Approximate
risk of seizure
in different situations |
General population
 | Lifetime risk of having a seizure: 10% |
 | Epilepsy at some point: 3-4% |
 | Epilepsy at any given time: 0.5-1% |
 | Acute reactive seizure: 3-4% |
 | Single unprovoked seizure: 1% |
 | Active epilepsy in age group over 55: 0.9% |
|
Acute Stroke
 | Lobar hemorrhage: 23% |
 | Subarachnoid hemorrhage: 26% |
 | Ischemic stroke: 6%, may be higher in embolic strokes |
|
Prior stroke
 | 9% probability over 10 years |
 | Early postinfarction seizure(within 2 weeks): risk of recurrent seizure
32% |
|
Brain tumor
 | Brain tumor: 30% has seizure as initial symptom |
 | Slow growing tumor tends to present with seizures |
 | More aggressive tumor usually presents with mass effect |
 | Brain mestastasis: 18% presents with seizures |
|
Infection
 | Bacterial meningitis: about 25% have seizures, abscess and encephalitis
higher |
 | Herpes encephalitis: 50% have seizures |
 | Late seizures:
 | Aseptic meningits: risk not increased |
 | Bacterial meningitis: risk is 5X of population |
 | Viral encephalitis: risk is 10X of population |
|
|
Head injury
 | Mild closed head injury: 0.4% |
 | Moderate injury (depressed skull fracture or LOC <24 hour: 2.4%, late
seizures 2% |
 | Severe head injury (with intracranial mass or LOC > 24 hr: 10.3%, 12%
chance of late seizures. Increase to 36% with presence of early seizure. |
 | Penetrating injury: 30-50% risk of late seizures |
|
Metabolic
 | Dialysis encephalopathy: 50% have seizures |
|
Alzheimer's disease
 | 16% has seizures |
|
Multiple sclerosis
 | 4% has seizures |
|
Neuroleptics
 | Neuroleptic at therapeutic dose: seizure risk 1.2%
 | Higher dose (1g/day of Chlorpromazine): ?9% |
 | Thioridazine (Mellaril) ? least epileptogenic |
|
 | Clozapine:
 | High dose (>600 mg/day): 4.4% |
 | Low dose (<300 mg/day): 1.0% |
 | rapid upward dosage titration increased the risk of
seizures. |
|
|
Antidepressant
 | Tricyclics at therapeutic dose: 0.3-0.6%
 | Tricyclics overdose: 8.4% have seizues |
|
 | Buproprion at usual dose:
 | at higher dose: increased risk, especially if patient has risk factors of
seizure |
|
|
Other medications
 | Imipenem may increase chance of seizure
 | at high dose, or dose not adjusted according to kidney function |
 | or given with theophylline & cyclosporine |
|
 | Aminophylline: in chronic treatment, level >30, may cause seizures,
especially in patients with underlying neuro disease. May be refractory to anticonvulsant.
|
 | Meperidine: 3% in certain population
 | related to the metabolite normeperidine, which has a half-life of 15 to
30 hours and accumulates faster in the setting of
 | renal insufficiency |
 | repeated dose |
 | hepatic enzyme inducing drugs |
|
|
 | Flumazenil
may precipitate seizure especially if
 | patient has overdose of tricyclics |
 | using benzodiazepine for epilepsy |
 | Avoid Flumazenil use in patient who is on tricyclic antidepressants,
cocaine, lithium, methylxanthines, isoniazid, propoxyphene, monoamine oxidase inhibitors,
buproprion HCl or cyclosporine |
|
 | Cyclosporine:
 | Seizures have been reported in transplant
recipients who were given cyclosporine but whose magnesium concentrations were normal. |
|
|
Alcohol
 | Dose dependent |
 | 50-100g/day (50g = 3.5 beer or 3 glasses of wine): risk for new seizures
3X of population |
 | 300g/day (1.5 pints of 40% ): 20X of population |
|
| Further reading
|