Brain venography performance following the pause of Ad.26.COV2.S COVID-19 vaccine administration
Cases of cerebral venous thrombosis (CVT) associated with vaccine induced thrombotic thrombocytopenia (VITT) were reported following administration of the adenoviral vector COVID-19 vaccines, resulting in a pause in Ad.26.COV2.S vaccine administration in the United States, beginning on April 14, 202...
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Veröffentlicht in: | Journal of thrombosis and thrombolysis 2022-02, Vol.53 (2), p.359-362 |
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creator | Long, Clayton V. Clemente, Jonathan D. Singh, Sam Strong, Dale Rhoten, Jeremy B. Prasad, Tanushree Asimos, Andrew W. |
description | Cases of cerebral venous thrombosis (CVT) associated with vaccine induced thrombotic thrombocytopenia (VITT) were reported following administration of the adenoviral vector COVID-19 vaccines, resulting in a pause in Ad.26.COV2.S vaccine administration in the United States, beginning on April 14, 2021. We aimed to quantify and characterize an anticipated increase in brain venograms performed in response to this pause. Brain venogram cases were retrospectively identified during the three-week period following the vaccine pause and during the same calendar period in 2019. For venograms performed in 2021, we compared COVID vaccinated to unvaccinated patients. There was a 262% increase in venograms performed between 2019 (n = 26) and 2021 (n = 94), compared to only a 19% increase in all radiologic studies. Fifty-seven percent of patients in 2021 had a history of COVID-19 vaccination, with the majority being Ad.26.COV2.S. All patients diagnosed with CVT were unvaccinated. COVID vaccinated patients lacked platelet or D-dimer measurements consistent with VITT. Significantly more vaccinated versus unvaccinated patients had a headache (94% vs 70%, p = 0.0014), but otherwise lacked compelling CVT presentations, such as decreased/altered consciousness (7% vs 23%, p = 0.036), neurologic deficit (28% vs 48%, p = 0.049), and current/recent pregnancy (2% vs 28%, p = 0.0003). We found a dramatic increase in brain venograms performed following publicity of rare COVID-19 vaccine associated CVT cases, with no CVTs identified in vaccinated patients. Clinicians should carefully consider if brain venogram performance is indicated in COVID-19 vaccinated patients lacking thrombocytopenia and D-dimer elevation, especially without other compelling CVT risk factors or symptoms. |
doi_str_mv | 10.1007/s11239-021-02592-3 |
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We aimed to quantify and characterize an anticipated increase in brain venograms performed in response to this pause. Brain venogram cases were retrospectively identified during the three-week period following the vaccine pause and during the same calendar period in 2019. For venograms performed in 2021, we compared COVID vaccinated to unvaccinated patients. There was a 262% increase in venograms performed between 2019 (n = 26) and 2021 (n = 94), compared to only a 19% increase in all radiologic studies. Fifty-seven percent of patients in 2021 had a history of COVID-19 vaccination, with the majority being Ad.26.COV2.S. All patients diagnosed with CVT were unvaccinated. COVID vaccinated patients lacked platelet or D-dimer measurements consistent with VITT. Significantly more vaccinated versus unvaccinated patients had a headache (94% vs 70%, p = 0.0014), but otherwise lacked compelling CVT presentations, such as decreased/altered consciousness (7% vs 23%, p = 0.036), neurologic deficit (28% vs 48%, p = 0.049), and current/recent pregnancy (2% vs 28%, p = 0.0003). We found a dramatic increase in brain venograms performed following publicity of rare COVID-19 vaccine associated CVT cases, with no CVTs identified in vaccinated patients. Clinicians should carefully consider if brain venogram performance is indicated in COVID-19 vaccinated patients lacking thrombocytopenia and D-dimer elevation, especially without other compelling CVT risk factors or symptoms.</description><identifier>ISSN: 0929-5305</identifier><identifier>EISSN: 1573-742X</identifier><identifier>DOI: 10.1007/s11239-021-02592-3</identifier><identifier>PMID: 34739662</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Brain ; Cardiology ; Coronaviruses ; COVID-19 - prevention & control ; COVID-19 vaccines ; COVID-19 Vaccines - adverse effects ; Hematology ; Humans ; Intracranial Thrombosis - etiology ; Medicine ; Medicine & Public Health ; Phlebography - adverse effects ; Retrospective Studies ; Risk factors ; Thrombocytopenia ; Thrombocytopenia - etiology ; Thrombosis ; Thrombosis - etiology ; United States ; Vaccination - adverse effects ; Vaccines</subject><ispartof>Journal of thrombosis and thrombolysis, 2022-02, Vol.53 (2), p.359-362</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021</rights><rights>2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-86674daed01e6c73cf382dbdad6a5c4b35b0827c34e2a1a495b62a4e0c4b8bc23</citedby><cites>FETCH-LOGICAL-c474t-86674daed01e6c73cf382dbdad6a5c4b35b0827c34e2a1a495b62a4e0c4b8bc23</cites><orcidid>0000-0002-5183-9004</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/s11239-021-02592-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11239-021-02592-3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34739662$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Long, Clayton V.