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BJA Advance Access published online on October 12, 2008

British Journal of Anaesthesia, doi:10.1093/bja/aen290
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© The Board of Management and Trustees of the British Journal of Anaesthesia 2008. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

Permutation entropy of the electroencephalogram: a measure of anaesthetic drug effect

E. Olofsen1, J. W. Sleigh2,* and A. Dahan1

1 Department of Anesthesiology, Leiden University Medical Center, Leiden University, Leiden, The Netherlands
2 Department of Anaesthesiology, Waikato Clinical School, University of Auckland, Hamilton, New Zealand

* Corresponding author. E-mail: sleighj{at}waikatodhb.govt.nz

Background: It would be useful to have an open-source electroencephalographic (EEG) index of {gamma}-amino-butyric acid (GABA)-ergic anaesthetic drug effect that is resistant to eye-blink artifact, responds rapidly to changes in EEG pattern, and can be linked to underlying neurophysiological and neuropharmacological mechanisms that control the conscious state.

Methods: The EEG waveform can be described as a sequence of ordinal patterns. The permutation entropy (PE) describes the relative occurrence of each of these patterns. It is high ({approx}1.0) when the signal has predominantly high frequencies and low ({approx}0.4) when the signal consists of only low frequencies. The response of the PE to various computer-generated EEG-like waveforms was assessed. A composite PE index (CPEI) was developed, which was the sum of two simple PEs and included a small measurement-noise threshold (0.5 µV). We also applied the CPEI to two small pilot EEG data sets from patients receiving sevoflurane (n=21) or propofol (n=9) anaesthesia.

Results: With minimal pre-processing or artifact rejection, the CPEI reliably tracked the anaesthetic-related EEG changes, namely loss of high frequencies, spindle-like waves, and delta waves. Using NONMEM, it was possible to construct adequate pharmacokinetic–pharmacodynamic models from the data. The CPEI was comparable with models derived using the bispectral index [BIS R2=0.88 (0.08) vs CPEI R2=0.91 (0.06) for the propofol data] and M-entropy indices [M-entropy R2=0.91 (0.06) vs CPEI R2=0.87 (0.09) for the sevoflurane data].

Conclusions: PE of the EEG shows promise as a simple measure of GABAergic anaesthetic drug effect.

Keywords: anaesthesia, general; monitoring, electroencephalography; pharmacodynamics


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