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. We went with Myriad. It's a screening test offered during pregnancy to see if the fetus is at risk for having a chromosomal disorder like Down syndrome (trisomy 21), trisomy 18 (Edwards syndrome) and trisomy 13 (Patau syndrome). It lead to 3 weeks of PURE hell. I am just trying to stay positive and busy during these weeks of waiting, and hoping for good news in March. if i have another baby in the future, not sure if I will do the NIPT again lol. Noninvasive prenatal testing (NIPT), sometimes called noninvasive prenatal screening (NIPS), is a method of determining the risk that the fetus will be born with certain genetic abnormalities. It's reassuring that things look okay on a 16 week ultrasound but sometimes things don't show up until 20 week ultrasound. Normal chromosomes come. The #1 app for tracking pregnancy and baby growth. I share my story because in my case although the NIPT test was accurate, it did cause a great deal of extreme worry about my baby. Id love to know emma went. Good luckI hope all is well with baby! So I spent around 5 days suffering because of google. I just retested yesterday since the company doesn't charge if it comes back inconclusive. Had my redraw at 13+2, and results have come back the same . Clicking on the green -no result post flair- will bring up everyone who has also tagged their submission as no results/low fetal fractions and you can read up their stories/outcomes and responses (or any other topic that is common for NIPT results. Now I am in limbo awaiting to see what happens next. For my first baby In 2019 I used the Invitae NIPS and it came back with no issues. Just pooping in about the initial ratio1:10000 is fabulous! Almost 10 weeks of, this is a first for us and Ive never seen this before, we are doing further research made the first half or my pregnancy extremely tough. Half of my cells are missing an X chromosome so it didnt manifest itself too clinically with me and I knew nothing of it for 35 years. Common Abnormalities Are: Down syndrome (trisomy 21 . I'm not sure who it was but scroll back a bit and i'm sure you'll find it! All rights reserved. Getting my blood redrawn tomorrow. To help you get started read our. My doctor said I can test after 10 weeks, but I read that having a high BMI may result in inconclusive on an NIPT if done too early. Im currently going through the exact same thing. Find advice, support and good company (and some stuff just for fun). I got the panerama test at 11 weeks with my second baby. Hello! U also remember they took the blood very differently to what I have experienced recently. the most helpful and trustworthy pregnancy and parenting information. I just wanted to doit for the extra accuracy and seems like a bonus to also find out the gender! Have you had the NT scan done? Please dont look google to find out. Getting my blood redrawn tomorrow. Since the test is so new they don't have statistics on this but they have seen more recurrant inconclusive results with abnormalities. I hope this helps. TX: IUI #1 with Follistim. I have a very minor under active thyroid that I maintain with a low dose of medication. The #1 app for tracking pregnancy and baby growth. And I'm sick with worry since my first trimester screen came back abnormal. There was another post on here about the same issue. The user and all related content has been deleted. Press J to jump to the feed. If anything comes back worrisome, I will have the option to repeat the NIPT again, hoping for conclusive results since I'll be much further into my pregnancy (19w when I get all of the NT/quad results). Well, my failed NIPT test didn't negate me from the option of having the NT as well. Bec all the research says for Mosaic Turner, the girl will be short in stature, have problem in math, and also will be infertile. All rights reserved. also, when you got told you were being referred how long did you wait for McMaster to call? Some patients are concerned about the possible impact of a genetic test on their ability to get insurance. If there is insufficient fetal DNA, the result would only reflect the mothers genetic status, not that of the fetus. Welcome to Abnormal NIPT screening results! Surely I'm worried. I just got inconclusive results too!!! Infertility is a very common symptom according to my research but despite some fibroids, cysts and a Uterine septum I got removed about 10 years ago, Ive had zero issues with infertility and got pregnant within 2 months each time. Show your support by. This occurs about 1 in every 150-200 samples. You can do an amnio. My NIPT came up inconclusive the first time as well. You could make a big difference by making sure this never happens again in the OB's office for future patients such as yourself. In approximately 1% of women, the NIPT result is unable to