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

Table 2.

Bivariate analyses between clusters S1, S2, and S3 upon SEB stimulation and clinical and biological parameters.

Cluster S1 (n = 16) Cluster S2 (n = 11) Cluster S3 (n = 12) p value
Status < 0.001
Healthy, n (%) 10 (62.5) 0 (0) 0 (0)
Patients, n (%) 6 (37.5) 11 (100) 12 (100)
Comorbidities*,a 0.171
No, n (%) 1 (16.7) 6 (54.5) 2 (16.7)
Yes, n (%) 5 (83.3) 5 (45.5) 10 (83.3)
Median SOFA* (day 1), [IQR] 7.5 [6.2–8] 8 [6.5–10.5] 8.5 [8–10] 0.574
Median ICU length of stay*, [IQR] 4.5 [4–5.8] 10 [7.5–24] 9 [6.5–12] 0.585
Mortality at day 28*, n (%) 0 (0) 4 (36.4) 0 (0) 0.034
Median mHLA-DR* (day 3–4) (Ab/C), [IQR] 10,938 [9456–14642] 7301 [4653–11673] 3839.5 [3444–6250] 0.007
Median TNFα secretion post-LPS stimulation (pg/mL), [IQR] 3799 [2067.2–5401.2] 282.7 [122.2–861.8] 700.8 [457.8–913.3] < 0.001

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 shock 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.