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Epilepsy

Chronic,recurrent, unprovoked

Hughlings – excessive & disorder discharge in
brains on muscles

Discharge – aura,ictal phase; instant loss of
consciousness,alteration of perception &
sensation,impaiment of psychic function,
convulsive movements; post ictal phase

Convulsions – involuntary repetitive muscular
contractions

Seizure – paroxysmal electrical discharge in
brain
causes

Idiopathic ;SNAC

Sleep deprivation, alcohol, stress

Vascular malformation (CT,MRI)

Infection (CBC)

Trauma

Alzheimer

Neoplasm

psychiatric
Grand Mal

Prodromal – apathic, depressed, ecstatic

Abdominal pains, jerks,headaches, jerks

Motor signs – flextion of trunk, open mouth,
eyelids, upward deviation,hands
pronated,elbows flexed, tonic phase – extended

Tonic spasm of respiratory muscles – breath on
hold – cyanotic

Urination, dilation of pupil

Clonic phase transistion

Generalized tremor mild

Violent flexor spasm at 8 -4 sec interval

Violaceous face, series of grimaces

Salivation,sweating, BP, Dilation of pupil

Deep inspiration

Violent contraction may result – vertebral body
crush, periorbital hemorrhages, subdural
hematoma
differentials

Stoke adams

Limb shaking

Basilar artery occlusion

Treatment – CBZ, valproate,phenytoin
Absence/ petitmal

Brevity, frequency & paucity of motor activity

Absent mindedness, day dreaming

Sudden interuption of consciuosness

Patient stares, briefly stops responding

Minor automatisms – lip smacking, chewing,
fumbling movements of fingers

Remain motionless movements of eyelids,
facial muscles or fingers

Voluntary hyperventilation - triggers
Absence variants

2-2.5 spike wave

Atypical; Long runs of slow waves – can be
interrupted

Lennox gastaut syndrome – serious

1-2 slow wave

Intellectual impairment, minor tonic,clonic,
partial seizures

valproate
Myoclonic

Brief myoclonic jerks involving one part of
muscle – 50 – 100 ms

Associated with GTC, petit mal

Childhood – lafora type, myoclonus
-opsoclonus- ataxia

uremia
Juvenile myoclonic epilepsy

15 yrs

Morning

4-6 HZ irregular polyspike interval

valproate
Focal/ partial

Focal lesion

Simple and complex

Simple – sensorimotor cortex

Complex – focal lesions in limbic, temporal lobe
Frontal/ focal motor jacksonian
seizures

Supplementary motor area

Head and eyes turn opposite side – adversive,
area 6

Extension of limbs before loss of
consciousness due to expansion to thalamus,
mid brain RF
Jacksonian

Muscles of fingers, foot, arm, face

Premotor – 6, jacksonian

Fencing posture, 4,6,(8 choreathetotic,dystonic
); tonic extension and elevation of contralateral
arm

Todds paralysis
SOMATOSENSOR, visual

Numbness, tingling, pins and needles

Sylvian fissure – head

Superior sagital fissure – legs

Visual seizures – striate cortex, antero, occipito
temporal lobe

Darkness, flashes of light – opp eye

Auditary – buzzing or roaring – temporary lobe

Gustatory, vertigenous
Complex partial seizures

Adolscence, following febrile convulsions,
Secondary GTC

Focal seizure; temporal lobe – hallucinations,
alterd behaviour

Illusions – macro,micropsia, tilting of visual
environment, hallucinations,

dyscognitive states – strangeness to
environment, unfamiliar

Fear, anxiety

Motor components – fumbling fingers,
chewing, lip smacking, daze walking,
unresponsiveness

Violence – temporal lobe

Gelastic epilepsy – no memory

Volvular – revolving in circles

Simple wndering aimless

No memory of aura, attack

Lesions in hippocampal,medial temporal
sclerosis

Disoriented to time and place – right sided
lesion

Non – fluent aphasia

Nose wiping -temporal
Transient amnesic epileptic
seizures

Temporal lobe

Tendency to occur on awakening, impaired
performance

Psychic, behavioural, personality
Status epilepticus

Seizure lasted 5-30 min with brief interval

Non compliance with antiepileptic drug regimen

ABC management

Iv lorazepam, fosphenytoin

Correct hypoglycemia

EKG monitoring

Continue treatment every,5,10,15 (IV
fosphenytoin),20 minutes ( IV Phenobarbital)

