Skip to main content

Table 1 Clinical and patient characteristics

From: A clinical evaluation of two central venous catheter stabilization systems

 

Suture group (n = 86 patients)

Suture-free group (n = 85 patients)

p value

Median (IQR) age (years)

66 (56.3; 74)

62 (51; 72)

0.222a

Median (IQR) APACHE II score

23 (15.5; 32)

21 (14; 29)

0.271a

Median (IQR) BMI

26.7 (23.0:31.9) (n = 80)

26.8 (24.3:30.5) (n = 73)

0.509a

Male-to-female ratio (%)

59:27 (68.6:31.4)

68:17 (80.0:20.0)

0.115b

Number of patients (%) receiving

Sedative agents

38 (44.2)

47 (55.3)

0.170b

Paralysing agents

11 (12.8)

7 (8.2)

0.456b

Endotracheal tube

43 (50.0)

50 (58.8)

0.284b

Tracheostomy

7 (8.1)

16 (18.8)

0.046b

Mechanical ventilation

46 (53.5)

55 (64.7)

0.162b

Non-invasive ventilation

18 (20.9)

15 (17.6)

0.699b

Haemodialysis

9 (10.5)

15 (17.6)

0.194b

ECMO

2 (2.3)

2 (2.4)

1.00b

RASS score (%)

(n = 494 catheter days)

(n = 580 catheter days)

 

1 or above

30 (6.1)

33 (5.7)

0.539b

0

227 (46.0)

249 (42.9)

 

− 1 or less

237 (48.0)

298 (51.4)

 
  1. Patients were randomized to receive either sutures and a Tegaderm™ IV Advanced dressing (suture group) or 3M™ PICC/CVC Securement Device + Tegaderm™ IV Advanced dressing (suture-free group) to secure a short-term central venous catheter (CVC) onto the skin [n = number of patients or catheter days (IQR or %)]
  2. APACHE II score, the acute physiology and chronic health evaluation score; BMI, body mass index; ECMO, extracorporeal membrane oxygenation; RASS score, the Richmond Agitation–Sedation Scale score
  3. aMann–Whitney test; bFisher’s exact test