17-Hydroxypregnenolone, Pre- and Post-ACTH Stimulation

TEST: 500770
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CPT: 84143(x2)
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Synonyms

  • 17-Hydroxypregnenolone (Two Specimens)
  • Pregnenolone, 17-Hydroxy (Two Specimens)

Special Instructions

Draw blood for baseline 17-OH pregnenolone. Inject cosyntropin 250 μg IM or IV (If IV, dilute cosyntropin in 2-5 mL of sterile saline and inject over two minutes). Draw blood for stimulated 17-OH pregnenolone 60 minutes after. See the online Endocrine Appendix: ACTH Stimulation for expected values for various steroids at baseline and after ACTH stimulation.

Expected Turnaround Time

7 - 12 days

Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.

Related Information

Related Documents

For more information, please view the literature below.

Adrenal Steroid Response to ACTH: Pediatrics

    Specimen Requirements

    Specimen

    Serum (preferred) or plasma, frozen

    Volume

    1 mL (each specimen)

    Minimum Volume

    0.4 mL (Note: This volume does not allow for repeat testing.)

    Container

    Red-top tube, gel-barrier tube, lavender-top (EDTA) tube, or green-top (heparin) tube

    Collection

    Transfer separated serum or plasma to a plastic transport tube. Note: Label each tube with patient's name, collection time, and date. Submit specimens simultaneously on the same test request form. To avoid delays in turnaround time when requesting multiple tests on frozen samples, please submit separate frozen specimens for each test requested.

    Storage Instructions

    Freeze

    Stability Requirements

    Temperature

    Period

    Refrigerated

    1 day

    Frozen

    2 years

    Causes for Rejection

    Non-EDTA/heparin plasma; recently administered isotopes

    Test Details

    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 involved. Every effort has been made to ensure accuracy in these recommendations, but clinicians must use their judgment and refer to specific pharmaceutical resources to determine appropriate drug dosages for their patients.

    Methodology

    High-pressure liquid chromatography (HPLC) tandem mass spectrometry

    LOINC® Map

    Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
    500770 17-OH Pregnenolone, ACTH Stim. 500771 17-OH Pregnenolone Baseline ng/dL 6765-2
    500770 17-OH Pregnenolone, ACTH Stim. 500772 17-OH Pregnenolone Stimulated ng/dL 13604-4

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