</creatorcontrib><creatorcontrib>Clemente, Jonathan D.</creatorcontrib><creatorcontrib>Singh, Sam</creatorcontrib><creatorcontrib>Strong, Dale</creatorcontrib><creatorcontrib>Rhoten, Jeremy B.</creatorcontrib><creatorcontrib>Prasad, Tanushree</creatorcontrib><creatorcontrib>Asimos, Andrew W.</creatorcontrib><title>Brain venography performance following the pause of Ad.26.COV2.S COVID-19 vaccine administration</title><title>Journal of thrombosis and thrombolysis</title><addtitle>J Thromb Thrombolysis</addtitle><addtitle>J Thromb Thrombolysis</addtitle><description>Cases of cerebral venous thrombosis (CVT) associated with vaccine induced thrombotic thrombocytopenia (VITT) were reported following administration of the adenoviral vector COVID-19 vaccines, resulting in a pause in Ad.26.COV2.S vaccine administration in the United States, beginning on April 14, 2021. We aimed to quantify and characterize an anticipated increase in brain venograms performed in response to this pause. Brain venogram cases were retrospectively identified during the three-week period following the vaccine pause and during the same calendar period in 2019. For venograms performed in 2021, we compared COVID vaccinated to unvaccinated patients. There was a 262% increase in venograms performed between 2019 (n = 26) and 2021 (n = 94), compared to only a 19% increase in all radiologic studies. Fifty-seven percent of patients in 2021 had a history of COVID-19 vaccination, with the majority being Ad.26.COV2.S. All patients diagnosed with CVT were unvaccinated. COVID vaccinated patients lacked platelet or D-dimer measurements consistent with VITT. Significantly more vaccinated versus unvaccinated patients had a headache (94% vs 70%, p = 0.0014), but otherwise lacked compelling CVT presentations, such as decreased/altered consciousness (7% vs 23%, p = 0.036), neurologic deficit (28% vs 48%, p = 0.049), and current/recent pregnancy (2% vs 28%, p = 0.0003). We found a dramatic increase in brain venograms performed following publicity of rare COVID-19 vaccine associated CVT cases, with no CVTs identified in vaccinated patients. Clinicians should carefully consider if brain venogram performance is indicated in COVID-19 vaccinated patients lacking thrombocytopenia and D-dimer elevation, especially without other compelling CVT risk factors or symptoms.</description><subject>Brain</subject><subject>Cardiology</subject><subject>Coronaviruses</subject><subject>COVID-19 - prevention & control</subject><subject>COVID-19 vaccines</subject><subject>COVID-19 Vaccines - adverse effects</subject><subject>Hematology</subject><subject>Humans</subject><subject>Intracranial Thrombosis - etiology</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Phlebography - adverse effects</subject><subject>Retrospective Studies</subject><subject>Risk factors</subject><subject>Thrombocytopenia</subject><subject>Thrombocytopenia - etiology</subject><subject>Thrombosis</subject><subject>Thrombosis - etiology</subject><subject>United States</subject><subject>Vaccination - adverse effects</subject><subject>Vaccines</subject><issn>0929-5305</issn><issn>1573-742X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kUtv1DAUhS1ERYfCH2CBLLFhk8Gv2PEGqQyvSpW64CF2xnFuZlwldrCTQf33uEwpLQsW1l2c7557rw9CzyhZU0LUq0wp47oijJZXa1bxB2hFa8UrJdi3h2hFNNNVzUl9jB7nfEkI0ZqwR-iYC8W1lGyFvr9J1ge8hxC3yU67KzxB6mMabXCA-zgM8acPWzzvAE92yYBjj0-7NZPrzcVXtv6ESzl7W1GN99Y5HwDbbvTB5znZ2cfwBB31dsjw9KaeoC_v333efKzOLz6cbU7PKyeUmKtGSiU6Cx2hIJ3irucN69rOdtLWTrS8bknDlOMCmKVW6LqVzAogRWtax_gJen3wnZZ2hM5BKAsMZkp-tOnKROvNfSX4ndnGvWlq2ZTZxeDljUGKPxbIsxl9djAMNkBcsik_LJiWWtOCvvgHvYxLCuU8wyRXdfGjqlDsQLkUc07Q3y5DibkO0BwCNCVA8ztAw0vT87tn3Lb8SawA_ADkIoUtpL-z_2P7Czy1plk</recordid><startdate>20220201</startdate><enddate>20220201</enddate><creator>Long, Clayton V.</creator><creator>Clemente, Jonathan D.</creator><creator>Singh, Sam</creator><creator>Strong, Dale</creator><creator>Rhoten, Jeremy B.</creator><creator>Prasad, Tanushree</creator><creator>Asimos, Andrew W.