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
FOCAL EPILEPTOGENESIS Asynchronous burst firing in some hypocampal and cortical neurons Generalized epileptogenesis : asynchronous burst firing in abnormal thalamocortical interaction EPIDEMIOLOGY Developed countries : annual incidence 50-70 cases per 100.000 Developing countries : prevalence 1% Incidence varies with age
ETIOLOGY Idiopathic Cryptogenic Symptomatic
Hypoxia Hypoglycaemia Hypocalcaemia Febrile Seizures Intracranial Infections Birth trauma Intracranial haemorrhage Congenital anomalies Tuberous sclerosis Storage diseases 1 5 10 0 20 Head Injuries Drugs and alcohol Genetic epilepsies Cerebral tumours 60 Cerebrovascular degenerations Age (years) Factors lowering seizure threshold Common Occasional Sleep deprivation Alcohol withdrawal Television flicker Epileptogenic drugs Systemic infection Head trauma Recreational drugs AED non-compliance Menstruation Barbiturate withdrawal Dehydration Benzodiazepine withdrawal Hyperventilation Flashing lights Diet and missed meals Specific reflex triggers Stress Intense exercise International Classification of Epileptic Seizures Partial seizures (beginning locally) Simple partial seizures (without impaired consciousness) with motor symptoms with somatosensory or special sensory symptoms Complex partial seizures (with impaired consciousness) simple partial onset followed by impaired consciousness impaired consciousness at onset Partial seizures evolving into secondary generalized seizures Generalized seizures (convulsive or non- convulsive) Absence seizures Typical Atypical Myoclonic seizures Clonic seizures Tonic seizures Tonic clonic seizures Atonic seizures Unclassified seizures Simplified Classification of Epileptic Seizures Partial seizures Simple preservation of awarness Complex impairment of consciousnesss Secondary generalized Generalized seizures Absence Myoclonic Tonic-clonic Tonic Atonic Diagnosis Interviews with patients or witness Circumstances surrounding the attacks idiopathic and generalized No seizure worning No underlying brain lesions Associated with a family history Symptomatic and localization related Aura Specific site of onset Identifiable cause Recurrent episodes of seizures Symptoms occured during and after seizures Recording symptomatic events with videocamera and continous ambulatory EEG monitoring
E E G 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 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
Functional cerebral changes Useful adjuncts in candidate epileptic surgery 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 Strategies for managing newly diagnosed epilepsy Newly diagnosed epilepsy First drug Second drug Refractory Rational duotherapy Surgical assessment Seizure-free Seizure-free 47% 13% 40% Drug choice in newly diagnosed epilepsy in adolescents and adults
Partial Carbamazepine Phenytoin Lamotrigine* Oxcarbamazepine* Sodium valproate Unclassifiable Sodium valproate Lamotrigine* *Lamotrigine and oxcarbamazepine are regarded as first-line drugs in some countries 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
Special Problems of Epilepsy Behavioral problem : -Label of epilepsy racial disadvantage -Brain function, medication, type of seizure -Attitudes of helpers and helped Education : -Discussion between doctors, families, schools teachers and the patient, steps which might be taken to promote normal education and personal development 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 Marriage and pregnancy Health education Impairment, disability and handicap