Background. Many anaesthetists are deterred from using total i.v. anaesthesia because of uncertainty over the concentration of propofol required to prevent awareness. We predicted blood and effect-site concentrations of propofol at two clinical end-points: loss of consciousness and no response to a painful stimulus. Methods. Forty unpremedicated Caucasian patients were anaesthetized with i.v. propofol delivered by a Diprifusor target-controlled infusion (TCI). Bispectral index (BIS) and auditory evoked potential index (AEPex) were measured and blood and effect-site propofol concentrations were predicted. Logistic regression was used to estimate population values for predicted blood and effect-site propofol concentrations at the clinical end-points and to correlate these with BIS and AEPex. Results. The effect-site EC50 at loss of consciousness was 2.8 μm ml-1 with an EC05 and an EC95 of 1.5 and 4.1 μm ml-1, respectively. The predicted EC50 when there was no response to a tetanic stimulus was 5.2 μm ml-1 with an EC05 and an EC95 of 3.1 and 7.2 μm ml-1, respectively. Conclusions. Unconsciousness and lack of response to a painful stimulus occur within a defined range of effect-site concentrations, predicted by Diprifusor TCI software.
CITATION STYLE
Milne, S. E., Troy, A., Irwin, M. G., & Kenny, G. N. C. (2003). Relationship between bispectral index, auditory evoked potential index and effect-site EC50 for propofol at two clinical end-points. British Journal of Anaesthesia, 90(2), 127–131. https://doi.org/10.1093/bja/aeg035
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