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Effects of Transcutaneous Aortic Valve Implantation on Aortic Valve Disease-Related Hemostatic Disorders Involving von Willebrand Factor
Abstract Background Aortic valve stenosis (AVS) can be complicated by bleeding associated with acquired type 2A von Willebrand syndrome. The association of AVS and gastrointestinal bleeding from angiodysplasia is defined as Heyde syndrome. We sought to evaluate the effect of transcutaneous aortic va...
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Published in: | Canadian journal of cardiology 2015-06, Vol.31 (6), p.738-743 |
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creator | Caspar, Thibault, MD Jesel, Laurence, MD Desprez, Dominique, MD Grunebaum, Lélia, MD Samet, Hafida, MD Trinh, Annie, MD Petit-Eisenmann, Hélène, MD Kindo, Michel, MD, PhD Ohlmann, Patrick, MD, PhD Morel, Olivier, MD, PhD |
description | Abstract Background Aortic valve stenosis (AVS) can be complicated by bleeding associated with acquired type 2A von Willebrand syndrome. The association of AVS and gastrointestinal bleeding from angiodysplasia is defined as Heyde syndrome. We sought to evaluate the effect of transcutaneous aortic valve implantation (TAVI) on hemostasis disorders and to assess its effectiveness to treat Heyde syndrome. Methods We prospectively enrolled 49 consecutive patients with severe AVS addressed for TAVI at our institution. Biological hemostasis parameters involving von Willebrand factor (vWF) were assessed at baseline and 1 week after the procedure. Results At baseline, a significant link between vWF abnormalities and the severity of AVS was evidenced: mean aortic transvalvular gradient was negatively correlated with the levels of vWF antigen (vWF:Ag) ( r = −0.29; P < 0.05), vWF ristocetin cofactor activity ( r = −0.402; P = 0.006), and vWF collagen-binding activity (vWF:CB; r = −0.441; P = 0.005). One week after the procedure, a significant increase of vWF:Ag, vWF ristocetin cofactor activity, and vWF:CB was evidenced in the whole cohort (respectively, 3.32 vs 2.29 IU/mL, P < 0.001; 2.98 vs 1.86 IU/mL, P < 0.001; and 3.16 vs 2.16 IU/mL, P < 0.001). Patients with pre-TAVI vWF abnormalities consistent with a type 2A vWF syndrome (ratio vWF:CB/vWF:Ag < 0.7) preferentially improved their vWF function with respect to patients with a normal ratio (relative increase of vWF:CB of 63.8% vs 3.5%). Conclusions Hemostasis parameters involving vWF are improved after TAVI, especially in patients with pre-existing abnormalities consistent with acquired type 2A von Willebrand syndrome. |
doi_str_mv | 10.1016/j.cjca.2015.01.012 |
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fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_01280438v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0828282X15000379</els_id><sourcerecordid>1684429043</sourcerecordid><originalsourceid>FETCH-LOGICAL-c511t-7e3989cfcc850d1dd96cae3773e162c0b0bcd296ec6cae25aca92cc8579abebb3</originalsourceid><addsrcrecordid>eNp9kl2L1TAQhoso7nH1D3ghvdSLHpP0KwERDuuu58ABQdePu5BOp5qaNmeTtrD_wJ9tQtcFvRAGApnnnYH3nSR5TsmWElq97rfQg9oyQsstoaHYg2RDBa2ymtTlw2RDOOMZ4-zbWfLE-56QgtZ19Tg5Y6XIS86LTfLrsusQJp_aLr12avQwT2pEO_t0Z92kIf2izILpYTgZNU5q0nZMQ_3VfKc9Ko_ZRzRqwjbd42B9ZCG2rGvR-fQwLtYsevyeLkH_VRuDTVjYplcKJuueJo86ZTw-u3vPk89Xl9cX--z44f3hYnfMoKR0ymrMBRfQAfCStLRtRQUK87rOkVYMSEMaaJmoEOI_KxUowSJcC9Vg0-Tnyat17g9l5MnpQblbaZWW-91Rxr9gIydFzhca2Jcre3L2ZkY_yUF7QGNWhySteFEwEeiAshUFZ7132N3PpkTGtGQvY1oyphV2xDVB9OJu_twM2N5L_sQTgDcrgMGRRaOTHjSOgK12ITXZWv3_-W__kYPRowZlfuIt-t7ObgxeSyo9k0R-ivcSz4WWhJC8Fvlvray9dA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1684429043</pqid></control><display><type>article</type><title>Effects of Transcutaneous