ESTRADIOL BY LCMSMS
$58.00
Also known as: E491, ESDPM Orderable Code: E491 Test Contains (LOINC): Estradiol (35384-7) Sample Type: Serum or Plasma Preferred Container: Serum Separator Tube (SST) Alternate Container: EDTA (Lavender Top) Tube or Heparin (Green Top) Tube…
Description
Also known as: E491, ESDPM
Orderable Code: E491
Test Contains (LOINC): Estradiol (35384-7)
Sample Type: Serum or Plasma
Preferred Container: Serum Separator Tube (SST)
Alternate Container: EDTA (Lavender Top) Tube or Heparin (Green Top) Tube
Sample Volume: 2.0 mL
Minimal Sample Volume: 0.5 mL (does not allow for repeat testing)
Handling Instructions
Collect specimen per tube manufacturer’s instructions. Centrifuge sample and separate serum or plasma from cells within 2 hours. Aliquot and refrigerate.
Specimen Stability: Ambient: 2 Days; Refrigerated: 7 Days; Frozen: 1 Month
Unsuitable Specimen: Grossly hemolyzed specimens
Frequency: Sunday, Monday, Tuesday, Wednesday, Thursday, Friday,Saturday
Expected Turn Around: 2 – 5 Days
Reference Range: Age and gender specific reference ranges will be applied per report
Referral Lab: SRL
Referral Lab Code: E491
CPT: 82670
Methodology: Liquid Chromatography/Tandem Mass Spectrometry (LC-MS/MS)
ADDITIONAL INFORMATION
Estrogens are steroids that are mainly produced in the ovaries and are crucial in the development and function of the female reproductive system. Synthesis of these steroids occurs via aromatase enzymatic activity from androgenic precursors. Measurement of estrogens is useful in diagnosing disorders of puberty, in identifying defects of sex-steroid metabolism, in monitoring low-dose hormone therapy, and in monitoring aromatase inhibitor therapy.
Ordering Recommendation: Useful in the diagnosis and workup of disorders of puberty, identifying defects in sex steroid metabolism, and in monitoring low-dose hormone therapy and aromatase inhibitor therapy.
Compliance Statement: This test was developed and its performance characteristics determined by Sonic Reference Laboratory (SRL). It has not been cleared or approved by the U.S. Food and Drug Administration (FDA). The FDA has determined that such clearance or approval is not necessary. This test is used for clinical purposes and should not be regarded as investigational or for research. SRL is qualified to perform high complexity testing under the Clinical Laboratory Improvement Amendments (CLIA).
AFFORDALAB™ of Wichita
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AFFORDALAB™ of Hays
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