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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