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SEIZURE DISORDERS
Saleh H. Al-Khalid
Supervised by Dr. Remma Hakim
Special Thanks to Dr. Hussein algahtani
OUTLINE
• Definition
• Epidemiology
• Classification
• Pathophysiology
• Etiology
• DDx
• Approach
• Management
• Prevention
• Cases
• MCQs
OUTLINE
•Definition
• Epidemiology
• Classification
• Pathophysiology
• Etiology
• DDx
• Approach
• Management
• Prevention
• Cases
• MCQs
DEFINITION
• Seizure is a sudden, involuntary, time-limited alteration in behavior
accompanied by an abnormal , synchronized electrical discharge of
cortical neurons.
• The Alteration in behavior may involve a change:
• Motor activity
• Autonomic function
• Consciousness
• Sensation
STATUS EPILEPTICUS
• Status epilepticus: is defined as:
More than 30 minutes of continuous seizure activity or
Two or more sequential seizures without recovery of consciousness
between seizures.
OUTLINE
• Definition
•Epidemiology
• Classification
• Pathophysiology
• Etiology
• DDx
• Approach
• Management
• Prevention
• Cases
• MCQs
WHO
• World Health Organization (WHO) estimates that 50 million people of
all ages are affected by epilepsy worldwide with more than 85% living
in the developing world.
• In developing countries, up to 90% of epileptic patients may not
receive the treatment they require and this wide treatment gap remains
a reason for tremendous individual, family, social and economic
burden.
EPIDEMIOLOGY IN SAUDI ARABIA (2001)
• Prevalence rate (PR) for active epilepsy was 6.54 /1000 population.
• 28% of the patients had partial seizures,
• 21% generalized seizures and in
• 51%, it was not possible to determine if the generalized seizures had focal onset or not.
• The epilepsy was symptomatic in 32% of the cases:
• Perinatal encephalopathy 23%,
• Head injury 4%,
• Childhood neurological infection 4%
• Stroke 1%.
• Febrile convulsions PR was 3.55 /1000 children under the age of 6 years
http://www.nsj.org.sa/
‫واألعصاب‬ ‫المخ‬ ‫لجراحة‬ ‫السعودية‬ ‫الجمعية‬
CONTINUE
• The rate of mortality from status epilepticus (defined
as death within 30 days of status epilepticus) is 22%.
• Mortality rate among children is 3 percent.
• Mortality rate among adults is 26 percent.
• Mortality rate in elderly is 38 percent.The highest
EPILEPSY STATISTICS
• One in 20 people will have a one-off epileptic seizure at some point in their life
(although this does not necessarily mean that they have epilepsy).
• One in 50 people will have epilepsy at some time in their life (not everyone with
epilepsy will have it for life).
• Around 87 people are diagnosed with epilepsy every day.
• There are around 60 million people with epilepsy in the world.
• Up to 3% of people with epilepsy will be affected by flashing lights (called
photosensitive epilepsy), so most people with epilepsy do not have seizures
triggered by flashing lights.
PEAKS
• The incidence varies greatly with age, with high rates occurring in early childhood ,
falling to low levels in early adult life, but with a second peak in those aged over 65
years.
OUTLINE
• Definition
• Epidemiology
•Classification
• Pathophysiology
• Etiology
• DDx
• Approach
• Management
• Prevention
• Cases
• MCQs
SEIZURES CLASSIFICATION (OLD)
• Partial: in start and involve part of the brain
• Simple: without impair of awareness
• Complex: with impaired awareness
• Generalized: bilateral abnormal electrical activity with bilateral motor
manifestation with impaired conscious
• Absence (Petit mal)
• Tonic
• Myoclonic
• Tonic-clonic (grand mal)
• Akinetic
• Unclassifiable: seizure that don’t fit with any class
Awareness
ANATOMICAL SITE
• Most of seizures begin in the
temporal lobe.
• Most temporal lobe seizures begin
in the mesial temporal lobe
structures.
• The frontal lobe is the next most
frequent site for CPS.
CONTINUE
Generalized seizures begin
in both hemispheres at
same time (i.e. seizures that
cannot be localized to one
cerebral hemisphere at
onset).
