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Test ID: VWPR    
von Willebrand Profile

Secondary ID A test code used for billing and in test definitions created prior to November 2011

83099

NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Useful For Suggests clinical disorders or settings where the test may be helpful

Detection of deficiency or abnormality of von Willebrand factor and related deficiency of factor VIII coagulant activity

 

Subtyping von Willebrand disease as Type 1 (most common), Type 2 variants (less common), or Type 3 (rare)

Profile Information A profile is a group of laboratory tests that are ordered and performed together under a single Mayo Test ID. Profile information lists the test performed, inclusive of the test fee, when a profile is ordered and includes reporting names and individual availability.

Test IDReporting NameAvailable SeparatelyAlways Performed
F8ACoag Factor VIII Activity Assay, PYesYes
VWAGvon Willebrand Factor Ag, PYesYes
VWFXvon Willebrand Factor Activity, PYesYes
CCC1InterpretationNoYes

Reflex Tests Lists test(s) that may or may not be performed, at an additional charge, depending on the result and interpretation of the initial test(s)

Test IDReporting NameAvailable SeparatelyAlways Performed
IBETHBethesda UnitsNoNo
F8ISCoag Factor VIII Assay Inhib Scrn,PNoNo
RISTRistocetin Cofactor, PNoNo
VWFMvon Willebrand Factor Multimer, PYes, (order #8844)No
CCC2Special Coagulation InterpretationNoNo

Testing Algorithm Delineates situation(s) when tests are added to the initial order. This includes reflex and additional tests.

Initial testing includes: coag factor VIII activity assay, von Willebrand factor (VWF) antigen, and VWF activity.  

If the factor VIII, VWF antigen, and VWF activity are normal, and VWF activity:VWF antigen ratio is > or =0.8, a computer-generated interpretive comment indicating no evidence of von Willebrand’s disease will be provided.

If VWF activity assay is <55%, VWF ristocetin cofactor activity assay will be performed. If VWF antigen is <55%, the VWF activity is <55%, or the VWF activity:VWF antigen ratio is <0.8, VWF multimer analysis will be performed.

If any test results are abnormal, all results will be reviewed by a coagulation consultant and a Special Coagulation Consultant Interpretation will be provided.

 

See von Willebrand Disease Profile in Special Instructions.

Special Instructions and Forms Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test

Method Name A short description of the method used to perform the test

F8A, F8IS, IBETH: Activated Partial Thromboplastin Time-Based Clotting Assay

VWAG: Automated Latex Immunoassay (LIA)

VWFX: Latex Particle Enhanced Immunoassay

RIST: Ristocetin Induced Aggregation of Washed Normal Platelets

VWFM: Agarose Gel Electrophoresis/Infrared Dye-Labeled Antibody Detection

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

von Willebrand Prof

Aliases Lists additional common names for a test, as an aid in searching

Coag
von Willebrand Profile