Find out more about cortisol deficiency and how it is treated. This page also contains information from Great Ormond Street Hospital (GOSH) about how to deal with illnesses, accidents and other stressful events in children on cortisol replacement.
Where are the adrenal glands and what do they do?
The adrenal glands rest on the tops of the kidneys. They are part of the endocrine system, which organises the release of hormones within the body (please see the diagram above). Hormones are chemical messengers that switch on and off processes in the body.
The adrenal glands consist of two parts:
- the medulla (inner section) which makes the hormone ‘adrenaline’ which is part of the ‘fight or flight’ response a person has when stressed.
- the cortex (outer section) which releases several hormones.
The two most important are:
- Aldosterone – this helps regulate the blood pressure by controlling how much salt is retained in the body. If a person is unable to make aldosterone themselves, they will need to take a tablet called ‘fludrocortisone’.
- Cortisol – this is the body’s natural steroid and has three main functions:
- helping to control the blood sugar level
- helping the body deal with stress
- helping to control blood pressure and blood circulation.
If the body does not make enough cortisol, a tablet version is given. This tablet is called ‘hydrocortisone’ and is given at regular intervals throughout the day. Without treatment your child will become very ill.
What is cortisol deficiency?
Cortisol deficiency occurs when the adrenal glands do not produce enough cortisol. This can happen for four main reasons:
- When the pituitary gland is unable to produce the chemicals needed to tell the adrenal glands to ‘switch on’ their cortisol production. The pituitary gland is the ‘master gland’ which controls other glands in the body.
- When there is a defect in the adrenal glands so they do not allow cortisol to be produced.
- If the adrenal gland itself fails or is removed.
- If adrenal glands stop producing cortisol because there are additional steroids in the body. The replacement steroid medicines should be withdrawn slowly to give the adrenal glands a chance to ‘wake up’ and start producing cortisol again.
For more information about your child’s condition, please ask your doctor or nurse specialist.
When to increase a child’s hydrocortisone dose
If a person with cortisol deficiency becomes very unwell, they are unable to increase the production of cortisol in their system, which is needed to help the body cope and which could be life threatening.
In these circumstances, the amount of hydrocortisone given needs to be increased quickly. This is done by, either:
- increasing the dose of oral hydrocortisone taken as tablets or
- giving an injection into the child’s thigh (intramuscular hydrocortisone).
It can be difficult to know when the child needs to increase their dose of hydrocortisone, but it may be necessary if they are ill, have an accident or injury or are going to have some medical treatments. Parents should follow the flow chart they have been provided to help them decide if this is required.
An extra dose will not do any harm, so if in doubt it is better to give it than not, and then contact the specialist treatment centre for advice about what to do next. If the child is unwell enough to require double dosing, an additional double normal morning dose of hydrocortisone should be given at 4am – set an alarm to remind you.
If the child is given a hydrocortisone injection, they must be admitted to hospital afterwards to be monitored. You should insist that this is for a minimum of 12 hours. This is because the effects of injection only lasts about six to eight hours and it is important to check that the child is stable on their normal oral dose before going home.
Diarrhoea and/or vomiting
It is important not to ignore diarrhoea and/or vomiting, especially if the child is also taking tablets such as fludrocortisone or DDAVP (desmopressin). Diarrhoea and/or vomiting can cause your child to become dehydrated with imbalanced salt levels. Please follow your flow chart for treating diarrhoea and/or vomiting.
Coughs and colds
If the child has a minor head cold with snuffles, runny nose and a cough but is otherwise well, there is usually no need to increase the oral hydrocortisone.
If the child has a raised temperature, this shows that they have some sort of infection and will need double dose oral hydrocortisone and the additional 4am dose. This will usually be for two to three days until the temperature is back to normal.
If the child has been prescribed antibiotics, parents will need to give them double doses of oral hydrocortisone and the 4 am dose until they are better. This can then be reduced to normal maintenance dosing. However, the child must still finish the course of antibiotics as prescribed even if they are feeling better.
- If the child has a dental appointment for a check-up or cleaning, they should not need any extra hydrocortisone.
- If the child has an appointment for fillings or other treatments which require a pain killing injection, parents should give them double the dose of oral hydrocortisone for the 24-hour period around the appointment.
- If the child unexpectedly needs an injection for fillings or other treatment for broken teeth for example, give them double the dose of oral hydrocortisone as soon as possible, and continue for the next 24 hours.
- Major dental work, such as having teeth removed, should only be carried out in hospital. Please call your specialist treatment centre for advice before the appointment.
If the child needs a general anaesthetic for any reason, they will need extra hydrocortisone given intravenously (IV) as they go to sleep. The endocrine registrars at GOSH and UCLH are available to advise your local team on the dose needed and can be contacted by your treatment centre. Advice is available 24 hours a day for emergency admissions.
At GOSH, the child will have an alert attached to their file to remind staff they are on hydrocortisone. It is still important to remind staff in all centres that the child needs their medication given regularly, on time and that it should not be omitted unless adequate IV cover is given.
Immunisations for childhood illnesses
Immunisations are not contraindicated while on replacement hydrocortisone therapy and we would encourage families to complete all routine immunisations.
