sepsis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: patients with sepsis diagnosed by Sepsis-3 admitted to Tohoku University Hospital
Exclusion criteria
Exclusion criteria: 1) Cases for which consent was not obtained from the patient or the patient's next of kin 2) Patients requiring mechanical assisted circulation (IABP, ECMO, LVAD) 3) Patients requiring acute blood purification therapy prior to the start of the study 4) Patients with infection more than 7 days prior to study enrollment or with unknown onset of infection 5) Pregnant
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint was the amount of Tissue factor bearing microparticles (TF banding MPs) at the first blood draw in the DIC and non-DIC groups. | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of the production of other MPs (monocyte-derived, endothelial cell-derived, platelet-derived, etc.) between DIC and non-DIC groups. Thrombin generation study. | — |
Countries
Japan
Contacts
Tohoku University Hospital department of Anesthesiology and preoperative medicine