ADAMTS13 Activity with Reflex to Inhibitor

Message

If the vWF Protease Activity result is < or = 40, vWF Protease Inhibitor will be performed at an additional charge (CPT: 85335).

SRHC Clients:

Outpatients:  Send patient to SRHC laboratory for collection due to processing and stability requirements

Inpatients:

 

  • 1 light blue top tube (3.2% Sodium Citrate)
  • Must be processed for platelet poor plasma and frozen within 1 hour of collection
  • Send to SRHC laboratory immediately for processing

 


 



Test Code
LAB70003


Quest Code
145328


Alias/See Also
ADAMTS
ADAMTS-13


CPT Codes
85397

Includes
If the ADAMTS13 Activity result is ≤0.30 IU/mL, then ADAMTS13 Inhibitor will be performed at an additional charge (CPT: 85335).


Preferred Specimen
1 mL frozen plasma collected in a 3.2% sodium citrate (light blue-top) tube


Minimum Volume
0.5 mL


Instructions
Please submit a separate, frozen vial for each special coagulation assay ordered. Draw blood in a light blue-top tube containing 3.2% sodium citrate, mix gently by inverting 3-4 times. Centrifuge 15 minutes at 1500 g within one hour of collection. Using a plastic pipette, remove plasma, taking care to avoid the WBC/platelet buffy layer and place into a plastic vial. Freeze immediately and transport on dry ice.


Transport Container
Transport tube


Transport Temperature
Frozen


Specimen Stability
Room temperature: Unacceptable
Refrigerated: Unacceptable
Frozen: 21 days


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Gross hemolysis • Grossly lipemic • Grossly icteric


Methodology
Immunoassay (IA)

Setup Schedule
Set up: Sun-Fri; Report available: 2-4 days


Reference Range
ADAMTS13 Activity 0.68-1.63 IU/mL
  ADAMTS13 Inhibitor <0.4 BEU


Clinical Significance
ADAMTS-13 is a zinc metalloprotease that cleaves ultra large vWF multimers. Studies have shown that low levels of ADAMTS-13 activity are associated with thrombotic thrombocytopenic purpura (TTP), a life-threatening hematological condition characterized by a low platelet count, microvascular thrombi, red cell fragmentation, and renal complications. Congenital TTP is a rare inherited disease caused by mutations within the ADAMTS-13 gene, which result in the production of non-functional protein. The acquired form of TTP is an autoimmune-like disorder caused by the development of autoantibodies to ADAMTS-13 that inhibits enzyme activity.


Performing Laboratory
Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly, VA 20153




The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.