Monday, June 04, 2012

Newborn screening tests

Table of Contents

How to prepare for the test

There is no preparation necessary for newborn screening tests. The tests are performed when the baby is between 24 hours and 7 days old, typically before the baby goes home from the hospital.


How the test will feel

The baby will most likely cry when his or her heel is pricked to obtain the small blood sample. Studies have shown that babies whose moms hold them skin-to-skin or breastfeed them during the procedure show less distress. Swaddling the baby, or offering a pacifier dipped in sugar water, also appear to help reduce pain.

The hearing test should not cause the baby to feel pain, cry, or respond.


Why the test is performed

Screening tests do not diagnose illnesses. They identify which babies need additional testing to confirm or rule out illnesses.

If follow-up testing confirms that the child has a disease, appropriate treatment can be started right away, before symptoms appear.

Screening tests are used to detect a number of disorders, including:

  • Amino acid metabolism disorders:
    • Arginosuccinic acidemia
    • Citrullinemia
    • Homocystinuria
    • Maple syrup urine disease
    • Phenylketonuria (PKU)
    • Tyrosinemia type I
  • Biotinidase deficiency
  • Congenital adrenal hyperplasia
  • Congenital hypothyroidism
  • Cystic fibrosis (see also: Neonatal cystic fibrosis screening)
  • Fatty acid metabolism disorders:
    • Carnitine uptake deficiency
    • Long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency
    • Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency
    • Trifunctional protein deficiency
    • Very long-chain acyl-CoA dehydrogenase deficiency (VLCAD)
  • Galactosemia
  • Glucose-6-phosphate dehydrogenase deficiency (G6PD)
  • Human immunodeficiency disease (HIV)
  • Organic acid metabolism disorders:
    • 3-Hydroxy-3-methylglutaric aciduria (HMG)
    • 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC)
    • Beta ketothiolase deficiency
    • Glutaric acidemia type I
    • Isovaleric acidemia
    • Methylmalonic acidemia
    • Multiple carboxylase deficiency (MCD)
    • Propionic acidemia
  • Sickle cell disease and other hemoglobinopathy disorders and traits
  • Toxoplasmosis

See also: Hearing loss - infants


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Review Date: 06/18/2011
Reviewed By: Kimberly G Lee, MD, MSc, IBCLC, Associate Professor of Pediatrics, Division of Neonatology, Medical University of South Carolina, Charleston, SC. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org)