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HelpEPIC ORDER CODE LAB3788 Sequential Maternal Screening, Part 1, Serum
Additional Codes
SQ: SEQAM
MAYO: SEQA
Ordering Guidance
When part 1 is negative, part 2 must be completed in order to receive an interpretable result. If collecting a second-trimester specimen is expected to be difficult, order first-trimester screening instead (1STT1 / First Trimester Maternal Screen, Serum).
If a stand-alone neural tube defect risk assessment is desired, order MAFP1 / Alpha-Fetoprotein (AFP), Single Marker Screen, Maternal, Serum.
Additional Testing Requirements
Sequential maternal screening is a 2-part test that includes a first-trimester sample (this test) and a second-trimester sample (SEQB / Sequential Maternal Screening, Part 2, Serum).
Necessary Information
Approval to send specimen for first-trimester screening is required and may take up to 5 business days to complete. Nuchal translucency (NT) measurements are only accepted from NT-certified sonographers. Do not send specimen to Mayo Clinic Laboratories if the sonographer is not NT-certified or before completing the application process. See Maternal Screening: Sonographer Approval Process. Complete the NT/CRL Data for First Trimester/Sequential Maternal Screening.
Specimen Required
Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. The ultrasound and blood draw must be completed within a gestational window of 10 weeks, 0 days and 13 weeks, 6 days, which corresponds to a crown-rump length range of 31 to 80 mm.
2. Centrifuge and aliquot serum into a plastic vial within 2 hours of collection.
Forms
First Trimester/Sequential Maternal Screening Patient Information (T593) is required.
Useful For
First-trimester prenatal screening for trisomy 21 (Down syndrome) and trisomy 18 (Edwards syndrome)
Testing Algorithm
Sequential maternal screening is a 2-step test, with first- and second-trimester components. It requires a nuchal translucency measurement and blood collection in the first trimester. If the result from part 1 indicates a risk for Down syndrome that is higher than the screen cutoff, the screen is completed, and a report is issued. If the results from part 1 are negative, an additional blood collection in the second trimester is required (SEQB / Sequential Maternal Screening, Part 2, Serum). If the second specimen is not received for sequential screening, the results are uninterpretable, and no maternal risk will be provided.
For additional information see Sequential Maternal Serum Screening Testing Algorithm.
Special Instructions
Method Name
Immunoenzymatic Assay
Reporting Name
Sequential Maternal Screen, Part 1Specimen Type
SerumSpecimen Minimum Volume
0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Serum | Refrigerated (preferred) | 7 days | |
| Frozen | 90 days | ||
| Ambient | 7 days |
Reject Due To
| Gross hemolysis | Reject |
| Gross lipemia | OK |
| Gross icterus | OK |
Clinical Information
Maternal serum screening is used to identify pregnancies that may have an increased risk for certain birth defects, such as trisomy 21 (Down syndrome), neural tube defects (NTD) and trisomy 18. Various options for maternal serum screening are available and include: first trimester, second trimester, and cross-trimester. Sequential screening is a type of cross-trimester screening that has an improved detection rate as compared to either first- or second-trimester screening. Sequential screening combines biochemical and ultrasound markers (nuchal translucency: NT) measured in both trimesters of the pregnancy.
This test involves an ultrasound and a blood draw. The ultrasound measurement, referred to as the NT measurement, is difficult to perform accurately. Therefore, NT data is accepted only from NT-certified sonographers. Along with the NT measurement, a maternal serum specimen is collected to measure pregnancy-associated plasma protein A (PAPP-A). The results of the ultrasound measurement and blood work, along with the maternal age and demographic information, are used to calculate trisomy 21 (Down syndrome) and trisomy 18 risk estimates.
If the result from part 1 indicates a risk for Down syndrome that is higher than the screen cutoff, the screen is completed, and a report is issued. In that event, the patient is typically offered counseling and diagnostic testing. When the part 1 screen is completed, NTD risk is not provided. For a stand-alone NTD-risk assessment, order MAFP1 / Alpha-Fetoprotein (AFP), Single Marker Screen, Maternal, Serum.
