The discovery that fetal DNA is present in the mother\u2019s blood during pregnancy has led to the development of a genomics-based maternal blood test called NIPS (non-invasive prenatal screening), which is a very reliable test for Down syndrome. In part due to its cost, NIPS is currently only used as a second-tier test, after a mother has tested positive on less costly and less accurate tests, to confirm the finding prior to resorting to amniocentesis.<\/p>\n\n\n\n
Making NIPS the entry-level test for Down syndrome could benefit women by more accurately detecting an affected pregnancy with less chance of a false positive result and by providing that result several weeks earlier in the pregnancy. As well, because NIPS can detect other chromosomal abnormalities, its use could enable screening for more conditions. The PEGASUS-2 project\u2019s goal is to provide high-quality evidence to support the use of NIPS instead of traditional screening tests by comparing its use as a first-tier and second-tier test in a large cohort of pregnant women. The project will also study the cost effectiveness of expanding screening to other conditions and the ethical, social and legal implications of doing so. It will also provide strategies to promote shared decision-making between couples and health-care professionals. Finally, it will further develop the NIPS technology to reduce its costs by 50 percent and expand its ability to detect other anomalies, as well as ensuring quality control for clinical NIPS testing in Canada and worldwide.<\/p>\n\n\n\n
PEGAGUS-2 will enable publicly funded access to a promising genomics technology for all interested pregnant women, while ensuring that couples have access to web-based tools to help their decision-making and that all health-care professionals are trained in shared decision-making for prenatal screening.<\/p>\n\n\n\n
Short version <\/strong><\/p>\n\n\n\n PEGAGUS-2 will provide the evidence needed to support the provision of a genomics-based prenatal screening test for Down syndrome as a first-tier test and to expand it to diagnose other chromosomal anomalies. Its work will enable earlier and more accurate detection of fetal chromosomal anomalies and support shared decision-making between couples and their health-care professionals.<\/p>\n\n\n\n To learn more about this project, click here<\/a><\/p>\n\n\n\n
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