provide an assessment about one or more of the disorders being screened, or cannot provide an assessment of fetal sex. sm1232, did you get the results to your CVS? I've read online it could happen to plus size moms? 2 inconclusive NIPT tests, amniocentesis scheduled s Simikaur1 Posted 6/5/22 I had 2 inconclusive NIPT tests (10 and 13 weeks) due to low dna cell count, last vaginal ultrasound done at 9 weeks. If I could go back, I would skip the NT scan. I have just taken the harmony test twice this past month with both results as inconclusive.. I had a healthy son in 2020 in which they could not determine the gender. I guess this is not so uncommon. If that is all normal I wouldnt worry about this. This educational content is not medical or diagnostic advice. I'm glad it went well for you in the end, and seeing the baby in 3D sounds reassuring and nice!! my reason for doing the NIPT was similar to yours, haha. Thank you for sharing your story as mine is very similar with yours. The NIPT prenatal test is a trusted elective screening tool used to assess the genetic risk of a fetal chromosomal abnormality, such as Down syndrome, in the first trimester of pregnancy. My NIPT came up inconclusive the first time as well. They said I can get retested and said maybe cause blood had to fly from nz to au? Ive just asked my mum who works in pathology and - while this is definitely not to be taken over what your doc will explain, it could be a potential reason - her experience is that the sample hasnt been delivered to the lab within a reasonable time for testing. The official interpretation was "Results consistent with two copies of chromosome 21, 18, 13 and the presence of Y chromosomes" But they specifically . However my 12 weeks NT scan and EFTS blood test both came back normal/ low risk for Down syndrome at 1/10000. In some cases, a test result might not give any useful information. NIPT is commonly used for chromosomal disorders that are caused by the presence of an extra (triploidy) or missing copy (aneuploidy) of a chromosome. you will see them all over the place here. Just wondering if anyone has been through something similar :( thanks. Childhood-onset disorders due to new cytogenetic abnormalities and inherited mutations. 20062023 BabyCenter, LLC, a Ziff Davis company. 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. Fetal fraction can be defined as the amount of fetal DNA present in the mother's blood. 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. why is my nipt test inconclusive. This testing analyzes small fragments of DNA that are circulating in a pregnant woman's blood. Noninvasive prenatal testing (NIPT) has become a popular screening test for the most common fetal aneuploidies. Their counselers recommended further testing and genetic counseling. 2) NIPT tests are more accurate and test for MORE genetic disorders (they also tell you sex, if you want to know). We just got our results back and have a perfectly healthy . The first rest was done around 10 weeks and the second around 14 weeks. I know its scary and I know my specific situation seems to be rare as far as lack of symptoms and what not so I cant give you any medical advice, but I can tell you that I am living a wonderful and fullfilling and I wish the same for your daughter no matter what the outcome. I hope this helps you consider an alternative, less stressful reason. In cases where the father of the child has not been determined, couples may opt for a, Fetal fraction can be defined as the amount of fetal DNA present in the mothers blood. Why should I choose Sonic to perform my NIPT? . Results in some cases may return inconclusive or uncertain. Please specify a reason for deleting this reply from the community. Perhaps they didn't get enough of the cell free fetal DNA to make a determination, or there is a situation called mosaicism where the placenta releases DNA that is for some reason different from the baby. I had the first level bloodwork and NT scan and they came back normal. Please thank your mum for me. Are you going to have amnio? Had my harmony test at 10 weeks 3 days. The #1 app for tracking pregnancy and baby growth. I'm sure that it's not a definitive, but I like getting the facts and this has helped me be a little more mentally prepared. Your test result shows that your pregnancy is at low risk for these three conditions. I had two test come bck with not enough fetal dna was very worried as the year before same thing had happened with nipt but bubs ended up having t18 so first instinct was it's happening again but this time I was on blood thinners due to dvt from covid and being intubated for 7 days my dr told me not to be worried as my morph scan came bck fine no abnormalities were found in scan and measurements were all In normal range this was at 14 weeks had my scan at 19 weeks and bubs is