Ordering Recommendation

New York DOH Approval Status

This test is not New York state approved. There are no New York state-approved laboratories available. Submit a Non-Permitted Laboratory Request Form (NPL) to the NYDOH prior to collection of specimen. If NPL is approved by NYDOH, and sample is received at ARUP, testing will be performed.

Specimen Required

Patient Preparation

Patient should not be on any corticosteroid, ACTH, estrogen, or gonadotropin medications, if possible, for at least 48 hours prior to collection of specimen.

Collect

24-hour urine. No special preservatives required.

Specimen Preparation

Mix specimen well. Refrigerate during collection. Transfer 10 mL aliquot of urine to ARUP Standard Transport Tubes. (Min: 5 mL) Submit total volume.
Test is not performed at ARUP; separate specimens must be submitted when multiple tests are ordered.

Storage/Transport Temperature

Frozen. On dry ice is preferred. Separate specimens must be submitted when multiple tests are ordered.

Unacceptable Conditions
Remarks
Stability

Ambient: 1 hour; Refrigerated: 4 days; Frozen: 6 months

Methodology

Quantitative Radioimmunoassay

Performed

Varies

Reported

7-10 days

Reference Interval

By report

Interpretive Data



Compliance Category

Performed by non-ARUP Laboratory

Note

Hotline History

N/A

CPT Codes

83498

Components

Component Test Code* Component Chart Name LOINC
0098378 Urine 17-Hydroxyprogesterone 1670-9
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

17-Hydroxyprogesterone, Urine

Interscience