EVALUATION & MANAGEMENT
OF EPILEPSY
DR SUDHIR KUMAR
MD (MEDICINE), DM (NEUROLOGY)
SENIOR CONSULTANT NEUROLOGIST
APOLLO HEALTH CITY, HYDERABAD
What is epilepsy?
• Occurrence of 2 or more seizures, at least 24
hours apart, is called epilepsy (=seizure
disorder or fits)
• Convulsions: tonic and/or clonic movements,
as part of seizures
• Seizure: an episode of epileptic attack
• Seizures occur due to abnormal electrical
discharges in the brain.
DEFINITIONS
• Idiopathic epilepsy- presumed to be of genetic
origin
• Cryptogenic epilepsy- epilepsy of unknown
cause
• Acute symptomatic seizure- occurs due to a
known acute cause, such as metabolic/toxic
insult, CNS infection, stroke, head injury, drug
toxicity, alcohol or medication withdrawal
• Remote symptomatic seizure- > 1 week after
the occurrence of underlying disorder
SEIZURE MIMICS
• Syncope
• Transient ischemic attack (TIA)
• Non-epileptic attack disorder (=psychogenic
seizures)
SYNCOPE vs SEIZURE
• Syncope occurs in specific circumstances such as
pain, extreme emotions, cough, micturition, hot
environment, prolonged standing, exercise, etc
• Pre-syncopal symptoms such as dizziness,
lightheadedness and h/o cardiovascular disease also
favor syncope
• Factors favoring seizures include tongue biting, head
turning, posturing, urinary incontinence, cyanosis,
prodromal deja-vu, and postictal confusion.
PSYCHOGENIC SEIZURES (NEAD)
• Common in younger people, women>men
• Should be considered only in patients with
recurrent seizures, and not the first episode
• Patients may have tongue bites (on tip of
tongue as compared to sides in true seizures),
and urinary incontinence; but they avoid self-
injury during episodes.
FIRST EPISODE OF SEIZURE
• Work-up for underlying causes
• Metabolic profile (electrolytes, calcium, glucose, etc)
• Toxicity/drug overdosage screening (in suspected
cases)
• ABG- if hypoxia suspected
• Brain imaging
• EEG
• CSF analysis (in selected cases)
TREATMENT OF FIRST SEIZURE
• Treatment of the underlying cause
• Correction of metabolic derangements is
sufficient in cases of acute symptomatic
seizures and long-term AEDs are not required.
• Risk of seizure recurrence after a single
seizure is 51%
• Anti-epileptic drug therapy is required in cases
with higher risk of recurrence
RISK FACTORS FOR RECURRENT SEIZURES
• Age <16
• Seizures occurring between 12 MN and 9 AM
• Remote symptomatic seizures
• Family history of epilepsy
• Status epilepticus or multiple seizures in 24 hours
• Todd’s paresis
• Abnormal neurological examination
• Abnormalities on CT or MRI scan
• Epileptiform discharges on EEG
WHEN TO START AED THERAPY?
• Occurrence of 2 or more seizures,
After first episode if:
• Positive family history of epilepsy,
• Abnormal neurological exam,
• Abnormal CT/MRI findings
• Epileptiform discharges on EEG
TYPES OF EPILEPSY
• Partial (or focal)- simple or complex partial
• Generalized
• Partial onset with secondary generalization
Subtypes of Generalized epilepsy
• Absence (or petit mal)
• Grand mal (or GTCS)
• Atonic
• Myoclonic
ANTIEPILEPTIC DRUGS
• Conventional- Phenobarbitone (PB),
phenytoin (PHT), carbamazepine (CBZ),
valproate (VPT)
• Newer AEDs- oxcarbazepine (OXC),
lamotrigine (LTG), topiramate (TPM),
levetiracetam (LEV), clobazam, zonisamide,
lacosamide, etc.
WHICH DRUG TO CHOOSE?
Depends on:
1. Type of epilepsy,
2. Age & sex of patient,
3. Presence of co-morbid conditions,
4. Need for IV formulation,
5. Tolerability,
6. Affordability.
DRUGS OF CHOICE
• Partial epilepsy- CBZ, OXC; alternative: VPT,
LEV
• Generalized epilepsy- VPT; alternatives- PB,
PHT, LEV
• Absence- VPT
• Myoclonic- VPT; alternatives- clonazepam, LEV
• Mixed seizure types- VPT
HOW TO START AEDs?
• Choose monotherapy
• Start the lowest therapeutic dose (based on body
weight),
• Gradually increase the dose based on efficacy and
tolerability,
• Watch for any adverse events,
• 2nd
AED can be added if seizure occurs despite being
on the maximum tolerable dose of single drug
• Adding 3rd
or 4th
AED usually does not help.
