Types of seizure Flashcards

1
Q

classification of seizures types

A

Focal onset
- Aware
- Impaired awareness

Generalised onset
- Always lose consciousness
- E.g. tonic-clonic, myoclonic, atonic, nonmotor

Unknown onset

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2
Q

Generalised seizures pathophysiology

A
  • Originate at a specific place in the brain and rapidly engage both hemispheres
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3
Q

focal seizures pathophysiology

A
  • Originate within networks limited to one hemisphere
  • May be discretely localized or more widely distributed….
  • Usually don’t lose consciousness due to usually affecting one side of the brain
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4
Q

provoked seizures

A

Seizure as a result of another medical condition

Examples include:
- Drug use or withdrawal
- Alcohol withdrawal
- Head trauma and intracranial bleeding
- Metabolic disturbances e.g hyponatraemia, hypoglycaemia
- CNS Infections: meningitis and encephalitis
- Febrile seizures in infants
- Uncontrolled hypertension
- Key is to treat both the seizure and the underlying condition. Unlikely to need ongoing AED treatment if cause treated

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5
Q

Types of Reflex Seizure

A

Seizure brought on by a particular stimulus (not provoked e.g. taking drugs )
- Photogenic (strobe lights)
- Musicogenic
- Thinking
- Eating
- Hot water immersion
- Reading
- Orgasm
- Movement

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6
Q

focal seizures types

A
  1. With impairment of consciousness (‘complex’)
  2. Without impairment of consciousness (‘simple’)
  3. Evolving to a bilateral, convulsive seizure (‘secondary generalised’)
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7
Q

Focal: With impairment of consciousness (‘complex’)

A

Patients lose consciousness either after an aura, or at seizure onset. These seizures most commonly originate at the temporal lobe

Post-ictal symptoms are common (eg. confusion in temporal lobe seizures).

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8
Q

Focal: Without impairment of consciousness (‘simple’)

A

Patients do not lose consciousness, and only experience focal symptoms.

Post-ictal symptoms do not occur.

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9
Q

Focal: Evolving to a bilateral, convulsive seizure (‘secondary generalised’)

A

Patients experience a focal seizure, which then evolves to a generalised seizure, which is typically tonic-clonic.

This occurs in 2/3 of patients with focal seizures.

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10
Q

features of focal seizures

A

Temporal lobe - Automatisms (eg. lip-smacking); déjà vu or jamais vu, emotional disturbance (eg. sudden terror); olfactory, gustatory, or auditory hallucinations.

Frontal lobe - Motor features such as Jacksonian features, dysphasia, or Todd’s palsy.

Parietal lobe - Sensory symptoms such as tingling and numbness; motor symptoms - due to spread of electrical activity to the pre-central gyrus in the frontal lobe.

Occipital lobe - Visual symptoms such as spots and lines in the visual field.

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11
Q

management of focal seizures

A

First line: Lamotrigine or Levetiracetam

Secod line: Carbamazepine, Oxcarbazepine or Zonisamide.

Third line: Lacosamide

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12
Q

main types of generalised seizures

A

Absence
Atypical absence
Myoclonic
Atonic
Tonic
Tonic-clonic.

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13
Q

Typical Absence Seizures features

A

Absence (petit mal) seizures are brief episodes, usually lasting 3–20 seconds, of staring with impairment of awareness and responsiveness.
- Seizures begin and end suddenly.
- There is no warning before the seizure, and immediately afterward the person is alert and attentive.
- If duration is >10 seconds, there are often accompanying motor phenomena (e.g., eye blinks, brief automatic mouth or hand movements, changes in muscle tone).
- These spells usually begin between ages 4 and 14 years, and usually resolve by age 18.

Provoking factures:
hyperventilation.

Investigation findings:
- The EEG signature of absence epilepsy is the generalized 3 Hz spike-wave discharge.
- Children with typical absence seizures usually have normal development and intelligence.

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14
Q

Atypical absence seizures features

A

Atypical absence seizures also occur predominantly in children, usually beginning before 6 years of age. Atypical absence seizures usually arise during childhood, but may persist into adulthood

  • Atypical absences may begin and end gradually (over seconds), usually last 5–30 seconds

Provoking factors:
Not generally provoked by rapid breathing.

