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Presenter
Dr berihu assefa (EMCC R2)
moderator
Dr selam (EMCC R3)
adviser
Dr weldesenbet ( EMCC consultant)
OUTLINE
 DEFINITION
 EPIDEMIOLOGY
 PATHOPHSYSIOLOGY
 CLINICAL FEUTURE
 DIFFERETIAL DIAGNOSIS
 CONVULSIVE STATUS EPILEPTICUS
 NONCONVULSIVE STATUS EPILEPTICUS
objectives
 To be able to know definition of seizure,GCSE,NCSE
 To understand epidiomology,clinical features of seizure &SE
 To know basic pathophysiology of seizure
 To identify major causes of provoked seizure
 To understand the management principles
DEFINITION
SEIZURE- are excessive abnormal neuronal activity associated with
alteration sensory , motor , autonomic dysfunction and/or
cognitive function.
CONVULSION- refers specifically to the motor manifestation of a
seizure
POSTICTAL PERIOD- an interval of altered mental status immediately
following a seizure, generally lasting less than 1hr.
EPILEPSY- refers to a condition of recurrent unprovoked seizures.
Cont..
 Acute symptomatic seizure-refers to
 a seizure that occurs at the time of a systemic insult or in close temporal
association with documented brain insult.
-within 01 wk. of stroke ,TBI , anoxic encephalopathy or intracranial
surgery
-during active phase of CNS infection
-within 24 hrs. of severe metabolic derangement
-account up to 25-30% of 1st seizure and has low risk for future
epilepsy
…
 Unprovoked seizures- seizure of unknown etiology as well as one that
occurs in r/n to a preexisting brain lesion or
progressive nervous system disorder
. Status epileptics - ≥ 5 min continuous seizure or
- ≥ 2 discrete seizure b/n w/c there is incomplete
recovery of consciousness
.
…
FOCAL SEIZURE WITH RETAINED AWARENESS
The symptoms vary from one patient to another and depends entirely on
the part of the cortex that is disrupted
occipital lobe - may result in flashing light
motor cortex- jacksonian march
parietal cortex-spatial perception
frontal lobe - sudden speech difficulties
temporal lobe- gustatory or olfactory hallucination
…
FOCAL SEIZURE WITH IMPAIRED AWARENESS
- the most common types of seizure in adults with epilepsy
- typically lasts less than 3 min and may begin with a preserved
awareness
-postictal phase- somnolence ,confusion and headache for up to
several hrs.
- symptom can be bizarre
Cont..
 Automatism - lip smacking , fiddling with cloth or button, repeating
short phrases
 Visceral - sensation of butterflies rising from epigastrium
 Hallucination- visual, olfactory ,auditory or gustatory
 Affective symptoms- fear, paranoia, depression, elation
 Memory disturbance
 Distorted perception
Cont..
 Absence or petit mal seizure - manifest as brief dissociative states,
often without muscle or postural change
- resume previous activity without postictal symptoms
- classic one occur on school age
- the attack can occur more than 100 within a day and affect school
performances
- usually resolve as a child mature
Cont..
 Generalized tonic-clonic seizure- most common types
Tonic phase- all muscle of the arm, legs, chest and back becomes
stiff. Patient become cyanotic during
this phase..20sec
Clonic phase- the muscle begin to jerk and twitch for additional
30sec-1min
Postictal phase- begin once twitching movement end
EPIDEMIOLOGY
 bimodal distribution among infant and > 75yrs old
 45% adult with 1st unprovoked seizure experience another within 2 years ,
most within 1 year
 Up to 50% of patients with epilepsy have recurrent seizure despite
initiation of therapy
 account for 1-2% of all emergency department visit
Etiology
- Withdrawal syndrome.....alcohol , antiepileptic , benzodiazepines
- Structural....stroke ,TBI , TB sclerosis
- Metabolic....hypoglycemia ,hyponatremia , uremia
- Intoxication....cefipime ,imipenem ,flouroquinolones ,isoniazide
TSA, chemotherapy
- Infectious....meningitis ,brain abscess, encephalitis ,
neurocysticercosis
Pathogenesis
Cont..
 typically seizure are self limited. This may be
- related to reflex inhibition
- loss of synchrony
- neuronal exhaustion
- alteration of local balance of NT in favor of inhibition
Clinical Feature
Is it a seizure?
