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. 2020 Sep 30;10:16136. doi: 10.1038/s41598-020-73014-2

Table 3.

Bivariate analyses between clusters SV1, SV2, and SV3 upon SEB stimulation and clinical and biological parameters.

Cluster SV1 (n = 11) Cluster SV2 (n = 14) Cluster SV3 (n = 15) p value
Status < 0.001
Healthy, n (%) 10 (91) 0 (0) 0 (0)
Sepsis patients, n (%) 0 (0) 6 (43) 4 (27)
Septic shock patients, n (%) 1 (8) 8 (57) 11 (73)
Comorbidities*,a 0.427
No, n (%) 0 (0) 5 (35.7) 3 (20)
Yes, n (%) 1 (100) 9 (64.3) 12 (80)
Day 1
Median SOFA*, [IQR] 8 9 [8–9.8] 9 [4.5–10.5] 0.335
Day 3–4
Median mHLA-DR (Ab/C), [IQR] 28,272 [18308–30940] 5098 [3544–8223] 4680 [3097–8709] < 0.001
Median TNFα secretion post-LPS stimulation (pg/mL), [IQR] 4176 [3644–5412] 1590 [1289–2442] 719 [474–1090] < 0.001
Outcomes
Hospital-acquired infections*, n (%) 0 (0) 1 (7.1) 7 (46.7) 0.035
Median ICU length of stay*, [IQR] 2 7.5 [5–9.8] 11 [7–16] 0.050
Mortality at day 28*, n (%) 0 (0) 3 (21.4) 0 (0) 0.053

For categorical variables Chi-squared test was used and for numerical variables, t test (parametric) or Wilcoxon (non-parametric) was used.

SOFA sequential organ failure assessment, ICU intensive care unit, HLA-DR human leukocyte antigen DR, TNFα tumour necrosis factor alpha, LPS lipopolysaccharide.

*Parameters measured exclusively for septic patients.

aPresence of comorbidities was affirmative when at least one of the following comorbidity was present in the patient: chronic pulmonary disease, heart failure, myocardial infarction, ulcer, diabetes, renal failure, or malign solid tumour.