If the risk from the first trimester is below the established cutoff, an additional serum specimen is collected in the second trimester for SEQB / Sequential Maternal Screen, Part 2, Serum. The blood specimen is tested for AFP, unconjugated estriol , human chorionic gonadotropin , and inhibin A. The information from both trimesters is combined and a report is issued. If results are positive, the patient is typically offered counseling and diagnostic testing.
NT:
The NT measurement, an ultrasound marker, is obtained by measuring the fluid-filled space within the nuchal region (back of the neck) of the fetus. While fetal NT measurements obtained by ultrasonography increase in normal pregnancies with advancing gestational age, Down syndrome and trisomy 18 fetuses have larger NT measurements than gestational age-matched normal fetuses. Increased fetal NT measurements can therefore serve as an indicator of an increased risk for Down syndrome and trisomy 18.
PAPP-A:
PAPP-A is a 187-kDa protein comprised of 4 subunits: 2 PAPP-A subunits and 2 pro-major basic protein subunits. PAPP-A is a metalloproteinase that cleaves insulin-like growth factor-binding protein-4 (IGFBP-4), dramatically reducing IGFBP-4 affinity for IGF1 and IGF2, thereby regulating the availability of these growth factors at the tissue level. PAPP-A is highly expressed in first-trimester trophoblasts, participating in regulation of fetal growth. Levels in maternal serum increase throughout pregnancy. Low PAPP-A levels before the fourteenth week of gestation are associated with an increased risk for Down syndrome and trisomy 18.
Reference Values
An interpretive report will be provided.
Interpretation
Maternal screens provide an estimation of risk, not a diagnosis. A negative result indicates that the estimated risk falls below the screen cutoff. A positive result indicates that the estimated risk exceeds the screen cutoff.
Trisomy 21 (Down Syndrome):
Second-trimester results are negative when the calculated risk is below 1/270 (0.37%). Negative results mean that the risk is less than the established cutoff; they do not guarantee the absence of Down syndrome.
Results are positive when the risk is greater than the established cutoff (ie, ≥1/50 in the first trimester and ≥1/270 in the second trimester). Positive results are not diagnostic.
When both sequential maternal screening parts 1 and 2 are performed with a screen cutoff of 1/270, the combination of maternal age, nuchal translucency (NT), pregnancy-associated plasma protein A , alpha-fetoprotein , unconjugated estriol , human chorionic gonadotropin , and inhibin A has an overall detection rate of approximately 90% with a false-positive rate of approximately 3% to 4%. In practice, both the detection rate and false-positive rate vary with maternal age.
Trisomy 18 (Edwards Syndrome):
In part 1, trisomy 18 results are only reported if the Down syndrome risk is positive.
In part 2, the screen cutoff for trisomy 18 is 1/100 (1%). Risks that are greater or equal to 1% are screen-positive; positive results are not diagnostic. Risks less than 1% are screen-negative; negative results do not guarantee the absence of trisomy 18.
Use caution when revising trisomy 18 positive results with earlier dating. Babies with trisomy 18 tend to be small, which can lead to underestimation of gestational age and an increased chance of missing a true-positive.
When sequential maternal screening parts 1 and 2 are performed, the overall detection rate is approximately 90% with a false-positive rate of approximately 0.1% using a screen cutoff of 1/100.
Neural Tube Defect:
Risk assessment for neural tube defects is only available after completion of part 2 of the sequential maternal screen. See SEQB / Sequential Maternal Screening, Part 2, Serum for details.
Follow-up:
Verify that all information used in the risk calculation is correct (maternal date of birth, gestational dating, etc). If any information is erroneous, contact the laboratory for a revision.
Screen-negative results typically do not warrant further evaluation.
If the results are positive, the patient is typically offered counseling, ultrasound, diagnostic testing, and possibly, referral to genetics counseling or a high-risk clinic.
