Test Code FMSI1 Maternal Serum Screening, Integrated, Specimen #1, PAPP-A, NT
Additional Codes
LIS Code |
FMSI1 |
Epice Code |
LAB3325 |
Mayo Code |
FFMSS |
Specimen Required
Specimen #1 collection must occur between 10 weeks, 0 days and 13 weeks, 6 days gestation. (If gestational age is based on Crown-Rump length (CRL), the specimen must be collected when the CRL is between 32.4 - 83.9 mm)
Draw blood in a plain red-top tube(s), serum gel tube is acceptable. Spin down and send 0.5 mL serum refrigerated in a plastic vial.
Separate from cells ASAP or within 2 hours of collection.
Note:
Submit with order: Patient's date of birth, current weight, number of fetuses present, patient's race, if the patient was diabetic at the time of conception, if there is a known family history of neural tube defects, if the patient has had a previous pregnancy with a trisomy, if the patient is currently smoking, if the patient is taking valproic acid or carbamazepine (Tegretol), if this is a repeat sample, and the age of the egg donor if in vitro fertilization.
In addition to the above:
If a NT measurement is performed: the date of ultrasound, the CRL measurement, the nuchal translucency (NT) measurement and the name and certification number of the sonographer is required. NT must be measured when the CRL is between 38-83.9mm.
Or
If no NT measurement is performed: a due date or CRL measurement with the date of ultrasound is required.
The NT measurement must also be performed by an ultrasonographer that is certified by one of the following agencies: Fetal Medicine Foundation (FMF) or Nuchal Translucency Quality Review (NTQR).
Useful For
Helpful to identify pregnancies at increased risk of having a child with Down Syndrome (DS), open neural tube defects (ONTD) and trisomy 18 (T18). This test is not diagnostic.
Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
FPATI | Patient Information | No | Yes |
FMAS1 | Maternal Screen INT-1 | No | Yes |
Special Instructions
Reporting Name
Maternal Serum Screen INT, Sp-1Specimen Type
SerumSpecimen Minimum Volume
0.3 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 14 days | |
Frozen | 90 days | ||
Ambient | 72 hours |
Reject Due To
Hemolysis | Mild reject/Gross reject |
Other | Plasma |
Reference Values
An interpretive report will be provided.
Part 2 must be completed in order to receive an interpretable result.
If the second specimen is not received for sequential screening, the results are uninterpretable and no maternal risk will be provided.
Performing Laboratory
ARUP LaboratoriesCPT Code Information
84163
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
FFMSS | Maternal Serum Screen INT, Sp-1 | Not Provided |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
Z5958 | PAPP-A Maternal | 48407-1 |
Z5959 | Nuchal Translucency (NT) | 12146-7 |
Z5960 | Nuchal Translucency (NT), Twin B | 12146-7 |
Z5961 | Maternal Screen Interpretation | 49586-1 |
Z5962 | Maternal Age At Delivery | 21612-7 |
Z5963 | Maternal Weight | 29463-7 |
Z5964 | Estimated Due Date | 11778-8 |
Z5965 | Gestational Age Calculated at Coll. | 18185-9 |
Z5966 | Dating | 21299-3 |
Z5967 | Number of Fetuses | 11878-6 |
Z5968 | Maternal Race | 21484-1 |
Z5969 | Smoking | 64234-8 |
Z5970 | Family History of Aneuploidy | 32435-0 |
Z5971 | Specimen | 19151-0 |
Z5972 | Crown Rump Length | 11957-8 |
Z5973 | Crown Rump Length, Twin B | 11957-8 |
Z5974 | Sonographer Certification Number | 49089-6 |
Z5975 | Sonographer Name | 49088-8 |
Z5976 | Ultrasound Date | 34970-4 |
Z5977 | Best date to draw sample nmb 2 by | 33882-2 |
Z5978 | EER Maternal Serum, Integrated, Sp1 | 11526-1 |
Day(s) Performed
Sunday through Saturday