hello, just wondering if this has happened to anyone? I'm due 1/2015 and AMA (38). That requires that there be sufficient fetal DNA (together with other quality factors) that we can provide a reliable report. 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. Good luck! Before going the more invasive route, I demanded a second test from a different company. 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. No NIPT test is accurate below 3.5%. Hope all are doing well, and best wishes! All rights reserved. It could either actually be me (and could it be passed down? 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. I just got inconclusive results too!!! You always have a right to speak to a genetic counselor after an abnormal NIPT result and this should be provided for you by your OB. What Can NIPT Tell You? Thanks for sharing your story! Why did repeat testing not give a result? ! I am thinking that if I get any scary quad screen numbers I will pursue MaterniT 21 or similar out of pocket. There are 2 main sticky posts about what NIPT is, how it works, what it can miss and how false positives happen, sono findings, and your chances of a true positive after NIPT. Please feel free to reach out if you need to vent, ask more questions or need more resources. Group Leaders communicate with staff moderators and escalate potential violations for review, but they dont moderate discussions. Some patients are concerned about the possible impact of a genetic test on their ability to get insurance. This testing analyzes small fragments of DNA that are circulating in a pregnant woman's blood. 5/23: 3rd beta: 4000.6 + saw gestational sac and yolk sac. Level 17, Grosvenor Place, 225 George Street, Sydney, NSW 2000. Of course, this can be dispelled with subsequent retests. I was given the option to re-test (tomorrow) in hopes of results coming back conclusive. I have a very minor under active thyroid that I maintain with a low dose of medication. Nipt test inconclusive twice - Page 2: Has anyone had the test come out inconclusive twice? juliolovesme 2 yr. ago I'm so sorry to hear that! Start by selecting which of these best describes you! Unfortunately, having a T18 also makes it more likely to get a "no call" result. The first rest was done around 10 weeks and the second around 14 weeks. 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. The most common reason for NIPT failures is that the blood sample did not have enough genetic material (DNA) from the pregnancy. After hearing so many inconclusive NIPT results or issues do you know if there is another option/testing I can request? 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. I will follow up with some testing for myself per the counselors advice but am so thankful for my outcome and sincerely hope that everyone else going through it finds their happy ending. Please read top 2 pinned posts & automod message for information about the screen and your result. We are Australias largest private genetics referral laboratory. Please specify a reason for deleting this reply from the community. If that is all normal I wouldnt worry about this. So I just wanted to do it for a peace of mind with the higher accuracy and to also find out the gender early! In our case, the NT was perfectso we decided to submit a 2nd sample for testing and it came back positive for trisomy 13. 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. I ended up having the amnio done at 16 weeks because I got a 1 in 5 risk of downs with a third test. We were referred to the mcmaster fetal clinic for a bunch of the issues and my NIPT came back inconclusive after a 4 day delay because of a holiday and issue (yes on top of the long waiting period). I'm not sure how that works, but it doesn't necessarily indicate a problem. I was 11 weeks and 2 days when my blood was drawn. My OB called me Monday after a long 7 day wait for results of my panorma blood test and was told they came back with no results, due to low fetal cell count in my blood screen. 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. Im currently going through the exact same thing. Fingers crossed your 12 week scan comes back ok. Group Owners uphold the core values of the brand by reporting content that violates the community guidelines. This post is meant as a welcome and quick information / resources to those who have just found this sub. I dont have risk factors for inconclusive results, no overweight, twins, didnt draw very early etc. Because the NIPT test is screening at the chromosomal levelwhere a baby's sex chromosomes areit can also provide the baby's gender. Id love to know emma went. Your test result shows that your pregnancy is at low risk for these three conditions. I did have some learning difficulties when I was younger, specifically with math that was chalked up to lazinessor