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Seizures
Prof.Dr.P.Soundararajan
seizure is a transient occurrence of signs and symptoms
resulting from abnormal excessive or synchronous
neuronal activity in the brain.
Febrile seizure; definition
• Between 6m to 60months
• Fever >38oc
• no CNS infection, no metabolic
imbalance
• No prior febrile seizure
SFS
• GTC
• <15mts
• No >1 episode <24hrs
• No postictal complications
CFS
• Focal
• >1 episode in 24hrs
• >15mts
• Post ictal abnormality
• 2-5% incident
• SFS; No risk of complications
• CFS; 2 fold increase in morbidity
Cause
• Autosomal dominant
• Many genes,
• sodium channel genes
• generalized epilepsy with febrile
seizures plus (GEFS+)
• severe myoclonic epilepsy of infancy
Recurrence
• <1yr age
• <24hr of fever
• Family h/o febrile fit or epilepsy
• CFS
• Male
• Low serum sodium
RISK FACTOR RISK FOR SUBSEQUENT EPILEPSY
Simple febrile seizure 1%
Neurodevelopmental abnormalities 33%
Focal complex febrile seizure 29%
Family history of epilepsy 18%
Fever <1 hr before febrile seizure 11%
Complex febrile seizure, any type 6%
Recurrent febrile seizures 4%
Workup
• Thorough history & examination
• LP [assess sensorium]
• Prior antibiotics?
EEG
• Normal CNS; no need
• Doesn’t predict epilepsy
• Spikes seen during drowsy
• To do >2 weeks
• To know type of epilepsy
• 30mts wakefulness & sleep
• Serum glucose
• CT or MRI
– Status epilepticus [hippocampal atrophy]
Management
• Counsel parent
• Antipyretics
• SFS; no drugs
• CFS; Diazepam, lorazepam, midazolam
• Rectal diazepam
• Intranasal midazolam
• Intermittent prophylaxis
– Diazepam, phenobarbitone, clobazam
• Iron deficiency?
Status epilepticus
• continuous seizure activity or recurrent
seizure activity without regaining of
consciousness lasting for >30 min.
• impending status epilepticus ; seizures
between 5 and 30 min.
• Nonconvulsive status epilepticus
• Refractory status epilepticus
Causes
• 30% 1st episode SFS
• CNS infection
• Trauma
• CVA
• Metabolic imbalance
• Poisoning
• Imbalance between excitation & inhibition
• Increased excitability [glutamate, aspartate]
• Decreased GABA mediated inhibition
• Inadequate O2 supply
• Hypoxia
• Cerebral edema
• Ca influx into neurons
• Neuronal death
Management
• A B C
• Detect underlying etiology
• Electrolytes, BUN, glucose
• CSF study
• EEG
• Imaging
Drugs
• IV lorazepam
• midazolam
• Fosphenytoin
• Phenobarbitone
• Valproate
• propofol, thiopentol
• Isoflorane
• Induced acidosis.
SE Protocol - 0 - 10 min
• Verify and describe seizure
• Airway - Positioning & suctioning
• O2 through mask, Attach pulse oxymeter
• NGT, BMV if needed
• Start IV / IO - IV lorazepam 0.1 mg / kg (1st dose)
• If no IV / IO, Midazolam IM 0.15 mg / kg
• Monitor HR, RR, perfusion, BP, SaO2
SE Protocol - 10 - 20 min
• Check Glucose - Dextrostix, IV dextrose
• Lab investigations
• IV lorazepam 0.1mg / kg (2nd dose)
• Monitor HR, RR, Perfusion, BP, SaO2
• BM ventilation if needed
• IV Phenytoin 20 mg / kg over 20 min. (1st dose)
• Fever reduction
SE Protocol - 40 - 50 min
• BM ventilation
• IV Phenytoin 10 mg / kg (2nd dose)
• If seizure still persists, IV Phenobarbitone
20mg / kg over 10 min.
• Intubate prior to Phenobarbitone
• Manage ICT
• Consider IV Pyridoxine if > 3 yrs old
SE Protocol - 60 min.
Refractory Status Epilepticus
• Admit in PICU
• Involve Anesthetist / PICU team
• Support circulation
• Correct metabolic problems (Hypoglycemia,
Hypocalcemia, Hypomagnesemia)
• IV Midazolam infusion, Pentothal, IV Sodium
valproate
• IV Midazolam 0.15 mg / kg stat. dose
Maintenance - 1 mcg / kg / min.
• Raise / 1 mcg / kg / min. every 15 min. if seizure
persists. Maximum 20 mcg / kg / min.
• Higher the dose, need for ventilation
• After control, same rate of infusion for 24 hours then
taper by 1 mcg every 2 hours
Approach to seizure
• Assess CVS, RS status
• Metabolic screen
• Head examination
• Eye ex
• NCM
• HSM
• FND
• EEG, imaging
Thank you

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Febrile seizures

  • 2. seizure is a transient occurrence of signs and symptoms resulting from abnormal excessive or synchronous neuronal activity in the brain.
