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Status epilepticus

You have status epilepticus if

  • you have a seizure that lasts 30 minutes or longer, or
  • you have a cluster of shorter seizures for 30 minutes or more, with little or no recovery in between.

Any type of seizure can become status epilepticus. Status epilepticus is a medical emergency because the longer a seizure lasts, the less likely it is to stop on its own. It’s also less likely to stop with emergency medicines. Status epilepticus can lead to brain damage, or even death.

Epilepsy Action has more information about seizure types.

Convulsive status epilepticus

During a long convulsive tonic-clonic seizure, your body struggles to circulate oxygen around your body. When this happens, your brain doesn’t get enough oxygen. Over a long period, this can lead to brain damage and death.

Epilepsy Action has more information about tonic-clonic seizures.

Non-convulsive status epilepticus

If you have a long seizure that is non-convulsive, for example a focal (partial) seizure, you may still need emergency medicines after five minutes. This is to prevent non-convulsive status epilepticus, which can cause brain damage. But, because you will still be breathing, it is not as dangerous as convulsive status epilepticus.

Epilepsy Action has more information about focal seizures.

Calling for an ambulance

For all types of seizure, call for an ambulance if…

  • You know it is the person’s first seizure, or
  • The seizure continues for more than five minutes, or
  • One tonic-clonic seizure follows another without the person regaining consciousness between seizures, or
  • The person is injured during the seizure, or
  • You believe the person needs urgent medical attention

Treatment for status epilepticus

The following information is about the treatment of status epilepticus in the UK. The treatment in other countries may be different.

When a person has status epilepticus, a medical professional will usually give them an injection of the drug diazepam, either at the scene of the seizure or in hospital.  Where diazepam is not suitable, other drugs, such as buccal midazolam, can be used. (See below.)           

Diazepam can also be given rectally (into the back passage). It doesn’t need to be given by a medically qualified person. However, it’s usual for some training to be given to people who may need to provide the drug. This training is usually given by a medically qualified person.

It’s essential for the person who needs emergency medication to have an individual care plan. This should show when, and how much, rectal diazepam is to be used, and what to do afterwards. If you would like a care plan template, please send an email asking for this to the Epilepsy Helpline

Rectal diazepam can be extremely effective in stopping seizures, but many people with epilepsy feel uneasy at the thought of being given medication this way.  It can also raise issues surrounding privacy, dignity and the law. (Local Education Authorities and Social Services Departments have their own rules as to whether their staff may give rectal diazepam.)

Some epilepsy clinics and centres are using an alternative drug. This is called midazolam. It is given by a dropper, inside the person’s cheek or nose. It’s not licensed to be used for epilepsy in the UK at the moment. However, some medical consultants prescribe it to individual patients, if they believe the drug would be helpful to them.

Further information

The following information about emergency treatment for epilepsy is available from Epilepsy Action. You can find further details about them in our online shop.

  • Rectal diazepam individual care plan
  • Buccal midazolam training DVD for parents and carers

We can provide references and information on the source material we use to write our epilepsy advice and information pages. Please contact our Epilepsy Helpline by email at helpline@epilepsy.org.uk.
Code: 
F84.01

Epilepsy Action would like to thank Dr Amanda Freeman, Consultant Paediatrician at Queen Alexandra Hospital, Portsmouth, UK for her contribution to this information.

Dr Amanda Freeman has no conflict of interest to declare.

This information has been produced under the terms of The Information Standard.

  • Updated August 2012
    To be reviewed August 2014

Comments: read the 5 comments or add yours

Comments

Thanks soooo much for this information page. I have uncontrolled epilepsy and I need to advise my friends and family of what to do if I have a seizure and this page is straight to the point and very factual. Thanks again epilepsy action:)

Submitted by Danielle burns on

my partner has been having seizures since she had a programmable shunt put in may 2011 charring cross hospital because her headaches were so severe, it became blocked after a short time and was replaced in March 2012, no one can tell us why this is happening or what type of seizures she is having they all have been just giving her more more pain killers nothing is helping they insist she is not epilectic and her headaches are still severe we are at our wits end as to what to do now?

Submitted by Kerry Rawlings on

Hi

What a terrible situation to be in, it must be very distressing for you both. I wonder why the doctors are insisting she doesn’t have epilepsy. Of course, it might be that she doesn’t. Could it be that the tests were clear? Tests can be clear even in people who have epilepsy. For example, an EEG only shows what is happening in your brain at the time the test is being done. It’s not able to show what has already happened or what is going to happen in the future. An MRI scan shows if there is anything in the brain that can cause epilepsy. Your partner has had a shunt fitted which can sometimes cause seizures

The difficulty when diagnosing epilepsy is that the symptoms of seizures can be similar to many other medical conditions, including migraine. If it is the shunt that could be causing your partner to have epileptic seizures, she would be having some type of focal seizure. Focal seizures may, or may not, spread to a tonic clonic] seizure.

Your partner might find it helpful to read our website information on seizures and their symptoms. If she finds any symptoms similar to hers, she could download, and highlight them, then talk to her GP. They might be more likely to refer her to an epilepsy specialist if she finds similar symptoms.

Advice and Information Team
Rosanna

Submitted by Rosanna@Epileps... on

would you say 50 was to old for the diet ?

Submitted by karen tidman on

Hi

At present, the ketogenic diet is not used for adults with epilepsy in the UK.  But Matthew's Friends have information on adult diets used to help adults with epilepsy. You will find this information using the dietary treatment tab on their home page.

 

If we can be of any more help, please feel free to contact us again, either by email or the Epilepsy Helpline freephone 0808 800 5050.

Regards

Diane
Advice and Information team

Submitted by Diane@Epilepsy ... on

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