Test Code ESTRCC Estradiol
Reference Values
Healthy Men: 0-39.8 pg/ml
Healthy Women:
Follicular phase 19.5-144.2 pg/mL
Mid cycle phase 63.9-356.7 pg/mL
Luteal Phase 55.8-214.2 pg/mL
Postmenopausal 0-32.2 pg/mL
Healthy Pregnant Women:
1st trimester 154.0-3243.0 pg/mL
2nd trimester 1561.0-21280.0 pg/mL
3rd trimester 8525.0->30000.0 pg/mL
Day(s) Test Performed
Tuesday and Friday
Specimen Requirement
Serum
Draw blood in a gold-top (serum separator) gel tube. Label the specimen with the patient’s name (first and last), date of birth, date and time of draw, phlebotomist’s initials, and as serum. Spin down and send 1 mL of serum refrigerated.
Specimen stability:
20 hours at room temperature when spun
2 days at 2-8°C
≤ -20°C for longer storage
Minimum volume: 0.5 mL
Specimen rejection criteria: High doses of biotin will affect this assay
CPT Codes
82670
Method
Electrochemiluminesence immunoassay
Useful For
All applications that require moderately sensitive measurement of estradiol:
- Evaluation of hypogonadism and oligo-amenorrhea in females
- Assessing ovarian status, including follicle development, for assisted reproduction protocols
- In conjunction with lutenizing hormone measurements, monitoring of estrogen replacement therapy in hypogonadal premenopausal women
- Evaluation of feminization, including gynecomastia, in males
- Diagnosis of estrogen-producing neoplasms in males, and to a lesser degree, females
- As part of the diagnosis and work-up of precocious and delayed puberty in females, and to a lesser degree, males
- As part of the diagnosis and work-up of suspected disorders of sex steroid metabolism, eg, aromatase deficiency and 17 alpha-hydroxylase deficiency
- As an adjunct to clinical assessment, imaging studies and bone mineral density measurement in the fracture risk assessment of postmenopausal women, and to a lesser degree, men
- Monitoring low-dose female hormone replacement therapy in post-menopausal women
- Monitoring antiestrogen therapy (eg, aromatase inhibitor therapy)