Appearance:
- The child stares, but the reduction in responsiveness is usually incomplete.
- Eye blinking or slight twitching movements of the lips may be seen.
- Because atypical absence seizures often occur in children with global cognitive impairment, the seizures may be difficult to distinguish from the child’s usual behaviour.

Investigations:
The EEG usually shows generalized “slow spike-wave” complexes (i.e., <2.5 Hz). .

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15
Q

Tonic-Clonic Seizures features

A

Primary generalized tonic-clonic (also called grand mal or convulsive seizures) seizures cause loss of consciousness associated with:
1) an initial tonic phase of stiffening, a fall, and often a cry evoked by air forced through contracted vocal cords. Legs are usually extended, and arms may be extended, flexed, or each in succession.
2) The subsequent clonic phase consists of jerking of the extremities which gradually increases in amplitude and decreases in frequency before stopping.
Other signs
There may be drooling or foaming resulting from lack of swallowing and excessive salivation; biting of the tongue, cheek, or lip, causing bleeding; and bladder or bowel incontinence.

Postictal lethargy and confusion often last minutes to hours, and may be followed by transient agitation.

Investigations
The EEG shows generalized polyspikes, but these are usually obscured by muscle artefact. Postictally, there is background suppression and then diffuse slowing

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16
Q

myoclonic seizure

A

Myoclonic seizures are characterized by brief, jerking spasms of a muscle or muscle group. They often occur with atonic seizures, which cause sudden muscle limpness.

Presentation
A person having a myoclonic seizure experiences a sudden increases in muscle tone as if they have been jolted with electricity.

The mechanism is similar to a myoclonic jerk, the sudden spasm occasionally experienced by people as they are falling asleep. However, unlike myoclonic jerks, the “jolts” of myoclonic seizures occur in bouts.

17
Q

atonic seizure

A

In an atonic seizure (or ‘drop attack’) the person’s muscles suddenly relax, and they become floppy. If they are standing they often fall, usually forwards, and may injure the front of their head or face. Like tonic seizures, atonic seizures tend to be brief and happen without warning. With both tonic and atonic seizures people usually recover quickly, apart from possible injuries.

18
Q

tonic seizure

A

A tonic seizure causes a sudden stiffness or tension in the muscles of the arms, legs or trunk. The stiffness lasts about 20 seconds and is most likely to happen during sleep. Tonic seizures that occur while the person is standing may cause them to fall. After the seizure, the person may feel tired or confused.

19
Q

complications of epilepsy

A

Status epilepticus - >5 minutes of continuous seizures; treat with IV Lorazepam/buccal Midazolam, then Phenytoin if that does not work and call the anaesthetist
Depression
Suicide
Sudden unexpected death in epilepsy (SUDEP) - thought to be due to excessive electrical activity causing a cardiac arrhythmia and death.

20
Q

summary of management of epilepsy

A

Initiation of medication is not always appropriate, especially after a “provoked” first seizure, and should be discussed with a specialist.

Choice of antiepileptic drugs is a complex area, and often involves a degree of trial and error as very few randomised trials compare different medications head-to-head, and no single drug is clearly more effective or better tolerated.

General rules of thumb:

Lamotrigine, levetiracetam and valproate are good for all seizure types.

Carbamazepine, gabapentin and phenytoin are better for focal (including secondary generalised) seizures.

Ethosuximide is the drug of choice for absence seizures.

Carbamazepine may worsen myoclonic seizures.

Interactions with other medications, seen particularly with phenytoin and carbamazepine, should be considered.

  • Issues regarding teratogenicity should also be considered, particularly in the context of valproate use which has a high risk of neural tube defects. Lamotrigine is a good choice for women of childbearing age.
21
Q

DVLA and epilepsy

A

Car/motorbike licence
- one off seizure (not diagnosed with epilepsy)= reapply in 6 months

  • epileptic who has had seizure = reapply in 12 months

seizure following change in antiepileptic medications = reapply to drive if seizure was more than 6 months ago or you’ve been back on previous medication for 6 months

Bus/coach/lorry licence
- one off seizure - reapply in 5 years or if you haven’t taken anti epileptic medications for 5 years
- more than one seizure = reapply once you haven’t had a seizure for 10 years or you haven’t taken any anti-epileptic medication for 10 years