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We used both primary and secondary inpatient diagnosis codes to identify the sample of shock patients.
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Second, the study was performed in a sample of septic shock patients from a single center, potentially limiting the generalizability of the results.
The sample of the hemorrhagic shock and obstructive shock was not usable for this calculation.
It has already been reported that the concentration of IP-10 was elevated in plasma samples of septic shock patients compared to SIRS patients and that IP-10 might serve as a diagnostic marker [ 39].
However, there was absolutely no correlation between the individually reinfused volume of blood and the level of citrate found afterward in blood samples taken following induction of shock (results not shown).
Finally, our observations were restricted to a small sample of patients in septic shock.
MBRRACE-UK CEMM: a sample of women with septic shock Are women cared for according to current guidelines?
Both proved to be the children from whom blood was sampled three days after the onset of shock, while the three DSS children sampled two days after shock onset still exhibited a typical DSS gene expression profile.
The ability of some genes transcripts or genes products to accurately predict progression to DSS should be evaluated by multivariate regression models [91] using blood samples collected before the onset of shock, while this proves to be difficult in the context of dengue outbreaks [28].
The first blood sample was collected at the onset of shock (i.e., within 30 min after the beginning of vasoactive treatment: 0, 24, and 48 h after (H0, H24, and H48)).
The prevalence of shock in our sample was 5.3% (36 cases).
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