Test Code AFPA Alpha-Fetoprotein, Amniotic Fluid
Reporting Name
Alpha Fetoprotein, AFUseful 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.
Method Name
AFPA: Immunoenzymatic Assay
ACHE_: Polyacrylamide Electrophoresis
Performing Laboratory
Mayo Clinic Laboratories in RochesterSpecimen Type
Amniotic FldNecessary 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
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Container/Tube: Plain, plastic, screw-top tube
Specimen Volume: 0.75 mL
Collection Instructions: Do not centrifuge.
Specimen 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.Special Instructions
Reference Values
< 2.0 multiples of median (MoM)
Day(s) Performed
Monday through Friday
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 |
Clinical Information
Alpha-fetoprotein (AFP) is a single polypeptide chain glycoprotein with a molecular weight of approximately 70,000 Da. Synthesis of AFP occurs primarily in the liver and yolk sac of the fetus. It is secreted in fetal serum, reaching a peak at approximately 13 weeks gestation, after which it rapidly declines until about 22 weeks gestation and then gradually declines until term. Transfer of AFP into maternal circulation is accomplished primarily through diffusion across the placenta. Maternal serum AFP levels rise from the normal non-pregnancy level of 0.20 ng/mL to about 250 ng/mL at 32 weeks gestation.
If the fetus has an open neural tube defect, AFP is thought to leak directly into the amniotic fluid, causing unexpectedly high concentrations of AFP. Other fetal abnormalities such as omphalocele, gastroschisis, congenital kidney disease, and esophageal atresia; and other fetal distress situations such as threatened abortion, prematurity, and fetal demise, may also show AFP elevations. Decreased amniotic fluid AFP values may be seen when gestational age has been overestimated.
Specimen Retention Time
2 weeksTest 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.Report Available
2 to 19 daysForms
Second Trimester Maternal Screening Alpha-Fetoprotein / Quad Screen Patient Information (T595) is required.