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Test ID BLOD0106 Thyrotropin Receptor Antibody, Serum

Useful For

Recommended first-line test for detection of thyrotropin receptor antibodies

 

Differential diagnosis of etiology of thyrotoxicosis in patients with ambiguous clinical findings and/or contraindicated (eg, pregnant or breast-feeding) or nondiagnostic thyroid radioisotope scans

 

Diagnosing clinically suspected Graves disease (GD) (eg, extrathyroidal manifestation of GD include endocrine exophthalmos, pretibial myxedema, thyroid acropachy) in patients with normal thyroid function tests

 

Determining the risk of neonatal thyrotoxicosis in a fetus of a pregnant female with active or past active GD

 

Differential diagnosis of gestational thyrotoxicosis versus first trimester manifestation or recurrence of GD

 

Assessing the risk of GD relapse after antithyroid drug treatment

Specimen Type

Serum


Specimen Required


Patient Preparation:

1. For 12 hours before specimen collection. patient should not take multivitamins or dietary supplements (eg, hair, skin, and nail supplements) containing biotin (vitamin B7).

2. Patient should not be receiving heparin treatment.

Supplies: Sarstedt Aliquot Tube, 5 mL (T914)

Collection Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Submission Container/Tube: Plastic vial

Specimen Volume: 1 mL

Collection Instructions: Centrifuge and aliquot serum into a plastic vial.


Reject Due To

Gross hemolysis Reject
Gross lipemia OK
Gross icterus Reject

Specimen Minimum Volume

0.75 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 7 days
  Frozen  90 days

Day(s) Performed

Monday through Saturday

Report Available

1 to 3 days

Method Name

Electrochemiluminescence Immunoassay

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

83520

Reporting Name

Thyrotropin Receptor Ab, S

Reference Values

≤1.75 IU/L

Test Classification

This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

Forms

If not ordering electronically, complete, print, and send a General Request (T239) with the specimen.

Secondary ID

81797
Sanford Laboratories - Enterprise Additional Information:

SANFORD LABORATORY INTERFACE BUILD INFORMATION

Result Code  Result Code Description 
13100 Thyrotropin Receptor Ab, S