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Correspondence |



* University of British Columbia, Vancouver, Canada
University of Ottawa, Ottawa, Canada
McMaster University, Hamilton, Canada E-mail: pchoi{at}vanhosp.bc.ca
We thank Dr. Donati for his interest in our study.1 The assessment of the intubating conditions in our study was based, in part, on the guidelines recommended at the 1994 consensus conference.2 In the interest of improving the interpretation of our results and permitting future comparisons, we have re-examined the data, which are reported as "excellent", "good", and "poor" based on the consensus conference definitions (Table
). Data on intubating conditions were incomplete in six patients (three in each group) and were excluded from the analysis. We did not find a statistically significant difference in the intubating conditions between the two groups (
2 = 1.273; P = 0.53). The type of surgery did not affect these findings. In addition, we performed sensitivity analyses in which we allocated the missing patients in the sevoflurane group to the "poor" category and the missing patients in the propofol group to the "excellent" category and vice versa. There were no statistically significant differences in intubating conditions between the two groups in both sensitivity analyses.
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References
1 Yang H, Choi PT, McChesney J, Buckley N. Induction with sevoflurane-remifentanil is comparable to propofol-fentanyl-rocuronium in PONV after laparoscopic surgery. Can J Anesth 2004; 51: 6607.
2 Viby-Mogensen J, Engbaek J, Eriksson LI, et al. Good clinical research practice (GCRP) in pharmacodynamic studies of neuromuscular blocking agents. Acta Anaesthesiol Scand 1996; 40: 5974.[Medline]
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