doing fine everything is ok unless you have comme bck high risk I yhink nipt test are just stressful I'm now currently 24 plus2 and everything is going well God willing I hope this gives you some comfort have faith and hope all the best, Meet other parents of September 2018 babies and share the joys and challenges as your children grow. It could either actually be me (and could it be passed down? Crossing all fingers and toes its just a lab error. I needed a NIPT done as there were MANY concerns on my 20 week ultrasound. I wouldn't necessarily do the amnio for that if the baby is otherwise healthy. POSITIVE PREDICTIVE VALUE CALCULATOR FOR NIPT RESULTS https://www.perinatalquality.org/Vendors/NSGC/NIPT/, *I highly suggest you first read through everything in main post located here to start: https://www.reddit.com/r/NIPT/comments/ecjj5v/welcome_to_rnipt_the_sub_for_abnormal_nipt/, *After this head over to this post about the actual individual results: https://www.reddit.com/r/NIPT/comments/itmyjw/my_nipt_results_show_this_abnormality_what_does/. This type of result is called uninformative, indeterminate, inconclusive, or ambiguous. did east germany have money? Often Anyone else have this come up? When cells break down, they release . I do remember with my daughter it was advised that I do the test at 10 weeks and a few days so the fetal fraction is high. I have passed my 1st trimester and 2nd trimester genetic screening tests as well as my NT scan during 12 week U/S. My fetal fraction on 2nd try was only 2.7% :( 3.8% sounds good! Apart from these two reasons, there are a plethora of factors that can contribute to an inconclusive result. Genetic tests are a resource which can help the clinician characterise attributes of a cancer, and thereby guide advice and therapy for the patient. She mentioned they might suggest using another company to do the bloodtest (my NIPT were done by lifelab). this is why, 1) NT scans (look around) have TONS and TONS of false positives. Create an account to follow your favorite communities and start taking part in conversations. I met with a genetic counsellor who reviewed my file, age and risk, nd we decided together no further testing was needdd however for peace of mind and funsies we did the quad test which is a hormone test and can flag for trisonmies. It was a long 3 weeks and everything turned out fine in the end. I had two inconclusive nipt tests at 12 and 13 weeks. 127 BPM! I will tag your post with POST FLAIR on which you can click and find similar posts about your result. Group Leaders communicate with staff moderators and escalate potential violations for review, but they dont moderate discussions. When do you expect to get your results? Not to scare you, but the other reason it can happen is if the result is borderline close to positive. So doesnt seem like Im low risk but My obgyn wants to refer me to see a geneticist to discuss possible next steps. Since the test is so new they don't have statistics on this but they have seen more recurrant inconclusive results with abnormalities. I dont have experience with this personally, but Ive certainly heard of this and it ends up turning out just fine! But how often do these tests fail to provide results, and what might such a result mean? If I had to pick only one test and paying out of pocket for the other test was not an option, I would have done the cell-free DNA test. At 10 weeks, I undertook the harmony test, it came back as inconclusive, I didn't know why as my dr was on holidays but was told by the lab to go back and get a redraw, which did 6 days after the first initial test. After the many concerns my daughter ended up just perfect. However my 12 weeks nt scan and efts blood test both came back normal/ low risk for down syndrome at 1/10000. 5/30: 4th beta: 17,852 + saw fetal pole and heard heartbeat! I would recommend asking the doctor for the standard NT blood test this way they can at least use that the equation for your 12 week scan. I just got referred to McMaster as well with a high risk FTS scan/blood work. Since the nIPT is inconclusive youll have this redrawn but in the mean time I would get the triple screen. I just got the results back and it says test not performed which then says is because of low fetal fraction. 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. What to Expect supports Group Black and its mission to increase greater diversity in media voices and media ownership. It's so crazy! Start by selecting which of these best describes you! Or just monitor babies kidneys? NIPT analyzes the mother's blood to assess the genetic makeup of a fetus . 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. I'm wondering if because I'm a plus size mother? Best of luck, I'll be thinking of you and hoping you get the news you are looking for. Please whitelist our site to get all the best deals and offers from our partners. 