Criteria

Commission for Classification and Terminology of the International League Against Epilepsy (ILAE)​[1][2]​​​​[3]​​

A generalised tonic-clonic seizure (GTCS) is clinically identified by a discrete and typically self-limiting episode involving convulsive activity on both sides of the body with impairment of consciousness, beginning with a tonic phase followed by a clonic phase. An electroencephalogram (EEG) may be utilised to confirm generalised epileptiform activity; however, given the limited time course of a GTCS, this is rarely employed.

A diagnosis of epilepsy is made after two seizures of any type that had no clear provoking factor. Even a single seizure warrants thorough investigation, and a diagnosis of epilepsy can be made after a first seizure if testing suggests the risk of recurrence is similar to that after a second unprovoked seizure (>60%).[53] Any abnormal study (e.g., EEG or magnetic resonance imaging [MRI]) indicates an increased likelihood of epilepsy, even if a second seizure has not yet occurred.

EEG and MRI are indicated for all patients with a GTCS in order to classify the epilepsy syndrome.[44]​​ An EEG may reveal evidence of lateralising or localising epileptiform abnormalities, which may suggest focal-onset epilepsy. The EEG can also provide evidence of symmetrical, widespread abnormalities that are suggestive of generalised-onset epilepsy. Similarly, MRI of the brain can reveal structural lesions that suggest certain epilepsy syndromes.

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