Newborn metabolic screening is a free test that screens for over 20 rare but potentially serious conditions that can affect your baby's health and development. These conditions are caused by problems with the way the body breaks down food, absorbs nutrients, or handles enzymes. Some examples of these conditions are:
- Phenylketonuria (PKU): a condition that prevents the body from processing a substance called phenylalanine, which is found in many foods. If left untreated, PKU can cause brain damage and intellectual disability.
- Cystic fibrosis: a condition that affects the lungs and digestive system, causing mucus to build up and block the airways and organs. If left untreated, cystic fibrosis can cause lung infections, malnutrition, and respiratory failure.
- Congenital hypothyroidism: a condition that affects the thyroid gland, which produces hormones that regulate metabolism and growth. If left untreated, congenital hypothyroidism can cause poor growth, developmental delay, and intellectual disability.
These are just some of the conditions that newborn metabolic screening can detect. The good news is that most of these conditions can be treated or managed with early diagnosis and intervention. This can prevent or reduce the risk of serious complications and improve your baby's quality of life.
So how is newborn metabolic screening done? It's very simple and painless. A blood sample is taken from your baby's heel at or as soon as possible after 48 hours of age (the 'heel prick' or 'Guthrie' test). The blood sample is then sent to a lab where it is screened for many disorders at once. You will also be asked to fill out a consent form and provide some information about your baby's health history and family background.
The results of the screening are usually available within a few weeks. If your baby's screening results are normal, you will not be contacted by the screening program. This means that your baby is not at increased risk for any of the screened conditions. However, this does not mean that your baby will never develop any health problems in the future. You should still monitor your baby's health and development and consult your doctor if you have any concerns.
If your baby's screening results are abnormal, you will be contacted by the screening program as soon as possible. This means that your baby may have one of the screened conditions or may be a carrier of a genetic condition. However, this does not mean that your baby definitely has the condition or will develop symptoms. You will be referred to a specialist who will confirm the diagnosis and provide you with more information and support.
One of the leading providers of newborn metabolic screening in India is Trivitron Healthcare. Trivitron Healthcare offers a comprehensive range of newborn metabolic screening products and services, including:
- Newborn Screening Kits: high-quality reagents and consumables for testing various metabolic disorders using different methods such as fluorometry, tandem mass spectrometry, immunoassay, and molecular diagnostics.
- Newborn Screening Instruments: advanced instruments for performing newborn metabolic screening tests with high accuracy, speed, and reliability.
- Newborn Screening Software: user-friendly software for managing newborn metabolic screening data and generating reports.
- Newborn Screening Services: end-to-end solutions for setting up and running newborn metabolic screening programs in hospitals and labs.
Trivitron Healthcare has been providing newborn metabolic screening solutions for over 20 years and has helped thousands of babies across India and other countries to get early diagnosis and treatment for various metabolic disorders. Trivitron Healthcare is committed to improving the health outcomes of newborns and their families through innovation, quality, and service.
If you want to learn more about newborn metabolic screening or Trivitron Healthcare's products and services, you can visit their website or contact at +98400 80008 Email: groupmarketing@trivitron.com
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