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Table 4 The Richmond Agitation Sedation scores at 10, 20, 30, and 60 min after extubation in the two groups. The RASS scores in the PRD group were significantly lower than that in the PR group at t1, t2, t3(P < 0.001). The incidence of EA was significantly lower in the PRD group than in the PR group at t1 (10.0% [6/54] vs. 40.0% [24/36]), t2 (3.3% [2/58] vs. 40.0% [24/36]), t3 (0.0% [0/60] vs. 23.3% [14/46])

From: The effects of remifentanil-propofol combined with dexmedetomidine on cognitive dysfunction in elderly patients after ureteroscopic holmium laser lithotripsy: a double-blind randomized controlled trial

Time points

Group

− 1

0

1

2

3

X2

P values

t1

PR

0

10

26

14

10

42.329

0.000*

PRD

12

25

17

6

0

t2

PR

0

17

19

16

8

54.262

0.000*

PRD

21

23

14

2

0

t3

PR

5

13

28

14

0

48.415

0.000*

PRD

14

38

8

0

0

t4

PR

7

36

17

0

0

2.930

0.231

PRD

7

42

9

0

0

  1. Number of patients
  2. PR propofol-remifentanil, PRD propofol-remifentanil and dexmedetomidine, t1 10 min after extubation, t2 20 min after extubation, t3 30 min after extubation, t4 60 min after extubation
  3. *P < 0.001 vs. the PR group