17-Hydroxyprogesterone Quantitative by HPLC-MS/MS, Serum or Plasma
Ordering Recommendation
Methodology
Quantitative High Performance Liquid Chromatography-Tandem Mass Spectrometry
Performed
Sun-Sat
Reported
1-4 days
New York DOH Approval Status
Specimen Required
Serum Separator Tube (SST). Also acceptable: Plain Red, Pink (K2EDTA), Plasma Separator Tube (PST), Green (Sodium Heparin), or Green (Lithium Heparin).
Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.3 mL)
Frozen. Also acceptable: Refrigerated.
Grossly hemolyzed specimens.
After separation from cells: Ambient: 3 Days; Refrigerated: 1 week; Frozen: 6 months
Reference Interval
Effective August 19, 2013
Age |
Female |
Male |
---|---|---|
Premature (26-28 weeks) | 124-841 ng/dL | 124-841 ng/dL |
Premature (29-35 weeks) | 26-568 ng/dL | 26-568 ng/dL |
Full term Day 3 | 7-77 ng/dL | 7-77 ng/dL |
4 days-30 days | 7-106 ng/dL | Less than 200 ng/dL |
1 month-2 months | 13-106 ng/dL | Less than 200 ng/dL |
3 months-5 months | 13-106 ng/dL | 3-90 ng/dL |
6 months-1 year | Less than or equal to 148 ng/dL | Less than or equal to 148 ng/dL |
2-3 years | Less than or equal to 256 ng/dL | Less than or equal to 228 ng/dL |
4-6 years | Less than or equal to 299 ng/dL | Less than or equal to 208 ng/dL |
7-9 years | Less than or equal to 71 ng/dL | Less than or equal to 63 ng/dL |
10-12 years | Less than or equal to 129 ng/dL | Less than or equal to 79 ng/dL |
13-15 years | 9-208 ng/dL | 9-140 ng/dL |
16-17 years | Less than or equal to 178 ng/dL | 24-192 ng/dL |
18 years and older | Less than 207 ng/dL | Less than 139 ng/dL |
Follicular | 15-70 ng/dL | Does Not Apply |
Luteal | 35-290 ng/dL | Does Not Apply |
Tanner Stage I | Less than or equal to 74 ng/dL | Less than or equal to 62 ng/dL |
Tanner Stage II | Less than or equal to 164 ng/dL | Less than or equal to 104 ng/dL |
Tanner Stage III | 13-209 ng/dL | Less than or equal to 151 ng/dL |
Tanner Stage IV-V | 7-170 ng/dL | 20-173 ng/dL |
Interpretive Data
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)
Note
Hotline History
CPT Codes
83498
Components
Component Test Code* | Component Chart Name | LOINC |
---|---|---|
0092332 | 17-Hydroxyprogesterone, HPLC-MS/MS | 1668-3 |
Aliases
- 17-OHP
- 17a
- 17a-OH
- Hydroxyprogesterone
- Progesterone