VIDEO
• Types of seizure
OUTLINE
• Definition
• Epidemiology
• Classification
•Pathophysiology
• Etiology
• DDx
• Approach
• Management
• Prevention
• Cases
• MCQs
PATHOPHYSIOLOGY
A seizure results from a paroxysmal high-frequency or
synchronous low-frequency electrical discharge that can arise
from almost any part of the cerebral cortex (i.e., Not the
cerebellum, brainstem, or spinal cord).
CONTINUE
Based on experimental models of epilepsy, the event is
thought to involve a reduction in cortical inhibition mediated
by GABA, combined with divergent excitation, probably
mediated by glutamate.
CONTINUE
In a partial seizure, the synchronously depolarizing neurons
remain localized, while in a generalized seizure, the
synchronous depolarizations are present throughout both
hemispheres.
OUTLINE
• Definition
• Epidemiology
• Classification
• Pathophysiology
•Etiology
• DDx
• Approach
• Management
• Prevention
• Cases
• MCQs
OUTLINE
• Definition
• Epidemiology
• Classification
• Pathophysiology
• Etiology
•DDx
• Approach
• Management
• Prevention
• Cases
• MCQs
DIFFERENTIAL DIAGNOSIS
• Syncope
 Transient ischemic attack
 Neurological vasovagal reflex
• Hypoglycemisa
• Psychlogical:
 Panic attacks,
 Hyperventilation,
 Narcolepsy with cataplexy,
 Psychogenic nonepileptic seizure
• Migraine
• Transient global amnesia
• Paroxysmal movement disorders
OUTLINE
• Definition
• Epidemiology
• Classification
• Pathophysiology
• Etiology
• DDx
•Approach
• Management
• Prevention
• Cases
• MCQs
CASE
3 MAIN STEPS
1. Is it seizure?
2. Partial vs generalized
3. Identify the underlying cause
IS IT SEIZURE?
IF YES
PARTIAL VS GENERALIZED
IDENTIFY THE UNDERLYING CAUSE
HISTORY
• Preictal
• Any warning? Abdominal pain, fear, unpleasant sensation
• What was patient doing
• Asleep or awake
• Triggers
• • Ictal
• Consciousness?
• Repetitive behaviors during spell – lip smacking, etc
• Body movements – part or all
• Cyanosis
• Incontinence
• How long, how many, how often
• Gaze deviation, eye rolling
• Post ictal
• How did patient feel after (Drowsy? Confused? Tired?)
• How long until return to baseline?
• Trauma
OUTLINE
• Definition
• Epidemiology
• Classification
• Pathophysiology
• Etiology
• DDx
• Approash
•Management
• Prevention
• Cases
• MCQs
WHEN TO START TREATMENT?
• People should be treated with A.E.D when the clinician
thinks that the person will probably have another seizure
without treatment.
• The seizure type or syndrome may help with this decision.
• For example, absence seizures are rarely isolated and so
require therapy, whereas febrile seizures are often isolated
and therapy is not indicated.
IN THESE CASES, IT IS REASONABLE TO
BEGIN A.E.D.
• Seizure recurrence is more likely if the patient has:
• Focal neurologic deficits
• Mental retardation
• EEG that demonstrates epileptiform abnormalities
• Structural brain lesion.
CONTINUE
• In patients with a well-defined provocative etiology, it
is best to treat the underlying process rather than the
seizures themselves.
NON-PHARMACOLOGICAL:
• Lifestyle modification
• Adequate sleep.
• Healthy diet.
• Avoidance of alcohol, stimulants, etc.
• Stress reduction.
• Ketogenic diet: high in fat and low in CHO
• Vagus nerve stimulation
• Implantable neurostimulation: Used when antiepileptic treatment have failed
• Surgery: It is a standard treatment for patients with partial seizures that are resistant to
medication.
• Anterior temporal lobectomy
• Amygdalohippocampectomy
• Laser therapy
PHARMACOLOGICAL
• To start pharmacological therapy consider the following:
• Start monotherapy
• Start low dose and slowly increase until resolve of seizure attacks
• Discontinuation of medication can be consider if more than 2-5
years seizure free
• Add second medication if the first medication partially effective or
significant side effect from first medication
TREATMENT
• Partial Seizure:
• First Line: Carbamazepine or Lamotrigine.
• Not tolerated: Levetiracetam, Oxcarbazepine, or Sodium valproate.
