Test Code PROG Progesterone
Additional Codes
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Cerner |
NextGen |
|
Progesterone |
Progesterone |
Methodology
Chemiluminescent Competitive Immunoassay
Patient Preparation
None
Collection Instructions
Standard phlebotomy practices.
Specimen Requirements
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Container |
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Stability |
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Rejection Criteria |
Gross Hemolysis Turbid Specimens |
Result Reporting and Reference Values
Reported in ng/mL
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Ovulatory Cycle: |
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|
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Normal Female follicular phase |
|
2.61 |
|
Normal Female Periovulatory phase |
|
5.86 |
|
Normal Female mid-luteal phase |
6.82 |
27.90 |
|
Normal Female luteal phase |
1.30 |
22.20 |
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Post Menopausal Female |
|
0.52 |
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Pregnant Females: |
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|
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1st Trimester (4-12 weeks gestation) |
3.85 |
35.70 |
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2nd Trimester (13-24 weeks gestation) |
15.3 |
|
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3rd Trimester (24-36 weeks gestation) |
39.8 |
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Normal Male |
|
0.79 |
Reflex Testing
None
Limitations
- Ortho reports a bias with the following:
- High Cholesterol can cause a negative bias
- High Lipids can cause a negative bias
- Low Protein can cause a negative bias
- Ortho reports no significant effect with the following:
- Bilirubin up to 40 mg/dL
- Hemoglobin up to 1000 mg/dL
Useful For
The main sites of progesterone production are the adrenal cortex, ovaries, and corpus luteum following ovulation and the placenta by the twelfth week of pregnancy. Circulating progesterone is bound to several serum proteins including albumin and corticosteroid binding globulin. Measurement of serum progesterone is useful in the investigation of ovarian function where disorders of ovulation are responsible for infertility in 15-20% of patients, and for predicting ovulation in induced cycles, where concentrations are generally higher than normal. Corpus luteum dysfunction is indicated by lower than normal progesterone concentrations.