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Published on: March 19, 2016
Pre-clinical study protocol: Blood transfusion in endotoxaemic shock
Nchafatso G Obonyo1,2, Liam Byrne1,3,4, John-Paul Tung1,5,6,7
1Critical Care Research Group, The Prince Charles Hospital, Brisbane, QLD, Australia.
This study protocol outlines a preclinical trial investigating early packed red blood cell (PRBC) transfusion for hemodynamic support in sepsis. It aims to clarify the volume expansion effects of PRBCs versus traditional fluids.
Area of Science:
- Critical Care Medicine
- Transfusion Medicine
- Hemodynamics
Background:
- Current sepsis guidelines offer varied recommendations for blood transfusion thresholds.
- Volume expansion with crystalloids/colloids in sepsis is linked to adverse outcomes.
- Hemodynamic effects of early packed red blood cell (PRBC) transfusion in sepsis remain unclear.
Purpose of the Study:
- To describe a preclinical randomized controlled trial protocol.
- To examine the hemodynamic effects of early PRBC transfusion as initial volume expansion in a sepsis model.
- To explore underlying physiological, hematological, immunological, and tissue-specific mechanisms of PRBC transfusion.
Main Methods:
- Utilizing a validated ovine model of hyperdynamic endotoxemic shock.
- Designing a preclinical randomized controlled trial.
- Comparing early PRBC transfusion (before crystalloids/colloids) with other resuscitation strategies.
- Investigating effects of short (≤5 days) versus long (≥30 days) PRBC storage durations.
Main Results:
- This section will report findings from the described preclinical trial once completed.
Conclusions:
- This study protocol provides a framework for investigating the role of early PRBC transfusion in sepsis resuscitation.
- Findings may inform future clinical guidelines on transfusion strategies for septic shock.
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