Newborn screening is a complicated system in a race against time. And if we lose the race, children can die from these disorders. If we can find affordable ways to make the system of newborn screening run the race faster, we can help save lives. With the help of the Robert Wood Johnson Foundation and experts across the University in health services, engineering and health policy, my research team is working to find a way to help us run a faster race.
What is newborn screening? Well, shortly after birth, every baby in the US is tested for a variety of inherited diseases. If babies who have these diseases are not found and started on treatment, they can become seriously ill, and, in some cases, die. This process of testing and treating children at birth for inherited diseases is called newborn screening. It is a 50 year-old public health program that is conducted in every state across the US. Continue reading