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Test Code LABFDXM Dexamethasone, Serum

Additional Codes

Test Name in EPIC

EPIC Test Code

Mnemonic

Mayo Test ID

Dexamethasone LABFDXM DEXA DEXA

 


Ordering Guidance


For synthetic glucocorticoid analyte screen, order SGSS / Synthetic Glucocorticoid Screen, Serum.



Specimen Required


Supplies: Sarstedt Aliquot Tube, 5 mL (T914)

Collection Container/Tube:

Preferred: Red top

Acceptable: Serum gel

Submission Container/Tube: Plastic vial

Specimen Volume: 0.5 mL serum

Collection Instructions:

1. Draw blood between 7:30 a.m. and 9:00 a.m. the morning following an evening dose.

2. Within 2 hours of collection, centrifuge and aliquot serum into a plastic vial and freeze immediately. Do not send in original tube.

3. Send frozen.


Useful For

Measuring dexamethasone concentrations in serum

 

Ensuring that dexamethasone concentrations are adequate when performing dexamethasone suppression testing

 

Confirming the cause of secondary adrenal insufficiency

 

This test is not useful as the sole basis for diagnosis or treatment decisions.

Method Name

Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)

Reporting Name

Dexamethasone, S

Specimen Type

Serum

Specimen Minimum Volume

Serum: 0.25 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Frozen (preferred) 28 days
  Refrigerated  14 days
  Ambient  72 hours

Reject Due To

Gross hemolysis OK
Gross lipemia OK
Gross icterus OK

Clinical Information

The primary use of this test is to ensure that dexamethasone concentrations are adequate for interpretation of cortisol concentrations following the overnight dexamethasone administration. Suboptimal dexamethasone concentrations may be seen when absorption of dexamethasone is impaired, when metabolism of dexamethasone is accelerated due to concomitant medications, or when instructions for taking or timing of dexamethasone are not followed.

 

Overnight dexamethasone suppression testing is a standard-of-care endocrine test for assessment of mild autonomous cortisol secretion in adrenal tumors or for evaluation of endogenous hypercortisolism (Cushing syndrome) of any kind (ectopic, pituitary, adrenal). Consensus guidelines recommend concomitant measurement of dexamethasone and cortisol to minimize the risk of false-positive results when performing dexamethasone suppression testing.(1)

 

An additional potential application of this test is to aid in the assessment of secondary adrenal insufficiency.

 

Synthetic glucocorticoids are widely used and have an important clinical utility both as anti-inflammatory and immunosuppressive agents. The medical use of these agents, as well as their surreptitious use, can sometimes lead to a confusing clinical presentation. Patients exposed to these steroids may present with clinical features of Cushing syndrome but with suppressed cortisol and corticotropin concentrations, ie, hypothalamus-pituitary-adrenal axis suppression. This test provides measurements of dexamethasone, a commonly used glucocorticoid. The synthetic glucocorticoid screen measures a broader spectrum of synthetic glucocorticoids and would be the recommended test when exogenous glucocorticoid exposure is suspected; see SGSS / Synthetic Glucocorticoid Screen, Serum.

Reference Values

Baseline: <30 ng/dL

8:00 a.m. following 1 mg Dexamethasone, previous evening: >100 ng/dL

8:00 a.m. following 8 mg Dexamethasone, (4 x 2 mg doses) previous day: >800 ng/dL

Interpretation

This test will screen for, and quantitate if present, the synthetic glucocorticoid, dexamethasone.

 

The presence of this synthetic glucocorticoid in serum indicates the current or recent use of this compound.

Cautions

Lack of detection does not preclude use of dexamethasone because adrenal suppression may persist for some time after the exogenous steroid is discontinued.

Method Description

Deuterated dexamethasone is added to serum as an internal standard. Dexamethasone and the deuterated internal standard are extracted from the specimens and analyzed by liquid chromatography tandem mass spectrometry (LC-MS/MS).(Unpublished Mayo method)

Day(s) Performed

Tuesday, Thursday

Report Available

2 to 10 days

Specimen Retention Time

3 months

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

80299

LOINC Code Information

Test ID Test Order Name Order LOINC Value
DEXA Dexamethasone, S 14062-4

 

Result ID Test Result Name Result LOINC Value
609439 Dexamethasone, S 14062-4

Forms

If not ordering electronically, complete, print, and send a Therapeutics Test Request (T831) with the specimen.