Test Code Progest Progesterone Level
Patient Preparation
No special patient preparation required
Collection Method
Venous collection
Minimum Volume
- Adults: 1 ml
- Pediatric: 0.8 mL
Container
Lt Green / Plasma Separator / Lithium Heparin
Preferred Specimen
Light Green Top (lithium heparin) plasma
Acceptable Specimens
Serum:
- Gold Top SST
- Red Top
Plasma:
- Light Geen Top (Lithium heparin)
- Purple or Pink Top(K2/K3 EDTA)
Reference or Target Ranges
Female | Follicular Phase | 0.20 – 1.50 ng/mL |
Ovulation Phase | 0.80 – 3.00 ng/mL | |
Luteal Phase | 1.70 – 27.00 ng/mL | |
Post-meopausal | 0.10 – 0.80 ng/mL | |
Oral Contraceptive | 0.20 – 8.11 ng/mL | |
Pregnancy | First Trimester | 11.00 – 44.30 ng/mL |
Second Trimester | 25.4 – 83.30 ng/mL | |
Third Trimester | 58.70 – 214.00 ng/mL | |
Male | 0.20 – 1.40 ng/mL |
Reportable Units
ng/mL
Critical Value
Not defined for this assay
Reasons for Rejection
<!-- Rejection-->
Hemolysis Threshold | 1000 mg/dL |
Icterus Threshold | 54 mg/dL |
Lipemia Threshold | 200 mg/dL |
Other | QNS, contaminated, improperly Labeled, improper specimen type |
Specimen Stability
<!-- Stability -->
Ambient | 1 day |
Refrigerated (4°C to 8°C) | 5 days |
Frozen(-40°C to 0°C) | 6 months |
Performance Information
<!-- Performance information -->
Days and Time Performed | 24/7 |
Expected Turn Around Time | Expedited: 2 hours Routine: 4 hours |
Stat Availability | No |
Performing Bench | WCH Chemistry |
Methodology/Method Description | Roche Cobas – Competition principle |
CPT Codes
84144