Epilepsy Flashcards
Describe an epileptic seizure
-Discrete episode of symptoms
-Reflecting brain disturbance
-Due to paroxysmal abnormal electrical activity (often presumed)
Describe epilepsy as a condition
-A continuing tendency to unprovoked (can have a event as trigger) epileptic seizures
Conditions associated with epilepsy
-cerebral palsy: around 30% have epilepsy
-tuberous sclerosis
-mitochondrial diseases
Classification of epileptic seizures
- Where seizures begin in the brain
- Level of awareness during a seizure (important as can affect safety during seizure)
- Other features of seizures
-Focal onset
=Features reflect site of origin, look for underlying focal cause
=Awareness: affected or not?
=Motor onset or other?
-Generalised onset
=Reflect generalised disorder e.g. genetics
=Motor: GTCS, GTS, GCS, other (myoclonic)
=Absences
Classification of epilepsy
-Primary
= Not a symptoms of underlying disease
=Generally genetic
-Secondary
= Due to some other disease (trauma, infection, tumour, stroke)
Describe auras
-Precede a seizure
-Due to focal epileptic disturbance which then spreads to become generalised
=Aura itself a seizure so a focal cause
Examples of epilepsy classification
Primary:
=Primary absence seizure disorder of childhood
=Juvenile Myoclonic Epilepsy
Secondary:
=Focal motor epilepsy with secondary generalisation due to glioma
=Temporal lobe seizures due to mesial temporal lobe sclerosis
Presentation of epilepsy
As well as the seizure activity described above patients who have had generalised seizures may
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.
Questions for diagnostic steps
-Episode(s) epileptic seizure(s) or not?
-If so, what types of seizures ?
-Is there a continuing tendency to unprovoked seizures ?
-Primary or Secondary ?
-If Primary: what is the Epilepsy Classification ?
-If Secondary: what is the Epilepsy classification & cause ?
Investigations for epilepsy
-Brain imaging (cause)
-Routine EEG (classification- where seizure began, level of awareness during seizure, other features), after second simple tonic-clonic, abnormal electrical activity
-Ambulatory EEG
-Video-Telemetry EEG recording
-MRI brain (first seizure under child 2yrs, focal, no response to first line antiepileptic)
-ECG to exclude heart problems, electrolytes, glucose, cultures, urine culture, LP.
Common triggers of epilepsy
Sleep deprivation
Excessive Alcohol
Intercurrent illness / pyrexia
Hormonal factors
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Management of epilepsy
-Antiepileptic after second seizure
=After 1st seizure of neurological deficit, structural abnormality in brain imaging
-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: the possible interactions of the contraceptive and anti-epileptic medication need to be considered
Examples of anti-epilepsy drugs
-Lamotrigine (female): sodium channel blocker
=SE: SJS
-Sodium Valproate (males): increases GABA activity, generalised seizures.
=SE: appetite and weight gain, alopecia, P450 enzyme inhibitor, ataxia, tremor hepatitis, pancreatitis, thrombocytopenia, teratogenic
-Carbamazepine: binds to sodium channels increasing refractory period, second line focal.
=SE: P450 enzyme inducer, dizziness and ataxia, drowsiness, leucopenia and agranulocytosis, SIADH, visual disturbances (diplopia)
-Levetiracetam
-Phenytoin: binds to sodium channels increasing refractory periods
=SE: P450 inducer, dizziness and ataxia, drowsiness, gingival hyperplasia, hirsutism, megaloblastic anaemia, peripheral neuropathy, osteomalacia, lymphadenopathy
-Phenobarbitone
For women taking phenytoin,carbamazepine, barbiturates, primidone, topiramate, oxcarbazepine:
UKMEC 3: the COCP and POP
UKMEC 2: implant
UKMEC 1: Depo-Provera, IUD, IUS
For lamotrigine:
UKMEC 3: the COCP
UKMEC 1: POP, implant, Depo-Provera, IUD, IUS
If a COCP is chosen then it should contain a minimum of 30 µg of ethinylestradiol.
Epilepsy: pregnancy and breastfeeding
-aim for monotherapy
-there is no indication to monitor antiepileptic drug levels
-sodium valproate: associated with neural tube defects, neurodevelopmental delay
-carbamazepine: often considered the least teratogenic of the older antiepileptics
-phenytoin: associated with cleft palate
-lamotrigine: studies to date suggest the rate of congenital malformations may be low. The dose of lamotrigine may need to be increased in pregnancy
-Breast feeding is generally considered safe for mothers taking antiepileptics with the possible exception of the barbiturates
-It is advised that pregnant women taking phenytoin are given vitamin K in the last month of pregnancy to prevent clotting disorders in the newborn
What is included in an assessment of drug therapy?
Seizure frequency
Seizure severity
Side effects
Quality of Life