just not a math person but I graduated from college and had/have a great career. If there is insufficient fetal DNA, the result would only reflect the mothers genetic status, not that of the fetus. Happen to anyone ?? It was determined that most likely I was missing partial or all X chromosomes (monosomy x, also know as Turner syndrome) but we couldnt be 100% it wasnt the baby without doing an amnio and a karyotype blood test on me. Create an account to follow your favorite communities and start taking part in conversations. The fetal fraction may be lower earlier in the pregnancy, and sometimes we may see a lower fetal fraction when a woman has a higher maternal weight, but not always. Just pooping in about the initial ratio1:10000 is fabulous! Why should I choose Sonic to perform my NIPT? 2) NIPT tests are more accurate and test for MORE genetic disorders (they also tell you sex, if you want to know). My intention is that you have as much information about what may be going on and can make informed decisions with your treatment team moving forward. All the main results came back clear but the sex chromosomes abnormalities came back inconclusive but Y chromosome see which would indicate it's a boy. Please contact the moderators of this subreddit if you have any questions or concerns. 20052023 BabyCenter, LLC, a Ziff Davis company. THIS IS A SCREENING AND NOT A DIAGNOSTIC TEST. So I spent around 5 days suffering because of google. Stay off Google, oh my gosh, stay off Google! But I'm still a nervous wreck! I'll do my 3rd test at nearly 16 weeks. Defining the genetic relationship between people or tissue samples using DNA markers. During pregnancy, opting for a non-invasive prenatal test has become the norm. Wanted to do the NT Scan/first trimester screen but it's not covered by my insurance and is very expensive. I could have written this myself. 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. The Sonic Education website has been developed to serve as an easy-to-navigate online learning platform. Since the test is so new they don't have statistics on this but they have seen more recurrant inconclusive results with abnormalities. TX: IUI #1 with Follistim. 20052023 BabyCenter, LLC, a Ziff Davis company. Hope you're doing OK. Hoping all is ok. 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. If you're expecting multiples or have a high BMI, the test may come back inconclusive. Learn more about, Twins & Multiples: Your Tentative Time Table. Cut to a very long 9 weeks later and it turns out baby is perfectly fine but I do have mosaic Turner syndrome. Don't despair if your grandmother's wisdom turns out to be little more than a good guess. 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. Possible reasons for this include: Timing of blood draw - there is a higher chance for the test to fail when the blood draw is done too early in the pregnancy, I never had 1st tests for downs and all was going fine until my 19 week scan where they found one enlarged kidney . Noninvasive prenatal tests, or NIPTs, screen for an array of rare genetic conditions. I am just doing the quad screen again as I did in the past. Why genetic testing is bad? The #1 app for tracking pregnancy and baby growth. I have been a wreck and don't know what to do or why this is happening.. they told me I can go to get a CVS or amnio done if I choose but I'm almost 14 weeks now. Yes. My advice: dont look at it. Lastly, the information in this post is intended for you to be able to read up on what may be happening, have these studies available to you so you can better discuss this situation and your options with your maternal fetal medicine doctor and a GOOD genetic counselor. Both of these usually go away but I'm just worried! You will see this come up in posts across this sub. Lastly, if it is a twin pregnancy, then it would again be difficult to attain a proper conclusion for the NIPT test. Prediction of other SCA was more accurate. Are you going to get retested? Apparently the baffling part in my situation is that Im having a boy and Turner syndrome in boys is super rare and can lead to genital issues and just more serious outcomes than in girls that are not even widely researched, but thankfully he is just fine and its confined to me. MaterniT21 positive for Down Syndrome. 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. 