TREATMENT
• Generalized Seizure:
• First Line: Sodium valproate, Lamotrigine.
• Not tolerated: Levetiracetam or Topiramate.
TREATMENT
• Absence seizures (non motor):
• First line: Ethosuximide or Sodium valproate.
• Not tolerated: Combination of Ethosuximide, Lamotrigine or Sodium
valproate.
STATUS EPILEPTICUS
MEDICAL EMERGENCY
• Once the diagnosis of status epilepticus is made, treatment should be initiated
immediately.
• Two or more sequential seizures without full recovery of consciousness between seizures, or more
than 30 minutes of continuous seizure activity.
• The goal of treatment always should be immediate diagnosis and termination of
seizures.
• The first step in managing status epilepticus is assessing the patient’s airway and
oxygenation.
• Start the protocol for management of status epilepticus
PROTOCOL FOR MANAGEMENT OF STATUS
EPILEPTICUS (1)
• At: zero minutes:
• Initiate general systemic support of the airway (insert nasal airway or intubate if
needed)
• Check blood pressure.
• Begin nasal oxygen.
• Monitor ECG and respiration.
• Check temperature frequently.
• Obtain quick history from relatives.
• Perform neurologic examination.
PROTOCOL FOR MANAGEMENT OF STATUS
EPILEPTICUS (2)
• Lab:
• Electrolytes,
• glucose level,
• complete blood cell count,
• toxic drug screen,
• anticonvulsant levels;
• check arterial blood gas values.
• Start IV line containing isotonic saline at a low infusion rate.
• Inject 50 mL of 50 percent glucose IV and 100 mg of thiamine IV or IM.
• Call EEG laboratory to start recording as soon as feasible.
PROTOCOL FOR MANAGEMENT OF STATUS
EPILEPTICUS (3)
o Administer
 Lorazepam (Ativan) at 0.1 per kg IV (2 mg per minute);
o If seizures persist,
 Fosphenytoin (Cerebyx) at 18 mg per kg IV (150 mg per minute).
o At: 20 to 30 minutes, if seizures persist
 Intubate, insert bladder catheter, start EEG recording, check temperature.
 Administer phenobarbital in a loading dose of 20 mg per kg IV (100 mg per minute).
o At: 40 to 60 minutes, if seizures persist
 Begin pentobarbital infusion at 5 mg per kg IV initial dose, then IV push until seizures have stopped, using EEG
monitoring
 Continue pentobarbital infusion at 1 mg per kg per hour; slow infusion rate every four to six hours to determine if
seizures have stopped, with EEG guidance; monitor blood pressure and respiration carefully.
 Support blood pressure with pressors if needed.
OUTLINE
• Definition
• Epidemiology
• Classification
• Pathophysiology
• Etiology
• DDx
• Approach
• Management
•Prevention
• Cases
• MCQs
PREVENTION
• Idiopathic epilepsy is not preventable. However, preventive measures can be applied
to the known causes of secondary epilepsy.
• Preventing head injury is the most effective way to prevent post-traumatic epilepsy.
• Adequate perinatal care can reduce new cases of epilepsy caused by birth injury.
• The use of drugs and other methods to lower the body temperature of a feverish child
can reduce the chance of febrile seizures.
• Avoid CNS infections
TIPS TO PREVENT SEIZURES
• Get plenty of sleep each night
• Learn stress management and relaxation techniques.
• Avoid drugs and alcohol.
• Take medications.
• Avoid bright, flashing lights and other visual stimuli.
• Skip TV and computer time whenever possible.
• Avoid playing video games.
• Eat a healthy diet.
FIRST AID IN SEIZURE
• Video
PROGNOSIS
• 60% of untreated patients have no further seizures during the two years
after their first seizure.
• 70 % go into remission, defined as being seizure-free for 5 years on or
off treatment.
• This leaves 20 to 30 % who develop chronic epilepsy, which is often
treated with multiple antiepileptic drugs.
OUTLINE
• Definition
• Epidemiology
• Classification
• Pathophysiology
• Etiology
• DDx
• Approach
• Management
• Prevention
• Real Case
• MCQs
CASE
• A 28-year-old woman is brought to the ED by ambulance after she
developed a generalized convulsive seizure at home.
• She has had neck stiffness and fever for the past several days and has
been somewhat confused and not “acting like herself.”
