4. Do NOT Take Notes
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5. Plan
Definitions
Aetiology
Classification
Clinical Manifestations
Investigations
Diagnosis
Treatment
Who to Treat?
6. Plan
Definitions
Aetiology
Classification
Clinical Manifestations
Investigations
Diagnosis
Treatment
Who to Treat?
7. Definitions
Seizure or Ictus:
Is the clinical manifestation of an abnormal,
excessive excitation and synchronization of a
population of cortical neurons
○ Clinically apparent – symptoms or signs
○ Subclinical – only seen on EEG
Epilepsy:
recurrent seizures (two or more) which are not
provoked by systemic or acute neurologic
insults
8. Definitions
Status Epilepticus:
Continuous convulsion lasting >30 minutes
OR
Occurrence of serial convulsions lasting >30 minutes
between which there is no return of consciousness
9. Famous People who had
Epilepsy
Definite Most Likely
Alexander of Macedon
Julius Caesar
Aristotle
Socrates
Martin Luther
Cardinal Richelieu
Leonardo da Vinci
Michelangelo
Isaac Newton
Alfred Nobel
Richard Burton
Leo Tolstoy
Alfred Tennyson
Ludwig van Beethoven
Karen Armstrong
Napoleon Bonaparte
Vincent van Gogh
10. Plan
Definitions
Aetiology
Classification
Clinical Manifestations
Investigations
Diagnosis
Treatment
Who to Treat?
11. Incidence and Prevalence
Seizure:
• Incidence: 80/100,000 per year
• Lifetime incidence: 9%
(1/3rd are febrile convulsions)
Epilepsy:
• Incidence: 45/100,000 per year
• Point prevalence: 0.5-1%
• Cumulative lifetime incidence: 3%
13. Plan
Definitions
Aetiology
Classification
Clinical Manifestations
Investigations
Diagnosis
Treatment
Who to Treat?
14. Classification
By symptoms
motor, sensory etc
By Age
Infantile, childhood adult
Pathophysiological
Not possible
Treatment Response
Controlled / uncontrolled
Anatomical / Connections
Thalamic, Limbic, Temporal Lobe, Motor Cortex
etc
15. Internationally Accepted
ILAE -
International League Against Epilepsy
First Proposed in 1981
Modified several Times
Latest Modifications 2010 & 2017
16. Terms to understand
Generalized
Whole of brain is involved
Partial or Focal
Part of brain is involved
Simple
Consciousness not lost
Complex
Consciousness is lost
Secondary Generalization
Starts as Focal but spreads to involve the whole
brain
17. ILAE Classification of
Seizures
C-Slide 17
Seizures
Partial Generalized
Simple Partial
Complex Partial
Secondarily
Generalized
Absence
Myoclonic
Atonic
Tonic / Clonic
Tonic-Clonic
ILAE – International League Against EpilepsyAmerican Epilepsy Society 2010
Reflex Status Epilepticus
18. ILAE Classification of
Seizures
C-Slide 18
Seizures
Partial Generalized
Simple Partial
With somatosensory
or special sensory
symptoms
With motor signs
With autonomic
symptoms or signs
With psychic or
experiential symptoms
American Epilepsy Society 2010
19. Plan
Definitions
Aetiology
Classification
Clinical Manifestations
Investigations
Diagnosis
Treatment
Who to Treat?
20. GTC Seizures
Aura + Tonic Phase Clonic Phase + Postictal
Aura +/-
Sudden sharp tonic
contraction of body
and respiratory muscle:
stridor / moan
Falls
“Cry”
Respiratory inhibition
cyanosis
Tongue biting
Urinary incontinence
Synchronized jerking of the
body
Small gusts of grunting
respiration
Frothing of saliva
Tongue biting
Urinary incontinence
Deep respiration
Muscle relaxation
Remains
unconscious/confused
Awakens feeling sore,
headaches
21. Absence seizures
Children
Sudden onset
Interruption of on-going activities
Blank stare
Brief upward rotation of eyes
Duration: Less than 10 seconds
No motor involvement
May develop generalized
convulsive seizure in later age
22. Other generalized
Epilepsies
Myoclonic seizures
‘Jerks’ take the form of
momentary brief
contractions of a muscle
or muscle groups
Often seen while going
to sleep or on waking up
Sudden involuntary
twitch of a finger or
hand.