-circumstance
-as general rule ,no single C/F or diagnostic modality is 100%
confirmatory for occurrence of neurologic seizures
-strong markers of seizure -post octal confusion
-tongue biting
-cyanosis
- confirmed unresponsiveness
-preceding dejavu or lamias vu
-head/eye turning to one side
-dystonic feature
Hx
 hx of trauma
 hx alcohol intoxication or abuse
 pregnancy
 fever or headache
 incidence of seizure with stroke-5-15%, epilepsy 4-9%
 non compliance with anticonvulsant
 hx of nonneurologic comorbid disease
P/E
 vital sign
 irregular heart rate
 pupillary rxn
 postictal confusion...failure to improved can be caused by
-NCSE -CNS infection
-metabolic encephalopathy -vascular event
-drug toxicity -migraine
-hypoglycemia
Cont..
 neurologic examination - GCS
-pupillary rxn
-neurologic deficit
 soft tissue and skeletal trauma - oral trauma
-tongue bite
-shoulder dislocation
DDX
 SYNCOPE- usually present with prodromal symptoms
- can be associated with injury,incontinence,or even breif
tonic clonic activity
- often has provocative cause, the LOC is brief and return
to full consciousness is prompt without a confusional
state
Pseudo seizure
o Psychogenic in origin associated with
 conversion disorders, malingering
 Brief psychosis, panic disorders
o Usually in response to emotion upset
o Often bizarre and highly variable
o Pt able to protect them selves
o Characteristic movements
 Side to side head thrashing, pelvic thrusting
Cont..
 Clonic alternating extremities movement
 Incontinence and injury are uncommon
 No postictal confusion
 Often stop seizure like activities on command
 Accurate diagnosis needs EEG and video monitoring
Cont..
 Movement disorders
 Dystonia, chorea &myoclonic jerks
 Tremor, tics
 Consciousness always preserved
 Movement temporary suppressed
Cont..
Hyperventilation syndrome
 Gradual onset of attacks with shortness of breath, anxiety &perioral
numbness.
 Post ictal symptoms are rare
 Asking the pt to hyperventilate will be reproduced.
INVESTIGATION
 RBS
 Metabolic panel...Na, Ca, Mg
 pregnancy test
 toxicology screen
 serum lactate and prolactin level
 serum anticonvulsant level....therapeutic level
Cont..
 Imaging...CT scan
...MRI
 Lumbar puncture...febrile,immunocompromised
possible SAH
 EEG...NCSE
...subtle SE
...ongoing SE despite TX
Empirical management
 Prehospital
 Prompt recognition of
 Hypoxia
 Hypotension
 Hypoglycemia
 Place in a lateral decubitus position
 Oral air way
 benzodiazepines
…
 Emergency treatment
 Place in monitoring bed
 Oral airway contraindication
 Administer O2
 Lorazepam iv,midazolam IM
 PHENYTOIN 20mg /Kg to max of 50 mg/min/
 Fosphenytoin 20 PE/Kg/max of 150/min/
 Valproic acid 20-40mg/Kg at 3-6mg/Kg/min
…
 If seizure continues
 Half loading phenytoin,fosphenytoin,valproic acid
 Levetiracetam iv bolus 1-3 gm./15 min
 At 20-60mg/kg
If seizure continues
 Rule out reversible causes
 Bleeding,drugoverdose
 Prepare for RSI &administer 3rd line therapy
…
 INH overdose cause refractory seizure to benzodiazepines
 Pyridoxine
 If Child bearing female is seizing
 Consider eclampsia which is mgso4 responsive.
 Children &psychiatric pts. at risk of water intoxication
 Hyponatremia requiring hypertonic saline
…
 Patient with Hx of seizure
-depends on the particular circumstance of of the case
-identify and correct potential precipitant that lower the thresholds
-medication nonadherance...serum anticonvulsant
-if they are adequate... no need of specific tx
-if anticonvulsant level not available- give the usual dose
-if precipitant cant found- change/adjust the dose
…
 Patient with 1st Unprovoked seizure
- as long as the patient returned to neurologic baseline , hospital
admission and initiation of anticonvulsant is not recommended
- predictors of seizure recurrence.. cause of the seizure
. result of EEG
-Ideal antiepileptic drug- single drug therapy with minimal toxicity
-drug selection based on seizure types
-precaution. Swimming, working with hazardous material/heights
driving license??
