EPILEPSY - كلية الطب · 2019-10-17 · Risk factors for epilepsy : 1. Family history...
Transcript of EPILEPSY - كلية الطب · 2019-10-17 · Risk factors for epilepsy : 1. Family history...
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EPILEPSY
Dr Sadik AL GhazawiAssociated professor
NeurologistMRCP,FRCP UK
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‘The Sacred Disease’
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‘The Sacred Disease’
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The term “epilepsy” is derived from Greek epilepsia: a taking hold of or seizing.
Ancient accounts over 2500 years ago by Babylonians and Egyptians.
Detailed descriptions in On the Sacred Disease attributed to Hippocrates in the 5th century BC. Use of “Sacred” possibly meant to be ironic.
Late 19th century:
-Jackson: Model of focal seizures; aura evolving to psychosomatic or convulsive seizure. Use of aura for localizing seizure onset.
Historical Background
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Late 20th century:
- Widespread use of simultaneous video-EEG .
- Neuroimaging
- Development of new antiepileptic drugs based on seizure mechanisms.
- Emergence of epileptology as a defined specialty within neurology and development of comprehensive epilepsy programs including epilepsy monitoring units and epilepsy surgery.
Historical Background
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21st century:
- Identification of genetic basis of many syndromic epilepsies.
- Neurostimulation devices: Vagus Nerve Stimulation (VNS), Responsive NeuroStimulation (RNS), Deep Brain Stimulation (DBS).
- Use of laser ablation in epilepsy surgery.
Historical Background
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Seizure
is the clinical manifestation of an abnormal,
excessive, and hypersynchronous electrical discharge of a population of cortical neurons.
Epilepsy:
A brain disease characterized by recurrent seizures
that are unprovoked by systemic or neurologic insults.
Definitions
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Epilepsy syndrome:
a particular form of epilepsy, often implying specific causes,
clinical manifestations, and prognosis.
Aura:
The earliest part of a seizure and typically the only
subjective experience recalled by the patient.
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Convulsion:
The motor manifestations of a seizure, usually consisting of rhythmic tonic followed by clonic movements andpostures.
Semiology:
Abnormal sensations, emotions, behaviors, loss of consciousness, muscle spasms, convulsions that accompany the brain seizure activity.
Definitions
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Postictal period:
Time between the end of the seizure and recovery to the
baseline state.
Status epilepticus:
Five or more minutes of continuous or recurrent seizures
without recovery.
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Sudden Unexpected Death in Epilepsy (SUDEP):
Sudden, unexpected , witnessed or unwitnessed, nontraumatic, and nondrowning death of patients with epilepsy with or without evidence of a seizure and in whom postmortem examination does not reveal a structural or toxicological causes.
Definitions
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Automatisms:
1- nonpurposeful, stereotyped, and repetitive behaviors that commonly accompany focal impaired awareness seizures (in the semiologic classification, they define automotor seizures).
2-The behavior is inappropriate for the situation. Patients are usually amnestic to their automatisms.
3-Automatisms could be oral or manual.
Definitions
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Epilepsy is a disease of the brain defined by any of the following conditions
1. A least two unprovoked (or reflex) seizures occurring >24 h apart
2. One unprovoked (or reflex) seizure and a probability of further seizures similar to
the general recurrence risk (at least 60%) after two unprovoked seizures, occurring
over the next 10 years.
3. Diagnosis of an epilepsy syndrome
Epilepsy is considered to be resolved for individuals who had an age-dependent
epilepsy syndrome but are now past the applicable age or those who have remained
seizure-free for the last 10 years, with no seizure medicines for the last 5 years.