HOW LONG TO CONTINUE AEDs?
• At least 3 seizure-free years.
• Attempt withdrawal at least once.
• There is a group of patients, where seizures recur
after or during withdrawal of AEDs.
• They need lifelong AEDs.
• Patients with structural brain lesions (such as
gliosis/scar/tumor/old infarcts/mesial temporal
sclerosis, etc) may need lifelong AEDs.
EEG in EPILEPSY
• Should be done for all cases,
• Helps in classifying epilepsy
• Helps in selecting the most appropriate AED,
• Can be diagnostic in some cases, such as
absence seizures, SSPE, etc
• Useful in diagnosing NEAD and non-convulsive
seizures.
BRAIN IMAGING in EPILEPSY
• Should be done for all cases
• Positive findings seen in about 30% of cases,
• Common findings include granulomas, old
infarcts, mesial temporal sclerosis.
• MRI is preferred,
• Contrast study should be performed if
suspecting infections/tumors.
SURGERY IN EPILEPSY
• Required for 10-15% of all cases,
• Offered to patients with medically-refractory
epilepsy,
• Also required for those with brain lesions
causing epilepsy (such as arachnoid cysts,
tumors, Rasmussen’s encephalitis, etc)
FEBRILE SEIZURES
• Occurs in children between age 6 months to 6 years,
• Associated with high fever,
• GTCS type,
• Single episode,
• No need of long-term AED
• Fever should be aggressively treated
• Intermittent clobazam may be used for prevention of
seizure.
EPILEPSY IN PREGNANCY
• Both epilepsy and AED can lead to adverse outcomes
in pregnancy.
• Single seizure during pregnancy is more harmful that
the intake of AEDs,
• AED should be withdrawn if woman is seizure-free
for 2 years,
• Use monotherapy if possible,
• Avoid VPT
• Use folic acid supplementation
• Risk of fetal malformations highest in 1st
trimester.
AEDs in specific situations
• Liver disease- avoid VPT
• Cardiac disease- avoid PHT
• Severe renal impairment- reduce LEV dose by
50%
• Porphyria- gabapentin and clobazam safe
• Children- avoid PB, as it leads to hyperactivity
and learning disability
• Hyponatremia- avoid CBZ, OXC
Any Questions?
Email: drsudhirkumar@yahoo.com
Facebook
http//www.facebook.com/bestneurologist/

Evaluation and Management of Epilepsy

  • 1.
    EVALUATION & MANAGEMENT OFEPILEPSY DR SUDHIR KUMAR MD (MEDICINE), DM (NEUROLOGY) SENIOR CONSULTANT NEUROLOGIST APOLLO HEALTH CITY, HYDERABAD
  • 2.
    What is epilepsy? •Occurrence of 2 or more seizures, at least 24 hours apart, is called epilepsy (=seizure disorder or fits) • Convulsions: tonic and/or clonic movements, as part of seizures • Seizure: an episode of epileptic attack • Seizures occur due to abnormal electrical discharges in the brain.
  • 3.
    DEFINITIONS • Idiopathic epilepsy-presumed to be of genetic origin • Cryptogenic epilepsy- epilepsy of unknown cause • Acute symptomatic seizure- occurs due to a known acute cause, such as metabolic/toxic insult, CNS infection, stroke, head injury, drug toxicity, alcohol or medication withdrawal • Remote symptomatic seizure- > 1 week after the occurrence of underlying disorder
  • 4.
    SEIZURE MIMICS • Syncope •Transient ischemic attack (TIA) • Non-epileptic attack disorder (=psychogenic seizures)
  • 5.
    SYNCOPE vs SEIZURE •Syncope occurs in specific circumstances such as pain, extreme emotions, cough, micturition, hot environment, prolonged standing, exercise, etc • Pre-syncopal symptoms such as dizziness, lightheadedness and h/o cardiovascular disease also favor syncope • Factors favoring seizures include tongue biting, head turning, posturing, urinary incontinence, cyanosis, prodromal deja-vu, and postictal confusion.
  • 6.
    PSYCHOGENIC SEIZURES (NEAD) •Common in younger people, women>men • Should be considered only in patients with recurrent seizures, and not the first episode • Patients may have tongue bites (on tip of tongue as compared to sides in true seizures), and urinary incontinence; but they avoid self- injury during episodes.
  • 7.
    FIRST EPISODE OFSEIZURE • Work-up for underlying causes • Metabolic profile (electrolytes, calcium, glucose, etc) • Toxicity/drug overdosage screening (in suspected cases) • ABG- if hypoxia suspected • Brain imaging • EEG • CSF analysis (in selected cases)
  • 8.