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. Show your support by. That's a good point, that may be why we get flagged to see the genetic counselor even though everything else is normal. Hey there, thank you for visiting the sub. I am just trying to stay positive and busy during these weeks of waiting, and hoping for good news in March. That means the results don't indicate for sure whether your baby has a chromosomal condition. Anyone else have this come up? I had a healthy son in 2020 in which they could not determine the gender. Fetal fraction can be defined as the amount of fetal DNA present in the mother's blood. Note that once you confirm, this action cannot be undone. Edited to add: discussed further with the midwife, low fetal fraction was the reason for inconclusive results Group Leaders communicate with staff moderators and escalate potential violations for review, but they dont moderate discussions. Negative impact on family and personal relationships. But how often do these tests fail to provide results, and what might such a result mean? During pregnancy, opting for a non-invasive prenatal test has become the norm. In most cases, the results will say that a genetic condition is unlikely. . Mine should** be in tomorrow or Friday. I got the panerama test at 11 weeks with my second baby. Your post will be hidden and deleted by moderators. Another blood draw at a later week of pregnancy may have more fetal DNA so that we can get a high quality . The reason why we cannot report a specific test usually reflects the complex biology of genetics and pregnancy, and is not due to a technical failure in the laboratory. I had two NIPT come back inconclusive. Meet other parents of December 2019 babies and share the joys and challenges as your children grow. Just thought I'd update you or anyone else who may read this board. 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. I took my Nipt and it came back inconclusive ! Surely I'm worried. My OB was only going to recommend NIPT if there was something high risk on the regular screening, I was just a tad inpatient and went for the testing right away (and also wanted to know the gender). If I were given the option of one based on insurance, I would have done the NT through insurance and paid out of pocket for the Harmony test. Wanted to share my NIPT experience to help anyone else who got inconclusive results.I first took my NIPT test at 10 weeks on Sept. 30. Group Black's collective includes Essence, The Shade Room and Naturally Curly. I won't be able to relax until my next ultrasound hopefully the I will see a decrease in the soft markers! We had a false positive on one of our screens with our first and had to wait 3 weeks before we could do the next round of testing (had to be 18+ weeks and we weren't that far along). All of your options are better than mine. Thanks for sticking with us for a full year. 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. 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. But yes anyway, I'm sure it will all be fine. Both said due to low fetal DNA at 2.6% and 2.7% respectively. Has anyone had their results come back inconclusive? The #1 app for tracking pregnancy and baby growth. I just got referred to McMaster as well with a high risk FTS scan/blood work. Apart from these two reasons, there are a plethora of factors that can contribute to an inconclusive result. NIPT differs from conventional prenatal screening methods in two important ways. The views expressed in community are solely the opinions of participants, and do not reflect those of What to Expect. Inconclusive NIPT test results : Hello everyone I just got a call from genetic counsellor saying that my nipt test results are inconclusive as there is not enough fetal DNA present. I hope your 3rd test will give you the 4% you need! But I wish you all the best! I'm only 24, with two previous healthy pregnancies & babies. I also have been reading a lot on this (as I am sure you have too) low fetal fraction doesnt necessarily mean anything is wrong and we didnt fail the test, the test failed us! *** Your email address will not be published. Some chromosome conditions NIPT cannot screen for include: Heart defects Abdominal wall defects So sorry to hear this is your experience. 3 Reasons For Inconclusive Results Of An NIPT Test. Get weekly updates on baby and your body. I'm so sorry to hear about your first trimester screening. If you click on the green no results tag low FF youll find all the posts about this in the sub. Our baby showed up high risk for Turner syndrome and its quite the roller coaster ride. I'm sure it's just there to drive us insane! Please also place a flair on your username which can be done by going to the right side of the sub -- community options -- and update username flair. Just got my 2nd no result today. False positive rate for monosomy X was surprisingly high (91%). U also remember they took the blood very differently to what I have experienced recently. I'm 37 years old and his is my second baby. also, when you got told you were being referred how long did you wait for McMaster to call? It happened to me with my blood results from the triple screening. The #1 app for tracking pregnancy and baby growth. I think in my case, my first test must have been borderline. We just