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Updated: Jan 12, 2026

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Fixed Volume or Fixed Pressure: A Murine Model of Hemorrhagic Shock
Published on: June 6, 2011
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Ongoing Endothelial Cell Dysfunction Following Hemorrhagic Shock: Crystalloids are the Culprit
Matthew Vasquez1, Sarah Abdullah1, Chavi Rehani1
1Program in Trauma, R Adams Cowley Shock Trauma Center, University of Maryland, Baltimore, Maryland.
Shock (Augusta, Ga.)
|October 30, 2025
Summary
Crystalloid fluid use after hemorrhage control is linked to ongoing endothelial and coagulation issues. This suggests a need for different resuscitation methods post-hemorrhage to improve patient outcomes.
Area of Science:
- Trauma Resuscitation
- Critical Care Medicine
- Hemorrhagic Shock Management
Background:
- Current trauma care emphasizes early blood product use and limited crystalloid administration to improve outcomes.
- Limited data exists on the impact of crystalloid use following successful hemorrhage control.
- This study investigates the hypothesis that crystalloid administration during early post-resuscitation care may exacerbate endothelial dysfunction.
Purpose of the Study:
- To examine the association between crystalloid fluid administration in the post-hemorrhage control period and markers of endothelial dysfunction, coagulation, and inflammation.
- To evaluate the correlation between crystalloid volume and clinical outcomes such as organ failure and length of stay in the intensive care unit (ICU).
Main Methods:
- Prospective observational study of 69 patients in hemorrhagic shock.
- Collection of crystalloid administration data at arrival, in the operating room (OR), and at 24, 48, and 72 hours post-resuscitation in the ICU.
- Analysis of blood samples for indicators of inflammation, endothelial dysfunction (e.g., syndecan-1), and coagulation (e.g., INR) using Luminex assays.
Main Results:
- Patients received a mean of 4.7L of crystalloid within the first 24 hours, with significant volumes administered in the OR and ICU.
- Elevated endothelial, coagulation, and inflammatory markers were observed on admission compared to controls.
- Crystalloid volume at 24 hours correlated with syndecan-1 and INR, indicating persistent endothelial dysfunction.
- Later crystalloid totals (48h and 72h) correlated with increased Sequential Organ Failure Assessment (SOFA) scores, longer ICU stays, and more ventilator days.
Conclusions:
- Crystalloid administration persists even after hemorrhage control in clinical practice.
- This practice is associated with ongoing endothelial and coagulation dysfunctions.
- Alternative resuscitation strategies are needed for the post-hemorrhagic phase to mitigate these adverse effects.
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