Ohg. Wildersmith et al., EEG AROUSAL DURING LARYNGOSCOPY AND INTUBATION - COMPARISON OF THIOPENTONE OR PROPOFOL SUPPLEMENTED WITH NITROUS-OXIDE, British Journal of Anaesthesia, 75(4), 1995, pp. 441-446
We studied EEG arousal after laryngoscopy and intubation with standard
ized bolus induction of anaesthesia. Twenty patients were prospectivel
y allocated randomly to induction with propofol 3 mg kg(-1) (n = 10) o
r thiopentone (6 mg kg(-1) (n = 10) and 50% nitrous oxide in oxygen. N
euromuscular block was produced with vecuronium 0.2 mg kg(-1) given 30
s after induction. Three minutes after induction, laryngoscopy was per
formed for 60 s, with intubation at 3 min 30 s, and study end at 5 min
. Nociception to laryngoscopy and intubation was followed by lass of l
ow (relative delta activity change: thiopentone -30%, propofol -7%; P
< 0.05) and a shift to higher frequency EEG activity (beta activity ch
ange: 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 intu
bation. 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 d
egree of cortical EEG depression seems less useful for predicting reac
tion to subsequent nociception, EEG arousal reactions may prove suitab
le for monitoring intra-anaesthetic nociception and its modulation.