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Toxoplasma gondii Antibody, IgM (8000100329)
Test Mnemonic:
Specimen Requirements:
Collection:

Serum separator tube (SST) 
Container:

Serum separator tube (SST)
Minimum Volume:

1mL of serum
Storage/Transport:

Refrigerate (2-8°C) up to 7 days; Samples should be frozen (<-20°C)
Specimen Preparation:

Within 2 hours of collection, centrifuge 
Stability:

Refrigerate (2-8°C) up to 7 days; Samples should be frozen (<-20°C)
Causes for Rejection:

Insufficient quantity, gross hemolysis, lipemia, specimen container unlabeled or labeled incorrectly, no date or time of collection on order. 
Reference Range:

Negative
Turnaround Time:

Test performed daily, Sunday through Friday
Methodology:

Multiplex bead immunoassay
Performed:

Clinical Microbiology
Synonyms:

Toxoplasma antibody, IgM, TOXOM
Clinical Indication:

Screen for TOXO antibodies, IgM
Patient Preparation :

Routine venipuncture
CPT 4 Code:

86778
Note:

Negative - No anti-Toxoplasma gondii IgM detected. A negative IgM result may be due to delayed seroconversion and does not rule out current infection.

Equivocal - A second sample should be sent.

Positive - Indicative of a current or recent infection with Toxoplasma gondii.  False positive results may occur.   The results of the test must be taken within the context of the patient's clinical history, symptomology, and other laboratory findings.

For additional information, refer to the CDC website (https://www.cdc.gov/dpdx/toxoplasmosis/index.html) or to PAMF website (http://www.pamf.org/serology).
When ordering tests for which Medicare or Medicaid reimbursement will be sought, physicians should only order tests that are medically necessary for the diagnosis or treatment of the patient. Components of the organ or disease panels may be ordered individually. The diagnostic information must substantiate all tests ordered and must be in the form of an ICD-10 code or its verbal equivalent.
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