Acquired von Willebrand syndrome in patients treated with veno-arterial extracorporeal membrane oxygenation
Veno-arterial extracorporeal membrane oxygenation (VA ECMO) is a powerful device for treatment of patients with life-threatening heart failure. Although bleeding is often associated with VA ECMO and sometimes results in a fatal outcome, its precise causes remain unknown. On the other hand, excessive...
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Veröffentlicht in: | Cardiovascular intervention and therapeutics 2019-10, Vol.34 (4), p.358-363 |
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creator | Tamura, Toshihiro Horiuchi, Hisanori Obayashi, Yuki Fuki, Masayuki Imanaka, Miyako Kuroda, Maiko Nishimura, Shunsuke Amano, Masashi Sakamoto, Jiro Tamaki, Yodo Enomoto, Soichiro Miyake, Makoto Kondo, Hirokazu Izumi, Chisato Nakagawa, Yoshihisa |
description | Veno-arterial extracorporeal membrane oxygenation (VA ECMO) is a powerful device for treatment of patients with life-threatening heart failure. Although bleeding is often associated with VA ECMO and sometimes results in a fatal outcome, its precise causes remain unknown. On the other hand, excessive high shear stress in the cardiovascular system causes acquired von Willebrand syndrome (aVWS), characterized by loss of von Willebrand factor (vWF) large multimers. vWF large multimers of five consecutive patients treated with VA ECMO were quantitatively evaluated using the vWF large multimer indices, defined as the ratio of the large multimer ratio of a patient to that of a healthy subject analyzed simultaneously. All 5 patients exhibited oozing type of bleeding at the skin insertion sites under treatment with PCPS at flow rates of 2.5–3.0 l/min/m
2
, including two severe cases of bleeding; one patient had massive gastrointestinal bleeding and another had hemothorax. Their vWF large multimer indices were 20.8, 28.8, 27.6, 51.0, and 31.0% (means 31.8 ± 11.4%). Surprisingly, these values are much lower than those observed in severe aortic stenosis reported previously by us (Tamura et al. in J Atheroscler Thromb 22:1115–1123,
2015
), where vWF multimer indices in 31 severe aortic stenosis patients with peak pressure gradient through the aortic valves of 85.1 ± 29.4 mmHg were 75.0 ± 21.7% (
p |
doi_str_mv | 10.1007/s12928-019-00568-y |
format | Article |
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2
, including two severe cases of bleeding; one patient had massive gastrointestinal bleeding and another had hemothorax. Their vWF large multimer indices were 20.8, 28.8, 27.6, 51.0, and 31.0% (means 31.8 ± 11.4%). Surprisingly, these values are much lower than those observed in severe aortic stenosis reported previously by us (Tamura et al. in J Atheroscler Thromb 22:1115–1123,
2015
), where vWF multimer indices in 31 severe aortic stenosis patients with peak pressure gradient through the aortic valves of 85.1 ± 29.4 mmHg were 75.0 ± 21.7% (
p
< 0.0001), indicating that much higher grade of aVWS occurred in patients with VA ECMO than severe aortic stenosis patients. All the 5 patients treated with VA ECMO developed aVWS that was much more severe than in patients with severe aortic stenosis.</description><identifier>ISSN: 1868-4300</identifier><identifier>EISSN: 1868-4297</identifier><identifier>DOI: 10.1007/s12928-019-00568-y</identifier><identifier>PMID: 30656612</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>Adult ; Aged ; Cardiology ; Extracorporeal Membrane Oxygenation - adverse effects ; Female ; Gastrointestinal Hemorrhage - etiology ; Hemothorax - etiology ; Humans ; Interventional Radiology ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Myocardial Infarction - therapy ; Myocarditis - therapy ; Original Article ; Pulmonary Embolism - therapy ; von Willebrand Diseases - etiology</subject><ispartof>Cardiovascular intervention and therapeutics, 2019-10, Vol.34 (4), p.358-363</ispartof><rights>Japanese Association of Cardiovascular Intervention and Therapeutics 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-7998c3b9a9b49c8ddf88a56cbf5079b0c150efa0c6fecf33559d059d2a7a9d6c3</citedby><cites>FETCH-LOGICAL-c371t-7998c3b9a9b49c8ddf88a56cbf5079b0c150efa0c6fecf33559d059d2a7a9d6c3</cites><orcidid>0000-0001-8655-0203</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12928-019-00568-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12928-019-00568-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30656612$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tamura, Toshihiro</creatorcontrib><creatorcontrib>Horiuchi, Hisanori</creatorcontrib><creatorcontrib>Obayashi, Yuki</creatorcontrib><creatorcontrib>Fuki, Masayuki</creatorcontrib><creatorcontrib>Imanaka, Miyako</creatorcontrib><creatorcontrib>Kuroda, Maiko</creatorcontrib><creatorcontrib>Nishimura, Shunsuke</creatorcontrib><creatorcontrib>Amano, Masashi</creatorcontrib><creatorcontrib>Sakamoto, Jiro</creatorcontrib><creatorcontrib>Tamaki, Yodo</creatorcontrib><creatorcontrib>Enomoto, Soichiro</creatorcontrib><creatorcontrib>Miyake, Makoto</creatorcontrib><creatorcontrib>Kondo, Hirokazu</creatorcontrib><creatorcontrib>Izumi, Chisato</creatorcontrib><creatorcontrib>Nakagawa, Yoshihisa</creatorcontrib><title>Acquired