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Automated quantification of spike-wave activity may be used to predict the development of electrical status epilepticus in sleep (ESES) in children with perinatal stroke.
- Source :
-
Clinical Neurophysiology . Jan2021, Vol. 132 Issue 1, p146-153. 8p. - Publication Year :
- 2021
-
Abstract
- • Patients with ESES show significantly higher pre-diagnosis spike-frequency than those without ESES. • Stroke patients with ESES show significantly lower pre-diagnosis delta power than those without ESES. • Using spike-frequency, clinicians may be able to identify patients at risk of developing ESES. Continuous spike and wave in slow-wave sleep (CSWS), an epileptic encephalopathy, occurs after perinatal stroke where it is associated with cognitive decline. CSWS features a distinct EEG pattern, electrical status epilepticus in sleep (ESES). Biomarkers for the prediction of ESES have not been identified but will facilitate earlier diagnosis and treatment. We hypothesized that spike-frequency and differences in power spectra would be predictive of subsequent ESES. A cross-sectional study comparing EEG spike-frequency and Power before the development of ESES in patients with perinatal stroke, patients with focal epilepsy, and appropriate controls. 43 patients met the inclusion criteria; 11 stroke-ESES, 10 stroke controls, 14 epilepsy-ESES, 8 epilepsy controls. ESES patients had higher pre-diagnosis mean spike-frequency (24.0 ± 24 versus 6.6 ± 9.1 SW/min, p = 0.002) than patients that did not develop ESES; these differences present ~ 3 years before ESES diagnosis. Pre-diagnosis, normalized delta power (1–4 Hz) was higher in the stroke-ESES group (105.7 ± 58 dB/Hz) compared to stroke controls (57.4 ± 45 dB/Hz, p = 0.036). Spike-frequency and delta power may represent EEG biomarkers of the risk of developing ESES in children with perinatal stroke. EEG biomarkers may be used by clinicians to assess which patients are more at-risk for ESES. Using spike-frequency, clinicians may be able to identify patients at risk of developing ESES. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 13882457
- Volume :
- 132
- Issue :
- 1
- Database :
- Academic Search Index
- Journal :
- Clinical Neurophysiology
- Publication Type :
- Academic Journal
- Accession number :
- 147964293
- Full Text :
- https://doi.org/10.1016/j.clinph.2020.11.003