…
Seizure Initial choice Second line
Tonic clonic Phenytoin/
Valproate/carbamazepine
Lamotrigine/ carbamazepine
Myoclonic Valproate Lamotrigine
Partial Carbamazepine / Phenytoin Valproate/Lamotrigine/
Oxcarbazine
Absence valproate Ethosuximide/ Lamotrigine
unclassified Valproate Lamotrigine
convulsive status epileptics
DEFINITION - ≥ 5 min continuous seizure or
- ≥ 2 discrete seizure b/n w/c there is incomplete
recovery of consciousness
The ILAE published conceptual defn of SE that incorporates two operational dimensions, t1
& t 2
- SE is a condition resulting from either the failure of the
mechanism responsible for seizure termination or from the
initiation of mechm that leads to abnormally prolonged sz. t1
- SE is a condition that can have long term consequence depending
on the type and duration of sz. t2
…
 For GCSE..t1 5min and t2 30 min
 Focal SE with impaired conciousness..t1 10 min and t2 > 60 min
 Absence seizure..t1- 10-15min
..t2 no data available
…
 EPIDEMIOLOGY- incidence follows U shaped distribution, highest in
<1yr and > 60 yr
- over a lifetime up to 10% adult with epilepsy and 20% of children
with epilepsy have one/more episodes SE
 ETIOLOGY - in children febrile seizure is the most common causes
- in adult, acute symptomatic seizure the most common
followed by remote symptomatic and low anti epileptic
drug
1. GCSE - the most dramatic form of SE ,with potential for serious
complications, morbidity and mortality
-includes both 1 and 2ry generalized
-there is always impaired consciousness and bilateral tonic
stiffening, followed by rhythmic jerking of the limbs
…
2. Focal motor SE -many clinical feuture and largely depends on
epileptogenic brain area
-in almost all cases there is associated focal lesion
EPC(epileptia partialis continua)- a particular refractory focal motor SE
with a very prolonged & very regular jerking activity
- EPC remarkably persistent lasting days , wks,or
even decades
- often restricted to one part of the body and slower than
most other forms focal motor SE
…
3. Myoclonic SE(MSE) - is characterized by frequent myoclonic jerks
that can be rhythmic or arrhythmic
- are often generalized but some are focal
- causes divided into epilepsy syndrome related
and symptomatic causes
1. primary epilepsy syndrome -myoclonus is characteristic finding
2. secondary epilepsy syndrome
3. symptomatic MSE- anoxia, encephalopathy
→
EEG
- During GCSE , EEG often obscured by muscle & movt artifact but it may
show continuous spike & wave activity indicative of generalized sz activity
- Once convulsion ceased EEG is crucial in determining whether SE is truly
ended
- During focal motor SE , EEG can be subtle or absent- deeper seizure
- orientation
- intermittent
- In myoclonic SE ,EEG helps to differentiate types of MSE
…
 Complication
- hyperthermia
- pulmonary edema
- aspiration pneumonia
- cardiac arrhythmias
- rhabdomyolysis
- long term neurologic complication
Treatment
 Early recognition & treatment are critically important
 mortality dramatically increase with delayed diagnosis and initiation of
treatment
 the goal of treatment is to control as soon as possible & within 30 min of
presentation
Initial management divided into three phases
1. Rapid assessment and support- attention to ABC is urgent
- supportive therapy( eg O2& MV)
-at least two iv catheter
-cardiac monitor, bp , pulse
…
 NM blocking agent facilitate intubation but can abolish the motor
manifestation of seizure & thus mask ongoing SE
 If NM agent used EEG monitoring is mandatory
 midazolam and thiopental are preferred to facilitate rapid intubation
…
2. Initial pharmacology treatment
Benzodiazepines are first line treatment
lorazepam - 0.1mg/kg ,max rate 2mg/min, or 4mg fixed dose loading
- repeat the dose if pt still seizing after one min
- no definitive maximum dose
- even if seizure stops following benzodiazepine loading dose
of antiepileptic should follow
…
 diazepam- has high lipid solubility and can rapidly cross BBB
- 0.1-0.3mg/kg IV
- an effect can be seen 10-20 sec and CSF concentration
reach maximum within 03 min
- 50 -80% of initial termination of seizure but 50% chance of
recurrence within 02hr if no antiepileptic given
…
 when IV access not available
- IM midazolam is safe and effective
- 10mg IM,nasally or bucal >40kg..5mg for pt 13-40kg
- rectal diazepam - onset 2-10min
…
 Complication of benzodiazepine
- respiratory depression
- seizures
- withdrawal symptoms
- dependency and abuse
- hypotension
- bradycardia
…
 Fosphenytoin- water soluble converted into phenytoin in the plasma
- similar onset and effectiveness as phenytoin
- fewer infusion site rxn and CV effect due to lack of
propylene glycol and ethanol as solvent
- may be infused quickly and can also given IM
- loading 20PE/kg, infusion 150PE/min over 10-15 min
…
 Phenytoin - typically infused not faster than 25mg/min due to
myocardial depression
- shouldn’t be given IM and with glucose solution
- contraindicated on 2nd & 3rd degree block
- stop and restart with lower dose if side effect occur
- both phenytoin and fosphenytoin intensify seizure caused
by cocaine, theophyline...
