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. Also horrible stats about high incidence of redraw samples being inconclusive too. Acosta decided to take advantage of non-invasive pregnancy testing, or NIPT, a relatively new prenatal screening method. Your post will be hidden and deleted by moderators. Diagnostic fetal chromosome analysis should be offered after abnormal NIPT or in the presence of cystic hygromas despite normal NIPT. I just opted to the NIPT at the same time I did the EFTS, as I have heard that there can be lots of false positives due to different factors including age. It has to be at least above 4 percent to give a conclusive result. I'm waiting on my nipt test results now too. Hopefully will have before weds next week. Results in some cases may return inconclusive or uncertain. 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). > This pageexplains some of these biological reasons. Are you going to try the blood test again? This occurs about 1 in every 150-200 samples. (High HCG, low PAAP-A, normal nuchal translucency.) Babies can be born with a change Hope you're doing OK. Hi all. It can come with its own set of risks. Try not to worry! Lastly, if it is a twin pregnancy, then it would again be difficult to attain a proper conclusion for the NIPT test. 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. Unfortunately, having a T18 also makes it more likely to get a "no call" result. Noninvasive prenatal testing (NIPT) has become a popular screening test for the most common fetal aneuploidies. You could make a big difference by making sure this never happens again in the OB's office for future patients such as yourself. Have you gotten your NIPT results back yet? Group Leaders arent expected to spend any additional time in the community, and are not held to a set schedule. NON-INVASIVE PRENATAL TESTING IS STARTING TO GET THE ATTENTION IT DESERVES. Thank you for replying. 5/23: 3rd beta: 4000.6 + saw gestational sac and yolk sac. My NIPT came up inconclusive the first time as well. Community for those with abnormal or discordant Noninvasive Prenatal Testing (NIPT/NIPS) screening results: FALSE POSITIVE, FALSE NEGATIVE, TRUE POSITIVE & those stuck in limbo. I could have written this myself. Collection centres for all other genetic tests, Genetic counselling for other heritable disorders, Genetic counselling for selected familial disorders, Reproductive carrier screening genetic counselling. You are right! Some disadvantages, or risks, that come from genetic testing can include: Testing may increase your stress and anxiety. Im currently going through the exact same thing. I have been feeling so worry and pessimistic ever since the NIPT result. Easy to overthink (I sure did) and assume the worst - feels like Sod's law at the . Seems unfair to leave you in limbo not knowing. 1997-2023 BabyCenter, LLC, a Ziff Davis company. Group Leaders arent expected to spend any additional time in the community, and are not held to a set schedule. versttning med sammanhang av "invasiva tester inte kan" i svenska-engelska frn Reverso Context: nr invasiva tester inte kan gras eller :). why is my nipt test inconclusive. sm1232, did you receive your results? Note that once you confirm, this action cannot be undone. I actually have an auto immune disease so they think thats why. 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. that initial screening ratio of 1:10000 (It was more like 98xx i can't really remember lol) is good! I'm due 1/2015 and AMA (38). 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. In 2015, the American. Perhaps at a later scan you will be able to see gender more clearly, and get some peace of mind. This usually happens when a, Non-Invasive Prenatal Baby Gender Blood Test. If you click on the green no results tag low FF youll find all the posts about this in the sub. Since the nIPT is inconclusive youll have this redrawn but in the mean time I would get the triple screen. Edited to add: discussed further with the midwife, low fetal fraction was the reason for inconclusive results. Please specify a reason for deleting this reply from the community. Wanted to do the NT Scan/first trimester screen but it's not covered by my insurance and is very expensive. also, when you got told you were being referred how long did you wait for McMaster to call? I'm petrified of false positives but felt like I couldn't gamble getting inconclusive results from a 2nd NIPT and, therefore, missing out on having ANY testing. If the concentration of fetal DNA is below this, then the test might prove to be inconclusive. Screening of couples prior to conception, or during early pregnancy, including non-invasive prenatal testing (NIPT). 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. It happened to me with my blood results from the triple screening. Now is the perfect time to start your Baby Registry! March 31, 2022 . I don't know what to do now? *** Your email address will not be published. Thus, if you received no result during your non-invasive prenatal paternity test, then it might be best to check if any of these 3 factors might be in play. Its nothing to worry about, it was probably just a bit too early! Update: my redraw came back low risk for everything! The #1 app for tracking pregnancy and baby growth. Fingers crossed your 12 week scan comes back ok. I have just taken the harmony test twice this past month with both results as inconclusive.. this is why, 1) NT scans (look around) have TONS and TONS of false positives. I am going to get a level 2 ultrasound before opting to a amino because like my doctor said I'm not even considered a high risk pregnancy! The NIPT shows that I am high risk for Turner Syndrome with my baby girl. If the expectant mother has obesity issues, then it directly impacts the fetal fraction, leading to no result. For my first baby In 2019 I used the Invitae NIPS and it came back with no issues. Im barely 53, but I have about a half an inch in my older sister and come. 