4.2 Article

Assessing the depth of dexmedetomidine-induced sedation with electroencephalogram (EEG)-based spectral entropy

Journal

ACTA ANAESTHESIOLOGICA SCANDINAVICA
Volume 51, Issue 1, Pages 22-30

Publisher

WILEY
DOI: 10.1111/j.1399-6576.2006.01174.x

Keywords

alpha(2)-adrenergic agonists; dexmedetomidine; electroencephalogram; electroencephalogram-based spectral entropy; intensive care unit; monitoring; sedation

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Background Adequate sedation of critically ill patients improves the outcome of intensive care. Maintaining an optimal level of sedation in the intensive care unit (ICU) is difficult because of a lack of appropriate monitoring methods to guide drug dosing. Dexmedetomidine, a selective alpha(2)-adrenoceptor agonist, has recently been introduced for the sedation of ICU patients. This study investigated the utility of electroencephalogram (EEG)-based spectral entropy monitoring (with M-ENTROPY (TM), GE Healthcare, Helsinki, Finland) for the assessment of dexmedetomidine-induced sedation. Methods Eleven healthy, non-smoking men, aged 23.9 +/- 2.5 years (mean +/- standard deviation), were recruited. Spectral entropy was recorded before and during low (0.5 ng/ml) and high (5 ng/ml) plasma concentrations of dexmedetomidine. At the end of the infusion, subjects were awakened by verbal command and light shaking. Results Spectral entropy decreased from 84 +/- 5 to 66 +/- 16 (P = 0.029) during low dexmedetomidine levels and from 84 +/- 5 to 20 +/- 12 (P < 0.001) during high dexmedetomidine levels. Transitions during loss and regaining of consciousness were analysed separately. Entropy decreased from 76 +/- 8 before to 43 +/- 10 (P < 0.001) after loss of consciousness, and increased from 14 +/- 4 to 63 +/- 13 (P < 0.001) on regaining of consciousness. These changes were consistent across all subjects. Prediction probability and sensitivity values indicated a high predictive performance of the method. Conclusion The depth of dexmedetomidine-induced sedation can be monitored with EEG-based spectral entropy. These results should be confirmed in a clinical setting.

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