…
 Valproate -available data suggest valproate is as effective as
phenytoin
- shouldn’t be administered along with phenytoin
- hepatic toxicity, hepatic encephalopathy, pancreatitis
- dose 20-40 mg/kg
. levitracetam - not yet FDA approved
. lacosmide
…
 Postictal recovery - most patient begin to recover within 20-30 min after
GCSE
- the two most important common reason for
postictal recovery are sedation & NC sz
- of 164 patients with GCSE EEG monitoring was done
postictal- 52% had no evidence of ongoing ictal
discharge- 13% mortality
- 14% had NCSE-51% mortality
- 34% non continuous rythimic discharge
32% mortality
…
3. secondary assessment
- Repeat full neurologic examination
- head CT,MRI
- lumbar puncture
Refractory SE
 IS defined as persistent seizure activity despite the IV administration of
adequate amount of two antiepileptic drugs
 usually exceed 60 min
 20-31% SE develop refractory SE
 single vs combination agents
…
 Propofol- can be started 2-10mg/kg/hr and titrated up to seizure
cessation
- has a short half life w/c allow quicker neurologic recovery
- propofol infusion syndrome
- if seizure are controlled with propofol ,effective effusion
should be maintained for 24 hr ,then tapper at dose of 5%
per hr
…
 Midazolam- water soluble
- initiated with 0.2mg bolus given at rate of 2mg/min
- additional bolus can be given every 05 min
- continuous infusion 0.1mg/kg/hr max 3mg/kg/hr
. Pentobarbital - initial dose 5mg/kg over 10 min
- infusion 1mg/kg/hr
. Ketamine - 3rd line agent
- dose bolus 0.5-4.5mg/kg or infusion 5mg/kg/hr
…
 Others - inhalational anesthetics eg isofuranane & desfuranane
- vagus stimulation
- surgical approach
- induced hypothermia
- ketogenic diet
- transcranial magnetic stimulation
Noncovulsive SE
 ILAE defines SE as a condition resulting either from failure the
mechanism responsible for seizure termination or from initiation
mechanism that leads to abnormally prolonged seizure
 the temporal threshold that define an abnormally prolonged seizure
depends on the type of seizure - convulsive- 05 min
- NCSE- 10min
…
 Electro clinical classification- NCSE is subdivided according to level of
consciousness & clinical & EEG features
1. NCSE without coma
A. Generalized NCSE - typical absence SE
- atypical absence SE
- myoclonic absence SE
B. Focal SE with/without impairment of SE
- aphasic SE
…
2. NCSE in coma - around 8-20% of comatose patient who have not had
any clinical seizure activity will have EEG finding
consistent with NCSE at the time of monitoring
- aftermath of CSE - 14%
…
 Etiology
- approximately 1/2-2/3 of pts. have a prior hex of seizure or epilepsy
- almost the same etiology with convulsive SE
- Drug induced NCSE on critical ill pts. & cancer pts. being treated with
multiagent chemotherapy should considered- beta lactam eg.cefipem
- New onset refractory SE( NORSE)- RSE for which no etiology
identified within 48hr
…
 C/F - impairment of consciousness ranges from mild confusion to coma
- other c/f divided into two general category
a. negative symptoms- aphasia, mutism, catatonia
b. positive symptoms- tonic eye deviation, lip smacking
trippus, nystagmoid eye jerking
- 3/4 of patients with NCSE have no discernable clinical correlation
& EEG monitoring for diagnosis
…
 DX
1 EEG - the diagnosis of NCSE requires EEG
- patient selection for EEG
. aftermath of GCSE
. critically ill who are obtunded or comatose
. duration of monitoring?
2 Acute IV ant seizure drug trial
3 Neuroimaging
…
 Treatment
- delay in dx & tx associated with higher mortality
- initial treatment benzodiazepines with non-coma inducing IV
ant seizure
- How aggressive should one treat?
