Factor VIII Inhibitor Panel

Factor VIII Inhibitor Panel

Test Code

40083
85240, 85335
40083
85240, 85335
Not offered in Quest Diagnostics Nichols Institute (IFD) – San Juan Capistrano. Please provide SERVICE AREA INFORMATION to find available tests you can order.
In-home collection is not available in your area through Quest Mobile.

Clinical Significance

Factor VIII Inhibitor Panel - The presence of alloantibodies against factor VIII activity is a complication of treatment in hemophilia A, while the presence of autoantibodies may develop spontaneously in patients with acquired Factor VIII-C deficiency. The presence of Factor VIII inhibitor may lead to the neutralization (inactivation) of transfused or endogenous Factor VIII activity. The detection and magnitude of Factor VIII inhibitor is of great importance in the care of these patients. Factor VIII inhibitor Chromogenic assay provides a quick method for the detection of Factor VIII inhibitor with less sample volume.

Test Details

Includes

  • Factor VIII Inhibitor, Chromogenic Screen
    Factor VIII Activity, Clotting

    If Factor VIII Inhibitor, Chromogenic Screen is Positive, then Nijmegen Assay will be performed at an additional charge (CPT code(s): 85335).

Methodology

Chromogenic • Photometric Clot Detection

Reference Range(s)

Factor VIII Inhibitor, Chromogenic ScreenNegative
Factor VIII Activity, Clotting50-180 % normal

Alternative Name(s)

FVIII Bethesda Inhibitor,Factor VIII Inactivity, Inhibitor APTT,Factor 8 Inhibitor Evaluation

LOINC® Codes, Performing Laboratory

Factor VIII Inhibitor, Chromogenic Screen
Factor VIII Activity, Clotting

If Factor VIII Inhibitor, Chromogenic Screen is Positive, then Nijmegen Assay will be performed at an additional charge (CPT code(s): 85335).

Methodology

Chromogenic • Photometric Clot Detection

Reference Range(s)

Factor VIII Inhibitor, Chromogenic ScreenNegative
Factor VIII Activity, Clotting50-180 % normal

Alternative Name(s)

FVIII Bethesda Inhibitor,Factor VIII Inactivity, Inhibitor APTT,Factor 8 Inhibitor Evaluation

Preferred Specimen(s)

2 mL plasma collected in 3.2% sodium citrate (light blue-top) in each of two separate tubes

Minimum Volume

1 mL (x2)

Collection Instructions

Submit a total of 4 mL (2 mL in each of 2 tubes).
Centrifuge light blue-top tube 15 minutes at approximately 1500 g within 60 minutes of collection. Using a plastic pipette, remove plasma, taking care to avoid the WBC/platelet buffy layer and place into a plastic vial. Centrifuge a second time and transfer platelet-poor plasma into a new plastic vial. Plasma must be free of platelets (<10,000/mcl). Freeze immediately and ship on dry ice.

Note: Storage of whole blood at refrigerated temperatures prior to processing may lead to cryoprecipitate formation and falsely low Factor VIII and von Willebrand Factor studies.

Transport Container

Transport tube(s)

Transport Temperature

Frozen

Specimen Stability

  • Room temperature: Unacceptable
  • Refrigerated: Unacceptable
  • Frozen: 14 days

Reject Criteria

Hemolysis • Received room temperature • Received refrigerated • Received thawed

Setup Schedule

2 mL plasma collected in 3.2% sodium citrate (light blue-top) in each of two separate tubes
1 mL (x2)
Submit a total of 4 mL (2 mL in each of 2 tubes).
Centrifuge light blue-top tube 15 minutes at approximately 1500 g within 60 minutes of collection. Using a plastic pipette, remove plasma, taking care to avoid the WBC/platelet buffy layer and place into a plastic vial. Centrifuge a second time and transfer platelet-poor plasma into a new plastic vial. Plasma must be free of platelets (<10,000/mcl). Freeze immediately and ship on dry ice.

Note: Storage of whole blood at refrigerated temperatures prior to processing may lead to cryoprecipitate formation and falsely low Factor VIII and von Willebrand Factor studies.
Transport tube(s)
Frozen
Room temperature: Unacceptable
Refrigerated: Unacceptable
Frozen: 14 days
Hemolysis • Received room temperature • Received refrigerated • Received thawed
Not offered in Quest Diagnostics Nichols Institute (IFD) – San Juan Capistrano. Please provide SERVICE AREA INFORMATION to find available tests you can order.
In-home collection is not available in your area through Quest Mobile.
Test Details

Clinical Significance

Test Resources

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.

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