• The patient is still convulsing when she arrives in the ED 20 minutes
later.
CONTINUE
• She was started on lorazepam 0.1 mg/kg intravenously (IV)
• The patient stops seizing with starting of anticonvulsant therapy.
• A lumbar puncture is emergently performed, and analysis of the CSF reveals 9 white
blood cells with a lymphocytic predominance, 32 red blood cells, a protein level of 63
mg/dl, and a glucose level of 65 mg/dl.
• An EEG shows sharp wave discharges in the temporal lobes but no electrographic
seizures.
HERPES SIMPLEX VIRUS (HSV) EEG
CHANGES
MRI
OUTLINE
• Definition
• Epidemiology
• Classification
• Pathophysiology
• Etiology
• DDx
• Approash
• Management
• Prevention
• Cases
•MCQs
MCQ1
• The commonest cause of seizure in adult above 35 and under 60 years is:
• (a) Tumor
• (b) Degenerative
• (c) CVA
• (d) Infection
CVA
MSQ2
• The commonest cause of seizure in children above 60 years is:
• (a) Unknown
• (b) Degenerative
• (c) Tumor
• (d) Stroke
Stroke
MCQ3
• Second most site which seizures begins from:
• (a) Frontal
• (b) Temporal
• (c) Occipital
• (d) Thymus
Frontal
MCQ4
• What is the first line therapy for the condition in the video?
• (a) Carbamazepine
• (b) Lamotrigine
• (c) Ethosuximide
• (d) No need for treatment
• Absence seizure
Ethosuximide
MCQ5
• What is the first line therapy for the condition in the video?
• (a) Carbamazepine
• (b) Sodium valproate
• (c) Ethosuximide
• (d) No need for treatment
• Simple partial
Carbamazepine
MCQ6
• What is the first line therapy for the condition in the video?
• (a) Carbamazepine
• (b) Sodium valproate
• (c) Ethosuximide
• (d) No need for treatment
• Generalized Tonic-Clonic Seizure
Sodium valproate
• A 23-year-old white female with a generalized seizure disorder is brought into the ED
in status epilepticus.Which one of the following drugs should be administered
initially?
• (a) Lorazepam
• (b) Fosphenytoin
• (c) Pentobarbital
• (d) Phenytoin
• (e) Phenobarbital
Lorazepam
REFERENCES
THANK YOU
Any questions?
Any point of improvement?

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Seizure Disorder.pdf

  • 1. SEIZURE DISORDERS Saleh H. Al-Khalid Supervised by Dr. Remma Hakim Special Thanks to Dr. Hussein algahtani
  • 2. OUTLINE • Definition • Epidemiology • Classification • Pathophysiology • Etiology • DDx • Approach • Management • Prevention • Cases • MCQs
  • 3. OUTLINE •Definition • Epidemiology • Classification • Pathophysiology • Etiology • DDx • Approach • Management • Prevention • Cases • MCQs
  • 4. DEFINITION • Seizure is a sudden, involuntary, time-limited alteration in behavior accompanied by an abnormal , synchronized electrical discharge of cortical neurons. • The Alteration in behavior may involve a change: • Motor activity • Autonomic function • Consciousness • Sensation
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  • 6. STATUS EPILEPTICUS • Status epilepticus: is defined as: More than 30 minutes of continuous seizure activity or Two or more sequential seizures without recovery of consciousness between seizures.
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  • 8. OUTLINE • Definition •Epidemiology • Classification • Pathophysiology • Etiology • DDx • Approach • Management • Prevention • Cases • MCQs
  • 9. WHO • World Health Organization (WHO) estimates that 50 million people of all ages are affected by epilepsy worldwide with more than 85% living in the developing world. • In developing countries, up to 90% of epileptic patients may not receive the treatment they require and this wide treatment gap remains a reason for tremendous individual, family, social and economic burden.
