Quantitative High Performance Liquid Chromatography/Tandem Mass Spectrometry
New York DOH Approval Status
Serum separator tube. Also acceptable: Plain red, pink (K2EDTA), plasma separator tube, green (sodium heparin), or green (lithium heparin).
Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.3 mL)
Refrigerated. Also acceptable: Frozen.
Grossly hemolyzed specimens.
After separation from cells: Ambient: Unacceptable; Refrigerated: 1 week; Frozen: 6 months
Reference ranges for 17-Hydroxyprogesterone following stimulation are not well defined, and are dependent on the stimulation method utilized.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Laboratory Developed Test (LDT)
|Component Test Code*||Component Chart Name||LOINC|
|2009479||17-Hydroxyprogesterone 30min, HPLC-MS/MS|