What does Florida newborn screening test for?

What does the newborn blood screening test for?

Newborn screening tests look for developmental, genetic, and metabolic disorders in the newborn baby. This allows steps to be taken before symptoms develop. Most of these illnesses are very rare, but can be treated if caught early. The types of newborn screening tests that are done vary from state to state.

What is included in the infant metabolic screen in Florida?

Some of these may include:

  • Amino acid metabolism disorders.
  • Biotinidase deficiency.
  • Congenital adrenal hyperplasia.
  • Congenital hypothyroidism.
  • Cystic fibrosis.
  • Fatty acid metabolism disorders.
  • Galactosemia.
  • Glucose-6-phosphate dehydrogenase deficiency (G6PD)


What conditions are newborns screened for?

Newborn Screening Tests

  • Phenylketonuria (PKU). PKU is an inherited disease in which the body cannot metabolize a protein called phenylalanine. …
  • Congenital hypothyroidism. …
  • Galactosemia. …
  • Sickle cell disease. …
  • Maple syrup urine disease. …
  • Homocystinuria. …
  • Biotinidase deficiency. …
  • Congenital adrenal hyperplasia.

Is newborn screening mandatory in Florida?

Per Florida Statute 383.14, all newborns must have a specimen collected before discharge, unless a parent or guardian objects to the screening test. A written statement of such objection must be presented to the physician or other person whose duty it is to administer and report tests and screenings.

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Can parents refuse newborn screening?

All states require screening to be performed on newborns, but most will allow parents to refuse for religious purposes. Any decision to decline or refuse testing should first be discussed with a health professional, since newborn screening is designed to protect the health of the baby.

Who will collect the sample of newborn screening?

The blood sample for ENBS may be collected by any of the following: physician, nurse, medical technologist or trained midwife.

What happens if a baby tests positive for PKU?

Newborn babies who test positive for PKU are placed on phenylalanine-free formula right away. As babies start to eat solid food, their diet will need to be restricted. This is because phenylalanine is found in many foods with protein. A child with PKU should not eat milk, fish, cheese, nuts, beans, or meat.

How accurate is newborn screening for cystic fibrosis?

The newborn screen is just a screen for cystic fibrosis. Those with an abnormal (screen positive) newborn screen do not necessarily have cystic fibrosis. Most times (approximately 90%), it is a false positive, meaning the screen was abnormal and the child does not have cystic fibrosis.

Will DCF take my newborn in Florida?

DCF will remove if they believe the newborn is at substantial risk of harm with you for any reason. You may want to consult with an attorney to further discuss your circumstances and develop a plan prior to your child’s birth.

Is blood type tested at birth?

The easiest way is to quickly check your birth certificate, since blood type is sometimes listed in birth records, Dr. Lee says.

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What does an abnormal newborn screening mean?

An “abnormal” result means that the test results were not normal. “Abnormal” results may appear on the newborn screening report for some of the disorders on the newborn screening panel.

How long do newborn screening results take?

It takes about three weeks for your doctor to receive your baby’s results. If your baby needs more testing, you will be notified by phone or letter in a few days after your baby’s blood spot is collected. How much does the Newborn Screening cost?

What test do hospitals run on newborns?

The newborn screening test, called the Recommended Uniform Screening Panel (RUSP), is done when your baby turns 24 hours old and is usually performed in the nursery at the hospital. The nurse will swab your baby’s heel, then prick the heel and blot five small blood samples on a testing paper.

Is newborn screening accurate?

For a screening test to be fully effective, its sensitivity should ideally approach 100%. The reasons for this are quite obvious; to assure that health care professionals and patients can depend on the newborn screening test result, it must reliably detect almost every case of the disease.

When should I get my newborn screened?

When does the screen happen? The blood test is generally performed when a baby is 24 to 48 hours old. This timing is important because certain conditions may go undetected if the blood sample is drawn before 24 hours of age.

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