2. WHAT IS EPILEPSY?
Epilepsy is a chronic neurological condition
characterized by recurrent, unprovoked
seizures, occurrence of at least 2 unprovoked
seizures 24 hours apart.
Epileptic seizure → clinical manifestation of
abnormal & excessive discharge of a set of neurons
in the brain
4. Seizures: Pathophysiology:
Sustained partial depolarisation in a group of
neurons -->excitability --> sudden
depolarisation in response to stimuli --
>conduction to surrounding cells, distant
synaptically connected cells & subcortical
neurons -->dissemination -->loss of
consciousness
11. Focal seizure-affect part of the brain
Aware:
Alert, involuntary movement, odd taste/smell,
fear/happiness, sweating/goose bumps
Impaired awareness:
Aura, unconscious, lip smacking, meaningless
movements, picking at clothing, wandering
around, repeating words
12.
13. SPECIAL EPILEPSY SYNDROME
1.INFANTILE SPASM:-
-Most cases appears in 1st yr of life.
- Single brief recurrent gross flexion movements of
the limb …rarely extension movements
-EEG shows multifocal,multiple small spikes.
-On maturity it disappears(4 to 5yr)
-CT & MRI mostly normal.
-Later progress to LENOX GASTAUT SYND.
14. HISTORY TAKING
HOPI:-
Two unprovoked seizures >24 hr apart suggest the presence of an
epileptic disorder
Any aura?change in the behaviour?
Types of seizures
-tonic clonic(tensing,then shaking,LOC)
-atonic(drop attack)
-absence(jus staring,not responding,blinking)
-partial(maybe consciouss,only ½ limbs shaking/jerking
How long did it last?frequency?time of day?precipatating factor?
Any loss of consciousness?tongue bitting?
What did you do for the child?(appropriate first aid measures)
Post ictal:drowsy?sleeping?vomiting?
17. The clinical diagnosis is more important then any tool…
(H/O, Eye witnesses, substantiated by video if available)
# EEG:-
EEG is most sensitive tool for diagnosis which shows
electrical activity changes in the brain but it also require
clinical correlation
Many children with epilepsy may have normal EEG and
many children who will never have epilepsy have EEG
abnormalities
Done for dx, classification, selection of anti-epileptic drugs
and prognosis
DIAGNOSIS
19. Management of Seizures
Initial assessment
Airway
Breathing
Circulation
Call for help
Hospitalist
Neuro
PICU/RRT
Ask for more history
How long has the
patient been seizing?
New-onset vs. known
seizure disorder
Baseline seizure
frequency, is this
typical or not?
Events leading up to
this episode
Meds/triggers
History of status
20. Management of Seizures
Consider rapid work-up for underlying
etiologies
CNS infection
Acute HIE
Metabolic disease
Electrolyte imbalance
TBI
Drugs, intoxications, poisonings
Cerebrovascular event
21. Seizures - Management
I Management of acute attack:
Calm down
Head down lateral position
Prevent hurt
If does'nt stop convulsing in 3-5 min,
Inj Diazepam 0.3 mg/kg slow iv bolus
Maybe repeated after 20 min
Effect lasts 0.5-3 hrs
SE- hypotension, respiratory depression,
secretions
or
Rectal diazepam 0.5 mg/kg dose/ nasal midzolam 0.2
mg/kg/dose
22. PRINCIPLES OF ANTICONVULSANT THERAPY
Treatment recommended if ≥ 2 episodes→ recurrence
risk 80%
Attempt to classify the seizure type & epileptic syndrome
Monotherapy as far as possible → most appropriate drug
→ increase dose gradually till epilepsy controlled,
maximum dose reached / side effects occur
Alternative monotherapy (Add on the 2nd drug if 1st drug
failed. Optimise 2 nd drug, then try to withdraw 1st drug.
Rational combination therapy (usually 2 or maximum 3
drugs )
Combines drugs with different mechanism of action &
consider their spectrum of efficacy, drug interactions &
adverse affects
23. Monitor drug levels (carbamazepine, phenytoin,
phenobarbitone) to check compliance → if seizures not
well controlled/in situations of polypharmacy where drug
interaction is suspected.