von Willebrand syndrome in patients treated with veno-arterial extracorporeal membrane oxygenation</title><title>Cardiovascular intervention and therapeutics</title><addtitle>Cardiovasc Interv and Ther</addtitle><addtitle>Cardiovasc Interv Ther</addtitle><description>Veno-arterial extracorporeal membrane oxygenation (VA ECMO) is a powerful device for treatment of patients with life-threatening heart failure. Although bleeding is often associated with VA ECMO and sometimes results in a fatal outcome, its precise causes remain unknown. On the other hand, excessive high shear stress in the cardiovascular system causes acquired von Willebrand syndrome (aVWS), characterized by loss of von Willebrand factor (vWF) large multimers. vWF large multimers of five consecutive patients treated with VA ECMO were quantitatively evaluated using the vWF large multimer indices, defined as the ratio of the large multimer ratio of a patient to that of a healthy subject analyzed simultaneously. All 5 patients exhibited oozing type of bleeding at the skin insertion sites under treatment with PCPS at flow rates of 2.5–3.0 l/min/m
2
, including two severe cases of bleeding; one patient had massive gastrointestinal bleeding and another had hemothorax. Their vWF large multimer indices were 20.8, 28.8, 27.6, 51.0, and 31.0% (means 31.8 ± 11.4%). Surprisingly, these values are much lower than those observed in severe aortic stenosis reported previously by us (Tamura et al. in J Atheroscler Thromb 22:1115–1123,
2015
), where vWF multimer indices in 31 severe aortic stenosis patients with peak pressure gradient through the aortic valves of 85.1 ± 29.4 mmHg were 75.0 ± 21.7% (
p
< 0.0001), indicating that much higher grade of aVWS occurred in patients with VA ECMO than severe aortic stenosis patients. All the 5 patients treated with VA ECMO developed aVWS that was much more severe than in patients with severe aortic stenosis.</description><subject>Adult</subject><subject>Aged</subject><subject>Cardiology</subject><subject>Extracorporeal Membrane Oxygenation - adverse effects</subject><subject>Female</subject><subject>Gastrointestinal Hemorrhage - etiology</subject><subject>Hemothorax - etiology</subject><subject>Humans</subject><subject>Interventional Radiology</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Myocardial Infarction - therapy</subject><subject>Myocarditis - therapy</subject><subject>Original Article</subject><subject>Pulmonary Embolism - therapy</subject><subject>von Willebrand Diseases - etiology</subject><issn>1868-4300</issn><issn>1868-4297</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMoKuof8CA5eqnmY_sxx2XxCxa8KB5Dmk612iZrkur235t11aOBIQPzzEvyEHLK2QVnrLwMXICoMsYhYywvqmzaIYe8Ss1MQLn720vGDshJCK8sHQEAM7lPDiQr8qLg4pC8zc372Hls6Iez9Knre6y9tg0Nk228G5B2lq507NDGQKNHHRP72cUX-oHWZdpH9J3uKa6j18b5lUtMTwccNjlI3Xp6RpsCnD0me63uA5783Efk8frqYXGbLe9v7hbzZWZkyWNWAlRG1qChnoGpmqatKp0Xpm5zVkLNDM8ZtpqZokXTSpnn0LBUQpcamsLII3K-zV159z5iiGrogsG-T-9xY1CClyCBg8gTKrao8S4Ej61a-W7QflKcqY1ntfWskmf17VlNaensJ3-sB2z-Vn6tJkBugZBG9hm9enWjt-nP_8V-AeT1jGo</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Tamura, Toshihiro</creator><creator>Horiuchi, Hisanori</creator><creator>Obayashi, Yuki</creator><creator>Fuki, Masayuki</creator><creator>Imanaka, Miyako</creator><creator>Kuroda, Maiko</creator><creator>Nishimura, Shunsuke</creator><creator>Amano, Masashi</creator><creator>Sakamoto, Jiro</creator><creator>Tamaki, Yodo</creator><creator>Enomoto, Soichiro</creator><creator>Miyake, Makoto</creator><creator>Kondo, Hirokazu</creator><creator>Izumi, Chisato</creator><creator>Nakagawa, Yoshihisa</creator><general>Springer Japan</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><orcidid>https://orcid.org/0000-0001-8655-0203</orcidid></search><sort><creationdate>20191001</creationdate><title>Acquired von Willebrand syndrome in patients treated with veno-arterial extracorporeal membrane oxygenation</title><author>Tamura, Toshihiro ; Horiuchi, Hisanori ; Obayashi, Yuki ; Fuki, Masayuki ; Imanaka, Miyako ; Kuroda, Maiko ; Nishimura, Shunsuke ; Amano, Masashi ; Sakamoto, Jiro ; Tamaki, Yodo ; Enomoto, Soichiro ; Miyake, Makoto ; Kondo, Hirokazu ; Izumi, Chisato ; Nakagawa, Yoshihisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-7998c3b9a9b49c8ddf88a56cbf5079b0c150efa0c6fecf33559d059d2a7a9d6c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Cardiology</topic><topic>Extracorporeal Membrane Oxygenation - adverse effects</topic><topic>Female</topic><topic>Gastrointestinal Hemorrhage - etiology</topic><topic>Hemothorax - etiology</topic><topic>Humans</topic><topic>Interventional Radiology</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Myocardial Infarction - therapy</topic><topic>Myocarditis - therapy</topic><topic>Original Article</topic><topic>Pulmonary Embolism - therapy</topic><topic>von Willebrand Diseases - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tamura, Toshihiro</creatorcontrib><creatorcontrib>Horiuchi, Hisanori</creatorcontrib><creatorcontrib>Obayashi, Yuki</creatorcontrib><creatorcontrib>Fuki, Masayuki</creatorcontrib><creatorcontrib>Imanaka, Miyako</creatorcontrib><creatorcontrib>Kuroda, Maiko</creatorcontrib><creatorcontrib>Nishimura, Shunsuke</creatorcontrib><creatorcontrib>Amano, Masashi</creatorcontrib><creatorcontrib>Sakamoto, Jiro</creatorcontrib><creatorcontrib>Tamaki, Yodo</creatorcontrib><creatorcontrib>Enomoto, Soichiro</creatorcontrib><creatorcontrib>Miyake, Makoto</creatorcontrib><creatorcontrib>Kondo, Hirokazu</creatorcontrib><creatorcontrib>Izumi, Chisato</creatorcontrib><creatorcontrib>Nakagawa, Yoshihisa</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><jtitle>Cardiovascular intervention and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tamura, Toshihiro</au><au>Horiuchi, Hisanori</au><au>Obayashi, Yuki</au><au>Fuki, Masayuki</au><au>Imanaka, Miyako</au><au>Kuroda, Maiko</au><au>Nishimura, Shunsuke</au><au>Amano, Masashi</au><au>Sakamoto, Jiro</au><au>Tamaki, Yodo</au><au>Enomoto, Soichiro</au><au>Miyake, Makoto</au><au>Kondo, Hirokazu</au><au>Izumi, Chisato</au><au>Nakagawa, Yoshihisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acquired von Willebrand syndrome in patients treated with veno-arterial extracorporeal membrane oxygenation</atitle><jtitle>Cardiovascular intervention and therapeutics</jtitle><stitle>Cardiovasc Interv and Ther</stitle><addtitle>Cardiovasc Interv Ther</addtitle><date>2019-10-01</date><risdate>2019</risdate><volume>34</volume><issue>4</issue><spage>358</spage><epage>363</epage><pages>358-363</pages><issn>1868-4300</issn><eissn>1868-4297</eissn><abstract>Veno-arterial extracorporeal membrane oxygenation (VA ECMO) is a powerful device for treatment of patients with life-threatening heart failure. Although bleeding is often associated with VA ECMO and sometimes results in a fatal outcome, its precise causes remain unknown. On the other hand, excessive high shear stress in the cardiovascular system causes acquired von Willebrand syndrome (aVWS), characterized by loss of von Willebrand factor (vWF) large multimers. vWF large multimers of five consecutive patients treated with VA ECMO were quantitatively evaluated using the vWF large multimer indices, defined as the ratio of the large multimer ratio of a patient to that of a healthy subject analyzed simultaneously. All 5 patients exhibited oozing type of bleeding at the skin insertion sites under treatment with PCPS at flow rates of 2.5–3.0 l/min/m
2
, including two severe cases of bleeding; one patient had massive gastrointestinal bleeding and another had hemothorax. Their vWF large multimer indices were 20.8, 28.8, 27.6, 51.0, and 31.0% (means 31.8 ± 11.4%). Surprisingly, these values are much lower than those observed in severe aortic stenosis reported previously by us (Tamura et al. in J Atheroscler Thromb 22:1115–1123,
2015
), where vWF multimer indices in 31 severe aortic stenosis patients with peak pressure gradient through the aortic valves of 85.1 ± 29.4 mmHg were 75.0 ± 21.7% (
p
< 0.0001), indicating that much higher grade of aVWS occurred in patients with VA ECMO than severe aortic stenosis patients. All the 5 patients treated with VA ECMO developed aVWS that was much more severe than in patients with severe aortic stenosis.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><pmid>30656612</pmid><doi>10.1007/s12928-019-00568-y</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-8655-0203</orcidid></addata></record> |
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subjects | Adult Aged Cardiology Extracorporeal Membrane Oxygenation - adverse effects Female Gastrointestinal Hemorrhage - etiology Hemothorax - etiology Humans Interventional Radiology Male Medicine Medicine & Public Health Middle Aged Myocardial Infarction - therapy Myocarditis - therapy Original Article Pulmonary Embolism - therapy von Willebrand Diseases - etiology |
title | Acquired von Willebrand syndrome in patients treated with veno-arterial extracorporeal membrane oxygenation |
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