1. subtle SE from generalized convulsive SE
2. NORSE
3. acute brain injury associated NCSE
References
 UpToDate 2018
 Tintinalis 9th Edition
 Rosen Emergency Medicine 9th Edition
 Adams and Victor Principles of Neurology 8th Edition
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seizure &status epilepticus.pptx

  • 1. Presenter Dr berihu assefa (EMCC R2) moderator Dr selam (EMCC R3) adviser Dr weldesenbet ( EMCC consultant)
  • 2. OUTLINE  DEFINITION  EPIDEMIOLOGY  PATHOPHSYSIOLOGY  CLINICAL FEUTURE  DIFFERETIAL DIAGNOSIS  CONVULSIVE STATUS EPILEPTICUS  NONCONVULSIVE STATUS EPILEPTICUS
  • 3. objectives  To be able to know definition of seizure,GCSE,NCSE  To understand epidiomology,clinical features of seizure &SE  To know basic pathophysiology of seizure  To identify major causes of provoked seizure  To understand the management principles
  • 4. DEFINITION SEIZURE- are excessive abnormal neuronal activity associated with alteration sensory , motor , autonomic dysfunction and/or cognitive function. CONVULSION- refers specifically to the motor manifestation of a seizure POSTICTAL PERIOD- an interval of altered mental status immediately following a seizure, generally lasting less than 1hr. EPILEPSY- refers to a condition of recurrent unprovoked seizures.
  • 5. Cont..  Acute symptomatic seizure-refers to  a seizure that occurs at the time of a systemic insult or in close temporal association with documented brain insult. -within 01 wk. of stroke ,TBI , anoxic encephalopathy or intracranial surgery -during active phase of CNS infection -within 24 hrs. of severe metabolic derangement -account up to 25-30% of 1st seizure and has low risk for future epilepsy
  • 6. …  Unprovoked seizures- seizure of unknown etiology as well as one that occurs in r/n to a preexisting brain lesion or progressive nervous system disorder . Status epileptics - ≥ 5 min continuous seizure or - ≥ 2 discrete seizure b/n w/c there is incomplete recovery of consciousness .
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  • 8. … FOCAL SEIZURE WITH RETAINED AWARENESS The symptoms vary from one patient to another and depends entirely on the part of the cortex that is disrupted occipital lobe - may result in flashing light motor cortex- jacksonian march parietal cortex-spatial perception frontal lobe - sudden speech difficulties temporal lobe- gustatory or olfactory hallucination
  • 9. … FOCAL SEIZURE WITH IMPAIRED AWARENESS - the most common types of seizure in adults with epilepsy - typically lasts less than 3 min and may begin with a preserved awareness -postictal phase- somnolence ,confusion and headache for up to several hrs. - symptom can be bizarre
  • 10. Cont..  Automatism - lip smacking , fiddling with cloth or button, repeating short phrases  Visceral - sensation of butterflies rising from epigastrium  Hallucination- visual, olfactory ,auditory or gustatory  Affective symptoms- fear, paranoia, depression, elation  Memory disturbance  Distorted perception
  • 11. Cont..  Absence or petit mal seizure - manifest as brief dissociative states, often without muscle or postural change - resume previous activity without postictal symptoms - classic one occur on school age - the attack can occur more than 100 within a day and affect school performances - usually resolve as a child mature
  • 12. Cont..  Generalized tonic-clonic seizure- most common types Tonic phase- all muscle of the arm, legs, chest and back becomes stiff. Patient become cyanotic during this phase..20sec Clonic phase- the muscle begin to jerk and twitch for additional 30sec-1min Postictal phase- begin once twitching movement end
  • 13. EPIDEMIOLOGY  bimodal distribution among infant and > 75yrs old  45% adult with 1st unprovoked seizure experience another within 2 years , most within 1 year  Up to 50% of patients with epilepsy have recurrent seizure despite initiation of therapy  account for 1-2% of all emergency department visit
  • 14. Etiology - Withdrawal syndrome.....alcohol , antiepileptic , benzodiazepines - Structural....stroke ,TBI , TB sclerosis - Metabolic....hypoglycemia ,hyponatremia , uremia - Intoxication....cefipime ,imipenem ,flouroquinolones ,isoniazide TSA, chemotherapy - Infectious....meningitis ,brain abscess, encephalitis , neurocysticercosis