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. The first draw I did at 12 weeks and second draw did at around 13 weeks 6 days. Thats when you are most likely to get an inconclusive result. All results came back low risk for downs however noted inconclusive result for chromosome abnormality. I'm not sure how that works, but it doesn't necessarily indicate a problem. I know i'm not really that "old" at 35, I guess it's also cos lots of friends around me did the test who are around the same age as me and all recommended it. Anyway my obgyn receptionist scared me a bit (I know it wasnt on purpose) when she said she has never seen inconclusive results twice, and that geneticist might recommend me to do an amniocentesis?? Thank you for sharing, as the Natera Panorama has really freaked me out. She actually specifically said that it didn't mean anything, bad or good. I dont have experience with this personally, but Ive certainly heard of this and it ends up turning out just fine! However, they got all the ones they needed for the NIPT which were good. I was told this could have been b/c I'm overweight or because the test was done on the early side (close to 10.5w). 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! It was a long 3 weeks and everything turned out fine in the end. Ugh. She should hopefully have a happy healthy baby now.. Hi guys, currently in the same boat. 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. Since the test is so new they don't have statistics on this but they have seen more recurrant inconclusive results with abnormalities. Create an account to follow your favorite communities and start taking part in conversations. I got the results yesterday and another inconclusive. 14/01/2022 22:06. So frustrating and upsetting for you! THIS IS A SCREENING AND NOT A DIAGNOSTIC TEST. for the test to get accurate results. 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. What Does NIPT Not Test For? My fetal fraction on 2nd try was only 2.7% :( 3.8% sounds good! During pregnancy, opting for a non-invasive prenatal test has become the norm. GAH! It was terrifiying, to say the least. 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. Please select a reason for escalating this post to the WTE moderators: Connect with our community members by starting a discussion. I had a healthy son in 2020 in which they could not determine the gender. Rarely, tests results can be false negative, which occur when the results indicate a decreased risk or a genetic condition when the person is actually affected. 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. Sex chromosome aneuploidy was frequently suspected on NIPT. The non-invasive prenatal test (NIPT) is an accurate screening test for common trisomies, sex chromosome aneuploidies and other selected chromosome abnormalities. 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. 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. did east germany have money? Often Your body then filters it out. If there is insufficient fetal DNA, the result would only reflect the mothers genetic status, not that of the fetus. They need 4% (DNA?) I'm panicking now because I'm so worried. . 20062023 BabyCenter, LLC, a Ziff Davis company. This means that the result is not clear and a result cannot be produced. So sorry, the waiting is so tough. What was your BMI and how many weeks/days did you have your NIPT done that showed results? 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? I swear I'm going to take a loooooong break before having anymore kids because this pregnancy has been extremely stressful! It has to be at least above 4 percent to give a conclusive result. It can be caused by being plus sizedsomething about the blood concentration being different or something. What to Expect supports Group Black and its mission to increase greater diversity in media voices and media ownership. 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. The Sonic Genetics website includes general information regarding genetic testing, as well as specific information about particular tests. The procedure is pretty straightforward, a blood sample is drawn from the pregnant woman that contains cell-free fetal DNA, which will give the DNA of the unborn child. We went with Myriad. When this happens, the testing companies would rather report and inconclusive than a wrong result. I took my Nipt and it came back inconclusive ! 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. Please guide us. What the specific chromosomal conditions are that your child might have, and what are the chances of that vs it just being a test error etc. Note that once you confirm, this action cannot be undone. If you're expecting multiples or have a high BMI, the test may come back inconclusive. Noninvasive prenatal testing (NIPT) has become popular with many physicians in screening pregnant patients. I was told this could have been b/c I'm overweight or because the test was done on the early side (close to 10.5w). . Their reasoning is that it affects their accuracy numbersand they don't want to skid away from the 99%. I'm so sorry to hear about your first trimester screening. It's so crazy! Thanks, I'm still waiting! They are up to 99% accurate for chromosomal abnormalities. What to Expect has thousands of open discussions happening each day. 