What is the Guthrie blood test for?

What is the Guthrie blood test for?

The Guthrie test, also called the PKU test, is a diagnostic tool to test infants for phenylketonuria a few days after birth. To administer the Guthrie test, doctors use Guthrie cards to collect capillary blood from an infant’s heel, and the cards are saved for later testing.

Why is it called a Guthrie test?

The classical Guthrie test is named after Robert Guthrie, an American bacteriologist and physician who devised it in 1962. The test has been widely used throughout North America and Europe as one of the core newborn screening tests since the late 1960s.

Why is the Guthrie test done after 48 hours?

12. Why is the test done at 48 hours or as soon as possible after this? When a baby with a metabolic disorder is in the womb, the placenta clears away any abnormal biochemical levels as the baby’s system produces them.

When is the Guthrie test performed?

The newborn heel prick test (Guthrie test) is a term used to describe the newborn blood spot screening test that is offered to all newborns at the age of 5-40 days.

When is a Guthrie done?

The screening works best when tests are done early, so the samples are collected 48 to 72 hours after birth.

How long does Guthrie test take?

Usually, a midwife takes a blood sample between 48 and 72 hours after the baby is born. The midwife pricks the baby’s heel and places a few drops of blood onto a piece of card. This can happen in the hospital or at home. The test is safe and will not harm your baby.

When should the Guthrie test be done?

The screening test is also called the ‘heel prick’, ‘Guthrie’ or ‘PKU’ test. The screening test is done when your baby is 48 hours (2 days) old or as soon as possible after this – it can be done in hospital or at home. Your midwife will collect a small amount of blood from your baby’s heel onto a blood spot card.

How long does it take for Guthrie test results?

The results are usually available within 6-8 weeks. The results are entered in the child’s medical records, which should be preserved for all future visits.

What are the symptoms of PKU if left untreated?

Untreated PKU can lead to:

  • Irreversible brain damage and marked intellectual disability beginning within the first few months of life.
  • Neurological problems such as seizures and tremors.
  • Behavioral, emotional and social problems in older children and adults.
  • Major health and developmental problems.

What happens if a baby doesn’t pass the hearing test?

If your baby doesn’t pass the second hearing test, they will be referred to a paediatric audiologist to test if they have a hearing problem. The audiologist will see your baby as soon as possible if they do not pass the follow-up hearing screen in both ears.

Can you live a normal life with PKU?

If PKU is confirmed, treatment will be given straight away to reduce the risk of serious complications. Treatment includes a special diet and regular blood tests. With early diagnosis and the correct treatment, most children with PKU are able to live healthy lives.

What is the Guthrie test?

The Guthrie test or “Heel Prick” test is routinely carried out on neonatal (newborn 48-72 hours of age) blood for a variety of known genetic disorders. The clinical term “phlebotomy” describes the act of drawing or removing blood from the circulatory system through an incision or puncture to obtain a sample for analysis and diagnosis.

What is the Guthrie test used to diagnose phenylketonuria?

By 1963 the test had become a routine neonatal test for phenylketonuria. The “Heel Prick” test. The Guthrie test or “Heel Prick” test is routinely carried out on neonatal (newborn 48-72 hours of age) blood for a variety of known genetic disorders.

What did Dr Guthrie do in Buffalo?

At Dr. Guthrie’s urging, adult participants in a sheltered workshop in Buffalo collated and packaged test kits.

What is a Guthrie card?

Dr Robert Guthrie (1916-1995) was an American microbiologist at University of Buffalo who developed the collection of whole blood on filter paper “Guthrie cards” for transportation, storage, and testing for metabolic and genetic disorders of the newborn.