Hi @Han1234,
Twin pregnancy here - 19 days from delivery now. One of the twins had NT of 1.9 and the other 3.9 at 12 weeks. Sent to a consultant the same day, following a number of scary meetings/bombardment of info immediately after the scan.
I wouldn’t believe myself if the me right now told the September me how much better I’d feel, but I do. Hopefully the below helps. 🤍
I went into a complete meltdown following the higher NT measurement and needed 1-2 weeks off work to sit and cry in bed. It was overwhelming and I totally feel for you going through this. Every scan since then has been positive and I was discharged from Fetal medicine in January.
We had an NIPT (Harmony) at 10 weeks, which made the 12 week news more shocking. Results were low probability for the three trisomys. Due to the nature of the pregnancy we decided against CVS or Amnio as there were no issues with the other twin.
Being totally clear, our worst case scenario was a severely disabled child over losing the pregnancy but we came to the conclusion that they’re so small around the 12 week mark and we’d get more answers between 17-24 weeks. If our NIPT had come back with any concerns or we weren’t able to have it, we would have proceeded with invasive testing.
The Fetal echo and anomaly scans were much more reassuring (loads between 18 and 26 weeks). One sonographer said they wouldn’t know why they were scanning me if they didn’t have my notes as the baby looked perfect.
What helped me was (slightly self-made) percentages and probabilities but also rationally breaking it down and trying not to let the anxiety take over.
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these are mm measurements so you’re 0.2mm over the threshold, which is tiny. Some countries have a cut off of 4mm.
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if NT stays high at future scans, that’s more concerning than if it falls to a normal bracket
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the probability of abnormalities increases per bracket (3.6-4.5mm / 4.6-5.5mm / 5.6-6.5mm / 6.6-7.5mm) etc
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95% ish of abnormalities are the three trisomys. Out of the remaining 5% (approx 500 abnormalities screened in the microarray) more than half* of those would go hand in hand with a serious heart defect, which would show on Fetal echo scans.
*I took this as 60% knocking off 3% of the 5% outstanding abnormalities and calculating my risk as 2%.
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I took comfort in the fact that the skeleton looks good, the baby was moving well and if something was seriously, seriously wrong, it’s likely my body would make the decision for me or there would be a large growth discrepancy between the twins.
Feel free to message me if you want to chat. It’s a worrying time but it’s also the hospital’s job to run through worst case scenarios, however unlikely. This is my last pregnancy and it’s been somewhat ruined by months of worry.
Plan of action for us now is physical checks on delivery and then we will have a blood test carried out on both babies to highlight any genetic issues. The other option is keeping a keen eye on twin 1’s milestones until they’re two but I feel, for me, I’d constantly be looking for something and comparing them to the other twin.
Good luck. Trust your gut, speak to your partner loads and loads about it. Discuss how conclusive information might change your path. Hold tight, the bigger the baby, the more they can see. 🫶🏻
Hope you get your microarray back soon @linz1987 Your amnio result should give you huge reassurance. It’s a conclusive, diagnostic test and your trisomy results are fab! Wishing you luck 🍀