Post-Transplant, Toxoplasma gondii DNA, Qualitative Real-Time PCR, Serum

Test Code

18154

CPT Codes
87798

Preferred Specimen

1 mL serum

Minimum Volume

0.5 mL

Instructions

For shipper collection please see detailed instructions in Test Resources.

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

Room temperature: 48 hours
Refrigerated: 7 days
Frozen: 30 days

Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)

Hemolysis

Methodology
Real-Time Polymerase Chain Reaction

FDA Status
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.

Setup Schedule

Monday-Sunday Morning Report available: Next Day

Reference Range

Not detected

Clinical Significance

Toxoplasma gondii, an obligate intracellular parasite, is an important opportunistic pathogen of immunosuppressed patients and pregnant women. Real-time PCR methods are useful in identifying T. gondii in clinical specimens of immunosuppressed patients or in the amniotic fluid of mothers thought to be recently infected.

The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.