Maternal Screening, Sequential, Specimen #2, Alpha Fetoprotein, hCG, Estriol, and Inhibin A
Second-trimester screening test for trisomy 21 (Down syndrome), trisomy 18, and open neural tube defects. Requires a previously submitted first-trimester specimen, Maternal Screening, Sequential, Specimen #1, hCG, PAPP-A, NT (3000146). Also requires nuchal translucency measurement performed by an ultrasonographer certified by the Fetal Medicine Foundation (FMF) or Nuchal Translucency Quality Review (NTQR). Risks provided in both first and second trimesters.
Quantitative Chemiluminescent Immunoassay
Specimen must be drawn between 14 weeks, 0 days and 24 weeks, 6 days gestation. The recommended time for maternal serum screening is 16 to 18 weeks gestation.
Serum Separator Tube (SST) or Plain Red.
Separate from cells ASAP or within 2 hours of collection. Transfer 3 mL serum to an ARUP Standard Transport Tube. (Min: 1 mL)
Plasma. Hemolyzed specimens.
Requires that a previous first trimester specimen, Maternal Screening, Sequential, Specimen #1, hCG, PAPP-A, NT (ARUP test code 3000146), has been performed.
After separation from cells: Ambient: 72 hours; Refrigerated: 2 weeks; Frozen: 1 year (Avoid repeated freeze/thaw cycles.)
Refer to report.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Laboratory Developed Test (LDT)
This test is used to screen for fetal risk of Down syndrome (trisomy 21), trisomy 18, and Open Neural Tube Defect (ONTD, spina bifida).
|Component Test Code*||Component Chart Name||LOINC|
|0080267||MoM for DIA||35738-4|
|0080918||MoM for AFP||20450-3|
|0080920||Maternal Screen Interpretation||49586-1|
|0080924||Insulin Req Maternal Diabetes||44877-9|
|0080925||Family Hx Neural Tube Defect||8670-2|
|0080927||Number of Fetuses||11878-6|
|0080932||Maternal Age At Delivery||21612-7|
|0080943||MoM for uE3||20466-9|
|0081065||Nuchal Translucency (NT)||12146-7|
|0081068||MoM for PAPP-A||32123-2|
|0081069||Sonographer Certification #||49089-6|
|0081074||MoM for NT||49035-9|
|0081158||Family History of Aneuploidy||32435-0|
|3000166||Crown Rump Length||11957-8|
|3000168||Nuchal Translucency (NT), Twin B|
|3000169||MoM for NT, Twin B||49035-9|
|3000170||Crown Rump Length, Twin B||11957-8|
|3000174||EER Maternal Serum, Sequential, Spcm2||11526-1|
|3000261||Patient's hCG, 2nd Trimester||19080-1|
|3000262||hCG MoM, 2nd Trimester||20465-1|
|3000390||Gestational Age for Second Specimen||18185-9|
- Maternal Serum Sequential Screen
- second trimester screen
- Sequential Screening
- Serum Stepwise Sequential Screen
- Stepwise Maternal Screen
- Stepwise Sequential, Contingent