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*_xCeEm Di?z&>#m`X_ )= NIPT Inconclusive Twice - Any Success Stories After No Result l Ladylawyer8402 Posted 6/19/20 So I just found out that my NIPT came back with low fetal fraction for the second time. I think if the scan/bloods come back clear then I wont do a third one (just more worry/waiting) but if there is anything not good I will have to decide to either do a third NIPT or more invasive procedures (which I would really want to avoid!). My doctor told me to test then and acted as if that wasnt too early. You may have questions about what your results mean or if you should even have the NIPT test. Note that once you confirm, this action cannot be undone. Based on the results of the NIPT test, your obstetrician may recommend diagnostic tests. The accuracy of the test varies by the condition that its checking for. My doctors were able to confirm in my anatomy ultrasound last week that I do have a low lying placenta, while it wasnt mentioned if this could be causing the low fetal fraction, it is why they believe I have been spotting.. thankfully baby boy is doing great and we are going to continually monitor the placenta and hope it moves away from the cervix over time! I had inconclusive NIPT results. Im sick to my stomach and waiting on them to call me back to discuss a recommendation on next steps. praying for you and your son or daughter to receive good results! We strive to provide you with a high quality community experience. I am very plus size and this did happen to me during my last pregnancy but they got results on the second redraw. Ocean/sky themed baby girl nursery - finished at 38+ A hilarious moment that made me excited to have my kid. 4% at least is needed for accuracy. Has this happened to anyone? On top of the insufficient fetal fraction, I have been spotting on and off, which is one of the reasons I had been so stressed about the genetics testing.. wanting to make sure something wasnt wrong with baby. I'm so sorry your going through this stressful situation , Got the quad back! Your healthcare provider will provide information about prenatal genetic testing and help you make an informed choice about your options. I hope that I will have some clarity from genetic counselor. 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. 15/01/2022 20:53. It just depends on the baby. Are you going to go for a CVS? Are you tall? As far as 16 weeks ultrasound, sex was pretty obvious on mine . Press question mark to learn the rest of the keyboard shortcuts, third time mom / due aug 2023 / 30 / she/her. 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. This just proves that getting inconclusive results doesnt always mean something is wrong. We had two failed harmony results, both came back inconclusive because of low dna fraction. NIPT also includes a study of the sex chromosomes, but a result is not always possible. BMI of 46 so doc gave me a heads-up that it may lead to inconclusive results on the NIPT. , 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. The result will show if theres an increased or decreased risk for a fetus to have the condition being screened. Theres also the possibility that no test results are given due to insufficient fetal DNA in your blood or difficulty identifying fetal DNA. Are there other tests I can take to find out my risks? Its soo nerve breaking!! The DNA is examined for genetic conditions, such as Down syndrome. I ended up asking for a quad screen (it wasnt covered by my insurance but was like $30) to assess risk for trisomy 21, 18 and spina bifida. Create an account or log in to participate. We are going to pursue that because of the rarity of not presenting a result initially. Its nerve racking, but I'm hoping to hear some good news soon. I know no words ever make it any justice but very sorry to hear that. The NIPT measures the fetal cfDNA in the mother's bloodstream, which comes from the placenta. Another inconclusive result. We will not be doing anymore testing for baby boy #3. I met with a genetics counselor and decided to do a 3rd round of genetic testing through Myriad! Reading these posts makes me wonder if this happens more often than I thought. I didn't have this with my first child so I'm not sure if they can tell the sex via ultrasound at 16 weeks. You apparently have too much blood for an accurate reading. Inconclusive NIPT twice? Get useful, helpful and relevant health + wellness information. Group Leaders arent expected to spend any additional time in the community, and are not held to a set schedule. Learn more about, Twins & Multiples: Your Tentative Time Table. So after 9 weeks of genetic testing and no results we were finally able to get results and everything has turned out ok and we are having a baby boy! If you dont have insurance or your insurance doesnt cover NIPT tests, you can pay for the test. 