Seizures and epilepsy Flashcards

1
Q

Define seizure?

A

Transient occurence of SS due to abnormal excessive or synchronous neuronal activity in the brain (not necessary convulsions –> motor seizure)
* Provoked seizure: occuring at the time or in close temporal association with documented brain insult. Arise from pathological lowering of seizure threshold (if temporary does not rise to epilepsy) e.g. fever, neurological (stroke, TBI, encephalopathy, SDH) or metabolic (hypogly, hypoCa, hypoNa)
* Unprovoked seizures: absence of temporary/reversible factor causing decreased seizure threshold. Cryptogenic seizure: seizure with a presumed yet unidentified structural cause. Remote symptomatic seziures due to chronic irreversible conditions that increase risk of seizures e.g. tumors, post stroke states, autoimmune diseases
* Reflex seizure: triggered by exintrinsic cause (light, tactile, acoustic stimulus)

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2
Q

Define epilepsy

A

An enduring tendency (>60% risk) to develop unprovoked seizures

Defined as
* >2 unprovoked/reflex seizures occuring >24h apart
* 1 unprovoked/reflex seizure with a >60% risk of seizure recurrence in next 10y
* Diagnosis of epilepsy syndrome

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3
Q

Pathogenesis of seizures?
Conditions that change seizure threshold?

A

Oscillations by cortical neurons within each network depends on activity of inhibitory neurons (GABA neurons), communication between different neurons (synaptic transmission), intrinsic neuronal properties (ability to maintain burst firing)
Acute symptomatic seizure caused by any acute brain insult e.g. stroke (esp lobar hemorrhage), SAH, SDH, TBI, brain abscess
Epilepsy due to underlying genetic, structural, metabolic, immune, infectious, unknown

Change in seizure threshold
* Increased connectivitiy
* Increased excitatory transmission +failure of inhibitory mechanisms
* Changes in intrinsic neuronal properties

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4
Q

Types of seizures

A
  • Focal seizures: originate within networks within 1 hemisphere. Usually due to underlying focal CNS lesiosn
  • Generalized seizures: originate and rapidly engaging bilateraly distributed networks. Usually with a strong genetic component. Discharges arise from subcortical location and spreads to bilateral cortex simultaneously
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5
Q

How to categorize focal seizures?

A
  • Focal aware seizure if no LOC
  • Focal impaired awareness seizure (prev complex partial): aura (same as focal aware seizure, represents phase before progressin to LOC), LOC (may be a/w behavioural arrest/staring, automatisms)
  • Focal to bilateral tonic clonic if focal progresses into a generalized seizure
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6
Q

How to localize focal seizures?

A

Mesial temporal lobe (commonest): complex aura +/-progression into impairment in consiousness
* Aura: visceral disturbances (gustatory and olfactory hallucinations, epigastric rising sensation), psychiatric symptoms (deja vu, jamais vu, depersonalization), sensory symptoms: visual/auditory hallucinations
* After progression into LOC (complex partial seizure/focal impaired awareness seizure): automatisms –> orobuccal movements (chewing, swallowing, sucking), complex motor phenomena (bicycling, kicking)

Frontal lobe: focal clonic movements
Jacksonian march: marching clonic movement with gradual anatomical spread
Parietal lobe (uncommon): focal/spreading paresthesia or tingling sensation
Occipital lobe: visual phenomena varying from simple flashes to complex hallucination

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7
Q

Types of generalized seizures?

A
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8
Q

Presentation of post ictal period of seizure?

A
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9
Q

ddx of epileptic seizures

A
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10
Q

Causes of epilepsy according to age

A
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11
Q

etiology of epilepsy
Structural
Genetic
Infectious
Other (metabolic, immune, unknown)

A
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12
Q

Epilepsy syndromes

A
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13
Q

Early infantile epileptic encephalopathy cause and features

A
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14
Q

Dravet syndrome cause and features

A
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15
Q

Infantile spasm cause and features

A
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16
Q

Lennox Gastaut syndrome cause and features

A
17
Q

Generalized epilepsy with febrile seizure plus (GEFS) cause and features

A
18
Q

Approach to epilepsy?

A
19
Q

Non pharmacological mx of epilepsy

A
20
Q

Indications for starting AED and types of antiepileptics

A
21
Q

Use of AEDs in types of seizures

A
22
Q

What cautions of AEDs in women?
What drugs need to be changed?

A
23
Q

Preop evaluation for epilepsy surgery

A

□ Video EEG ± invasive intracranial EEG
□ Neuroimaging
□ WADA test: determine language lateralization and memory fx of each temporal lobe→ sedating agent injected into ICA → determine dominance to prepare for TLE surgery
□ Cortical mapping

24
Q

Temporal lobe epilepsy surgery and S/E

A
25
Q

Neurostimulation mx in epilepsy

A

 Vagus nerve stimulation (VNS): regular pulsed stimulation via vagus nerve → desynchronize cerebral activity + ↑synthesis of inhibitory neurotransmission
 Deep brain stimulation (DBS): usually at anterior thalamus to abort seizure spread

26
Q

Define status epilepticus

A
27
Q

Types of status epilepticus

A
28
Q

Causes of status epilepticus

A

□ Acute cerebral insult due to
→ CNS infections (classically encephalitis)
→ Neurotoxins incl. drugs, eg. lignocaine, amphetamine
□ Rapid withdrawal of AEDs

29
Q

General mx of status epilepticus

A
30
Q

Acute mx of status epilepticus

A