  • 10. EPIDEMIOLOGY IN SAUDI ARABIA (2001) • Prevalence rate (PR) for active epilepsy was 6.54 /1000 population. • 28% of the patients had partial seizures, • 21% generalized seizures and in • 51%, it was not possible to determine if the generalized seizures had focal onset or not. • The epilepsy was symptomatic in 32% of the cases: • Perinatal encephalopathy 23%, • Head injury 4%, • Childhood neurological infection 4% • Stroke 1%. • Febrile convulsions PR was 3.55 /1000 children under the age of 6 years http://www.nsj.org.sa/ ‫واألعصاب‬ ‫المخ‬ ‫لجراحة‬ ‫السعودية‬ ‫الجمعية‬
  • 11. CONTINUE • The rate of mortality from status epilepticus (defined as death within 30 days of status epilepticus) is 22%. • Mortality rate among children is 3 percent. • Mortality rate among adults is 26 percent. • Mortality rate in elderly is 38 percent.The highest
  • 12. EPILEPSY STATISTICS • One in 20 people will have a one-off epileptic seizure at some point in their life (although this does not necessarily mean that they have epilepsy). • One in 50 people will have epilepsy at some time in their life (not everyone with epilepsy will have it for life). • Around 87 people are diagnosed with epilepsy every day. • There are around 60 million people with epilepsy in the world. • Up to 3% of people with epilepsy will be affected by flashing lights (called photosensitive epilepsy), so most people with epilepsy do not have seizures triggered by flashing lights.
  • 13. PEAKS • The incidence varies greatly with age, with high rates occurring in early childhood , falling to low levels in early adult life, but with a second peak in those aged over 65 years.
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  • 15. OUTLINE • Definition • Epidemiology •Classification • Pathophysiology • Etiology • DDx • Approach • Management • Prevention • Cases • MCQs
  • 16. SEIZURES CLASSIFICATION (OLD) • Partial: in start and involve part of the brain • Simple: without impair of awareness • Complex: with impaired awareness • Generalized: bilateral abnormal electrical activity with bilateral motor manifestation with impaired conscious • Absence (Petit mal) • Tonic • Myoclonic • Tonic-clonic (grand mal) • Akinetic • Unclassifiable: seizure that don’t fit with any class Awareness
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  • 20. ANATOMICAL SITE • Most of seizures begin in the temporal lobe. • Most temporal lobe seizures begin in the mesial temporal lobe structures. • The frontal lobe is the next most frequent site for CPS.
  • 21. CONTINUE Generalized seizures begin in both hemispheres at same time (i.e. seizures that cannot be localized to one cerebral hemisphere at onset).
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  • 25. OUTLINE • Definition • Epidemiology • Classification •Pathophysiology • Etiology • DDx • Approach • Management • Prevention • Cases • MCQs
  • 26. PATHOPHYSIOLOGY A seizure results from a paroxysmal high-frequency or synchronous low-frequency electrical discharge that can arise from almost any part of the cerebral cortex (i.e., Not the cerebellum, brainstem, or spinal cord).
  • 27. CONTINUE Based on experimental models of epilepsy, the event is thought to involve a reduction in cortical inhibition mediated by GABA, combined with divergent excitation, probably mediated by glutamate.
  • 28. CONTINUE In a partial seizure, the synchronously depolarizing neurons remain localized, while in a generalized seizure, the synchronous depolarizations are present throughout both hemispheres.
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  • 30. OUTLINE • Definition • Epidemiology • Classification • Pathophysiology •Etiology • DDx • Approach • Management • Prevention • Cases • MCQs
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  • 36. OUTLINE • Definition • Epidemiology • Classification • Pathophysiology • Etiology •DDx • Approach • Management • Prevention • Cases • MCQs
  • 37. DIFFERENTIAL DIAGNOSIS • Syncope  Transient ischemic attack  Neurological vasovagal reflex • Hypoglycemisa • Psychlogical:  Panic attacks,  Hyperventilation,  Narcolepsy with cataplexy,  Psychogenic nonepileptic seizure • Migraine • Transient global amnesia • Paroxysmal movement disorders
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  • 39. OUTLINE • Definition • Epidemiology • Classification • Pathophysiology • Etiology • DDx •Approach • Management • Prevention • Cases • MCQs
  • 40. CASE
  • 41. 3 MAIN STEPS 1. Is it seizure? 2. Partial vs generalized 3. Identify the underlying cause
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  • 47. HISTORY • Preictal • Any warning? Abdominal pain, fear, unpleasant sensation • What was patient doing • Asleep or awake • Triggers
  • 48. • • Ictal • Consciousness? • Repetitive behaviors during spell – lip smacking, etc • Body movements – part or all • Cyanosis • Incontinence • How long, how many, how often • Gaze deviation, eye rolling
  • 49. • Post ictal • How did patient feel after (Drowsy? Confused? Tired?) • How long until return to baseline? • Trauma
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  • 51. OUTLINE • Definition • Epidemiology • Classification • Pathophysiology • Etiology • DDx • Approash •Management • Prevention • Cases • MCQs
  • 52. WHEN TO START TREATMENT? • People should be treated with A.E.D when the clinician thinks that the person will probably have another seizure without treatment. • The seizure type or syndrome may help with this decision. • For example, absence seizures are rarely isolated and so require therapy, whereas febrile seizures are often isolated and therapy is not indicated.
