Test Directory
| Test Code | |||
| TXGWB | |||
| Test Name | |||
| Toxoplasma gondii PCR, B | |||
| CPT Codes | |||
| 87798 | |||
| Expected Turnaround Time | |||
| 1 - 4 days | |||
| Clinical Utility | |||
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Useful for supporting the diagnosis of active toxoplasmosis, particularly in immunocompromised individuals. |
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| Specimen and Container Info | |||
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Specimen Type: Whole Blood Collection Container: Lavender Top (EDTA) Desired Specimen Volume: 1 mL |
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| Collection Instructions | |||
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| Processing and Submission Instructions | |||
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| Transport Instructions | |||
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Transport to the laboratory refrigerated. |
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| Stability Requirements | |||
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| Methodology | |||
| Polymerase Chain Reaction (PCR)/DNA Probe Hybridization | |||
| Reference Intervals | |||
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See patient report. |
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| Limitations | |||
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This assay is designed for use in patients with a clinical history and symptoms consistent with toxoplasmosis. This test should not be used to screen healthy patients. Blood may not be a sensitive specimen for detecting organ specific disease (eg, ocular or cerebral toxoplasmosis). In this case, other specimens (eg, ocular fluid, spinal fluid, fresh tissue) should be considered. Results should be interpreted with consideration of clinical and laboratory findings. A negative result does not indicate absence of disease. Reliable results depend on adequate specimen collection and the absence of inhibiting substances. |
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| Alternate Names | |||
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| Reference Lab | |||
| Mayo Clinic Laboratories | |||
| Testing Schedule | |||
| Routine, Monday - Saturday | |||
The American Medical Association (AMA) Current Procedural Terminology (CPT) codes published by HNL Lab Medicine are guidelines and are intended for informational purposes only. CPT coding is the exclusive responsibility of the billing entity. View the Terms.
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