Tonic seizures
stiffening of the body,
not followed by jerking.
Clonic Seizures
Jerking of the body, not
preceded by stiffening
Atonic seizures
A sudden collapse with
loss of muscle tone and
consciousness.
23. **
During sleep a patient can have only two
abnormal movements
GTC Seizures
Myoclonic Jerks
24. Simple Partial Epilepsy
focal motor seizure (Jacksonian)
Originate within the motor cortex
Jerking typically begins on one side of
the mouth or in one hand,
march of a seizure : Jacksonian
Local temporary paralysis of the limbs
affected sometimes follows – Todd’s
paralysis.
25. Complex Partial Epilepsy
Arise from the temporal lobe (60%) or the
frontal lobe.
Preceding aura
Epigastric sensation and nausea with a wide
variety of possible psychic phenomena or
hallucinations
Déjà vu, Olfactory or visual hallucinations or
misperceptions like micropsia or macropsia
Period of complete or partial loss of
awareness of surroundings, lasting for 1–2
minutes
26. Complex Partial Epilepsy
Speech arrest
Automatism – semi-purposeful
stereotyped motions such as lip
smacking or dystonic limb posturing
Complex motor behaviours such as
walking in a circle
Short period of post-ictal confusion or
may develop into a secondary
generalized convulsive seizure.
27. Complex Partial Seizures
Impaired consciousness
Clinical manifestations
vary with site of origin
and degree of spread
• Presence and nature of aura
• Automatisms
• Other motor activity
Duration typically < 2
minutes
C-Slide 27
Seizures
Partial Generalized
Complex
Partial
28. Secondarily Generalized
Seizures
Begins focally, with or
without focal neurological
symptoms
Variable symmetry, intensity,
and duration of tonic
(stiffening) and clonic
(jerking) phases
Typical duration 1-3 minutes
Postictal confusion,
somnolence, with or
without transient focal
deficit
C-Slide 28
Seizures
Partial Generalized
Secondarily
Generalized
American Epilepsy Society 2010
29. Plan
Definitions
Aetiology
Classification
Clinical Manifestations
Investigations
Diagnosis
Treatment
Who to Treat?
30. Investigations
Blood CBC
Urinalysis + Ketones
LFTs + Albumen
Na K Ca Mg
RFTs
Blood Sugar R
Lipid Profile R
ABGs
Drug Levels
Toxicology Screen
Chest X Ray
CT Scan Head
MRI Brain
SPECT Brain
EEG
With hyperventilation
ECG
2 D Echo
Tumour Markers
CSF Examination
31. Investigations
Neuroimaging can
be:
Static
CT Scan
MRI Scan
Dynamic
Electrphysiological
Neuroimaging ENI
Electromagnetic
Source Imaging
(EMSI)
EEG
10 – 20 eelectrodes
in the head
Records electrical
activity
32.
33.
34. Plan
Definitions
Aetiology
Classification
Clinical Manifestations
Investigations
Diagnosis
Treatment
Who to Treat?
36. Plan
Definitions
Aetiology
Classification
Clinical Manifestations
Investigations
Diagnosis
Treatment
Who to Treat?
37. Treatment
General Measures
Reassurance
Education
○ Patient, family, Parents, Teachers etc
Precautions
Specific Treatment
Medical Management
Surgery
38. Precautions while on
treatment
Driving
Can be allowed after 2 years FIT FREE
while on drugs, OR
3 years with only nocturnal fits
Heights – mountains, cliffs, roof edges
Water – pools, lakes etc
Fires – large fires, bonfires etc
Moving Heavy Machinery – eg thrasher
39.
40. Mechanism of Action
Suppress repetitive action potentials in
epileptic foci in the brain
Sodium channel blockade
GABA-related targets
Calcium channel blockade
Others: neuronal membrane
hyperpolarisation
42. Special Considerations
Women
Pregnancy – up to 7% teratogenecity
Lactation – some drugs excreted in milk
Children
Growth, activities and psychological
development
Drug-Drug Interactions
Liver based metabolism and detoxification
Can Either suppress or activate P-450
enzyme systems
43. Surgery
Curative
Catastrophic unilateral or secondary
generalised epilepsies of infants and young
children
○ Sturge-Weber syndrome
○ Large unilateral developmental abnormalities
Palliative
Vagal nerve stimulation
44. Plan
Definitions
Aetiology
Classification
Clinical Manifestations
Investigations
Diagnosis
Treatment
Who to Treat?
