Epilepsy Flashcards

1
Q

Ix for epilepsy

A

EEG

MRI brain

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2
Q

What is a generalised tonic-clonic seizure

A

There is loss of consciousness and tonic (muscle tensing) and clonic (muscle jerking) episodes.

Typically the tonic phase comes before the clonic phase.

There may be associated tongue biting, incontinence, groaning and irregular breathing.

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3
Q

What is the post-ictal period in generalised tonic-clonic seizures

A

After the seizure there is a prolonged post-ictal period where the person is confused, drowsy and feels irritable or depressed.

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4
Q

Mx of generalised tonic-clonic seizures

A

First line: sodium valproate

Second line: lamotrigine or carbamazepine

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5
Q

What are focal seizures

A

Focal seizures start in temporal lobes. They affect hearing, speech, memory and emotions. There are various ways that focal seizures can present:

Hallucinations
Memory flashbacks
Déjà vu
Doing strange things on autopilot

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6
Q

Mx of focal seizures

A

First line: carbamazepine or lamotrigine
Second line: sodium valproate or levetiracetam

Reverse of GTCS

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7
Q

What are absence seizures

A

Absence seizures typically happen in children. The patient becomes blank, stares into space and then abruptly returns to normal.

During the episode they are unaware of their surroundings and won’t respond. These typically only lasts 10-20 seconds.

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8
Q

Mx of absence seizures

A

First line: sodium valproate or ethosuximide

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9
Q

What are atonic seizures

A

also known as “drop attacks”. They are characterised by brief lapses in muscle tone. These don’t usually last more than 3 minutes. They typically begin in childhood.

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10
Q

Syndrome associated with atonic seizures

A

Lennox-gastaut syndrome

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11
Q

Mx of atonic seizures

A

First line: sodium valproate

Second line: lamotrigine

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12
Q

What are myoclonic seizures

A

Myoclonic seizures present as sudden brief muscle contractions, like a sudden “jump”.

The patient usually remains awake during the episode. They occur in various forms of epilepsy but typically happen in children as part of juvenile myoclonic epilepsy

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13
Q

Mx of myoclonic seizures

A

First line: sodium valproate

Other options: lamotrigine, levetiracetam or topiramate

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14
Q

What are infantile spasms

A

This is also known as West syndrome

It is characterised by clusters of full body spasms. There is a poor prognosis

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15
Q

Mx of infantile spasms

A

Prednisolone

Vigabatrin

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16
Q

Maintenance option for epilepsy

A

Sodium valproate - all forms of epilepsy except focal

17
Q

Side effects of sodium valproate

A

Teratogenic so patients need careful advice about contraception
Liver damage and hepatitis
Hair loss
Tremor

18
Q

1st line maintenance therapy for focal seizures

A

Carbamazepine

19
Q

Notable side effects of carbamazepine

A

Agranulocytosis
Aplastic anaemia
Induces the P450 system so there are many drug interactions

20
Q

Notable side effects of phenytoin

A
Folate and vitamin D deficiency
Megaloblastic anaemia (folate deficiency)
Osteomalacia (vitamin D deficiency)
21
Q

Notable side effects of ethosuximide

A

Night terrors

Rashes

22
Q

Notable side effects of lamotrigine

A

Stevens-Johnson syndrome or DRESS syndrome. These are life threatening skin rashes.
Leukopenia

23
Q

Definition of status epilepticus

A

Seizures lasting more than 5 minutes or more than 3 seizures in one hour

24
Q

Mx of status epilepticus

A

A-E
IV lorazepam 4mg - repeat after 10 mins if seizure continues
If seizures persist - IV phenobarbital or phenytoin

25
Q

Medical options for management of status epilepticus in the community

A

Buccal midazolam

Rectal diazepam

26
Q

Factors which support pseudo seizures

A
pelvic thrusting
family member with epilepsy
much more common in females
crying after seizure
don't occur when alone
gradual onset
27
Q

Factors favouring true epileptic seizures

A

tongue biting
raised serum prolactin*

Video telemetry is useful for differentiating

28
Q

DVLA advice - first unprovoked/isolated seizure

A

6 months off if there are no relevant structural abnormalities on brain imaging and no definite epileptiform activity on EEG. If these conditions are not met then this is increased to 12 months

29
Q

DVLA advice - established epilepsy or those with multiple unprovoked seizures

A

may qualify for a driving licence if they have been free from any seizure for 12 months
if there have been no seizures for 5 years (with medication if necessary) a ’til 70 licence is usually restored

30
Q

DVLA advice - withdrawal of epilepsy medication

A

should not drive whilst anti-epilepsy medication is being withdrawn and for 6 months after the last dose

31
Q

When do NICE recommend initiating anti-epileptic treatment after a first seizure

A

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

32
Q

Specific features of temporal lobe seizures

A

HEAD

Hallucinations (auditory/gustatory/olfactory), Epigastric rising/Emotional, Automatisms (lip smacking/grabbing/plucking), Deja vu/Dysphasia post-ictal)

33
Q

Specific features of frontal lobe seizures

A

Motor

Head/leg movements, posturing, post-ictal weakness, Jacksonian march

34
Q

Specific features of parietal lobe seizures

A

Sensory

Paraesthesia

35
Q

Specific features of occipital lobe seizures

A

Floaters/flashes