Newborn Screening
The video explains the process of newborn screening, which involves tests to detect certain metabolic disorders in newborns. The first screening occurs within the first 24 hours after birth, requiring the baby to be at least 12 hours old. This involves a heel prick to collect blood, which is applied to a card. The second screening takes place at two weeks of age. These tests check for rare but serious conditions like PKU and hypothyroidism. The results are reviewed initially at the birth site and followed up with a call after the two-week screening if any issues are detected.