Archive for the ‘neonata heel prick’ Category
Neonatal heel prick
The neonatal heel prick is a common for taking a blood sample from the heel of newborns infants. A pinprick puncture is made in the heel of the infant’s foot, and blood from the foot is soaked into pre-printed collection cards known as Guthrie cards.
The blood samples can be used for a variety of genetic tests, including:
- Thyroid stimulating hormone (TSH) to detect hypothyroidism and hence prevent cretinism.
- Trypsin to detect cystic fibrosis.
- Detection of phenylketonuria, an enzyme deficiency that can impair brain development.
Other potential tests include:
- A test for galactosemia
It is recommended that the screening test be performed when the infant is between 48 and 72 hours of age. False positives and negatives can sometimes occur when the screening tests are performed before 48 hours.
With genetic tests becoming more common, a wide variety of tests may use the blood drawn by this method. Many neonatal units (SCBUs) now use this method to carry out the daily blood tests (blood count, electrolytes) required to check the progress of ill neonates.
The NHS test for:
- Hypothyroidism
- Cystic fibrosis
- Phenylketonuria
- Medium Chain Acyl Co-A Dehydrogenase Deficiency (MCADD)
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