ILAE OFFICIAL
REPORT
ILAE: International League Against Epilepsy
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Asses Risk of further seizures
Single Seizure Recurrence Risk (2 years)
All patients 20-60%
No risk factors, normal EEG, normal MRI
20-30%
Abnormal EEG (epileptiformdischarges)
60-70%
Focal structural lesion on imaging
>60%
Two seizures 73%
Berg AT, Shinnar S. Neurology 1991; 41:965-972
Hauser WA et al. N Engl J Med 1998; 338:429-434
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Seizures: Classification
Generalized or Focal
•Generalized abnormalities on
EEG
•1-No lesion or diffuse
abnormalities on MRI
•2-No aura
•3-Bilaterally symmetrical
onset
•4-Often < 30 seconds
•Focal abnormalities on EEG
•1-May have focal lesion on MRI
•2-Auras sometimes present
•3-Focal clinical features during
seizure
•4-May be longer (1-2 minutes)
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Motortonic-clonic
clonic
tonic
myoclonic
myoclonic-tonic-clonic
myoclonic-atonic
atonic
epileptic spasms2
Non-Motor (absence)typical
atypical
myoclonic
eyelid myoclonia
Unknown Onset
Motor Onsetautomatisms
atonic2
clonic
epileptic spasms2
hyperkinetic
myoclonic
tonic
Non-Motor Onset
autonomic
behavior arrest
cognitive
emotional
sensory
focal to bilateral tonic-clonic
Generalized OnsetFocal Onset
Aware Impaired
Awareness Motor
tonic-clonic
epileptic spasms
Non-Motor
behavior arrest
ILAE 2017 Classification of Seizure Types Expanded Version1
Unclassified3
1 Definitions, other seizure types and descriptors are listed in the
accompanying paper and glossary of terms.
2 These could be focal or generalized, with or without alteration of awareness
3 Due to inadequate information or inability to place in other categories
From Fisher et al. Instruction manual for the ILAE 2017 operational
classification of seizure types. Epilepsia doi: 10.1111/epi.13671
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Temporal
Frontal
Parietal
Occipital
Location of Focal Epilepsy
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Focal ---- Simple Partial ---- Focal without impairment--- Focal Awareof awareness
Psychomotor---- Complex Partial--- Focal with impairment--- Focal impaired of awareness awareness
Grand Mal---- Tonic-Clonic----- Tonic-Clonic -------- Tonic-ClonicOR OR focal to
Focal evolving to bilateral tonic-clonica bilateral, convulsive
seizure
Petit Mal Absence---- Absence ----- Non-Motor (Absence)
Fisher et al. Instruction manual for the ILAE 2017 operational classification of seizure types. Epilepsia doi: 10.1111/epi.13671.
Berg AT, et al. Epilepsia 2010; 51(4): 676-85
Past Recent Current 2017
Terminology
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1-Genetic (previously called idiopathic)
2-Structural/Metabolic (previously called symptomatic)
3-Unknown cause (previously called cryptogenic)
Etiology of Epilepsies
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1-
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2-
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4- conditions associated with seizures but not a diagnosis of epilepsy
A- febrile seizures
B- benign neonatal seizures
5- Epilepsies of unkown cause.
Epilepsy syndromes per ILAE
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Provoking factors include acute CNS or systemic
alterations that lead to increased excitation of the
brain resulting in a seizure.
Provoked seizures
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50 million people worldwide are affected by epilepsy.
In 30% of these patients, the seizures are not controlled by any available medical therapy.
Even among patients whose seizures are controlled, significant medication side effects are common.
In addition to the medical burden of epilepsy, the social and economic stress of refractory epilepsy can be devastating to the patient and family.
1-2% of World’s population affected ~50 Million worldwide.
Epidemiology
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Epidemiology
There is a bimodal incidence for both seizures and epilepsy with
highest rate in the( first year) of life and increasing again (after age 60).
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1. 2.
3. 4.
History from Patient ?
Routine EEG
MRI
History from witness of event
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Risk factors for epilepsy :
1. Family history (genetic predisposition to seizure disorder)
2. Birth history and complications, cognitive and motor development
3. Infant or childhood seizures (e.g. febrile seizures are associated with temporal lobe epilepsy)
4. Past history of CNS infections, stroke, head trauma, cancer.
History:
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Detailed description of the event: Seizures are generally brief and have stereotyped patterns.