  • 53. IN THESE CASES, IT IS REASONABLE TO BEGIN A.E.D. • Seizure recurrence is more likely if the patient has: • Focal neurologic deficits • Mental retardation • EEG that demonstrates epileptiform abnormalities • Structural brain lesion.
  • 54. CONTINUE • In patients with a well-defined provocative etiology, it is best to treat the underlying process rather than the seizures themselves.
  • 55. NON-PHARMACOLOGICAL: • Lifestyle modification • Adequate sleep. • Healthy diet. • Avoidance of alcohol, stimulants, etc. • Stress reduction. • Ketogenic diet: high in fat and low in CHO • Vagus nerve stimulation • Implantable neurostimulation: Used when antiepileptic treatment have failed • Surgery: It is a standard treatment for patients with partial seizures that are resistant to medication. • Anterior temporal lobectomy • Amygdalohippocampectomy • Laser therapy
  • 56. PHARMACOLOGICAL • To start pharmacological therapy consider the following: • Start monotherapy • Start low dose and slowly increase until resolve of seizure attacks • Discontinuation of medication can be consider if more than 2-5 years seizure free • Add second medication if the first medication partially effective or significant side effect from first medication
  • 57. TREATMENT • Partial Seizure: • First Line: Carbamazepine or Lamotrigine. • Not tolerated: Levetiracetam, Oxcarbazepine, or Sodium valproate.
  • 58. TREATMENT • Generalized Seizure: • First Line: Sodium valproate, Lamotrigine. • Not tolerated: Levetiracetam or Topiramate.
  • 59. TREATMENT • Absence seizures (non motor): • First line: Ethosuximide or Sodium valproate. • Not tolerated: Combination of Ethosuximide, Lamotrigine or Sodium valproate.
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  • 61. STATUS EPILEPTICUS MEDICAL EMERGENCY • Once the diagnosis of status epilepticus is made, treatment should be initiated immediately. • Two or more sequential seizures without full recovery of consciousness between seizures, or more than 30 minutes of continuous seizure activity. • The goal of treatment always should be immediate diagnosis and termination of seizures. • The first step in managing status epilepticus is assessing the patient’s airway and oxygenation. • Start the protocol for management of status epilepticus
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  • 63. PROTOCOL FOR MANAGEMENT OF STATUS EPILEPTICUS (1) • At: zero minutes: • Initiate general systemic support of the airway (insert nasal airway or intubate if needed) • Check blood pressure. • Begin nasal oxygen. • Monitor ECG and respiration. • Check temperature frequently. • Obtain quick history from relatives. • Perform neurologic examination.
  • 64. PROTOCOL FOR MANAGEMENT OF STATUS EPILEPTICUS (2) • Lab: • Electrolytes, • glucose level, • complete blood cell count, • toxic drug screen, • anticonvulsant levels; • check arterial blood gas values. • Start IV line containing isotonic saline at a low infusion rate. • Inject 50 mL of 50 percent glucose IV and 100 mg of thiamine IV or IM. • Call EEG laboratory to start recording as soon as feasible.
  • 65. PROTOCOL FOR MANAGEMENT OF STATUS EPILEPTICUS (3) o Administer  Lorazepam (Ativan) at 0.1 per kg IV (2 mg per minute); o If seizures persist,  Fosphenytoin (Cerebyx) at 18 mg per kg IV (150 mg per minute). o At: 20 to 30 minutes, if seizures persist  Intubate, insert bladder catheter, start EEG recording, check temperature.  Administer phenobarbital in a loading dose of 20 mg per kg IV (100 mg per minute). o At: 40 to 60 minutes, if seizures persist  Begin pentobarbital infusion at 5 mg per kg IV initial dose, then IV push until seizures have stopped, using EEG monitoring  Continue pentobarbital infusion at 1 mg per kg per hour; slow infusion rate every four to six hours to determine if seizures have stopped, with EEG guidance; monitor blood pressure and respiration carefully.  Support blood pressure with pressors if needed.
