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Table 1 Baseline demographic data and clinical characteristics of patients included in the study

From: The effect of dobutamine in sepsis: a propensity score matched analysis

Covariate

Original patients (before matching)

Missing data (%)

Non-dobutamine group (Nā€‰=ā€‰2165)

Dobutamine group (Nā€‰=ā€‰121)

P value

Age (years)

66.63ā€‰Ā±ā€‰17.06

68.57ā€‰Ā±ā€‰16.44

0.222

0.0

Gender (Male), n (%)

1208 (55.8%)

74 (61.2%)

0.248

0.0

Height (cm)

168.76ā€‰Ā±ā€‰11.00

168.61ā€‰Ā±ā€‰9.68

0.883

0.0

Weight (kg)

82.65ā€‰Ā±ā€‰27.00

83.26ā€‰Ā±ā€‰21.95

0.808

0.0

BMI (kg/m [2])

29.00ā€‰Ā±ā€‰9.00

29.13ā€‰Ā±ā€‰6.72

0.871

0.0

Temperature (ā„ƒ)

37.71ā€‰Ā±ā€‰1.04

37.87ā€‰Ā±ā€‰1.11

0.108

0.4

MAP (mmHg)

51.63ā€‰Ā±ā€‰14.01

46.44ā€‰Ā±ā€‰15.51

0.000

0.0

HR (beats mināˆ’1)

112.71ā€‰Ā±ā€‰22.97

118.60ā€‰Ā±ā€‰23.46

0.006

0.0

RR (mināˆ’1)

30.23ā€‰Ā±ā€‰7.11

31.78ā€‰Ā±ā€‰8.00

0.020

0.0

SOFA score

7.22ā€‰Ā±ā€‰4.00

9.91ā€‰Ā±ā€‰3.73

0.000

0.0

SOFA-cardiovascular score

2.26ā€‰Ā±ā€‰1.45

3.23ā€‰Ā±ā€‰1.20

0.000

0.0

SAPS-I score

21.46ā€‰Ā±ā€‰5.68

24.86ā€‰Ā±ā€‰5.64

0.000

0.0

SAPS-II score

46.76ā€‰Ā±ā€‰16.66

56.59ā€‰Ā±ā€‰14.83

0.000

0.0

ECI

10.36ā€‰Ā±ā€‰7.91

11.06ā€‰Ā±ā€‰7.92

0.342

0.0

Norepinephrine dose (mg)

58.30ā€‰Ā±ā€‰82.56

79.89ā€‰Ā±ā€‰96.44

0.004

0.0

Norepinephrine use

1269 (58.6%)

110 (90.9%)

0.000

0.0

Urine volume (ml, 1st day)

1565.61ā€‰Ā±ā€‰1333.18

1083.63ā€‰Ā±ā€‰1005.80

0.000

1.0

Input volume (ml, 1st day)

8209.26ā€‰Ā±ā€‰6142.67

9471.47ā€‰Ā±ā€‰7166.17

0.069

4.3

Microbiology, n (%)

Ā Positive (%)

1719 (79.4%)

99 (81.8%)

0.521

0.0

Ā Negative

446 (20.6%)

22 (18.2%)

Interventions, n (%)

Ā Renal replacement use (1st day)

170 (7.9%)

15 (12.4%)

0.074

0.0

Ā Mechanical ventilation use (1st day)

1128 (52.1%)

95 (78.5%)

0.000

0.0

Comorbidities, n (%)

Ā Congestive heart failure

780 (36.0%)

75 (62.0%)

0.000

0.0

Ā Pulmonary circulation disease

168 (7.8%)

10 (8.3%)

0.840

0.0

Ā Renal failure

469 (21.7%)

23 (19.0%)

0.489

0.0

Ā Diabetes

676 (31.2%)

44 (36.4%)

0.236

0.0

Ā COPD

496 (22.9%)

33 (27.3%)

0.268

0.0

Ā Coagulopathy

614 (28.4%)

53 (43.8%)

0.000

0.0

Ā Fluid electrolyte disorder

1204 (55.6%)

66 (54.5%)

0.818

0.0

Admission type, n (%)

Ā Emergency

2106 (97.3%)

113 (93.4%)

0.014

0.0

Ā Elective

59 (2.7%)

8 (6.6%)

0.0

Sepsis type, n (%)

Ā Sepsis

451 (20.8%)

7 (5.8%)

0.000

0.0

Ā Severe sepsis

896 (41.4%)

50 (41.3%)

0.0

Ā Septic shock

818 (37.8%)

64 (52.9%)

0.0

Laboratory Tests

Ā Lactate (mmol/L)

2.59ā€‰Ā±ā€‰2.19

3.50ā€‰Ā±ā€‰2.86

0.001

48.4

Ā Glucose-min

106.90ā€‰Ā±ā€‰38.77

108.06ā€‰Ā±ā€‰48.17

0.753

0.5

Ā Glucose-max

190.70ā€‰Ā±ā€‰94.38

227.50ā€‰Ā±ā€‰93.32

0.000

0.5

  1. Data are meanā€‰Ā±ā€‰SD, median (interquartile) or n (%). SOFA Sequential Organ Failure Assessment, ranging from 0 to 24, with higher scores indicating a greater degree of organ failure; ECI Elixhauser comorbidity index, and we used the modified vanWalraven Elixhauser comorbidity score in our study, which consists of 30 comorbidity diseases, range from āˆ’Ā 19 to 89 points, with higher scores indicating a greater risk of hospital mortality, MAP mean arterial pressure; HR: heart rate, RR respiratory rate, SAPS-I simplified acute physiologic score-I, SAPS-II simplified acute physiologic score-II, ICU intensive care unit, COPD chronic obstructive pulmonary disease. The definitions and diagnositic criteria for sepsis, severe sepsis and septic shock were made according to the Surviving Sepsis Campaign Guidelines [1, 13, 14]