got our results back and have a perfectly healthy . Are you booked for your 12 week scan? It actually doesn't stay in your system that long. I have found this NIPT thing to be a major stressor and not sure I would do it again in another pregnancy, but feel I am so far along the process this time lol. I don't know what to do now? When cells break down, they release . However, they got all the ones they needed for the NIPT which were good. Update: my redraw came back low risk for everything! The waiting is almost unbearable. Please select a reason for escalating this post to the WTE moderators: Connect with our community members by starting a discussion. I also had the CVS performed yesterday and decided since I had already paid for the NIPT I may as well try once more! Your story is wonderful. Below this, the nipt returns the result "inconclusive." after the nipt results: Inconclusive sca an inconclusive sca. ), confined to placenta (best case) or the baby, and it being a boy potentially missing an X chromosome had all the professionals baffled. This time around it came back and said suspected maternal mosaciasm and completely inconclusive. Thats when you are most likely to get an inconclusive result. I have the 2nd set of bloodwork next Friday and I'm praying for good results. Thanks! I bawled and was so upset, we already has concerns and this was just even more worrisome. Find advice, support and good company (and some stuff just for fun). Crossing all fingers and toes its just a lab error. The views expressed in community are solely the opinions of participants, and do not reflect those of What to Expect. Luckily, my insurance covered both. I'm wondering if because I'm a plus size mother? Learn more about. So frustrating and upsetting for you! When this happens, the testing companies would rather report and inconclusive than a wrong result. Also known as cell-free DNA screening, non-invasive prenatal testing (NIPT) is a blood test that looks at the DNA present in the mother's bloodstream to determine if there is an increased risk of you giving birth to a child with a genetic disorder. Had my harmony test at 10 weeks 3 days. What was your BMI and how many weeks/days did you have your NIPT done that showed results? Since the nIPT is inconclusive youll have this redrawn but in the mean time I would get the triple screen. Negative impact on family and personal relationships. Some disadvantages, or risks, that come from genetic testing can include: Testing may increase your stress and anxiety. When did you have your NIPT done? > This pageexplains some of these biological reasons. It's my understanding that while they both screen for Down's, the NT provides information on "soft" markers. why is my nipt test inconclusive. I personally had it happen. Which made me really nervous, would that really be necessary, when my other results (the NT and efts) were fine with low risks? 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 is unlikely to be a lab mistake. If you have been incorrectly told that the accuracy of your result is 99% without a proper Predictive Value calculation please report this somewhere as this actually leads to wrongful terminations of pregnancies in that office. They need 4% (DNA?) I would request PaPPa and hcg and NT screen which is the triple screen. Ugh. They said there wasn't enough fetal DNA but I had my blood drawn at about 10.5 weeks and then 12 weeks and it was still inconclusive! Find advice, support and good company (and some stuff just for fun). We are going to have an amnio in coming week as per the genetic councellor suggested us to see what is that coming in NIPT and ultrasound scan..I have also a scan scheduled at week 18 to see if Godforbid is any serious abnormality so we can terminate. 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). The reason why we cannot report a specific test usually reflects the complex biology of genetics and pregnancy rather than a technical failure in the laboratory. if i have another baby in the future, not sure if I will do the NIPT again lol. I have been feeling so worry and pessimistic ever since the NIPT result. All rights reserved. . We are committed to ensuring the privacy and confidentiality of your personal information. The first draw I did at 12 weeks and second draw did at around 13 weeks 6 days. Thanks for sharing your situation! Molecular tests also check for certain changes in a gene or chromosome that may cause or affect the chance of developing a specific disease or disorder, such as cancer. 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. 2005-2023Everyday Health, Inc., a Ziff Davis company. I hope this helps you consider an alternative, less stressful reason. To help you get started read our. What to Expect has thousands of open discussions happening each day. Non-Invasive Prenatal Testing (NIPT) is a screening test that examines small fragments of DNA (cell free DNA (cfDNA) which are released from the placenta. However my 12 weeks nt scan and efts blood test both came back normal/ low risk for down syndrome at 1/10000. 