17-OH Progesterone, LC/MS, Eight Specimens
Use
The 17-OH Progesterone, LC/MS, Eight Specimens test is used to assess adrenal gland function and to evaluate conditions such as congenital adrenal hyperplasia (CAH). This test monitors the level of 17-OH progesterone, a steroid hormone involved in the biosynthesis of other important hormones, which can provide insights into various hormonal imbalances and disorders. The test is particularly significant for diagnosing and managing conditions that affect hormone production, balancing adrenal functions, and guiding appropriate treatment plans.
Special Instructions
This panel requires multiple specimens to be collected at different time points. It includes an initial baseline specimen, followed by others after administering a treatment like medication or glucola. It is essential to coordinate with the clinician before use, ensuring that it is appropriate for the patient. Do not use this panel unless a sequential collection is needed post-treatment.
Limitations
The test is not FDA cleared or approved; it is developed and its performance characteristics determined by LabCorp. Interpretation of the results should consider patient-specific factors and may require follow-up testing for confirmation or further investigation. Variability in collection times and insufficient specimen volumes can affect the accuracy of results. Adherence to specified collection and treatment protocols is crucial for reliable outcomes.
Methodology
Mass Spectrometry
Biomarkers
LOINC Codes
- 27996-8
- 46963-5
- 51680-7
- 12716-7
- 12717-5
- 12718-3
- 12719-1
- 51679-9
- 51681-5
Result Turnaround Time
3-7 days
Related Documents
For more information, please review the documents below
Specimen
Whole Blood
Volume
Not provided
Minimum Volume
Not provided
Collection Instructions
Refer to the Endocrine Appendix of the LabCorp Directory for instructions on multiple specimen testing. Specimens must be collected at specified intervals following treatment administration.
Causes for Rejection
Deviation from the collection protocol, improper labeling, or inadequate volume.