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, SSpecimen Type
SerumSpecimen 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 daysSpecimen Retention Time
3 monthsPerforming 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.