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Test Code LAB529 Progesterone, Plasma or Serum

Reporting Title

Progesterone

Methodology

Roche Diagnostics, Elecsys®/Electrochemiluminescence Immunoassay

Performing Laboratory

OhioHealth Laboratory Services - RMH and MH Core Laboratories

Specimen Requirements

Due to interference, patients receiving high doses of biotin (>5 mg/day) should wait at least 8 hours after dose before having blood drawn.

Collection Instructions:

1. Serum and Plasma gel tubes should be centrifuged within 2 hours of collection.

2. Red-top tubes should be centrifuged and aliquoted within 2 hours of collection.

 

 

Submit only 1 of the following specimens:

 

Preferred:

Serum

Draw blood in a gold-top serum gel tube(s). Spin down and send 1 mL of serum refrigerated.
Note:

1. A speckled-top serum gel tube (s) or a plain, red-top tube(s) is also acceptable.

2. Patients receiving therapy with mouse monoclonal antibodies may have erroneous results.

3. Indicate serum on request form.

4. Label specimen appropriately (serum).

 

Alternate: 

Plasma

Draw blood in a mint green-top (heparin) gel tube(s). Spin down and send 1 mL of heparinized plasma refrigerated.

Note:  1. Patients receiving therapy with mouse monoclonal antibodies may have erroneous results.

2. Indicate plasma on request form.

3. Label specimen appropriately (plasma).

 

Specimen Stability Information

Specimen Type Temperature Time
Serum or plasma Refrigerated 5 days
  Ambient   
  Frozen  6 months

 

Specimen Transport Temperature

Refrigerate/Ambient OK/Frozen OK

Reference Values

Roche

Males:  0-0.6 ng/mL

Nonpregnant females

Follicular phase:  0-1.5 ng/mL

Luteal phase:  2.3-25.0 ng/mL

Midluteal phase:  3.5-25.0 ng/mL

Postmenopausal:  0-0.7 ng/mL

Oral contraceptives:  0-0.4 ng/mL

Pregnant females

First trimester:  8.1-42.0 ng/mL

Day(s) Test Set Up

Monday through Sunday; Continuously

Test Classification and CPT Coding

84144