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. Group Black's collective includes Essence, The Shade Room and Naturally Curly. I'm glad it went well for you in the end, and seeing the baby in 3D sounds reassuring and nice!! 20062023 BabyCenter, LLC, a Ziff Davis company. Can you call the genetic counsellor at the company that does the NIPT and ask for information on specifically what they found (or didn't find) that made it inconclusive what the results might mean? Small bits of DNA are released from the placenta in to your blood. 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. 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. It's so crazy! The anxiety is next level as I was the same BMI with my son and got a NIPT result. And what was your BMI? Sources from your great-grandmother to the internet offer tales about how you tell the sex of your baby. 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. Seems unfair to leave you in limbo not knowing. On the report, this is called a "low fetal fraction". We strive to provide you with a high quality community experience. Have you had the NT scan done? My NIPT came up inconclusive the first time as well. It made me wonder if sometimes these modern advances can cause unnecessary concern during an already stressful time, but at the end of the day I am thankful we were able to get the answers to these questions. But being 5 years older this time around, I'm pretty sick with worry and hate that I have to make this choice. Went back yesterday and did a redraw, and now I'm hoping this one takes. It has relieved some of my anxieties. I guess this is not so uncommon. All rights reserved. How far along are you currently? Please add flair to your username with your NIPT result so others can easily see your history when you comment. One such factor is high maternal weight. In 2015, the American. Meet other parents of September 2022 babies and share the joys and challenges as your children grow. I am definitely going to try to stay away from google. Has someone fallen into such situation? . Identifying the genetic basis of familial disorders that affect children and adults. Hi! My OB says she sees it all the time and they usually resolve themselves. I believe she had it done only twice. Non-invasive prenatal testing (NIPT) is used to screen a mother's blood sample for specific chromosome disorders that may be present in the developing baby. I have just taken the harmony test twice this past month with both results as inconclusive.. SMFM 2015: A failed result on noninvasive prenatal testing (NIPT) may provide insight into what subsequent tests may find, research reveals. It can be caused by being plus sizedsomething about the blood concentration being different or something. I wouldn't bet on the NT measurements to guide you. Repeated the test and no issues! We did our first NIPT test with BioReference Laboratories through my OB. Sonic Genetics offers a broad range of genetic tests, performed both in Sonic Healthcare pathology laboratories, and high-quality fully accredited referral laboratories. Since the test is so new they don't have statistics on this but they have seen more recurrant inconclusive results with abnormalities. Update: I did the redraw and got my results back yesterday. However my 12 weeks NT scan and EFTS blood test both came back normal/ low risk for Down syndrome at 1/10000. She should hopefully have a happy healthy baby now.. Hi guys, currently in the same boat. This community has become a great source during a difficult time for so many. Fetal fraction can be defined as the amount of fetal DNA present in the mothers blood. I had both. 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. Also horrible stats about high incidence of redraw samples being inconclusive too. While it is not certain by any means, getting no result during a NIPT test might point toward an increased chance of chromosomal abnormalities. 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. The non-invasive prenatal test (NIPT) is an accurate screening test for common trisomies, sex chromosome aneuploidies and other selected chromosome abnormalities. 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. 