Specimen Collection Manual and Test Catalog
TOXOPLASMA GONDII DNA, QUALITATIVE REAL-TIME PCR
Geisinger Epic Procedure Code: LAB1287 Geisinger Epic ID: 53073Amniotic fluid, CSF, or tissue (preferred) OR serum, whole blood, plasma, amniotic fluid supernatant, or vitreous fluid
1 mL amniotic fluid, CSF, serum, whole blood, plasma, amniotic fluid supernatant (minimum 0.3 mL), 3 mm tissue or 0.2 mL vitreous fluid
Raw vitreous fluid specimens: Do not dilute collected specimen with additional saline.
Serum or plasma: Centrifuge and aliquot.
Refrigerated (cold packs).
Whole blood: Room temperature: 48 hours. Refrigerated: 7 days. Frozen: Unacceptable.
All other specimens: Room temperature: 48 hours. Refrigerated: 7 days. Frozen: 30 days.
Hemolyzed whole blood
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
The CPT codes provided by GML are based on AMA guidelines and are for informational purposes only.
Quest test code 34451, Tgon-QL PCR
Toxoplasma gondii, an obligate intracellular parasite, is an important opportunistic pathogen of immunosuppressed patients. In AIDS patients and transplant patients, this infection may result in a life-threatening encephalitis. T. gondii can also cause a fatal infection of the fetus if an infection is acquired during pregnancy. Fetal death or major abnormalities such as blindness and mental retardation may occur when infection is acquired during the first trimester. PCR methods may be useful in identifying T. gondii in CSF of immunosuppressed patients or in the amniotic fluid of mothers thought to be recently infected.