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The Effects of Transfusion of Red blood cells In the critically ill II

The Effects of Transfusion of Red blood cells In the critically ill II - TETRIS2

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON48722
Enrollment
86
Registered
2017-07-21
Start date
2017-08-24
Completion date
Unknown
Last updated
2024-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anemia blood deficiency

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients who will receive an erythrocyte transfusion in the ICU (to correct for anemia) and are not suspected of an active bleeding.

Exclusion criteria

Exclusion criteria: * Patients who have not given informed consent * Patients who pose difficulties in securing blood products (e.g. rare blood groups) * Patients who receive more than 1 unit of RBCs in 1 transfusion episode * No arterial catheter in situ

Design outcomes

Primary

MeasureTime frame
Change in the expression of PS on erythrocytes before and after RBC transfusion and the influence of an inflammatory state in the receiver.

Secondary

MeasureTime frame
* Clearance rate of erythrocytes - expression of clearance markers, other than PS * markers of immune cell and endothelial cell activation and adhesion * complete blood count * Levels of fibrinogen, APTT, PTT and D-dimers in blood (to calculate DIC score) * markers of inflammatory host respons * Sublingual microcirculatory density and perfusion velocity, as visualized with SDF * Tissue oxygenation, as measured with NIRS * VO2 (oxygen uptake), DO2 (oxygen delivery), O2ER (oxygen extraction ratio) * Time on mechanical ventilation * Duration of ICU stay * Duration of hospital stay * 28 day mortality * DNA staining on residual red blood cell material, * Red blood cell deformability, activation status and cell-binding ability

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)