Screening Programmes Congenital hypothyroidism and your child What is congenital hypothyroidism (CHT)? About 1 in 3000 babies born in the UK has CHT. Congenital means the baby is born with the condition. Babies with CHT do not make enough of the hormone thyroxine, an important chemical made in the body. Thyroxine is produced by a gland in the neck called the thyroid. Without thyroxine, babies do not grow properly and can develop permanent physical and mental disabilities. Although CHT cannot be cured, it can be treated simply and successfully.
Newborn blood spot screening is vital because it helps to identify babies with CHT before they start to show symptoms. A few babies born with CHT may have symptoms such as jaundice, dry skin, puffy eyelids, a large tongue, a hoarse cry, feeding problems, constipation and sleepiness. How do children get CHT? The thyroid gland usually starts working in the unborn baby when the mother is about 20 weeks pregnant. There is currently no reliable way to detect CHT before birth and no way to prevent babies being born with CHT. In most cases CHT happens by chance and the specific cause is not known. There is nothing the parents of a baby with CHT could have done to prevent it.
Babies may develop CHT for different reasons: 1. Abnormal development of the thyroid gland: The thyroid gland may not reach its proper place in the neck during development in the womb, or it may be too small, or even missing completely. There is usually no family history of CHT in these babies. The chance of a parent having another baby with CHT is very low. 2. Thyroid gland does not make thyroxine: In 10-20% of babies with CHT the thyroid gland is in the normal place and might even be enlarged, but it still does not produce enough thyroxine. In these families, there may be other relatives with thyroid conditions and there is a chance of having another baby with CHT. If you plan to have more children you may wish to discuss this with your healthcare team. What is life like for children with CHT? Children with CHT are able to live full and active lives, like other children, as long as treatment is taken every day. A few children may develop problems with learning and clumsiness, and may need extra help. There may be a slightly increased risk of hearing problems, so talk to your healthcare team if you have any concerns about your child s hearing. Your child should have all the usual immunisations or medical treatment needed for other conditions. He or she does not need to eat any special diet because of CHT. If you have any other concerns about your baby s health, please ask your healthcare team.
How is CHT diagnosed? CHT is diagnosed by measuring the levels of free thyroxine (free T4) and thyroid stimulating hormone (TSH) in the baby s blood. Some babies will also have a scan of the neck to look at the thyroid gland. 1. Newborn blood spot ( heel prick test ) The newborn blood spot screening test measures the level of TSH in the baby s blood. TSH triggers the thyroid gland to make more thyroxine. A high level of TSH suggests that the baby s thyroid is not working properly to make enough thyroxine. Further blood tests may need to be done. 2. Other blood tests A repeat blood test is done to check the results of the newborn blood spot screening test. This measures the level of TSH again and also the level of free T4 in the blood. A high level of TSH together with a low level of free T4 helps to confirm the diagnosis of CHT. 3. Thyroid scans A thyroid scan may be recommended. Thyroid scans are very safe and they can give information about the type of CHT and whether this is likely to be permanent. They can be helpful in deciding whether there is a chance of CHT occurring in future children.
There are different types of scans: a) Thyroid uptake scan - This test can provide a picture of the thyroid gland and can help to see how it is working. A small dose of a chemical (radioiodine or technetium) is injected into the blood before a scan of the neck is done. An active thyroid gland takes up the chemical and its position can be seen on the scan. An underactive thyroid may not take up much chemical. b) Ultrasound scan of the neck - This is to look at the thyroid position, shape and size. No injection is required and this is completely pain-free. 4. Tests for the Mother The baby s mother may also have some blood tests to aid diagnosis.
What treatment is available for CHT? The treatment for CHT is to take levothyroxine by mouth once a day. This replaces the thyroxine that the body cannot make. Babies should start their treatment promptly, during the first few weeks after birth. Most children will need to continue it throughout life. Studies of children taking levothyroxine show that this treatment is safe and effective because it is putting back what the body isn t making properly. How do I give Levothyroxine? It is very important for your baby to begin taking levothyroxine as soon as possible and to continue to take it for as long as your healthcare team advises. In some babies it may be possible to discontinue levothyroxine after two to three years if tests show it is not needed. Most babies with CHT never stop treatment and take levothyroxine for life. Levothyroxine should be given every day by mouth. It is available in tablets or as a solution and is prescribed in an amount that is measured in micrograms. As levothyroxine is simply replacing a normal body chemical, giving the correct dose every day should not have any side effects. Tablets Thyroxine tablets are small and tasteless. For very young babies, the tablets can be crushed and dissolved in a little breast milk, formula milk or water. This can then be given from a small syringe or a spoon. Most babies accept the medication quite easily in this way. Solution Levothyroxine may also be prescribed as an oral solution. The solution comes in different strengths so it is important to make sure you are given the correct one when collecting a new supply. The solution can be given in the same way as a crushed tablet, using a syringe or a spoon. Other important things to remember about giving levothyroxine:
Tablets should not be mixed into a bottle feed because if the baby does not finish the bottle, he or she will not receive the full dose. If you forget a dose of thyroxine give it as soon as you remember. Do not give a double dose. If your baby vomits immediately after taking the tablet, you will need to give another dose. A suspension is not the same as a solution. Do not use a suspension. If you are in doubt, please speak to a healthcare professional. Older babies can have their tablets crushed into a spoonful of cereal, mashed vegetables or fruit. Certain foods such as soya products and iron medications may alter the amount of thyroxine that gets into the blood. Check with your healthcare team if you are unsure about anything you are giving your baby. Talk to your healthcare team about how to manage your baby s thyroxine treatment in special situations, e.g. if your baby is ill. What follow up checks will my baby need? Your baby will need regular blood tests to make sure that he or she is receiving the correct dose of levothyroxine for their age and size. The dose will be increased over time, as your baby grows up and several dose changes will be needed. The first blood tests are usually 2 weeks after treatment starts and then 4 weeks, 8 weeks, 3 months, and every 3 months until the baby is a year old. Blood tests will be needed more frequently during the first year of life as your baby will be growing fast. Testing then tends to be less frequent in the next two years but should not be less than twice a year. The healthcare team will also carefully monitor your child s growth.
