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Spike-Wave Index Assessment and Electro-Clinical Correlation in Patients with Encephalopathy Associated with Epileptic State During Slow Sleep (ESES / CSWS); Single-Center Experience.
Öztoprak, Ülkühan; Yayici Köken, Özlem; Aksoy, Erhan; Yüksel, Deniz.
Afiliação
  • Öztoprak Ü; University of Health Sciences, Dr. Sami Ulus Training and Research Hospital, Department of Pediatric Neurology, Ankara, Turkey. Electronic address: ulkuhantoprak@yahoo.com.
  • Yayici Köken Ö; Ankara City Hospital, Children's Hospital, Department of Pediatric Neurology, Ankara, Turkey. Electronic address: drozlemkoken@gmail.com.
  • Aksoy E; University of Health Sciences, Dr. Sami Ulus Training and Research Hospital, Department of Pediatric Neurology, Ankara, Turkey. Electronic address: aksoyerhan24@gmail.com.
  • Yüksel D; University of Health Sciences, Dr. Sami Ulus Training and Research Hospital, Department of Pediatric Neurology, Ankara, Turkey. Electronic address: drdeniz_yuksel@yahoo.com.tr.
Epilepsy Res ; 170: 106549, 2021 02.
Article em En | MEDLINE | ID: mdl-33450525
ABSTRACT

PURPOSE:

This study aimed to describe the electroclinical spectrum and neurocognitive outcome in children with epileptic encephalopathy with status epilepticus during sleep (ESES) according to the EEG patterns.

METHODS:

Records of 48 (19 males, 29 females) patients with ESES/CSWS syndrome were retrospectively evaluated for data on sleep and awake EEGs, psychometric tests, and brain MRI. Patients with a spike-wave index (SWI) of at least 50 % in the NREM sleep EEG were included in the study. Electrophysiologic findings were separated into two groups based on SWI SWI>85-100 % (typical ESES) and SWI < 85 % (atypical ESES). The neurocognitive prognosis was also evaluated in two groups; favorable and unfavorable.

RESULTS:

The median age at the onset of ESES was 6 years and 5 months and ranged from 3 to 13 years. The median duration of follow-up after the ESES diagnosis was 57 months (range 24-150 months). Etiology was evaluated in three groups symptomatic/structural, idiopathic, and unknown (cryptogenic). Twenty-seven (56.25 %) patients had atypical ESES patterns and 21 patients (43.75 %) had typical ESES patterns. Twenty-eight patients (58.3 %) had cognitive deterioration. Long term neurocognitive outcome was unfavorable in half of the patients. Symptomatic/structural etiology was more common in patients with unfavorable (p < 0.001) outcomes. The median age at the diagnosis of ESES (p < 0.001) was significantly earlier in the patients with unfavorable neurocognitive outcomes. The longer duration of ESES(p < 0.001), and the longer time between the onset of epilepsy and ESES (p = 0.039) was significantly associated with unfavorable outcomes. We found that patients with typical ESES had a higher risk for poor neurocognitive outcomes than patients with atypical ESES (OR 31.096 [1.565-617.696]).

CONCLUSION:

The long-term outcome of ESES is exceedingly variable. An unfavorable neurocognitive outcome seems to be related to ESES with a long-duration and early-onset epileptic activity, SWI ≥ 85 %, and etiology.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estado Epiléptico / Encefalopatias / Epilepsia Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estado Epiléptico / Encefalopatias / Epilepsia Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article