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). Look up their websites and they will tell you the disorders they test for and the accuracy. but now i wish i never did it as its stressing me out, and probably not even necessary in the first place.. anyways good luck to the both of us :). NIPT analyzes fragments of the baby's DNA found circulating in a pregnant person's blood. So as others have said, keep the faith if your first test is inconclusive! We keep them up because there are a ton of great conversations here and we believe you deserve to see them all. 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. Just got this email from the lab doing my test!!! Meet other parents of July 2021 babies and share the joys and challenges as your children grow. Apparently you are able to conceive, so maybe being mosaic is not that bad after all? Common Abnormalities Are: Down syndrome (trisomy 21 . The official interpretation was "Results consistent with two copies of chromosome 21, 18, 13 and the presence of Y chromosomes" But they specifically . Its been very interesting learning this for sure and although my symptoms are extremely mild and nothing showed up for my daughters testing last year when I was pregnant with her I still of course hope this wasnt passed down. 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. Below this, the nipt returns the result "inconclusive." after the nipt results: Inconclusive sca an inconclusive sca. Good luck! They have offered me a redraw. If the concentration of fetal DNA is below this, then the test might prove to be inconclusive. Do your OB rooms have an on call service you can call? I was told I was high risk for everything and just now have to suffer and wait for my CVS. Confirmed by amnio a week later. 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. Costs about 50 bucks. juliolovesme 2 yr. ago I'm so sorry to hear that! The #1 app for tracking pregnancy and baby growth. Makes me worried about why they can't pick up enough fetal DNA. unfortunately, I called the company and they won't give me any information! What company did your test? Certain prenatal screening tests like NIPT are very accurate for conditions such as Down syndrome, but less so for rare genetic conditions. Now I am in limbo awaiting to see what happens next. Luckily, my insurance covered both. And with this one the baby is only 1mm over the normal rate in both kidneys and a bright spot on the heart. My ex husband and I struggled to conceive for years. This message is automatically generated for all submissions and might sometimes get it wrong. They said I can get retested and said maybe cause blood had to fly from nz to au? Which according the clinical labs, they can taste at this rate. Yes. I will keep you all informed about this issue. No? Has anyone else had this happen to them? Cut to a very long 9 weeks later and it turns out baby is perfectly fine but I do have mosaic Turner syndrome. Identifying the genetic basis of familial disorders that affect children and adults. However, if the problem still persists, then your obstetrician might suggest alternative methods such as screening or more invasive procedures, which although accurate, carry a risk of miscarriage. I personally had it happen. Research suggests that about 5 percent of women get no result at all. They all came back negative ! I really do feel for those that don't have as many affordable options. Please specify a reason for deleting this reply from the community. For some patients, however, results are not reported because of laboratory technical issues such as low fetal fraction and sequencing failures. When do you expect to get your results? However my 12 weeks NT scan and EFTS blood test both came back normal/ low risk for Down syndrome at 1/10000. I'll do my 3rd test at nearly 16 weeks. Use of this site is subject to our terms of use and privacy policy. 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. Are you going to get retested? We strive to provide you with a high quality community experience. Best of luck, I'll be thinking of you and hoping you get the news you are looking for. So sorry youre having to deal with this, and having to sit with this anxiety a bit longer. 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. 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. 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. NIPT (also called prenatal cell-free DNA screening) is a screening test that estimates the risk that your baby will be born with a genetic abnormality, including Down syndrome . Then 12 week scan showed 3mm NT. I'm only 24, with two previous healthy pregnancies & babies. The test can also determine the sex of the fetus. 20062023 BabyCenter, LLC, a Ziff Davis company. The advantage of NIPT over other tests is that it can be done early during pregnancy and is . Is the NIPT test conclusive? Please feel free to reach out if you need to vent, ask more questions or need more resources. We work hard to share our most timely and active conversations with you. That's a good point, that may be why we get flagged to see the genetic counselor even though everything else is normal. Science has produced many safe, medically sound, and accurate methods to determine the sex of a fetus during pregnancy. This educational content is not medical or diagnostic advice. 