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DEFINITION
Abnormal and recurrent excessive synchronized discharge of cerebral neuron with clinical manifestation of epileptic seizure which are an intermittent stereotypical behavior, emotion, motor function or sensation
PATHOPHYSIOLOGY
Paroxysmal depolarization shift (PDS) of the resting membrane potential, which triggers a brief rapid burst of action potentials terminated by a sustained after hyperpolarization PDS : result of imbalance between excitatory (glutamate and aspartate) and inhibitory (GABA) neurotransmitters Abnormalities of voltage controlled membrane ion channels Imbalance between endogenous neuromodulators, acetylcholine favoring depolarization and dopamine enhancing neuronal membrane stability
FOCAL EPILEPTOGENESIS Asynchronous burst firing in some hypocampal and cortical neurons
EPIDEMIOLOGY
Developed countries : annual incidence 50-70 cases per 100.000 Developing countries : prevalence 1% Incidence varies with age
ETIOLOGY
Idiopathic Cryptogenic Symptomatic
Congenital anomalies
Tuberous sclerosis Storage diseases
Birth trauma
Intracranial haemorrhage
Genetic epilepsies
Cerebral tumours
Head Injuries
Hypoxia
Drugs and
Cerebrovascular degenerations
Hypoglycaemia
Hypocalcaemia
alcohol
10 20 Age (years)
60
Occasional
Barbiturate withdrawal Dehydration Benzodiazepine withdrawal Hyperventilation Flashing lights Diet and missed meals Specific reflex triggers Stress Intense exercise
Myoclonic seizures Clonic seizures Tonic seizures Tonic clonic seizures Atonic seizures Unclassified seizures
Generalized epilepsies and syndromes Idiopathic epilepsy with age-related onset (listed in order of age at onset) - benign neonatal familial convulsions - benign neonatal non-familial convulsions - benign myoclonic epilepsy in infancy - childhood absence epilepsy (formerly known as pyknolepsy) - juvenile absence epilepsy - juvenile myoclonic epilepsy (formerly known as impulsive petit mal) - epilepsy with generalized tonic-clonic seizures on awaking Other idiopathic epilepsies
Idiopathic or symptomatic epilepsy (listed in order of age at onset) - West syndrome (infantile spasms) - Lennox-Gastaut syndrome (childhood epileptic encephalopathy) - epilepsy with myoclonic-astatic seizures - epilepsy with myoclonic absence seizures Symptomatic epilepsy Non-specific syndromes - early myoclonic encephalopathy - early infantile epileptic encephalopathy Specific syndromes (epileptic seizures as a complication of a disease, such as phenylketonuria, juvenile Gauchers disease or Lundborgs progressive myoclonic epilepsy)
Epilepsies and syndromes with both generalized and focal seizures Neonatal seizures Severe myoclonic epilepsy in infancy Epilepsy with continuous spike waves during slow-wave sleep Acquired epileptic aphasia (LandauKleffner syndrome)
Epilepsies without unequivocal generalized or focal features Special syndromes Situation-related seizures - febrile convulsions - seizures related to other identifiable situations, such as stress, hormonal changes, drugs, alcohol withdrawal or sleep deprivation Isolated, apparently unprovoked epileptic events Epilepsies characterized by specific modes of seizure precipitation Chronic progressive epilepsia partialis continua of childhood
Diagnosis
idiopathic and generalized No seizure worning No underlying brain lesions Associated with a family history
Symptomatic and localization related
Recording symptomatic events with videocamera and continous ambulatory EEG monitoring
To confirm the clinical diagnosis To support the classification of partial or generalized seizures Routine trace 50% normal Diagnostic in non convulsion state epileptic activities : Hyperventilation Photic stimulations Sleep deprivation
EEG
EEG
EEG
BRAIN IMAGING
Essential, particularly in partial onset seizures Computerized tomography (CT) Magnetic resonance imaging (MRI)
Structural lesion
MRI
MRI
MRI
Scan
Scan should be repeated periodically : Suspicion of a tumour Worsening in neurological examination or cognitive function Deterioration in the frequency or severity of the seizures
