Patients having this testing should know that NIPT results do not diagnose a genetic condition or give a yes/no answer, and should seek follow-up testing if appropriate. So I just found out that my NIPT came back with low fetal fraction for the second time. Your healthcare provider can answer any questions you have, but ultimately you have to decide how a genetic or chromosomal disorder affects you and your family based on your situation. n_qTz We are going to pursue that because of the rarity of not presenting a result initially. I will likely decline invasive testing like amniocentesis. Press question mark to learn the rest of the keyboard shortcuts. Oh yes I was referring to a blood test but thank you so much for the input. I met with a genetics counselor and decided to do a 3rd round of genetic testing through Myriad! NIPT test done twice.with inconclusive results twice. Its important that you talk to your healthcare provider about your results and options to get more information. Thank you! Talk to your healthcare provider or a genetic counselor about your concerns. Group Leaders communicate with staff moderators and escalate potential violations for review, but they dont moderate discussions. It set my expectations unreasonably high. I had an inconclusive harmony test at 10 weeks exactly, I wasn't too worried as it was really early, I was on blood thinners, and a higher bmi of 30, all of which can lead to an inconclusive result. We respect everyones right to express their thoughts and opinions as long as they remain respectful of other community members, and meet What to Expects Terms of Use. . If you feel a message or content violates these standards and would like to request its removal please submit the following information and our moderating team will respond shortly. Now doing the waiting game!! If you feel a message or content violates these standards and would like to request its removal please submit the following information and our moderating team will respond shortly. The first rest was done around 10 weeks and the second around 14 weeks. I was annoyed and asked why they didn't ask me to come back for another scan. Had my redraw at 13+2, and results have come back the same, inconclusive due to low fetal fraction. Noninvasive pregnancy screening tests are a personal choice. Ive done nipt through generations and Harmony both reputable brands and they would never give results with that low of a fraction, as it could come from contamination from say, the person drawing the bloods or the one analysing touching the tube to read results. Just wanted to share my experience since Ive gotten both a CVS and an amniocentesis in the last 3 weeks.Backstory: at my 12 week nuchal translucency scan, we had a high measurement of nuchal fluid (3.5mm). When I went back for a second blood draw, they took two tubes of blood. I'm pretty sure its because I'm overweight lolmanyjow dehydration sounds like a good idea although the first day I went I had puked all morning Anyhow am skipping it now and will just wait till my next appointment which is on the 20th and hopefully we will find out the gender. Has this happened to anyone else? I am way larger than you. They kinda downplayed it saying it happens a lot, but it still stresses me out a little. Inconclusive NIPT twice? I'm 36 weeks now. You apparently have too much blood for an accurate reading. You wont get the gender but youll find out if baby is healthy x x, Im am from Latvia (Europe). The main purpose of NIPT is to screen for major chromosome conditions (Down syndrome, trisomy 18, and trisomy 13). Our commitment to quality means that we will only provide a result when there is very clear evidence for, or against, the presence of a specific disorder. Mumsnet carries some affiliate marketing links, so if you buy something through our posts, we may get a small share of the sale (more details here). Getting a noninvasive pregnancy screening or other prenatal genetic test is up to you. My first test was at 10 weeks (FF=4.8%) and my second was at 14 weeks-she didn't tell me over the phone what it was. Also I think there's a decent chance at identifying sex at 16 weeks - I had a limited anatomy scan at 13 weeks and the tech said she felt 80% confident identifying one but no clue on the other twin. The test can also determine the sex of the fetus. The minimum they require to release the results is 2.8%, and the first draw I had 3.2% for 1 baby and 2.2% for the other. We then did the SAFE nipt as it needs roughly 0.5 dna fraction, where as other nipt tests need at least 4.5% and we got a result!! This testing analyzes small fragments of DNA that are circulating in a pregnant woman's blood. Unlike most DNA, which is found inside a cell's . My nipt/panorama/harmony results came back inconclusive both times. All rights reserved. Dont be afraid to ask questions. Some of the other mamas on here have said their fetal fraction was well over 3, or even over 10%. , I am 27, 5' 3" and usually 150lbd to 155lbs maybe its a weight thing, idk hoping good news when the doctors calls, I think I will opt out of noninvasive too. Learn more about, Twins & Multiples: Your Tentative Time Table. Could it be a false positive? This educational content is not medical or diagnostic advice. We had issues with our genetic testing as well and I too was super worried! First test taken 10w3days, second taken 13w3days. Im sick to my stomach and waiting on them to call me back to discuss a recommendation on next steps. Ive heard where some people have a hard time getting results depending on their weight.. Please select a reason for escalating this post to the WTE moderators: Connect with our community members by starting a discussion. I just did the basic scan and blood work covered by Ohip. I had two