Platelet function analyser (PFA-100) results and von Willebrand factor deficiency: a 16-year 'real-world' experience

Summary The platelet function analyser (PFA‐100) is a biological tool designed to explore primary haemostasis. This system has thus been widely demonstrated as reliable in detecting von Willebrand factor (VWF) deficiency. However, most studies were based on patients benefitting from regular medical...

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Veröffentlicht in:Haemophilia : the official journal of the World Federation of Hemophilia 2015-09, Vol.21 (5), p.646-652
Hauptverfasser: Ardillon, L., Ternisien, C., Fouassier, M., Sigaud, M., Lefrançois, A., Pacault, M., Ribeyrol, O., Fressinaud, E., Boisseau, P., Trossaërt, M.
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container_issue 5
container_start_page 646
container_title Haemophilia : the official journal of the World Federation of Hemophilia
container_volume 21
creator Ardillon, L.
Ternisien, C.
Fouassier, M.
Sigaud, M.
Lefrançois, A.
Pacault, M.
Ribeyrol, O.
Fressinaud, E.
Boisseau, P.
Trossaërt, M.
description Summary The platelet function analyser (PFA‐100) is a biological tool designed to explore primary haemostasis. This system has thus been widely demonstrated as reliable in detecting von Willebrand factor (VWF) deficiency. However, most studies were based on patients benefitting from regular medical care and accurate diagnosis, and it would seem probable that the results were somewhat optimistic, and do not reflect its performances in ‘real‐world’ situations. We have chosen to study the reliability of PFA‐100 for screening VWF ristocetin cofactor (VWF:RCo) deficiency. We retrospectively analysed the results (n = 6431) of 4027 patients referred to our centre between October 1997 and June 2013 and in whom PFA‐Epi, PFA‐ADP, and VWF:RCo activity had been evaluated. We studied the influence of blood group on the results and the performances of each method in a subgroup of 213 patients with genetically confirmed von Willebrand disease. We have shown that the PFA‐100 system, in our experience, constitutes an excellent screening test for detecting VWF:RCo deficiency, whatever the clinical situation, in ‘real‐world’ conditions. The negative predictive value (NPV), the positive predictive value, the sensitivity and the specificity were respectively: 0.98, 0.51, 0.98 and 0.40. When values adjusted for blood group are used, NPV and sensitivity are inferior to those using normal values which have not been adjusted for blood group. We have shown the PFA‐100 method to be more efficient in screening for VWF deficiency than the VWF:RCo technique.
doi_str_mv 10.1111/hae.12653
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This system has thus been widely demonstrated as reliable in detecting von Willebrand factor (VWF) deficiency. However, most studies were based on patients benefitting from regular medical care and accurate diagnosis, and it would seem probable that the results were somewhat optimistic, and do not reflect its performances in ‘real‐world’ situations. We have chosen to study the reliability of PFA‐100 for screening VWF ristocetin cofactor (VWF:RCo) deficiency. We retrospectively analysed the results (n = 6431) of 4027 patients referred to our centre between October 1997 and June 2013 and in whom PFA‐Epi, PFA‐ADP, and VWF:RCo activity had been evaluated. We studied the influence of blood group on the results and the performances of each method in a subgroup of 213 patients with genetically confirmed von Willebrand disease. We have shown that the PFA‐100 system, in our experience, constitutes an excellent screening test for detecting VWF:RCo deficiency, whatever the clinical situation, in ‘real‐world’ conditions. The negative predictive value (NPV), the positive predictive value, the sensitivity and the specificity were respectively: 0.98, 0.51, 0.98 and 0.40. When values adjusted for blood group are used, NPV and sensitivity are inferior to those using normal values which have not been adjusted for blood group. 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We have shown that the PFA‐100 system, in our experience, constitutes an excellent screening test for detecting VWF:RCo deficiency, whatever the clinical situation, in ‘real‐world’ conditions. The negative predictive value (NPV), the positive predictive value, the sensitivity and the specificity were respectively: 0.98, 0.51, 0.98 and 0.40. When values adjusted for blood group are used, NPV and sensitivity are inferior to those using normal values which have not been adjusted for blood group. We have shown the PFA‐100 method to be more efficient in screening for VWF deficiency than the VWF:RCo technique.