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Table 3 Secondary endpoints of the study

From: Application of a protective sleeve is associated with decreased occupational anxiety during endotracheal intubation: a randomized controlled trial

Variables

Protective sleeve group (n = 30)

Control group (n = 30)

P- value

Patients’ oppressed feeling

0 (0)

0 (0)

1.000

Baseline oral odour score, n (%)

  

0.704

 0 to 2

27(90.00)

25(83.33)

 

 3 to 5

3(10.00)

5(16.67)

 

Perception of patients’ oral malodour

0 (0)

5 (16.67)

0.02*

Intubation time(s)

93 (75.75,125.50)

54 (41,83)

< 0.001*

MN distance (cm)

33 (30, 38.25)

36.5 (30.75,42)

0.122

Lifting strength scale, n (%)

  

0.182

 0 to 3

23 (76.67)

16 (53.33)

 

 4 to 6

4 (13.33)

10 (33.33)

 

 7 to 10

3 (10.00)

4 (13.33)

 

Waist discomfort, n (%)

  

1.000

 No

28 (93.33)

27 (90.00)

 

 Mild

2 (6.67)

3 (10.00)

 

 Moderate

0 (0)

0 (0)

 

 Severe

0 (0)

0 (0)

 

Shoulder discomfort, n (%)

  

0.237

 No

30 (100)

27 (90.00)

 

 Mild

0 (0)

3 (10.00)

 

 Moderate

0 (0)

0 (0)

 

 Severe

0 (0)

0 (0)

 

Satisfaction degree of operators, n (%)

  

0.016*

 Totally satisfied

8 (26.67)

1 (3.33)

 

 Relatively satisfied

22 (13.33)

28 (30.00)

 

 Unsatisfied

0(0)

1(3.33)

 
  1. Lifting strength was assessed by VAS: from 0 (no exertion) to 10 (maximal exertion)
  2. Waist and shoulder discomfort were judged by the 4-point scale: No, Mild, Moderate and Severe
  3. Satisfaction degree was graded as Totally satisfied, Relatively satisfied and Unsatisfied
  4. Values are mean ± SD, median (inter-quartile range) or n (%), *P-value < 0.05