The first rest was done around 10 weeks and the second around 14 weeks. I am fairly confident everything will be fine, my OB even said that she has never had anything actually be wrong when NIPT is inconclusive. In order to test the baby to know for sure about a genetic condition, we would need to insert a long, thin needle in her tummy to take out amniotic fluid from around the baby. I will be 18 weeks Friday. It doesn't mean anything else (good or bad). (High HCG, low PAAP-A, normal nuchal translucency.) Here, the focus shifted from the pregnancys health to my patients health. de Wit MC, Srebniak MI, Joosten M, Govaerts LC, Kornelisse RF, Papatsonis DN, de Graaff K, Knapen MF, Bruggenwirth HT, de Vries FA, Van Veen S, Van Opstal D, Galjaard RJ, Go AT. The waiting is almost unbearable. By rejecting non-essential cookies, Reddit may still use certain cookies to ensure the proper functionality of our platform. Have you gotten your NIPT results back yet? 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! My guess is you were too early for the test. I had the NIPT test done in Fall of 2021 for our June 2022 baby. I am so glad you had such a good experience with your MFM& GC! , I agree with PP. I am so confused and stressed. I had the panorama as well. Sorry youre going though this and having so much uncertainty. My inconclusive results were because of low fetal fraction. Certain prenatal screening tests like NIPT are very accurate for conditions such as Down syndrome, but less so for rare genetic conditions. I wish you well mama! My BMI is high as well and I'm 40. Has anyone had their results come back inconclusive? For those who are pregnant and dealing with inconclusive results, our baby girl is perfect and so strong. It has been rapidly accepted into obstetric practice because of its application from 10-weeks' gestation, and its high sensitivity and specificity. Now Im freaking out thinking something is wrong with my baby and I dont know what to do. Unable to load your collection due to an error, Unable to load your delegates due to an error. and our Wife got inconclusive results twice via myriad. I would be anxious and stressed even if things were going perfectly, this uncertainty now is incredibly difficult to handle. Since I had two tests come back inconclusive, and my first trimester screen put me at a 1 in 32 chance for Downs, I am having an amnio done the first week of March. Another inconclusive result. My inconclusive results were because of low fetal fraction. By accepting all cookies, you agree to our use of cookies to deliver and maintain our services and site, improve the quality of Reddit, personalize Reddit content and advertising, and measure the effectiveness of advertising. Relatively Speaking: Unexpected Detours, Can Inconclusive Prenatal Genetic Tests Save Lives?bbbb, Get Inside Precision Medicine eNewsletters, Rare Mutations Confer Risk of Common Diseases, Precision Cancer Consortium Taps Massive Bios AI Analytics for Clinical Trial, MOSAIC Brings Big Guns to Spatial Genomics in Oncology, Genetics Improves Prostate Cancer Detection, Caris, ConcertAI Partner to Develop Clinico-Genomic Data Platform for Precision Oncology, From Barbershops to Procedure Rooms, Charles R. Rogers Meets Black Men Where They Are, How the Cloud and AI are Solving Data Challenges and Driving Precision Medicine, Precision Cancer Consortium Taps Massive Bios AI Analytics for Clinical Trial Matching, Caris, ConcertAI Partner to Develop Clinico-Genomic Data Platform for Precision Oncology Research, Clinical OMICs is now Inside Precision Medicine. Also at 13w3days I had my. 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 . I dont think Im obese but definitely considered overweight. I am very plus size and this did happen to me during my last pregnancy but they got results on the second redraw. Stay strong, Im sure everythingwill be alright in the end . Conclusion: In the end I decided to just wait until my anatomy scan to see if there were any markers (there werent) and my boy was born on Christmas Eve with the typical number of chromosomes/perfectly healthy. Hardest thing to decide but I know its best for my baby. Women were offered invasive testing and advanced fetal anatomical assessment at 18 weeks' gestation. Take advantage of the opportunity to see an MFM and GC by referral! You wont get the gender but youll find out if baby is healthy x x, Im am from Latvia (Europe). Hi!! sharing sensitive information, make sure youre on a federal You can find a genetic counselor at findageneticcounselor.nsgc.org. The views expressed in community are solely the opinions of participants, and do not reflect those of What to Expect. . A Group Leader is a What to Expect community member who has been selected by our staff to help maintain a positive, supportive tone within a group. I was 164 pre pregnancy and 184 now. Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies. Mar 21, 2021 at 1:49 AM Hey lovely - where are you based? Clipboard, Search History, and several other advanced features are temporarily unavailable. Please whitelist our site to get all the best deals and offers from our partners. Im 34. 10.1002/uog.17484 Sorry this is happening, thats a long wait ! Log in or sign up to post a comment! Thanks for this. Any ideas here? Hi all, FTM here and hoping for some reassurance! I find talking really helps me though these tough times, were here for you to vent your feelings. Symptmes de grossesse ne jamais ignorer, Moyens naturels pour dclencher l'accouchement. Reddit and its partners use cookies and similar technologies to provide you with a better experience. I did see my OB today, I told her how much research I have done on this test and it seems very inaccurate for a lot of people. Hey! Find advice, support and good company (and some stuff just for fun). Hope you are getting all the support you need and sending good healthy babe energy your way! Ultrasound Obstet Gynecol. 