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Mycobacterium tuberculosis Complex, PCR, Non-Respiratory
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Test Code
MTBNON
CPT Codes
87556
Preferred Specimen
1 mL CSF, gastric lavage, pericardial fluid, peritoneal fluid, pleural fluid, synovial fluid, abscess fluid or urine collected in a sterile, plastic leak-proof container or whole blood collected in an EDTA lavender top tube. Also acceptable 2 grams fresh (unfixed) tissue collected in a sterile, plastic leak-proof container or with a small amount of saline with no fixatives or preservatives or 0.5 mL vitreous (eye) fluid.
Minimum Volume
0.5 mL, 2 grams tissue, 0.2 mL vitreous fluid
Other Acceptable Specimens
0.5 mL vitreous (eye) fluid in a sterile leak-proof container
Instructions
Gastric lavage: Sterile leak-proof container. Must be neutralized with sodium bicarbonate within 4 hours of collection and store refrigerated.
Tissue: Fresh (unfixed) tissue submitted in a sterile, plastic, leak-proof container or Fresh (unfixed) tissue in a sterile plastic leak-proof container with a small amount of saline with no fixatives or preservatives and store refrigerated or frozen.
Tissue: Fresh (unfixed) tissue submitted in a sterile, plastic, leak-proof container or Fresh (unfixed) tissue in a sterile plastic leak-proof container with a small amount of saline with no fixatives or preservatives and store refrigerated or frozen.
Transport Temperature
Vitreous (eye) fluid: Frozen
All other samples: Refrigerated (cold packs)
All other samples: Refrigerated (cold packs)
Specimen Stability
Room temperature: 48 hours
Refrigerated: 14 days
Frozen: 30 days
Vitreous (eye) fluid must be frozen
Refrigerated: 14 days
Frozen: 30 days
Vitreous (eye) fluid must be frozen
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Sputum, specimen received in formalin and/or alcohol, processed/concentrated specimen from client; swabs, formalin-fixed paraffin-embedded tissue, culture isolates, non-neutralized gastric lavage
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. This test should not be used for diagnosis without confirmation by other medically established means.
Setup Schedule
Set up: Daily; Report available: 1-3 days
Reference Range
Not detected
Clinical Significance
Used to aid the physician in the rapid diagnosis and treatment of a possible tuberculosis infection.
Performing Laboratory
Quest Diagnostics Nichols Institute |
33608 Ortega Highway |
San Juan Capistrano, CA 92675-2042 |
Last Updated: April 2, 2024