Epilepsy and seizures Flashcards

1
Q

What is the definition of a seizure?

A
  • The action of capturing someone or something using force

Medical definition : The manifestation of an abnormal hypersynchronous discharge of a population of cortical neurones

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the definition of epilepsy?

A

A disorder of the brain characterised by an enduring predisposition to generate seizures and the neurobiologic, cognitive, pyschological and social consequences of this condition

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

When do seizures occur?

A
  • When you have excessive brain electrical activity
  • The propensity for recurrent, unprovoked seizures
  • Tonic - clonic seizure =
  • Tonic : tense or rigid muscles
  • Clonic : sustained rhythmical jerking movements
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Explain epilepsy

A
  • The tendency for recurrent unprovoked seizures
  • More of a symptom of disease than a disease itself
  • Epiletics have more excitable brains due to:
  • Structural abnormality (tumours, scars)
  • Cogenital anomaly :
  • Channelopathies (ion channel dysfunction)
  • Abnrmal cortical neural networks
  • Provoked seizures = single seizure events that result from an immediately recognisable stimulus or cause e.g. head injury, strokem alcohol/ drug withdrawl, fever, hypoglycaemia, brain infection. Seizures do not happen in the absence of the stimulus and thus are not epilepsy.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are epilepsy syndromes defined by?

A

Defined by a group of features usually occurring
together e.g.
* Age when seizures begin
Genetics
Responses to medication
* Clinical course
* Brain focus involved
* EEG findings
Seizure type
Juvenile myoclonic syndrome
*
* Childhood & juvenile absence
epilepsy
Temporal lobe epilepsy
*
Benign Rolandic Epilepsy
*

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Why is it important to be able to classify seizures?

A
  • Management - choice of medication
  • Prognostication
  • Investigation (could provide a useful link to specific syndromes)
  • Trials and research
  • Provides words to patients to describe their disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the diffferent classification of seizure types?

A
  1. Focal onset : Aware/ Impaired awareness . Motor/ Non motor - focal to bilateral tonic-clonic (Starts at a focal point and spreads to opposite hemisphere). Arises from a discrte cortical focus .
  2. Generalised onset : Impaired awareness. Motor. Tonic-clonic or other motor, Non motor (abscence) . Affects both hemispheres of the brain at the same time.
  3. Unknown onset : Motor : Tonic- clonic , other motor, non-motor (abscence) = beginning of seizure is unknown. Not witnessed by anyone.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are the different symptoms that happen during a seizurre?

A

For focal onset seizures:
Motor symptoms may include:
* Jerking (clonic)
* Muscles becoming limp or weak (atonic)
* Tense or rigid muscles (tonic)
* Brief muscle twitching (myoclonus)
* Epileptic spasms (body flexes and extends repeatedly).
* Automatisms or repeated automatic movements, like clapping or rubbing
of hands, lip-smacking or chewing, or running.
*Non-motor symptoms:
* Changes in sensation,
* Changes in emotions
* Changes in thinking or cognition
* Changes in autonomic functions (such as gastrointestinal sensations,
waves of heat or cold, goosebumps, heart racing, etc.),
* Lack of movement (called behavior arrest).

For generalized onset seizures:
*Motor symptoms may include:
* Sustained rhythmical jerking movements (clonic)
* Muscles becoming weak or limp (atonic)
* Muscles becoming tense or rigid (tonic)
* Brief muscle twitching (myoclonus)
* Epileptic spasms (body flexes and extends repeatedly).
*Non-motor symptoms are usually called absence seizures. These can be
typical or atypical absence seizures (staring spells). Absence seizures can also
have brief twitches (myoclonus) that can affect a specific part of the body or
just the eyelids.
For unknown onset seizures:
*Motor seizures are described as either tonic- clonic epileptic spasms.
*Non-motor seizures usually include a behavior arrest. This means that movement stops —
the person may just stare and not make any other movements.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is consciousness?

