Platelet Antibody, Indirect (IgG)

Test Code

91805

CPT Code(s)

86022

Test Code

91805

CPT Code(s)

86022

In-home collection is not available in your area through Quest Mobile.

Clinical Significance

Platelet Antibody, Indirect (IgG) - The identification of circulating platelet antibodies is useful in order to identify immune-mediated platelet destruction. Disorders associated with immune platelet destruction include isoimmune neonatal thrombocytopenia, drug induced thrombocytopenia, drug sensitivities, allergies and post transfusion purpura. The destruction is either autoimmune, where a malfunction in the immune response results in the production of antibodies directed against 'self' platelet specific antigens; or else platelet destruction occurs when the patient received platelet-specific antibodies from an outside source such ...

Test Resources

None found for this test
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Test Details

Methodology

Flow Cytometry (FC)

Assay Category

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

Negative

Alternative Name(s)

Platelet Associated Antibody,Flow,Platelet-Bound Platelet Antibody,Platelet Bound Antibody

LOINC® Codes, Performing Laboratory

Service Area must be determined

Methodology

Flow Cytometry (FC)

Assay Category

Reference Range(s)

Negative

Alternative Name(s)

Platelet Associated Antibody,Flow,Platelet-Bound Platelet Antibody,Platelet Bound Antibody

LOINC® Codes, Performing Laboratory

Service Area must be determined

Preferred Specimen(s)

2 mL serum

Minimum Volume

1 mL

Collection Instructions

Collect 5 mL whole blood in a serum separator tube (SST) and separate serum before submitting

Transport Container

Transport tube

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

Room temperature: Unacceptable
Refrigerated: 21 days
Frozen: Unacceptable

Reject Criteria

Hemolysis • Lipemia • Icteric • Anticoagulant samples

Setup Schedule

Service Area must be determined

Preferred Specimen(s)

2 mL serum

Minimum Volume

1 mL

Collection Instructions

Collect 5 mL whole blood in a serum separator tube (SST) and separate serum before submitting

Transport Container

Transport tube

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

Room temperature: Unacceptable
Refrigerated: 21 days
Frozen: Unacceptable

Reject Criteria

Hemolysis • Lipemia • Icteric • Anticoagulant samples

Setup Schedule

Service Area must be determined

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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