1. What was the patient doing at time of the event (e.g. occur out of sleep)?
2. Were there any warning symptoms/aura and were they focal ?
3. Did he/she loose consciousness?
4. What other symptoms were present? (SOB, chest pain, etc. may suggest different diagnosis )
History:
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5. How long did the events last (most seizure last < 3
minutes)?
6. Description of the movements; falling to the ground,
convulsion/myoclonus/posturing, head turn, eye
movements , automatisms.
7. Did he/she loose bowel/bladder control or bite their
tongue?
8. Was there postictal confusion, hemi-paresis,
aphasia?
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Generalized Tonic-Clonic seizures:
1-Can arise from a partial seizure (focal to bilateral tonic clonic) or as a generalized seizure from the beginning (primarily generalized)
2-Strained cry---------
3-Generalized tonic-------- then clonic activity
4-Duration: 1-2 minutes
5-Post-ictal phase
History
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Absence Seizures:
1-Cessation of activity, staring, clonic twitches of perioral and eyelid muscles
2-Brief: 10-20 seconds
3-No post-ictal period
4-Multiple per day
5-No associated developmental delay
6-EEG: 3 Hz spike and wave ++++++++
7-Can be confused with focal impaired awareness seizures.
History
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Semiology of focal epilepsies:
Temporal lobe:
Déjà vu, Epigastric rising sensation, oral and manual
automatisms, olfactory or auditory hallucinations, impaired consciousness, impaired language if dominant side.
History
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Frontal lobe:
hypermotor activity, bicycling, brief, recurrent, out of sleep,
quick regain of consciousness.
Occipital lobe:
elementary visual hallucinations.
Parietal lobe:
Quick propagation to other areas causes different
semiologies.
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DD,The history can suggest other possible diagnosis for transient neurological symptoms and/or loss of consciousness.
1. Syncope (presyncopal symptoms, precipitating maneuvers, orthostatic BP, abnormal ECG)
2. Sleep disorders such as narcolepsy/cataplexy
3. Stroke ( is rare in stroke, but can occur with posterior circulation stroke)
4. Migraine
History
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5. Paroxysmal Vertigo
6. Transient global amnesia
7. /drug related “blackouts”
8. Movement disorder (e.g. myoclonus, dyskinesias)
9-Psychiatric (nonepileptic seizures, panic attacks, hyperventilation)
History
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1-Duration: 1-2 minutes
2-Clustering
3-Tongue-biting
4-Incontinence
5-Stereotyped
6-Amnesia
7-Arising out of true sleep
8-Eyes open
9-Post-ictal dysfunction
Suggestive of a Seizure
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Seizure vs Syncope
Seizure 1-aura
2-duration: 1-2 min
3-post-ictal phase x several minutes
4-tonic-clonic activity, limb posturing
5-tongue-biting
6-Incontinence
7-Guttural, strained cry
Syncope
1-visual, auditory fading
2-10-30 seconds
3-minimal post-ictal phase
4-pallor & diaphoresis
5-flaccidity
6-Provocation by prolonged standing, hunger, heat, pain, micturition, cough
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1-Mental status
2-Focal features
3-Signs of tongue biting
4-Signs of infection or trauma
Physical Exam
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1-Labs: Electrolytes, glucose, LFT, KFT, CBC, toxic screen ?, CPK ? , CSF ?
2-Imaging: MRI preferred to CT scan.
3-EEG: as soon as available.
