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Table 1 Baseline characteristics, use of organ support and outcome of patients included in the per-protocol analyses

From: Co-administration of iloprost and eptifibatide in septic shock (CO-ILEPSS)—a randomised, controlled, double-blind investigator-initiated trial investigating safety and efficacy

Variable

Active treatment

Placebo treatment

Median (IQR)

Median (IQR)

n

12

6

Age, years

61.5 (54.2–68.6)

71.3 (64.2–75)

Male gender, n (%)

8 (66.7%)

6 (100%)

BMI, kg/m2

24.5 (22.1–28.7)

27.8 (22.8–30.4)

Infectious focus

 CNS, n (%)

0 (0%)

0 (0%)

 Lungs, n (%)

10 (83.3%)

4 (66.7%)

 Gastrointestinal, n (%)

0 (0%)

2 (33.3%)

 Urogenital, n (%)

0 (0%)

0 (0%)

 Skins and soft tissue, n (%)

2 (16.7%)

1 (16.7%)

 Blood, n (%)

0 (0%)

1 (16.7%)

 Unknown, n (%)

1 (8.3%)

0 (0%)

 Identified pathogen (microbiology), n (%)

9 (75%)

5 (83.3%)

Comorbidity

 Chronic diagnosis, n (%)

9 (75%)

6 (100%)

Admitted from

 Acute medical care unit, n (%)

6 (50%)

3 (50%)

 Medical department, n (%)

3 (25%)

1 (16.7%)

Disease severity, physiology and biochemistry

 SOFA (first)

9.0 (7.8–12.0)

9.5 (7.3–13.3)

 SAPS II

46 (42–57)

48 (39–55)

 Systolic blood pressure, mmHg

113 (100–120)

123 (104–145)

 Lactate, mmol/l

1.4 (1.3–3.1)

3.5 (1.9–3.9)

 pH

7.35 (7.3–7.41)

7.41 (7.39–7.41)

 Haemoglobin, mmol/l

6.9 (6.4–7.7)

6.5 (5.8–7)

 White blood cell count, × 109/l

15 (9.8–19.1)

17.2 (8.8–23.1)

 Platelet count, ×109/l

188 (130–255)

212 (149–295)

 INR

1.2 (1.1–1.2)

1.3 (1.1–2)

 Antithrombin

0.64 (0.52–0.76)

0.58 (0.37–0.82)

 D-dimer

4.6 (2.4–19.9)

14.4 (3.4–15.3)

 Creatinine, μmol/l

97 (67–242)

126 (114–189)

 Blood urea nitrogen (BUN), mmol/l

7.9 (5.3–13.2)

13.5 (8.6–17.9)

 ALAT, U/l

35 (26–62)

35 (23–169)

 Bilirubin, μmol/l

11 (5–24)

16 (8–29)

 Basic phosphatase, U/l

64 (57–84)

149 (76–242)

 C-reactive protein, mg/l

172 (129–244)

138 (89–169)

Therapy and outcome

 Ventilator days, n (%)

5 (3–6)

6 (4–6)

 Ventilator-free days, n (%)

25 (24–27)

24 (6–24)

 RRT days, n (%)

0 (0–0)

0 (0–0)

 RRT-free days, n (%)

30 (29–30)

30 (8–30)

 Vasopressor days, n (%)

5 (5–5)

5 (4–5)

 Vasopressor-free days, n (%)

25 (24–25)

25 (6–25)

 Discharged to admitting dept., n (%)

9 (75%)

3 (50%)

 Discharged to other hosp., n (%)

1 (8.3%)

1 (16.7%)

 Discharged to other ICU, n (%)

1 (8.3%)

1 (16.7%)

 Active stop therapy, n (%)

2 (16.7%)

1 (16.7%)

 7-day mortality, n (%)

0 (0%)

1 (16.7%)

 30-day mortality, n (%)

1 (8.3%)

2 (33.3%)

 90-day mortality, n (%)

3 (25%)

3 (50%)

  1. IQR interquartile range, BMI body mass index, CNS central nervous system, SOFA Sequential Organ Failure Assessment, SAPS II Simplified Acute Physiology Score II, INR international normalised ratio, ALAT alanine aminotransferase, RRT renal replacement therapy, ICU intensive care unit, NS non-significant