Epilepsy Flashcards
Definition of epilepsy
Sudden paroxysmal uncontrolled synchronous discharge of cerebral neurons which produces symptoms either visible to patient or observer
Excludes gradual onset and discharge without symptoms
Prevelance
0.7-0.8% - higher in developing countries
Most common epilepsy causes in children
Perinatal problems, genetic or congenital disorders
Most common epilepsy causes in adults
Trauma, alcohol abuse, drugs, brain infection
Most common epilepsy causes in elderly
Cerebrovascular disease and mass lesions
Pre and perinatal risk factors x4
Intrauterine infections (including rubella, toxoplasmosis) maternal drug abuse, irradiation in early gestation, severe perinatal trauma or anoxia
Trauma/surgery and epilepsy
Highest risk with depressed skull fracture, penetrating injury or intracranial haemorrhage
Can be early or late when chronic epilepsy is most common
Metabolic causes of epilepsy x5
Electrolyte: Hyponatraemia, hypocalcaemia, hypomagnesaemia and hypoglycaemia
Uraemia
Hepatic failure
Acute hypoxia
Porphyria
Main pathological cause of temporal lobe epilepsy
Hippocampal sclerosis -childhood febrile convulsions are big risk factor - can treat surgically if medical not effective
Drugs which increase risk of epilepsy - 6x medication
3 x poisoning
Phenothiazines, tricyclics, MAO inhibitors, amphetamines, lidocaine and nalidixic acid
Lead, CO, Mercury
Infectious/inflammatory causes of epilepsy x6
Encephalitis Meningitis Tuberculomas Cerebral abscess Neurosyphilis
Neurocysticercosis - tapeworm - in countries where it is epidemic - major cause of epilepsy
Circulatory cause of epilepsy
Anoxic encephalopathy due to cardiac arrest or respiratory arrest
Seizure triggers
Photosensitivity, stress, sleep deprivation
Partial (focal) seizure definition
Electrical discharge limited to one region of cortex. Simple = no LOA, Complex = LOA
Generalised seizure definition
Simultaneous involvement of both hemispheres always associated with LOC or LOA
Focal can become secondary generalised
Features of absence seizures
Age of onset typically 4-12 - rarely beyond adolescence
Family history in 40% of patients
30% get TC in adolescence
Loss of awareness and vacant expression for
Tonic Clonic seizures features
Prodrome - no warning or may be an aura including tingling
Sudden LOC and drop to ground
Epileptic cry
Tonic - body stiff, elbows flexed, arms extended, eyes open, jaw clenched, pupils dilated - about 10 seconds - associated with rapid neuronal discharge
Clonic - neuronal discharge slows, jerking of limbs, increasing size but decreasing frequency, eyes open and roll backwards, might bite tongue and have urinary/faecal incontinence - lasts about 1-2mins
Post-ictal phase - flaccid unresponsiveness, confusion and drowsiness (15mins-1hour), headache, feel exhausted for days after including muscle ache due to CPK
What are myoclonic jerks?
Momentary brief contractions of a muscle or muscle group - commonest disorder = benign juvenile myoclonic epilepsy - onset in puberty - typically in the morning and affecting the upper limb.
Family hx may be present as is hereditary
What are tonic seizures?
Stiffening of the body - sustained muscle contraction - no jerking afterwards just LOC
Atonic seizures?
Sudden collapse with loss of muscle tone and LOC