Toxoplasma Antibody, IgM
Label Mnemonic: | TOXOM |
Epic code: | LAB8776 |
Downtime form: | Doctor/Provider Orders - Pathology Core and Specialty Care Nursery |
Chemistry
6240 RCP
356-3527
6240 RCP
356-3527
Specimen(s):
Plasma
Collection Medium:
![]() |
Plasma Separator Tube 4.5 mL |
Minimum:
3.0 mL whole blood from PST tube or TWO Microtainer devices
Testing Schedule:
24 hrs/day, 7 days a week, including holidays.
Turn Around
Time:
1 hour (upon receipt in laboratory)
Reference Range:
Negative
Interpretive Data:
Negative - Toxoplasma IgM antibodies were not detected. False
negatives can occur early in infection or in immunocompromised
patients.
Equivocal - Equivocal results: Toxoplasma IgM status not determined. If clinically indicated, obtain an additional specimen within 2-3 weeks.
Positive - Toxoplasma IgM antibodies detected which may indicate a current or recent infection. False positive results can occur. The results of the test must be taken within the context of the patient's clinical history, symptomology, and other laboratory findings.
Equivocal - Equivocal results: Toxoplasma IgM status not determined. If clinically indicated, obtain an additional specimen within 2-3 weeks.
Positive - Toxoplasma IgM antibodies detected which may indicate a current or recent infection. False positive results can occur. The results of the test must be taken within the context of the patient's clinical history, symptomology, and other laboratory findings.
Methodology:
Multiplex Flow Immunoassay
CPT Code:
86778
The results of this test should be taken within the context of the patient's clinical history, symptomatology, and other laboratory findings. This testing is not intended for use and screening blood or plasma donors. Performance characteristics have not been established for cord blood testing and neonates or for body fluids other than serum or plasma. Contaminated, icteric, lipemic, hemolyzed, or heat‑inactivated sera may cause erroneous results and should be avoided. Immune complexes or other immunoglobulin aggregates present in patient samples may cause increased non-specific findings and produce false positive results.