Long-term evolution of neuropsychological competences in encephalopathy with status epilepticus during sleep: A variable prognosis
Articolo
Data di Pubblicazione:
2013
Abstract:
PURPOSE:
The aim of this study was to evaluate the long-term cognitive outcome in children with continuous spikes and waves during slow wave sleep (CSWS syndrome).
METHODS:
We reviewed the neuropsychological tests of 25 children diagnosed with CSWS between 1987 and 2010 and with a mean follow-up of 13.5 years.
KEY FINDINGS:
Cognitive performances worsened during CSWS in virtually all patients. Seven patients (28%) with nonlesional epilepsy had a positive outcome; three patients (12%) showed persistence of motor deficit without involvement of cognitive functions; and seven patients (28%) who presented a long duration of CSWS (mean = 28.1 months) had a negative cognitive outcome. In 6 patients (24%) with structural or metabolic disorders before CSWS onset cognitive outcomes did not change; 2 patients (8%) had a negative outcome irrespective of the duration or presence of other neurologic disorders before CSWS onset. Forty-four percent of children with CSWS demonstrated permanent cognitive impairment.
SIGNIFICANCE:
The long-term outcome of CSWS syndrome is variable and seems to depend on treatment response, disease duration, and underlying etiology
The aim of this study was to evaluate the long-term cognitive outcome in children with continuous spikes and waves during slow wave sleep (CSWS syndrome).
METHODS:
We reviewed the neuropsychological tests of 25 children diagnosed with CSWS between 1987 and 2010 and with a mean follow-up of 13.5 years.
KEY FINDINGS:
Cognitive performances worsened during CSWS in virtually all patients. Seven patients (28%) with nonlesional epilepsy had a positive outcome; three patients (12%) showed persistence of motor deficit without involvement of cognitive functions; and seven patients (28%) who presented a long duration of CSWS (mean = 28.1 months) had a negative cognitive outcome. In 6 patients (24%) with structural or metabolic disorders before CSWS onset cognitive outcomes did not change; 2 patients (8%) had a negative outcome irrespective of the duration or presence of other neurologic disorders before CSWS onset. Forty-four percent of children with CSWS demonstrated permanent cognitive impairment.
SIGNIFICANCE:
The long-term outcome of CSWS syndrome is variable and seems to depend on treatment response, disease duration, and underlying etiology
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
CSWS; ESES; Epilepsy; Neuropsychological evaluation; Outcome
Elenco autori:
Maria C., Pera; Daniela, Brazzo; Nausicaa, Altieri; Balottin, Umberto; Veggiotti, Pierangelo
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