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From the Epilepsy Unit (Drs. Semah, Adam, Broglin, Arzimanoglou, Bazin, Cavalcanti, and Baulac), Clinique P. Castaigne, Hôpital de la Salpêtrière, Paris; SHFJ (Dr. Semah), CEA, Orsay; and the Department of Medical Information (Dr. Picot), Hôpital Lapeyronie, Montpellier, France.
Address correspondence and reprint requests to Dr. Franck Semah, SHFJ, CEA, 4 Place du Général Leclerc, 91401 Orsay Cedex, France.
Background: We investigated the prognostic value of the type of epilepsies and epileptic syndromes for seizure recurrence. In patients with partial epilepsy, we focused on the prognostic value of any structural brain abnormality and of the location of the epileptogenic region.
Methods: A total of 2,200 adult outpatients were included in a hospital-based observational survey, with a follow-up of 1 to 7 years. Twenty-two percent of the patients exhibited generalized epilepsy, 62% partial epilepsy, and 16% undetermined epilepsy.
Results: Seizure control (>1 year without seizure) was achieved in 82% of patients who had idiopathic generalized epilepsy, 35% of those with symptomatic partial epilepsy, 45% of those with cryptogenic partial epilepsy, and 11% of those with partial epilepsy associated with hippocampal sclerosis (HS). Temporal lobe epilepsy (TLE) was the most refractory partial epilepsy, with only 20% of such patients remaining seizure free, compared with 36% of extra-TLE patients. In partial epilepsy, HS, cerebral dysgenesis, and dual pathology (HS and another lesion) were associated with a low rate of seizure-free patients (11%, 24%, and 3%, respectively). No significant difference in seizure control was found between patients with extra-TLE and those with TLE and no HS.
Conclusions: In adults, partial epilepsy is more difficult to treat than idiopathic generalized epilepsy. In patients who have partial epilepsy, the location of the epileptogenic zone does not seem to be a determining factor. Brain abnormalities-especially HS, either alone or associated with another lesion-are a major prognostic factor.
Received December 3, 1997. Accepted in final form July 2, 1998.
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