Thyroglobulin, Serum or Plasma with Reflex to LC-MS/MS or CIA

2006685
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Additional Technical Information

Ordering Recommendation

Recommended test for the surveillance of residual/recurrent thyroid cancer. Accurately measures thyroglobulin levels in serum or plasma.

Mnemonic

THYROGRFX

Methodology

Quantitative Chemiluminescent Immunoassay/High Performance Chromatography-Tandem Mass

Performed

Sun-Sat

Reported

1-7 days

New York DOH Approval Status

This test is New York DOH approved.

Specimen Required

Patient Preparation
Collect

Serum Separator Tube (SST). Also acceptable: Green (Sodium or Lithium Heparin).

Specimen Preparation

Transfer 3 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 1.5 mL)

Storage/Transport Temperature

Frozen.

Unacceptable Conditions

EDTA or K2EDTA plasma. Grossly lipemic samples. Any fluid other than noted above. (See Thyroglobulin, Fine Needle Aspiration (FNA) (ARUP test code 0020753) for ordering alternate fluids).

Remarks
Stability

After separation from cells: Ambient: 8 hours; Refrigerated: 1 week; Frozen: 6 months

Reference Interval

Test Number
 Components
 Reference Interval
  Thyroglobulin Antibody 0.0-4.0 IU/mL
  Thyroglobulin, Serum or Plasma
Age
 ng/mL
6 months - 3 years 7.4-48.7
4-7 years 4.1-40.5
8-17 years 0.8-29.4
18 years and older 1.3-31.8

  Thyroglobulin by LC-MS/MS, Serum/Plasma
Age ng/mL
6 months - 3 years 7.4-48.7
4-7 years 4.1-40.5
8-17 years 0.8-29.4
18 years and older 1.3-31.8

Interpretive Data

Specimens negative for thyroglobulin antibodies (TgAb) are tested for thyroglobulin (Tg) by chemiluminescent immunoassay (CIA) using the Beckman Coulter Access DxI method. Specimens with TgAb results above the upper reference limit are tested for Tg by high-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS). Results obtained with different test methods or kits cannot be used interchangeably. Tg results, regardless of concentration, should not be interpreted as absolute evidence for the presence or absence of papillary or follicular thyroid cancer. Tg testing is not recommended for use as a screening procedure to detect the presence of thyroid cancer in the general population.

Lower limit of detection for Thyroglobulin by LC-MS/MS is 0.5 ng/mL.

Compliance Category

FDA

Note

The reflex testing method (CIA or LC-MS/MS) is determined by the TgAb result. Additional charges apply.

Hotline History

View Hotline History

 

Hotline History

Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
05/16/2022
X
N/A

CPT Codes

86800; if reflexed, add 84432

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Components

Component Test Code* Component Chart Name LOINC
0050105 Thyroglobulin Antibody 8098-6
0070420 Thyroglobulin, Serum or Plasma 3013-0
2007078 Thyroglobulin by LC-MS/MS, Serum/Plasma 3013-0
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

  • Anti Thyroglobulin Antibody
  • HTG
  • Human Thyroglobulin
  • TATC
  • Tg
  • Thyroglobulin
  • Thyroglobulin Antibody
  • Thyroglobulin Assay for Thyroid Cancer
  • Thyroglobulin HTC
Thyroglobulin, Serum or Plasma with Reflex to LC-MS/MS or CIA