Useful terms Agenesis The complete absence of the thyroid gland. Congenital Congenital means the baby is born with the condition. Congenital hypothyroidism (CHT) A condition where, for one of a number of reasons, the thyroid gland does not work properly and fails to make the thyroid hormone called thyroxine. Dyshormonogenesis The thyroid gland is of normal size and position, or may even be enlarged, but it still does not produce enough thyroxine. Dysgenesis The thyroid gland is missing, ectopic (in the wrong place) or underdeveloped (small). Endocrinology A branch of medicine dealing with disorders of the glands and hormones of the body, e.g. CHT. Ectopic thyroid The thyroid gland is in the wrong place or position. Healthcare team Health professionals caring for your child: e.g. paediatric endocrinologist, paediatrician, GP, specialist nurse, health visitor Hypothyroidism Babies with hypothyroidism do not make enough of the hormone thyroxine, a natural chemical made in the body. Levothyroxine The full name for the medication given to babies with CHT. Levothyroxine medicine is sometimes just called thyroxine. Levothyroxine replaces the thyroxine that the body cannot produce.
Paediatric endocrinologist A doctor who specialises in treating endocrine (hormone) disorders in children, such as CHT. Radioiodine A form of iodine (a chemical) that has a very small amount of radioactivity. It is used for thyroid uptake scans. Sporadic CHT When CHT occurs by chance in babies with no CHT in their family, it is called sporadic. T4 (free T4) A measure of the level of thyroxine (or free thyroxine) in the blood. In children with CHT who need treatment, T4 levels are lower than they should be. Technetium A chemical with a very small amount of radioactivity used for thyroid uptake scans. Thyroid uptake scans A safe test to help get a good picture of the thyroid gland and look at its activity. A small dose of a chemical (radioiodine or technetium) is injected into the blood before a scan of the neck is done. Thyroxine TSH The thyroid hormone (a special body chemical) produced by the thyroid gland. Children with CHT take a thyroxine or levothyroxine tablet or liquid solution once a day by mouth. This replaces the thyroxine that the body cannot produce. Thyroid stimulating hormone is produced by the body to tell the thyroid gland how much thyroxine to make. In children with CHT who are not getting the right treatment, TSH levels in the blood are higher than normal.
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Contact details For leaflets on screening: You can visit the UK Newborn Screening Programme Centre (UKNSPC website at: www.newbornbloodspot.screening.nhs.uk/ Follow the link named Leaflets and Booklets on the Home Page. UK Newborn Screening Programme Centre Level 5, Frontage Building Great Ormond Street Hospital For Children NHS Foundation Trust Great Ormond Street London WC1N 3JH Tel: 0207 829 7883/4 Email: uknewbornscreen@gosh.nhs.uk The following organisations provide information and support for people with CHT and their families: British Thyroid Foundation 2nd Floor 3 Devonshire Place Harrogate HG1 4AA Tel/Fax: 01423 709707 or 01423 709448 Email: info@btf-thyroid.org Web: www.btf-thyroid.org The Child Growth Foundation 21 Malvern Drive Sutton Coldfield B76 1PZ Tel/Fax: 020 8995 0257 or 020 8995 9075 Email: info@childgrowthfoundation.org Web: www.childgrowthfoundation.org British Society for Paediatric Endocrinology and Diabetes BSPED Secretariat c/o BioScientifica Ltd. Euro House, 22 Apex Court Woodlands Bristol BS32 4JT Tel: 01454 642258 Email: BSPED @endocrinology.org Web: www.bsped.org.uk A UK National Screening Committee publication 1st edition February 2007. Updated August 2012. Review date August 2015.