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epilepsy
A tendency towards recurrent seizures.
Defined as >= 2 unprovoked seizures > 24 hours apart or
1 unprovoked seizure with a risk of further seizures of >= 60% [2]
Classification:
Epilepsy syndromes:
1) benign childhood epilepsy
2) juvenile myoclonic epilepsy
- epilepsy prior to age 18
3) idiopathic generalized epilepsy
4) focal epilepsy, epilepsia partialis continuans
5) temporal lobe epilepsy (most common syndrome in adults)
6) post-traumatic epilepsy
7) febrile seizures
* International League Against Epilepsy has updated its system for classifying epilepsies [16]
- focal is now used instead of partial
- focal seizures are now classified by awareness
- the terms dyscognitive, simple partial, complex partial, psychic, & secondarily generalized are no longer used [16]
Etiology:
- inherited syndromes
- congenital brain malformations
- focal cortical dysplasia
- infection
- head trauma (most common cause in children)* [14]
- brain tumors
- stroke (most common in elderly) [14,22]
- neurodegenerative disease, dementia [14,22]
- risk factors for late-life epilepsy [22]
- hypertension
- diabetes mellitus
- highest risk: black patients with diabetes
- smoking
- apoE4 allele [22]
- reduced risk associated with
- physical activity is a negative risk factor
- moderate alcohol consumption is a negative risk factor [22]
* no mention of febrile seizures [14]
Epidemiology:
- cumulative lifetime incidence in U.S. is 3% [2]
- 44% of patients with epilepsy report seizures under control [21]
Clinical manifestations:
- risk of recurrent seizures is > 60% [2]
Diagnostic criteria:
- diagnosis of epilepsy requires 2 or more unprovoked seizures 24 hours apart [2,8], or
- one unprovoked seizure plus >= 60% likelihood of additional seizure(s) within 10 years (a single seizure 1 month after a stroke), or
- presence of an epilepsy syndrome
* resolution of epilepsy may be considered if
- a patient has outgrown an age-dependent epilepsy syndrome
- 10 years without a seizure & off anticonvulsants for 5 years [8]
Laboratory:
- avoid routine drug levels in patients with epilepsy [23]
- see ARUP consult [3]
Special laboratory:
- electroencephalogram (EEG)
- do not routinely order EEG as initial part of syncope workup [23]
- negative results do not exclude epilepsy [2]
- electroencephalography is 40-50% sensitive in diagnosing epilepsy [2]
- EEG not useful in assessing need for continuation of anticonvulsants in patients who respond to combination of 2 anticonvulsants [2]
- video EEG monitoring should be considered
- patients not responding to 2 or more anticonvulsants
- seizures requiring further characterization [2]
- gold standard for classifying type of epilepsy
Radiology:
- magnetic resonance imaging
- negative results do not exclude epilepsy [2]
- do not routinely obtain neuroimaging after an acute seizure in a patient with established epilepsy [23]
Complications:
- major depression
- bipolar disorder
- cognitive impairment
- increased risk of bone fractures
- increased risk of sudden, unexplained death [2,6,9]
- 11 year mortality ~ 0.9% [9]
- up to 1% with intractable seizures, multiple anticonvulsants [2]
- 3-fold risk of unnatural mortality [20]
- 5-fold risk of unintentional medication overdose
- opioid & psychotropic major implicated drugs
- anticonvulsants not implicated in overdoses [20]
- increased risk of major cardiovascular events (RR=1.6) [25,26]
Management:
- see specific form of seizure
- anticonvulsant therapy
- avoid valproic acid in women of child-bearing age [23]
- levetiracetam or lamotrigine*
- anticonvulsants of choice in women of child-bearing age
- discovery of pregnancy is not reason enough to stop anticonvulsant [2]
- uncontrolled seizure can result in fetal anoxia & death [2]
- no significant interactions with hormonal contraceptives [2]
- dosage reduction in patients with renal failure [2]
- levetiracetam, lamotrigine & gabapentin are anticonvulsants of choice in older patients [2]
- do not prescribe long-term anticonvulsant therapy to patients with withdrawal seizures [23]
- patients who do not respond to combination of 2 anticonvulsants are considered refractory [2]
- lifelong therapy of at least 2 anticonvulsants in patients who respond to combination of 2 anticonvulsants [2]
- patients with refractory epilepsy should be referred to an epilepsy center for evaluation [2]
- avoid drugs the lower seizure threshold
- among antibiotics Zosyn with lower risk of triggering seizures than levofloxacin, cefepime, imipenem
- medical marijuana may improve seizure control & quality of life in refractory epilepsy [17]
- high out-of-pocket costs & inconvenient access cited as reasons for discontinuation
- behavioral interventions can reduce seizures in patients with refractory epilepsy [19]
- muscle relaxation with diaphragmatic breathing (29%)
- control focused-attention activity with extremity movements (25%)
- neurosurgery to remove epileptic focus for patients with refractory focal seizures [2]
- laser ablation when location of seizure activity can be pinpointed is FDA-approved but not approved by Aetna [18]
* avoid valproic acid, phenobarbital, phenytoin, topiramate, carbamazepine in pregnant women & women of child-bearing age
Interactions
disease interactions
Related
hormonal effects on epilepsy
Specific
Amish infantile epilepsy syndrome
benign familial infantile convulsions
benign familial neonatal epilepsy
catamenial epilepsy; menstruation-associated seizures
childhood absence epilepsy
epilepsy during pregnancy
epilepsy female-restricted with mental retardation (convulsive disorder & mental retardation)
epilepsy X-linked with variable learning disabilities & behavior disorders (XELBD)
epileptic encephalopathy early infantile type 2; atypical CDKL5-related Rett syndrome
focal epilepsy
generalized epilepsy & paroxysmal dyskinesia
generalized epilepsy with febrile seizures (GEFS)
idiopathic generalized epilepsy
infantile epileptic encephalopathy
intractable childhood epilepsy with generalized tonic-clonic seizures (ICEGTC)
myoclonic epilepsy
myoclonic epilepsy with ragged-red fibers (MERRF) syndrome
nocturnal epilepsy
pyridoxine-dependent epilepsy; neonatal epileptic encephalopathy; pyridoxine-5'-phosphate oxidase deficiency; PNPO deficiency
status epilepticus
General
chronic neurologic disease
seizure; epileptic seizure
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