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. (1/19). We aim to be fair and reasonable with our fee structure. What if NIPT cannot make an assessment? I don't think i would want to do an amnio either as I am not even high risk. Use of this site is subject to our terms of use and privacy policy. your gp will sort it out for you love. They told me there wasn't enough fetal DNA in my blood to accurately complete the test. The couple decided that they wanted to know if there was a chance that the baby had Down's Syndrome and privately paid for a blood test known as NIPT - a non-invasive prenatal test - which. I just got referred to McMaster as well with a high risk FTS scan/blood work. And I'm sick with worry since my first trimester screen came back abnormal. Start by selecting which of these best describes you! They need 4% (DNA?) Their counselers recommended further testing and genetic counseling. But higher weight makes NIPT more likely to come back with a "no call" result (although generally not until >180 kg). Reasons behind an inconclusive prenatal paternity test. Symptmes de grossesse ne jamais ignorer, Moyens naturels pour dclencher l'accouchement. 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. My OB says she sees it all the time and they usually resolve themselves. I appreciate those who chime in as we all remember how difficult to be in this situation. 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. Archived discussions are usually a bit older and not as active as other community content. I'm grateful insurance pays for both. My NIPT came up inconclusive the first time as well. I would DEFINITELY choose the NIPT test. Create an account or log in to participate. Results in some cases may return inconclusive or uncertain. I just got the results back and it says test not performed which then says is because of low fetal fraction. Surely I'm worried. Please whitelist our site to get all the best deals and offers from our partners. Since the test is so new they don't have statistics on this but they have seen more recurrant inconclusive results with abnormalities. NIPT Test Results Inconclusive! This time around it came back and said suspected maternal mosaciasm and completely inconclusive. Contact us today to learn more about everything that we can do for you. I hope this helps. my reason for doing the NIPT was similar to yours, haha. It's new. The #1 app for tracking pregnancy and baby growth. harry hill family. Hoping all is ok. My nipt/panorama/harmony results came back inconclusive both times. 127 BPM! I had my blood drawn for the NIPT test on 12/28. The OB said that for some reason they couldn't test because of my blood sequence or something? Please contact the moderators of this subreddit if you have any questions or concerns. Which made me really nervous, would that really be necessary, when my other results (the NT and efts) were fine with low risks? 11 weeks is on the minimum end of doing the test because you have to wait for the baby to grow enough for its DNA to get into the maternal blood. Of course, this can be dispelled with subsequent retests. Just got my 2nd no result today. The cell-free DNA tests also screen for other chromosomal abnormalities other than Down's, such as Edward's syndrome. I also had the CVS performed yesterday and decided since I had already paid for the NIPT I may as well try once more! The #1 app for tracking pregnancy and baby growth. Its 100% accurate (I believe). I had the first level bloodwork and NT scan and they came back normal. Getting my blood redrawn tomorrow. I finally decided to do the Amnio yesterday and now anxiously waiting forresults and am so scare for her to even be Mosaic Turner. 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/. Just waiting for the office to call back to rebook. While it is not certain by any means, getting no result during a NIPT test might point toward an increased chance of chromosomal abnormalities. Thank you for sharing your story as mine is very similar with yours. The DNA sample of the potential father is collected through a buccal swab, and the two samples are compared to determine paternity. Like dont they know us preggers are already stressing?!? Just pooping in about the initial ratio1:10000 is fabulous! Genetic tests are a resource which can help the clinician characterise attributes of a cancer, and thereby guide advice and therapy for the patient. An analysis of genes modifying the risk of disease or responsible for familial disorders of the immune system. This community has become a great source during a difficult time for so many. Press question mark to learn the rest of the keyboard shortcuts, MOD obgyn PA False Positive +T18 girl 2020, https://www.perinatalquality.org/Vendors/NSGC/NIPT/, https://www.reddit.com/r/NIPT/comments/ecjj5v/welcome_to_rnipt_the_sub_for_abnormal_nipt/, https://www.reddit.com/r/NIPT/comments/itmyjw/my_nipt_results_show_this_abnormality_what_does/. 