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Table 1 Baseline characteristics and macrolide use

From: Effect of erythromycin on mortality and the host response in critically ill patients with sepsis: a target trial emulation

 

Erythromycin (n = 235)

Controls (n = 470)

P-value

SMD*

Demographics

 Age, years

60.8 (13.6)

60.9 (15.3)

0.98

0.002

 Sex, male

162 (68.9)

285 (60.6)

0.031

0.174

 Body mass index, kg m−2

25.5 [23.0, 29.3]

25.5 [22.9, 29.1]

0.63

0.062

 Race, white

208 (88.9)

417 (88.9)

> 0.99

0.001

Admission data

 Hospital A

149 (63.4)

233 (49.6)

0.001

0.282

 Admission type, surgical

75 (31.9)

114 (24.3)

0.038

0.171

 SDD use during admission

181 (77.0)

325 (69.1)

0.033

0.178

Chronic comorbidities

 Charlson Comorbidity Index (without age)

2 [0, 4]

2 [0, 3]

0.31

0.066

 Any malignancy

58 (24.7)

103 (21.9)

0.45

0.065

  Non-metastatic solid tumor

33 (14.0)

49 (10.4)

0.17

0.111

  Metastatic malignancy

6 (2.6)

19 (4.0)

0.39

0.083

  Hematologic malignancy

23 (9.8)

37 (7.9)

0.39

0.068

 Diabetes mellitus (type 1 or type 2)

49 (20.9)

100 (21.3)

0.92

0.010

 Cerebrovascular disease

28 (11.9)

45 (9.6)

0.36

0.076

 Hemiplegia

6 (2.6)

17 (3.6)

0.51

0.062

Chronic medication

 Any immunosuppressant

32 (13.7)

72 (15.8)

0.50

0.061

 Antiplatelet drugs

63 (26.9)

123 (27.0)

> 0.99

0.002

 Calcium-entry blockers

43 (18.3)

80 (17.1)

0.68

0.033

 Beta-adrenergic blockers

65 (27.7)

129 (27.5)

> 0.99

0.003

 Oral antidiabetic drugs

29 (12.3)

65 (13.9)

0.64

0.045

 Insulin

26 (11.1)

52 (11.1)

> 0.99

0.001

Disease severity at ICU admission

 APACHE IV score

90.9 (28.5)

85.0 (28.4)

0.010

0.207

 Acute physiology score

78.2 (26.4)

72.1 (26.4)

0.004

0.231

 mSOFA score

8 [6, 11]

7 [5, 9]

< 0.001

0.455

 Shock

176 (75.5)

242 (51.6)

< 0.001

0.514

 ARDS

78 (33.2)

132 (28.1)

0.16

0.111

 Mechanical ventilation

225 (96.6)

419 (89.3)

0.001

0.285

 PaO2/FiO2 ratio

148 [99, 230]

156 [108, 217]

0.49

0.052

 AKI

117 (49.8)

187 (39.8)

0.012

0.202

 Gastrointestinal failure score

  

< 0.001

0.456

  0—Normal gastrointestinal function

86 (36.6)

269 (57.2)

  

  1—Reduced/delayed enteral feeding§

112 (47.7)

133 (28.3)

  

  2—Food intolerance or IAH

35 (14.9)

65 (13.8)

  

  3—Food intolerance and IAH

2 (0.9)

2 (0.4)

  

  4—Abdominal compartment syndrome

0 (0.0)

0 (0.0)

  

 Gastrointestinal failure score >  = 1

149 (63.4)

200 (42.6)

< 0.001

0.425

 Gastrointestinal bleeding

7 (3.0)

8 (1.7)

0.28

0.085

Source of infection

    

 Pulmonary tract

119 (50.6)

252 (53.6)

0.47

0.060

 Abdominal tract

48 (20.4)

83 (17.7)

0.41

0.070

 Urinary tract

20 (8.5)

26 (5.5)

0.15

0.117

 Cardiovascular

15 (6.4)

16 (3.4)

0.08

0.138

 Skin

17 (7.2)

16 (3.4)

0.036

0.171

 Central nervous system

6 (2.6)

29 (6.2)

0.042

0.178

 Other or unknown

30 (12.8)

75 (16.0)

0.31

0.091

Erythromycin use

    

 First administration from admission, hours

38 [25, 52]

   

 Duration of the first course, hours

42 [24, 69]

   

 No. of administrations (first course)

5 [3, 8]

   

 Median dose per administration (first course), mg

200 [125, 200]

   

 Cumulative dose (first course), mg

800 [600, 1400]

   

 No. of courses during ICU stay

    

  1

182 (77.4)

   

  2

46 (19.6)

   

  3+

7 (3.0)

   

Other macrolides

    

 High-dose erythromycin > 72 h after admission

0 (0.0)

1 (0.2)

  

 Azithromycin or clarithromycin > 72 h after admission

1 (0.4)

2 (0.4)

  
  1. AKI acute kidney injury, APACHE-IV acute physiology and chronic health evaluation IV, ARDS acute respiratory distress syndrome, IAH intraabdominal hypertension, ICU intensive care unit, mSOFA modified sequential organ failure assessment score (without the central nervous system component), SDD selective decontamination of the digestive tract, SMD standardized mean difference
  2. *SMD > 0.2 indicates a substantial imbalance between groups; < 0.1 indicates a negligible difference
  3. Patients who did not receive SDD received selective oropharyngeal decontamination as part of a clinical trial [64]
  4. Missing in 10/235 (4.3%) in the erythromycin group and 50/470 (10.6%) in the control group, see Additional file 1: Methods and Additional file 1: Table 3 for details
  5. §“Enteral feeding < 50% of calculated needs or no feeding 3 days after abdominal surgery” in the original paper [44]
  6. Categorical data are displayed as count (percentage) and compared using Fisher's exact test
  7. Normally distributed continuous data are displayed as mean (standard deviation) and compared using Welch's t-test
  8. Non-normally distributed continuous data are displayed as median [interquartile range] and compared using Wilcoxon's rank-sum test