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Tetanus Antibody Post IgG

Test Code: 921
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Clinical Utility

A common method for evaluating suspected antibody deficiency is to immunize the patient with an appropriately selected vaccine, such as Tetanus, and determine vaccine-specific antibody concentrations in a serum sample 3-4 weeks post-immunization compared to a pre-immunization sample.

Procedure

Tetanus Toxoid is used as a solid phase antigen in a sensitive microtiter EIA. Calibrators are referenced to the antitoxin reference preparation 76/589. The recommended protective level is greater than or equal to 0.10 IU/mL. This test has not been cleared or approved for diagnostic use by the U.S. Food and Drug Administration.

2-3 business days from receipt of specimen

Specimen Type Order Code CPT Code NY Approved Volume Assay Range Special Instructions
serum 921 86774 Yes

1 mL (min. 500 uL)

0.01-7.0 IU/mL

  • Collect 1 mL, ambient, no special shipping requirements.

Specimens are approved for testing in New York only when indicated in the Specimen Information field above.

The CPT codes provided are based on Viracor Eurofins' interpretation of the American Medical Association's Current Procedural Terminology (CPT) codes and are provided for general informational purposes only. CPT coding is the sole responsibility of the billing party. Questions regarding coding should be addressed to your local Medicare carrier. Viracor Eurofins assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.

References

Smith TF J Resp Dis 1989;10: 12-29

Shapiro G. et al. Pediatrics 1991; 87: 311-316

Halsey, J. F. et al. J Allergy and Clin Immunol (abstr),1992;89:272

Siber G, et al Ped Infect. Dis. Journal 1989;8:S84-S91

Popa V, Kim K, Heiner D. Annals of Allergy 1993; 70:418 - 424.

Kilpatrick DC. Transfusion Medicine 2002; 121: 335-351.

Akira S et al. Nature Immunol 2002; 2: 675-680.

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