Quiz: Test Your Knowledge of Epilepsy and Seizure-related Conditions
Amy Kao, MD
|January 12, 2016
Epilepsy is a medical disorder marked by recurrent, unprovoked seizures. Epilepsy is defined as a brain disorder characterized by an enduring predisposition to generate epileptic seizures and by the neurobiologic, cognitive, psychological, and social consequences of this condition. In 2014, the International League Against Epilepsy Epilepsy Guidelines Task Force expanded the practical definition of epilepsy to include having at least two unprovoked seizures more than 24 hours apart, having one unprovoked seizure and a probability of further seizures of at least 60%, and a diagnosis of an epilepsy syndrome. The clinical signs and symptoms of seizures depend on the location of the epileptic discharges in the cerebral cortex and the extent and pattern of the propagation of the epileptic discharges in the brain. Do you know what to look for and best practices? Test yourself with our short quiz.
Which of the following is the most common known cause of epilepsy in young adults?
Strokes
Head trauma
Tumors
Infection
In a substantial number of cases, the cause of epilepsy remains unknown. Identified causes tend to vary with patient age. Inherited syndromes, congenital brain malformations, infection, and head trauma are leading causes in children. Head trauma is the most common known cause in young adults. Strokes, tumors, and head trauma become more frequent in middle age, with stroke becoming the most common cause in the elderly, along with Alzheimer disease and other degenerative conditions.
Which of the following types of seizures consist of brief episodes (< 20 sec) of impaired consciousness with no aura or postictal confusion?
Myoclonic seizures
Atonic seizures
Absence seizures
Primary generalized tonic-clonic seizures
Absence seizures are brief episodes of impaired consciousness with no aura or postictal confusion. They typically last less than 20 seconds and are accompanied by few or no automatisms. Myoclonic seizures consist of brief arrhythmic jerking motor movements that last less than 1 second and often cluster within a few minutes. If the seizures evolve into rhythmic jerking movements, they are classified as evolving into a clonic seizure. Clonic seizures consist of rhythmic jerking motor movements with or without impairment of consciousness; they can have a focal origin. Focal seizures are classified as simple or complex partial seizures. The typical generalized clonic seizures simultaneously involve the upper and lower extremities. Tonic seizures consist of sudden-onset tonic extension or flexion of the head, trunk, and/or extremities for several seconds. These seizures typically occur in relation to drowsiness, shortly after patients fall asleep, or just after they awaken. Atonic seizures are also called "drop attacks." These seizures typically occur in people with clinically significant neurologic abnormalities (although they may occur in developmentally normal children as part of an idiopathic epilepsy syndrome) and consist of brief loss of postural tone, often resulting in falls and injuries (hence, some patients need helmets).
For more on the presentation of epilepsy, read here.
Which of the following is considered to be a localization-related epileptic syndrome?
Mesial temporal lobe sclerosis
Juvenile absence epilepsy
Lennox-Gastaut syndrome
Juvenile myoclonic epilepsy
The current system comprises two major categories: localization-related syndromes and generalized-onset syndromes. Physicians ideally would classify their patients' seizures by using the classification for seizure types and make a syndromic diagnosis, if possible.
Localization-related epilepsies and syndromes include the following:
Idiopathic, with age-related onset
Benign childhood epilepsy with centrotemporal spikes
Childhood epilepsy with occipital paroxysms
Symptomatic
Mesial temporal lobe sclerosis
Generalized epilepsies and syndromes include the following:
Idiopathic, with age-related onset
Benign neonatal familial convulsions
Benign neonatal convulsions
Benign myoclonic epilepsy of infancy
Childhood absence epilepsy (pyknolepsy)
Juvenile absence epilepsy
Juvenile myoclonic epilepsy (JME)
Epilepsy with grand mal seizures on awakening
Idiopathic and/or symptomatic infantile spasms
Lennox-Gastaut syndrome
Epilepsy with myoclonic astatic seizures
Epilepsy with myoclonic absences
Symptomatic
For more on the presentation of epilepsy, read here.
Which of the following is the criterion standard for classifying the type of seizure or syndrome or for diagnosing pseudoseizures?
MRI
CT scanning
Positron emission tomography (PET) scanning
Video electroencephalography (video EEG)
Video EEG monitoring is the criterion standard for classifying the type of seizure or syndrome or for diagnosing pseudoseizures. This study can be performed to rule out an epileptic etiology with a high degree of confidence if the patient has demonstrable impairment of consciousness during the spell in question, without abnormality on the EEG. Video EEG is also used to characterize the type of seizure and epileptic syndrome to optimize pharmacologic treatment and for presurgical workup.
Which of the following is not indicated in the treatment of absence seizures?
Ethosuximide
Valproic acid
Carbamazepine
Topiramate
A recent study determined that ethosuximide and valproic acid are superior in effectiveness compared with lamotrigine; valproic acid was found to have a higher rate of side effects. If absence seizures are present along with other seizure types (eg, generalized tonic-clonic seizures, myoclonic seizures), many neurologists would choose valproic acid, lamotrigine, or topiramate. Do not use carbamazepine, gabapentin, or tiagabine because these drugs may exacerbate absence seizures. It is uncertain whether pregabalin, a medication related to gabapentin, has the same risk.