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Outcomes of newly diagnosed idiopathic generalized epilepsy syndromes in a non-pediatric setting

Authors


Martin J. Brodie, Epilepsy Unit, Western Infirmary, Glasgow G11 6NT, UK
Tel.: +44 141 211 2572
Fax: +44 141 334 9329
e-mail: martin.j.brodie@clinmed.gla.ac.uk

Abstract

Introduction –  The prognosis of idiopathic generalized epilepsy syndromes (IGES) in the adult setting may vary from that in children owing to differences in genetic, environmental and lifestyle factors.

Methods –  All patients diagnosed with epilepsy at the Epilepsy Unit, Western Infirmary, Glasgow, between 1981 and 2001 were reviewed.

Results –  Of 890 patients, 118 (13%) met the criteria for IGES. Outcomes were known for 103, 66 (64%) of whom achieved remission. The responder rate with sodium valproate was superior (66% vs 45%, P = 0.073) to that with lamotrigine (LTG) particularly in patients with juvenile myoclonic epilepsies (75% vs 39%, P = 0.014). History of febrile seizures was the only factor associated with reduced likelihood of remission (P = 0.032)

Conclusions –  Idiopathic generalized epilepsy syndromes constituted 13% of cases in a largely adult cohort of newly diagnosed epilepsy, most of whom achieved remission usually with a single antiepileptic drug. History of febrile seizures was associated with a poorer outcome.

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