17-Hydroxyprogesterone

Overview

  • EPIC Code:
  • LAB720
  • Soft Test Code:
  • 17PRO
  • Send Out Test Code:
  • 17180
Alternate Names
  • 17-OHProgesterone
Clinical Significance

17-Hydroxyprogesterone is elevated in patients with Congenital Adrenal Hyperplasia (CAH). CAH is a group of autosomal recessive diseases characterized by a deficiency of cortisol and an excess of ACTH concentration. 17-Hydroxyprogesterone is also useful in monitoring cortisol replacement therapy and in evaluating infertility and adrenal and ovarian neoplasms.


Specimen Collection & Preparation

Specimen Requirements

0.5 mL Serum from a Red Top Tube in a Plastic Vial


Alternate Specimen

0.5 mL Plasma from a Lavender Top Tube - EDTA in a Plastic Vial 
or
0.5 mL Plasma from a Navy Blue Top Tube - EDTA in a Plastic Vial 
or
0.5 mL Plasma from a Green Top Tube - Li Heparin in a Plastic Vial  
or 
0.5 mL Plasma from a Green Top Tube - Na Heparin in a Plastic Vial


TransportAndStorage

48 hours Ambient
7 days Refrigerated (Transport)
2 years Frozen


Collection Instructions

Separate serum after clotting. Ship serum refrigerated or frozen


Minimum Volume

0.25 mL Serum


Neonatal Volumne

Clinical Interpretation

Reference Range:

Adult Male    
18-30 Years 32-307 ng/dL
31-40 Years 42-196 ng/dL
41-50 Years 33-195 ng/dL
51-60 Years 37-129 ng/dL
Adult Female    
Follicular Phase ≤185 ng/dL
Luteal Phase ≤285 ng/dL
Postmenopausal ≤45 ng/dL
Pregnancy    
  First Trimester 78-457 ng/dL
  Second Trimester 90-357 ng/dL
  Third Trimester 144-578 ng/dL
Pediatric    
1-12 Months 11-170 ng/dL
1-4 Years 4-115 ng/dL
5-9 Years ≤90 ng/dL
10-13 Years ≤169 ng/dL
14-17 Years 16-283 ng/dL
Infant    
Premature (31-35 Weeks) ≤360 ng/dL
Term (3 Days) ≤420 ng/dL
Tanner Stages    
II-III Male 12-130 ng/dL
II-III Female 18-220 ng/dL
IV-V Male 51-190 ng/dL
IV-V Female 36-200 ng/dL


Methodology:
  • Liquid Chromatography / Tandem Mass Spectrometry (LC-MS/MS)

Clinical Significance

17-Hydroxyprogesterone is elevated in patients with Congenital Adrenal Hyperplasia (CAH). CAH is a group of autosomal recessive diseases characterized by a deficiency of cortisol and an excess of ACTH concentration. 17-Hydroxyprogesterone is also useful in monitoring cortisol replacement therapy and in evaluating infertility and adrenal and ovarian neoplasms.


Production Schedule

Sites Performed
  • Quest - Chantilly
Days Performed
Sunday
Monday
Tuesday
Wednesday
Thursday
Friday
Saturday
Departments
  • Sendouts - Clinical
Turn Around Time

2 to 5 days


Coding & Compliance

CDM

01422803


CPT Coding

83498