The role of the platelet function analyser (PFA-100TM) in the characterization of patients with von Willebrand's disease and its relationships with von Willebrand factor and the ABO blood group

Determination of the closure time (CT) with the platelet function analyser (PFA‐100TM) is a useful screening test for von Willebrand's disease (VWD) but its role in the characterization of VWD is not well established. We studied the relationship between the prolongation of the CT with adenosine...

Full description

Saved in:
Bibliographic Details
Published inHaemophilia : the official journal of the World Federation of Hemophilia Vol. 9; no. 3; pp. 298 - 302
Main Authors Nitu-Whalley, I. C., Lee, C. A., Brown, S. A., Riddell, A., Hermans, C.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science Ltd 01.05.2003
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Determination of the closure time (CT) with the platelet function analyser (PFA‐100TM) is a useful screening test for von Willebrand's disease (VWD) but its role in the characterization of VWD is not well established. We studied the relationship between the prolongation of the CT with adenosine diphosphate (ADP) (CT‐ADP) and epinephrine (CT‐EPI) cartridges and the von Willebrand factor (VWF) in 53 patients with VWD. We found that a relatively small percentage of the prolongation of the CT‐ADR and CT‐ADP (16 and 29%, respectively) was determined by a reduction in VWF levels. The CT‐ADP was significantly more prolonged in the presence of qualitative defects in VWF but could not discriminate between the VWD subtypes. The ABO blood group had no effect on the prolongation of the CT or the bleeding time. In conclusion, the PFA‐100TM appears of little use in the characterization of severity and subtype of VWD.
Bibliography:ark:/67375/WNG-X2VXWVZZ-4
ArticleID:HAE755
istex:170F09E3514323C937C70F50AD69393F3D81E324
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1351-8216
1365-2516
DOI:10.1046/j.1365-2516.2003.00755.x