Sign in →

Test Code LABPAIG Platelet Associated Antibodies, Direct Assay

Important Note

Support the diagnosis of autoimmune thrombocytopenia (AITP).

Specimens must be analyzed within 48 hours of collection. Required amount of blood may be dependent on platelet count.

 

Additional Codes

Test Name in EPIC EPIC Test Code Mnemonic ARUP Test ID
Platelet Associated Antibodies, Direct Assay LABPAIG PAIG 0095614

 

Methodology

Qualitative Flow Cytometry

Specimen Requirements

Collect
Lavender (EDTA) or pink (K2EDTA).

Specimen Preparation
Transport 4 mL whole blood. (Min: 1 mL)

Storage/Transport Temperature
CRITICAL ROOM TEMPERATURE.

Unacceptable Conditions
Clotted, hemolyzed, frozen, or refrigerated specimens. Specimens older than 48 hours.

Remarks
Specimens must be analyzed within 48 hours of collection. Required amount of blood may be dependent on platelet count.

Specimen Transport Temperature

Stability
Ambient: 48 hours; Refrigerated: Unacceptable; Frozen: Unacceptable

 

 

Performing Laboratory

ARUP Laboratories

500 Chipeta Way

Salt Lake City, Utah 84108

Test Classification and CPT Coding

Component Test Code* Component Chart Name              LOINC
0095612                         Platelet Antibodies Direct, IgG    29497-5
0095613                         Platelet Antibodies Direct, IgM    29498-3

CPT 86023 x 2

Interpretive Data

Negative (IgG & IgM): No excess antibodies were associated with the patient's platelets. An immune cause of thrombocytopenia is unlikely.
Positive (IgG and/or IgM): An increase in platelet associated immunoglobulin is noted. An immune cause of thrombocytopenia should be considered. However, many conditions can result in an increase in platelet associated antibodies; for example, IgM rheumatoid factor antibodies.
Strong Positive (IgG and/or IgM): A definite increase in platelet associated immunoglobulin is noted and an immune cause of thrombocytopenia should be considered. However, many conditions can result in an increase in platelet associated antibodies; for example, IgM rheumatoid factor antibodies.

This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.


Compliance Category
Analyte Specific Reagent (ASR)

Note:  More information
Detection of platelet-associated IgG and/or IgM may be used to separate thrombocytopenia of immune origin from nonimmune origin. Most patients with ITP have abnormally high levels of IgG associated with their platelets. Occasionally patients will have normal IgG levels but abnormally high levels of IgM. Dual staining and flow cytometric analysis ensures that only platelets are analyzed and relatively small volumes of blood are required. This assay does not distinguish between autoantibodies and alloantibodies, nor does it identify specific types of antiplatelet antibodies, such as those against HPA-1a.

 

 

Performed and Reported

Performed Reported
Sunday-Saturday 2-3 days