2009
DOI: 10.1016/j.surg.2009.04.007
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Surviving blood loss without blood transfusion in a swine poly-trauma model

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Cited by 88 publications
(108 citation statements)
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“…Furthermore, the model may be stringent. Valproic acid (400 mg/kg), which prolonged survival in Yorkshire pigs in a polytrauma model 25 consisting of femur fracture, 60% hemorrhage and 30 minutes of shock followed by fluid resuscitation, and Grade V liver injury, did not promote survival in the present model: median survival for valproic acid was 6 minutes compared with 92 minutes in vehicle controls. 26 An additional limitation of our experiments is the use of five to seven of these expensive animals per treatment group; however, the combined analysis of both experiments involved 12 animals in each of the 1-mg/kg and vehicle control groups.…”
Section: Discussioncontrasting
confidence: 53%
“…Furthermore, the model may be stringent. Valproic acid (400 mg/kg), which prolonged survival in Yorkshire pigs in a polytrauma model 25 consisting of femur fracture, 60% hemorrhage and 30 minutes of shock followed by fluid resuscitation, and Grade V liver injury, did not promote survival in the present model: median survival for valproic acid was 6 minutes compared with 92 minutes in vehicle controls. 26 An additional limitation of our experiments is the use of five to seven of these expensive animals per treatment group; however, the combined analysis of both experiments involved 12 animals in each of the 1-mg/kg and vehicle control groups.…”
Section: Discussioncontrasting
confidence: 53%
“…Currently, there has been much focus on VPA because this agent has shown promise in cellular protection after periods of ischemia or hemorrhage, but these pathways are largely unknown. [23][24][25] Our results have identified factors related to apoptosis/ cell death and angiogenesis/vascular development as being among the major pharmacologic targets of VPA after a severe ischemia-reperfusion injury, particularly VEGF and TGF-␤. Although it is possible that changes in hemodynamic factors and other aspects of the injury contributed to the changes in gene expression in the VPA-treated animals, the genes we discovered that changed have been identified as transcriptional targets of VPA in several in vitro models.…”
Section: Discussionmentioning
confidence: 75%
“…Howes et al [121] investigated the effect of recombinant factor VIIa in a polytraumatic (femur fracture, liver laceration and soft tissue crush injury) pig model. Alam et al [122] examined the efficacy of treatment with valproic acid in pigs using a highly lethal polytrauma and hemorrhagic shock model [femur fracture, 60% hemorrhage (mean arterial pressure 25-30 mm Hg) and grade V liver injury].…”
Section: Types Of Modelsmentioning
confidence: 99%