First-line test for identifying visceral T. gondii infection. CDC suggests equivocal or positive results should be retested using a different assay from another reference laboratory specializing in toxoplasmosis testing (IgG dye test, IgM ELISA, reflex to avidity and/or other tests).
Semi-Quantitative Chemiluminescent Immunoassay
Within 24 hours
New York DOH Approval Status
Serum Separator Tube (SST).
Allow specimen to clot completely at room temperature. Separate from cells ASAP or within 2 hours of collection. Transfer 2 mL serum to an ARUP Standard Transport Tube. (Min: 0.5 mL) Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens.
Plasma or urine. Contaminated, heat-inactivated or grossly hemolyzed specimens.
Label specimens plainly as "acute" or "convalescent."
After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles)
|0050770||Toxoplasma gondii Antibody, IgG||Effective March 3, 2014
|0050557||Toxoplasma gondii Antibody, IgM||
Refer to report.
This test should not be used for blood donor screening, associated re-entry protocols, or for screening Human Cell, Tissues and Cellular and Tissue-Based Products (HCT/P).
|Component Test Code*||Component Chart Name||LOINC|
|0050557||Toxoplasma gondii Ab, IgM||8040-8|
|0050770||Toxoplasma gondii Ab, IgG||8039-0|
- CMV Antibody IgM
- HSV 1 and/or 2 Abs, IgM by ELISA’ TORCH IgM panel
- Rubella Antibody IgM
- Toxoplasma gondii Ab, IgM