- Patient/Guest
- Phlebotomist
- Updates
| Quad Screen NT | - |
|---|
|
Assess fetal aneuploidy with NT |
||
| Synonym | See updates | |
| Test Code | CDBIOPR0043 | |
| Test Type | Biochemistry | |
| Pre-Test Condition | See updates | |
| Report Availability | 3 D(s) | |
| # Test(s) | Multiple | |
| Test details | Sample Report |
|---|---|
| Quad Screen NT |
|
| Synonym | See updates | ||
| Test Code | CDBIOPR0043 | ||
| Test Category | Fetal aneuploidy | ||
| Pre-Test Condition | See updates | ||
| |
Medical History | See updates | |
| Report Availability | 3 D(s) | ||
| Specimen/Sample | Serum; 2 mL; SST | ||
| Stability @21-26 deg. C | 6 Hr(s) | ||
| Stability @ 2-8 deg. C | 7 D(s) | ||
| Stability @ Frozen | 1 M(s) | ||
| # Test(s) | Multiple | ||
| Processing Method | Immunoassay | ||
| **First Trimester Quad Screen and NT****FDA Status**: FDA-approved for prenatal screening.**Other Names**: First Trimester Quad Marker Test, Combined Quad Screening.**Historical Breakthrough**: Developed in the 2000s for enhanced prenatal screening, advancing obstetrics.**Key Purpose and Impact**: Measures PAPP-A, free β-hCG, AFP, inhibin-A, and NT to assess Down syndrome and other risks.**Preparation and Patient History**: Blood and ultrasound; report pregnancy history or family history.**Consent Requirement**: Standard consent with prenatal counseling.**Clinical Value**: Sensitivity ~95%; specificity ~95%; detects abnormalities in ~90% of cases; guides further testing.**References Cited**: Testing.com Prenatal Tests 2023; Labcorp Quad Screen 2025; UpToDate Prenatal Screening 2025 |
