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Het effect van een bloedtransfusie bij kritiek zieke patiënte

Conditions
EN: red blood cell transfusion, clearance, microcirculation, sepsis, intensive care medicineNL: rode bloedcel transfusie, klaring, microcirculatie, sepsis, intensive care
Registration Number
NL-OMON27009
Lead Sponsor
Academic medical centre Amsterdam
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
86
Inclusion Criteria

Patients must receive an erythrocyte transfusion on the ICU, to correct for anemia

- Patients may not have received a transfusion with red blood cells, plasma or thrombocytes in the previous 24 hours

Exclusion Criteria

- Patients who have not given informed consent

- Patients who pose difficulties in securing blood products (e.g. rare blood groups)

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Phosphatidylserine exposure on donor RBCs
Secondary Outcome Measures
NameTimeMethod
- Clearance of erythrocytes<br /><br>- Expression of clearance markers other than PS <br /><br>- Markers of immune cell and endothelial cell activation and adhesion <br /><br>- Complete blood count<br /><br>- Levels of fibrinogen, APTT, PTT and D-dimers in blood (to calculate DIC score)<br /><br>- Markers of inflammatory host respons <br /><br>- Sublingual microcirculatory density and perfusion velocity, as visualized with SDF <br /><br>- Tissue oxygenation, as measured with NIRS<br /><br>- Time on mechanical ventilation<br /><br>- Duration of ICU stay<br /><br>- Duration of hospital stay<br /><br>- 28 day mortality<br /><br>- DNA staining on residual red blood cell material, <br /><br>- Red blood cell deformability, activation status and cell-binding ability<br /><br>- Oxygen tension in the mitochondria (MitoPO2)<br>
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