Normal saline influences coagulation and endothelial function after traumatic brain injury and hemorrhagic shock in pigs

Surgery. 2014 Sep;156(3):556-63. doi: 10.1016/j.surg.2014.04.016. Epub 2014 Jun 19.

Abstract

Background: Traumatic brain injury (TBI) and hemorrhagic shock (HS) are the leading causes of trauma-related deaths. These insults disrupt coagulation and endothelial systems. This study investigated whether previously reported differences in lesion size and brain swelling during normal saline (NS), colloids (Hextend [HEX]), and fresh frozen plasma (FFP) resuscitation are associated with differential effects on coagulation and endothelial systems.

Methods: We subjected 15 Yorkshire swine to TBI and HS (40% blood volume), and kept in HS for 2 hours before resuscitation with NS, HEX, or FFP. Markers of endothelial activation (E-selectin, Intercellular adhesion molecule [ICAM]-1), coagulation activation (prothrombin fragment 1 + 2), and natural anticoagulation (activated protein C [aPC]) were determined in serum and brain whole cell lysates.

Results: Serum levels of aPC were greater in the NS group (203 ± 30 pg/mL) compared with HEX (77 ± 28 pg/mL; P = .02) and FFP (110 ± 28 pg/mL; P = .09), as was PF 1 + 2 in the brain when compared with FFP (PF 1 + 2, 89 ± 46 vs 37 ± 14 ng/mL; P = .035). Brain E-selectin was greater in the NS group compared with FFP (3.36 ± 0.02 vs 3.31 ± 0.01 ng/mL; P = .029). Circulating ICAM-1 levels were increased in the NS group (151 ± 9 ng/mL) compared with the HEX (100 ± 9 ng/mL; P < .01) and FFP (108 ± 9 ng/mL; P = .01).

Conclusion: In this clinically realistic large animal model of TBI + HS, NS resuscitation was associated with an early activation of coagulation, natural anticoagulation, and endothelial systems, compared with HEX and FFP.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Blood Coagulation*
  • Brain / metabolism
  • Brain Injuries / blood
  • Brain Injuries / physiopathology*
  • Brain Injuries / therapy*
  • Colloids / therapeutic use
  • E-Selectin / blood
  • E-Selectin / metabolism
  • Endothelium, Vascular / physiopathology*
  • Female
  • Fibrinolysis
  • Intercellular Adhesion Molecule-1 / blood
  • Intercellular Adhesion Molecule-1 / metabolism
  • Isotonic Solutions / therapeutic use
  • Peptide Fragments / blood
  • Peptide Fragments / metabolism
  • Plasma
  • Protein C / metabolism
  • Prothrombin / metabolism
  • Resuscitation / methods
  • Shock, Hemorrhagic / blood
  • Shock, Hemorrhagic / physiopathology*
  • Shock, Hemorrhagic / therapy*
  • Sodium Chloride / therapeutic use*
  • Sus scrofa

Substances

  • Biomarkers
  • Colloids
  • E-Selectin
  • Isotonic Solutions
  • Peptide Fragments
  • Protein C
  • prothrombin fragment 1.2
  • Intercellular Adhesion Molecule-1
  • Sodium Chloride
  • Prothrombin