Introduction
Classification
- 1. Where seizures begin in the brain
- 2. Level of awareness during a seizure (important as can affect safety during seizure)
- 3. Other features of seizures
Focal seizures
- previously termed partial seizures
- these start in a specific area, on one side of the brain
- the level of awareness can vary in focal seizures. The terms focal aware (previously termed 'simple partial'), focal impaired awareness (previously termed 'complex partial') and awareness unknown are used to further describe focal seizures
- further to this, focal seizures can be classified as being motor (e.g. Jacksonian march), non-motor (e.g. déjà vu, jamais vu; ) or having other features such as aura
Generalised
- these engage or involve networks on both sides of the brain at the onset
- consciousness lost immediately. The level of awareness in the above classification is therefore not needed, as all patients lose consciousness
- generalised seizures can be further subdivided into motor (e.g. tonic-clonic) and non-motor (e.g. absence)
- specific types include:
- → tonic-clonic (grand mal)
- → tonic
- → clonic
- → typical absence (petit mal)
- → myoclonic: brief, rapid muscle jerks
- → atonic
Unknown onset
- this termed is reserved for when the origin of the seizure is unknown
Focal to bilateral seizure
- starts on one side of the brain in a specific area before spreading to both lobes
- previously termed secondary generalized seizures
In addition a number of special forms of epilepsy are recognised in children:
Syndrome | Notes |
---|---|
Infantile spasms (West's syndrome) | Brief spasms beginning in first few months of life
|
Lennox-Gastaut syndrome | May be extension of infantile spasms (50% have hx)
|
Benign rolandic epilepsy |
|
Juvenile myoclonic epilepsy (Janz syndrome) | Typical onset in the teens, more common in girls
|
Epidemiology
- Incidence: 50.00 cases per 100,000 person-years
- Most commonly see in infants
- Sex ratio: 1:1
Condition | Relative incidence |
---|---|
Febrile convulsions | 42.00 |
Epilepsy: first seizure | 1 |
<1 | 1-5 | 6+ | 16+ | 30+ | 40+ | 50+ | 60+ | 70+ | 80+ |
Aetiology
- cerebral palsy: around 30% have epilepsy
- tuberous sclerosis
- mitochondrial diseases
Clinical features
- bite their tongue
- experience incontinence of urine
Asking about such features can be useful way of detecting epileptic seizures when taking a history from a patient who presents with a 'blackout' or 'collapse'.
Following a seizure patients typically have a postictal phase where they feel drowsy and tired for around 15 minutes.
Investigations
Differential diagnosis
Disorder | Notes |
---|---|
Febrile convulsions |
|
Alcohol withdrawal seizures |
|
Psychogenic non-epileptic seizures |
|
Management
Antiepileptics are one of the few drugs where it is recommended that we prescribe by brand, rather than generically, due to the risk of slightly different bioavailability resulting in a lowered seizure threshold.
It is useful when thinking about the management of epilepsy to consider certain groups of patients:
- patients who drive: generally patients cannot drive for 6 months following a seizure. For patients with established epilepsy they must be fit free for 12 months before being able to drive
- patients taking other medications: antiepileptics can induce/inhibit the P450 system resulting in varied metabolism of other medications, for example warfarin
- women wishing to get pregnant: antiepileptics are generally teratogenic, particularly sodium valproate. It is important that women take advice from a neurologist prior to becoming pregnant, to ensure they are on the most suitable antiepileptic medication. Breastfeeding is generally considered safe for mothers taking antiepileptics with the possible exception of the barbiturates
- women taking contraception: both the effect of the contraceptive on the effectiveness of the anti-epileptic medication and the effect of the anti-epileptic on the effectiveness of the contraceptive need to be considered
Most neurologists now start antiepileptics following a second epileptic seizure. NICE guidelines suggest starting antiepileptics after the first seizure if any of the following are present:
- the patient has a neurological deficit
- brain imaging shows a structural abnormality
- the EEG shows unequivocal epileptic activity
- the patient or their family or carers consider the risk of having a further seizure unacceptable
Sodium valproate is considered the first line treatment for patients with generalised seizures with carbamazepine used for focal seizures.
Generalised tonic-clonic seizures
- sodium valproate
- second line: lamotrigine, carbamazepine
Absence seizures* (Petit mal)
- sodium valproate or ethosuximide
- sodium valproate particularly effective if co-existent tonic-clonic seizures in primary generalised epilepsy
Myoclonic seizures**
- sodium valproate
- second line: clonazepam, lamotrigine
Focal seizures
- carbamazepine or lamotrigine
- second line: levetiracetam, oxcarbazepine or sodium valproate
*carbamazepine may exacerbate absence seizures
**carbamazepine may exacerbate myoclonic seizures
Acute management of seizures
Most seizures terminate spontaneously. When seizures don't terminate after 5-10 minutes then it is often appropriate to administer medication to terminate the seizure. Patients are often prescribed these so family members may administer them in this eventuality, often termed 'rescue medication'. Benzodiazepines such as diazepam are typically used are may be administered rectally or intranasally/under the tongue.
If a patient continues to fit despite such measures then they are termed to have status epilepticus. This is a medical emergency requiring hospital treatment. Management options include further benzodiazepine medication, infusions of antiepileptics or even the use of general anaesthetic agents.