Sixth Åland Island Conference on von Willebrand disease

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Berntorp , E , Trakymiene , S S , Federici , A B , Holstein , K , Corrales-Medina , F F , Pierce , G F , Srivastava , A , Prondzinski , M V D , Johnsen , J M , Zupan , I P , Halimeh , S , Nummi , V & Roberts , J C 2022 , ' Sixth Åland Island Conference on von Willebrand disease ' , Haemophilia , vol. 28 , no. S5 , pp. 3-15 .

Title: Sixth Åland Island Conference on von Willebrand disease
Author: Berntorp, Erik; Trakymiene, Sonata S.; Federici, Augusto B.; Holstein, Katharina; Corrales-Medina, Fernando F.; Pierce, Glenn F.; Srivastava, Alok; Prondzinski, Mario von Depka; Johnsen, Jill M.; Zupan, Irena P.; Halimeh, Susan; Nummi, Vuokko; Roberts, Jonathan C.
Contributor organization: HUS Helsinki and Uusimaa Hospital District
Date: 2022-07
Language: eng
Number of pages: 13
Belongs to series: Haemophilia
ISSN: 1351-8216
Abstract: Introduction The sixth angstrom land Islands Conference on von Willebrand disease (VWD) on the angstrom land Islands, Finland, was held from 20 to 22 September 2018. Aim The meeting brought together experts in the field of VWD from around the world to share the latest advances and knowledge in VWD. Results and discussion The topics covered both clinical aspects of disease management, and biochemical and laboratory insights into the disease. The clinical topics discussed included epidemiology, diagnosis and treatment of VWD in different countries, management of children with VWD, bleeding control during surgery, specific considerations for the management of type 3 VWD and bleeding control in women with VWD. Current approaches to the management of acquired von Willebrand syndrome were also discussed. Despite significant advances in the understanding and therapeutic options for VWD, there remain many challenges to be overcome in order to optimise patient care. In comparison with haemophilia A, there are very few registries of VWD patients, which would be a valuable source of data on the condition and its management. VWD is still underdiagnosed, and many patients suffer recurrent or severe bleeding that could be prevented. Awareness of VWD among healthcare practitioners, including non-haematologists, should be improved to allow timely diagnosis and intervention. Diagnosis remains challenging, and the development of fast, simple assays may help to facilitate accurate and rapid diagnosis of VWD.
Subject: diagnosis
von Willebrand disease
von Willebrand factor
Peer reviewed: Yes
Rights: cc_by_nc_nd
Usage restriction: openAccess
Self-archived version: publishedVersion

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