Epilepsy Flashcards

1
Q

What is Epilepsy?

A

A disease of the brain defined by the following:

  • At least two unprovoked siezures occuring more than 24 hours apart
  • One unprovoked seizure and a probability of further seizures similar to the general recurrence risk, after two unprovoked seizures, occurring over the next 10 years
  • Diagonsis of an epilepsy syndrome
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2
Q

Does a single seizure mean epilepsy?

A

No
As a seizure can be caused by many different factors includi g toxins, infections and metabolic disturbances.

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3
Q

What is the definition of a seizure?

A

A seizure is the transient occurrence of signs or symptoms due to abnormal excessive or synchronous neuronal activity in the brain.

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4
Q

What are the potential causes of Epilepsy?

A
  • Structural abnormalities within the brain
  • Genetic mutations resulting in epilepsy (not necessarily inherited genetics)
  • Infectious causes in which seizures are a core symptom of the disorder, e.g. cerebral malaria,
    tuberculosis
  • Metabolic issues such as porphyria or pyridoxine deficiency
  • Immune disorders in which seizures are a core symptom of the disorder, e.g. anti-NMDA receptor
    encephalitis
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5
Q

What are some complications of Epilepsy?

A
  • Sudden Unexpected Death in Epilepsy (SUDEP)
  • Injuries and accidents (e.g. drowning, road traffic accidents, falls)
  • Depression and Anxiety
  • Absence from work and / or school
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6
Q

What are the factors that differeniate seizures?

A
  • Their onset
  • If the patient has awareness or not
  • Other symptoms
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7
Q

What are the three broad categories of seizures?

A
  • Focal Onset Seizures
  • Generalised Onset Seizure
  • Unknown Onset Seizure

They are classified by their location of onset

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8
Q

What are Focal onset seizures?

A

Seizures that originate in networks limited to one hemisphere of the brain, and may be localised (a small part of the hemisphere) or more widely distributed (a large part of the hemisphere effected).

Sometimes a focal onset seizure can spread to both sides of the brain, called a focal to bilateral tonic-clonic seizure (aka secondarily generalised seizures).

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9
Q

What are the sub-classifications for Focal onset seizures?

A
  • Focal aware seizures aka simple partial seizures
  • Focal impaired awareness seizures aka complex partial seizures

This is where the patient is aware of what is happening to them or not

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10
Q

What is the second classification for Focal onset seizures?

A

After awareness, the seizures are classified into motor onset and non-motor onset.

Motor onset is with physical symptoms and non-motor onset is without physical symptoms.

What happens during focal aware and focal impaired awareness depends on what part of the brain the focus is.

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11
Q

What kind of symptoms are involved in motor onset?

A

Automatisms

Atonic

Clonic

Epileptic spasms

Hyperkinetic

Myoclonic

Tonic

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12
Q

What kind of symptoms are involved in non-motor onset?

A

Autonomic

Behavior arrest

Cognitive

Sensory

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13
Q

Examples of what motor symptoms focal seizures can include?

A
  • making lip-smacking or chewing movements
  • repeatedly picking up objects or pulling at clothes;
  • suddenly losing muscle tone and limbs going limp or floppy, or limbs suddenly becoming stiff;
  • repetitive jerking movements that affect one or both sides of the body;
  • making a loud cry or scream
  • making strange postures or repetitive movements such as cycling or kicking.
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14
Q

Examples of what non-motor symptoms focal seizures can include?

A
  • changes or a ‘rising’ feeling in the stomach or déjà vu (feeling like you’ve ‘been here
    before’)
  • getting an unusual smell or taste
  • a sudden intense feeling of fear or joy
  • a strange feeling like a ‘wave’ going through the head;
  • stiffness or twitching in part of the body, (such as an arm or hand);
  • a feeling of numbness or tingling;
  • a sensation that an arm or leg feels bigger or smaller
    than it actually is
  • visual disturbances such as coloured or flashing lights or hallucinations (seeing something that isn’t actually there).
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15
Q

What are generalised onset seizures?

A

Siezures that originate in bilaterally distributed networks (affect both sides of the brain), and can include cortical and subcortical structures (but not necessarily the whole cortex). These happen without warning.

So start somewhere and affects both sides of the brain at once, happening without warning.

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16
Q

What are the sub-classifications for Generalised onset seizures?

A

Motor and non-motor seizures

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17
Q

Examples of generalised motor seizures?

A

Tonic-clonic

Tonic

Atonic

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18
Q

What are unknown onset seizures?