Single Photon Emission CT (SPECT) Positron Emission Tomography (PET) MRI spectroscopy Functional MRI
DIFFERENTIAL DIAGNOSIS
Migraine Transient Ischaemic Attacks Hyperventilation Tics Myoclonus Hemifacial spasm Syncope Sleep disorders Non Epileptic Attacks Narcolepsy Metabolic disorders Transient global amnesia
Management
Medical treatment : Establish a correct diagnosis of epileptic seizure type and epileptic syndrome Decide treatment with epileptic drugs is necessary Decide which drug should be used Patients and their families should receive counselling regarding :
Aims of treatment Prognosis and duration of the expected treatment Importance of compliance Side effects
Surgical treatment
Proposed Indications for resective epileptic surgery
Intractable seizures Resectable structural abnormality as identified on magnetic resonance imaging Confirmation that seizures arise from a visible lesion (using video telemetry) Over 20% of seizures arising from the contralateral temporal lobe in temporal lobe seizures Intelligence quotient > 70 points No significant psychiatry morbidity No medical contraindications Age < 45 years
Rational duotherapy
Surgical assessment
Ten commandments in the pharmacological treatment of epilepsy Choose the correct drug for the seizure type or epilepsy syndrome Start at low dosage and increase incrementally Titrate slowly to allow tolerance to central nervous system side-effects Keep the regiment simple with once- or twice-daily dosing, if possible Measure drug concentration when seizures are controlled or if control is not readily obtained (if possible)
Counsel the patient early regarding the implications of the diagnosis and the prophylactic nature of drug therapy Try two reasonable monotherapy options before adding a second drug When seizures persist, combine the best tolerated first-line drug with one of the newer agents depending on seizure type and mechanism of action Simplify dose schedules and drug regimens as much as possible in patients receiving polypharmacy Aim for the best seizure control consistent with the optimal quality of life in patients with refractory epilepsy
Drug choice in newly diagnosed epilepsy in adolescents and adults Seizure type
Tonic clonic Absence Myoclonic
First line
Sodium valproate Carbamazepine Phenytoin
Sodium valproate Sodium valproate Carbamazepine Phenytoin
Second line
Lamotrigine* Oxcarbamazepine*
Ethosuximide Lamotrigine* Lamotrigine* Lamotrigine* Oxcarbamazepine* Sodium valproate Lamotrigine*
Partial
Myoclonic
Tonic
Sodium valproate
Sodium valproate
Lamotrigine*
Lamotrigine*
Clobazam Phenobarbital
Clobazam Topiramate
Absence
Sodium valproate
Carbamazepine Phenytoin
Lamotrigine* Ethosuximide
Sodium valproate Gabapentin Oxcarbazepine* Sodium valproate Nitrazepam Lamotrigine* Topiramate
Clobazam
Lamotrigine* Vigabatrin Clobazam Topiramate Lamotrigine* Clobazam Felbamate
Partial
Status Epilepticus
Life threatening medical defined as frequent and / or prolonged epileptic seizure
Prognosis
Dependent with underlying syndrome and / or its cause Patients compliance Reciprocal illness or medications 60-70% controlled by first-line drug of epilepsy 10% of the rest controlled by new drugs The rest : surgery Institution
Employment : -Personal and racial states as well as financial reward -Understanding of the employee of their illness in the context of particular employment, safety for their selves and environment -People around in working hours need to know what to do if the attack occurred The law
Driving lisence
Free of seizure after 6 months controlled epilepsy
No permitting to drive if :
Have suffered of epileptic attack at the age before adolescent Medical condition caused driving a source of danger to them selves and to the public
Leisure :
Swimming, water sport, cycling, horse riding in groups with safety controlled Boxing, climbing, sport with body contact are prohibited Television and video games, avoid flickering of the screen