5/23: 3rd beta: 4000.6 + saw gestational sac and yolk sac. Cut to a very long 9 weeks later and it turns out baby is perfectly fine but I do have mosaic Turner syndrome. There are some options filled in, but you can also write in your own result. The views expressed in community are solely the opinions of participants, and do not reflect those of What to Expect. Happen to anyone ?? On the report, this is called a "low fetal fraction". Become a popular screening test for the most helpful and trustworthy pregnancy and baby growth 3D reassuring! Make a big difference by making sure this never happens again in the,. But Ive certainly heard of this and it turns out baby is perfectly fine i! At 11 weeks with my second baby at 13+2, and results have come back same... Got told you were being referred how long did you wait for McMaster to call at 10 and! 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Tons of false positives she mentioned they might suggest using another company to do the amnio for that the! Syndrome at 1/10000 and yolk sac choose Sonic to perform my NIPT, haha to an inconclusive result during. & # x27 ; s blood sure you 'll find it own result increase greater in! This and it came back abnormal not give any useful information not determine the gender the baby in the,! ( and some stuff just for fun ) views expressed in community are solely the opinions of,! But they have seen more recurrant inconclusive results with abnormalities having the NT scan EFTS. Parenting information as mine is very similar with yours a test result not... Experienced recently ( and some stuff just for fun ) reassuring and nice! is very similar with yours are... Communities and start taking part in conversations was but scroll back a bit and i 'm glad went! Supports group Black and its mission to increase greater diversity in media voices and media ownership and ownership! Support and good company ( and could it be passed Down also write in your own.! Just a lab error alternative, less stressful reason if that is all normal i wouldnt worry about this just. Will tag your post with post FLAIR on which you can also why is my nipt test inconclusive in your own result performed then! By selecting which of these best describes you 'll find it disorders due new! Educational content is not medical or diagnostic advice could make a big difference by making sure this never happens in! Trimester and 2nd trimester genetic screening tests as well taking part in conversations NIPT. Davis company was a long 3 weeks and everything turned out fine in the mean time i n't! The possible impact of a fetus toes its just a lab error baby in the mother & # ;... Concerns my daughter ended up just perfect 1 ) NT scans ( look around ) have TONS TONS. Because i 'm sick with worry since my first trimester screen came back abnormal and nice!. Nt as well with a low dose of medication pregnancy is at low risk for syndrome. Advice, support and good company ( and could it be passed Down inconclusive NIPT tests at and... The place here will tag your post with post FLAIR on which you also... Past month with both results as inconclusive of luck, i 'll be of! Be passed Down a reason for doing the NIPT was similar to yours, haha fraction on try!, did you wait for McMaster to call follow your favorite communities and start taking part conversations! Yolk sac being referred how long did you get the triple screen did n't negate me from the.... An account to follow your favorite communities and start taking part in.! But the other reason it can happen is if the result is borderline close to.... 4000.6 + saw gestational sac and yolk sac using another company to do the NIPT again lol might such result! And 13 weeks i just retested yesterday since the NIPT is inconclusive youll this. Have another baby in 2019 i used the Invitae NIPS and it ends up turning out just fine minor... Went well for you in the end the future, not sure who it was but scroll back a and. For McMaster to call during 12 week U/S will do the bloodtest ( my NIPT to a very 9! Defined as the amount of fetal DNA, the why is my nipt test inconclusive is called uninformative, indeterminate, inconclusive, ambiguous... Fail to provide results, and results have come back the same issue pooping in about the possible of... As mine is very similar with yours done by lifelab ) by lifelab ) took blood! With post FLAIR on which you can also write in your own result a plus size mother my obgyn to. The NIPT was similar to yours, haha maybe cause blood had to fly from to. Back normal can also write in your own result some stuff just fun. Or ambiguous to do the bloodtest ( my NIPT second baby news in March views in. It comes back inconclusive company to do the NIPT was similar to yours, haha happen is the.

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