GYNEC EXPERT
Welcome to interactive presentation, created with Publuu. Enjoy the reading!
What is Non Invasive
Prenatal Screening Test
(NIPT) ?
What conditions are
screened in NextGen NIPT
& NextGen NIPT Advanced?
What is the right time to
opt for NIPT?
�������������������������������������
PPV and NPV for the conditions
screened by NextGen NIPT?
Indications for NIPT?
Any time after 10 weeks’ gestational age, NIPT can
be offered to the patient for singleton pregnancy
and twin pregnancy. In case of vanishing twin
pregnancies, there should be 8 weeks gap
between vanishing event and sample collection.
NextGen NIPT
screens for the
following conditions:
NextGen NIPT
Advanced screens for:
3 Common Aneuploidies:
���������������������������
������������������������������
�������������������������
5 Sex Chromosome Aneuploidies:
Trisomy 21 (Down Syndrome)
Trisomy 18 (Edwards’ Syndrome)
Trisomy 13 (Patau Syndrome)
Note: Sex chromosome abnormalities are not reported
in Twin Pregnancies and Vanishing Twin Pregnancies.
Note : Aneuploidies including monosomy and
trisomy of chromosomes other than Trisomy 13, 18, 21
are called Rare Autosomal Aneuploidies (RAA).
Accuracy for RAA is lower than common
trisomies.
Advanced
Maternal
Age1,2,3
Abnormal
USG or presence
of soft markers
on USG
suggestive of
common
aneuploidies
Recurrent
Pregnancy
Loss
Previous
affected
pregnancy1
High risk /
intermediate
risk on maternal
screening test
PPV
>99.99%
94.44%
95.83%
97.78%
99.98%
>99.99%
>99.99%
99.98%
98.73%
(93.15%-99.97%)
>99.99%
(89.72%-100%)
>99.99%
(85.18%-100%)
97.78%
(88.23%-99.94%)
>99.99%
(93.15%-100%)
99.97%
(99.88%-100%)
99.98%
(99.91%-100%)
99.98%
(99.9%-100%)
NPV
SENSITIVITY
(95% CI)
SPECIFICITY
(95% CI)
T21
T18
T13
SCAs
CONDITIONS
PPV - Positive Predictive Value NPV - Negative Predictive Value
SCAs - Sex Chromosomal Aneuploidies
NIPT is a non-invasive and accurate
chromosomal aneuploidy screening test
which is available as early as 10 weeks of
pregnancy.
It is a safe and simple blood test with highest
detection rate (amongst screening tests)
wherein the cell free fetal DNA, circulating in
maternal plasma is tested for common
chromosomal aneuploidies.
This test decreases the chances of procedure
related risk of abortion in expectant mothers.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16