID-19). However, ECMO management can cause both bleeding and thrombotic complications. There are insufficient coagulofibrinolytic data for appropriate ECMO management in patients with COVID-19.
A 48-year-old man with severe COVID-19-acute respiratory distress syndrome underwent long-term venovenous ECMO management for 48 days. Refractory oronasal bleeding developed on day 13, so the administration of unfractionated heparin was ceased for 29 days.
The patient showed dynamic coagulofibrinolytic responses associated with ECMO management, as shown by fibrin/fibrinogen degradation products, soluble fibrin, thrombin-antithrombin complex, and plasmin-α2-plasmin inhibitor complex elevations, suggesting the development of ECMO-induced coagulopathy.
We assessed coagulofibrinolytic markers to decide the appropriate timing for controlling excessive activation of coagulation by exchanging ECMO circuits. Moreover, viscoelastic hemostatic assays were used for adequate transfusion of blood products.
Safe long-term ECMO management was completed, which was withdrawn on day 48. The patient was weaned off mechanical ventilation on day 57 and was transferred to another hospital for rehabilitation.
Monitoring the coagulofibrinolytic status using markers and viscoelastic hemostatic assays may be effective for safe long-term ECMO management even without anticoagulant therapy.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins</pub><pmid>36705388</pmid><doi>10.1097/MD.0000000000032817</doi><orcidid>https://orcid.org/0000-0002-6728-4605</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anticoagulants Clinical Case Report COVID-19 - complications COVID-19 - therapy Extracorporeal Membrane Oxygenation - adverse effects Fibrin Fibrinogen Degradation Products Hemorrhage - etiology Hemostatics Heparin Humans Male Middle Aged Respiratory Distress Syndrome - etiology Respiratory Distress Syndrome - therapy |
title | Dynamic coagulofibrinolytic responses under long-term VV-ECMO management without anticoagulation in a COVID-19-ARDS patient: A case report |
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