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  • 18. Cont..  typically seizure are self limited. This may be - related to reflex inhibition - loss of synchrony - neuronal exhaustion - alteration of local balance of NT in favor of inhibition
  • 19. Clinical Feature Is it a seizure? -circumstance -as general rule ,no single C/F or diagnostic modality is 100% confirmatory for occurrence of neurologic seizures -strong markers of seizure -post octal confusion -tongue biting -cyanosis - confirmed unresponsiveness -preceding dejavu or lamias vu -head/eye turning to one side -dystonic feature
  • 20. Hx  hx of trauma  hx alcohol intoxication or abuse  pregnancy  fever or headache  incidence of seizure with stroke-5-15%, epilepsy 4-9%  non compliance with anticonvulsant  hx of nonneurologic comorbid disease
  • 21. P/E  vital sign  irregular heart rate  pupillary rxn  postictal confusion...failure to improved can be caused by -NCSE -CNS infection -metabolic encephalopathy -vascular event -drug toxicity -migraine -hypoglycemia
  • 22. Cont..  neurologic examination - GCS -pupillary rxn -neurologic deficit  soft tissue and skeletal trauma - oral trauma -tongue bite -shoulder dislocation
  • 23. DDX  SYNCOPE- usually present with prodromal symptoms - can be associated with injury,incontinence,or even breif tonic clonic activity - often has provocative cause, the LOC is brief and return to full consciousness is prompt without a confusional state
  • 24. Pseudo seizure o Psychogenic in origin associated with  conversion disorders, malingering  Brief psychosis, panic disorders o Usually in response to emotion upset o Often bizarre and highly variable o Pt able to protect them selves o Characteristic movements  Side to side head thrashing, pelvic thrusting
  • 25. Cont..  Clonic alternating extremities movement  Incontinence and injury are uncommon  No postictal confusion  Often stop seizure like activities on command  Accurate diagnosis needs EEG and video monitoring
  • 26. Cont..  Movement disorders  Dystonia, chorea &myoclonic jerks  Tremor, tics  Consciousness always preserved  Movement temporary suppressed
  • 27. Cont.. Hyperventilation syndrome  Gradual onset of attacks with shortness of breath, anxiety &perioral numbness.  Post ictal symptoms are rare  Asking the pt to hyperventilate will be reproduced.
  • 28. INVESTIGATION  RBS  Metabolic panel...Na, Ca, Mg  pregnancy test  toxicology screen  serum lactate and prolactin level  serum anticonvulsant level....therapeutic level
  • 29. Cont..  Imaging...CT scan ...MRI  Lumbar puncture...febrile,immunocompromised possible SAH  EEG...NCSE ...subtle SE ...ongoing SE despite TX
  • 30. Empirical management  Prehospital  Prompt recognition of  Hypoxia  Hypotension  Hypoglycemia  Place in a lateral decubitus position  Oral air way  benzodiazepines
  • 31. …  Emergency treatment  Place in monitoring bed  Oral airway contraindication  Administer O2  Lorazepam iv,midazolam IM  PHENYTOIN 20mg /Kg to max of 50 mg/min/  Fosphenytoin 20 PE/Kg/max of 150/min/  Valproic acid 20-40mg/Kg at 3-6mg/Kg/min
  • 32. …  If seizure continues  Half loading phenytoin,fosphenytoin,valproic acid  Levetiracetam iv bolus 1-3 gm./15 min  At 20-60mg/kg If seizure continues  Rule out reversible causes  Bleeding,drugoverdose  Prepare for RSI &administer 3rd line therapy
  • 33. …  INH overdose cause refractory seizure to benzodiazepines  Pyridoxine  If Child bearing female is seizing  Consider eclampsia which is mgso4 responsive.  Children &psychiatric pts. at risk of water intoxication  Hyponatremia requiring hypertonic saline
  • 34. …  Patient with Hx of seizure -depends on the particular circumstance of of the case -identify and correct potential precipitant that lower the thresholds -medication nonadherance...serum anticonvulsant -if they are adequate... no need of specific tx -if anticonvulsant level not available- give the usual dose -if precipitant cant found- change/adjust the dose
  • 35. …  Patient with 1st Unprovoked seizure - as long as the patient returned to neurologic baseline , hospital admission and initiation of anticonvulsant is not recommended - predictors of seizure recurrence.. cause of the seizure . result of EEG -Ideal antiepileptic drug- single drug therapy with minimal toxicity -drug selection based on seizure types -precaution. Swimming, working with hazardous material/heights driving license??
