MaterniT21 PLUS Core+Sex Chromosome Aneuploidy (SINGLETON ONLY)

Synonyms

  • LAB4154
  • MATERNIT
  • MATERNIT21 PLUS CORE+SCA
  • NIPS
  • NIPT

Cerner Name

MaterniT21 PLUS Core+SCA

Clinical Info

For (SINGLETON ONLY) pregnancies at increased risk of fetal abnormalities, the MaterniT21 PLUS test delivers a comprehensive NIPT for the analysis of chromosomal regions including trisomies 21, 18, and 13, fetal sex, and sex chromosome aneuploidies.

Specimen Sources

Blood, Arterial Blood, Capillary Blood, Central Line Blood, Venous

Specimen Types

Blood

Specimen Volume

10 ml Whole Blood ( 8 mL min)

Container

Streck Tube

Collection Instructions

Container/Tube:  Streck Tube 
Specimen:  10 ml Whole Blood ( 8 mL min)
Special InstructionsThe following information must be provided with the test request form: patient's date of birth, gestational age, additional patient demographic information, pregnancy type (singleton or multiple), donor egg status and the clinical indications (including advanced maternal age, abnormal ultrasound, history suggestive of increased risk for aneuploidy, positive serum screen, or other indications).

Transport Instructions

Room Temperature

Specimen Stability

7 Days Room temperature

Methodology

Cell- free DNA

Days Performed

TAT 4-6 Days

Performing Laboratories

LabCorp- Sequenom

CPT

81420

PDM

245606

Results
Component Name Base Name Common Name External Name
E DUE DATE EDUEDT E DUE DATE Estimated Due Date
GESTATION GESTATION GESTATION Gestation
FETAL FRACTION FETALFRACT FETAL FRACTION Fetal Fraction
GESTATIONAL AGE > OR = 9W: GESTAGE GESTATIONAL AGE GREATER THAN OR EQUAL TO 9W Gestational Age > or = 9w:
TEST RESULT TESTRESULT TEST RESULT Test Result
LAB DIRECTOR COMMENTS LABDIRCOM LAB DIRECTOR COMMENTS Lab Director Comments
APPROVED BY APPORVEDBY APPROVED BY Approved By
TRISOMY 21 (DOWN SYND) TRISOMY21 TRISOMY 21 (DOWN SYND) Trisomy 21 (Down Syndrome)
TRISOMY 18 (EDWARDS SYND) TRISOMY18 TRISOMY 18 (EDWARDS SYND) Trisomy 18 (Edwards Syndrome)
TRISOMY 13 (PATAU SYND) TRISOMY13 TRISOMY 13 (PATAU SYND) Trisomy 13 (Patau Syndrome)
FETAL SEX FETALSEX FETAL SEX Fetal Sex
MONOSOMY X (TURNER SYNDROME) MONOSOMYX MONOSOMY X TURNER SYNDROME Monosomy X (Turner Syndrome)
XYY (JACOBS SYNDROME) XYY XYY JACOBS SYNDROME XYY (Jacobs Syndrome)
XXY (KLINEFELTER SYNDROME) XXY XXY KLINEFELTER SYNDROME XXY (Klinefelter Syndrome)
XXX (TRIPLE X SYNDROME) XXX XXX TRIPLE X SYNDROME XXX (Triple X Syndrome)
NEGATIVE PREDICTIVE VALUE NEGPREDVAL NEGATIVE PREDICTIVE VALUE Negative Predictive Value
POSITIVE PREDICTIVE VALUE POSPREDVAL POSITIVE PREDICTIVE VALUE Positive Predictive Value
ABOUT THE TEST ABOUTTEST ABOUT THE TEST About the Test
TEST METHOD TESTMETH TEST METHOD Test Method
PERFORMANCE PERFORMANCE PERFORMANCE Performance
PERFORMANCE CHARACTERISTICS PERFOMCHAR PERFORMANCE CHARACTERISTICS Performance Characteristics
LIMITATIONS OF THE TEST LIMITOFTEST LIMITATIONS OF THE TEST Limitations of the Test
NOTE NOTE NOTE Note
REFERENCES REFERENCES REFERENCES References
PDF AFP RESULT PDF PDF, RESULT PDF

Result Interpretation

See Report

Forms
Molecular-Send Outs LAB4154 build edit