  • 3. Febrile seizure; definition • Between 6m to 60months • Fever >38oc • no CNS infection, no metabolic imbalance • No prior febrile seizure
  • 4. SFS • GTC • <15mts • No >1 episode <24hrs • No postictal complications
  • 5. CFS • Focal • >1 episode in 24hrs • >15mts • Post ictal abnormality
  • 6. • 2-5% incident • SFS; No risk of complications • CFS; 2 fold increase in morbidity
  • 7. Cause • Autosomal dominant • Many genes, • sodium channel genes • generalized epilepsy with febrile seizures plus (GEFS+) • severe myoclonic epilepsy of infancy
  • 8. Recurrence • <1yr age • <24hr of fever • Family h/o febrile fit or epilepsy • CFS • Male • Low serum sodium
  • 9. RISK FACTOR RISK FOR SUBSEQUENT EPILEPSY Simple febrile seizure 1% Neurodevelopmental abnormalities 33% Focal complex febrile seizure 29% Family history of epilepsy 18% Fever <1 hr before febrile seizure 11% Complex febrile seizure, any type 6% Recurrent febrile seizures 4%
  • 10. Workup • Thorough history & examination • LP [assess sensorium] • Prior antibiotics?
  • 11. EEG • Normal CNS; no need • Doesn’t predict epilepsy • Spikes seen during drowsy • To do >2 weeks • To know type of epilepsy • 30mts wakefulness & sleep
  • 12. • Serum glucose • CT or MRI – Status epilepticus [hippocampal atrophy]
  • 13. Management • Counsel parent • Antipyretics • SFS; no drugs • CFS; Diazepam, lorazepam, midazolam • Rectal diazepam • Intranasal midazolam • Intermittent prophylaxis – Diazepam, phenobarbitone, clobazam • Iron deficiency?
  • 14. Status epilepticus • continuous seizure activity or recurrent seizure activity without regaining of consciousness lasting for >30 min. • impending status epilepticus ; seizures between 5 and 30 min. • Nonconvulsive status epilepticus • Refractory status epilepticus
  • 15. Causes • 30% 1st episode SFS • CNS infection • Trauma • CVA • Metabolic imbalance • Poisoning
  • 16. • Imbalance between excitation & inhibition • Increased excitability [glutamate, aspartate] • Decreased GABA mediated inhibition • Inadequate O2 supply • Hypoxia • Cerebral edema • Ca influx into neurons • Neuronal death
  • 17. Management • A B C • Detect underlying etiology • Electrolytes, BUN, glucose • CSF study • EEG • Imaging
  • 18. Drugs • IV lorazepam • midazolam • Fosphenytoin • Phenobarbitone • Valproate • propofol, thiopentol • Isoflorane • Induced acidosis.
  • 19. SE Protocol - 0 - 10 min • Verify and describe seizure • Airway - Positioning & suctioning • O2 through mask, Attach pulse oxymeter • NGT, BMV if needed • Start IV / IO - IV lorazepam 0.1 mg / kg (1st dose) • If no IV / IO, Midazolam IM 0.15 mg / kg • Monitor HR, RR, perfusion, BP, SaO2
  • 20. SE Protocol - 10 - 20 min • Check Glucose - Dextrostix, IV dextrose • Lab investigations • IV lorazepam 0.1mg / kg (2nd dose) • Monitor HR, RR, Perfusion, BP, SaO2 • BM ventilation if needed • IV Phenytoin 20 mg / kg over 20 min. (1st dose) • Fever reduction
  • 21. SE Protocol - 40 - 50 min • BM ventilation • IV Phenytoin 10 mg / kg (2nd dose) • If seizure still persists, IV Phenobarbitone 20mg / kg over 10 min. • Intubate prior to Phenobarbitone • Manage ICT • Consider IV Pyridoxine if > 3 yrs old
  • 22. SE Protocol - 60 min. Refractory Status Epilepticus • Admit in PICU • Involve Anesthetist / PICU team • Support circulation • Correct metabolic problems (Hypoglycemia, Hypocalcemia, Hypomagnesemia) • IV Midazolam infusion, Pentothal, IV Sodium valproate
  • 23. • IV Midazolam 0.15 mg / kg stat. dose Maintenance - 1 mcg / kg / min. • Raise / 1 mcg / kg / min. every 15 min. if seizure persists. Maximum 20 mcg / kg / min. • Higher the dose, need for ventilation • After control, same rate of infusion for 24 hours then taper by 1 mcg every 2 hours
  • 24. Approach to seizure • Assess CVS, RS status • Metabolic screen • Head examination • Eye ex • NCM • HSM • FND • EEG, imaging
  • 25.