ABSTRACT
The laboratory diagnosis of von Willebrand disease (vWD) is complex and requires a
panel of different laboratory tests. Because of this complexity, a proper quality
control process is necessary. Since 2003, the European Concerted Action on Thrombosis
and Disabilities Foundation has provided an external quality control program for several
laboratory tests included in the diagnosis of vWD. Currently, ~180 different laboratories
participate in this program, of which the vast majority perform both von Willebrand
factor (vWF):antigen (Ag) and activity tests. The lowest between-laboratory variation
was observed for the vWF antigen assay (10 to 24%), with a better performance for
the latex immunoassay (8 to 24%) than the enzyme immunoassay (13 to 25%). Both the
ristocetin cofactor activity assay (RCo) and the collagen-binding assay showed a higher
between-laboratory variation (20 to 40% and 17 to 29%, respectively). We have observed
that the within-laboratory repeatability for normal samples ranged from 0 to 40% for
the antigen assay and from 0 to 86% for the ristocetin cofactor activity assay. Normal
samples were interpreted correctly by the majority of the participants. However, type
1 vWD samples were wrongly interpreted by 20 to 40% of the participants, which was
mainly caused by a discordance in the vWF:RCo/vWF:Ag ratio. It can be concluded that
further improvement in the laboratory diagnosis of vWD is necessary.
KEYWORDS
von Willebrand disease - von Willebrand factor - von Willebrand factor activity -
von Willebrand factor antigen - quality control program
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Piet MeijerPh.D.
ECAT Foundation, P.O. Box 2215
2301 CE Leiden, The Netherlands
eMail: P.Meijer@ecat.nl