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 had two NIPT come back inconclusive. Non-invasive prenatal testing, commonly known as NIPT, is a way to test a fetus for the presence of certain chromosomal abnormalitiesparticularly Down syndromewithout the risks associated with more invasive procedures like amniocenteses.The necessary information can be obtained from a sample of the mother's blood, which contains some of the fetus' DNA. No NIPT test is accurate below 3.5%. I was 11 weeks and 2 days when my blood was drawn. I thought I would share my story in case it helps anyone else! We are repeating the assay on the same sample you have already sent and we should have that result on Wednesday. Noninvasive prenatal testing (NIPT), is a screening test for determining the risk of certain chromosomal abnormalities in the fetus. During pregnancy, opting for a non-invasive prenatal test has become the norm. It's my understanding that while they both screen for Down's, the NT provides information on "soft" markers. Have you had the NT scan done? NIPT analyzes the mother's blood to assess the genetic makeup of a fetus . I read some said that could be a factor? Your post will be hidden and deleted by moderators. Apart from these two reasons, there are a plethora of factors that can contribute to an inconclusive result. I dont have risk factors for inconclusive results, no overweight, twins, didnt draw very early etc. Both of these usually go away but I'm just worried! They said since they dont know which of my cells are missing the X because they only take a sample size, its hard to pinpoint what is impacted or not. Please dont look google to find out. Hope you get your peace of mind as well! 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. 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'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. 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 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. Defining the genetic relationship between people or tissue samples using DNA markers. 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. How far along are you currently? 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 your 3rd test will give you the 4% you need! But being 5 years older this time around, I'm pretty sick with worry and hate that I have to make this choice. Edited to add: discussed further with the midwife, low fetal fraction was the reason for inconclusive results Hope you get some answers soon. We are Australias largest private genetics referral laboratory. Someone please help calm my nerves! With my first daughter there was an ECF as well that resolved itself. 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. Negative impact on family and personal relationships. Please place POST FLAIR on your actual post. 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. NIPT also includes a study of the sex chromosomes, but a result is not always possible. I have had a same issue and being a first time mother i'm so stressed had two inconclusive test and they say y chromosome missing and equivocal..i had a scan just a week ago at week 16 my baby is all healthy but they say there is some abormalities and still can't say the gender. Your story is wonderful. No, I am a public patient. sm1232, did you get the results to your CVS? Hope all are doing well, and best wishes! Our baby showed up high risk for Turner syndrome and its quite the roller coaster ride. This is unlikely to be a lab mistake. Welcome to Abnormal NIPT screening results! Wouldn't that give you the results you're looking for? Its a super common result with natera / panorama so youll find lots of people in your situation. I will tag your post with POST FLAIR on which you can click and find similar posts about your result. Update: I did the redraw and got my results back yesterday. It definitely makes me feel better with whatever the outcome may be. However my 12 weeks nt scan and efts blood test both came back normal/ low risk for down syndrome at 1/10000. MaterniT21 positive for Down Syndrome. Please whitelist our site to get all the best deals and offers from our partners. Find advice, support and good company (and some stuff just for fun). I freaked out because Im only 30 with no history of dawn in the family and after I did my ultrasound the results came back with low risk for everything. The first rest was done around 10 weeks and the second around 14 weeks. 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. Normal chromosomes come. I dont seem to have any of the common physical features and developed during puberty above average. 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! the test and lead to no result. I'm sure it's just there to drive us insane! 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. Had my harmony test at 10 weeks 3 days. Non-invasive prenatal testing (NIPT) using cell-free DNA in maternal blood is a relatively new screening modality for the common trisomies of chromosomes 21, 18 and 13 and sex chromosome aneuploidies. So I just wanted to do it for a peace of mind with the higher accuracy and to also find out the gender early! I was worried too, so I did a bit of research on it. Some radiologists like to comment on ALL the scans the technicians provided even the poor quality ones. Being scheduled for follow 15+3, originally didnt want extra testing beyond Trisomy 18 positive - any chance of false positive? I had both. The views expressed in community are solely the opinions of participants, and do not reflect those of What to Expect. When did you have your NIPT done? Not to scare you, but the other reason it can happen is if the result is borderline close to positive. Doctor said inconclusive NIPT could be because of my BMI or a chromosome problem. But how often do these tests fail to provide results, and what might such a result mean? My NT ultrasound was normal but they didnt do the blood draw portion because I was getting the nipt, I should ask if they want to do that as well as I may be past the dates for the triple screen draw if I wait for results from my 2nd nipt, Im already 13+2. I have passed my 1st trimester and 2nd trimester genetic screening tests as well as my NT scan during 12 week U/S. 