Literature DB >> 24368352

Assessment of coagulopathy, endothelial injury, and inflammation after traumatic brain injury and hemorrhage in a porcine model.

Martin Sillesen1, Lars S Rasmussen, Guang Jin, Cecilie H Jepsen, Ayesha Imam, John O Hwabejire, Ihab Halaweish, Marc DeMoya, George Velmahos, Pär I Johansson, Hasan B Alam.   

Abstract

BACKGROUND: Traumatic brain injury (TBI) and hemorrhagic shock (HS) can be associated with coagulopathy and inflammation, but the mechanisms are poorly understood. We hypothesized that a combination of TBI and HS would disturb coagulation, damage the endothelium, and activate inflammatory and complement systems.
METHODS: A total of 33 swine were allocated to either TBI + HS (n = 27, TBI and volume-controlled 40% blood loss) or controls (n = 6, anesthesia and instrumentation). TBI + HS animals were left hypotensive (mean arterial pressure, 30-35 mm Hg) for 2 hours. Blood samples were drawn at baseline, 3 minutes and 15 minutes after injury, as well as following 2 hours of hypotension. Markers of coagulation, anticoagulation, endothelial activation/glycocalyx shedding, inflammation, complement, and sympathoadrenal function were measured.
RESULTS: The TBI + HS group demonstrated an immediate (3 minutes after injury) activation of coagulation (prothrombin fragment 1 + 2, 289 ng/mL vs. 232 ng/mL, p = 0.03) and complement (C5a, 2.83 ng/mL vs. 2.05 ng/mL, p = 0.05). Shedding of the endothelial glycocalyx (syndecan 1) was evident 15 minutes after injury (851.0 ng/ml vs. 715.5 ng/ml, p = 0.03) while inflammation (tumor necrosis factor α [TNF-α], 81.1 pg/mL vs. 50.8 pg/mL, p = 0.03) and activation of the protein C system (activated protein C, 56.7 ng/mL vs. 26.1 ng/mL, p = 0.01) were evident following the 2-hour hypotension phase.
CONCLUSION: The combination of TBI and shock results in an immediate activation of coagulation and complement systems with subsequent endothelial shedding, protein C activation, and inflammation.

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Year:  2014        PMID: 24368352     DOI: 10.1097/TA.0b013e3182aaa675

Source DB:  PubMed          Journal:  J Trauma Acute Care Surg        ISSN: 2163-0755            Impact factor:   3.313


  25 in total

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Authors:  Monisha A Kumar; Wenjing Cao; Huy P Pham; Dheeraj Raju; Kelsey Nawalinski; Eileen Maloney-Wilensky; James Schuster; X Long Zheng
Journal:  J Neurotrauma       Date:  2018-08-14       Impact factor: 5.269

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3.  Lung Protective Effects of Low-Volume Resuscitation and Pharmacologic Treatment of Swine Subjected to Polytrauma and Hemorrhagic Shock.

Authors:  Vahagn C Nikolian; Baihong Pan; Tomaz Mesar; Isabel S Dennahy; Patrick E Georgoff; Xiuzhen Duan; Baoling Liu; Xizi Wu; Michael J Duggan; Hasan B Alam; Yongqing Li
Journal:  Inflammation       Date:  2017-08       Impact factor: 4.092

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Authors:  J N Luker; M Vigiola Cruz; B C Carney; A Day; L T Moffatt; L S Johnson; J W Shupp
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Authors:  Alexis L Cralley; Ernest E Moore; Daniel Kissau; Julia R Coleman; Navin Vigneshwar; Margot DeBot; Terry R Schaid; Hunter B Moore; Mitchell J Cohen; Kirk Hansen; Christopher C Silliman; Angela Sauaia; Charles J Fox
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Review 6.  Proteoglycans and glycosaminoglycans in central nervous system injury.

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8.  Modern resuscitation of hemorrhagic shock: what is on the horizon?

Authors:  D T Martin; M A Schreiber
Journal:  Eur J Trauma Emerg Surg       Date:  2014-06-17       Impact factor: 3.693

9.  TLR2 Regulates Complement-Mediated Inflammation Induced by Blood Loss During Hemorrhage.

Authors:  Jeremy Goering; Michael R Pope; Sherry D Fleming
Journal:  Shock       Date:  2016-01       Impact factor: 3.454

10.  A systematic review of large animal models of combined traumatic brain injury and hemorrhagic shock.

Authors:  Andrew R Mayer; Andrew B Dodd; Meghan S Vermillion; David D Stephenson; Irshad H Chaudry; Denis E Bragin; Andrew P Gigliotti; Rebecca J Dodd; Benjamin C Wasserott; Priyank Shukla; Rachel Kinsler; Sheila M Alonzo
Journal:  Neurosci Biobehav Rev       Date:  2019-06-27       Impact factor: 8.989

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