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Table 3 Bispectral index and haemodynamic data in the two study groups

From: Effect-site concentration of propofol required for LMA-Supreme™ insertion with and without remifentanil: a randomized controlled trial

Variable

 

Propofol + saline

Propofol + remifentanil

(n = 32) [Mean % difference from baseline]

(n = 26) [Mean % difference from baseline]

BIS

Baseline

96 (3)

97 (2)

Before SLMA insertion*, **

36 (12) [63 %]

53 (14) [45 %]

1 min after SLMA insertion*, **

37 (15) [64 %]

51 (15) [47 %]

6 min after SLMA insertion*, **

28 (9) [71 %]

42 (16) [57 %]

Systolic BP (mmHg)

Baseline

125 (15)

131 (15)

Before SLMA insertion*, **

108 (13) [14 %]

95 (15) [27 %]

1 min after SLMA insertion*, **

111 (17) [11 %]

94 (15) [27 %]

6 min after SLMA insertion*

97 (14) [23 %]

92 (11) [29 %]

Diastolic BP (mmHg)

Baseline

76 (10)

78 (12)

Before SLMA insertion*, **

66 (11) [12 %]

54 (12) [29 %]

1 min after SLMA insertion*, **

68 (11) [12 %]

56 (12) [29 %]

6 min after SLMA insertion*

56 (11) [26 %]

55 (9) [28 %]

Heart rate (bpm)

Baseline

72 (18)

71 (10)

Before SLMA insertion*, **

71 (8) [0.01 %]

58 (9) [18 %]

1 min after SLMA insertion*, **

74 (12) [0,03 %]

58 (10) [18 %]

6 min after SLMA insertion*, **

62 (10) [14 %]

54 (8) [24 %]

  1. Data are expressed as mean (SD)
  2. BIS bispectral index, BP blood pressure, SD standard deviation
  3. *p < 0.05; significant difference from baseline (difference within the group)
  4. **p < 0.05; significant difference between the propofol + saline and propofol + remifentanil groups by ANOVA with repeated measurements