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  • 40. … Seizure Initial choice Second line Tonic clonic Phenytoin/ Valproate/carbamazepine Lamotrigine/ carbamazepine Myoclonic Valproate Lamotrigine Partial Carbamazepine / Phenytoin Valproate/Lamotrigine/ Oxcarbazine Absence valproate Ethosuximide/ Lamotrigine unclassified Valproate Lamotrigine
  • 41. convulsive status epileptics DEFINITION - ≥ 5 min continuous seizure or - ≥ 2 discrete seizure b/n w/c there is incomplete recovery of consciousness The ILAE published conceptual defn of SE that incorporates two operational dimensions, t1 & t 2 - SE is a condition resulting from either the failure of the mechanism responsible for seizure termination or from the initiation of mechm that leads to abnormally prolonged sz. t1 - SE is a condition that can have long term consequence depending on the type and duration of sz. t2
  • 42. …  For GCSE..t1 5min and t2 30 min  Focal SE with impaired conciousness..t1 10 min and t2 > 60 min  Absence seizure..t1- 10-15min ..t2 no data available
  • 43. …  EPIDEMIOLOGY- incidence follows U shaped distribution, highest in <1yr and > 60 yr - over a lifetime up to 10% adult with epilepsy and 20% of children with epilepsy have one/more episodes SE  ETIOLOGY - in children febrile seizure is the most common causes - in adult, acute symptomatic seizure the most common followed by remote symptomatic and low anti epileptic drug
  • 44.
  • 45. 1. GCSE - the most dramatic form of SE ,with potential for serious complications, morbidity and mortality -includes both 1 and 2ry generalized -there is always impaired consciousness and bilateral tonic stiffening, followed by rhythmic jerking of the limbs
  • 46. … 2. Focal motor SE -many clinical feuture and largely depends on epileptogenic brain area -in almost all cases there is associated focal lesion EPC(epileptia partialis continua)- a particular refractory focal motor SE with a very prolonged & very regular jerking activity - EPC remarkably persistent lasting days , wks,or even decades - often restricted to one part of the body and slower than most other forms focal motor SE
  • 47. … 3. Myoclonic SE(MSE) - is characterized by frequent myoclonic jerks that can be rhythmic or arrhythmic - are often generalized but some are focal - causes divided into epilepsy syndrome related and symptomatic causes 1. primary epilepsy syndrome -myoclonus is characteristic finding 2. secondary epilepsy syndrome 3. symptomatic MSE- anoxia, encephalopathy →
  • 48. EEG - During GCSE , EEG often obscured by muscle & movt artifact but it may show continuous spike & wave activity indicative of generalized sz activity - Once convulsion ceased EEG is crucial in determining whether SE is truly ended - During focal motor SE , EEG can be subtle or absent- deeper seizure - orientation - intermittent - In myoclonic SE ,EEG helps to differentiate types of MSE
  • 49. …  Complication - hyperthermia - pulmonary edema - aspiration pneumonia - cardiac arrhythmias - rhabdomyolysis - long term neurologic complication
  • 50. Treatment  Early recognition & treatment are critically important  mortality dramatically increase with delayed diagnosis and initiation of treatment  the goal of treatment is to control as soon as possible & within 30 min of presentation Initial management divided into three phases 1. Rapid assessment and support- attention to ABC is urgent - supportive therapy( eg O2& MV) -at least two iv catheter -cardiac monitor, bp , pulse
  • 51. …  NM blocking agent facilitate intubation but can abolish the motor manifestation of seizure & thus mask ongoing SE  If NM agent used EEG monitoring is mandatory  midazolam and thiopental are preferred to facilitate rapid intubation
  • 52. … 2. Initial pharmacology treatment Benzodiazepines are first line treatment lorazepam - 0.1mg/kg ,max rate 2mg/min, or 4mg fixed dose loading - repeat the dose if pt still seizing after one min - no definitive maximum dose - even if seizure stops following benzodiazepine loading dose of antiepileptic should follow
  • 53. …  diazepam- has high lipid solubility and can rapidly cross BBB - 0.1-0.3mg/kg IV - an effect can be seen 10-20 sec and CSF concentration reach maximum within 03 min - 50 -80% of initial termination of seizure but 50% chance of recurrence within 02hr if no antiepileptic given
  • 54. …  when IV access not available - IM midazolam is safe and effective - 10mg IM,nasally or bucal >40kg..5mg for pt 13-40kg - rectal diazepam - onset 2-10min
  • 55. …  Complication of benzodiazepine - respiratory depression - seizures - withdrawal symptoms - dependency and abuse - hypotension - bradycardia
  • 56. …  Fosphenytoin- water soluble converted into phenytoin in the plasma - similar onset and effectiveness as phenytoin - fewer infusion site rxn and CV effect due to lack of propylene glycol and ethanol as solvent - may be infused quickly and can also given IM - loading 20PE/kg, infusion 150PE/min over 10-15 min
  • 57. …  Phenytoin - typically infused not faster than 25mg/min due to myocardial depression - shouldn’t be given IM and with glucose solution - contraindicated on 2nd & 3rd degree block - stop and restart with lower dose if side effect occur - both phenytoin and fosphenytoin intensify seizure caused by cocaine, theophyline...
