Electrodiagnostic applications of somatosensory evoked high-frequency EEG oscillations: Technical considerations.

Brain Res Bull

Institute of Neuroscience, The Medical School, Newcastle University, NE2 4HH, UK; Department of Neurology, Royal Victoria Infirmary, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, NE1 4LP, UK; Department of Clinical Neurophysiology, Royal Victoria Infirmary, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, NE1 4LP, UK. Electronic address:

Published: March 2018

AI Article Synopsis

  • High frequency oscillations (HFOs) in somatosensory evoked potentials (SEPs) are often overlooked in standard clinical recordings, but they could offer valuable diagnostic insights for patients, especially those with hypoxic ischemic encephalopathy (HIE) in the ICU.
  • In a study with 17 healthy subjects, standard clinical recording techniques detected SEP-HFOs in 65% of participants, but when more sensitive methods were used, all subjects showed HFOs, indicating that current techniques may miss important data.
  • Enhancing the sensitivity of SEP recordings through better electrode density could help in identifying HFOs more reliably, potentially improving the understanding and treatment of neurological conditions like HIE.

Article Abstract

Introduction: High frequency oscillations (HFOs) embedded within the somatosensory evoked potential (SEP) are not routinely recorded/measured as part of standard clinical SEPs. However, HFOs could provide important additional diagnostic/prognostic information in various patient groups in whom SEPs are tested routinely. One area is the management of patients with hypoxic ischaemic encephalopathy (HIE) in the intensive care unit (ICU). However, the sensitivity of standard clinical SEP recording techniques for detecting HFOs is unknown.

Methods: SEPs were recorded using routine clinical methods in 17 healthy subjects (median nerve stimulation; 0.5 ms pulse width; 5 Hz; maximum 4000 stimuli) in an unshielded laboratory. Bipolar EEG recordings were acquired (gain 50 k; bandpass 3Hz-2 kHz; sampling rate 5 kHz; non-inverting electrode 2 cm anterior to C3/C4; inverting electrode 2 cm posterior to C3/C4). Data analysis was performed in MATLAB.

Results: SEP-HFOs were detected in 65% of controls using standard clinical recording techniques. In 3 controls without significant HFOs, experiments were repeated using a linear electrode array with higher spatial sampling frequency. SEP-HFOs were observed in all 3 subjects.

Conclusions: Currently standard clinical methods of recording SEPs are not sufficiently sensitive to permit the inclusion of SEP-HFOs in routine clinical diagnostic/prognostic assessments. Whilst an increase in the number/density of EEG electrodes should improve the sensitivity for detecting SEP-HFOs, this requires confirmation. By improving and standardising clinical SEP recording protocols to permit the acquisition/analysis of SEP-HFOs, it should be possible to gain important insights into the pathophysiology of neurological disorders and refine the management of conditions such as HIE.

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http://dx.doi.org/10.1016/j.brainresbull.2018.01.011DOI Listing

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