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Table 2
PROPOSED DIAGNOSTIC SCHEME FOR PEOPLE WITH EPILEPTIC
SEIZURES AND WITH EPILEPSY
Epileptic seizures and epilepsy syndromes are to be described and categorized
according to a system that utilizes standardized terminology, and that
is sufficiently flexible to take into account the following practical
and dynamic aspects of epilepsy diagnosis:
- Some patients cannot be given a recognized syndromic diagnosis.
- Seizure types and syndromes change as new information is obtained.
- Complete and detailed descriptions of ictal phenomenology are not
always necessary.
- Multiple classification schemes can, and should, be designed for specific
purposes (e.g. communication and teaching; therapeutic trials; epidemiological
investigations; selection of surgical candidates; basic research; genetic
characterizations).
This diagnostic scheme is divided into five parts, or Axes, organized
to facilitate a logical clinical approach to the development of hypotheses
necessary to determine the diagnostic studies and therapeutic strategies
to be undertaken in individual patients:
Axis 1: Ictal phenomenology - from the Glossary of Descriptive Ictal
Terminology can be used to describe ictal events with any degree of detail
needed.
Axis 2: Seizure type - from the List of Epileptic Seizures. Localization
within the brain and precipitating stimuli for reflex seizures should
be specified when appropriate.
Axis 3: Syndrome - from the List of Epilepsy Syndromes, with the understanding
that a syndromic diagnosis may not always be possible.
Axis 4: Etiology - from a Classification of Diseases Frequently Associated
with Epileptic Seizures or epilepsy syndromes when possible, genetic defects,
or specific pathological substrates for symptomatic focal epilepsies.
Axis 5: Impairment - this optional, but often useful, additional diagnostic
parameter can be derived from an impairment classification adapted from
the WHO ICIDH-2.
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