Test ID: FRT4
T4 (Thyroxine), Free, Serum
Secondary ID
A test code used for billing and in test definitions created prior to November 2011
NY State Approved
Indicates the status of NY State approval and if the test is orderable for NY State clients.
Useful For
Suggests clinical disorders or settings where the test may be helpful
The test generally is used as a second-line test after thyroid-stimulating hormone (TSH) to help evaluate TSH changes.
The free thyroxine value, combined with the TSH value, gives a more accurate picture of the thyroid status in patients with abnormal thyroid-binding globulin levels such as those who are pregnant or those who are receiving treatment with estrogens, androgens, phenytoin, or salicylates.
Testing Algorithm
Delineates situation(s) when tests are added to the initial order. This includes reflex and additional tests.
See Thyroid Function Ordering Algorithm in Special Instructions.
Special Instructions and Forms
Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test
Method Name
A short description of the method used to perform the test
Chemiluminometric Immunoassay
Reporting Name
A shorter/abbreviated version of the Published Name for a test; an abbreviated test name
Aliases
Lists additional common names for a test, as an aid in searching
Free Thyroxine
FT4, Serum
Non-Protein Bound Tetraiodothyronine
T4 Free, Serum
Thyroid Function Cascade ORDER 80683
Thyroxine, Free
Specimen Type
Describes the specimen type needed for testing
Specimen Required
Defines the optimal specimen. This field describes the type of specimen required to perform the test and the preferred volume to complete testing. The volume allows automated processing, fastest throughput and, when indicated, repeat or reflex testing.
Container/Tube:
Preferred: Red top
Acceptable: Serum gel
Specimen Volume: 0.5 mL
Forms: If not ordering electronically, submit a General Request Form (Supply T239) with the specimen.
Specimen Minimum Volume
Defines the amount of specimen required to perform an assay once, including instrument and container dead space. Submitting the minimum specimen volume makes it impossible to repeat the test or perform confirmatory or perform reflex testing. In some situations, a minimum specimen volume may result in a QNS (quantity not sufficient) result, requiring a second specimen to be collected.
Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected
| Hemolysis | Mild OK; Gross reject |
| Lipemia | NA |
| Icterus | NA |
| Other | NA |
Specimen Stability Information
Provides a description of the temperatures required to transport a specimen to the laboratory. Alternate acceptable temperature(s) are also included.
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Refrigerated (preferred) | 7 days |
| Frozen | 30 days | |
| Ambient | 8 hours |
Clinical Information
Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test
Free thyroxine comprises a small fraction of total thyroxine. The free T4 (FT4) is available to the tissues and is, therefore, the metabolically active fraction.
Elevations in FT4 cause hyperthyroidism, while decreases cause hypothyroidism.
Reference Values
Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.
0.8-1.8 ng/dL
Elevated values are seen in patients on thyroxine therapy.
Interpretation
Provides information to assist in interpretation of the test results
Elevated values suggest hyperthyroidism or exogenous thyroxine (T4).
Decreased values suggest hypothyroidism.
Free T4 works well to correct total T4 values for thyroid-binding globulin alterations, but may give misleading values when abnormal binding proteins are present or the patient has other major illnesses (Euthyroid Sick Syndrome).
Cautions
Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances
Heparin, free fatty acids, and autoantibodies to thyroxine (T4) can cause misleading values.
Phenytoin may interfere with free T4 levels due to competition with T4 for thyroid-binding globulin binding sites.
Clinical Reference
Provides recommendations for further in-depth reading of a clinical nature
1. Klee GG, Hay ID: Biochemical thyroid function testing. Mayo Clin Proc 1994;69:469-470
2. Klee GG, Hinz VS: The Ciba Corning ACS:180 Plus. In Immunoassay Automation: An Updated Guide to Systems. San Diego, CA, Academic Press, Inc., 1996, pp 63-102
Method Description
Describes how the test is performed and provides a method-specific reference
This is a chemiluminometric immunoassay. Free thyroxine (FT4) is measured using an automated, competitive, chemiluminescent immunoassay on the Advia: Centaur instrument. FT4 in the specimen competes with an acridinium ester-labeled analog of thyroxine (T4) for a limited amount of polyclonal rabbit anti-T4 antibody, which is covalently coupled to paramagnetic particles. An inverse relationship exists between the amount of FT4 in the patient specimen and the amount of relative light units detected by the system.(Package insert: Bayer Advia: Centaur. Bayer Diagnostics. East Walpole, MA)
Day(s) and Time(s) Test Performed
Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.
Monday through Friday, Sunday; 6 a.m.-3 p.m.
Analytic Time
Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.
Maximum Laboratory Time
Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result
Specimen Retention Time
Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded
Performing Laboratory Location
The location of the laboratory that performs the test
Test Classification
Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer's instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR), Investigation Use Only (IUO) product, or a Research Use Only (RUO) product.
CPT Code Information
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.
84439
LOINC® Code Information
Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the result codes returned for this test or profile.
| Result ID | Reporting Name | LOINC Code |
|---|---|---|
| FRT4 | T4 (Thyroxine), Free, S | 3024-7 |