A
  • A system of cortical and sub cortical brain networks that work to maintain :
  • Alertness
  • Attention
  • Awareness
  • Disruption (impairement or complete loss of consciousness) = can be severely debilitating
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Describe consciousness in focal onset seizures

A

Focal onset aware seizure (previously
simple partial seizures)
Consciousness is unaffected (person is
awake and aware) = EPILEPTIC AURA
Mainly seen in frontal lobe, occipital lobe
seizures

Focal onset Aware Can be motor or non-motor

  • Focal epileptic discharge
    — Motor (Jacksonian march)
    — Sensory (tingling, burning)
    e.g. disturbance of motor,
    sensory, cognitive or autonomic
    function
    (déjå vu, hallucinations)
    — Psychic
    — Special sense (metallic taste, flashing lights, unpleasant smell)
    — Autonomic (epigastric rising sensation)
  • Often there is a deficit after attack- Todd’s palsy
    e.g. limb weakness in affected limb, speech aphasia
    (Broca’s), visual field defects (occipital) or loss of sensation

Focal onset impaired awareness
(previously complex partial seizures)
Consciousness is affected (person is
confused or their awareness is affected)
Mainly seen in temporal lobe seizures

Often preceded by an aura
Often originate in the temporal lobe :

  • Vocalisations (grunting etc)
  • Posturing
  • Wandering
  • Automatisms - semi-purposeful movements
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the 3 As of epilepsy?

A
  • Aura (i.e may be initially fully conscious)
    Altered consciousness (but usually partially responsive)
  • Automatisms (characteristic)
    — Lip smacking
    — Teeth grinding
    — Fiddling with clothes, objects
    Wandering, pacing, circling
    ‘Absence’ common, but typically not the sole feature
    Typically the longest in duration
    — Can be several minutes up to even an hour
  • Variable disorientation afterwards, amnesia for the event
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is myoclonus (generalised onset motor seizure)?

A

e.g. myoclonus (= generalised onset motor)
Myo = muscle
Clonic = jerks
Very brief (1 second)
* Shock-like
Muscle contraction
Usually bilateral
Falls
Full immediate recovery
* Loss of consciousness too brief to be appreciated
Occur in a number of epilepsy syndromes
Benign myoclonus occurs in healthy people e.g when falling asleep or hiccups.
This is not a myoclonic seizure.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the absence (generalised onset non motor)?

A

Typical
Most common
Brief (< 10 seconds)
Abrupt loss of consciousness
Unaware of episode
Full, immediate recovery
Vacant stare
Speech arrest
Tone usually unaffected
— If seated, maintain posture
— If walking, keep walking
No aura
Often missed / misinterpreted
(‘daydreaming’)
More common in children
Formerly petit mal

Atypical
Atypical because they may be
longer (20+seconds), have a
slower onset and offset,
involves different symptoms
Usually a change in muscle
tone and movement e.g.
Blinking/eyes flickering
Lip-smacking/chewing
Rubbing fingers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is tonic - clonic (generalised onset motor)?

A

e.g. tonic-clonic (generalized onset motor)
Formerly grand mal
Possible aura (varied)
Ictus
— Tonic (rigid) phase (seconds) — driven by intense neuronal discharge from cerebral
cortex
* Flexion of arms -entire body become rigid
Cry — laryngeal and respiratory muscles force air out of the chest
Cyanosis — breathing ceases temporarily
— Clonic (jerking) phase (minutes)
* Jerking of limbs (muscular contraction and relaxation)
* Reducing frequency
* Intermittent/suspended breathing, hypersalivation appears as frothing at mouth
* Tongue biting (side of tongue)
* Urinary incontinence
Post-ictal period
Drowsy, disorientated
— Out of sorts for the rest of the day

T-C seizure lasting more than 5 minutes
is a medical emergency. Call 999.
A seizure that lasts more than 10
minutes, or three seizures in a row
without the person coming to between
them, is a dangerous condition. This is
called status epilepticus; emergency
treatment in a hospital is needed.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the structural aetiology of epilepsy?

A

Structural
Epilepsy can be symptomatic of a structural lesion e.g.
. Congenital
Acquired
-Tumour
-Vascular malformation
-Abscess
-Stroke
-Scarring
-Cysts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the genetic ateiology of epilepsy?

A

Genetic factors
Can be inherited OR spontaneous mutation.
Heritable component can be autosomal dominant or autosomal
recessive.
Heritable component can by complex and polygenic
Most known mutations affect ion channels (sodium, potassium,
calcium, chloride) = channelopathies
Thought to alter the balance of excitatory and inhibitory
influences — associated with focal or generalised seizures

17
Q

What are some metabolic / immune disorders that cause epilepsy?