    TREATMENT OF FIRSTSEIZURE • Treatment of the underlying cause • Correction of metabolic derangements is sufficient in cases of acute symptomatic seizures and long-term AEDs are not required. • Risk of seizure recurrence after a single seizure is 51% • Anti-epileptic drug therapy is required in cases with higher risk of recurrence
  • 9.
    RISK FACTORS FORRECURRENT SEIZURES • Age <16 • Seizures occurring between 12 MN and 9 AM • Remote symptomatic seizures • Family history of epilepsy • Status epilepticus or multiple seizures in 24 hours • Todd’s paresis • Abnormal neurological examination • Abnormalities on CT or MRI scan • Epileptiform discharges on EEG
  • 10.
    WHEN TO STARTAED THERAPY? • Occurrence of 2 or more seizures, After first episode if: • Positive family history of epilepsy, • Abnormal neurological exam, • Abnormal CT/MRI findings • Epileptiform discharges on EEG
  • 11.
    TYPES OF EPILEPSY •Partial (or focal)- simple or complex partial • Generalized • Partial onset with secondary generalization
  • 12.
    Subtypes of Generalizedepilepsy • Absence (or petit mal) • Grand mal (or GTCS) • Atonic • Myoclonic
  • 13.
    ANTIEPILEPTIC DRUGS • Conventional-Phenobarbitone (PB), phenytoin (PHT), carbamazepine (CBZ), valproate (VPT) • Newer AEDs- oxcarbazepine (OXC), lamotrigine (LTG), topiramate (TPM), levetiracetam (LEV), clobazam, zonisamide, lacosamide, etc.
  • 14.
    WHICH DRUG TOCHOOSE? Depends on: 1. Type of epilepsy, 2. Age & sex of patient, 3. Presence of co-morbid conditions, 4. Need for IV formulation, 5. Tolerability, 6. Affordability.
  • 15.
    DRUGS OF CHOICE •Partial epilepsy- CBZ, OXC; alternative: VPT, LEV • Generalized epilepsy- VPT; alternatives- PB, PHT, LEV • Absence- VPT • Myoclonic- VPT; alternatives- clonazepam, LEV • Mixed seizure types- VPT
  • 16.
    HOW TO STARTAEDs? • Choose monotherapy • Start the lowest therapeutic dose (based on body weight), • Gradually increase the dose based on efficacy and tolerability, • Watch for any adverse events, • 2nd AED can be added if seizure occurs despite being on the maximum tolerable dose of single drug • Adding 3rd or 4th AED usually does not help.
  • 17.
    HOW LONG TOCONTINUE AEDs? • At least 3 seizure-free years. • Attempt withdrawal at least once. • There is a group of patients, where seizures recur after or during withdrawal of AEDs. • They need lifelong AEDs. • Patients with structural brain lesions (such as gliosis/scar/tumor/old infarcts/mesial temporal sclerosis, etc) may need lifelong AEDs.
  • 18.
    EEG in EPILEPSY •Should be done for all cases, • Helps in classifying epilepsy • Helps in selecting the most appropriate AED, • Can be diagnostic in some cases, such as absence seizures, SSPE, etc • Useful in diagnosing NEAD and non-convulsive seizures.
  • 19.
    BRAIN IMAGING inEPILEPSY • Should be done for all cases • Positive findings seen in about 30% of cases, • Common findings include granulomas, old infarcts, mesial temporal sclerosis. • MRI is preferred, • Contrast study should be performed if suspecting infections/tumors.
  • 20.
    SURGERY IN EPILEPSY •Required for 10-15% of all cases, • Offered to patients with medically-refractory epilepsy, • Also required for those with brain lesions causing epilepsy (such as arachnoid cysts, tumors, Rasmussen’s encephalitis, etc)
  • 21.
    FEBRILE SEIZURES • Occursin children between age 6 months to 6 years, • Associated with high fever, • GTCS type, • Single episode, • No need of long-term AED • Fever should be aggressively treated • Intermittent clobazam may be used for prevention of seizure.
  • 22.
    EPILEPSY IN PREGNANCY •Both epilepsy and AED can lead to adverse outcomes in pregnancy. • Single seizure during pregnancy is more harmful that the intake of AEDs, • AED should be withdrawn if woman is seizure-free for 2 years, • Use monotherapy if possible, • Avoid VPT • Use folic acid supplementation • Risk of fetal malformations highest in 1st trimester.
  • 23.
    AEDs in specificsituations • Liver disease- avoid VPT • Cardiac disease- avoid PHT • Severe renal impairment- reduce LEV dose by 50% • Porphyria- gabapentin and clobazam safe • Children- avoid PB, as it leads to hyperactivity and learning disability • Hyponatremia- avoid CBZ, OXC
  • 24.