Besides NIPT (Non-Invasive Prenatal Testing), the OSCAR test (One-Stop Clinic for Assessment of Risk) is another common option for first-trimester screening. While both tests aim to evaluate the risk of chromosomal conditions, they work in different ways. NIPT is a simple blood test performed from 10 weeks of pregnancy that analyses fetal DNA in maternal blood to estimate the risk of chromosomal conditions such as Down syndrome, with higher accuracy than conventional screening. The OSCAR test, typically performed between 11 and 14 weeks, combines a maternal blood test with an ultrasound scan that measures nuchal translucency to calculate chromosomal risk and assess early fetal development.
Although NIPT provides more precise risk estimates, it remains a screening test and may be followed by diagnostic procedures, such as amniocentesis, if the results indicate a higher risk. The OSCAR test, on the other hand, provides broader early pregnancy information, including a structural evaluation of the fetus; however, its accuracy for chromosomal conditions is slightly lower compared to NIPT.
The OSCAR Test incorporates multiple elements in its risk assessment. The biochemical component measures two pregnancy-related hormones in maternal blood: free beta-hCG (human chorionic gonadotropin) and PAPP-A (pregnancy-associated plasma protein A). These markers, combined with ultrasound findings and maternal factors, form the overall risk calculation.
Additionally, 3D fetal ultrasound technology enhances conventional screening by providing three-dimensional images of the fetus’s anatomy. This imaging allows visualisation of facial features, limb development, and organ formation, offering both medical insights and meaningful bonding opportunities for parents as they see their baby’s features in greater detail.