Relationship between serum neuron-specific enolase and EEG after cardiac arrest: A reappraisal

Clin Neurophysiol. 2023 Jul:151:100-106. doi: 10.1016/j.clinph.2023.05.001. Epub 2023 May 12.

Abstract

Objective: Electroencephalogram (EEG) and serum neuron specific enolase (NSE) are frequently used prognosticators after cardiac arrest (CA). This study explored the association between NSE and EEG, considering the role of EEG timing, its background continuity, reactivity, occurrence of epileptiform discharges, and pre-defined malignancy degree.

Methods: Retrospective analysis including 445 consecutive adults from a prospective registry, surviving the first 24 hours after CA and undergoing multimodal evaluation. EEG were interpreted blinded to NSE results.

Results: Higher NSE was associated with poor EEG prognosticators, such as increasing malignancy, repetitive epileptiform discharges and lack of background reactivity, independently of EEG timing (including sedation and temperature). When stratified for background continuity, NSE was higher with repetitive epileptiform discharges, except in the case of suppressed EEGs. This relationship showed some variation according to the recording time.

Conclusions: Neuronal injury after CA, reflected by NSE, correlates with several EEG features: increasing EEG malignancy, lack of background reactivity, and presence of repetitive epileptiform discharges. The correlation between epileptiform discharges and NSE is influenced by underlying EEG background and timing.

Significance: This study, describing the complex interplay between serum NSE and epileptiform features, suggests that epileptiform discharges reflect neuronal injury particularly in non-suppressed EEG.

Keywords: Anoxic-ischemic encephalopathy; Background; Epileptiform; Prognosis; Reactivity.

MeSH terms

  • Adult
  • Coma*
  • Electroencephalography / methods
  • Heart Arrest* / complications
  • Heart Arrest* / diagnosis
  • Humans
  • Phosphopyruvate Hydratase
  • Prognosis
  • Retrospective Studies

Substances

  • Phosphopyruvate Hydratase