Volume 40, Issue 11 pp. 1593-1601

Continuous Spike-and-Wave Activity During Slow-Wave Sleep: Syndrome or EEG Pattern?

Pierangelo Veggiotti

Corresponding Author

Pierangelo Veggiotti

Child Neuropsychiatry Division, Neurological Institute Casimiro Mondino Foundation IRCCS, University of Pavia, Pavia

Address correspondence and reprint requests to Dr. P. Veggiotti at Child Neuropsychiatry Division, Neurological Institute Casimiro Mondino Foundation University of Pavia, Via Palestro n 3, 27100 Pavia, Italy. E-mail:[email protected]Search for more papers by this author
Francesca Beccaria

Francesca Beccaria

Child Neuropsychiatry Division, Ospedale C. Poma, Mantova

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Renzo Guerrini

Renzo Guerrini

Institute of Child Neurology and Psychiatry, University of Pisa-IRCCS Stella Maris Foundation, Pisa, Italy

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Giuseppe Capovilla

Giuseppe Capovilla

Child Neuropsychiatry Division, Ospedale C. Poma, Mantova

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Giovanni Lanzi

Giovanni Lanzi

Child Neuropsychiatry Division, Neurological Institute Casimiro Mondino Foundation IRCCS, University of Pavia, Pavia

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First published: 02 August 2005
Citations: 82

Abstract

Summary: Purpose: We reviewed the electroclinical pictures and clinical characteristics of 32 patients with continuous spike-and-wave activity during slow sleep (CSWS) to ascertain to what extent this electroencephalogram (EEG) pattern is associated with the age-related CSWS syndrome as defined by the International League Against Epilepsy (ILAE) International Classification or with different clinical settings.

Methods: We reviewed clinical and EEG characteristics of 32 CSWS patients.

Results: In all patients, detection of CSWS coincided with a worsening of neurologic status. Ten (34%) patients had the typical features of CSWS syndrome, four were classified as having Landau-Kleffner syndrome, and three had acquired opercular syndromes. The remaining 15 patients, all with symptomatic epilepsy, had CSWS, which lasted for variable periods and might be related to inappropriate drug choice. Three patients of this group had unilateral CSWS and exhibited worsening of spontaneous movements in the hemibody contra-lateral to CSWS activity lasting for a few hours after awakening.

Conclusions: Our data show that a number of factors can intervene in the genesis of CSWS, which may explain the variability of the associated clinical conditions. In view of this etiologic heterogeneity, it is not possible to classify all the patients with CSWS as having the CSWS syndrome. Therefore, the CSWS syndrome should be considered a category embracing a limited group of patients, whereas the EEG pattern of CSWS is seen commonly in various clinical conditions.

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