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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z # |
T-SPOT®.TB
Test Code38702
CPT Codes
86481<br>Restricted Client Code
Preferred Specimen
Adults and children ≥ 10 Years:
6 mL whole blood collected in Greiner 9 mL lithium heparin (green-top) tube
Pediatric 2-9 Years of Age:
4 mL whole blood collected in a Greiner 9 mL lithium heparin (green-top) tube
Pediatric < 2 Years of Age:
2 mL whole blood collected in a Greiner 9 mL lithium heparin (green-top) tube
Immunocompromised individuals
Adults and children ≥ 10 Years:
9 mL whole blood collected in a Greiner 9 mL lithium heparin (green-top) tube
6 mL whole blood collected in Greiner 9 mL lithium heparin (green-top) tube
Pediatric 2-9 Years of Age:
4 mL whole blood collected in a Greiner 9 mL lithium heparin (green-top) tube
Pediatric < 2 Years of Age:
2 mL whole blood collected in a Greiner 9 mL lithium heparin (green-top) tube
Immunocompromised individuals
Adults and children ≥ 10 Years:
9 mL whole blood collected in a Greiner 9 mL lithium heparin (green-top) tube
Instructions
Collect blood by venipuncture into a Quest-provided Greiner 9 mL lithium heparin (green-top) tube. The tube contents must be inverted (8-10 times) to ensure that the whole blood is mixed thoroughly with the anticoagulant. Specimens must be shipped in accordance to the pre-approved logistics process established for your site. Samples received >39 hours after collection will be rejected. Date and time of draw are required and must be provided.
Note: *****This is a short stability test and requires special handling. Please see above for special collection instructions. If you have any questions, please contact Customer Service 1-800-336-3718 option 1.*****
Note: *****This is a short stability test and requires special handling. Please see above for special collection instructions. If you have any questions, please contact Customer Service 1-800-336-3718 option 1.*****
Transport Container
See instructions
Transport Temperature
Room temperature
Specimen Stability
Room temperature: 39 hours
Refrigerated: Unacceptable
Frozen: Unacceptable
Refrigerated: Unacceptable
Frozen: Unacceptable
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Anticoagulants other than lithium heparin or sodium heparin • Hemolyzed • Centrifuged • Samples received > 32 hours after collection • Samples not received in TSPOT ®.TB insulated shipper • Frozen or refrigerated samples
Methodology
Enzyme-Linked Immunosorbent Assay
Setup Schedule
Set up: Daily; Report available: Next day
Reference Range
See Laboratory Report
Clinical Significance
The T-SPOT®.TB test is an in vitro diagnostic test for the detection of effector T cells that respond to stimulation by Mycobacterium tuberculosis antigens ESAT-6 and CFP 10 by capturing interferon gamma (IFN-y) in the vicinity of T cells in human whole blood collected in lithium heparin. It is intended for use as an aid in the diagnosis of M. tuberculosis infection. The T-SPOT.TB test is an indirect test for M. tuberculosis infection (including disease) and is intended for use in conjunction with risk assessment, radiography and other medical and diagnostic evaluations.