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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
Main Authors: 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
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container_title Canadian journal of cardiology
container_volume 31
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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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 &lt; 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 &lt; 0.001; 2.98 vs 1.86 IU/mL, P &lt; 0.001; and 3.16 vs 2.16 IU/mL, P &lt; 0.001). Patients with pre-TAVI vWF abnormalities consistent with a type 2A vWF syndrome (ratio vWF:CB/vWF:Ag &lt; 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 &lt; 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 &lt; 0.001; 2.98 vs 1.86 IU/mL, P &lt; 0.001; and 3.16 vs 2.16 IU/mL, P &lt; 0.001). Patients with pre-TAVI vWF abnormalities consistent with a type 2A vWF syndrome (ratio vWF:CB/vWF:Ag &lt; 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 &lt; 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 &lt; 0.001; 2.98 vs 1.86 IU/mL, P &lt; 0.001; and 3.16 vs 2.16 IU/mL, P &lt; 0.001). Patients with pre-TAVI vWF abnormalities consistent with a type 2A vWF syndrome (ratio vWF:CB/vWF:Ag &lt; 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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