Toxoplasma gondii, Molecular Detection, PCR, Blood
Use
Supporting the diagnosis of active toxoplasmosis, particularly in immunocompromised individuals. Detection of T gondii DNA by PCR on blood may confirm or support serologic testing results; however, blood may not be sensitive for organ‑specific disease such as ocular or cerebral toxoplasmosis, so other specimens such as ocular fluid, spinal fluid, or fresh tissue should be considered.
Special Instructions
Not provided.
Limitations
This assay is designed for use in patients with a clinical history and symptoms consistent with toxoplasmosis and should not be used to screen healthy patients. A negative result does not exclude disease, especially for organ‑specific involvement; blood may not be a sensitive specimen, and results depend on adequate collection and absence of interfering substances.
New York Approved
Methodology
PCR-based (PCR)
Biomarkers
LOINC Codes
- 16279-2 - T gondii DNA Bld Ql NAA+probe
- 16279-2 - T gondii DNA Bld Ql NAA+probe
Result Turnaround Time
1-4 days
Related Documents
For more information, please review the documents below
Specimen
Whole Blood
Volume
1 mL
Minimum Volume
0.3 mL
Container
Lavender top (EDTA)
Collection Instructions
Send whole blood specimen in original tube. Do not aliquot.
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 7 days |
| Frozen | 7 days |