45. Who To Treat?
First Seizure – no treatment needed
Second Seizure – Treat
Precipitating cause recognized
Treat cause
Once on treatment - continue for 2 years
Check drug levels for compliance
Taper off after 2 years – in months
Editor's Notes
Seizures can be classified based on their clinical and electrographic features. The diagnosis of a patient’s epilepsy syndrome is based on their clinical history and their seizure type(s).
The diverse range of simple partial seizures gives rise to diagnostic challenges. For example, paresthesias (tingling sensations) in the fifth finger spreading to the forearm can result from a seizure, migraine, transient ischemic attack, or ulnar nerve disorder. Sudden abdominal discomfort may be produced by a gastrointestinal disorder as well as by a seizure arising from brain structures subserving autonomic or visceral function. When occurring in isolation, these symptoms may not be recognized as seizures by the patient or doctor.
Motor seizures alter muscle activity. Localized tonic posturing (stiffening) or clonic movements (twitching, jerking) can occur. Abnormal movements may be restricted to one body part or involve gradual spread to adjacent areas on the same side of the body (Jacksonian seizure) or both sides of the body with loss of consciousness (secondarily generalized seizure).
Epileptic discharges that occur in the sensory cortex may produce sensory seizures that manifest as hallucinations or illusions, for example; a sensation of something that is not there or distortion of a true sensation. Hallucinations may remain restricted to one area (e.g., paresthesias in a finger) or spread to other areas (e.g., entire upper extremity or entire side in a Jacksonian sensory march). Hallucinations and illusions can involve any sensory modality, including touch (e.g., pins and needles, electrical sensations), smell or taste (e.g., chemical or metallic sensations, often unpleasant), vision (e.g., flashing lights, complex scene), and hearing (e.g., buzzing, person’s voice).
Autonomic seizures are common, evoking changes in autonomic activity (e.g., altered heart or breathing rate, sweating) or visceral sensations (e.g., in abdomen or chest)
Psychic seizures affect how we feel, think, and experience things. Patients may report a “dreamy state,” transitional between waking and unconsciousness. Psychic seizures can alter language function, perception or memory. They can also evoke spontaneous emotions (e.g., fear, anxiety, or depression), altered perceptions of time or familiarity (time slowing down or speeding up; deja vu—new experiences appear familiar, jamais vu—familiar things appear foreign), depersonalization (feeling one is not oneself), derealization (the world seems unreal, dream-like), or autoscopy (viewing one’s body from outside).
Complex partial seizures are seizures which are associated with impairment of consciousness. A common misunderstanding is that this requires seizure spread to both sides of the brain. The majority of complex partial seizures originate in the temporal lobe and can affect consciousness while still remaining focal. During complex partial seizures the patient tends to stare off. This is accompanied by impaired responsiveness, cognitive function, and recall, although some degree of responsiveness may be preserved (e.g., orienting toward a stimulus). Automatic movements (automatisms) are common and involve the mouth (e.g., lip smacking, chewing, swallowing), upper extremities (e.g., fumbling, picking), vocalization/verbalization (e.g., grunts, repeating a phrase), or complex acts (e.g., shuffling cards). More dramatic automatisms occasionally occur (e.g., screaming, running, disrobing, pelvic thrusting). Complex partial seizures usually last from 15 seconds to 3 minutes. After the seizure, postictal confusion is common, usually lasting less than 15 minutes, although other symptoms, such as fatigue, may persist for hours.
Partial seizures can progress to generalized seizures with tonic-clonic activity. Once a partial seizure secondarily generalizes it is generally impossible to differentiate from a primarily generalized seizure. The history, electroencephalogram (EEG), neurologic exam (especially postictally), and neuroimaging tests (CT or MRI) often help distinguish these seizure types. In secondarily generalized seizures, patients may recall an aura prior to the convulsive activity or witnesses may observe a simple partial or complex partial seizure prior to generalization. In addition, following a secondarily generalized seizure, the patient may have focal weakness (Todd’s paralysis) on the side contralateral to seizure onset.