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). It has relieved some of my anxieties. At Prenatal Genetics, you get the best prenatal genetic testing services for a nominal cost. I wish you and your baby boy all the best too! Are you booked for your 12 week scan? 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. Reason being: the labs offering these tests seem to only bill people paying out of pocket $250. To help you get started read our. Had my redraw at 13+2, and results have come back the same . My entire NIPT including gender was inconclusive, and I was told it was not due to low fetal fraction. Did you opt for an amnio? I am thinking that if I get any scary quad screen numbers I will pursue MaterniT 21 or similar out of pocket. jenesiso member. Sounds right on the money, I got turned away for my first babys boot as it was a Friday an they send the test on the Monday and they said they would have it sitting there all weekend its not recommended. What to Expect supports Group Black and its mission to increase greater diversity in media voices and media ownership. 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. Please read top 2 pinned posts & automod message for information about the screen and your result. I wouldn't bet on the NT measurements to guide you. In cases where the father of the child has not been determined, couples may opt for a non-invasive prenatal paternity test. Inconclusive NIPT results. Getting my blood redrawn tomorrow. 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. We are committed to ensuring the privacy and confidentiality of your personal information. Nipt test inconclusive twice - Page 2: Has anyone had the test come out inconclusive twice? This testing analyzes small fragments of DNA that are circulating in a pregnant woman's blood. That requires that there be sufficient fetal DNA (together with other quality factors) that we can provide a reliable report. Why should I choose Sonic to perform my NIPT? Hi! 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. Thank you, I am hoping it's just a silly lab error. It's. My advice: dont look at it. Show your support by. This is the route I took with my son (now 4.5) so I'm familiar with it. PlayRightParent 11.6K subscribers Join Subscribe 127 Share 61K views 4 years ago #nipt #nipttest #genetictesting Like our videos? Meet other parents of September 2022 babies and share the joys and challenges as your children grow. Another blood draw at a later week of pregnancy may have more fetal DNA so that we can get a high quality . This is so when you speak to others, they immediately understand your situation AND you can see their situation summary. Meet other parents of December 2019 babies and share the joys and challenges as your children grow. Hope you're doing OK. 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. But I'm still a nervous wreck! This was simply a technical issue within the laboratory. This discussion is archived and locked for posting. I guess this is not so uncommon. It can be caused by being plus sized.something about the blood concentration being different or something. 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. 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, All rights reserved. Level 17, Grosvenor Place, 225 George Street, Sydney, NSW 2000. On the report, this is called a "low fetal fraction". Just thought I'd update you or anyone else who may read this board. TX: IUI #1 with Follistim. I had the same thing on my panorama test but I was 9 weeks. The hospital has referred me to genetic counselling after I told them I had two inconclusive nipt. 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. Keep us posted! I needed a NIPT done as there were MANY concerns on my 20 week ultrasound. 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. 2005-2023Everyday Health, Inc., a Ziff Davis company. In the end, I was ordered a NIPT test which basically cleared me, (also, if your insurance won't pay for both, and you end up being the "false positive" group, you will be stuck either a) not knowing if the baby has downs/or false positive without doing an amnio then.or waiting for much more testing as your pregnancy progresses). Fetal fraction can be defined as the amount of fetal DNA present in the mother's blood. Reason being: these tests utilize actual DNA and not soft markers. 1 DNA is usually located within cells. 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. . Anyone else have this come up? No, NIPT is a screening test, not a diagnostic test. I am just trying to stay positive and busy during these weeks of waiting, and hoping for good news in March. If the concentration of fetal DNA is below this, then the test might prove to be inconclusive. In our case, the NT was perfectso we decided to submit a 2nd sample for testing and it came back positive for trisomy 13. Symptmes de grossesse ne jamais ignorer, Moyens naturels pour dclencher l'accouchement. 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. 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.
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