Inpatient and Outpatient Orderable
MaterniT21 PLUS Core+Sex Chromosome Aneuploidy (SINGLETON ONLY)
Synonyms
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- LAB4154
- MATERNIT
- MATERNIT21 PLUS CORE+SCA
- NIPS
- NIPT
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Cerner Name
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MaterniT21 PLUS Core+SCA
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Clinical Info
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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.
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Specimen Sources
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Blood, Arterial
Blood, Capillary
Blood, Central Line
Blood, Venous
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Specimen Types
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Blood
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Specimen Volume
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10 ml Whole Blood ( 8 mL min)
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Container
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Streck Tube
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Collection Instructions
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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).
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Transport Instructions
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Room Temperature
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Specimen Stability
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7 Days Room temperature
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Methodology
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Cell- free DNA
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Days Performed
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TAT 4-6 Days
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Performing Laboratory
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LabCorp- Sequenom
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CPT
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81420
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PDM
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245606
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Only Orderable at Locations:
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Orderable Everywhere
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Results
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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 |
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Result Interpretation
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Forms
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LAB4154