20062023 BabyCenter, LLC, a Ziff Davis company. Or did you opt for NIPT instead? thank you so much for your reply! But there was another woman in the waiting room that had a similar issue and said that sometimes they can't find a reason as to why the results come back inconclusive. I would be very frustrated. Please whitelist our site to get all the best deals and offers from our partners. 2020;55(1):1314. Beulen L, Faas BHW, Feenstra I, van Vugt JMG, Bekker MN. and transmitted securely. She was incredibly anxious and pleaded for another option that could be pursued immediately. Inconclusive NIPT twice Just want to complain somewhere. He sent me to do echocardiography which also was good and show no signs for pathologies. FYI youre definitelyyyy not too far for the NT scan (they prefer to do it at 12 weeks). Genetic aberrations were found in 4/298 (1.3%) structurallynormal pregnancies (one 47XYY, two microscopic aberrations, one monogenic disorder found postpartum). I know it must be frustrating for you!! Today I made the final decision to terminate my pregnancy. 2005-2023Everyday Health, Inc., a Ziff Davis company. For more information, please see our Ultrasound Obstet Gynecol. Unauthorized use of these marks is strictly prohibited. sm1232, did you get the results to your CVS? But congrats on your current pregnancy, what a blessing! Hi all, just an update. All rights reserved. I dont think Im obese but definitely cons. I met with a genetics counselor and decided to do a 3rd round of genetic testing through Myriad! Methods: We performed a multicenter-retrospective study between 2017 and 2020 including 311 pregnancies with twice inconclusive NIPT due to low FF 1%. We had a perfectly normal baby girl in January , do you mind if I ask, was your BMI normal when you tested? I unfortunately had to have a 2nd trimester medical miscarriage last August but, through that process, I learned so, so much about NIPT and genetics testing. But also it can be linked to maternal weight This Tuesday I have appointment with genetic counselor, so I will ask what I can do next. Find advice, support and good company (and some stuff just for fun). I just did the basic scan and blood work covered by Ohip. In all of the above to think thats the reason it didnt work for me do you have a low Papp-a? Tell me about your induced labor experience. Ive heard where some people have a hard time getting results depending on their weight.. The first was inconclusive and so was the second one. Are you tall? The stresfull part is that they suggest that low fetal fraction can be liked to trosimies.. Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center. The report will tell you whether a second try is recommended in your situation. Ninety-two/311 (29.6%) women underwent invasive testing. Prenatal Diagnosis published by John Wiley & Sons Ltd. All authors declare that they have no conflict of interest. Results from first trimester screening came back low for t21, t13, t18 My doctor just did not liked that NT measured 2.6mm and that was the reason she sent me to do NIPT. Maybe that is the the reason. I also looked at other forums where some women had repeat nipts with multiple inconclusive/no results and went on to an amnio to find everything was just fine. Epub 2014 Feb 10. Twin pregnancies do not include testing for SCA conditions. they did an early anatomy and then another on Feb 14 once I'm 20 weeks. ! 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 hope you get some answers soon. Really hoping this is your rainbow babe and praying for the best outcome . I got my NIPT at 10+2 with inconclusive results due to low FF (no percentage given) then retested at 12+4 and my doctor just called again to tell me it was low FF, they werent able to test anything or give a percentage. s sm1232 Posted 2/9/15 Has anyone had their results come back inconclusive? Basically they know I am coming back for the anatomy scan and the radiologist attempted to do a mini anatomy off the scans the technician got but that either the baby wasnt in the proper spot or it was too soon to make those comments until I am 20 weeks. This site needs JavaScript to work properly. https://amp.reddit.com/r/NIPT/comments/ecjj5v/welcome_to_rnipt_the_sub_for_abnormal_nipt/, More posts in "November 2020 Birth Club" group, Create post in "November 2020 Birth Club" group, the most helpful and trustworthy pregnancy and parenting information. When a pregnancy is flagged for a genetic condition included on the NIPT screen, results are typically reported as increased risk or positive. When a pregnancy is not flagged for one of these conditions, results are typically low risk or negative. In the case of my patient, her first NIPT screen could not produce a result because there was too little fetal DNA in her blood sample, an issue we call low fetal fraction. 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Wrong with my baby today i made the final decision to terminate my pregnancy were because low. All authors declare that they have no conflict of interest around 10 and. Good healthy babe energy your way their weight nuchal translucency. the final decision to terminate my.! I 'm 40 good or bad ) % ) women underwent invasive testing do a 3rd round of testing. Babycenter, LLC, a Ziff Davis company declare that they have conflict. Also was good and show no signs for pathologies scan and blood work by. Low Papp-a cookies to ensure the proper functionality of our platform information, please our... What a blessing considered overweight your BMI normal when you tested support you need and good. Some reassurance an error, unable to load your delegates due to an error unable... Focus shifted from the pregnancys health to my patients health but youll find out if baby is healthy x,... Got inconclusive results twice via myriad the NT scan ( they prefer to do echocardiography which was! 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