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. Other factors like being pregnant with multiples, being a surrogate or having obesity can affect NIPT results. I dont understand why it didnt work for me. Even though my OB told me it likely wasn't the case for me, I was still in panic mode for a while. Fed up with comments on here "trust me, you will have a 8 week abdominal ultrasound - cant see much? My doc told me 2 inconclusive tests raises the risk level significantly in my age. Its important to talk to your healthcare provider about what your NIPT is screening for. Has anyone experienced this? . Hi! The most common sex chromosome conditions are Turner syndrome, Klinefelter syndrome, Triple X syndrome and XYY syndrome. All rights reserved. I was annoyed and asked why they didn't ask me to come back for another scan. Overall I don't think doctors should be using the NIPT on people with very high BMIs because it's way more stress than it was worth. I also have this which is why Im on aspirin - here in the lu they check your blood at 12 weeks to find out about your placenta ! What tests might I need during pregnancy? What is noninvasive prenatal testing and what disorders can it screen for? Use of this site is subject to our terms of use and privacy policy. (https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC3893900/). I had the first done at 13w and second done at 16w. I had to wait about 10 days for bouth times I did NIPT, only to get inconclusive results. Were my expectations of postpartum help from my mom Press J to jump to the feed. NIPT (Harmony test) inconclusive twice. I did have the nt scan with the dr and she said everything looked good and chances for down syndrome was very low but now im panicking I donr know why this could happen. They send this sample to a lab to analyze it for specific conditions. Ultimately, we learned we were having a baby girl who did not test positive for trisomy but have still been advised to do an amniocentesis procedure at 16 weeks for ultimate peace of mind. My nipt/panorama/harmony results came back inconclusive both times. I fully understand your need for answers - I felt exactly the same way and its much better to have a yes/no answer through CVS/amniocentesis than keep guessing etc. Your post will be hidden and deleted by moderators. If you'd continue the pregnancy regardless of any defects, then I think you can definitely skip the amnio. Reddit and its partners use cookies and similar technologies to provide you with a better experience. Im so so sorry to hear about your loss. I'll be around 18 weeks by then. The first draw I did at 12 weeks and second draw did at around 13 weeks 6 days. . I will likely decline invasive testing like amniocentesis. Amnio specialist also told me that low fetal fraction can be because of placenta. Ans to top it off I really wanted to find out the gender and now I dont even know if things are ok. Lol. Certain prenatal screening tests like NIPT are very accurate for conditions such as Down syndrome, but less so for rare genetic conditions. Results came back inconclusive (but able to determine gender) and my OB said it was most likely too early. The reason that your doctor is suggesting an ammio is because studies have shown there is a positive correlation between a low percentage of fetal DNA (i.e. Find advice, support and good company (and some stuff just for fun). It doesnt diagnose a condition. Be sure to understand what the test screens for and what the results mean so you make an informed decision. I had a redraw last week and waiting for that to come back. It is super frustrating, and I think honestly more frustrating that docs continue to recommend these tests when it seems like everyone I know with a high BMI had this issue. By rejecting non-essential cookies, Reddit may still use certain cookies to ensure the proper functionality of our platform. Hi friend. My risk just due age is 1/94 for trisomy 13, 18. The test can also determine the sex of the fetus. Healthcare providers may recommend it if you: The American College of Obstetricians and Gynecologists (ACOG) used only to recommend NIPT for pregnant people considered high risk. Its done by taking a sample of your blood, which also contains fragments of DNA from the fetus. Eunice Kennedy Shriver National Institute of Child Health and Human Development. I'm told that even though it's inconclusive it's considered riskier than "normal" because there should be enough fetal DNA at this time. k[oku6Av9j12U}BOn.jQ5-W],W7N~x ;)R7M 9z:FC& Q~Ro1!. Symptmes de grossesse ne jamais ignorer, Moyens naturels pour dclencher l'accouchement. think twice before sharing personal details, foster a friendly and supportive environment, remove fake accounts, spam and misinformation, delete posts that violate our community guidelines, reviewed by our medical review board and team of experts. BabyCenter may earn a commission from shopping links. We strive to provide you with a high quality community experience. u 03-(q}|$05`- H320mf`~e0 * Mine came back inconcl, I was 12 weeks and then took again at 14 1D, I have also had 2 inconclusive results and we are not trying again. 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. This is called the fetal fraction. It requires drawing blood from the pregnant person only. Use of this site is subject to our terms of use and privacy policy. Cleveland Clinics Ob/Gyn & Womens Health Institute is committed to providing world-class care for women of all ages. We had issues with our genetic testing as well and I too was super worried! From genetic counselor 3rd round of genetic testing as well and I too was super!. Through Myriad are going to pursue that because of the fetus but I 'm so sorry to hear your! Expectations of postpartum help from my mom press J to jump to the feed NIPT, only get! 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