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Table 1 Characteristics of the study population (ICUs), outcomes and crude incidence rate ratios of intervention versus baseline periods, according to the study group

From: Central-line associated bloodstream infections in intensive care units before and after implementation of daily antiseptic bathing with chlorhexidine or octenidine: a post-hoc analysis of a cluster-randomised controlled trial

Parameter

Description

Study group

Chlorhexidine

Octenidine

Routine care (control arm)

Baseline

Intervention

Baseline

Intervention

Baseline

Intervention

ICUs

N

24

24

24

24

24

24

Patients

N

21,346

22,897

26,095

25,127

28,698

28,791

Patient days

N

75,593

85,135

92,597

90,820

98,726

103,356

CL days

N

46,011

54,305

60,430

58,656

66,670

70,068

Length of stay (days)b

Pooled mean

3.5

3.6

3.7

3.4

3.5

3.6

Median (IQR), P valuea

3.7 (2.6–4.6)

3.6 (2.7–4.2), 0.9179a

3.6 (2.7–4.5)

3.6 (2.7–4.5), 1.000a

3.3 (2.9–4.2)

3.3 (2.9–4.6), 0.7880a

CL use (%)b

Pooled mean

60.9

64.6

63.8

67.53

65.3

67.8

Median (IQR), P valuea

63.4 (55.6–77.5)

67.9 (55.8–77.6), 0.8366a

68.4 (45.3–78.5)

64.9 (43.7–77.5), 0.8528a

68.5 (60.0–76.8)

65.3 (58.6–79.1), 0.8200a

Mechanical ventilation (%)b

Pooled mean

34.4

30.8

37.7

35.5

31.9

36.9

Median (IQR), P valuea

33.2 (24.6–45.9)

33.1 (26.7–47.4), 0.8206a

28.2 (17.9–41.3)

30.1 (16.6–39.5), 0.9671a

32.2 (24.4–44.9)

34.5 (24.6–48.1), 0.8850a

Outcomes

       

 CLABSI with any pathogen

N

68

49

76

86

80

82

ID/1000 CL days (95% CI)

1.48 (1.15–1.87)

0.90 (0.67–1.19)

1.26 (0.99–1.57)

1.47 (1.17–1.81)

1.20 (0.95–1.49)

1.17 (0.93–1.45)

  Compared to baseline in each study group

IRR (95% CI), P value

1 = reference

0.61 (0.42–0.88), 0.0085

1 = reference

1.17 (0.86–1.59), 0.3298

1 = reference

0.98 (0.72–1.33), 0.8735

 CLABSI with gram-positive bacteria

N

45

28

51

72

52

55

ID/1000 CL days (95% CI)

0.98 (0.71–1.31)

0.52 (0.34–0.75)

0.84 (0.63–1.11)

1.23 (0.96–1.55)

0.78 (0.58–1.02)

0.79 (0.59–1.02)

  Compared to baseline in each study group

IRR (95% CI), P value

1 = reference

0.53 (0.33–0.85), 0.0078*

1 = reference

1.45 (1.02–2.08), 0.0407*

1 = reference

1.01 (0.69–1.47), 0.9737

 CLABSI with CoNS

N

25

11

31

43

25

26

ID/1000 CL days (95% CI)

0.54 (0.35–0.80)

0.20 (0.10–0.36)

0.51 (0.35–0.73)

0.73 (0.53–0.98)

0.38 (0.24–0.55)

0.37 (0.24–0.564)

  Compared to baseline in each study group

IRR (95% CI), P value

1 = reference

0.37 (0.18–0.76), 0.0064*

1 = reference

1.43 (0.90–2.27), 0.1297

1 = reference

0.99 (0.57–1.71), 0.9701

 CLABSI with gram-negative bacteria

N

11

12

16

12

14

22

ID/1000 CL days (95% CI)

0.24 (0.12–0.43)

0.22 (0.11–0.39)

0.27 (0.15–0.43)

0.21 (0.11–0.36)

0.21 (0.12–0.35)

0.31 (0.20–0.48)

  Compared to baseline in each study group

IRR (95% CI), P value

1 = reference

0.92 (0.41–2.10), 0.8504

1 = reference

0.77 (0.37–1.63), 0.4995

1 = reference

1.50 (0.77–2.92), 0.2393

  1. Baseline period included 12 months before the intervention was started. Parts of  the intervention period have been shown elsewhere [15]. CLABSI, central line associated bloodstream infection. CL, central line. 95% CI, 95% confidence interval. ID, incidence densities per 1000 CL days. IRR, incidence rate ratios calculated by Poisson regression comparing intervention period to baseline period in each study group. CoNS, coagulase-negative staphylococci. aP values based on comparison of intervention period to baseline period in each study group. bP values were not shown because there were no differences between the three groups during the intervention period. *P values < 0.05 were considered significant