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Whats a harmony test12/31/2023 ![]() ![]() NIPT is not recommended for all pregnant women, but it may be offered to women who are at increased risk of having a baby with a chromosomal abnormality due to their age or other risk factors. Is NIPT recommended for all pregnant women? The technician will require basic details, such as Ultra Sound report (USG), Dual and Quadruple Marker Report, Photo Identification Proof, etc. The blood sample is collected in a streak tube, about 10 ml, and your sample is then sent for quality testing and analysis. The sample collection is done at your residence, making it a highly convenient way of screening. The NIPT test is performed at a National Accreditation Board for Testing and Calibration Laboratories (NABL) certified laboratory. ![]() You can get further testing done to determine whether your foetus is testing positive for a specific condition. While not all tests are 100% accurate, the NIPT test will be able to provide critical insights on your pre-screening risk. If the NIPT results indicate a high risk for a chromosomal abnormality, it means that the risk of the baby having the condition is higher than average If the NIPT results indicate a low risk for a chromosomal abnormality, it means that the risk of the baby having the condition is very low. In general, NIPT results are reported as low risk or high risk for a specific chromosomal abnormality. There are several different NIPT tests available, and the specific test used will determine the results of the test. This means that NIPT is very good at identifying women who are at low risk of having a baby with a chromosomal abnormality. Overall, NIPT has a high sensitivity (the ability to correctly identify individuals with the condition being tested for) and a high negative predictive value (the ability to correctly identify individuals without the condition). The accuracy of NIPT depends on several factors, including the stage of pregnancy, the specific condition being tested for, and the specific NIPT test being used. Pls ask for Sample report to confirm your requirements. NIPT does not test for the gender of the fetus Whats the difference between NIPT Basic v/s NIPT Advanced If the NIPT results indicate an increased risk of a chromosomal abnormality, the healthcare provider may recommend further testing to confirm the diagnosis. NIPT can provide valuable information about the risk of certain chromosomal abnormalities in a developing fetus. The test is considered to be non-invasive because it does not involve any risk to the fetus and does not require a procedure such as amniocentesis (a procedure in which a sample of amniotic fluid is taken for testing). NIPT is a blood test that analyzes fetal DNA that is present in the mother's bloodstream. NIPT is typically performed during the f irst or second trimester of pregnancy / gestational age 11 to 17 weeks, and is used to screen for conditions such as Down syndrome (trisomy 21), trisomy 13, and trisomy 18. Non-invasive prenatal testing (NIPT) is a screening test that is used to assess the risk of certain chromosomal abnormalities in a developing fetus. ![]()
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