Newborn screening for hearing loss, PKU, congenital heart disease, congenital hypothyroidism, low thyroid hormone, congenital adrenal hyperplasia, galactosemia, Sickle Cell disease and related red blood cell disorder, biotinidase deficiency, amino acid disorders, fatty acid oxidation disorders, organic acid disorders and cystic fibrosis are routine in Alabama. Testing starts in the hospital and results are usually available at the two week checkup. Newborn screening tests and abnormal hearing tests are repeated at the two week checkup.
An abnormal screen DOES NOT MEAN something is wrong with your baby, only that follow-up is important to make sure that the test is normal. All of these conditions can be treated if detected early, giving babies the best outcomes. That is why we screen!
If you do not see the physicians at Smart Start Pediatrics for your two week checkup, please ensure that your baby’s doctor follows up on these screenings and gives your baby a Hepatitis B vaccination at two weeks of age, if they did not receive it while in the hospital.
You should be notified of your infant’s hearing screen results before leaving the hospital. These screens are often abnormal because infants have fluid in the middle ear space. This does not mean your child has hearing problems. Follow-up is very important.

