The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization

Laffan, M., Brown, S. A., Collins, Peter William ORCID: https://orcid.org/0000-0002-6410-1324, Cumming, A. M., Hill, F. G. H., Keeling, D., Peake, I. R. and Pasi, K. J. 2004. The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization. Haemophilia 10 (3) , pp. 199-217. 10.1111/j.1365-2516.2004.00894.x

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Abstract

von Willebrand disease (VWD) is the commonest inherited bleeding disorder. However, despite an increasing understanding of the pathophysiology of VWD, the diagnosis of VWD is frequently difficult because of uncertainty regarding the relationship between laboratory assays and function in vivo. The objective of this guideline is to provide contemporary advice on a rational approach to the diagnosis of VWD. This is the second edition of this UK Haemophilia Centre Doctors’ Organisation (UKHCDO) guideline and supersedes the previous edition which was published in 1997.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Medicine Systems Immunity Research Institute (SIURI)
Subjects:	R Medicine > R Medicine (General)
Uncontrolled Keywords:	bleeding; diagnosis; guidelines; haemostasis; UKHCDO; von Willebrand
Publisher:	Wiley-Blackwell
ISSN:	1351-8216
Last Modified:	25 Oct 2022 09:55
URI:	https://orca.cardiff.ac.uk/id/eprint/60486

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