A

Metabolic disorders
Alteration of intracellular osmolality
Depletion of substrates essential for cellular metabolism or
membrane function
Intracellular accumulation of toxic substances

Immune disorder
Antibodies
Autoimmune-mediated CNS inflammation

18
Q

What is the most common cause of epilepsy?

A
  • Infections
  • Neurocysticercosis - a parasitic brain infection caused by ingestion of eggs from the pork tapeworm
  • 3/4 people with epilepsy in low income countries do not get the treatment they need
19
Q

What is the electrical basis of epilepsy?

A
  • Network phenomenon that arises from
    abnormal synchronised discharges in large
    neuronal assemblies
  • There are associated changes in synaptic
    connectivity, receptor subunit composition
    and ion channels
    Abrupt shifts in resting membrane potential:
    Inward sodium current (mediated by voltage gated ion channels) is followed by
    prolonged, calcium-dependent depolarisation.
    — Lasts 10x longer than normal action potential
    — Terminated by calcium-sensitive potassium channels which repolarise
    neurone
    — Prelonged period of after-hyperpolarisation follows
    A hyper excitable state can result from:
    Increased excitatory synaptic neurotransmission
    Decreased inhibitory neurotransmission
    An alteration in voltage-gated ion channels
    An alteration of intra- or extra-cellular ion concentrations in favour of membrane
    depolarization
    Can also result when several synchronous subthreshold excitatory stimuli occur,
    allowing their temporal summation in the post synaptic neurons.
    If abnormal activity spreads over large enough area (more than a few cm in
    humans) it may develop into a seizure.
20
Q

How is epilepsy diagnosed?

A

Detailed eye witness account
* Electroencephalogram (EEG). When synchronised discharges occur simultaneously in several million cortical neurons it can be detected by scalp electrodes
* In some cases not possible to record epileptiform discharges if seizure focus is too deep (muscular interference can also interfere with EEG trace)
* Telemetry (EEG combined with video) in difficult cases

21
Q

How is epilepsy treated?

A

Treatment
Anti-epileptic drugs
Vagus nerve stimulation. Stimulation of cranial
nerve X
*We don’t know exactly how VNS works. It may:
*Increase blood flow in key brain areas
*Raising levels of some brain substances
neurotransmitters
Surgery
A pacemaker-like device
(called a generator) sends
stimulation through a flexible
wire (called a lead)

The lead connects to the
vagus nerve, which then
carries this stimulation the
rest of the way to the brain

-About 10% of drug-resistant focal epilepsy may benefit from neurosurgical procedure
-Before any surgery FMRI carried out to assess potential impact on memory, language &
intellect
-Aim is to remove causative lesion or interrupt white matterto prevent electrical spread
-Partial or complete removal of a lobe (lobectomy) may be appropriate for a focal lesion
-Division of corpus callosum can prevent interhemisphericspread of seizures

22
Q

What is differntial diagnosis of epilepsy?

A

Where there is loss of consciousness
* Main differentials
— Syncope (faint)
— Psychogenic non-epileptic
attack
— Transient ischaemic attack

23
Q

What is syncope?

A

Syncope
* Brain hypoperfusion
* Causes include:
— Vasovagal attack
— Cardiac arrythmias
— Cardiac output failure
— Autonomic dysfunction
— Metabolic causes
Examples
‘Common faint’
Heart block, SVTs
(supraventricular tachycardia)
HOCM
(hypertrophic cardiomyopathy)
Postural hypotension
Hypoglycaemia

  • Results from temporarily depressed cortical activity
24
Q

What are epileptic features in the history?

A

Features in the history
* Predispositions
— Upright, hot day, dehydration, queasy, exertion
— Fasting
* Prodrome
— sweating, palpitations
— light-headed
— Pallor
— ‘Greying out’ of vision
— Briefly unconscious, usually motionless
May have convulsions +/- incontinence
* Post-ictal
— Rapid recovery (if recumbent) < 1 min
— minimal confusion

Consciousness restored when perfusion is resumed

25
Q

How do we differentiate from Fit vs Faint?

A
  • History is key - eyewitness account that is :
  • detailed
  • blow by blow
  • Ideally : video of the event
  • If not : witness should attend consultation or at least be telephoned
  • Written account