Androstenedione, ACTH Stimulation

Also known as: 17-Dione (Two Specimens), δ4-Androstene, 3

Clinical Use

Use

This test may involve significant risk and should be performed only by qualified personnel who are familiar with the test and who have taken adequate precautions to protect the safety of the patient. Every effort has been made to ensure accuracy in these recommendations, but clinicians must use their judgement and refer to specific pharmaceutical resources to determine appropriate drug dosages for their patients.

Special Instructions

Not provided.

Limitations

The test may not provide accurate results if specimens are not handled properly, such as using gel-barrier tubes, which can cause significant absorption and affect results. Factors such as time of day and recent glucocorticoid administration can influence androgen levels and result interpretation. Thus, sample consistency regarding these parameters is crucial for accurate assessments.

Test Details

Methodology

Mass Spectrometry

Biomarkers

Androstenedione

Analyte

Concentration / Level

Concentration / Level • Quantitative (Continuous) (e.g., copies/mL, % expression)

LOINC Codes

Order Codes

13857-8 - Androst 1h p 250 ug ACTH IM SerPl-mCnc
24407-9 - Androst BS SerPl-mCnc

Result Codes

24407-9 - Androst BS SerPl-mCnc
13857-8 - Androst 1h p 250 ug ACTH IM SerPl-mCnc

Result Turnaround Time

4-6 days

Specimen

Serum

Volume

1 mL (each specimen)

Minimum Volume

0.5 mL (each specimen)

Container

Red-top tube

Collection Instructions

Transfer separated serum to a plastic transport tube. Label each tube with the patient's name, collection time, and date. Submit specimens simultaneously on the same test request form.