Hi All.. I'm (33 F) currently 17 weeks pregnant with my second baby. We live in Canada.
My 12th week ultrasound did not check for NT but the overall growth looked normal for the gestational age and the heart beat was good. I didn't have any concerning symptoms so far, no bleeding or abnormal blood pressure. I have also been feeling some baby movements for about a week and my fundal height measured appropriate for 16 weeks (last Doctor appointment).
However, I got a call from my doctor last Thursday informing that my numbers from prenatal screening requires further analysis. I have NIPT scheduled in another two days but we are really freaked out about the odds. Here is the screenshot of my results, 1:8 for Trisomy 21 and 1:100 for Trisomy 18.
Does the low PAPP-A of 0.14 and the HCG of 8.76 MoM mean that I should be directly looking for a Amnio ? or if I should wait for the NIPT results which may take another 2 weeks?