- If the child is taking medications other than hydrocortisone, you should ask your specialist treatment centre for advice.
- Parents should give double the dose of oral hydrocortisone for the 24-hour period around the injection. If you have any worries, please ring the specialist treatment centre for advice before the child is due to have the immunisation.
Children may develop a high temperature and/or a rash several days after some immunisations, particularly the MMR vaccine. Parents should keep a close eye on their child after the immunisation and follow the advice under ‘temperatures’ if they become unwell.
Accidents and injuries
If the child has a fall, bump or bruise, but immediately recovers and carries on what they were doing before, they may not need any extra hydrocortisone, but do contact your specialist treatment centre if you have any worries.
However, if they have a serious injury, for example, bump their head and become unconscious, or show signs of shock/hypoglycaemia for any reason, parents will need to give them an intramuscular injection of hydrocortisone and call an ambulance to take them to hospital immediately.
The child may not necessarily need the extra dose of hydrocortisone, but it will do no harm. It is always better that they have the injection as more serious problems may occur if they do not get it when needed.
If for any reason a parent finds their child with symptoms of hypoglycaemia (low blood sugar) for instance, they are:
- not responding as they would normally
parents should give the child the intramuscular injection of hydrocortisone and call an ambulance to take them to hospital immediately.
While waiting for the ambulance, if the child is conscious, give them a glucose gel. Give this by squirting the gel in their mouth between the gums and the inside of the cheek and then rub the cheek gently to help the gel become absorbed.
If the child is unresponsive, never give them anything to eat or drink, including glucose gel.
We provide information packs for schools and are happy for schools to contact us for information. Please let the CNS team know about all changes of school.
Special note for children with diabetes insipidus who are taking DDAVP
If the child needs:
Extra oral hydrocortisone for vomiting and/or diarrhoea, you should:
- Give them double doses of hydrocortisone and add in the 4am dose
- Do not give them any more DDAVP
- Allow them to drink if thirsty
- Take them to hospital for a blood test to check their plasma electrolytesIntramuscular hydrocortisone for any reason, you should:
- Give them an intramuscular injection of hydrocortisone
- Do not give them any more DDAVP
- Call an ambulance to take them to hospital immediately
Your specialist treatment centre will issue you with three emergency medication kits, one of which your child should carry at all times. Others should be kept at home and at your child’s nursery, school or college.
You should make these up as emergency kits in a box or a tin that closes securely.
Each kit should contain:
- 1 x vial of 100mg/1ml hydrocortisone sodium phosphate
- 1 x 2ml syringe
- 2 x blue needles
- 1 x tube of glucose gel with instructions for use
- 1 x leaflet ‘How to give an emergency injection of hydrocortisone®
- 1 x steroid card filled in with child’s details
- A copy of your ambulance protocol
- Some spare oral tablets of hydrocortisone
- You should check the expiry dates of hydrocortisone tablets, injection and glucose gel and order replacements from your family doctor (GP) before they pass their expiry date.
We recommend that all children on steroid replacement therapy wear a medical identity bracelet or necklace at all times. Further information about these can be obtained from the clinical nurse specialists.
If the child is just on hydrocortisone then the alert should say ’cortisol deficient; at risk of adrenal crisis’. If they are on other medications, please contact the Clinical Nurse Specialist (CNS) team for advice.
With parental permission, the child will have an ambulance alert put in place for your home and their school address. It is essential that parents contact the CNS team to update any change to these addresses so the protocols can be resubmitted.
The child needs to carry a 'Steroid card for patients on hydrocortisone replacement' at all times. Parents can get these cards from the CNS team.
App for your mobile phone
When travelling there are a few things to consider:
Book in the child’s travel vaccines with the GP and follow the immunisations advice earlier in the leaflet.
Parents will need to request a customs letter. Email firstname.lastname@example.org a minimum of two weeks before the holiday with all flight information including transfers, a customs letters and often an emergency protocol in the language of your destination can be sent to you.
- Ensure there is enough medication that if needed, to double dose the whole holiday you would not run short and add a few days extra in case of delays. This must be kept in hand luggage with an emergency hydrocortisone kit.
- When changing time zones, it is safest to give the normal morning dose then repeat eight-hourly (if on three times a day) or six-hourly (if on four times a day) until the morning of your destination’s time zone and then commence at normal times and doses from that point.
- If the child is also on DDAVP please call the endocrine CNS team for advice.
- Ensure your travel insurance company is aware of the child’s cortisol deficiency as this will need to be registered as a pre-existing condition.
- Find out how to contact an ambulance and where the local hospital is located near your destination before you travel. If your child is unwell, you do not want to be finding out this information at that point.
Many of our patients move to UCLH for their care once they reach adolescence. We work closely with the Endocrine team at UCLH to ensure transition is completed when it is appropriate for the child and happens as smoothly as possible. Parents will be given a leaflet introducing the service with contact information when the time comes.
Results from admission
The child’s results take time to collate and be reviewed. Parents will be contacted if changes to medications are needed. If no changes are needed, results will be discussed with in the next clinic appointment.
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