Antiphospholipid Syndrome Diagnostic Panel

Antiphospholipid Syndrome Diagnostic Panel

Test Code

19872
86147 (x3), 86146 (x3), 85730, 85613
CPT Code is subject to a Medicare Limited Coverage Policy and may require a signed ABN when ordering.
19872
86147 (x3), 86146 (x3), 85730, 85613
CPT Code is subject to a Medicare Limited Coverage Policy and may require a signed ABN when ordering.
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

Antiphospholipid Syndrome Diagnostic Panel - This assay may be useful in supporting or ruling out a diagnosis of antiphospholipid syndrome.

Test Resources

None found for this test
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Test Details

Includes

  • Cardiolipin Antibodies (IgA, IgG, IgM)
    Beta-2-Glycoprotein I Antibodies (IgG, IgA, IgM)
    Lupus Anticoagulant Evaluation with Reflex (PTT-LA and dRVVT with Reflex Confirmations)

    If PTT-LA Screen is prolonged (>40 seconds), then Hexagonal Phase Confirm is performed at an additional charge (CPT code(s): 85598).
    If Hexagonal Phase Confirm is positive or weakly positive, then Thrombin Clotting Time will be performed at an additional charge (CPT code(s): 85670).
    If dRVVT Screen is prolonged (>45 seconds), then dRVVT Confirmation will be performed at an additional charge (CPT code(s): 85597).
    If dRVVT Confirm is positive, then dRVVT 1:1 Mix will be performed at an additional charge (CPT code(s): 85613).

Methodology

Immunoassay (IA) • Photo-Optical Clot Detection

Reference Range(s)

See individual tests

LOINC® Codes, Performing Laboratory

Cardiolipin Antibodies (IgA, IgG, IgM)
Beta-2-Glycoprotein I Antibodies (IgG, IgA, IgM)
Lupus Anticoagulant Evaluation with Reflex (PTT-LA and dRVVT with Reflex Confirmations)

If PTT-LA Screen is prolonged (>40 seconds), then Hexagonal Phase Confirm is performed at an additional charge (CPT code(s): 85598).
If Hexagonal Phase Confirm is positive or weakly positive, then Thrombin Clotting Time will be performed at an additional charge (CPT code(s): 85670).
If dRVVT Screen is prolonged (>45 seconds), then dRVVT Confirmation will be performed at an additional charge (CPT code(s): 85597).
If dRVVT Confirm is positive, then dRVVT 1:1 Mix will be performed at an additional charge (CPT code(s): 85613).

Methodology

Immunoassay (IA) • Photo-Optical Clot Detection

Reference Range(s)

See individual tests

Preferred Specimen(s)

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

Minimum Volume

2 mL

Collection Instructions

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.

Transport Container

Transport tube

Transport Temperature

Frozen

Specimen Stability

  • Room temperature: Unacceptable
  • Refrigerated: Unacceptable
  • Frozen: 30 days

Reject Criteria

Hemolysis • Grossly lipemic • Received room temperature • Received refrigerated • Serum

Setup Schedule

3 mL frozen plasma collected in a 3.2% sodium citrate (light blue-top) tube
2 mL
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.
Transport tube
Frozen
Room temperature: Unacceptable
Refrigerated: Unacceptable
Frozen: 30 days
Hemolysis • Grossly lipemic • Received room temperature • Received refrigerated • Serum
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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