Toxoplasma gondii by PCR
Also known as: TOXOPCR
Use
This test is used to confirm toxoplasmosis infection in immunocompromised hosts as well as fetuses and newborns. It may also be used to confirm equivocal antibody testing results, providing a definitive diagnosis for patients at risk of severe complications from Toxoplasma gondii.
Special Instructions
This test is New York state approved. Specimen source is required when submitting samples. Ensure the correct type of specimen and compliance with preparation instructions to avoid rejection. Tissue samples should be frozen immediately after collection.
Limitations
A negative test result does not preclude the presence of Toxoplasma gondii DNA, as inhibitors or levels below the assay's detection limit may lead to undetectable concentrations. The test is a Laboratory Developed Test (LDT) and has not been cleared or approved by the FDA, though it is performed in a CLIA certified laboratory.
New York Approved
Methodology
PCR-based (PCR)
Biomarkers
LOINC Codes
- 31208-2
- 29904-0
Result Turnaround Time
1-5 days
Related Documents
For more information, please review the documents below
Specimen
Whole Blood
Volume
1 mL
Minimum Volume
0.5 mL
Container
Lavender (EDTA), pink (K2EDTA), or serum separator tube
Collection Instructions
Separate serum or plasma from cells and transfer to a sterile container. For tissue, transfer immediately to a sterile container and freeze.
Storage Instructions
Specimens should be stored and transported frozen.
Causes for Rejection
Heparinized specimens, tissues in optimal cutting temperature compound.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 8 hours |
| Refrigerated | 5 days |
| Frozen | 3 months |
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