Aortic Valve Implantation on Aortic Valve Disease-Related Hemostatic Disorders Involving von Willebrand Factor</title><source>Elsevier</source><creator>Caspar, Thibault, MD ; Jesel, Laurence, MD ; Desprez, Dominique, MD ; Grunebaum, Lélia, MD ; Samet, Hafida, MD ; Trinh, Annie, MD ; Petit-Eisenmann, Hélène, MD ; Kindo, Michel, MD, PhD ; Ohlmann, Patrick, MD, PhD ; Morel, Olivier, MD, PhD</creator><creatorcontrib>Caspar, Thibault, MD ; Jesel, Laurence, MD ; Desprez, Dominique, MD ; Grunebaum, Lélia, MD ; Samet, Hafida, MD ; Trinh, Annie, MD ; Petit-Eisenmann, Hélène, MD ; Kindo, Michel, MD, PhD ; Ohlmann, Patrick, MD, PhD ; Morel, Olivier, MD, PhD</creatorcontrib><description>Abstract Background Aortic valve stenosis (AVS) can be complicated by bleeding associated with acquired type 2A von Willebrand syndrome. The association of AVS and gastrointestinal bleeding from angiodysplasia is defined as Heyde syndrome. We sought to evaluate the effect of transcutaneous aortic valve implantation (TAVI) on hemostasis disorders and to assess its effectiveness to treat Heyde syndrome. Methods We prospectively enrolled 49 consecutive patients with severe AVS addressed for TAVI at our institution. Biological hemostasis parameters involving von Willebrand factor (vWF) were assessed at baseline and 1 week after the procedure. Results At baseline, a significant link between vWF abnormalities and the severity of AVS was evidenced: mean aortic transvalvular gradient was negatively correlated with the levels of vWF antigen (vWF:Ag) ( r = −0.29; P < 0.05), vWF ristocetin cofactor activity ( r = −0.402; P = 0.006), and vWF collagen-binding activity (vWF:CB; r = −0.441; P = 0.005). One week after the procedure, a significant increase of vWF:Ag, vWF ristocetin cofactor activity, and vWF:CB was evidenced in the whole cohort (respectively, 3.32 vs 2.29 IU/mL, P < 0.001; 2.98 vs 1.86 IU/mL, P < 0.001; and 3.16 vs 2.16 IU/mL, P < 0.001). Patients with pre-TAVI vWF abnormalities consistent with a type 2A vWF syndrome (ratio vWF:CB/vWF:Ag < 0.7) preferentially improved their vWF function with respect to patients with a normal ratio (relative increase of vWF:CB of 63.8% vs 3.5%). Conclusions Hemostasis parameters involving vWF are improved after TAVI, especially in patients with pre-existing abnormalities consistent with acquired type 2A von Willebrand syndrome.</description><identifier>ISSN: 0828-282X</identifier><identifier>EISSN: 1916-7075</identifier><identifier>DOI: 10.1016/j.cjca.2015.01.012</identifier><identifier>PMID: 25935884</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Aged ; Aged, 80 and over ; Aortic Valve Stenosis - complications ; Aortic Valve Stenosis - diagnostic imaging ; Aortic Valve Stenosis - surgery ; Cardiovascular ; Cohort Studies ; Female ; Follow-Up Studies ; Hemostatic Disorders - diagnosis ; Hemostatic Disorders - therapy ; Humans ; Life Sciences ; Male ; Postoperative Complications - diagnosis ; Postoperative Complications - mortality ; Postoperative Complications - therapy ; Prospective Studies ; Risk Assessment ; Statistics, Nonparametric ; Survival Rate ; Transcatheter Aortic Valve Replacement - methods ; Transcatheter Aortic Valve Replacement - mortality ; Treatment Outcome ; Ultrasonography, Doppler ; von Willebrand Diseases - complications ; von Willebrand Diseases - diagnosis ; von Willebrand Factor - analysis</subject><ispartof>Canadian journal of cardiology, 2015-06, Vol.31 (6), p.738-743</ispartof><rights>Canadian Cardiovascular Society</rights><rights>2015 Canadian Cardiovascular Society</rights><rights>Copyright © 2015 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-7e3989cfcc850d1dd96cae3773e162c0b0bcd296ec6cae25aca92cc8579abebb3</citedby><cites>FETCH-LOGICAL-c511t-7e3989cfcc850d1dd96cae3773e162c0b0bcd296ec6cae25aca92cc8579abebb3</cites><orcidid>0000-0001-8884-4395 ; 0000-0002-8021-2737</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25935884$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01280438$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Caspar, Thibault, MD</creatorcontrib><creatorcontrib>Jesel, Laurence, MD</creatorcontrib><creatorcontrib>Desprez, Dominique, MD</creatorcontrib><creatorcontrib>Grunebaum, Lélia, MD</creatorcontrib><creatorcontrib>Samet, Hafida, MD</creatorcontrib><creatorcontrib>Trinh, Annie, MD</creatorcontrib><creatorcontrib>Petit-Eisenmann, Hélène, MD</creatorcontrib><creatorcontrib>Kindo, Michel, MD, PhD</creatorcontrib><creatorcontrib>Ohlmann, Patrick, MD, PhD</creatorcontrib><creatorcontrib>Morel, Olivier, MD, PhD</creatorcontrib><title>Effects of Transcutaneous Aortic Valve Implantation on Aortic Valve Disease-Related Hemostatic Disorders Involving von Willebrand Factor</title><title>Canadian journal of cardiology</title><addtitle>Can J Cardiol</addtitle><description>Abstract Background Aortic valve stenosis (AVS) can be complicated by bleeding associated with acquired type 2A von Willebrand syndrome. The association of AVS and gastrointestinal bleeding from angiodysplasia is defined as Heyde syndrome. We sought to evaluate the effect of transcutaneous aortic valve implantation (TAVI) on hemostasis disorders and to assess its effectiveness to treat Heyde syndrome. Methods We prospectively enrolled 49 consecutive patients with severe AVS addressed for TAVI at our institution. Biological hemostasis parameters involving von Willebrand factor (vWF) were assessed at baseline and 1 week after the procedure. Results At baseline, a significant link between vWF abnormalities and the severity of AVS was evidenced: mean aortic transvalvular gradient was negatively correlated with the levels of vWF antigen (vWF:Ag) ( r = −0.29; P < 0.05), vWF ristocetin cofactor activity ( r = −0.402; P = 0.006), and vWF collagen-binding activity (vWF:CB; r = −0.441; P = 0.005). One week after the procedure, a significant increase of vWF:Ag, vWF ristocetin cofactor activity, and vWF:CB was evidenced in the whole cohort (respectively, 3.32 vs 2.29 IU/mL, P < 0.001; 2.98 vs 1.86 IU/mL, P < 0.001; and 3.16 vs 2.16 IU/mL, P < 0.001). Patients with pre-TAVI vWF abnormalities consistent with a type 2A vWF syndrome (ratio vWF:CB/vWF:Ag < 0.7) preferentially improved their vWF function with respect to patients with a normal ratio (relative increase of vWF:CB of 63.8% vs 3.5%). Conclusions Hemostasis parameters involving vWF are improved after TAVI, especially in patients with pre-existing abnormalities consistent with acquired type 2A von Willebrand syndrome.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aortic Valve Stenosis - complications</subject><subject>Aortic Valve Stenosis - diagnostic imaging</subject><subject>Aortic Valve Stenosis - surgery</subject><subject>Cardiovascular</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hemostatic Disorders - diagnosis</subject><subject>Hemostatic Disorders - therapy</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Postoperative Complications - diagnosis</subject><subject>Postoperative Complications - mortality</subject><subject>Postoperative Complications - therapy</subject><subject>Prospective Studies</subject><subject>Risk Assessment</subject><subject>Statistics, Nonparametric</subject><subject>Survival Rate</subject><subject>Transcatheter Aortic Valve Replacement - methods</subject><subject>Transcatheter Aortic Valve Replacement - mortality</subject><subject>Treatment Outcome</subject><subject>Ultrasonography, Doppler</subject><subject>von Willebrand