Test Code AFPA Alpha-Fetoprotein, Amniotic Fluid
Necessary Information
The following information is required:
1. Estimated due date by ultrasound
2. Collection date
3. Gestational age must be between 13 and 24 weeks; 16 to 18 weeks preferred.
If not ordering electronically, provide information on Second Trimester Maternal Screening Alpha-Fetoprotein / Quad Screen Patient Information (T595) and send with specimen.
Specimen Required
Container/Tube: Amniotic fluid container
Specimen Volume: 0.75 mL
Collection Instructions: Do not centrifuge.
Forms
Second Trimester Maternal Screening Alpha-Fetoprotein / Quad Screen Patient Information (T595) is required.
Useful For
Screening for open neural tube defects or other fetal abnormalities
Follow-up testing for patients with elevated serum alpha-fetoprotein results or in conjunction with cytogenetic testing
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
ACHE_ | Acetylcholinesterase, AF | Yes | No |
Testing Algorithm
If alpha-fetoprotein is positive, then acetylcholinesterase will be performed at an additional charge.
Special Instructions
Method Name
AFPA: Immunoenzymatic Assay
ACHE_: Polyacrylamide Electrophoresis
Reporting Name
Alpha Fetoprotein, AFSpecimen Type
Amniotic FldSpecimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Amniotic Fld | Refrigerated (preferred) | 7 days | |
Ambient | 7 days |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
< 2.0 multiples of median (MoM)
Day(s) Performed
Monday through Friday
Report Available
2 to 19 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
82106
82013 (if appropriate)
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
AFPA | Alpha Fetoprotein, AF | 58735-2 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
6739 | Collection Date | 58734-5 |
DAT15 | EDD by US Scan | 11781-2 |
6740 | Last Menstrual Period (LMP) | 8665-2 |
24233 | EDD by LMP | 11779-6 |
24239 | GA at Collection by Scan | 11888-5 |
24240 | GA at Collection by Dates | 11885-1 |
24234 | GA Used | 21299-3 |
9950 | Alpha Fetoprotein, AF | 1832-5 |
24241 | Results | 29595-6 |
24235 | Interpretation | 59462-2 |
24236 | Additional Comments | 48767-8 |
24237 | Follow up | 80615-8 |
24238 | General Test Info | 48767-8 |