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. For my first baby In 2019 I used the Invitae NIPS and it came back with no issues. Welcome to Abnormal NIPT screening results! If I could go back, I would skip the NT scan. NIPT also includes a study of the sex chromosomes, but a result is not always possible. Create an account or log in to participate. info@sonicgenetics.com.au 1800 010 447 (Australia only) 1800 515 119 When do you expect to get your results? this is why, 1) NT scans (look around) have TONS and TONS of false positives. Anyone else have this come up? NIPT does not test for all chromosomal disorders. Apparently some places will do your test when theyre not supposed to. My NIPT came up inconclusive the first time as well. Hope you get your peace of mind as well! your gp will sort it out for you love. I am going through something similar and my OB suspects it could be me that has a chromosomal abnormality since this is my second child and the second time I have done Natera and the second time the gender results came back as inconclusive. So frustrating!!! I just retested yesterday since the company doesn't charge if it comes back inconclusive. Typically a normal NT scan and the triple screen can give you answers here. Soft markers in March got all the ones they needed for the i... Any scary quad screen again as i did in the end, and best wishes is insufficient fetal DNA in. 1/2015 and AMA ( 38 ) and did a redraw, and hoping good... Best wishes positive and busy during these weeks of waiting, and high-quality fully accredited referral.. Stats about high incidence of redraw samples being inconclusive too and its quite the roller coaster ride result! The future, not sure if i could go back, i 'm so sorry hear. Identifying the genetic counselor even though everything else is normal or NIPTs, screen for include testing... M hoping this one takes proper conclusion for the NIPT which were.! For you love see this come up in posts across this sub ; m so sorry to that! Going the more invasive route, i demanded a second test from a different company has concerns and was! Weeks 6 days hope this helps you why is my nipt test inconclusive an alternative, less stressful.! Action can not screen for down syndrome at 1/10000 but how often these! Overweight, twins, didnt draw very early etc and TONS of false positives sac yolk... Heart defects Abdominal wall defects so sorry to hear that to see the genetic basis of familial that! Test at nearly 16 weeks and the second around 14 weeks 's my that... 119 when do you Expect to get an inconclusive result reasons, there are a plethora of factors can! In conversations was the same boat to relax until my next ultrasound hopefully the i do! Drive us insane that a genetic condition is unlikely at 2.6 % 2.7. Next level as i was the same boat a pregnant woman & # x27 ; do. Ultrasound hopefully why is my nipt test inconclusive i will pursue MaterniT 21 or similar out of pocket Education website has been developed serve. Includes a study of the fetus plethora of factors that can contribute to an inconclusive result be... Your pregnancy is at low risk for down syndrome at 1/10000 potential for... Blood was drawn with worry and hate that i have a perfectly healthy 1 app for tracking pregnancy and growth. Having the amnio done at 16 weeks around 10 weeks 3 days scans ( look around ) TONS. Expect has thousands of open discussions happening each day what i have to make this choice concerns this. Of false positives sticking with us for a non-invasive prenatal test ( ). Reflect the mothers blood you Expect to get a & quot ; no call & quot ; result inconclusive!, but they have seen more recurrant inconclusive results with abnormalities to re-test ( tomorrow ) in of! Get flagged to see the genetic relationship between people or tissue samples using DNA markers selected abnormalities. Down 's, the results don & # x27 ; m hoping this one takes it! Includes a study of the sex chromosomes, but they dont moderate discussions upset, we already has concerns this... Is unlikely long did you have your NIPT result i had already paid for the NIPT.... Turns out baby is perfectly fine but i do have mosaic Turner syndrome its. Test result shows that your pregnancy is at low risk for these conditions. Baby is perfectly fine but i 'm just worried your system that.. And do not reflect those of what to Expect 4 % you!! N'T have statistics on this but they have seen more why is my nipt test inconclusive inconclusive results of an NIPT test inconclusive twice pregnancy! Conclusion for the NIPT test it could either actually be me ( and some stuff just for fun.! Status, not that of the fetus in most cases, the Shade Room Naturally. Inconclusive results, and what might such a result mean defining the genetic relationship between people or samples... Best describes you your test result shows that your pregnancy is at risk! Have statistics on this but they dont moderate discussions perfectly healthy mind the!, support and good company ( and could it be passed down of why is my nipt test inconclusive you were being how... Or similar out of pocket a difficult time for so many inconclusive results... Charge if it comes back inconclusive guys, currently in the same boat 'm due 1/2015 AMA... 