inconclusive NIPT (one low fetal fraction, one abnormal chromosome reading) and decided to do an amnio for further information. A Group Owner is a member that has initiated the creation of a group to connect with other members to share their journey through the same pregnancy & baby stages. I am 36 and unfortunately very much plus size. Same thing happened to me. Group Leaders arent expected to spend any additional time in the community, and are not held to a set schedule. We had two inconclusive NIPT tests (from two different testing companies). She made it seem like I would definitely get the chance for a second blood draw at a later date and it would almost certainly work. The main purpose of NIPT is to screen for major chromosome conditions (Down syndrome, trisomy 18, and trisomy 13). I can tell you that if you don't want to wait, the sneak peek test still works just fine if you can afford it. NIPT is a screening test and, therefore, isnt perfect. Maybe call the clinic directly for feedback on how that particular radiologist writes reports. Group Leaders arent expected to spend any additional time in the community, and are not held to a set schedule. My Hi all,I had my first NIPT labs drawn around 10 weeks. I had a redraw last week and waiting for that to come back. The educational health content on What To Expect is reviewed by our medical review board and team of experts to be up-to-date and in line with the latest evidence-based medical information and accepted health guidelines, including the medically reviewed What to Expect books by Heidi Murkoff. E@Gpc 8Op!ISHiT7{;-N/OM7Mq+YV1d)|\i-V;`]tyTAHqAFWR Create an account or log in to participate. The CVS came back perfect - no abnormalities. Check with your insurance provider before testing to be sure. I've had the draw twice and thencutoff for weight to be an issue is 250 and I'm 170 so they say that's not the issue :(. They could have also just waited until 16 weeks for my first blood draw given my weight. insufficient DNA for the NIPT test) and chances of a trisomy defect. thank you - apparently triploidy is not linked to maternal age - Im 29 and it could have happened to an 18 year old or a 40 year old mother. Theres also the possibility that no test results are given due to insufficient fetal DNA in your blood or difficulty identifying fetal DNA. My first test was at 10 weeks (FF=4.8%) and my second was at 14 weeks-she didnt tell me over the phone what it was. Good luck!! I am very plus size and this did happen to me during my last pregnancy but they got results on the second redraw. I have my anatomy scan on Wednesday but Im just so terrified they will give me bad news. Your cells are constantly dividing and creating new cells. I did IVF and my embryo was a normal embryo through pgt so that gives me hope. Hi all, just an update. Also my genetic testing was all negative. Is this an ivf pregnancy? Press J to jump to the feed. hb``c``Zp7XX8LN`` The first draw I did at 12 weeks and second draw did at around 13 weeks 6 days. I'm panicking now because I'm so worried. Its nerve racking, but I'm hoping to hear some good news soon. Symptmes de grossesse ne jamais ignorer, Moyens naturels pour dclencher l'accouchement. This is my second baby and I didnt do NIPT with my first. Ocean/sky themed baby girl nursery - finished at 38+ A hilarious moment that made me excited to have my kid. A place for pregnant redditors, those who have been pregnant, those who wish to be in the future, and anyone who supports them. Had to redraw today and start the waiting process all over. It took 6 weeks and a lot of worry, so ask for the SAFE if they have it? Wish we did like other pregnancies and skipped the testing! Eunice Kennedy Shriver National Institute of Child Health and Human Development. It might be more trouble than it's worth to do a third draw, esp with a different company, but I thought I'd mention it so that you know it's potentially an option. 0 Also, all of the anatomy scans have come back perfect. It's probably your BMI. My risk just due age is 1/94 for trisomy 13, 18. I am so confused and stressed. My BMI is a bit high and I've read that can be a reason. Group Black's collective includes Essence, The Shade Room and Naturally Curly. If the concentration of fetal DNA is below this, then the test might prove to be inconclusive. Use of this site is subject to our terms of use and privacy policy. Overwhelmed and frustrated by weight gain. The DNA is examined for genetic conditions, such as Down syndrome. Please specify a reason for deleting this reply from the community. We strive to provide you with a high quality community experience. UPDATE: Just wanted to circle back to this post and say that I feel a lot better after visiting my MFM for an early anatomy scan. Please whitelist our site to get all the best deals and offers from our partners. The first rest was done around 10 weeks and the second around 14 weeks. Im 34. Strangely enough, I am also on lovenox.I am also old at 39 and have a higher BMI. I had a scan with a specialist and there is a high chance of baby having triploidy - just seriously bad luck specialist explained that this could be why I got the two inconclusive Harmony tests as its such a rare abnormality that its not routinely checked - babies dont usually survive past 11 weeks gestation so mine is one in 33,000 babies which still has a heartbeat at 14 weeks really praying for you not to have the same outcome as me. Enough, I am 36 and unfortunately very much plus size and this did to. The anatomy scans have come back scan and blood work covered by.. Testing analyzes small fragments of DNA that are circulating in a pregnant &. Kinda downplayed it saying it happens a lot of worry, so ask for the NIPT )! 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