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By
Dr Junaid Saleem
MBBS FCPS Med
Consultant Physician and Hepatologist
Hearts International Hospital
The Mall Rawalpindi
Conflicts of interest
 NONE
Do NOT Take Notes
 This slide set is free for all to copy
Plan
 Definitions
 Aetiology
 Classification
 Clinical Manifestations
 Investigations
 Diagnosis
 Treatment
 Who to Treat?
Plan
 Definitions
 Aetiology
 Classification
 Clinical Manifestations
 Investigations
 Diagnosis
 Treatment
 Who to Treat?
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
Definitions
 Status Epilepticus:
 Continuous convulsion lasting >30 minutes
OR
 Occurrence of serial convulsions lasting >30 minutes
between which there is no return of consciousness
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
Plan
 Definitions
 Aetiology
 Classification
 Clinical Manifestations
 Investigations
 Diagnosis
 Treatment
 Who to Treat?
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%
Aetiology
 Mostly cause
unknown
 Genetic Disorders
 Metabolic
 Tumours
 Trauma
 Toxins and drugs
 Degenerative
 Demyelinating
Disorders
 Vascular
 Infections (including
Venereal)
 Infestations
 Inflammations
Plan
 Definitions
 Aetiology
 Classification
 Clinical Manifestations
 Investigations
 Diagnosis
 Treatment
 Who to Treat?
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
Internationally Accepted
 ILAE -
 International League Against Epilepsy
 First Proposed in 1981
 Modified several Times
 Latest Modifications 2010 & 2017
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
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
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
Plan
 Definitions
 Aetiology
 Classification
 Clinical Manifestations
 Investigations
 Diagnosis
 Treatment
 Who to Treat?
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
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
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.
**
 During sleep a patient can have only two
abnormal movements
 GTC Seizures
 Myoclonic Jerks
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.
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
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.
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
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
Plan
 Definitions
 Aetiology
 Classification
 Clinical Manifestations
 Investigations
 Diagnosis
 Treatment
 Who to Treat?
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
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
Plan
 Definitions
 Aetiology
 Classification
 Clinical Manifestations
 Investigations
 Diagnosis
 Treatment
 Who to Treat?
Diagnosis
 History
 Clinical Examination
 Investigations
Plan
 Definitions
 Aetiology
 Classification
 Clinical Manifestations
 Investigations
 Diagnosis
 Treatment
 Who to Treat?
Treatment
 General Measures
 Reassurance
 Education
○ Patient, family, Parents, Teachers etc
 Precautions
 Specific Treatment
 Medical Management
 Surgery
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
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
Adverse Effects
 Teratogenicity
 Neural tube defects
 Fetal hydantoin syndrome
 Overdosage toxicity
 Life-threatening toxicity
 Hepatotoxicity
 Stevens-Johnson syndrome
 Abrupt withdrawal
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
Surgery
 Curative
 Catastrophic unilateral or secondary
generalised epilepsies of infants and young
children
○ Sturge-Weber syndrome
○ Large unilateral developmental abnormalities
 Palliative
 Vagal nerve stimulation
Plan
 Definitions
 Aetiology
 Classification
 Clinical Manifestations
 Investigations
 Diagnosis
 Treatment
 Who to Treat?
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
Epilpepsy iimc 8th mar 3rd year

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Epilpepsy iimc 8th mar 3rd year

  • 1. By Dr Junaid Saleem MBBS FCPS Med Consultant Physician and Hepatologist Hearts International Hospital The Mall Rawalpindi
  • 2.
  • 4. Do NOT Take Notes  This slide set is free for all to copy
  • 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%
  • 12. Aetiology  Mostly cause unknown  Genetic Disorders  Metabolic  Tumours  Trauma  Toxins and drugs  Degenerative  Demyelinating Disorders  Vascular  Infections (including Venereal)  Infestations  Inflammations
  • 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?
  • 35. Diagnosis  History  Clinical Examination  Investigations
  • 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
  • 41. Adverse Effects  Teratogenicity  Neural tube defects  Fetal hydantoin syndrome  Overdosage toxicity  Life-threatening toxicity  Hepatotoxicity  Stevens-Johnson syndrome  Abrupt withdrawal
  • 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

  1. 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).
  2. 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).
  3. 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.
  4. 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.