Clinical Reference
1. Malone FD, Canick JA, Ball RH, et al: First-trimester or second-trimester screening, or both, for Down's syndrome. N Engl J Med. 2005 Nov 10;353(19):2001-2011
2. Prenatal Diagnostic Testing for Genetic Disorders. ACOG Practice Bulletin No. 163. American College of Obstetricians and Gynecologists. Obstet Gynecol. 2016 May;127(5):979-981. doi: 10.1097/AOG.0000000000001439
3. Wald NJ, Rodeck C, Hackshaw AK, et al: SURUSS in Perspective. Semin Perinatol. 2005 Aug;29(4):225-235
4. Palomaki GE, Steinort K, Knight GJ, et al: Comparing three screening strategies for combining first- and second-trimester Down syndrome markers. Obstet Gynecol. 2006 Feb;107(2 Pt 1):367-375
5. Palomaki GE, Neveux LM, Knight GJ, et al: Maternal serum-integrated screening for trisomy 18 using both first- and second-trimester markers. Prenat Diagn. 2003 Mar;23(3):243-247
6. Yarbrough ML, Stout M, Gronowski AM: Pregnancy and its disorders. In: Rifai N, Horvath AR, Wittwer CT, eds. Tietz Textbook of Clinical Chemistry and Molecular Diagnostics. 6th ed.. Elsevier; 2018:1655-1696
Method Description
This test includes measuring the nuchal translucency (NT) and pregnancy-associated plasma protein A (PAPP-A). The NT and PAPP-A are compared to median values for a given gestational age and a multiple-of-the-median (MoM) is calculated for each. The MoM results are entered into a multivariate algorithm that includes the mother's age to derive risk factors for Down syndrome and trisomy 18. If the calculated risks exceed the screen cutoff, the results are reported and the screen is ended. If the results from the first part of screening fall below the screen cutoff, the results are held until the second sample is analyzed. PAPP-A is performed on the Beckman Access using an automated immunoenzymatic assay with paramagnetic separation and chemiluminescent detection.(Unpublished Mayo method)
Day(s) Performed
Monday through Friday
Report Available
4 to 6 daysSpecimen Retention Time
14 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
84163
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| SEQA | Sequential Maternal Screen, Part 1 | 49086-2 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 29451 | Recalculated Maternal Serum Screen | 43995-0 |
| 601802 | Results Summary | 50679-0 |
| 29469 | Down Syndrome Screen Risk Estimate | 43995-0 |
| 29470 | Down Syndrome Maternal Age Risk | 49090-4 |
| 29471 | Trisomy 18 Screen Risk Estimate | 43994-3 |
| 29468 | PAPP-A | 48407-1 |
| 601799 | PAPP-A MoM | 76348-2 |
| NT1 | NT | 33069-6 |
| 601800 | NT MoM | 49035-9 |
| NTTB1 | NT Twin | 33069-6 |
| 601801 | NT Twin MoM | 49035-9 |
| 29472 | Interpretation | 49586-1 |
| 29474 | Recommended Follow Up | 80615-8 |
| 29473 | Additional Comments | 48767-8 |
| 29452 | Specimen Collection Date | 33882-2 |
| 29453 | Maternal Date of Birth | 21112-8 |
| 29890 | Calculated Age at EDD | 43993-5 |
| 29454 | Maternal Weight | 29463-7 |
| 29455 | Maternal Weight | 29463-7 |
| DIAB1 | Insulin Dependent Diabetes | 33248-6 |
| RACE_ | Patient Race | 32624-9 |
| SMKN2 | Current cigarette smoking status | 72166-2 |
| SNDT1 | Scan Date | 34970-4 |
| CRL1A | CRL | 11957-8 |
| CRL2A | CRL Twin | 11957-8 |
| 29891 | GA on Collection by U/S Scan | 11888-5 |
| FET1 | Number of Fetuses | 11878-6 |
| CHOR1 | Chorions | 92568-5 |
| IVF1 | IVF | 47224-1 |
| PRHIX | Prev Down (T21) / Trisomy Pregnancy | 53826-4 |
| PRNTA | Prev Pregnancy w/ Neural Tube Defect | 53827-2 |
| PTNTA | Patient or father of baby has a NTD | 53827-2 |
| INTL2 | Initial or repeat testing | 86955-2 |
| SONOM | Sonographer Name | 49088-8 |
| SNCD1 | Sonographer Code | No LOINC Needed |
| SONO1 | Sonographer Reviewer ID | 49089-6 |
| DRPH2 | Physician Phone Number | 68340-9 |
| 29487 | General Test Information | 62364-5 |