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Test Code AVWPQ von Willebrand Disease Profile Interpretation


Specimen Required


 


Useful For

Interpretation of testing performed as part of a profile for detection of deficiency or abnormality of von Willebrand factor (VWF) and related deficiency of factor VIII coagulant activity

 

Interpretation of testing performed as part of a profile for subtyping von Willebrand disease (VWD) as type 1 (most common), type 2 variants (less common), or type 3 (rare)

 

This test is not useful for detection of hemophilia carriers.

 

This test is not useful for differentiating type 2A versus 2B VWD or platelet-type VWD (pseudo-VWD).

Method Name

Only orderable as a reflex. For more information see AVWPR / von Willebrand Disease Profile, Plasma.

 

Medical Interpretation

Reporting Name

von Willebrand Disease Interp

Specimen Type

Plasma Na Cit

Specimen Stability Information

Specimen Type Temperature Time Special Container
Plasma Na Cit Frozen 14 days

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject
Gross icterus Reject

Reference Values

Only orderable as part of a profile. For more information see AVWPR / von Willebrand Disease Profile, Plasma.

 

An interpretive report will be provided.

Day(s) Performed

Monday through Friday

Report Available

7 to 12 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

85390-26 Special Coagulation Interpretation

LOINC Code Information

Test ID Test Order Name Order LOINC Value
AVWPQ von Willebrand Disease Interp 48595-3

 

Result ID Test Result Name Result LOINC Value
603179 Reviewed by 18771-6
603186 von Willebrand Disease Interp 48595-3

NY State Approved

Yes

Test Classification

Not Applicable