When withdrawal of medication is planned → seizure
free for 2 years, consideration should be given to
epilepsy syndrome, likely prognosis & individual
circumstances before attempting slow withdrawal of
medication over 3-6 months (longer if clonazepam/
phenobarbitone)
If seizures recur → last dose reduction is reversed &
medical advice sought
32. Newer AEDs/ Other modalities
Topiramate:
Ind: Partial, generalised, drop attacks, LG syndrome
SE: ?cognitive impairment
Vigabatrine:
Ind: Partial, infantile spasms
Dose: 40-80 mg/kg/d
SE: Drowsiness, agitation, confusion
Oxcarbazepine:
Derivative of carbamazepine
Ketogenic diet
Surgery
33. Seizures: Status epilepticus:
Prolonged seizure for >20 min or repeated
seizures without regaining consciousness
Persistent seizure activity hypoxia,
hypoglycemia, hyperthermia, cerebral
edema & vasomotor instability
Life threatening
Risk of permanent brain damage
Medical emergency
34. Mx of Status epilepticus
ICU, monitoring
IV dextrose drip
Oxygen
IV Inj Diazepam 0.3 mg/kg or Lorazepam 0.1 mg/kg (longer action)
or Midzolam (lesser respiratory depression)
Inj phenytoin 15-20 mg/kg iv at a rate of <1mk/kg/min
Inj Phenobarbitone 20 mg/kg iv at a rate of 1 mg/kg/min or
IV Valproate 20 mg/kg as infusion in 50 ml NS over 30 min
Ventilatory support + diazepam/midzolam infusion
`` Thiopental infusion
35. INTRACTABLE EPILEPSY?
Re- evaluate the following possibilities
Is it a seizure /non epileptic event
Anticonvulsant dose not optimized
Poor compliance to anticonvulsant
Wrong classification of epilepsy syndrome → wrong
anticonvulsant
Anticonvulsant aggravating seizures
Lesional epilepsy, hence a potential epilepsy surgery
candidate
Progressive epilepsy or neurodegenerative disorder
36. Non-medication therapies
Vagus Nerve Stimulator (VNS)-prevents
seizures by sending regular, mild pulses of
electrical energy to the brain via the vagus
nerve
Deep Brain Stimulation (DBS)-electrodes placed
in target areas in the brain provide brain
stimulation to help stop the spread of seizures
Ketogenic Diet- 3-4 gms of fat for every 1 gm
carb and protein
37. Seizure Triggers
Missed dose of medication
Sleep deprivation
Illness
Stress, anxiety, overstimulation
Hormonal changes
Alcohol and drugs of abuse
Hyperventilation
Flashing lights
Temperature extremes
dehydration
38. Seizure Remission
The International League Against Epilepsy
(ILAE) has proposed to expand the
definition of remission to 10 years seizure-
free with the last 5 years off antiepileptic
drugs (AEDs).
39. ADVICE FOR PATIENTS
Educate and counsel on epilepsy.
Emphasize compliance if on anticonvulsant.
Don’t stop the medication by themselves.this may
precipitate breakthrough seizures.
In photosensitive seizures-watch tv in brightly lit
room.avoid sleep deprivation.
Use a shower with bathroom door unlocked
No cycling in traffic,climbing sports or swimming
alone.
Know emergency treatment for seizure
Inform teachers and school abt the condition.
40. Caleb is a 3 month old male who presents to your clinic with his
parents. They state over the past couple of weeks Caleb has been
having “weird movements”. Upon further questioning they report
that the movements consist of flexion of his trunk and extension of
his extremities in clusters particularly upon early morning
wakening.
A: Reassure them that babies sometimes have strange
movements
B: Refer them immediately to neurology for workup
including an EEG and to consider ACTH or high dose
steroids
C: Start them on Keppra and give them Diastat for
emergencies
Case Study 1
41. Brady is a 7 yo male who was brought into your clinic for evaluation
of inattention. His parents state he will often stop and stare for
about 30 seconds as if he is day dreaming. It occurs multiple times
a day and his teacher is reporting he is not listening in class and
his grades are dropping.
A: put him on Adderall for ADHD
B: tell him they need to discipline him better
C: Refer him to neurology for an EEG and to consider
treatment with Ethosuximide
Case Study 2
Describe the episode
What happened? Was there focality? What was moving and how was it moving? Were there other symptoms? Color? How long did the episode last?
Setting in which the seizure occurs
Nocturnal? Medications? Illness/fever?
What happened before the event?
Precipitants? Headache, anorexia, nausea, vomiting, breath-holding? Certain activities? Aura?
What happened after the event?
Immediate recovery? Confusion/somnolence? How long did this last? Ability to speak/follow commands? Not moving limbs?
Other important tidbits –
Has the patient had these episodes before?
What has been done to evaluate/treat these episodes? How many? How often? Has the patient ever been in status epilepticus?
Normal development? Social stressors? Previous history of neurological illness (infection, HIE, trauma)? Drug use? (especially in adolescents)
FAMILY HISTORY!!!!!
Seizure, developmental delay , genetic/metabolic problems, consanguinuity