</description><subject>ABO Blood-Group System - metabolism</subject><subject>Adult</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>platelet function analyser-100</subject><subject>Platelet Function Tests - instrumentation</subject><subject>Predictive Value of Tests</subject><subject>ristocetin cofactor activity</subject><subject>von Willebrand Diseases - blood</subject><subject>von Willebrand factor</subject><subject>von Willebrand Factor - metabolism</subject><issn>1351-8216</issn><issn>1365-2516</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1P3DAQhi1EVSjtgT-AfAMOBn_E9obbQvmohCgHKo7WxJ6IgDfZ2kkh_54sC9w6l5nRPPMcXkJ2BT8SUx0_AB4JabTaINtCGc2kFmZzNWvBZlKYLfIt50fOhZLcfCVbUlut7Exvk_42Qo8Re1oPre-brqXQQhwzJnpwezFngvNDmjAPsc_TKdB_E3LfxIhVWq01-L5LNGDd-AZbP55QoMKwESHR_YQQ2XOXYtin-LLEtELwO_lSQ8z4473vkD8X53dnV-z69-Wvs_k188ooxSpTlRqCMVwYAdJDXVQKfVFwDt4UwWgvQxmUtbwIwUOluZQAtlAzL4tJsUMO1t5l6v4OmHu3aLLHGKHFbshOWKGNnpWqnNDDNepTl3PC2i1Ts4A0OsHdKmQ3hezeQp7YvXftUC0wfJIfqU7A8Rp4biKO_ze5q_n5h5KtP5rc48vnB6QnZ6yy2t3fXLrT01Lf6DvrfqpXDG-Tvg</recordid><startdate>201509</startdate><enddate>201509</enddate><creator>Ardillon, L.</creator><creator>Ternisien, C.</creator><creator>Fouassier, M.</creator><creator>Sigaud, M.</creator><creator>Lefrançois, A.</creator><creator>Pacault, M.</creator><creator>Ribeyrol, O.</creator><creator>Fressinaud, E.</creator><creator>Boisseau, P.</creator><creator>Trossaërt, M.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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></search><sort><creationdate>201509</creationdate><title>Platelet function analyser (PFA-100) results and von Willebrand factor deficiency: a 16-year 'real-world' experience</title><author>Ardillon, L. ; Ternisien, C. ; Fouassier, M. ; Sigaud, M. ; Lefrançois, A. ; Pacault, M. ; Ribeyrol, O. ; Fressinaud, E. ; Boisseau, P. ; Trossaërt, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3633-b6b95ad660161a2caf4b3ec4400ac64d65c2d9d37704ddcab5022aa7438c24363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>ABO Blood-Group System - metabolism</topic><topic>Adult</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>platelet function analyser-100</topic><topic>Platelet Function Tests - instrumentation</topic><topic>Predictive Value of Tests</topic><topic>ristocetin cofactor activity</topic><topic>von Willebrand Diseases - blood</topic><topic>von Willebrand factor</topic><topic>von Willebrand Factor - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ardillon, L.</creatorcontrib><creatorcontrib>Ternisien, C.</creatorcontrib><creatorcontrib>Fouassier, M.</creatorcontrib><creatorcontrib>Sigaud, M.</creatorcontrib><creatorcontrib>Lefrançois, A.</creatorcontrib><creatorcontrib>Pacault, M.</creatorcontrib><creatorcontrib>Ribeyrol, O.</creatorcontrib><creatorcontrib>Fressinaud, E.</creatorcontrib><creatorcontrib>Boisseau, P.</creatorcontrib><creatorcontrib>Trossaërt, M.</creatorcontrib><collection>Istex</collection><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>Haemophilia : the official journal of the World Federation of Hemophilia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ardillon, L.</au><au>Ternisien, C.</au><au>Fouassier, M.</au><au>Sigaud, M.</au><au>Lefrançois, A.</au><au>Pacault, M.</au><au>Ribeyrol, O.</au><au>Fressinaud, E.</au><au>Boisseau, P.</au><au>Trossaërt, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Platelet function analyser (PFA-100) results and von Willebrand factor deficiency: a 16-year 'real-world' experience</atitle><jtitle>Haemophilia : the official journal of the World Federation of Hemophilia</jtitle><addtitle>Haemophilia</addtitle><date>2015-09</date><risdate>2015</risdate><volume>21</volume><issue>5</issue><spage>646</spage><epage>652</epage><pages>646-652</pages><issn>1351-8216</issn><eissn>1365-2516</eissn><abstract>Summary The platelet function analyser (PFA‐100) is a biological tool designed to explore primary haemostasis. This system has thus been widely demonstrated as reliable in detecting von Willebrand factor (VWF) deficiency. However, most studies were based on patients benefitting from regular medical care and accurate diagnosis, and it would seem probable that the results were somewhat optimistic, and do not reflect its performances in ‘real‐world’ situations. We have chosen to study the reliability of PFA‐100 for screening VWF ristocetin cofactor (VWF:RCo) deficiency. We retrospectively analysed the results (n = 6431) of 4027 patients referred to our centre between October 1997 and June 2013 and in whom PFA‐Epi, PFA‐ADP, and VWF:RCo activity had been evaluated. We studied the influence of blood group on the results and the performances of each method in a subgroup of 213 patients with genetically confirmed von Willebrand disease. 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subjects ABO Blood-Group System - metabolism
Adult
Female
Humans
Male
platelet function analyser-100
Platelet Function Tests - instrumentation
Predictive Value of Tests
ristocetin cofactor activity
von Willebrand Diseases - blood
von Willebrand factor
von Willebrand Factor - metabolism
title Platelet function analyser (PFA-100) results and von Willebrand factor deficiency: a 16-year 'real-world' experience
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