ABSTRACT
Regular multilaboratory surveys of laboratories derived primarily from Australia,
New Zealand, and Southeast Asia have been conducted during the last 8 years to evaluate
testing proficiency in the diagnosis of von Willebrand disease (vWD). We summarize
and update the findings of these surveys with a particular emphasis on diagnostic
errors and error rates associated with particular tests or test panel limitations.
A total of 43 plasma samples have been dispatched to survey participants. These have
included 13 normal samples, five type 1 vWD samples, eight type 2 vWD samples (three
2A, three 2B, one 2M, and one 2N), and four type 3 vWD samples. In addition to numerical
test results, participant laboratories (currently, n = 49) were asked to provide diagnostic
interpretations regarding results, and whether or not vWD was suggested, and if so,
a probable subtype. Although laboratories usually provided correct interpretative
responses, diagnostic errors occurred in a substantial number of cases. On average,
type 1 vWD plasma was misidentified as type 2 vWD in 13.3% of cases, and laboratories
performing von Willebrand factor (vWF):ristocetin cofactor activity (RCo) without
vWF:collagen-binding activity (CB) were seven times more likely to make such an error
compared with those performing vWF:CB. Similarly, type 2 vWD plasma was misidentified
as type 1 or type 3 vWD in an average of 20.1% of cases, and laboratories performing
vWF:RCo without vWF:CB were three times more likely to make such an error compared
with those performing vWF:CB. Finally, normal plasma was misidentified as vWD in an
average of 6.7% of cases, and laboratories performing vWF:RCo without vWF:CB were
four times more likely to make such an error compared with those performing vWF:CB.
We conclude that although laboratories are generally proficient in tests for vWD,
diagnostic errors do occur and error rates are substantially reduced when test panels
are more comprehensive and include the vWF:CB.
KEYWORDS
von Willebrand factor (vWF) - von Willebrand disorder - von Willebrand disease (vWD)
- laboratory assessment - survey - hemostasis testing - diagnostic practice - quality
control - quality assurance
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Dr. Emmanuel J Favaloro
Department of Haematology, Institute of Clinical Pathology and Medical Research (ICPMR)
SWAHS, Westmead Hospital, Westmead, New South Wales, 2145, Australia
Email: emmanuel@icpmr.wsahs.nsw.gov.au