Download Unconjugated Estriol (e3) Test Visual Guide infographic (PNG)
Unconjugated Estriol (e3) is a laboratory test that measures a result in a Blood sample. It may be ordered to investigate symptoms, support a diagnosis or monitor a condition, depending on your clinician's advice.
The current booking price is shown at Rs. 307, inclusive of taxes where applicable.
No fasting is required for this test alone. If another test in the same order requires fasting, follow its preparation instructions. Home sample collection is available in serviceable cities. A trained phlebotomist collects the sample using sterile equipment, and the report is shared online after processing.
Reference ranges vary by laboratory and method. Use the range printed on your final report. The information below is educational only.
| Measure | Typical guide | Note |
|---|---|---|
| Result format | MoM or risk-adjusted value | Interpretation depends on pregnancy week and maternal factors. |
| Screen positive | Higher risk estimate | Screening is not a diagnosis. |
| Panel value | Best read together | Markers are interpreted as a combined risk screen. |
| Reason | Description |
|---|---|
| Pregnancy risk screening | Supports chromosomal or placental-risk assessment. |
| Placental function context | Some markers reflect placental growth or blood-vessel signalling. |
| Follow-up planning | May guide ultrasound or specialist follow-up. |
| Situation | Description |
|---|---|
| Pregnancy context | Used during a specific gestational window. |
| Risk context | Maternal age, ultrasound findings or prior pregnancy history. |
| Follow-up users | People under obstetric care. |
| Topic | Guidance |
|---|---|
| Fasting | No fasting is required for this test alone. If another test in the same order requires fasting, follow its preparation instructions. |
| Timing | Pregnancy week is critical. |
| Do not read alone | Use with ultrasound and obstetric risk calculation. |
| Interpretation | Screening result should be reviewed by the obstetrician. |
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Your sample is collected by a trained phlebotomist and sent to the partner laboratory for analysis. The laboratory processes the sample using its validated procedures and quality controls. Your final report shows the result, unit and reference range used for that test. Discuss an unexpected or abnormal result with your clinician.