The efficacy and safety of the routine use of target-controlled infusion of propofol for the sedation of patients undergoing transrectal ultrasound-guided prostate biopsy were assessed. The optimal level of sedation was also evaluated. A total of 250 patients were randomized into five groups according to sedation level determined by the Observer's Assessment of Alertness/Sedation (OAA/S) scale. As the level of sedation was increased, the overall pain and discomfort score decreased and the satisfaction rate tended to: increase, although hypoxia meant that intervention occurred more frequently at higher sedation levels. Target-controlled infusion of propofol provided safe and effective sedation during transrectal ultrasound-guided prostate biopsy, particularly if moderate sedation (OAA/S score of 3) was achieved. The effect-site concentration of propofol for this level of sedation was about 1.5 μg/ml. Copyright © 2007 Field House Publishing LLP.
CITATION STYLE
Park, J. Y., Park, S. J., Choi, S. U., Shin, H. W., Lee, H. W., Lim, H. J., … Chang, S. H. (2007). Target-controlled propofol infusion for sedation in patients undergoing transrectal ultrasound-guided prostate biopsy. Journal of International Medical Research, 35(6), 773–780. https://doi.org/10.1177/147323000703500605
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