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. 2023 May 31;131(2):348–359. doi: 10.1016/j.bja.2023.04.026

Table 2.

Experiment 1: awakenings and interviews, and achieved states, with mean measured drug plasma concentrations for those participants who achieved the state. ∗Four dexmedetomidine and four propofol experiments were terminated before UR3. R, responsiveness; sd, standard deviation; UR, unresponsiveness.

UR1, N of interviews/UR1, N of achieved states (%) UR1, mean drug concentration (sd) UR2, N of interviews/UR2, N of achieved states (%) UR2, mean drug concentration (sd) UR3, N of interviews/UR3, N of achieved states (%) UR3, mean drug concentration (sd) R3, mean drug concentration (sd) All R periods, N of interviews/all UR periods, N of achieved states (%)
Both drugs 29/39 (74.4) 16/17 (94.1) 31/31 (100) 76/87 (87.4)
Dexmedetomidine 16/20 (80.0) 1.80 (0.84) ng ml−1 14/15 (93.3) 1.65 (0.38) ng ml−1 16/16∗(100) 3.27 (1.32) ng ml−1 1.64 (0.64) ng ml−1 46/51 (90.2)
Propofol 13/19 (68.4) 1.48 (0.60) μg ml−1 2/2 (100) 0.96 (0.20) μg ml−1 15/15∗(100) 2.46 (0.77) μg ml−1 1.11 (0.28) μg ml−1 30/36 (83.3)