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. 2004 Dec;8(6):R483-90.
doi: 10.1186/cc2984. Epub 2004 Oct 22.

The effect of interruption to propofol sedation on auditory event-related potentials and electroencephalogram in intensive care patients

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The effect of interruption to propofol sedation on auditory event-related potentials and electroencephalogram in intensive care patients

Heidi Yppärilä et al. Crit Care. 2004 Dec.

Abstract

Introduction: In this observational pilot study we evaluated the electroencephalogram (EEG) and auditory event-related potentials (ERPs) before and after discontinuation of propofol sedation in neurologically intact intensive care patients.

Methods: Nineteen intensive care unit patients received a propofol infusion in accordance with a sedation protocol. The EEG signal and the ERPs were measured at the frontal region (Fz) and central region (Cz), both during propofol sedation and after cessation of infusion when the sedative effects had subsided. The EEG signal was subjected to power spectral estimation, and the total root mean squared power and spectral edge frequency 95% were computed. For ERPs, we used an oddball paradigm to obtain the N100 and the mismatch negativity components.

Results: Despite considerable individual variability, the root mean squared power at Cz and Fz (P = 0.004 and P = 0.005, respectively) and the amplitude of the N100 component in response to the standard stimulus at Fz (P = 0.022) increased significantly after interruption to sedation. The amplitude of the N100 component (at Cz and Fz) was the only parameter that differed between sedation levels during propofol sedation (deep versus moderate versus light sedation: P = 0.016 and P = 0.008 for Cz and Fz, respectively). None of the computed parameters correlated with duration of propofol infusion.

Conclusion: Our findings suggest that use of ERPs, especially the N100 potential, may help to differentiate between levels of sedation. Thus, they may represent a useful complement to clinical sedation scales in the monitoring of sedation status over time in a heterogeneous group of neurologically intact intensive care patients.

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Figures

Figure 1
Figure 1
(a) The middle-latency auditory evoked potential (MLAEP) components Na, Pa, and Nb appear 10–50 ms after the onset of auditory stimulus. (b) N100 is the most prominent event-related potential (ERP) component. The thick line is the N100 for standard stimuli (N100 S) and the thin line is the N100 for deviant stimuli (N100 D). (c) The mismatch negativity (MMN) curve is obtained as a difference curve N100 D–N100 S. The MMN is the negative area under the curve between 100 and 250 ms.
Figure 2
Figure 2
Average and individual root mean squared (RMS) power and spectral edge frequency 95% (SEF95) values during and after discontinuation of propofol infusion in the (a, c) frontal (Fz) and (b, d) central (Cz) regions. Lines connect values obtained from the same patient; black squares with vertical lines indicate the mean ± standard deviation. Individual sedation levels obtained with the Sedation–Agitation Scale (SAS): white spheres: SAS 4, gray spheres: SAS 3, black spheres: SAS2. *Significantly different from 'propofol on'.
Figure 3
Figure 3
Average and individual N100 standard amplitude and mismatch negativity (MMN) values during and after discontinuation of propofol infusion in the (a, c) frontal (Fz) and (b, d) central (Cz) regions. Lines connect values obtained from the same patient; black squares with vertical lines indicate the mean ± standard deviation. Individual sedation levels obtained with the Sedation–Agitation Scale (SAS): white spheres: SAS 4, gray spheres: SAS 3, black spheres: SAS2. *Significantly different from 'propofol on'.

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