Dr Lal PathLabs Presents First Trimester Screening Test# for Screening Prenatal Disorders (Trisomy 21, 18 & 13)
FIRST TRIMESTER SCREENING, FMF Test#
First trimester screen is done on Fetal Medicine Foundation, UK, accredited platform for screening Prenatal disorders (trisomy 21, 18, & 13) to identify those women who are at sufficient risk for a congenital anomaly in the fetus to warrant further evaluation & follow up. The risk is calculated using SsDwLab6 software.
Advantages of FIRST TRIMESTER SCREENING, FMF Test#
- Detection rate is high
- If the observed risk is low, the patient can be put at ease early in her pregnancy
- In the event of high risk, more time is available to decide on the diagnostic possibilities
- Should the patient decide to terminate, procedure is safer when performed in early pregnancy
Added advantages of SsdwLab6 software
- Type of twinning (Monochorionic & dichorionic twins): The software uses chorionicity-specific medians for calculating MoM [Generation of chorionicity-specific medians* for the biochemical markers and their use in risk assessment improves the performance of first trimester screening for chromosomal abnormalities in twins to a level comparable with that in singleton pregnancies]
- Fetal dichotomous markers [Short femur, pyelectasis, echogenic cardiac foci, echogenic bowel, ventriculomegaly, abnormal ductal flow, Tricuspid regurgitation, single choroid plexus cyst, single umbilical artery] can be included for risk calculation
*Reference – Ultrasound Obstet Gynecol 2011;37, 38-474
#Kit is approved by FMF
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