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  • 67. OUTLINE • Definition • Epidemiology • Classification • Pathophysiology • Etiology • DDx • Approach • Management •Prevention • Cases • MCQs
  • 68. PREVENTION • Idiopathic epilepsy is not preventable. However, preventive measures can be applied to the known causes of secondary epilepsy. • Preventing head injury is the most effective way to prevent post-traumatic epilepsy. • Adequate perinatal care can reduce new cases of epilepsy caused by birth injury. • The use of drugs and other methods to lower the body temperature of a feverish child can reduce the chance of febrile seizures. • Avoid CNS infections
  • 69. TIPS TO PREVENT SEIZURES • Get plenty of sleep each night • Learn stress management and relaxation techniques. • Avoid drugs and alcohol. • Take medications. • Avoid bright, flashing lights and other visual stimuli. • Skip TV and computer time whenever possible. • Avoid playing video games. • Eat a healthy diet.
  • 70. FIRST AID IN SEIZURE • Video
  • 71. PROGNOSIS • 60% of untreated patients have no further seizures during the two years after their first seizure. • 70 % go into remission, defined as being seizure-free for 5 years on or off treatment. • This leaves 20 to 30 % who develop chronic epilepsy, which is often treated with multiple antiepileptic drugs.
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  • 73. OUTLINE • Definition • Epidemiology • Classification • Pathophysiology • Etiology • DDx • Approach • Management • Prevention • Real Case • MCQs
  • 74. CASE • A 28-year-old woman is brought to the ED by ambulance after she developed a generalized convulsive seizure at home. • She has had neck stiffness and fever for the past several days and has been somewhat confused and not “acting like herself.” • The patient is still convulsing when she arrives in the ED 20 minutes later.
  • 75. CONTINUE • She was started on lorazepam 0.1 mg/kg intravenously (IV) • The patient stops seizing with starting of anticonvulsant therapy. • A lumbar puncture is emergently performed, and analysis of the CSF reveals 9 white blood cells with a lymphocytic predominance, 32 red blood cells, a protein level of 63 mg/dl, and a glucose level of 65 mg/dl. • An EEG shows sharp wave discharges in the temporal lobes but no electrographic seizures.
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  • 77. HERPES SIMPLEX VIRUS (HSV) EEG CHANGES
  • 78. MRI
  • 79. OUTLINE • Definition • Epidemiology • Classification • Pathophysiology • Etiology • DDx • Approash • Management • Prevention • Cases •MCQs
  • 80. MCQ1 • The commonest cause of seizure in adult above 35 and under 60 years is: • (a) Tumor • (b) Degenerative • (c) CVA • (d) Infection
  • 81. CVA
  • 82. MSQ2 • The commonest cause of seizure in children above 60 years is: • (a) Unknown • (b) Degenerative • (c) Tumor • (d) Stroke
  • 84. MCQ3 • Second most site which seizures begins from: • (a) Frontal • (b) Temporal • (c) Occipital • (d) Thymus
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  • 87. MCQ4 • What is the first line therapy for the condition in the video? • (a) Carbamazepine • (b) Lamotrigine • (c) Ethosuximide • (d) No need for treatment
  • 89. MCQ5 • What is the first line therapy for the condition in the video? • (a) Carbamazepine • (b) Sodium valproate • (c) Ethosuximide • (d) No need for treatment
  • 91. MCQ6 • What is the first line therapy for the condition in the video? • (a) Carbamazepine • (b) Sodium valproate • (c) Ethosuximide • (d) No need for treatment
  • 92. • Generalized Tonic-Clonic Seizure Sodium valproate
  • 93. • A 23-year-old white female with a generalized seizure disorder is brought into the ED in status epilepticus.Which one of the following drugs should be administered initially? • (a) Lorazepam • (b) Fosphenytoin • (c) Pentobarbital • (d) Phenytoin • (e) Phenobarbital
  • 96. THANK YOU Any questions? Any point of improvement?