Diseases - complications</subject><subject>von Willebrand Diseases - diagnosis</subject><subject>von Willebrand Factor - analysis</subject><issn>0828-282X</issn><issn>1916-7075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kl2L1TAQhoso7nH1D3ghvdSLHpP0KwERDuuu58ABQdePu5BOp5qaNmeTtrD_wJ9tQtcFvRAGApnnnYH3nSR5TsmWElq97rfQg9oyQsstoaHYg2RDBa2ymtTlw2RDOOMZ4-zbWfLE-56QgtZ19Tg5Y6XIS86LTfLrsusQJp_aLr12avQwT2pEO_t0Z92kIf2izILpYTgZNU5q0nZMQ_3VfKc9Ko_ZRzRqwjbd42B9ZCG2rGvR-fQwLtYsevyeLkH_VRuDTVjYplcKJuueJo86ZTw-u3vPk89Xl9cX--z44f3hYnfMoKR0ymrMBRfQAfCStLRtRQUK87rOkVYMSEMaaJmoEOI_KxUowSJcC9Vg0-Tnyat17g9l5MnpQblbaZWW-91Rxr9gIydFzhca2Jcre3L2ZkY_yUF7QGNWhySteFEwEeiAshUFZ7132N3PpkTGtGQvY1oyphV2xDVB9OJu_twM2N5L_sQTgDcrgMGRRaOTHjSOgK12ITXZWv3_-W__kYPRowZlfuIt-t7ObgxeSyo9k0R-ivcSz4WWhJC8Fvlvray9dA</recordid><startdate>20150601</startdate><enddate>20150601</enddate><creator>Caspar, Thibault, MD</creator><creator>Jesel, Laurence, MD</creator><creator>Desprez, Dominique, MD</creator><creator>Grunebaum, Lélia, MD</creator><creator>Samet, Hafida, MD</creator><creator>Trinh, Annie, MD</creator><creator>Petit-Eisenmann, Hélène, MD</creator><creator>Kindo, Michel, MD, PhD</creator><creator>Ohlmann, Patrick, MD, PhD</creator><creator>Morel, Olivier, MD, PhD</creator><general>Elsevier Inc</general><general>Elsevier</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>1XC</scope><orcidid>https://orcid.org/0000-0001-8884-4395</orcidid><orcidid>https://orcid.org/0000-0002-8021-2737</orcidid></search><sort><creationdate>20150601</creationdate><title>Effects of Transcutaneous Aortic Valve Implantation on Aortic Valve Disease-Related Hemostatic Disorders Involving von Willebrand Factor</title><author>Caspar, Thibault, MD ; Jesel, Laurence, MD ; Desprez, Dominique, MD ; Grunebaum, Lélia, MD ; Samet, Hafida, MD ; Trinh, Annie, MD ; Petit-Eisenmann, Hélène, MD ; Kindo, Michel, MD, PhD ; Ohlmann, Patrick, MD, PhD ; Morel, Olivier, MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-7e3989cfcc850d1dd96cae3773e162c0b0bcd296ec6cae25aca92cc8579abebb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aortic Valve Stenosis - complications</topic><topic>Aortic Valve Stenosis - diagnostic imaging</topic><topic>Aortic Valve Stenosis - surgery</topic><topic>Cardiovascular</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Hemostatic Disorders - diagnosis</topic><topic>Hemostatic Disorders - therapy</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Postoperative Complications - diagnosis</topic><topic>Postoperative Complications - mortality</topic><topic>Postoperative Complications - therapy</topic><topic>Prospective Studies</topic><topic>Risk Assessment</topic><topic>Statistics, Nonparametric</topic><topic>Survival Rate</topic><topic>Transcatheter Aortic Valve Replacement - methods</topic><topic>Transcatheter Aortic Valve Replacement - mortality</topic><topic>Treatment Outcome</topic><topic>Ultrasonography, Doppler</topic><topic>von Willebrand Diseases - complications</topic><topic>von Willebrand Diseases - diagnosis</topic><topic>von Willebrand Factor - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Caspar, Thibault, MD</creatorcontrib><creatorcontrib>Jesel, Laurence, MD</creatorcontrib><creatorcontrib>Desprez, Dominique, MD</creatorcontrib><creatorcontrib>Grunebaum, Lélia, MD</creatorcontrib><creatorcontrib>Samet, Hafida, MD</creatorcontrib><creatorcontrib>Trinh, Annie, MD</creatorcontrib><creatorcontrib>Petit-Eisenmann, Hélène, MD</creatorcontrib><creatorcontrib>Kindo, Michel, MD, PhD</creatorcontrib><creatorcontrib>Ohlmann, Patrick, MD, PhD</creatorcontrib><creatorcontrib>Morel, Olivier, MD, PhD</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>Hyper Article en Ligne (HAL)</collection><jtitle>Canadian journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Caspar, Thibault, MD</au><au>Jesel, Laurence, MD</au><au>Desprez, Dominique, MD</au><au>Grunebaum, Lélia, MD</au><au>Samet, Hafida, MD</au><au>Trinh, Annie, MD</au><au>Petit-Eisenmann, Hélène, MD</au><au>Kindo, Michel, MD, PhD</au><au>Ohlmann, Patrick, MD, PhD</au><au>Morel, Olivier, MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Transcutaneous Aortic Valve Implantation on Aortic Valve Disease-Related Hemostatic Disorders Involving von Willebrand Factor</atitle><jtitle>Canadian journal of cardiology</jtitle><addtitle>Can J Cardiol</addtitle><date>2015-06-01</date><risdate>2015</risdate><volume>31</volume><issue>6</issue><spage>738</spage><epage>743</epage><pages>738-743</pages><issn>0828-282X</issn><eissn>1916-7075</eissn><abstract>Abstract Background Aortic valve stenosis (AVS) can be complicated by bleeding associated with acquired type 2A von Willebrand syndrome. The association of AVS and gastrointestinal bleeding from angiodysplasia is defined as Heyde syndrome. We sought to evaluate the effect of transcutaneous aortic valve implantation (TAVI) on hemostasis disorders and to assess its effectiveness to treat Heyde syndrome. Methods We prospectively enrolled 49 consecutive patients with severe AVS addressed for TAVI at our institution. Biological hemostasis parameters involving von Willebrand factor (vWF) were assessed at baseline and 1 week after the procedure. Results At baseline, a significant link between vWF abnormalities and the severity of AVS was evidenced: mean aortic transvalvular gradient was negatively correlated with the levels of vWF antigen (vWF:Ag) ( r = −0.29; P < 0.05), vWF ristocetin cofactor activity ( r = −0.402; P = 0.006), and vWF collagen-binding activity (vWF:CB; r = −0.441; P = 0.005). One week after the procedure, a significant increase of vWF:Ag, vWF ristocetin cofactor activity, and vWF:CB was evidenced in the whole cohort (respectively, 3.32 vs 2.29 IU/mL, P < 0.001; 2.98 vs 1.86 IU/mL, P < 0.001; and 3.16 vs 2.16 IU/mL, P < 0.001). Patients with pre-TAVI vWF abnormalities consistent with a type 2A vWF syndrome (ratio vWF:CB/vWF:Ag < 0.7) preferentially improved their vWF function with respect to patients with a normal ratio (relative increase of vWF:CB of 63.8% vs 3.5%). Conclusions Hemostasis parameters involving vWF are improved after TAVI, especially in patients with pre-existing abnormalities consistent with acquired type 2A von Willebrand syndrome.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>25935884</pmid><doi>10.1016/j.cjca.2015.01.012</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-8884-4395</orcidid><orcidid>https://orcid.org/0000-0002-8021-2737</orcidid></addata></record> |
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subjects | Aged Aged, 80 and over Aortic Valve Stenosis - complications Aortic Valve Stenosis - diagnostic imaging Aortic Valve Stenosis - surgery Cardiovascular Cohort Studies Female Follow-Up Studies Hemostatic Disorders - diagnosis Hemostatic Disorders - therapy Humans Life Sciences Male Postoperative Complications - diagnosis Postoperative Complications - mortality Postoperative Complications - therapy Prospective Studies Risk Assessment Statistics, Nonparametric Survival Rate Transcatheter Aortic Valve Replacement - methods Transcatheter Aortic Valve Replacement - mortality Treatment Outcome Ultrasonography, Doppler von Willebrand Diseases - complications von Willebrand Diseases - diagnosis von Willebrand Factor - analysis |
title | Effects of Transcutaneous Aortic Valve Implantation on Aortic Valve Disease-Related Hemostatic Disorders Involving von Willebrand Factor |
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