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Newborn Screening Tests

What are newborn screening tests?

Newborn screening tests are blood tests given to infants just after they are born. These tests check for certain disorders before they cause serious damage. Newborns can then be treated to prevent problems later in life. The tests are provided by state departments of health. Different states have different rules about which tests are done.

Newborn screening tests are not perfect. Sometimes they show that a child has a disease that the child does not actually have. All children who test positively for a disease should be tested again. Rarely, the tests do not identify children who actually do have the disease.

What diseases are tested for?

All states in the U.S. test for 4 diseases:

  • hypothyroidism. If babies do not have enough thyroid hormone, they may not develop normally.
  • phenylketonuria (PKU). This can cause mental retardation if not treated early.
  • galactosemia. This condition can cause blindness, mental retardation, and growth problems if not treated.
  • hemoglobinopathy, including sickle-cell disease. Blood diseases may cause newborns to be at risk for dangerous infections.

Many but not all states test for:

  • homocystinuria. This disorder can cause mental retardation, blood clotting problems, and skeletal problems.
  • congenital adrenal hyperplasia. This disorder may cause death if not treated.
  • biotinidase deficiency. This disorder may lead to seizures, hearing loss, mental retardation, and problems with the immune system.

If these rare diseases are diagnosed early, they can be treated. Some can be completely cured.

Some states test for amino acid, organic acid, and fatty acid oxidation defects. In other states these tests are only available through private testing labs. Early diagnosis and treatment of these disorders may help to prevent serious problems like mental retardation. Ask your health care provider about these screening tests.

How are the tests done?

Your child's health care provider makes a tiny cut in the baby's heel to get a small amount of blood to test. Well infants are usually tested just before they go home from the hospital, but not later than 72 hours after birth. Sick or premature infants are tested at 1 week of age, or earlier if a screenable disease is suspected.

If a test suggests your child has a disease, the health department will contact you and your baby's doctor. If the tests do not show any diseases, you will generally not be contacted. Your baby's doctor usually has copies of the newborn screening test results.

If your baby needs a blood transfusion, blood tests should be done before the transfusion.

Some states provide a second set of newborn screening tests between 1 and 2 weeks of age. This is important if the newborn leaves the hospital less than 24 hours after birth.

Parents may refuse to have their newborn screened because of religious beliefs or personal beliefs. Parents who refuse to have the testing done must sign waiver forms.

Additional information on newborn screening is available from your health care provider or from the state health department.

Written by Robert Brayden, MD, Associate Professor of Pediatrics, University of Colorado School of Medicine.
Published by McKesson Provider Technologies.
Last modified: 2006-10-26
Last reviewed: 2006-08-22
This content is reviewed periodically and is subject to change as new health information becomes available. The information is intended to inform and educate and is not a replacement for medical evaluation, advice, diagnosis or treatment by a healthcare professional.
Copyright 2006 McKesson Corporation and/or one of its subsidiaries. All Rights Reserved.
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