</creator><general>Springer US</general><general>Springer Nature B.V</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>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5183-9004</orcidid></search><sort><creationdate>20220201</creationdate><title>Brain venography performance following the pause of Ad.26.COV2.S COVID-19 vaccine administration</title><author>Long, Clayton V. ; Clemente, Jonathan D. ; Singh, Sam ; Strong, Dale ; Rhoten, Jeremy B. ; Prasad, Tanushree ; Asimos, Andrew W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-86674daed01e6c73cf382dbdad6a5c4b35b0827c34e2a1a495b62a4e0c4b8bc23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Brain</topic><topic>Cardiology</topic><topic>Coronaviruses</topic><topic>COVID-19 - prevention & control</topic><topic>COVID-19 vaccines</topic><topic>COVID-19 Vaccines - adverse effects</topic><topic>Hematology</topic><topic>Humans</topic><topic>Intracranial Thrombosis - etiology</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Phlebography - adverse effects</topic><topic>Retrospective Studies</topic><topic>Risk factors</topic><topic>Thrombocytopenia</topic><topic>Thrombocytopenia - etiology</topic><topic>Thrombosis</topic><topic>Thrombosis - etiology</topic><topic>United States</topic><topic>Vaccination - adverse effects</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Long, Clayton V.</creatorcontrib><creatorcontrib>Clemente, Jonathan D.</creatorcontrib><creatorcontrib>Singh, Sam</creatorcontrib><creatorcontrib>Strong, Dale</creatorcontrib><creatorcontrib>Rhoten, Jeremy B.</creatorcontrib><creatorcontrib>Prasad, Tanushree</creatorcontrib><creatorcontrib>Asimos, Andrew W.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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><jtitle>Journal of thrombosis and thrombolysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Long, Clayton V.</au><au>Clemente, Jonathan D.</au><au>Singh, Sam</au><au>Strong, Dale</au><au>Rhoten, Jeremy B.</au><au>Prasad, Tanushree</au><au>Asimos, Andrew W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brain venography performance following the pause of Ad.26.COV2.S COVID-19 vaccine administration</atitle><jtitle>Journal of thrombosis and thrombolysis</jtitle><stitle>J Thromb Thrombolysis</stitle><addtitle>J Thromb Thrombolysis</addtitle><date>2022-02-01</date><risdate>2022</risdate><volume>53</volume><issue>2</issue><spage>359</spage><epage>362</epage><pages>359-362</pages><issn>0929-5305</issn><eissn>1573-742X</eissn><abstract>Cases of cerebral venous thrombosis (CVT) associated with vaccine induced thrombotic thrombocytopenia (VITT) were reported following administration of the adenoviral vector COVID-19 vaccines, resulting in a pause in Ad.26.COV2.S vaccine administration in the United States, beginning on April 14, 2021. We aimed to quantify and characterize an anticipated increase in brain venograms performed in response to this pause. Brain venogram cases were retrospectively identified during the three-week period following the vaccine pause and during the same calendar period in 2019. For venograms performed in 2021, we compared COVID vaccinated to unvaccinated patients. There was a 262% increase in venograms performed between 2019 (n = 26) and 2021 (n = 94), compared to only a 19% increase in all radiologic studies. Fifty-seven percent of patients in 2021 had a history of COVID-19 vaccination, with the majority being Ad.26.COV2.S. All patients diagnosed with CVT were unvaccinated. COVID vaccinated patients lacked platelet or D-dimer measurements consistent with VITT. Significantly more vaccinated versus unvaccinated patients had a headache (94% vs 70%, p = 0.0014), but otherwise lacked compelling CVT presentations, such as decreased/altered consciousness (7% vs 23%, p = 0.036), neurologic deficit (28% vs 48%, p = 0.049), and current/recent pregnancy (2% vs 28%, p = 0.0003). We found a dramatic increase in brain venograms performed following publicity of rare COVID-19 vaccine associated CVT cases, with no CVTs identified in vaccinated patients. Clinicians should carefully consider if brain venogram performance is indicated in COVID-19 vaccinated patients lacking thrombocytopenia and D-dimer elevation, especially without other compelling CVT risk factors or symptoms.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>34739662</pmid><doi>10.1007/s11239-021-02592-3</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-5183-9004</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Brain Cardiology Coronaviruses COVID-19 - prevention & control COVID-19 vaccines COVID-19 Vaccines - adverse effects Hematology Humans Intracranial Thrombosis - etiology Medicine Medicine & Public Health Phlebography - adverse effects Retrospective Studies Risk factors Thrombocytopenia Thrombocytopenia - etiology Thrombosis Thrombosis - etiology United States Vaccination - adverse effects Vaccines |
title | Brain venography performance following the pause of Ad.26.COV2.S COVID-19 vaccine administration |
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