Call anesthesia - propofol

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Epilepsy

  • 2.  Chronic,recurrent, unprovoked  Hughlings – excessive & disorder discharge in brains on muscles  Discharge – aura,ictal phase; instant loss of consciousness,alteration of perception & sensation,impaiment of psychic function, convulsive movements; post ictal phase  Convulsions – involuntary repetitive muscular contractions  Seizure – paroxysmal electrical discharge in brain
  • 3. causes  Idiopathic ;SNAC  Sleep deprivation, alcohol, stress  Vascular malformation (CT,MRI)  Infection (CBC)  Trauma  Alzheimer  Neoplasm  psychiatric
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10. Grand Mal  Prodromal – apathic, depressed, ecstatic  Abdominal pains, jerks,headaches, jerks  Motor signs – flextion of trunk, open mouth, eyelids, upward deviation,hands pronated,elbows flexed, tonic phase – extended  Tonic spasm of respiratory muscles – breath on hold – cyanotic  Urination, dilation of pupil  Clonic phase transistion
  • 11.  Generalized tremor mild  Violent flexor spasm at 8 -4 sec interval  Violaceous face, series of grimaces  Salivation,sweating, BP, Dilation of pupil  Deep inspiration  Violent contraction may result – vertebral body crush, periorbital hemorrhages, subdural hematoma
  • 12.
  • 13. differentials  Stoke adams  Limb shaking  Basilar artery occlusion  Treatment – CBZ, valproate,phenytoin
  • 14. Absence/ petitmal  Brevity, frequency & paucity of motor activity  Absent mindedness, day dreaming  Sudden interuption of consciuosness  Patient stares, briefly stops responding  Minor automatisms – lip smacking, chewing, fumbling movements of fingers  Remain motionless movements of eyelids, facial muscles or fingers  Voluntary hyperventilation - triggers
  • 15.
  • 16.
  • 17. Absence variants  2-2.5 spike wave  Atypical; Long runs of slow waves – can be interrupted  Lennox gastaut syndrome – serious  1-2 slow wave  Intellectual impairment, minor tonic,clonic, partial seizures  valproate
  • 18. Myoclonic  Brief myoclonic jerks involving one part of muscle – 50 – 100 ms  Associated with GTC, petit mal  Childhood – lafora type, myoclonus -opsoclonus- ataxia  uremia
  • 19. Juvenile myoclonic epilepsy  15 yrs  Morning  4-6 HZ irregular polyspike interval  valproate
  • 20. Focal/ partial  Focal lesion  Simple and complex  Simple – sensorimotor cortex  Complex – focal lesions in limbic, temporal lobe
  • 21. Frontal/ focal motor jacksonian seizures  Supplementary motor area  Head and eyes turn opposite side – adversive, area 6  Extension of limbs before loss of consciousness due to expansion to thalamus, mid brain RF
  • 22. Jacksonian  Muscles of fingers, foot, arm, face  Premotor – 6, jacksonian  Fencing posture, 4,6,(8 choreathetotic,dystonic ); tonic extension and elevation of contralateral arm  Todds paralysis
  • 23. SOMATOSENSOR, visual  Numbness, tingling, pins and needles  Sylvian fissure – head  Superior sagital fissure – legs  Visual seizures – striate cortex, antero, occipito temporal lobe  Darkness, flashes of light – opp eye  Auditary – buzzing or roaring – temporary lobe  Gustatory, vertigenous
  • 24. Complex partial seizures  Adolscence, following febrile convulsions, Secondary GTC  Focal seizure; temporal lobe – hallucinations, alterd behaviour  Illusions – macro,micropsia, tilting of visual environment, hallucinations,  dyscognitive states – strangeness to environment, unfamiliar  Fear, anxiety
  • 25.  Motor components – fumbling fingers, chewing, lip smacking, daze walking, unresponsiveness  Violence – temporal lobe  Gelastic epilepsy – no memory  Volvular – revolving in circles  Simple wndering aimless  No memory of aura, attack  Lesions in hippocampal,medial temporal sclerosis
  • 26.  Disoriented to time and place – right sided lesion  Non – fluent aphasia  Nose wiping -temporal
  • 27. Transient amnesic epileptic seizures  Temporal lobe  Tendency to occur on awakening, impaired performance  Psychic, behavioural, personality
  • 28. Status epilepticus  Seizure lasted 5-30 min with brief interval  Non compliance with antiepileptic drug regimen  ABC management  Iv lorazepam, fosphenytoin  Correct hypoglycemia  EKG monitoring  Continue treatment every,5,10,15 (IV fosphenytoin),20 minutes ( IV Phenobarbital)  Call anesthesia - propofol