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Table 3 Univariable comparisons of clinical characteristics in patients with hypotension according to the vasopressor tapered immediately before developing hypotension

From: Incidence of hypotension according to the discontinuation order of vasopressors in the management of septic shock: a prospective randomized trial (DOVSS)

Variables

Hypotension on tapering of AVP (nā€‰=ā€‰12)

Hypotension on tapering of NE (nā€‰=ā€‰46)

P value

Age

67 (59 ā€“ 69)

65 (56 ā€“ 73)

0.773

Gender, male

10 (83.3)

30 (65.2)

0.307

Causes of septic shocka

Ā Ā 

0.246

ā€ƒPneumonia

8 (66.7)

20 (43.5)

Ā 

ā€ƒIntraabdominal infection

2 (16.7)

14 (30.4)

Ā 

ā€ƒUrogenital infection

3 (25.0)

6 (13.0)

Ā 

ā€ƒCather related infection

0 (0.0)

4 (8.7)

Ā 

ā€ƒEndocarditis

0 (0.0)

2 (4.3)

Ā 

ā€ƒOthersb

0 (0.0)

3 (6.5)

Ā 

MAP before initial resuscitation, mmHg

53 (47 ā€“ 57)

51 (42 ā€“ 57)

0.214

CVP before initial resuscitation, mmHg

7 (3 ā€“ 10)

6 (6 ā€“ 8)

0.161

MAP at the time of vasopressor initiated, mmHg

55 (47 ā€“ 57)

55 (52 ā€“ 60)

0.612

CVP at the time of vasopressor initiated, mmHg

11 (10 ā€“ 13)

11 (8 ā€“ 14)

0.669

Total bilirubin, mg/dL

0.90 (0.35 ā€“ 3.05)

1.20 (0.50 ā€“ 2.70)

0.382

Serum creatinine, mg/dL

1.47 (0.71 ā€“ 2.01)

1.42 (0.97 ā€“ 2.32)

0.687

Lactic acid, mmol/L (nā€‰=ā€‰57)

3.27 (1.91 ā€“ 4.62)

4.31 (2.67 ā€“ 6.32)

0.229

Procalcitonin, ng/mL (nā€‰=ā€‰53)

13.09 (4.18 ā€“ 81.53)

11.01 (2.61 ā€“ 30.97)

0.602

C-reactive protein, mg/mL

14.87 (8.51 ā€“ 29.72)

12.57 (5.59 ā€“ 19.42)

0.129

Maximum NE dose during study period, ug/kg/min

0.74 (0.54 ā€“ 1.56)

0.70 (0.46 ā€“ 1.20)

0.448

SAPS3

74 (62 ā€“ 86)

73 (62 ā€“ 84)

0.931

SOFA

9 (8 ā€“ 13)

10 (8 ā€“ 12)

0.601

Clinical status on randomization

ā€ƒMAP, mmHg

72 (70 ā€“ 78)

77 (73 ā€“ 81)

0.138

ā€ƒCVP, mmHg

10 (8 ā€“ 12)

10 (8 ā€“ 14)

0.420

ā€ƒNeed for mechanical ventilation

10 (83.3)

31 (67.4)

0.478

ā€ƒNeed for renal replacement therapy

4 (33.3)

14 (30.4)

1.000

ā€ƒNeed for dobutamine

1 (8.3)

3 (6.5)

1.000

ā€ƒSOFA

13(11 ā€“ 16)

12 (9 ā€“ 15)

0.255

ā€ƒPF ratio

118.8 (81.9 ā€“ 177.9)

186.9 (105.4 ā€“ 278.0)

0.110

ā€ƒTotal bilirubin, mg/dL

1.35 (0.53 ā€“ 3.68)

1.40 (0.80 ā€“ 3.88)

0.744

ā€ƒSerum creatinine, mg/dL

1.25 (0.60 ā€“ 1.99)

1.26 (0.81 ā€“ 2.21)

0.508

ā€ƒCorticosteroid treatment

10 (90.9)

42 (95.5)

0.495

ā€ƒCopeptin, pg/mL (nā€‰=ā€‰56)

77 (67 ā€“ 90)

168 (131 ā€“ 207)

<ā€‰0.001

ā€ƒTime to randomization, hours

25.1 (14.1 ā€“ 41.8)

21.1 (11.8 ā€“ 46.2)

0.818

Time to discontinuation of vasopressors just before hypotension developed

28.8 (18.5-44.3)

22.0 (13.6-47.2)

0.946

Time to hypotension after discontinuation of vasopressor, hours

2.5 (1.1 ā€“ 3.3)

2.5 (1.9 ā€“ 4.7)

0.442

ā€ƒMAP at the time of hypotension developed on tapering of vasopressor, mmHg

61 (57 ā€“ 63)

62 (59 ā€“ 63)

0.214

ā€ƒCVP at the time of hypotension developed on tapering of vasopressor, mmHg

10 (6 ā€“ 12)

10 (7 ā€“ 14)

0.735

Total vasopressor duration, hours

63.4 (38.9 ā€“ 122.6)

57.8 (38.9 ā€“ 88.0)

0.578

Clinical outcomes

ā€ƒICU mortality

5 (41.7)

13 (28.3)

0.486

ā€ƒICU length of stay, days

12 (8 ā€“ 22)

8 (3 ā€“ 12)

0.108

ā€ƒ28-day mortality

5 (41.7)

17 (37.8)

1.000

ā€ƒHospital mortality

6 (50.0)

20 (46.5)

0.686

ā€ƒHospital stay, days

27 (19 ā€“ 30)

22 (14 ā€“ 39)

0.617

  1. Data are presented as frequencies (number of patients), with the percentage in parenthesis, or as medians with interquartile ranges (IQR) in parenthesis
  2. aMore than one criterion can be used
  3. bOthers included meningitis (nā€‰=ā€‰1) and deep neck (nā€‰=ā€‰1) and soft tissue infections (nā€‰=ā€‰1)
  4. AVP, vasopressin; CVP, central venous pressure; MAP, mean arterial pressure; NE, norepinephrine; PF ratio, arterial partial pressure of oxygen (PaO2)/fraction of inspired oxygen (FiO2) ratio; SAPS3, simplified acute physiology score 3; SOFA, sequential organ failure assessment