We are Australias largest private genetics referral laboratory. Thank you for sharing your story as mine is very similar with yours. Noninvasive prenatal testing (NIPT) has become a popular screening test for the most common fetal aneuploidies. You have all been so supportive, thank you so much. Note that once you confirm, this action cannot be undone. and mine came back at 3.7% and couldn't be read. This testing analyzes small fragments of DNA that are circulating in a pregnant woman's blood. Canceled due to too many follicles (10 + that were large); BENCHED. Surely I'm worried. Sources from your great-grandmother to the internet offer tales about how you tell the sex of your baby. Please dont look google to find out. 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. During pregnancy, opting for a non-invasive prenatal test has become the norm. Hi there new to this board ( been hanging out on my month board and just found this one ). You're doing a great job, mama! 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! Ugh. 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. They could well be inaccurate- most companies require at least 3%. We are committed to ensuring the privacy and confidentiality of your personal information. As always, take any information given here and online for what it is - information - and always discuss further treatment plans with your physicians, however with caution. 3) anything that the NT scan would show (that NIPT wouldnt), the anatomy scan will also show in 20 weeks and that is a standard test for AMA people, as well. Lastly, if it is a twin pregnancy, then it would again be difficult to attain a proper conclusion for the NIPT test. 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. NIPT Test Results Inconclusive! Genetic tests are frequently not covered by Medicare or private health insurance, Every sample from a patient is tested to determine whether there is sufficient feto-placental DNA to provide a reliable result. There are some options filled in, but you can also write in your own result. I am a bot, and this action was performed automatically. Create an account to follow your favorite communities and start taking part in conversations. It can be caused by being plus sized.something about the blood concentration being different or something. Someone please help calm my nerves! 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. 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. I'm due 1/2015 and AMA (38). In medicine, a laboratory test that checks for certain genes, proteins, or other molecules in a sample of tissue, blood, or other body fluid. Your test result shows that your pregnancy is at low risk for these three conditions. Thats when you are most likely to get an inconclusive result. 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. The performance of NIPT is affected by several factors including maternal obesity, which results in a greater rate of no-calls for obese pregnant women. I'm sure it's just there to drive us insane! 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. Create an account or log in to participate. Just tonight I found out the second draw of blood for the Harmony test came back inconclusive. 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. Group Owners uphold the core values of the brand by reporting content that violates the community guidelines. I would DEFINITELY choose the NIPT test. Contact us today to learn more about everything that we can do for you. Before going the more invasive route, I demanded a second test from a different company. NIPT stands for noninvasive prenatal testing. But I'm still a nervous wreck! They are up to 99% accurate for chromosomal abnormalities. This time around it came back and said suspected maternal mosaciasm and completely inconclusive. This is a newish kind of screening test in which a blood sample from a pregnant woman is used to test for a range of genetic conditions in the fetus, with varying levels of certainty. Sorry youve gone through this stress xx. 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. Thanks for sticking with us for a full year. It's new. Had my redraw at 13+2, and results have come back the same . This educational content is not medical or diagnostic advice. Seems unfair to leave you in limbo not knowing. No, NIPT is a screening test, not a diagnostic test. The NIPT shows that I am high risk for Turner Syndrome with my baby girl. haha our timing for the tests sound quite similar, i am waiting for the referral to see the genetic counselor, so for now will have to wait and see what they recommend. I'm so sorry to hear about your first trimester screening. Hey there, thank you for visiting the sub. Alternatively, if the child is conceived through IVF, then it can also result in a similar situation. Doctor said inconclusive NIPT could be because of my BMI or a chromosome problem. Negative impact on family and personal relationships. Why genetic testing is bad? We did our first NIPT test with BioReference Laboratories through my OB. No, I am a public patient. Small bits of DNA are released from the placenta in to your blood. I wouldn't necessarily do the amnio for that if the baby is otherwise healthy. I don't think i would want to do an amnio either as I am not even high risk. Anyone else have this come up? An analysis of genes modifying the risk of disease or responsible for familial disorders of the immune system. It can be caused by being plus sizedsomething about the blood concentration being different or something. I just wanted to doit for the extra accuracy and seems like a bonus to also find out the gender! Yes. I think in my case, my first test must have been borderline. The non-invasive prenatal test (NIPT) is an accurate screening test for common trisomies, sex chromosome aneuploidies and other selected chromosome abnormalities. 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. It's so crazy! Getting my blood redrawn tomorrow. It has relieved some of my anxieties. Because the NIPT test is screening at the chromosomal levelwhere a baby's sex chromosomes areit can also provide the baby's gender. 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. The first rest was done around 10 weeks and the second around 14 weeks. 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. Thanks for sharing your story! Hope all are doing well, and best wishes! I am booked for a 12 week scan this week. 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. How far along are you currently? versttning med sammanhang av "invasiva tester inte kan" i svenska-engelska frn Reverso Context: nr invasiva tester inte kan gras eller Thanks for sharing your situation! 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 was just so surprised to get an "inconclusive" a second time- the woman in the lab who drew my blood said she had never seen it come back that way twice! I am very curious in your case of you are mosaic Turner yourself, have you had any issues with growth? During pregnancy, opting for a non-invasive prenatal test has become the norm. Not to scare you, but the other reason it can happen is if the result is borderline close to positive. One such factor is high maternal weight. 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! No? Try not to worry! Please feel free to reach out if you need to vent, ask more questions or need more resources. I just retested yesterday since the company doesn't charge if it comes back inconclusive. I had the first level bloodwork and NT scan and they came back normal. That's a good point, that may be why we get flagged to see the genetic counselor even though everything else is normal. A failed test result will only be reported after testing of both samples) Inconclusive result. So frustrating and upsetting for you! That OB needs further education about NIPT positives and how to present such information as well as knowledge of the Positive Predictive Value of NIPT based on age. It happened to me with my blood results from the triple screening. Are you booked for your 12 week scan? Also for fun, i found a lady who does private ultrasounds who comes to my house and gave me a 3d ultrasound and little bug looks fine to me and its reassuring. Best of luck! Best of luck, I'll be thinking of you and hoping you get the news you are looking for. Create an account or log in to participate. If I could go back, I would skip the NT scan. 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). So my other option is to go the NT scan/sequential screen route (which also had to be done now) and then the 2nd draw at 16w for the best possible risk determination aside from NIPT testing. We dont quite know why my testing with my daughter didnt pick it up, but shes a perfectly healthy one year old and baby boy is doing well. 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. Keep us posted! 5/23: 3rd beta: 4000.6 + saw gestational sac and yolk sac. Pregnancy. Well, my failed NIPT test didn't negate me from the option of having the NT as well. What Does NIPT Not Test For? I personally had it happen. 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. Reasons behind an inconclusive prenatal paternity test. Why did repeat testing not give a result? It lead to 3 weeks of PURE hell. 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! Please specify a reason for deleting this reply from the community. 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. Costs about 50 bucks. 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. No NIPT test is accurate below 3.5%. 16 week ultrasound scheduled for Monday, June 6 and Amniocentesis scheduled for Wednesday, June 8. My fetal fraction on 2nd try was only 2.7% :( 3.8% sounds good! I was 11 weeks and 2 days when my blood was drawn. 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. This time they are sending me to a high risk doctor. In 2015, the American. Because NIPT consists of a simple blood test, it doesn't create a risk for you or your baby. 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