A

Seizures where the focus hasn’t been confirmed.
This may happen when the patient was asleep, alone or the seizure was not witnessed.

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19
Q

What are unclassified seizures?

A

Seizures where there is not enough information available about the person’s seizure or because of the unusal nature of the seizure.

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20
Q

Explain the breakdown of a generalized onset seizure?

A

Generalized onset - seizures start and affect both sides of the brain at once and happen without warning.
These can be motor or non-motor. Motor is with visible physical movement and non-motor is the opposite.

This is then broken down into unknown onset or unclassified.

Unknown onset is used to describe a seizure where doctors are not sure where in the brain the seizure starts. This breaks down again into motor or non-motor.

Unclassified is used if there is not enough information available or the nature of the seizure is unusual.

21
Q

What are the different types of seizures?

A
  • Absence seizures
  • Tonic-clonic seizures
  • Tonic seizures
  • Atonic seizures (drop attacks)
  • Myoclonic seizures
  • Status Epilepticus
22
Q

What are absence seizures?

A

This is a type of generalized onset non-motor seizure.
This is separated into typical and atypical absence seizures.

Typical is characterized by a patient becoming blank and unresponsive for a few second (daydreaming look) - they are very brief.

Atypical is the same but start and end more slowly and last longer.

However, this is more common children
Previously called Petit-Mal

23
Q

What are tonic-clonic seizures?

A

The muscles contract and the body goes stiff, crying and loosing consciousness and fall to the floor. The muscles alternate between contraction and relaxation, resulting in jerk movements.
Might bite their tongue or cheek.
Then go limp. When waking up, they’ll have aching head and limbs.

They are brief and happen without warning.

24
Q

What are atonic seizures?

A

When a person goes limp and drops to the ground suddenly.

Might have head injury as they often fall forward.

25
Q

What are myoclonic seizures?

A

When the person has jerk movements but does not loose consciousness or awareness. This is also known as myolonic jerks.

Usually happens in the morning and in clusters.
Can be focal or generalized in onset.

The person is likely to have other seizures.

26
Q

What is Status Epilepticus?

A

This is a prolonged seizure lasting 5 minutes or longer, or recurrent seizures one after the other without recovery in between.

This can happen in any type or seizure.

27
Q

What are the first line treatments for focal seizures?

A

Levetiracetam or Lamotrigine

28
Q

What is the first line treatment for generalized tonic-clonic seizures?

A

Sodium Valproate

If not suitable for patient, Levetiracetam or Lamotrigine (but could make myoclonic seizures worse).

29
Q

What are the rules for Valproate?

A

Only give to: boys and men, girls under 10 and unlikely to need treatment when older and women who cannot have children.

Do not give to pregnant women or those able to become pregnant, unless other options are not suitable. If you really have to give, a highly effective contraception must be used and a valproate annual risk acknowledgement form must be completed.

30
Q

What is the first, second and third line treatment for absence seizures?

A

Ethosuximide

If ethosuximide is unsuccessful, offer sodium valproate as second-line monotherapy (is suitable to patient) or add-on treatment.

Third line is levetiracetam or lamotrigine as a third-line monotherapy or add-on treatment option.

31
Q

What is the first and second line treatment for myoclonic seizures?

A

First line - Sodium valproate or levetiracetam

Second line is levetiracetam as monotherapy or add-on treatment

32
Q

What is the first and second line treatment for atonic and tonic seizures?

A

Second - Sodium valproate

First - Lamotrigine

33
Q

What are the treatments for Status Epilepticus?

A

Buccal midazolam or rectal diazepam solution (if there’s not already an emergency management plan in place)

If in hospital - Intravenous lorazepam

If no response: IV levetiracetam, IV phenytoin, IV sodium valproate

Third line option: Phenobarbital or general anesthesia

34
Q

Which seizures have sodium valproate as their first line treatment?

A
  • Generalised tonic-clonic seizures
  • Myoclonic seizures
  • Atonic and tonic seizures
35
Q

What are the three risk-based categories for Anti-epileptic medications?

A

Category 1 – phenytoin, carbamazepine, phenobarbital, primidone

  • For these, patient must be maintained on a specific manufacturer’s product

Category 2 – valproate, lamotrigine, perampanel, retigabine, rufinamide, clobazam, clonazepam, oxcarbazepine, eslicarbazepine, zonisamide, topiramate

  • For these, the need for continued supply of a particular manufacturer’s product should be based on clinical judgement and consultation with patient and/or carer, taking into account factors such as seizure frequency and treatment history

Category 3 - levetiracetam, lacosamide, tiagabine, gabapentin, pregabalin, ethosuximide, vigabatrin

  • For these, ensure that patients are maintained on a
    specific manufacturer’s product unless there are specific reasons such as patient anxiety and risk of confusion or dosing errors
36
Q

What are the general considerations for Carbamazepine?

