Epilepsy Flashcards

1
Q

Definition (epilepsy)

A

· A tendency to recurrent unprovoked seizures

· You need to have had > 2 seizures for epilepsy to be diagnosed

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2
Q

Definition (seizure)

A

paroxysmal synchronised cortical electrical discharges

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3
Q

Types of seizure

A

o Focal Seizure: seizure localised to specific cortical regions (e.g. temporal lobe seizure). These can be further divided into:
· COMPLEX partial seizure: consciousness is affected
· SIMPLE partial seizure: consciousness is NOT affected

o Generalised Seizure: seizures that affect the whole of the brain. It also affects consciousness. There are different types of generalised seizure:
· Tonic-clonic
· Absence
· Myoclonic
· Atonic
· Tonic
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4
Q

Aetiology/Risk factors

A

· Most cases are IDIOPATHIC

· Primary epilepsy syndromes (e.g. idiopathic generalised epilepsy)

· Secondary Seizures
o Tumour
o Infection (e.g. meningitis)
o Inflammation (e.g. vasculitis)
o Toxic/Metabolic (e.g. sodium imbalance)
o Drugs (e.g. alcohol withdrawal)
o Vascular (e.g. haemorrhage)
o Congenital abnormalities (e.g. cortical dysplasia)
o Neurodegenerative disease (e.g. Alzheimer’s disease)
o Malignant hypertension or eclampsia
o Trauma

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5
Q

Things which look like seizures

A

o Syncope

o Migraine

o Non-epileptiform seizure disorder (e.g. dissociative disorder)

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6
Q

Pathophysiology of seizures

A

o Result from an imbalance in the inhibitory and excitatory currents or neurotransmission in the brain

o Precipitants include anything that promotes excitation of the cerebral cortex

o Often it is unclear why the precipitants cause seizures

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7
Q

Epidemiology

A

· COMMON

· 1% of the general population

· Typical age of onset: CHILDREN and ELDERLY

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8
Q

History taking

A

· NOTE: try and obtain a collateral history from a witness as well as the patient

· Key features to consider when taking a history from a potential epilepsy patient:

o Rapidity of onset
o Duration of episode
o Any alteration in consciousness?
o Any tongue-biting or incontinence?
o Any rhythmic synchronous limb jerking?
o Any post-ictal abnormalities (e.g. exhaustion, confusion)?
o Drug history (alcohol, recreational drugs)

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9
Q

Presenting symptoms (focal seizures)

A

o Frontal Lobe Focal Motor Seizure
· Motor convulsions
· May show a Jacksonian march (when the muscular spasm caused by the simple partial seizure spreads from affecting the distal part of the limb towards the ipsilateral face)
· May show post-ictal flaccid weakness (Todd’s paralysis)

o Temporal Lobe Seizures
· Aura (visceral or psychic symptoms)
· Hallucinations (usually olfactory or affecting taste)

o Frontal Lobe Complex Partial Seizure
· Loss of consciousness
· Involuntary actions/disinhibition
· Rapid recovery

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10
Q

Presenting symptoms (generalised seizures)

A

o Tonic-Clonic (Grand Mal)
· Vague symptoms before attack (e.g. irritability)
· Tonic phase (generalised muscle spasm)
· Clonic phase (repetitive synchronous jerks)
· Faecal/urinary incontinence
· Tongue biting
· Post-ictal phase: impaired consciousness, lethargy, confusion, headache, back pain, stiffness

o Absence (Petit Mal)
· Onset in CHILDHOOD
· Loss of consciousness but MAINTAINTED POSTURE
· The patient will appear to stop talking and stare into space for a few seconds
· NO post-ictal phase

o Non-Convulsive Status Epilepticus
· Acute confusional state
· Often fluctuating
· Difficult to distinguish from dementia

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11
Q

Signs on physical examination

A

· Depends on aetiology

· Patients tend to be normal in between seizures

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12
Q

Investigations

A
· Bloods
o FBC
o U&E
o LFTs
o Glucose
o Calcium
o Magnesium
o ABG
o Toxicology screen
o Prolactin - shows a transient increase shortly after seizures

· EEG
o Helps to confirm diagnosis
o Helps classify the epilepsy
o Ictal EEGs are particularly useful (i.e. during a seizure)

· CT/MRI
o Shows structural, space-occupying or vascular lesions

· Other investigations
o If it is suspected to be a secondary seizure (e.g. due to infection)

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13
Q

Management plan (status epilepticus)

A

DEFINITION of Status Epilepticus: a seizure lasting > 5 mins or repeated seizure without recovery and regain of consciousness in between

o Treatment is usually initiated early (after around 5-10 mins)

o ABC approach

o Check GLUCOSE (give glucose if hypoglycaemic)

o IV lorazepam OR IV/PR diazepam - REPEAT again after 10 mins if seizure does not terminate

o If seizures recur following the next dose of lorazepam or diazepam, consider IV phenytoin - an ECG monitor is required
· NOTE: other agents include phenobarbitone, levetiracetam and sodium valproate

o If this also fails, consider general anaesthesia (e.g. thiopentone) - intubation and mechanical ventilation required

o Treat the CAUSE (e.g. hypoglycaemia or hyponatraemia)

o Check plasma levels of anticonvulsants (because status epilepticus is often caused by lack of compliance with anti-epileptic medications)

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14
Q

Management plan (newly diagnosed)

A

o Only start anti-convulsant treatment after > 2 unprovoked seizures

o FOCAL Seizure 1st Line: lamotrigine or carbamazepine

o GENERALISED Seizure 1st Line: sodium valproate

o Start treatment with only ONE anti-epileptic drug

o Other anti-convulsants: phenytoin, levetiracetam, clobazam, topiramate, gabapentin, vigabatrin

Surgery may be considered for refractory epilepsy

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15
Q

Management plan (patient education)

A

o Avoid triggers

o Use seizure diaries

o Particular consideration for women of child-bearing age because the anti-epileptic drugs can have teratogenic effects

o Be careful of drug interactions (e.g. AEDs can reduce the effectiveness of the oral contraceptive pill)

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16
Q

Possible complications

A

· Fractures from tonic-clonic seizures

· Behavioural problems

· Sudden death in epilepsy (SUDEP)

· Complications of anti-epileptic drugs:
o Gingival hypertrophy (phenytoin)
o Neutropaenia and osteoporosis (carbamazepine)
o Stevens-Johnson syndrome (lamotrigine)

17
Q

Prognosis

A

50% remission at 1 year