Diagnostic Workup
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Electroencephalogram EEG right temporal
lobe epilepsy- T6 sharp waves
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Electroencephalogram EEG childhood abcense epilepsy – 3 Hz spike and wave
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Electroencephalogram EEG Lennox-
Gastaut syndrome – slow (<3 Hz) spike and wave and slow background ( and developmental delay and refractory seizures)
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Lowenstein in 1999
Defined status has having a seizure for 5 minutes or
longer or multiple seizures without full return to
baseline
Status Epilepticus
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Treatment of Epilepsy
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1-Don't hold the person down or try to stop his movements.
2-Time the seizure with your watch.
3-Clear the area around the person of anything hard or sharp.
4-Loosen ties or anything around the neck.
5-Put something flat and soft, like a folded jacket, under the head.
6-Turn him or her gently onto one side.
7-Do not try to force the mouth open with any hard implement or with fingers.
8-Be friendly and reassuring as consciousness returns.
Seizure First Aid
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1-Type of seizures (generalized vs. focal) 2-Can medication be loaded? 3-Other comorbidities 4-Medication interactions (including
contraceptives) 5-Short and Long Term Adverse Effects 6-Teratogenicity 7-Daily, BID, or TID dosing 8-Cost and Insurance coverage 9-Formulation (liquids, crushable, sprinkles,
etc.)
Choosing an Anti-Epileptic Drug (AED)
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Medications for seizure type
Carbamazepin
e
Oxcarbazepin
e Phenytoin
Phenobarbital
Gabapentin
Lacosamide
Pregabalin
Tiagabine
Vigabatrin
Valproate
Lamotrigine
Levetiracetam
Topirimate
Zonsiamide
Felbamate
Ethosuximid
e
(Absence)
Rufinamide
(Tonic)
Focal Generalized
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Carbamazepine :
Rash, neutropenia , hyponatremia, Stevens Johnson syndrome, osteoporosis, numerous drug interactions.
May make myoclonus worse. Liver enzyme inducing.
Will reduce effi cacy of oral contraceptive pills (OCPs)
Common Antiepileptic Drugs (AEDs) side effects
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Oxcarbazepine:
Hyponatremia, rash, Stevens Johnson syndrome. Mild
induction of hepatic enzymes. Will reduce efficacy of OCPs
Sodium valproate:
Rash, tremor, weight gain, hair loss, menstrual changes,
thrombocytopenia, hyperammonemia, pancreatitis.
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Lamotrigine : Rash, Stevens-Johnson syndrome, toxic
epidermolysis. Risk of adverse events increased with valproic acid.
Topiramate : Weight loss, cognitive impairment, renal calculi, metabolic acidosis.
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Levetiracetam:
Drowsiness, irritability, mood swings
Pregabalin:
Weight gain, peripheral edema
Phenytoin:
Gum hypertrophy, acne, hirsuitism, coarse facies,
osteoporosis, ataxia (cerebellar atrophy). Note: Zero-order
kinetics: small dose increase may produce large changes in
levels.
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Safety and EpilepsyKnow the Driving laws
Epilepsy Foundation: www.efa.org
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Fetal malformations
1-Occur in first trimester
2-Background risk 2-3%
3-In Epilepsy risk ~4-7%
Risk increases with:1- Valproic acid >> other anti-epileptic drugs (AEDs).
2- Polytherapy3- High Drug levels
Women, Epilepsy and Pregnancy
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Up to 30% of persons with epilepsy have pharomacoresistant epilepsies.
Many of them can be candidates for epilepsy surgery (resection of the epileptogenic focus) and this can be done after a comprehensive evaluation using non-invasive and invasive EEG monitoring, advanced neuroimaging (MRI with epilepsy protocol, PET, SPECT), and functional brain mapping.
Best outcome is seen in lesional temporal lobe epilepsies (up to 70-90% cure rate).
Epilepsy Surgery
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Vagus Nerve Stimulation (VNS)
Brain stimulation devices:Responsive NeuroStimulation (RNS), Deep Brain Stimulation (DBS).
Ketogenic or Low carbohydrate diet Palliative surgeries: Corpus Callosotomy; Subpial
transections
Other options
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The END
Thanks