A

Different formulations of oral preparations may vary in bioavailability - so use the same manufacturer.

Patients or their carers should be told how to recognize signs of blood, liver, or skin disorders, and advised to seek immediate medical attention if symptoms such as fever, rash,
mouth ulcers, bruising, or bleeding develop.

37
Q

What are the general considerations for Carbamazepine?

A

Different formulations of oral preparations may vary in bioavailability - so use the same manufacturer.

Patients or their carers should be told how to recognize signs of blood, liver, or skin disorders, and advised to seek immediate medical attention if symptoms such as fever, rash,
mouth ulcers, bruising, or bleeding develop.

38
Q

What are the general considerations for Valproate?

A

Different brands of valproate are available but not all are licensed for epilepsy.

Valproate must not be used in women and girls of childbearing potential.

39
Q

What are the general considerations for Topiramate?

A

An increased risk of major congenital malformations and intra-uterine growth restriction has been seen with topiramate

40
Q

What are the general considerations for Lamotrigine?

A

Advise them to see their doctor if rash appears or symptoms of hypersensitivity syndrome. Advice about symptoms and signs for bone-marrow failure aswell.

There are strict titration regimes that must be followed to reduce this risk.

Dose adjustments are required if it is considered essential to prescribe lamotrigine with valproate

41
Q

What are the common side effects of anti-epileptic medications?

A

Somnolence, headache & dizziness

All anti-epileptic drugs may be associated with a small increased risk of suicidal thoughts and
behaviour.

42
Q

Which anti-epileptic medications are associated with osteomalacia and osteoporosis?

A

Phenytoin, primidone, valproate & carbamazepine

43
Q

What are the serious side effects of Carbamazepine, Lamotrigine, Levetiracetam, Phenytoin, Topiramate, Valporate?

A

Carbamazepine - Blood, hepatic and skin disorders
Lamotrigine - Serious skin reactions and blood disorders
Levetiracetam - Drug reactions with Eosinophilia and systemic symptoms
Phenytoin - Blood and skin disorders
Topiramate - Increased intraocular pressure
Valporate - Hepatic and blood disorders, pancreatitis

44
Q

What are the interactions with anti-epileptic medications?

A

Most interactions are with enzyme-induction AEDs.
They interact with: anticoagulants, antibiotics, antidepressants, antipsychotics, oestrogens & progestogens

45
Q

Which anti-epileptic medication is TDM most useful for?

A

Phenytoin as small increases in dose can result in large increases in blood concentration

46
Q

What are the key tips for withdrawing from anti-epileptic medications?

A

Withdrawal must be slow (could take months). Abrupt cessation could cause status epilepticus.
Therefore withdrawal should be performed gradually over at least 3 months.

If they are taking more than one anti-epileptic medication, withdraw one at a time.
If seizure recurs, reverse the last dose reduction.

47
Q

What are the considerations for contraception and anti-epileptic medications?

A

Enzyme -inducing antiepileptic drugs (AEDs) may reduce the effectiveness of some combined hormonal contraceptives (CHC) and progestogen-only preparations.

Enzyme-inducing AEDs increase the metabolism of oestrogen and progestogen.

  • Preparations affected include CHC as the pill, patch, and vaginal ring. Progestogen only preparations affected are the progestogen-only pills (POPs) and progestogen implants.

If a woman wishes to continue taking the combined oral contraceptive pill (COC) then it is
recommended that two COC pills at a time are taken containing at least 50 micrograms of
ethinyloestradiol.

48
Q

Which contraception is unaffected by AEDs?

A

IDU or Progestogen-only injectable and condoms.

49
Q

What are the considerations for pregnancy and anti-epileptic medications?

A

Most seizures do not adversely affect foetus. With tonic‐clonic seizure, the foetus is at higher risk of
harm, but still very low risk, There is a risk of falling though, that’s when foetus can be injured.

Folic acid 5mg to be taken 3 months prior to conception to end of first trimester.

Some antiepileptic levels can be decreased, especially in second and third trimester, leading
to breakthrough seizures.

Enzyme‐inducing anti-epileptics may cause haemorrhagic disease of new-born - vitamin K
should be administered at birth.