Von Willebrand Factor Multimeric Assay in Acquired von Willebrand Disease Diagnosis: A Report of Experience from North Estonia Medical Centre

Author:

Pikta Marika12ORCID,Banys Valdas3,Szanto Timea4,Joutsi-Korhonen Lotta5,Vaide Ines6,Varik Mirja7,Lehtinen Anna-Elina8,Giangrande Paul9,Laane Edward6

Affiliation:

1. Department of Health Technologies, Tallinn University of Technology, Tallinn, Estonia

2. Department of Laboratory Medicine, North Estonia Medical Centre, Tallinn, Estonia

3. Department of Physiology, Biochemistry, Microbiology and Laboratory Medicine, Faculty of Medicine, Institute of Biomedical Sciences, Vilnius University, Vilnius, Lithuania

4. Research Program Unit of Systems Oncology, Helsinki University Hospital, Unit of Coagulation Disorders, Helsinki, Finland

5. Department of Clinical Chemistry, Unit of Coagulation Disorders, HUSLAB Laboratory Services, Helsinki University Hospital and University of Helsinki, Helsinki, Finland

6. Hemato-Oncology Clinic, Institute of Clinical Medicine, Tartu University, Tartu, Estonia

7. Hematology Department, North Estonia Medical Centre, Tallinn, Estonia

8. Department of Hematology, Unit of Coagulation Disorders, Helsinki University Hospital Comprehensive Cancer Center and University of Helsinki, Helsinki, Finland

9. Green Templeton College, University of Oxford, Oxford, United Kingdom

Abstract

Abstract Objectives Acquired von Willebrand syndrome (AVWS) is a rare and frequently underdiagnosed bleeding disorder with an unknown prevalence. The diagnosis of AVWS is made based on laboratory investigations and the presence of clinical symptoms. Evaluation and management of affected patients are complex due to the need for multiple laboratory assays. Materials and Methods Here, we describe the clinical and laboratory data of seven patients with a diagnosis of AVWS. All patients met the criteria for AVWS based on laboratory findings, bleeding symptoms, and the absence of any previous history of a bleeding disorder. Results In all cases, the laboratory findings, lack of bleeding anamnesis, and family history suggested the presence of AVWS. Von Willebrand factor multimeric analysis showed decreased high-molecular weight (HMW) multimers in six cases. Patients with lower HMW multimers experienced more severe bleeding complications. Conclusions The diagnosis of AVWS is complex and requires extensive laboratory evaluation. Interdisciplinary collaboration and complex laboratory evaluations are of paramount importance for the early recognition of AVWS and optimal AVWS diagnosis as well as successful clinical management.

Publisher

Georg Thieme Verlag KG

Reference30 articles.

1. Acquired von Willebrand syndromes: clinical features, aetiology, pathophysiology, classification and management;J J Michiels;Best Pract Res Clin Haematol,2001

2. Subcommittee on von Willebrand Factor. Acquired von Willebrand syndrome: data from an international registry;A B Federici;Thromb Haemost,2000

3. State of the art: von Willebrand disease;A H James;Haemophilia,2016

4. Epidemiology and general guidelines of the management of acquired haemophilia and von Willebrand syndrome;P Collins;Haemophilia,2008

5. Implementation and verification of new VWF: Ac assay system with components from different manufacturers;M Pikta;Laboratorine Medicina,2016

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3