Neonatal testing is an important part of infant care and is often used to identify potential issues, such as metabolic, congenital, or haematological disorders. Early detection of these problems could help improve results through the early administration of treatment.
An Overview of the Test Procedure
This type of testing is usually done within the first few days after a child is born. It involves obtaining a small amount of blood from the baby’s heel. This is why it is commonly referred to as the blood spot or heel prick test.
After that, the sample is examined for indicators linked to different illnesses. Oximetry screening and hearing tests may also be required to assess the baby’s health.
What Conditions Are Generally Tested for?
Here are a few examples of the conditions that are typically tested for:
• Phenylketonuria (PKU). This inherited disorder renders a child unable to properly use phenylalanine. It affects the brain and can cause the baby to have learning disabilities in addition to behavioural issues.
• Congenital hypothyroidism (CHT). When babies suffer from CHT, they have underdeveloped thyroid glands. Fortunately, this condition is treatable, and kids can live normal lives with the proper medication.
• Cystic fibrosis (CF). The mucus that is produced in the respiratory tract and intestines is thicker than usual in those who have cystic fibrosis. Infections of the lungs and problems with digestion typically result.
• Galactosaemia. This incurable genetic disorder causes an accumulation of galactose in the affected child’s blood. By avoiding milk and, later, food that contains this sugar, those who suffer from this condition can lead a normal life.
Get Quality Neonatal Test Kits
If your job involves neonatal testing, then it’s important that you have access to reliable test equipment to ensure reliable results. At Trinity Biotech, we offer reliable products to help you reach your goals.
Contact Trinity Biotech today to learn more about our products!
