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Estrone, by Tandem Mass Spectrometry
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Rarely indicated. If serum estrone measurement is needed, preferred test is Estrogens, Fractionated by Tandem Mass Spectrometry (0093248).
Quantitative High Performance Liquid Chromatography-Tandem Mass Spectrometry
Sun-Sat
1-4 days
Serum separator tube, lavender (EDTA), pink (K2EDTA), or green (sodium or lithium heparin).
Separate serum or plasma from cells within 2 hours of collection. Transfer 0.5 mL serum or plasma to an ARUP Standard Transport Tube. (Min 0.3 mL)
Refrigerated.
After separation from cells: Ambient: 48 hours; Refrigerated: 1 week; Frozen: 1 month
| Reference Intervals for Estrone-Children |
||
|---|---|---|
| Tanner Stages: I II III IV and V |
Males less than 7.0 pg/mL less than 11.0 pg/mL 1.0-31.0 pg/mL 2.0-30.0 pg/mL |
Females less than 27.0 pg/mL 1.0-39.0 pg/mL 8.0-117.0 pg/mL 4.0-109.0 pg/mL |
| Age Group 7-9 10-12 13-15 16-17 |
Males less than 7.0 pg/mL less than 11.0 pg/mL 1.0-30.0 pg/mL 1.0-32.0 pg/mL |
Females less than 20.0 pg/mL 1.0-40.0 pg/mL 8.0-105.0 pg/mL 4.0-133.0 pg/mL |
| Reference Intervals for Estrone-Adults |
|
|---|---|
| Females 18 Years and Older |
Males 18 Years and Older |
| Premenopausal: Early Follicular: less than 150.0 pg/mL Late Follicular: 100.0-250.0 pg/mL Luteal: less than 200.0 pg/mL |
9.0-36.0 pg/mL |
| Postmenopausal: 3.0-32.0 pg/mL | |
Compliance Statement B: For laboratory developed tests not using a RUO kit, and for FDA approved, cleared or 510(k) exempt assays with alterations. This test was developed and its performance characteristics determined by ARUP Laboratories. The U. S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.
82679
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 0093249 | Estrone by TMS | 2258-2 |
- Estrone (E1)
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