  • 58. …  Valproate -available data suggest valproate is as effective as phenytoin - shouldn’t be administered along with phenytoin - hepatic toxicity, hepatic encephalopathy, pancreatitis - dose 20-40 mg/kg . levitracetam - not yet FDA approved . lacosmide
  • 59. …  Postictal recovery - most patient begin to recover within 20-30 min after GCSE - the two most important common reason for postictal recovery are sedation & NC sz - of 164 patients with GCSE EEG monitoring was done postictal- 52% had no evidence of ongoing ictal discharge- 13% mortality - 14% had NCSE-51% mortality - 34% non continuous rythimic discharge 32% mortality
  • 60. … 3. secondary assessment - Repeat full neurologic examination - head CT,MRI - lumbar puncture
  • 61. Refractory SE  IS defined as persistent seizure activity despite the IV administration of adequate amount of two antiepileptic drugs  usually exceed 60 min  20-31% SE develop refractory SE  single vs combination agents
  • 62. …  Propofol- can be started 2-10mg/kg/hr and titrated up to seizure cessation - has a short half life w/c allow quicker neurologic recovery - propofol infusion syndrome - if seizure are controlled with propofol ,effective effusion should be maintained for 24 hr ,then tapper at dose of 5% per hr
  • 63. …  Midazolam- water soluble - initiated with 0.2mg bolus given at rate of 2mg/min - additional bolus can be given every 05 min - continuous infusion 0.1mg/kg/hr max 3mg/kg/hr . Pentobarbital - initial dose 5mg/kg over 10 min - infusion 1mg/kg/hr . Ketamine - 3rd line agent - dose bolus 0.5-4.5mg/kg or infusion 5mg/kg/hr
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  • 65. …  Others - inhalational anesthetics eg isofuranane & desfuranane - vagus stimulation - surgical approach - induced hypothermia - ketogenic diet - transcranial magnetic stimulation
  • 66. Noncovulsive SE  ILAE defines SE as a condition resulting either from failure the mechanism responsible for seizure termination or from initiation mechanism that leads to abnormally prolonged seizure  the temporal threshold that define an abnormally prolonged seizure depends on the type of seizure - convulsive- 05 min - NCSE- 10min
  • 67. …  Electro clinical classification- NCSE is subdivided according to level of consciousness & clinical & EEG features 1. NCSE without coma A. Generalized NCSE - typical absence SE - atypical absence SE - myoclonic absence SE B. Focal SE with/without impairment of SE - aphasic SE
  • 68. … 2. NCSE in coma - around 8-20% of comatose patient who have not had any clinical seizure activity will have EEG finding consistent with NCSE at the time of monitoring - aftermath of CSE - 14%
  • 69. …  Etiology - approximately 1/2-2/3 of pts. have a prior hex of seizure or epilepsy - almost the same etiology with convulsive SE - Drug induced NCSE on critical ill pts. & cancer pts. being treated with multiagent chemotherapy should considered- beta lactam eg.cefipem - New onset refractory SE( NORSE)- RSE for which no etiology identified within 48hr
  • 70. …  C/F - impairment of consciousness ranges from mild confusion to coma - other c/f divided into two general category a. negative symptoms- aphasia, mutism, catatonia b. positive symptoms- tonic eye deviation, lip smacking trippus, nystagmoid eye jerking - 3/4 of patients with NCSE have no discernable clinical correlation & EEG monitoring for diagnosis
  • 71. …  DX 1 EEG - the diagnosis of NCSE requires EEG - patient selection for EEG . aftermath of GCSE . critically ill who are obtunded or comatose . duration of monitoring? 2 Acute IV ant seizure drug trial 3 Neuroimaging
  • 72. …  Treatment - delay in dx & tx associated with higher mortality - initial treatment benzodiazepines with non-coma inducing IV ant seizure - How aggressive should one treat? 1. subtle SE from generalized convulsive SE 2. NORSE 3. acute brain injury associated NCSE
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  • 74. References  UpToDate 2018  Tintinalis 9th Edition  Rosen Emergency Medicine 9th Edition  Adams and Victor Principles of Neurology 8th Edition