Septic shock is still a major cause of death in ICU. Sepsis diagnosis is linked with many clinical, hemodynamic and biological criteria which have a low sensitivity and specificity if they are considered separately. The extensive experimental data which have been published contrast with the hematological data collected by the physician at patient's bedside especially regarding neutrophils and platelets levels. When there is no obvious clinical sign, a biological tool reflecting the patient's immune status could be useful to understand the physiopathology of Sepsis and to predict the progression of the disease in the patient. On the long-term it could also help to define management strategies.
Study Type
OBSERVATIONAL
Enrollment
1,000
Residue of blood further to NFS.
CHU Bordeaux - Service Réanimation Médicale
Bordeaux, France
CHU Henri MONDOR - Service Réanimation
Créteil, France
CHU Dijon - Service Réanimation Médicale
Dijon, France
CHU Limoges - Service de réanimation polyvalente
Limoges, France
CHU Orléans - Service de Réanimation Médicale
Orléans, France
Hôpital Cochin - service de Réanimation
Paris, France
CHU Poitiers - Service Réanimation
Poitiers, France
CHU Rennes - service de Réanimation
Rennes, France
CHU Tours - Service de Réanimation
Tours, France
expression of the marker CD10
Expression of CD10 on granulocytes.
Time frame: 28 days
Progession of SOFA score
Time frame: 48 hours
Expression of the marker CD16
Expression of CD16 on granulocytes and on monocytes.
Time frame: 28 days
Expression of the marker CD24
Expression of CD24 on granulocytes.
Time frame: 28 days
Expression of the marker CD64
Expression of CD64 on granulocytes.
Time frame: 28 days
Expression of the marker CD14
Expression of CD14 on monocytes.
Time frame: 28 days
Expression of the marker CD3
Expression of CD3 on T lymphocytes.
Time frame: 28 days
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