Epic Code LAB1230502 Anti-Mullerian Hormone (AMH)
Interface Order Alias
1230502
Ordering Instructions
Samples for AMH levels should be drawn on days 2-4 of the menstrual cycle
Collection Instructions
Specimen Collection: Blood
Container(s): Red top (plain, no additive) or Gold top (serum separator-SST Gel)
Preferred Volume to Collect: 2.0 mL
Minimum Volume to Collect: 1.0 mL
Neonate Volume to Collect: 1.0 mL
Capillary collect ok? Yes
Microtainer acceptable: Yes
Collection Instructions:
- Samples for AMH levels should be drawn on days 2-4 of the menstrual cycle
- Gently invert red or gold tube(s) 8 - 10 times to mix clot activator with blood.
- Specimen should be processed within 30 minutes – See Processing Instructions.
Processing Instructions (Laboratory, Outpatient or Off-site collection)
Processed Specimen: Serum
Centrifuge/Spin: Yes
Aliquot: Yes
Processing Instructions:
- When tubes are clotted (30 minutes), centrifuge specimens.
- Pour serum into aliquot tubes and refrigerate.
Transport Temperature: Refrigerate
Specimen Stability
Ambient: 8 hours
Refrigerate: 72 hours
Frozen: Freeze for longer storage
Laboratory Retention: 72 hours
Test Frequency
Available daily, usual TAT 1 day
Reference Range
Female
- 20 up to 25 Years: 1.22 - 11.40 ng/mL
- 25 up to 30 Years: 0.89 - 9.85 ng/mL
- 30 up to 35 Years: 0.58 - 8.13 ng/mL
- 35 up to 40 Years: 0.15 - 7.49 ng/mL
- 40 up to 45 Years: 0.03 - 5.47 ng/mL
This testing was designed for assessment of ovarian reserve in females ages 20-44. Reference range values for male patients or for female patients <20 years or >44 years have not been established in this laboratory. AMH values must be interpreted in conjunction with other clinical and laboratory findings. This testing is not intended to be used for monitoring of controlled ovarian stimulation or as a tumor marker for diagnosis or monitoring of AMH-secreting tumors.
Performing Department
Chemistry
Performing Department Laboratory Location
Corewell Health Reference Laboratory, Grand Rapids, MI
Methodology
Method is Roche cobas Electrochemiluminescense Immunoassay.
Patient results determined by assays using different manufacturers for methods may not be comparable.
CPT
83516
CDM Code
3018351615
Epic Test ID
1230102124
LOINC
Not available
Mayo Access Code
Not available
Reviewed Date
3/7/2024
Updated Date
3/14/2024 - Reference Range