British Journal of Anaesthesia, Vol 75, Issue 4 441-446, Copyright © 1995 by The Board of Management and Trustees of the British Journal of Anaesthesia
OHG. Wilder-Smith, O. Hagon and E. Tassonyi
We studied EEG arousal after laryngoscopy and intubation with standardized
bolus induction of anaesthesia. Twenty patients were prospectively
allocated randomly to induction with propofol 3 mg kg-1 (n = 10) or
thiopentone (6 mg kg-1 (n = 10) and 50% nitrous oxide in oxygen.
Neuromuscular block was produced with vecuronium 0.2 mg kg-1 given 30 s
after induction. Three minutes after induction, laryngoscopy was performed
for 60 s, with intubation at 3 min 30 s, and study end at 5 min.
Nociception to laryngoscopy and intubation was followed by loss of low
(relative delta activity change: thiopentone -30%, propofol -7%; P <
0.05) and a shift to higher frequency EEG activity (beta activity change:
thiopentone +647%, propofol +61%; P < 0.05). This EEG arousal was
greater in the thiopentone group, despite the fact that EEG depression was
similar to that produced by propofol before laryngoscopy and intubation.
Propofol and thiopentone in combination with nitrous oxide had similar
cortical depressant effects, but propofol appeared to depress subcortical
nociceptive processing more than thiopentone. While the degree of cortical
EEG depression seems less useful for predicting reaction to subsequent
nociception, EEG arousal reactions may prove suitable for monitoring
intra-anaesthetic nociception and its modulation.
CLINICAL INVESTIGATIONS
EEG arousal during laryngoscopy and intubation: comparison of thiopentone or propofol supplemented with nitrous oxide
Department of Anaesthesiology, Geneva University Hospital, 24 rue Micheli-du-Crest, CH-1211 Geneva 14, Switzerland
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