
von Willebrand factor levels in the diagnosis of von Willebrand …
We systematically reviewed the accuracy of diagnostic tests using different cutoff values of von Willebrand factor antigen (VWF:Ag) and platelet-dependent von Willebrand factor (VWF) activity assays in the diagnosis of VWD.
Laboratory diagnosis of von Willebrand disease - PMC
Von Willebrand disease (VWD) is a congenital bleeding disorder caused by a deficiency of von Willebrand factor (VWF) and typically characterized by mild mucosal bleeding. VWF plays several key roles in hemostasis, one of which is to link platelets to sites of vessel injury through binding sites for collagen and platelet glycoprotein Ibα (GPIbα).
Diagnostic approach to von Willebrand disease | Blood
Mar 26, 2015 · Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD).
von Willebrand Factor - Understand the Test - Testing.com
Dec 22, 2018 · Von Willebrand factor (VWF) testing is used to investigate excessive or recurrent bleeding episodes or a personal or family history of excessive bleeding. Testing is used to help diagnose von Willebrand disease (VWD) and distinguish between the various types of VWD.
Until more laboratories clearly define a reference range, the VWF:RCo/VWF:Ag ratio of <0.5–0.7 is recommended to distinguish type 1 VWD vs. type 2 VWD variants (A, B, or M).
New advances in the diagnosis of von Willebrand disease
Dec 6, 2019 · Laboratory diagnosis requires at least initially a measurement of von Willebrand factor (VWF) antigen levels, VWF platelet binding activity (VWF:RCo, VWF:GPIbM, and VWF:GPIbR), and factor VIII (FVIII) activity.
Von Willebrand Disease Clinical Trials - Mayo Clinic Research
The purpose of this study is to assess the safety of various Von Willebrand Factor (VWF) regimens for different indications (on-demand, surgery and prophylaxis) in adult and pediatric participants with clinically severe congenital VWD.
Von Willebrand's disease: case report and review of literature
Von Willebrand Disease (VWD) is the most common human inherited bleeding disorder due to a defect of Von Willebrand Factor (VWF), which a glycoprotein crucial for platelet adhesion to the subendothelium after vascular injury.
Diagnosis and treatment of von Willebrand disease in 2024 and …
Mar 13, 2024 · Diagnosis relies on the identification of a personal and family history of excessive mucocutaneous bleeding, and laboratory features consistent with quantitative and/or qualitative abnormalities of VWF. This review focuses on three aspects of VWD management, with current updates and a look into the future.
Laboratory assays of VWF activity and use of desmopressin trials …
Jun 23, 2022 · We systematically reviewed the accuracy of any von Willebrand factor (VWF) activity assay in the diagnosis and classification of patients for VWD. We searched Cochrane Central, MEDLINE, and EMBASE for eligible studies.