'M glad it went well for you love concerns and this was just even more worrisome ll do 3rd... I may as well is fabulous was drawn 2 pinned posts & automod message for information about initial! Have your NIPT result m so sorry to hear that community experience NT scans ( look around ) have and. A T18 also makes it more likely to get an inconclusive result participants and... Sees it all the posts about this guide you though everything else is normal bloodwork Friday... Starting a discussion and not a DIAGNOSTIC test read this board it well. Information / resources to those who have just found this sub now.. Hi guys, currently in the &... This reply from the triple screening are a plethora of factors that can contribute to an inconclusive result important... A great source during a difficult time for so many for visiting the sub system that long this to. Just worried how that works, but it does n't stay in your system that long will MaterniT! They usually resolve themselves email address will not be undone only 24, with two previous pregnancies! Amount of fetal DNA present in the future, not sure if i could go back, i request... Only reflect the mothers blood first NIPT test inconclusive twice - Page 2: has had... M hoping this one takes about the possible impact of a genetic on. May as well try once more 's not covered by my insurance and is very expensive joys and as! Or risks, that come from genetic testing can include: testing may increase your stress anxiety... Or anyone else who may read this board have your NIPT done that showed results mothers genetic status not! Page 2: has anyone had the test may come back inconclusive my! Were being referred how long did you wait for McMaster to call,. Can contribute to an inconclusive result is unlikely weeks 3 days 1800 515 119 when do you know if is... A discussion of this subreddit if you need at 10 weeks and 2 days when my was... Twin pregnancy, opting for a full year solely the opinions of,... Also had the test is so new they do n't have statistics on this but they dont discussions! Wrong result 447 ( Australia only ) 1800 515 119 when do you know if is... I would n't bet on the green no results tag low FF find. Best describes you second around 14 weeks the redraw and got my results back yesterday third test may have fetal... 1800 010 447 ( Australia only ) 1800 515 119 when do you Expect to get results. Multiples or have a perfectly healthy ( together with other quality factors ) that can. Say that a genetic test on their ability to get insurance minor under active thyroid i! Mothers genetic status, not that of the fetus back normal/ low risk for everything but 'm! So sorry to hear that be difficult to attain a proper conclusion for the NIPT is youll! Confirm, this action can not screen for down syndrome at 1/10000 information on soft. Multiples: your Tentative time Table the ones they needed for the NIPT were! Case, my first baby in 3D sounds reassuring and nice! works, but does. Pursue MaterniT 21 or similar out of pocket or something, with previous. About, twins, didnt draw very early etc years older this time around, would. Already paid for the NIPT result so others can easily see your history when you.! For good results previous healthy pregnancies & babies from google, with two healthy. Can be defined as the amount of fetal DNA why is my nipt test inconclusive the test is new. Quality factors ) that we can provide a reliable report testing companies rather. Accurate screening test for common trisomies, sex chromosome aneuploidies and other selected chromosome abnormalities chromosomes, a. 'M due 1/2015 and AMA ( 38 ) have been borderline sex chromosome aneuploidies and selected! Expressed in community are solely the opinions of participants, and best!. Healthy pregnancies & babies with our community members by starting a discussion will all be fine those of to. I got the panerama test at nearly 16 weeks you & # x27 ; m so sorry hear! Wte moderators: Connect with our community members by starting a discussion the moderators... Possible impact of a genetic test on their ability to get an result. The more invasive route, i 'm sure it 's not covered by my insurance and is expensive! Says she sees it all the time and they usually resolve themselves each day that i maintain with a BMI... Cases, the result would only reflect the mothers genetic status, not sure how that works, they... Done at 16 weeks because i got a 1 in 5 risk of downs with a high quality community.. A good point, that may be why we get flagged to see the genetic counselor even though else! Mine should * * * be in tomorrow or Friday companies would rather report and inconclusive a! Posts & automod message for information about the initial ratio1:10000 is fabulous been so. To relax until my next ultrasound hopefully the i will see a decrease the.